TruthArchive.ai - Tweets Saved By @MeasslainteIRL

Saved - February 4, 2026 at 10:32 PM
reSee.it AI Summary
I question the link between Gates and Epstein, noting Gates’s mosquito gene drive tech came from Harvard’s PDE funded by Epstein, then applying it to humans. I’ve heard claims vaccines shed and act as a depopulation tool, with spikes in testes and ovaries causing infertility. I wonder why people don’t care, and I’m told to connect the dots. Others mention gene-drive infertility, and I say I reached out years ago with no response.

@JesseMatchey - Jesse Matchey

Idk how we get people to look a the science between Bill Gates & Epstein… Example: Gates’s Mosquito Gene drive tech came outta Harvard’s Program for Evolutionary Dynamics - which was founded & funded by Jeffrey Epstein Apply it to humans…

Video Transcript AI Summary
A gene drive is described as a mechanism that guarantees a specific gene will be inherited. It attaches to the chosen gene and is introduced into the organism. The concept begins with the fact that a single gene can have different versions, and each organism possesses two copies of every gene. Under normal circumstances, when parents carry different versions of a gene, each version is inherited by only half of the offspring, following traditional Mendelian inheritance. With a gene drive, the inheritance pattern changes: when parents have different versions of the gene, essentially all offspring will inherit the gene with the drive. This effect persists generation after generation, continuing to bias inheritance in favor of the drive-carrying gene. The gene drive contains instructions for a molecular tool that is designed to target the other versions of the chosen gene. This tool scans the organism’s DNA to locate the other versions of the gene. Once it finds a different version, the tool cuts it out, creating a gap or “hole” in the DNA where the other version used to be. After the cut, the organism’s cellular machinery uses the gene with the gene drive as a template to repair the hole. As a result of this repair process, the organism ends up with two copies of the gene that contains the drive, rather than one copy with the drive and one without. This duplication ensures that the drive-carrying gene is the version passed on to the next generation, reinforcing the drive’s presence in the population across generations. In summary, a gene drive biases inheritance so that nearly all offspring inherit the drive, by using a molecular tool to cut other gene versions and repair the DNA with the drive-containing gene as the template, thereby converting heterozygous individuals into homozygous drive carriers and ensuring two copies are passed forward.
Full Transcript
Speaker 0: A gene drive guarantees that a specific gene will be inherited. Gene drives are attached to the chosen gene and put into the organism. One gene can have different versions. Each organism gets two copies of each gene. Without a gene drive, when parents with different versions of a gene pass on their DNA, each version gets inherited by only half of the offspring. With a gene drive, when parents with different versions of a gene pass on their DNA, essentially all offspring will inherit the gene with the drive. Generation, after generation, after generation. A gene drive contains instructions for a molecular tool that targets other versions of the chosen gene. The tool scans the organism's DNA and looks for other versions of the gene. Once it finds another version, the tool cuts it out. Left with a hole, the body uses the gene with the gene drive as a template to patch it up. The organism now has two copies to pass on to the next generation.

@elitesbewarned - Dr. Nick's Red Pills 💊™

@EthicalSkeptic I believe the vaccine was made to replicate and shed through contact. This was a depopulation tool. Spike builds up in testes and fallopian tubes, attacking eggs and sperm. I think the next gen is going to be infertile from birth... if they survive to a child bearing age.

@JesseMatchey - Jesse Matchey

Yeah, connect the fking dots Why don’t people care about this?

@ErikEtv - ETV

@CoyoteSanctuary @CatsRule2023 @EddieGreen96162 @AllBiteNoBark88 Sounds like gene drive infertility

@JesseMatchey - Jesse Matchey

@swani741 I reached out years ago. No response.

Saved - January 31, 2026 at 10:26 PM
reSee.it AI Summary
From BioNtech (Lenk et al) and Sutton (1997), I note RNA:DNA hybrids inhibit DNaseI. Even less known: quadruplex Gs inhibit DNaseI too; some exist in SV40, and my qPCR amplicon gives the strongest signal. Two DNaseI-inhibition mechanisms mean plasmid fragmentation in mRNA vaccines isn’t uniform, so there could be ~100-fold more spike than vector. I overlay the spike map with GAA repeats and quadruplex Gs and show my primers.

@Kevin_McKernan - Kevin McKernan

It is well known from BioNtech (Lenk et al) and Sutton et al (1997) that RNA:DNA hybrids inhibit DNaseI. What is less known is that Quadruplex Gs also inhibit DNaseI. Some exist in SV40 and we get the most signal from this qPCR amplicon. 2 Different mechanisms of DNaseI inhibition = plasmid fragmentation cannot be assumed to be uniform in the mRNA vaccines. Hence 100 fold more spike than parts of the vector. Below is a map of the codon optimized spike where Quadruplex Gs are overlaid with GAA repeats. GAA's are stickier RNA:DNA hybrids. Our qPCR primers are overlayed as well. @RetsefL @KUPERWASSERLAB @weldeiry @JesslovesMJK @DJSpeicher @TracyBethHoeg @DrJBhattacharya

@Kevin_McKernan - Kevin McKernan

Evans et al demonstrate DNaseI is resistant to quadruplex Gs. They also move to alternative enzymes. https://www.nature.com/articles/s41522-025-00694-x

@Kevin_McKernan - Kevin McKernan

This is from Lenk et al (BioNtech). Note the concern over GAA sequences and RNA:DNA hybrids. Our spike qPCR primers happen to land on GAA rich and quadruplex G rich regions of Spike. https://www.frontiersin.org/journals/molecular-biosciences/articles/10.3389/fmolb.2024.1426129/full https://t.co/ww9Tf84ZHG

@Kevin_McKernan - Kevin McKernan

Transfected RNA:DNA hybrids trigger different Toll Like Receptors than mRNA alone (cGAS, TLR9, NLRP3) which induce cytokine, chemokine and Type I interferon responses. Entirely, avoidable if they use the proper enzyme for DNA removal.

@Kevin_McKernan - Kevin McKernan

Happy Caturday https://t.co/JcRxNsveCr

Saved - January 18, 2026 at 10:14 PM
reSee.it AI Summary
I describe post-vaccination syndrome (PVS) after mRNA vaccines, explored 2022–2026. Reports suggest spike protein may persist, amyloid fibrin microclots can form, and prion‑like domains may promote misfolding. Immune dysregulation—cytokine elevation and T-cell exhaustion—is noted. Investigations include DFPP and stem‑cell therapies; concerns about residual vaccine DNA are discussed. PVS is understudied and not yet recognized by major authorities, but some data show physiological changes in a subset.

@MeasslainteIRL - Thomas Emmett III 🐺🐭🦝 Snr mouse clicker™

Post-vaccination syndrome (PVS), also referred to as post-acute sequelae following COVID-19 vaccination, describes a set of persistent symptoms reported by a subset of individuals after receiving mRNA COVID-19 vaccines. Emerging research from 2022–2026 explores potential biological mechanisms behind these symptoms in affected people. This overview synthesizes peer-reviewed evidence, including studies on spike protein dynamics, microclots, prion-like elements, immune changes, and manufacturing concerns. It draws from a range of sources, to provide a balanced view. Note that PVS remains understudied and is not formally recognized by major health authorities like the FDA or WHO, but preliminary data suggest real physiological changes in some cases. I dont know anyone who regrets not taking the jabs :)

@KevinMcCairnPhD - Kevin W. McCairn PhD

McCairn Protocol Slays Biowarfare Amyloids

@MeasslainteIRL - Thomas Emmett III 🐺🐭🦝 Snr mouse clicker™

Understanding Post-Vaccination Syndrome: A Science-Based Overview When COVID-19 mRNA vaccines were introduced, they were designed to deliver temporary instructions for cells to produce the spike protein, triggering an immune response. However, emerging research suggests that for some individuals, this process may not follow the expected trajectory. This has led researchers to investigate a constellation of symptoms now being studied as "post-vaccination syndrome" or "post-acute sequelae" following vaccination. This explanation draws from peer-reviewed research published between 2022 and 2026 to help understand what scientists are currently investigating.

@MeasslainteIRL - Thomas Emmett III 🐺🐭🦝 Snr mouse clicker™

Core Concepts 1. Spike Protein Persistence The Expected Process: After mRNA vaccination, the spike protein should be cleared from the body within days to weeks. Think of it like a temporary instruction manual that gets used and discarded. What Research Shows: Studies indicate that for some people, spike protein may persist far longer than anticipated: "Expression of SARS-CoV-2 spike protein in cerebral arteries" (https://pubmed.ncbi.nlm.nih.gov/40184822/) detected spike protein in brain blood vessels months after vaccination. Similarly, https://news.yale.edu/2025/02/19/immune-markers-post-vaccination-syndrome- indicate-future-research-directions is investigating persistent spike protein in individuals with post-vaccination syndrome. A https://www.nature.com/articles/s41541-023-00742-7 confirmed mRNA can persist up to 30 days, while https://www.cell.com/cell-host-microbe/fulltext/S1931-3128(24)00438-4 found spike protein at the skull-meninges-brain interface, potentially linked to ongoing neuroinflammation. Analogy: Imagine leaving your car running after you arrive at your destination. The engine (spike protein) was meant to shut off, but it's still idling—and in some cases, revving—in ways that may cause problems.

Expression of SARS-CoV-2 spike protein in cerebral Arteries: Implications for hemorrhagic stroke Post-mRNA vaccination - PubMed Although the possibility of spike protein expression due to asymptomatic SARS-CoV-2 infection cannot be entirely excluded, this study demonstrated prolonged presence of SARS-CoV-2 spike protein in the cerebral arteries following mRNA vaccination. Additionally, some inflammatory cell infiltration was … pubmed.ncbi.nlm.nih.gov
Page not found | Yale News news.yale.edu
Duration of SARS-CoV-2 mRNA vaccine persistence and factors associated with cardiac involvement in recently vaccinated patients - npj Vaccines At the start of the COVID-19 pandemic, the BNT162b2 (BioNTech-Pfizer) and mRNA-1273 (Moderna) mRNA vaccines were expediently designed and mass produced. Both vaccines produce the full-length SARS-CoV-2 spike protein for gain of immunity and have greatly reduced mortality and morbidity from SARS-CoV-2 infection. The distribution and duration of SARS-CoV-2 mRNA vaccine persistence in human tissues is unclear. Here, we developed specific RT-qPCR-based assays to detect each mRNA vaccine and screened lymph nodes, liver, spleen, and myocardium from recently vaccinated deceased patients. Vaccine was detected in the axillary lymph nodes in the majority of patients dying within 30 days of vaccination, but not in patients dying more than 30 days from vaccination. Vaccine was not detected in the mediastinal lymph nodes, spleen, or liver. Vaccine was detected in the myocardium in a subset of patients vaccinated within 30 days of death. Cardiac ventricles in which vaccine was detected had healing myocardial injury at the time of vaccination and had more myocardial macrophages than the cardiac ventricles in which vaccine was not detected. These results suggest that SARS-CoV-2 mRNA vaccines routinely persist up to 30 days from vaccination and can be detected in the heart. nature.com

@MeasslainteIRL - Thomas Emmett III 🐺🐭🦝 Snr mouse clicker™

2. Amyloid Fibrin Microclots What They Are: Under a microscope, researchers have observed unusual clot-like structures in the blood of people with Long COVID and post-vaccination symptoms. These are not typical blood clots but tangled masses of fibrin (a protein involved in normal clotting) that has misfolded into an amyloid form—similar to what happens in Alzheimer's disease. The Research: Multiple studies using Thioflavin T staining (a fluorescent dye that lights up when it binds to amyloid) have detected these microclots in people with Long COVID. One review assessed the evidence (https://pmc.ncbi.nlm.nih.gov/articles/PMC11491705/), while another described their properties and diagnostic potential (https://www.thieme-connect.com/products/ejournals/pdf/10.1055/s-0043-1774796.pdf). Additional research (https://www.sciencedirect.com/science/article/pii/S2473952924001642 and https://onlinelibrary.wiley.com/doi/10.1002/jmv.70613) further documents these findings. Why It Matters: These microclots may: - Obstruct tiny blood vessels (capillaries) - Impede oxygen delivery to tissues - Contribute to fatigue, brain fog, and exercise intolerance Analogy: Think of your bloodstream as a highway system. Microclots are like roadblocks too small to close the whole road but large enough to cause traffic jams, slowing down essential deliveries (oxygen and nutrients) throughout your body.

Fibrinaloid microclots in long COVID: assessing the actual evidence properly pmc.ncbi.nlm.nih.gov
Microclots, as defined by amyloid-fibrinogen aggregates, predict risks of disseminated intravascular coagulation and mortality Microclots have been associated with various conditions, including postacute sequelae of severe acute respiratory syndrome coronavirus 2 infection. Th… sciencedirect.com

@MeasslainteIRL - Thomas Emmett III 🐺🐭🦝 Snr mouse clicker™

3. Prion-like Domains The Concern: Prion proteins are notorious for causing misfolding diseases like Creutzfeldt-Jakob disease. They propagate by inducing normal proteins to misfold in a chain reaction. Research (https://pmc.ncbi.nlm.nih.gov/articles/PMC8878784/) identified prion-like domains in the SARS-CoV-2 spike protein. These regions can rapidly shift shapes and may interact with cellular proteins to promote misfolding. https://www.news-medical.net/news/20220131/Prion-like-domains-in-SARS-CoV-2-RBD-and-ACE2-play-important-functional-roles-in-viral-adhesion-and-entry.aspx explains their important roles in viral adhesion and entry. Important Context: The presence of prion-like domains does not mean vaccines cause prion disease. It suggests a potential mechanism for protein aggregation and persistent symptoms in some individuals.

Prion-like Domains in Spike Protein of SARS-CoV-2 Differ across Its Variants and Enable Changes in Affinity to ACE2 Currently, the world is struggling with the coronavirus disease 2019 (COVID-19) pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Prions are proteins that possess a unique conformational conversion, with the ability ... pmc.ncbi.nlm.nih.gov
Prion-like domains in SARS-CoV-2 RBD and ACE2 play important functional roles in viral adhesion and entry Scientists have recently detected and analyzed viral PrDs in the S protein of SARS-CoV-2, which are the novel regulators of virion assembly. news-medical.net

@MeasslainteIRL - Thomas Emmett III 🐺🐭🦝 Snr mouse clicker™

4. Immune Dysregulation Cytokine Elevation: Cytokines are signaling molecules that coordinate immune responses. Studies show elevated cytokines in Long COVID (https://www.nature.com/articles/s41590-023-01724-6), indicating ongoing immune activation. https://www.mdpi.com/1422-0067/26/15/7258 details T-cell dynamics, while https://www.cell.com/cell/fulltext/S0092-8674(24)00886-9 reviews mechanisms of Long COVID. Additionally, https://pubmed.ncbi.nlm.nih.gov/39403255/ found elevated MMP-9 and microglia activation linked to spike protein stimulation. T-Cell Exhaustion: Nature research found that people with Long COVID exhibit T-cell dysregulation—immune cells worn out from chronic activation, reducing their ability to fight infections and regulate inflammation. Analogy: The immune system is like an army. Cytokine elevation is like constantly sounding alarms even without an enemy. T-cell exhaustion is like soldiers on duty too long without rest—they're present but less effective.

Long COVID manifests with T cell dysregulation, inflammation and an uncoordinated adaptive immune response to SARS-CoV-2 - Nature Immunology Long COVID (LC) occurs after at least 10% of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections, yet its etiology remains poorly understood. We used ‘omic” assays and serology to deeply characterize the global and SARS-CoV-2-specific immunity in the blood of individuals with clear LC and non-LC clinical trajectories, 8 months postinfection. We found that LC individuals exhibited systemic inflammation and immune dysregulation. This was evidenced by global differences in T cell subset distribution implying ongoing immune responses, as well as by sex-specific perturbations in cytolytic subsets. LC individuals displayed increased frequencies of CD4+ T cells poised to migrate to inflamed tissues and exhausted SARS-CoV-2-specific CD8+ T cells, higher levels of SARS-CoV-2 antibodies and a mis-coordination between their SARS-CoV-2-specific T and B cell responses. Our analysis suggested an improper crosstalk between the cellular and humoral adaptive immunity in LC, which can lead to immune dysregulation, inflammation and clinical symptoms associated with this debilitating condition. Roan et al. use Olink and single‐cell RNA sequencing (scRNA-seq) to show a dysregulated crosstalk between the cellular and humoral immune responses in individuals with long COVID 8 months postinfection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). nature.com
Long COVID elevated MMP-9 and release from microglia by SARS-CoV-2 Spike protein - PubMed MMP-9 from Spike protein-stimulated microglia could contribute to the development of long COVID and may serve as a target for treatment including the use of luteolin. pubmed.ncbi.nlm.nih.gov

@MeasslainteIRL - Thomas Emmett III 🐺🐭🦝 Snr mouse clicker™

Fibrinogen as a Protective Factor The Silver Lining: https://pmc.ncbi.nlm.nih.gov/articles/PMC8977893/ may help protect against prion-related toxicity. Research shows it can bind to problematic proteins and act as a "sink," sequestering them away from causing damage. A https://molmed.biomedcentral.com/articles/10.2119/molmed.2016.00003 confirms fibrinogen inhibits amyloid-β-induced toxicity, and https://pubmed.ncbi.nlm.nih.gov/32697670/ documents fibrinogen-cellular prion protein complex formation. This suggests potential therapeutic approaches—perhaps boosting fibrinogen or developing molecules that mimic its protective binding.

Fibrinogen Mitigates Prion-Mediated Platelet Activation and Neuronal Cell Toxicity Prion peptide (PrP) misfolds to infectious scrapie isoform, the β pleat-rich insoluble fibrils responsible for neurodegeneration and fatal conformational diseases in humans. The amino acid sequence 106–126 from prion proteins, PrP(106–126), is ... pmc.ncbi.nlm.nih.gov
Plasma Fibrinogen Is a Natural Deterrent to Amyloid β-Induced Platelet Activation and Neuronal Toxicity - Molecular Medicine Alzheimer’s disease (AD) is a devastating neurodegenerative disorder, characterized by extensive loss of neurons and deposition of amyloid β (A& link.springer.com
Fibrinogen-cellular prion protein complex formation on astrocytes - PubMed Traumatic brain injury (TBI) is one of the most common neurological disorders causing memory reduction, particularly short-term memory (STM). We showed that, during TBI-induced inflammation, increased blood content of fibrinogen (Fg) enhanced vascular protein transcytosis and deposition of extravasa … pubmed.ncbi.nlm.nih.gov

@MeasslainteIRL - Thomas Emmett III 🐺🐭🦝 Snr mouse clicker™

6. Investigational Treatments DFPP (Double Filtration Plasmapheresis): This blood filtration technique, used in Japan for conditions like CIDP and GBS, shows promise for filtering out microclots and inflammatory proteins. It is designed for this purpose (https://www.asahi-kasei.co.jp/medical/en/apheresis/cure/), with details at https://www.asahi-kasei.co.jp/medical/en/apheresis/product/plasma/about/cure.html#h2-2. Stem Cell Therapy: Mesenchymal stem cells (MSCs) have anti-inflammatory properties and may help repair damaged tissue. Trials are underway (https://clinicaltrials.gov/study/NCT06492798); https://clinicaltrials.gov/study/NCT05669261 is evaluating ATCell™ autologous stem cells. Early results (https://pmc.ncbi.nlm.nih.gov/articles/PMC11863646/) show potential for lung recovery in Long COVID patients. https://www.nature.com/articles/s41392-025-02313-9 discusses MSCs for inflammatory diseases, and https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11499875/ shows cord blood MSCs reducing Long COVID symptoms.

Applied Diseases | Asahi Kasei Medical Co., Ltd. Therapeutic Apheresis products info by applied diseases - Please select a department or a name of disease to refer treatment applications. Asahi Kasei Medical Co., Ltd. asahi-kasei.co.jp
Plasmapheresis | Asahi Kasei Medical Co., Ltd. Therapeutic Apheresis products info by therapies - Plasmapheresis modalities: Plasma Exchange (PE), Double Filtration Plasmapheresis (DFPP), Immunoadsorption (IA), Plasma Adsorption (PA). Asahi Kasei Medical Co., Ltd. asahi-kasei.co.jp
Long-term outcomes of mesenchymal stem cell therapy in severe COVID-19 patients: 3-year follow-up of a randomized, double-blind, placebo-controlled trial The long-term effects and outcomes of human mesenchymal stem cell (MSC) therapy in patients with severe coronavirus disease 2019 (COVID-19) remain poorly understood. This study aimed to evaluate the extended safety and efficacy of MSC treatment in ... pmc.ncbi.nlm.nih.gov
Mesenchymal stem cells in treating human diseases: molecular mechanisms and clinical studies - Signal Transduction and Targeted Therapy Mesenchymal stem cells (MSCs) have emerged as a highly promising strategy in regenerative medicine due to their self-renewal, pluripotency and immunomodulatory properties. MSCs are nonhematopoietic, multipotent stem cells that can differentiate into various mesodermal lineages and modulate the immune system. The therapeutic potential of MSCs from different tissues has been widely explored in preclinical models and clinical trials for human diseases, ranging from autoimmune diseases and inflammatory disorders to neurodegenerative diseases and orthopedic injuries. The therapeutic effects of MSCs can be mediated through the release of bioactive molecules, including growth factors, cytokines, and extracellular vesicles, which play crucial roles in modulating the local cellular environment, promoting tissue repair, angiogenesis, and cell survival, and exerting anti-inflammatory effects. MSCs can also interact with various immune cells, such as T cells, B cells, dendritic cells, and macrophages, modulating the immune response through both direct cell‒cell interactions and the release of immunoregulatory molecules. This review delves into the molecular mechanisms, signaling pathways, and regulatory factors that underpin the therapeutic effects of MSCs. This review also highlights the clinical applications and challenges associated with the use of MSC-based drugs to promote the safety and efficacy of MSC-based therapies. Overall, this comprehensive review provides valuable insights into the current state of MSC research and its potential for transforming the field of regenerative medicine as well as immune-mediated inflammatory diseases. nature.com
Integrated ensemble CNN and explainable AI for COVID-19 diagnosis from CT scan and X-ray images In light of the ongoing battle against COVID-19, while the pandemic may eventually subside, sporadic cases may still emerge, underscoring the need for accurate detection from radiological images. However, the limited explainability of current deep ... pmc.ncbi.nlm.nih.gov

@MeasslainteIRL - Thomas Emmett III 🐺🐭🦝 Snr mouse clicker™

7. DNA Contamination Concerns The Issue: Recent research has detected residual DNA plasmids in some mRNA vaccines, including SV40 promoter sequences. SV40 is a viral promoter sequence used in laboratory DNA work. The Debate: A study (https://www.tandfonline.com/doi/full/10.1080/08916934.2025.2551517) reports DNA levels up to 153-fold above regulatory limits, raising theoretical concerns about: - Integration into human DNA - Unintended immune effects - Long-term consequences Additional research (https://hal.science/hal-04778576v2/document) confirms residual DNA above limits, (https://www.researchgate.net/publication/386414408_BioNTech_RNA-Based_COVID-19_Injections_Contain_Large_Amounts_Of_Residual_DNA_Including_An_SV40_PromoterEnhancer_Sequence) documents large amounts of residual DNA including SV40, and (https://www.preprints.org/manuscript/202501.1462) discusses DNA contaminants as potential causes of adverse events. Current Status: This is an active area of research and debate. More studies are needed to determine clinical significance.

@MeasslainteIRL - Thomas Emmett III 🐺🐭🦝 Snr mouse clicker™

Post-vaccination syndrome is an emerging area of research investigating why some individuals experience persistent symptoms after mRNA COVID-19 vaccination. Key areas of investigation include: 1. Spike protein persistence beyond the expected duration 2. Amyloid fibrin microclots that may impair circulation 3. Prion-like domains that could promote protein misfolding 4. Immune dysregulation, including cytokine elevation and T-cell exhaustion 5. Potential treatments, including DFPP and stem cell therapy 6. Manufacturing concerns, including residual DNA components Research is ongoing, and many questions remain unanswered. What is clear is that a subset of individuals experiences real, measurable physiological changes that warrant serious scientific investigation and clinical attention.

@MeasslainteIRL - Thomas Emmett III 🐺🐭🦝 Snr mouse clicker™

@reseeit save thread

Saved - January 17, 2026 at 12:41 AM
reSee.it AI Summary
We analyzed pre-pandemic POTS and Long COVID, focusing on insoluble fibrinaloid microclot complexes (FMCs). Protein abundance differed little, but post-translational modifications (PTMs) were disease-specific and biologically meaningful. Long COVID showed extensive AGE/oxidation PTMs, amyloid signatures, and coagulation pathology; pre-pandemic POTS showed immune/complement PTMs with limited fibrinogen modification. LC-POTS appeared hybrid. PTMs reveal biology unseen by standard assays, with biomarker potential and therapy targets.

@resiapretorius - Resia Pretorius

🧵 1/10 We are excited to share our preprint examining pre-pandemic POTS and Long COVID, using deep analysis of the insoluble microclot fraction of blood. Our study shows that the key pathology lies not in protein levels, but in post-translational modifications (PTMs) hidden within fibrinaloid microclot complexes (FMCs). With @Renata_MBooyens, Satish Raj, @dbkell and others. Funded by @POTSActivist https://www.biorxiv.org/content/10.64898/2025.12.29.696828v1.full.pdf

@resiapretorius - Resia Pretorius

🧵 2/10 Why pre-pandemic POTS matters: A unique strength of this study is the inclusion of POTS samples collected before the COVID-19 pandemic in the Raj lab. This allowed us to define the baseline molecular signature in controls and classical POTS (entirely independent of SARS-CoV-2); and to distinguish which molecular features in LC-POTS are similar to POTS biology versus acquired through Long COVID.

@resiapretorius - Resia Pretorius

🧵 3/10 What we measured: We quantified fibrinaloid microclot complexes (FMCs) using fluorescence imaging flow cytometry, then performed deep proteomics on the insoluble FMC fraction using LC-MS/MS. This allowed us to move beyond how much protein is present → to how proteins are post-translationally modified.

@resiapretorius - Resia Pretorius

🧵 4/10 Key insight: At the protein level, differences between groups were minimal. At the PTM (post-translational modification) level, differences were extensive, disease-specific, and biologically meaningful.

@resiapretorius - Resia Pretorius

🧵 5/10 Long COVID FMCs showed dominant coagulation pathology: • Extensive AGE- and oxidation-based PTMs on fibrinogen • Strong amyloidogenic signatures • Patterns resembling diabetic glycation ➡️ Consistent with microvascular damage (thrombotic endothelialitis)

@resiapretorius - Resia Pretorius

6/10 Pre-pandemic POTS showed a very different signature: • Prominent immune and complement PTMs • Oxidised apolipoproteins (apoA1, apoB) • Relatively limited fibrinogen modification ➡️ An intrinsic POTS biology, independent of SARS-CoV-2.

@resiapretorius - Resia Pretorius

🧵 7/10 Long COVID–POTS displayed a hybrid molecular phenotype: • Coagulation PTMs resembling Long COVID • Immune PTMs resembling classical POTS ➡️ Providing a molecular explanation for why LC-POTS behaves differently from either condition alone.

@resiapretorius - Resia Pretorius

🧵 8/10 Why PTMs matter: Many dysregulated peptides were highly amyloidogenic, supporting FMCs as β-sheet-rich, fibrinolysis-resistant aggregates. Crucially, these PTM signatures are invisible to standard soluble plasma assays.

@resiapretorius - Resia Pretorius

🧵 9/10 Clinical relevance: PTM profiling within FMCs opens new avenues for: • Biomarker-driven diagnosis • Patient stratification • Targeted therapies addressing glycation, oxidative stress, and complement activation This is mechanism-based medicine, not symptom-based.

@resiapretorius - Resia Pretorius

🧵 10/10 Take-home message Long COVID, POTS, and LC-POTS are biochemically distinct diseases. Their differences are encoded in post-translational modifications inside fibrinaloid microclot complexes; not in protein abundance. https://t.co/OeRL5KjRWb

Saved - December 14, 2025 at 1:37 AM
reSee.it AI Summary
I report that Zhengli Shi of the WIV built a dangerous Gain of Function MERS chimera that contaminated pre-pandemic Wuhan rice datasets; potential violation of the Biological Weapons Convention; NIAID and USAID funded; parallels with SARS2; DRASTIC.

@stevenemassey - Steve Massey

Zhengli Shi of the WIV constructed a dangerous Gain of Function MERS chimera that contaminated pre-pandemic rice sequence datasets from Wuhan Potential violation of the Biological Weapons Convention NIAID + USAID provided funding Parallels with SARS2 🧵 #DRASTIC https://t.co/mrFgW2eSR3

Saved - November 1, 2025 at 8:55 AM
reSee.it AI Summary
I submitted a paper on the Bayes Lines Tool (BLT), a SQL-script that back-solves disease prevalence, test sensitivity, and specificity from government test results. By building confusion matrices (TP, FP, TN, FN) and testing many parameter combinations, BLT identifies likely values and evaluates policy relevance. For Jan 11, 2021 in the UK, I estimate prevalence ~4%, sensitivity ~80.5%, specificity ~92.5%, implying many false positives and overestimated prevalence.

@goddeketal - Dr. Simon Goddek

1/ Happy to announce that we have submitted our #paper ‘Bayes Lines Tool (BLT) - A SQL-script for analyzing diagnostic test results with an application to SARS-CoV-2-testing’. In this ⬇️thread⬇️, I will explain why our tool is that powerful for decision makers. #UnbiasedScience

@goddeketal - Dr. Simon Goddek

2/ In the meantime, the submitted paper is available on the preprint platform @zenodo_org. Factual criticism is highly desired and encouraged. The publication itself presents a seminal Bayesian calculator, the Bayes Lines Tool (BLT). (Petje af, @waukema!) https://zenodo.org/record/4459271#.YAwjxhYxk2w

Bayes Lines Tool (BLT) - A SQL-script for analyzing diagnostic test results with an application to SARS-CoV-2-testing The performance of diagnostic tests crucially depends on the disease prevalence, test sensitivity, and test specificity. However, these quantities are often not well known when tests are performed outside clinical practice which makes the rating of the test results somewhat problematic. A current example is the mass testing taking place within the context of the world-wide SARS-CoV-2 crisis. Here, for the first time in history, the test results have a dramatic impact on political decisions. Therefore, transparent, comprehensible, and reliable data is mandatory. It is in the nature of wet lab tests that their quality and outcome are influenced by multiple factors reducing their performance by handling procedures, underlying test protocols, and analytical reagents. These limitations in sensitivity and specificity have to be taken into account when calculating the real test results. As a resolution method, we have developed a seminal Bayesian calculator, the Bayes Lines Tool (BLT), for back-solving disease prevalence, test sensitivity, test specificity, and, therefore, true positive, false positive, true negative and false negative numbers, from official test outcome reports. The calculator performs a simple SQL query and can easily be implemented on any system supporting SQL. We provide three examples of SARS-CoV-2 test results from official government reports from the Netherlands, Germany, and the United Kingdom to illustrate the possible parameter space of prevalence, sensitivity, and specificity consistent with the observed data. Finally, we discuss this tool’s multiple applications, including its putative importance for informing policy decisions. zenodo.org

@goddeketal - Dr. Simon Goddek

3/ The Bayes Line Tool (available on https://bayeslines.org) is able to back-solve disease #prevalence, test #sensitivity, test #specificity, and therefore, true positive, false positive, true negative and false negative numbers from official governmental test outcome reports.

@goddeketal - Dr. Simon Goddek

4/ This is done by creating confusion matrices with four variables. Namely: TP, FP, TN, FN. In order to calculate the matrices, we need prevalence, specificity, and sensitivity as well as the number of people that got tested (within a given period) and the number of positives.

@goddeketal - Dr. Simon Goddek

5/ The number of positives and the number of tests are given by the government. Prevalence, specificity, and sensitivity are unknown. So we assume any combination of them ranging from 0-99%. These three combinations can amount up to #millions of #combinations.

@goddeketal - Dr. Simon Goddek

6/ Typically, we calculate with 7 million combinations. Of these 7 million combinations, only 1-100 usually match the numbers that the government gave us (e.g. TRUE Positives + FALSE Positives = amount of performed tests).

@goddeketal - Dr. Simon Goddek

7/ For the 11 Jan 2021, 536,947 tests were performed, resulting in 56,733 reported positives. The confusion matrices contained 21 possible matches for that day, represented in the #columns. We have sorted the columns by ‘prevalence’, as marked in red.

@goddeketal - Dr. Simon Goddek

8/ The prevalence in the UK is currently presumed to be 1,52% (https://bit.ly/3sRFSmw). Given the fact that reported positives dropped by 43% since January 8, we are looking at a prevalence of around 3%, but definitely lower than 12%, leaving us with the following options:

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@goddeketal - Dr. Simon Goddek

9/ Looking at the bars will already give you a good #indication on the test result in the context of everyone else who got tested in the population. This means that the model tells us whether the test results are/were #relevant.

@goddeketal - Dr. Simon Goddek

10/ In the next steps, I will show you how to figure out which event might most likely have been the one that occurred that day, figuring out the real TP/FP rate, test specificity and sensitivity and prevalence. For this, let’s take a look at the tests' sensitivity.

@goddeketal - Dr. Simon Goddek

11/ In the UK antigen and PCR tests are used. Antigen tests have a sensitivity between .664 (66.4%) and .738 (73.8%) (https://bit.ly/2Y5konY). PCR tests about .842 (84.2%) (https://bit.ly/3ogUAj7). PCR tests constitute the majority of tests that are used in the UK.

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Bitly | Page Not Found | 404 bit.ly

@goddeketal - Dr. Simon Goddek

12/ We are consequently looking for a sensitivity value just below .842. #BINGO! By just getting the amount of performed tests and number of reported positives from the government, we can conclude the actual specificity, sensitivity, and prevalence.

@goddeketal - Dr. Simon Goddek

13/ So on January 11th, the prevalence was most likely about 4%, the tests’ sensitivity about 80.5%, and the tests’ specificity about 92.5% (which is much lower than the claimed 98.9%: https://bit.ly/2Y5nEjf). The false-positive rate that day would consequently have been 68%!

Bitly | Page Not Found | 404 bit.ly

@goddeketal - Dr. Simon Goddek

14/ Let’s have a look at the calculated data that the Netherlands are providing.

@goddeketal - Dr. Simon Goddek

15/ AFAIK, the #Dutch government did not make a recent comment about prevalence, but we can assume a similar one as in the UK. Also, the sensitivity should be in the range of 75-85%, leaving us with the following possible scenarios. Remark: note the low #specificities < 90%.

@goddeketal - Dr. Simon Goddek

16/ The model’s outcomes are extremely valuable in that they can provide a decision-making tool for people in charge (i.e. #politicians, #physicians, #policymakers etc.) and support them in evaluating their strategy for fighting the disease. #COVID

@goddeketal - Dr. Simon Goddek

17/ This time-series can be further back-solved by solving single events following the #exclusionprinciple and consequently receiving insights with respect to the tests’ specificity/sensitivity or the prevalence within the population.

@goddeketal - Dr. Simon Goddek

18/ This method provides the light (i.e. better insights) for individuals, authorities and governmental agencies that are currently in the dark with measuring problems and often using imprecise prediction models.

@goddeketal - Dr. Simon Goddek

19/ Furthermore, the outcomes can provide a better insight into the expectable operational effectiveness of the tests (specificity/sensitivity) compared to the theoretical commercial claims of the manufacturers (equipment, primers, probes, supplies etc.).

@goddeketal - Dr. Simon Goddek

20 Last but not least, the tool can also be used to provide extensive time-series (see graph). If you want to be the first to receive updates around our Bayes Lines Tool feel free to join our #UnbiasedScience-Telegram channel via the following link: https://t.me/unbiasedscience

Telegram: Contact @unbiasedscience t.me

@goddeketal - Dr. Simon Goddek

21/ P.S. Here is another brilliant thread on Bayes’ Theorem that you might want to read. (Outstanding work @robinmonotti) https://threadreaderapp.com/thread/1336593397608542208.html

Read and Share Twitter Threads easily! Thread Reader helps you discover and read the best of Twitter Threads threadreaderapp.com

@goddeketal - Dr. Simon Goddek

Take-away message for the layperson. What we see is most likely the following: - Extremely high rate of false positives - Much lower test specificity than reported by the test manufacturers - Overestimation of the prevalence

@goddeketal - Dr. Simon Goddek

@AlexTweetyC Link?

Saved - October 12, 2025 at 5:36 AM
reSee.it AI Summary
Concern raised about DNA contamination, autopsies showing spike protein in tumors, and alleged vaccine–cancer links, tied to NIHGate and Senator Ron Johnson. A responder, MeasslainteIRL, replied several times with links to related content.

@BrokenTruthTV - Broken Truth

"I'm highly concerned. The DNA contamination, the autopsies where they have spike protein inside tumors, the turbo cancer reports, no I'm highly concerned about this" Discussing the Covid Vaccine Cancer connection and http://NIHGate.com with Senator Ron Johnson.

Video Transcript AI Summary
Speaker 0 thanks the guest for advocating vaccine research and asks about alleged cancer increases since the COVID nineteen vaccine. Speaker 1 replies: "No. I'm I'm highly concerned. You know, the DNA contamination, the autopsies where they have spike protein inside tumors, you know, the turbo cancer reports." He says "nobody wants to admit they're wrong here" and claims that "the federal agencies... what they were pushing might have resulted in the adverse events that are undeniable, the deaths that are undeniable" and warns of "changing the human basic genome by integration of the cell or you know, fostering these turbo cancers." He cites "doctor Sun Shiang" on cancers in very young patients and says the issue is "not being reported because... it's just way too scary." Speaker 0 recalls a FOIA in 2021/22: "'NIH gate'—'National Cancer Institute employees were aware that there were cancers being enabled by the spike protein in the vaccine, and they covered it up'—with '490 pages of completely redacted documents.' " Speaker 1 notes redactions now are "a white piece of paper" and jokes "eco friendly," mentioning "Tom Wrens" and a military cancer increase "covered up," concluding, "the deep state does not give up its secrets."
Full Transcript
Speaker 0: One last thing. It's just a transition to a different topic. Your advocacy and willingness to spend your political clout on vaccine research and injuries and investigations has has made you a big fan from people like me, and also the families who've who suffered from these injuries. Have you heard anything about these supposed cancer increases since the COVID nineteen vaccine? Speaker 1: Oh, I've heard about them for a number of years now. No. I'm I'm highly concerned. You know, the DNA contamination, the the autopsies where they have spike protein inside tumors, you know, the turbo cancer reports. No. I'm I'm I'm highly concerned about this. Again, I I don't don't have a whole lot of information on it. I'm not a medical doctor myself, but, no, I've been following this very closely. I've been highly concerned about it. I know a limited number of people are concerned as well. I mean, that's part of our problem is nobody wants to admit they're wrong here. The federal agencies, the the people that push the injections, doctors who push it on their patients, and nobody wants to admit that what they were suggesting, what they what they were pushing might have resulted in the adverse events that are undeniable, the deaths that are undeniable. They still don't want to be talking about how we we may be changing the human basic genome by integration of the cell or you know, fostering these turbo cancers. Mean, but you have doctor Sun Shiang, you know, highly alarmed about, you know, cancers in very young patients he's never seen before. I mean, it's it's getting to be kinda like the the unusual clotting that the coroners were seeing. It's just like it's we know about it. It's just not being reported because quite honestly, it's just way too scary. Speaker 0: Yeah. One of the my earliest alerts to this was in 2021, I submitted, I think. Maybe it's '22. I submitted a FOIA request for something that we call NIH gate. Basically, National Cancer Institute employees were aware that there were cancers being enabled by the spike protein in the vaccine, and they covered it up. And the DOD was apparently involved, and I had 490 pages of completely redacted documents. They wouldn't even release the blacked out pages. Speaker 1: Yeah. Now the the now way they're doing the redactions, they just give you a white piece of paper. Speaker 0: Oh, that's nice. Speaker 1: They don't even so you don't even know was this a, you know, bunch of paragraphs or just one thing redacted. Speaker 0: Well, it's less ink, so it's eco friendly. Speaker 1: Plus, you know, we had Tom Wrens, and I think this is my COVID nineteen second opinion event that talked about d med. And the whistleblower's there and then the, you know, all of a sudden there were apparently a glitch, but the initial data there showed a pretty significant increase in different types of malignancies as well within the military. But again, that's that's all been covered up. We have not got to the bottom of that. Again, it's it's even with the republican president in charge, even with people like Bobby Kennedy that is dedicated to radical transparency, the deep state does not give up its secrets. You still have the partisan actors. Even if they're not partisan, the the you know, won't admit they're they were wrong, that what they pushed, that they're covered up. That they're gonna try and bury that truth as as for as long as they possibly can.
BrokenTruth.TV | Broken Truth | Substack Broken Truth (BT) is an American online news and research website based in California. Broken Truth covers domestic, national, and international news, and publishes opinion pieces, investigative reports, documentaries, and interviews. Click to read BrokenTruth.TV, by Broken Truth, a Substack publication with thousands of subscribers. brokentruth.tv

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@BrokenTruthTV

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

🧬 DNA Contamination & mRNA Vaccine Biology Curated Reference Roadmap (all links are PubMed, PMC, DOI, or regulator FOI — stable, citable sources) 1️⃣ DNA Contamination & Quality Control McKernan et al. (2023) – Sequencing of Moderna & Pfizer bivalent mRNA vaccines reveals nanogram–microgram dsDNA per dose 🔗 OSF Preprint: https://osf.io/b9t7m/ König & Kirchner (2024) – Methodological considerations regarding DNA impurities in Comirnaty® 🔗 MDPI: https://www.mdpi.com/2409-9279/7/3/41 ⚠️ Expression of Concern: https://www.mdpi.com/2409-9279/8/4/68 Speicher, D.W. et al. (2023) – DNA fragments detected in Pfizer/Moderna mRNA vaccines from Ontario, Canada: Exploratory dose-response relationship with serious adverse events 🔗 OSF: https://osf.io/mjc97/ Kammerer, U. (2024) – BioNTech RNA-Based COVID-19 Injections Contain Large Amounts Of Residual DNA Including An SV40 Promoter/Enhancer Sequence https://publichealthpolicyjournal.com/biontech-rna-based-covid-19-injections-contain-large-amounts-of-residual-dna-including-an-sv40-promoter-enhancer-sequence/ Kaiser vs. König Debate (2025) – Recap of methodological flaws in Kaiser’s “no-DNA problem” rebuttal 🔗 Substack: https://open.substack.com/pub/anandamide/p/the-konig-vs-kaiser-debate-continues TGA FOI Docs (2024) – Internal correspondence on DNA contamination in mRNA vaccines 🔗 FOI PDF: https://www.tga.gov.au/sites/default/files/2024-12/FOI%2025-0070.pdf 2️⃣ Persistence, Immunology & Oncogenic Risk Strayer et al. (2002) – Durability of transgene expression and vector integration: SV40-derived vectors 🔗 PubMed: https://pubmed.ncbi.nlm.nih.gov/12161189/ Aldén et al. (2022) – BNT162b2 mRNA reverse transcribed into DNA in human liver cell line (Huh7) 🔗 DOI: https://doi.org/10.3390/cimb44030073 Mörz, M. (2022) – Case report: Necrotizing encephalitis & myocarditis after BNT162b2, spike protein detected by IHC 🔗 DOI: https://doi.org/10.3390/vaccines10101651 🔗 PubMed: https://pubmed.ncbi.nlm.nih.gov/36298516/ Schwab, C. et al. (2023) – Autopsy-based histopathological characterization of myocarditis after anti-SARS-CoV-2 vaccination 🔗 PMC: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9702955/ 🔗 PubMed: https://pubmed.ncbi.nlm.nih.gov/36436002/ (Optional supporting autopsies) Gill, J.R. et al. (2022) – Cardiac findings in 2 adolescents following second Pfizer dose 🔗 PubMed: https://pubmed.ncbi.nlm.nih.gov/35157759/ Choi, S. et al. (2021) – Myocarditis-induced sudden death after BNT162b2 🔗 PMC: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8524235/ Röltgen et al. (2022) – Immune imprinting and germinal center response in SARS-CoV-2 infection and vaccination 🔗 DOI: https://doi.org/10.1016/j.cell.2022.01.018 Patterson et al. (2021) – Persistence of SARS-CoV-2 S1 protein in CD16+ monocytes in PASC up to 15 months 🔗 DOI: https://doi.org/10.3389/fimmu.2021.746021 Castrucci et al. (2019) – Clonal persistence of influenza B virus antibodies (comparative baseline) 🔗 DOI: https://doi.org/10.1128/mBio.00066-19 Irrgang et al. (2022/23) – Class switch toward IgG4 after repeated mRNA vaccination 🔗 DOI: https://doi.org/10.1126/sciimmunol.ade2798 🔗 PubMed: https://pubmed.ncbi.nlm.nih.gov/36548397/ 3️⃣ Related / Corroborating Evidence Chakraborty (2023) – DNA vector fragments detected in bloodstream of vaccinated individuals 🔗 OSF: https://osf.io/hzyn3/ Buckhaults, P. (2023) – SC Senate testimony on plasmid DNA contamination in Pfizer vaccines 🎥 Video: https://www.scstatehouse.gov/video/archives.php?key=18538 📄 Transcript PDF: https://www.scstatehouse.gov/CommitteeInfo/SenateMedicalAffairsCommittee/PandemicPreparedness/Phillip-Buckhaults-SC-Senate-09122023-final.pdf EMA (ICH Q6B, 1999 / still current) – Specifications: Biotechnological/biological products → Residual DNA <10 ng/dose; no oncogenic sequences permitted 🔗 EMA Guideline: https://www.ema.europa.eu/en/documents/scientific-guideline/ich-q6b-specifications-biotechnological-biological-products_en.pdf Quantification of residual plasmid DNA and SV40 promoter-enhancer sequences in Pfizer/BioNTech and Moderna modRNA COVID-19 vaccines from Ontario, Canada David J. Speicher,Jessica Rose &Kevin McKernan https://www.tandfonline.com/doi/full/10.1080/08916934.2025.2551517 @Kevin_McKernan did I miss anything 🙏

DNA fragments detected in monovalent and bivalent Pfizer/BioNTech and Moderna modRNA COVID-19 vaccines from Ontario, Canada: Exploratory dose response relationship with serious adverse events. Background: In vitro transcription (IVT) reactions used to generate nucleoside modified RNA (modRNA) for SARS-CoV-2 vaccines currently rely on an RNA polymerase transcribing from a DNA template. Production of modRNA used in the original Pfizer randomized clinical trial (RCT) utilized a PCR-generated DNA template (Process 1). To generate billions of vaccine doses, this DNA was cloned into a bacterial plasmid vector for amplification in Escherichia coli before linearization (Process 2), expanding the size and complexity of potential residual DNA and introducing sequences not present in the Process 1 template. It appears that Moderna used a similar plasmid-based process for both clinical trial and post-trial use vaccines. Recently, DNA sequencing studies have revealed this plasmid DNA at significant levels in both Pfizer-BioNTech and Moderna modRNA vaccines. These studies surveyed a limited number of lots and questions remain regarding the variance in residual DNA observed internationally. Methods: Using previously published primer and probe sequences, quantitative polymerase chain reaction (qPCR) and Qubit® fluorometry was performed on an additional 27 mRNA vials obtained in Canada and drawn from 12 unique lots (5 lots of Moderna child/adult monovalent, 1 lot of Moderna adult bivalent BA.4/5, 1 lot of Moderna child/adult bivalent BA.1, 1 lot of Moderna XBB.1.5 monovalent, 3 lots of Pfizer adult monovalent, and 1 lot of Pfizer adult bivalent BA.4/5). The Vaccine Adverse Events Reporting System (VAERS) database was queried for the number and categorization of adverse events (AEs) reported for each of the lots tested. The content of one previously studied vial of Pfizer COVID-19 vaccine was examined by Oxford Nanopore sequencing to determine the size distribution of DNA fragments. This sample was also used to determine if the residual DNA is packaged in the lipid nanoparticles (LNPs) and thus resistant to DNaseI or if the DNA resides outside of the LNP and is DNaseI labile.  Results: Quantification cycle (Cq) values (1:10 dilution) for the plasmid origin of replication (ori) and spike sequences ranged from 18.44 - 24.87 and 18.03 - 23.83 and for Pfizer, and 22.52 – 24.53 and 25.24 – 30.10 for Moderna, respectively. These values correspond to 0.28 – 4.27 ng/dose and 0.22 - 2.43 ng/dose (Pfizer), and 0.01 -0.34 ng/dose and 0.25 – 0.78 ng/dose (Moderna), for ori and spike respectively measured by qPCR, and 1,896 – 3,720 ng/dose and 3,270 – 5,100 ng/dose measured by Qubit® fluorometry for Pfizer and Moderna, respectfully. The SV40 promoter-enhancer-ori was only detected in Pfizer vials with Cq scores ranging from 16.64 – 22.59. In an exploratory analysis, we found preliminary evidence of a dose response relationship of the amount of DNA per dose and the frequency of serious adverse events (SAEs). This relationship was different for the Pfizer and Moderna products. Size distribution analysis found mean and maximum DNA fragment lengths of 214 base pairs (bp) and 3.5 kb, respectively. The plasmid DNA is likely inside the LNPs and is protected from nucleases. Conclusion: These data demonstrate the presence of billions to hundreds of billions of DNA molecules per dose in these vaccines. Using fluorometry, all vaccines exceed the guidelines for residual DNA set by FDA and WHO of 10 ng/dose by 188 – 509-fold. However, qPCR residual DNA content in all vaccines were below these guidelines emphasizing the importance of methodological clarity and consistency when interpreting quantitative guidelines. The preliminary evidence of a dose-response effect of residual DNA measured with qPCR and SAEs warrant confirmation and further investigation. Our findings extend existing concerns about vaccine safety and call into question the relevance of guidelines conceived before the introduction of efficient transfection using LNPs. With several obvious limitations, we urge that our work is replicated under forensic conditions and that guidelines be revised to account for highly efficient DNA transfection and cumulative dosing. osf.io
BioNTech RNA-Based COVID-19 Injections Contain Large Amounts Of Residual DNA Including An SV40 Promoter/Enhancer Sequence - Science, Public Health Policy and the Law Background: BNT162b2 RNA-based COVID-19 injections are specified to transfect human cells to efficiently produce spike proteins for an immune response. publichealthpolicyjournal.com
The Konig vs Kaiser debate continues And the Corruption Carries On. anandamide.substack.com
Durability of transgene expression and vector integration: recombinant SV40-derived gene therapy vectors - PubMed Many applications of gene delivery require long-term transgene expression. In dividing cells, this result necessitates vector genome persistence, usually by integrating into cellular DNA. Since recombinant gene delivery vectors derived from tag-deleted, replication-incompetent simian virus-40 (SV40) … pubmed.ncbi.nlm.nih.gov
A Case Report: Multifocal Necrotizing Encephalitis and Myocarditis after BNT162b2 mRNA Vaccination against COVID-19 - PubMed The current report presents the case of a 76-year-old man with Parkinson's disease (PD) who died three weeks after receiving his third COVID-19 vaccination. The patient was first vaccinated in May 2021 with the ChAdOx1 nCov-19 vector vaccine, followed by two doses of the BNT162b2 mRNA vaccine in Jul … pubmed.ncbi.nlm.nih.gov
Autopsy-based histopathological characterization of myocarditis after anti-SARS-CoV-2-vaccination Cases of myocarditis, diagnosed clinically by laboratory tests and imaging have been described in the context of mRNA-based anti-SARS-CoV-2 vaccination. Autopsy-based description of detailed histological features of vaccine-induced myocarditis is ... pmc.ncbi.nlm.nih.gov
Autopsy-based histopathological characterization of myocarditis after anti-SARS-CoV-2-vaccination - PubMed Cases of myocarditis, diagnosed clinically by laboratory tests and imaging have been described in the context of mRNA-based anti-SARS-CoV-2 vaccination. Autopsy-based description of detailed histological features of vaccine-induced myocarditis is lacking. We describe the autopsy findings and common … pubmed.ncbi.nlm.nih.gov
Autopsy Histopathologic Cardiac Findings in 2 Adolescents Following the Second COVID-19 Vaccine Dose - PubMed The myocardial injury seen in these postvaccine hearts is different from typical myocarditis and has an appearance most closely resembling a catecholamine-mediated stress (toxic) cardiomyopathy. Understanding that these instances are different from typical myocarditis and that cytokine storm has a k … pubmed.ncbi.nlm.nih.gov
Myocarditis-induced Sudden Death after BNT162b2 mRNA COVID-19 Vaccination in Korea: Case Report Focusing on Histopathological Findings We present autopsy findings of a 22-year-old man who developed chest pain 5 days after the first dose of the BNT162b2 mRNA vaccine and died 7 hours later. Histological examination of the heart revealed isolated atrial myocarditis, with neutrophil ... pmc.ncbi.nlm.nih.gov
Immune imprinting, breadth of variant recognition, and germinal center response in human SARS-CoV-2 infection and vaccination During the SARS-CoV-2 pandemic, novel and traditional vaccine strategies have been deployed globally. We investigated whether antibodies stimulated by… sciencedirect.com
Frontiers | Persistence of SARS CoV-2 S1 Protein in CD16+ Monocytes in Post-Acute Sequelae of COVID-19 (PASC) up to 15 Months Post-Infection The recent COVID-19 pandemic is a treatment challenge in the acute infection stage but the recognition of chronic COVID-19 symptoms termed post-acute sequela... frontiersin.org
Class switch toward noninflammatory, spike-specific IgG4 antibodies after repeated SARS-CoV-2 mRNA vaccination - PubMed RNA vaccines are efficient preventive measures to combat the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic. High levels of neutralizing SARS-CoV-2 antibodies are an important component of vaccine-induced immunity. Shortly after the initial two mRNA vaccine doses, the immunogl … pubmed.ncbi.nlm.nih.gov
South Carolina Legislature Video Archives scstatehouse.gov
South Carolina Legislature Online - Error scstatehouse.gov
Page or document not found | European Medicines Agency (EMA) We are sorry, but the content you tried to access is unavailable at the link you used, which was either incorrect or out-of-date. To help you find what you are looking for, we have included some useful tips. ema.europa.eu

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

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@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@JillianMichaels DNA contamination with SV40 promoters, brewed in vats of E. coli poop soup. Sounds so “safe & effective.” 🤡 https://t.co/96OgCAHqMQ

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@BrokenTruthTV https://t.co/DNiBLgAkxQ

@JesslovesMJK - Jessica Rose 🤙

Speicher, D. J., Rose, J., & McKernan, K. (2025). Quantification of residual plasmid DNA and SV40 promoter-enhancer sequences in Pfizer/BioNTech and Moderna modRNA COVID-19 vaccines from Ontario, Canada. Autoimmunity, 58(1). https://doi.org/10.1080/08916934.2025.2551517

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@BrokenTruthTV https://t.co/iaMSVSxCgI

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@BrokenTruthTV https://t.co/ALQAS24QT7

@JesslovesMJK - Jessica Rose 🤙

"...mitochondria tend to be farther from [skin fibroblast] cell border[s] for patients who experience psychosis" Is that not the most fascinating observation ever?? https://www.biorxiv.org/content/10.1101/2025.10.08.676630v1 https://t.co/JMGPk4Uhvv

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@BrokenTruthTV https://t.co/rgfUu4FNWt

@DJSpeicher - David J Speicher PhD DTM

Nice to see an updated table of all the studies on plasmid DNA. Reproducibility trumps publication.

@hudikaha - 藤川賢治(FUJIKAWA Kenji)@小金井市議 Koganei City Councillor

I have added a row for the brand-new peer-reviewed paper by @DJSpeicher @JesslovesMJK and @Kevin_McKernan to the table "Verifications of mRNA Vaccine DNA Contamination Worldwide (as of 2025-09-06)." https://t.co/zhfOpreF6E

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@BrokenTruthTV https://t.co/F5KMVFxL42

@DJSpeicher - David J Speicher PhD DTM

New Study on Lipid Nanoparticles🎉 Congrats to @CanningPharm on her publication, "Complexity, unpredictability and safety challenges of lipid nanoparticles"‼️ This manuscript examines lipid nanoparticles (LNPs), tiny fat particles used in mRNA vaccines like those for COVID-19. This manuscript highlights several important items. Complex Behavior: LNPs are unpredictable due to varying structure and interactions in the body, affecting how well they work. Safety Risks: They can cause immune reactions or interact with drugs like clozapine, potentially leading to side effects. Delivery Issues: Only 1-15% of LNPs successfully deliver mRNA into cells, reducing vaccine effectiveness. Protein Coating: A protein layer forms on LNPs in the body, varying by person and impacting how they function. Need for Better Testing: The study calls for improved methods to study LNPs to ensure safety and effectiveness. This work highlights LNP risks and pushes for better designs and regulations to make mRNA vaccines safer and more reliable. The manuscript can be found here: https://www.researchgate.net/publication/396321059_Complexity_unpredictability_and_safety_challenges_of_lipid_nanoparticles_-A_multidisciplinary_narrative_review Congratulations Maria. You have worked tirelessly on this for the past several years and it's nice to see the document public. @JesslovesMJK @Kevin_McKernan @AdhesionsOrg @jimmy_dore @FLSurgeonGen @liz_churchill10 @natalimorris @NicHulscher @P_McCulloughMD @Double_Christ @MaryanneDemasi @hervk102 @TheRebelPatient @nzdsos @NG_Northgroup @cccalliance24 @SenseReceptor @VigilantFox @Fynnderella1 @IamBrookJackson @LynneBr37562004

Saved - October 11, 2025 at 10:19 PM
reSee.it AI Summary
I present “The Burger Logic”: when data align with common sense, we pause and investigate. I outline Step 1: the obvious truth; Step 2: a parallel pattern after vaccination; Step 3–6: Dutch and other data show a consistent ~10-week lag and repeatable signal; Step 7–9: why rollout continues—costs, contracts, careers, politics; Step 10–12: moral logic and informed choice over mandates; Step 14–19: a roadmap to acknowledge, pause, investigate, restore freedom; Step 23: disclaimer.

@ThomasEJnr - Thomas Emmett

🍔 The Burger Logic: When Common Sense Meets the Data Sometimes truth is so simple it becomes invisible buried under jargon, politics, and billions of dollars. But every so often, a simple analogy cuts through the noise. Let’s call it “The Burger Logic.”

@ThomasEJnr - Thomas Emmett

🎯 Step 1: The Obvious Truth > If a new burger hit the market and people consistently died after eating it we’d stop selling the burger. No committees. No “risk–benefit” panels. Just common sense. Stop serving the experimental burger.

@ThomasEJnr - Thomas Emmett

Step 2: The Parallel We’re Not Allowed to Make > After each COVID vaccination wave, all-cause mortality quietly ticks up. About 8–10 weeks later, deaths peak and then fall back again.

@ThomasEJnr - Thomas Emmett

The pattern is consistent, across multiple campaigns. Temporary but repeatable. Real, not random. Yet instead of asking why, health authorities doubled down more doses, more pressure, more silence.

@ThomasEJnr - Thomas Emmett

Step 3: What the Data Show Independent analyses of Dutch mortality data (and others) reveal: Clear temporal correlation: deaths rise shortly after vaccination waves.

@ThomasEJnr - Thomas Emmett

Consistent lag: around 10 weeks from peak injections to peak deaths. Transient pattern: mortality normalizes afterward. Statistical significance: signal repeats beyond random chance.

@ThomasEJnr - Thomas Emmett

If this were any other product, the question would be obvious: > “Why are more people dying after we introduce this?” But here, the data get buried under “safe and effective” slogans.

@ThomasEJnr - Thomas Emmett

Step 4: Why It Continues Stopping would mean admitting a mistake and for too many, that’s not an option. Billions invested in development and procurement Contracts locked with indemnities and guarantees

@ThomasEJnr - Thomas Emmett

Officials’ careers and reputations on the line Pharma profits dependent on continued rollout It’s not medicine anymore. It’s sunk-cost politics with a syringe.

@ThomasEJnr - Thomas Emmett

Step 5: The Moral Logic In every other aspect of life, when harm patterns emerge, we pause. We investigate. We protect people first. Except here where we’re told to look away and “trust the science,” even when the science itself says stop.

@ThomasEJnr - Thomas Emmett

🍔 Step 6: The “Owner’s Choice” Principle Imagine McDonald’s rolls out the experimental burger. The owner can eat it. Customers can choose the regular one. No one is forced to eat what they don’t trust.

@ThomasEJnr - Thomas Emmett

That’s how #informedchoice works. Now apply that same logic to vaccines: Individuals decide based on their own health and risk. Healthcare workers use professional judgment. #vulnerable populations are protected, not #coerced.

@ThomasEJnr - Thomas Emmett

No #mandates. No #threats. No #shaming. Just freedom the foundation of #ethicalmedicine.

@ThomasEJnr - Thomas Emmett

Step 7: The Common-Sense Path Forward 1. Acknowledge the pattern mortality rises after vaccination waves. 2. Pause the rollout stop experimental products pending review.

@ThomasEJnr - Thomas Emmett

3. Investigate transparently full #accesstodata, #contracts, and #autopsies. 4. Restore #medicalfreedom no more coercion disguised as care.

@ThomasEJnr - Thomas Emmett

❌ Step 8: The Current Reality 1. The pattern is #observed. 2. The pattern is #Denied 3. The #rollout continues. 4. Choice #disappears.

@ThomasEJnr - Thomas Emmett

Step 9: The #Takeaway If this were a burger, it would’ve been recalled years ago. But because it’s a #multibilliondollar #geneticproduct, logic is suspended, accountability disappears, and silence is #enforced.

@ThomasEJnr - Thomas Emmett

The #BurgerLogic exposes the #absurdity of it all: > If something consistently harms people stop doing it. If something is experimental don’t force it on everyone. If choice exists let people #choose. That’s not #conspiracy. That’s #CommonSense. 🧭

@ThomasEJnr - Thomas Emmett

The Bottom Line The data are speaking. The people are noticing. And the old excuses are running out. Because no amount of PR spin can hide what every honest eye can see: > After every experimental wave, more people die. And no one in power seems to care enough to ask why.

@ThomasEJnr - Thomas Emmett

Credit to Mark on this and his #GutMindSynergy site too https://gutmindsynergy.com/vitamin-b12-immune-system-boost-immunity/

Vitamin B12 and Immune System: The Essential Nutrient for Robust Immunity & Gut Health | GutMindSynergy Discover the science-backed role of Vitamin B12 in immune function, from supporting white blood cell production to regulating inflammation. Learn how B12 deficiency impacts immunity and whether supplementation can enhance your body's defenses. gutmindsynergy.com

@ThomasEJnr - Thomas Emmett

@Grok Translate the entire thread into Dutch, German, and French, keeping tone, structure, and emotion intact. Use natural phrasing (not literal). Preserve markdown, emojis, and headings. Label each section 🇳🇱 🇩🇪 🇫🇷.

@ThomasEJnr - Thomas Emmett

https://github.com/markfietje/health-data-causal-analyzer/blob/main/output/real_ireland_data.csv

health-data-causal-analyzer/output/real_ireland_data.csv at main · markfietje/health-data-causal-analyzer Comprehensive cross-country health data analysis examining 70-day mortality signals in Netherlands and Ireland vaccination data with official statistics from CBS, RIVM, CSO, and HPSC - health-data-causal-analyzer/output/real_ireland_data.csv at main · markfietje/health-data-causal-analyzer github.com

@ThomasEJnr - Thomas Emmett

“Disclaimer: This analysis represents independent research using publicly available official statistics. All findings are based on correlation analysis and do not imply causation. The precautionary principle suggests further investigation is warranted.”

Saved - September 19, 2025 at 1:43 PM
reSee.it AI Summary
I've shared some crucial links that are almost as important as our paper. Check out the paper itself, an article from Retraction Watch, a Senate hearing, and the original paper for more context.

@JesslovesMJK - Jessica Rose 🤙

link to paper: https://pubmed.ncbi.nlm.nih.gov/40913499/

Quantification of residual plasmid DNA and SV40 promoter-enhancer sequences in Pfizer/BioNTech and Moderna modRNA COVID-19 vaccines from Ontario, Canada - PubMed For some of the COVID-19 vaccines, the drug substances released to market were manufactured differently than those used in clinical trials. Manufacturing nucleoside-modified mRNA (modRNA) for commercial COVID-19 vaccines relies on RNA polymerase transcription of a plasmid DNA template. Previous stud … pubmed.ncbi.nlm.nih.gov

@JesslovesMJK - Jessica Rose 🤙

link to Retraction Watch article: https://retractionwatch.com/2025/09/18/covid-vaccine-safety-acip-dna-contamination-study-autoimmunity/

Exclusive: Publisher investigating DNA contamination paper that authors say CDC vaccine committee will consider The publisher Taylor & Francis is investigating concerns raised on PubPeer about a paper claiming to find DNA contamination in COVID-19 vaccines beyond regulators’ recommended amounts.  The move comes as the U.S. body tasked with making recommendations for vaccine use is scheduled to consider the safety of COVID-19 shots, and two of the study’s authors… retractionwatch.com

@JesslovesMJK - Jessica Rose 🤙

link to Senate hearing: https://www.hsgac.senate.gov/subcommittees/investigations/hearings/how-the-corruption-of-science-has-impacted-public-perception-and-policies-regarding-vaccines/

How the Corruption of Science has Impacted Public Perception and Policies Regarding Vaccines - Committee on Homeland Security & Governmental Affairs hsgac.senate.gov

@JesslovesMJK - Jessica Rose 🤙

link to original paper: https://www.tandfonline.com/doi/full/10.1080/08916934.2025.2551517#abstract

Saved - September 15, 2025 at 10:55 AM
reSee.it AI Summary
Both the SARS-CoV-2 virus and mRNA vaccines have significant effects on the brain and vascular system. Evidence shows increased psychiatric risks, including depression and anxiety, linked to both infection and vaccination. The spike protein is implicated in causing microclots, blood-brain barrier damage, and amyloid formation, contributing to symptoms like brain fog and strokes. Current data suggests that more vaccine doses do not equate to better protection and may even increase risks. Millions are affected by long COVID and vaccine-related injuries, warranting careful monitoring and reconsideration of public health policies.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Both the SARS-CoV-2 virus and the mRNA vaccines impact the brain & vascular system. I'll share the peer reviewed evidence in this thread 🧵 Large cohorts show ↑ psychiatric risks. Labs show the mechanism: microclots, BBB leakage, amyloid formation. Public health policy must face this evidence.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Thread to read 🧵! "Alabama-based physician Dr. Jordan Vaughn followed up with a chilling estimate—up to 15 million Americans may be suffering from long COVID or COVID vaccine injuries. He now treats teenagers who can’t stand up and previously healthy adults who are suffering strokes with no clear cause. According to Vaughn, the spike protein’s S1 subunit is far from harmless. 'It triggers inflammation, it disrupts endothelial barriers, it induces fibrin resistant to breakdown, and it promotes a lot of amyloid aggregates,' he said. These effects impair oxygen delivery, damage blood vessels, and trigger a wave of symptoms—racing heart, brain fog, shortness of breath, and post-exertional crashes. In his clinic, Vaughn uses immunofluorescent microscopy to detect the spike protein’s damage, showing up in patients who were once thriving. He warned that the mRNA injections led to uncontrolled spike protein production, which spread throughout the body, reaching the heart, brain, ovaries, and testes." This speech is a BOMBSHELL. Why? Because indeed, there is formation of fibrinaloids (deposition of fibrin in degenerative form), production and aggregation of degenerative fibers like Abeta42 (Alzheimer's), platelet activation, inflammation of blood vessels with permeabilization of the blood-brain barrier (BBB)... This is exactly what I describe in this document posted online on April 26, 2025. cf. photo. But the worst is that these degenerative fibers, particularly Abeta42, are linked to immune tolerance. Why? Abeta42 activates RAGE, which will induce alarmins (including HMGB1), recruiting MDSCs (anti-inflammatory immune cells) and the production of IL-10 (anti-inflammatory cytokine). Role of RAGE in Alzheimer’s Disease - PMC HMGB1 and RAGE in inflammation and cancer - PubMed HMGB1 enhances immune suppression by facilitating the differentiation and suppressive activity of myeloid-derived suppressor cells - PubMed IL-10 induces an increase in ACE2 expression... Facilitating infection by SARS-CoV-2 via... THE SPIKE. Preliminary Evidence for IL-10-Induced ACE2 mRNA Expression in Lung-Derived and Endothelial Cells: Implications for SARS-Cov-2 ARDS Pathogenesis - PMC Preliminary Evidence for IL-10-Induced ACE2 mRNA Expression in Lung-Derived and Endothelial Cells: Implications for SARS-Cov-2 ARDS Pathogenesis - PMC I don't know how to say it anymore: double amyloid effect! - Not only is the Spike amyloid (degenerative in itself), but it induces the production of amyloid fibers including Abeta, and... - The SPIKE allows for inducing immune tolerance via amyloid fibers, - And the SPIKE can use these amyloid fibers to spread throughout the body. That's the full set of amyloid properties of the Spike. Cherry on the plum tart: Conclusions: - Wave of degenerative pathologies... And it's not JUST in the brain. - The more you come into contact with the Spike, the more your body will react to be "better" contaminated and "better" host the virus - The more your immune system will be out of service (and therefore you will be vulnerable) - 10 to 15 million just in the USA... Where are we at in France and Europe? What does that represent in 2025? Huh. And yes, new variants are coming. I repeat: it stinks. Thank you very much. PS: The amyloid properties of the Spike are also linked to the carcinogenic properties of the Spike. Why? p53/mitochondries/Spike

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Space du SAMEDI 26 AVRIL... Space international... anglais/français... Avec un document original. https://acrobat.adobe.com/id/urn:aaid:sc:EU:24cc46bf-bf95-4e5d-9b3e-7d82a221abf8 Je dois encore améliorer mon approche pour vulgariser un maximum.

Space international 26 avril 2025-1 (1).pdf View this file, and add comments too. acrobat.adobe.com

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

RAGE, le VIH, la latence, la réactivation... et plus si affinité... SARS-CoV-2, un VIH-like. https://pmc.ncbi.nlm.nih.gov/articles/PMC7926981/ TOX - ou la boîte du groupe de haute mobilité associée à la sélection des thymocytes (TOX) - joue un rôle important dans la différenciation des cellules T en

HIV-1 Latency and Viral Reservoirs: Existing Reversal Approaches and Potential Technologies, Targets, and Pathways Involved in HIV Latency Studies Eradication of latent human immunodeficiency virus (HIV) infection is a global health challenge. Reactivation of HIV latency and killing of virus-infected cells, the so-called “kick and kill” or “shock and kill” approaches, are a popular strategy ... pmc.ncbi.nlm.nih.gov

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

@vieil_garde_ph @tatiann69922625 @KevinMcCairnPhD https://pmc.ncbi.nlm.nih.gov/articles/PMC10732518/ "These data suggest that caspase cleavage of GSDME, leading to pore formation in the plasma membrane or other intracellular compartments, facilitates calcium accumulation in the cytoplasm and PAD4 activation." https://pmc.ncbi.nlm.nih.gov/articles/PMC10121894/ "Given the ability of

NET formation is a default epigenetic program controlled by PAD4 in apoptotic neutrophils Neutrophil extracellular traps (NETs) not only counteract bacterial and fungal pathogens but can also promote thrombosis, autoimmunity, and sterile inflammation. The presence of citrullinated histones, generated by the peptidylarginine deiminase 4 ... pmc.ncbi.nlm.nih.gov
Gasdermin-E mediates mitochondrial damage in axons and neurodegeneration Mitochondrial dysfunction and axon loss are hallmarks of neurologic diseases. Gasdermin (GSDM) proteins are executioner pore-forming molecules that mediate cell death, yet their roles in the central nervous system (CNS) are not well understood. ... pmc.ncbi.nlm.nih.gov

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

P53, propriétés amyloides et cancers... Et oui... la p53, le gardien de notre génome, possède des propriétés amyloides et... prion-like. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596421/ On pense que l'agrégation de la p53 sous forme de dépôts amyloides est un mécanisme impliqué dans les cancers. En

p53 amyloid formation leading to its loss of function: implications in cancer pathogenesis The transcriptional regulator p53 has an essential role in tumor suppression. Almost 50% of human cancers are associated with the loss of p53 functions, where p53 often accumulates in the nucleus as well as in cytoplasm. Although it has been ... pmc.ncbi.nlm.nih.gov

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Spike, p53 et mitochondries... Allez, je vais essayer de vulgariser. 1. Interaction Spike/p53 et immunité : La Spike pourrait interagir avec p53, qui est un régulateur clé de l’immunité innée et adaptative, notamment via la production d’interférons (IFN) de type I et de gènes

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Thread à lire 🧵! "Le Dr Jordan Vaughn, médecin basé en Alabama, a ensuite fourni une estimation effrayante : jusqu'à 15 millions d'Américains pourraient souffrir de blessures liées à la COVID longue ou au vaccin contre la COVID. Il traite désormais des adolescents qui ne

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Seoul cohort (~2M adults, 2024): Post-vax hazards: • Depression HR=1.68 • Anxiety HR=1.44 • Sleep disorders HR=1.93 Authors: “Special cautions are necessary for giving additional doses.” 🔗 https://www.nature.com/articles/s41380-024-02627-0

Psychiatric adverse events following COVID-19 vaccination: a population-based cohort study in Seoul, South Korea - Molecular Psychiatry Evidence has suggested an increased risk of psychiatric manifestations following viral infections including coronavirus disease-2019 (COVID-19). However, psychiatric adverse events (AEs) after COVID-19 vaccination, which were documented in case reports and case series, remain unclear. This study is aimed to investigate the psychiatric AEs after COVID-19 vaccination from a large population-based cohort in Seoul, South Korea. We recruited 50% of the Seoul-resident population randomly selected from the Korean National Health Insurance Service (KNHIS) claims database on 1, January, 2021. The included participants (n = 2,027,353) from the Korean National Health Insurance Service claims database were divided into two groups according to COVID-19 vaccination. The cumulative incidences per 10,000 of psychiatric AEs were assessed on one week, two weeks, one month, and three months after COVID-19 vaccination. Hazard ratios (HRs) and 95% Confidence interval (CIs) of psychiatric AEs were measured for the vaccinated population. The cumulative incidence of depression, anxiety, dissociative, stress-related, and somatoform disorders, sleep disorders, and sexual disorders at three months following COVID-19 vaccination were higher in the vaccination group than no vaccination group. However, schizophrenia and bipolar disorders showed lower cumulative incidence in the vaccination group than in the non-vaccinated group. Depression (HR [95% CI] = 1.683 [1.520–1.863]), anxiety, dissociative, stress-related, and somatoform disorders (HR [95% CI] = 1.439 [1.322–1.568]), and sleep disorders (HR [95% CI] = 1.934 [1.738–2.152]) showed increased risks after COVID-19 vaccination, whereas the risks of schizophrenia (HR [95% CI] = 0.231 [0.164–0.326]) and bipolar disorder (HR [95% CI] = 0.672 [0.470–0.962]). COVID-19 vaccination increased the risks of depression, anxiety, dissociative, stress-related, and somatoform disorders, and sleep disorders while reducing the risk of schizophrenia and bipolar disorder. Therefore, special cautions are necessary for administering additional COVID-19 vaccinations to populations vulnerable to psychiatric AEs. nature.com

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Murata 2024 (Brain, Behavior & Immunity): Psychiatric disorders remain elevated after infection. Vaccination did not erase these risks effects varied by variant (Delta vs Omicron). 🔗 https://www.sciencedirect.com/science/article/pii/S088915912400254X

Associations between COVID-19 vaccination and incident psychiatric disorders after breakthrough SARS-CoV-2 infection: The VENUS Study The associations between COVID-19 vaccination and post-COVID psychiatric disorders are unclear. Furthermore, it is uncertain if these associations dif… sciencedirect.com

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Spike drives clotting & vessel injury: • Platelet hyperreactivity • Fibrin(oid) microclots resistant to breakdown • Endothelial dysfunction → brain fog, dysautonomia 🔗 https://pmc.ncbi.nlm.nih.gov/articles/PMC8705864/ 🔗 https://pubmed.ncbi.nlm.nih.gov/38549864/

SARS-CoV-2 Exacerbates Beta-Amyloid Neurotoxicity, Inflammation and Oxidative Stress in Alzheimer’s Disease Patients Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) triggered the pandemic Coronavirus Disease 19 (COVID-19), causing millions of deaths. The elderly and those already living with comorbidity are likely to die after SARS-CoV-2 infection. ... pmc.ncbi.nlm.nih.gov
Impact of the SARS-CoV-2 Spike Protein on the Innate Immune System: A Review - PubMed The Spike protein enables the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection by binding to multiple receptors, including the angiotensin-converting enzyme 2 (ACE2). Scientific studies also indicate that Spike is involved in severe forms of coronavirus disease 2019 (COVID-19), … pubmed.ncbi.nlm.nih.gov

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Amyloid properties (loss of proteostasis): Spike & fragments are amyloidogenic, promoting Aβ build-up. This links spike exposure to Alzheimer’s-like changes. 🔗 https://pubs.acs.org/doi/10.1021/jacs.2c03925 🔗 https://medicine.yale.edu/news-article/sars-cov-2-causes-buildup-of-alzheimers-related-peptides-in-the-retina/

SARS-CoV-2 Causes Buildup of Alzheimer’s-Related Peptides in the Retina A new study reveals a promising target for reducing amyloid beta buildup and preventing Alzheimer’s disease-like symptoms, such as brain fog, caused by COVID-19 medicine.yale.edu

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

State of the image from chatgpt 🤣🤣 I will fix it later 🤣

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Blood–brain barrier disruption (BBB): Spike damages endothelial junctions → BBB leakage, neuroinflammation, cognitive & mood symptoms. 🔗 https://pmc.ncbi.nlm.nih.gov/articles/PMC9239981/

Neuroinflammation and COVID-19 Coronavirus disease 2019 (COVID-19) has caused a historic pandemic of respiratory disease. COVID-19 also causes acute and post-acute neurological symptoms, which range from mild, such as headaches, to severe, including hemorrhages. Current evidence ... pmc.ncbi.nlm.nih.gov

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

More doses ≠ less infection (real-world data). Cleveland Clinic employees (2023-24): “The risk of COVID-19 also increased with the number of prior vaccine doses.” Current-season VE modest (≈42% → 19% after JN.1). 🔗 https://academic.oup.com/cid/article-abstract/79/2/405/7625220

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

#youwontgetsickifyougetthevaccine Swiss healthcare workers (2025, Nature): Recent boosters linked to: • ↑ influenza-like illness (ILI) • ↑ workdays lost Workforce sickness rose after boosting. 🔗 https://www.nature.com/articles/s43856-025-01046-8

Association of SARS-CoV-2 vaccination status with risk of influenza-like illness and loss of workdays in healthcare workers - Communications Medicine In the post-pandemic phase, the value of annual SARS-CoV-2 booster vaccination in healthcare-workers is unclear. In this multicentre cohort study, we sought to determine the association of SARS-CoV-2 vaccination status and other risk factors with the occurrence of influenza-like respiratory illness and workdays lost due to influenza-like respiratory illness. During a period of high SARS-CoV-2 community transmission (November 2023 to May 2024), we collected weekly data on symptoms and sick day leave and used negative binomial regression to identify risk factors for these outcomes among 1745 healthcare workers. To single out the effect of the vaccine and account for potential confounding, additional inverse probability weighted analysis was performed. In both analyses, we show that more SARS-CoV-2 vaccinations are associated with a higher risk of influenza-like respiratory illness and workdays lost. For influenza-like respiratory illness, the association is stronger with a more recent timing of the vaccination rather than the number of vaccinations, which suggests that the effect wanes over time. In contrast, seasonal influenza vaccination is associated with a decreased risk for both outcomes. Based on our data, we conclude that SARS-CoV-2 booster vaccination does not contribute to the protection of the healthcare workforce in a post-pandemic setting. SARS-CoV-2 vaccination may even temporarily increase the likelihood of symptomatic infection and workday loss. In the years following the COVID-19 pandemic, it is still unclear whether annual COVID booster vaccines are necessary for low-risk populations such as healthcare workers. In this study, 1745 healthcare workers in Switzerland were followed over several months to see how their vaccination status affected their chances of getting flu-like illnesses and missing work. The study found that those who recently received a COVID-19 booster were more likely to report symptoms and take sick leave. In contrast, people who received the seasonal flu vaccine were less likely to report symptoms or miss work. These findings suggest that COVID-19 boosters may not offer clear short-term benefits in a post-pandemic setting, and may even increase short-term illness risk. This raises questions about the best use of booster vaccines moving forward. Dörr, Lacy et al. evaluate the association between SARS-CoV-2 vaccination status and influenza-like illness and sick leave among 1745 Swiss healthcare workers. SARS CoV-2 vaccination is associated with increased illness symptoms and more days of sick leave, while influenza vaccination is associated with a decreased risk of both outcomes. nature.com

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Psychiatric outcomes corroborated: Multiple reviews show elevated neuropsychiatric risks post-COVID & mixed post-vax outcomes. 🔗 https://bmcmedicine.biomedcentral.com/articles/10.1186/s12916-025-03952-z 🔗 https://www.frontiersin.org/journals/psychiatry/articles/10.3389/fpsyt.2024.1360338/full

Psychiatric and neuropsychiatric sequelae of COVID-19 within 2 years: a multinational cohort study - BMC Medicine The long-term psychiatric and neuropsychiatric sequelae of COVID-19 across diverse populations remain not fully understood. This cohort study aims to investigate the short-, medium-, and long-term risks of psychiatric and neuropsychiatric disorders following COVID-19 infection in five countries. This population-based multinational network study used electronic medical records from France, Italy, Germany, and the UK and claims data from the USA. The initial target and comparator cohorts were identified using an exact matching approach based on age and sex. Individuals diagnosed with COVID-19 or those with a positive SARS-CoV-2 screening test between December 1, 2019, and December 1, 2020, were included as targets. Up to ten comparators without COVID-19 for each target were selected using the propensity score matching approach. All individuals were followed from the index date until the end of continuous enrolment or the last healthcare encounter. Cox proportional hazard regression models were fitted to estimate the risk of incident diagnosis of depression, anxiety disorders, alcohol misuse or dependence, substance misuse or dependence, bipolar disorders, psychoses, personality disorders, self-harm and suicide, sleep disorders, dementia, and neurodevelopmental disorders within the first 6 months (short-term), 6 months to 1 year (medium-term), and 1 to 2 years (long-term) post-infection. A total of 303,251 individuals with COVID-19 and 22,108,925 individuals without COVID-19 from five countries were originally included. Within the first 6 months, individuals with COVID-19 had a significantly higher risk of any studied disorders in all databases, with Hazard Ratios (HRs) ranging from 1.14 (95% CI, 1.07–1.22) in Germany to 1.89 (1.64–2.17) in Italy. Increased risks were consistently observed for depression, anxiety disorders, and sleep disorders across almost all countries. During the medium- and long-term periods, higher risks were observed only for depression (medium-term: 1.29, 1.18–1.41; long-term: 1.36, 1.25–1.47), anxiety disorders (medium-term: 1.29, 1.20–1.38; long-term: 1.37, 1.29–1.47), and sleep disorders (medium-term: 1.10, 1.01–1.21; long-term: 1.14, 1.05–1.24) in France, and dementia (medium-term: 1.65, 1.28–2.10) in the UK. Our study suggests that increased risks of psychiatric and neuropsychiatric outcomes were consistently observed only within, and not after, the 6-month observation period across all databases, except for certain conditions in specific countries. bmcmedicine.biomedcentral.com
Frontiers | New-onset psychosis following COVID-19 vaccination: a systematic review Background: The emergence of a new coronavirus strain caused the COVID-19 pandemic. While vaccines effectively control the infection, it's important to ackno... frontiersin.org

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Immune tolerance pathway explains persistence: RAGE–HMGB1 → MDSCs → IL-10 ↑ → ACE2 ↑ → viral entry + ongoing neuroinflammation. 🔗 https://pubmed.ncbi.nlm.nih.gov/17099778/ 🔗 https://pmc.ncbi.nlm.nih.gov/articles/PMC8823909/

TRPC6 fulfills a calcineurin signaling circuit during pathologic cardiac remodeling - PubMed The heart responds to injury and chronic pressure overload by pathologic growth and remodeling, which frequently result in heart failure and sudden death. Calcium-dependent signaling pathways promote cardiac growth and associated changes in gene expression in response to stress. The calcium/calmodul … pubmed.ncbi.nlm.nih.gov
Effect of Arterial Stiffness and Carotid Intima-Media Thickness Progression on the Risk of Dysglycemia, Insulin Resistance, and Dyslipidemia: a Temporal Causal Longitudinal Study Supplemental Digital Content is available in the text. Keywords: adolescent; atherosclerosis; causality; diabetes mellitus, type 2; hyperglycemia; metabolic syndrome; young adult pmc.ncbi.nlm.nih.gov

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Autopsy evidence (rare but real): Post-mRNA myocarditis cases show myocyte necrosis on histopathology. 🔗 https://pmc.ncbi.nlm.nih.gov/articles/PMC9922164/

A Potential Role of the Spike Protein in Neurodegenerative Diseases: A Narrative Review Human prion protein and prion-like protein misfolding are widely recognized as playing a causal role in many neurodegenerative diseases. Based on in vitro and in vivo experimental evidence relating to prion and prion-like disease, we extrapolate ... pmc.ncbi.nlm.nih.gov

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Long COVID = neuro + vascular burden: Millions now suffer brain fog, POTS, strokes, dementia-like decline post-infection. Vaccine-injury prevalence uncertain, but signals overlap & warrant monitoring. 🔗 https://polybio.org/projects/impact-of-sars-cov-2-infection-on-alzheimers-and-neurodegenerative-disease/

Impact of SARS-CoV-2 infection on Alzheimer's and neurodegenerative disease - PolyBio Research Foundation Project summary: The project will determine if live SARS-CoV-2 infection of human brain cell models leads to protein formation and gene... polybio.org

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Cancer-adjacent mechanisms: Spike linked to p53 disruption, mitochondrial stress, chronic inflammation. Early mechanistic evidence → oncogenic potential cannot be ignored. 🔗 https://www.mdpi.com/1999-4915/17/5/617

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

BBB disruption confirmed in long COVID: Nature Neuroscience 2024: persistent BBB leakage in patients with cognitive impairment (“brain fog”). 🔗 https://www.nature.com/articles/s41593-024-01576-9

Blood–brain barrier disruption and sustained systemic inflammation in individuals with long COVID-associated cognitive impairment - Nature Neuroscience Vascular disruption has been implicated in coronavirus disease 2019 (COVID-19) pathogenesis and may predispose to the neurological sequelae associated with long COVID, yet it is unclear how blood–brain barrier (BBB) function is affected in these conditions. Here we show that BBB disruption is evident during acute infection and in patients with long COVID with cognitive impairment, commonly referred to as brain fog. Using dynamic contrast-enhanced magnetic resonance imaging, we show BBB disruption in patients with long COVID-associated brain fog. Transcriptomic analysis of peripheral blood mononuclear cells revealed dysregulation of the coagulation system and a dampened adaptive immune response in individuals with brain fog. Accordingly, peripheral blood mononuclear cells showed increased adhesion to human brain endothelial cells in vitro, while exposure of brain endothelial cells to serum from patients with long COVID induced expression of inflammatory markers. Together, our data suggest that sustained systemic inflammation and persistent localized BBB dysfunction is a key feature of long COVID-associated brain fog. Long COVID is a major public health issue since 2020 and exhibits frequent neurological symptoms. Greene et al. propose that brain fog results from leaky brain blood vessels and a hyperactive immune system, shedding light on this phenomenon. nature.com

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Man every time I do one of these threads it feels like I'm repeating myself all the time Cohorts + labs show: • Vaccination = ↑ depression, anxiety, sleep disorders • Infection = psych harm persists • More doses = not always more protection • Spike = amyloid, microclots, BBB damage 👉 Until transparent data disproves these signals, stop blanket repeat-dose pushes. #LongCOVID #VaccineInjuries #SpikeProtein #end #Stoptheshots

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@grok please play devil's advocate and show the problems if any in this thread.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@reseeit save thread

Saved - September 14, 2025 at 1:55 PM
reSee.it AI Summary
I’ve analyzed the EHA documents and found significant misconduct by Peter Daszak. He actively obstructed investigations into EcoHealth Alliance’s ties to the Wuhan Institute of Virology, orchestrating support coalitions and lobbying against funding cuts. Daszak misled Congress, reported investigators to the FBI, and ignored oversight failures regarding risky research. His connections with Chinese officials and attempts to manipulate narratives raise serious concerns about EHA's transparency and integrity. The evidence suggests a calculated effort to protect funding and discredit scrutiny.

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

🧵My comments and some conclusions regarding the EHA documents we found: 1. Peter Daszak actively schemed to foil congressional and other investigations into EcoHealth Alliance (EHA) and its ties to the Wuhan Institute of Virology, as revealed in the DRASTIC document stash.

@gdemaneuf - Gilles Demaneuf

DRASTIC Working Notes: Findings from EHA documents made public by Congress in December 2024. 1️⃣ How the folder was made public: @RandPaul @thackerpd @SenJoniErnst @BillyBostickson @RogerPielkeJr https://t.co/9pTmdeUJaq

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

2⃣ He orchestrated a “Coalition of Support” with former USAID officials like Dennis Carroll and NGOs like the Smithsonian, which sent letters (e.g., April 24, 2020, to NIH) decrying grant cuts as political attacks to deflect scrutiny (Part 6, p.35-36).

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

3⃣ Daszak hired the Kyle House Group (KHG) to lobby against NDAA defunding amendments, with KHG’s Porter joining meetings like one on August 4, 2023, with Rep. Adam Smith’s staff to kill Sen. Joni Ernst’s provisions (Part 7, p.52).

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

4⃣🚨Perjury He also misled Congress by perjuring himself in testimony, falsely attributing the Latinne paper delay to grant issues while omitting Chinese pressure to suppress bat-origin data (Daszak-TI-Transcript.pdf, p.233; Part 10, p.79).

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

5⃣ Additionally, Daszak reported DRASTIC investigators to the FBI as “QAnon conspiracists” (May 21, 2020, FBI Daszak.pdf, p.39-40), attempting to discredit their probes into WIV’s role. These moves show a calculated effort to obstruct investigations and protect EHA’s funding.

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

6⃣ GoF Denials & Oversight Failures (Part 9, p.68; Part 10, p.76) Daszak claimed NIH’s GoF pause (2014-2017) was irrelevant to WIV’s work, implying compliance with Chinese laws, despite Baric’s 2015 concerns & 2018 warning against wildtype SARS-CoV work without U.S. registration

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

7⃣ Oversight Failures The above, coupled with WIV ignoring Baric’s GoF restrictions, exposes EHA’s lax oversight & complicity in risky research. His April 2015 note to check WIV’s GoF with Baric & WIV selling Baric’s mice, hints at deeper WIV misconduct which PD didn't address.

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

8⃣ DEFUSE and DARPA Ties (Part 1, p.4-8) Daszak and Shi Zhengli’s Jun 2017 DARPA/NIAID meetings to shape PREEMPT (p.4, 7) reveal the deep influence of EHA on US funding priorities. Secondly, Shi’s presence raises red flags about Chinese access to sensitive programs.

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

9⃣ Baric and DEFUSE The full 8-page Baric DEFUSE contribution (Mar 2018, p.4) (which is more complete than the @USRightToKnow version) and its accidental omission in the final proposal highlight EHA’s incompetence, potentially costing approval. https://draftable.com/compare/etsiSgBltbIi

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

@USRightToKnow 🔟 Daszak’s 2020 recycling of DEFUSE His attempt to recycle parts of DEFUSE into $300K/$500K DARPA grants (p.6) shows his opportunistic pivoting to COVID-19 concerns, while leveraging the prior WIV linked work of concern.

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

@USRightToKnow 1⃣1⃣ WIV Data Access Issues (Part 10, p.80) EHA’s lack of access to WIV’s bat CoV database (Mar 2018, DEFUSE proposal) and Zhengli’s refusal to share without approval (Part 10, p.79) confirm EHA’s limited control over WIV’s data, contradicting PD's claims of transparency.

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

@USRightToKnow 1⃣2⃣ PREDICT Narrative Flip (Part 10, p.76) Andrew Clements (USAID) initially pushed to claim RaTG13 as a PREDICT virus (May 2021), then distanced PREDICT from origins after scrutiny, with PD acquiescing, showing a coordinated effort to manipulate the lab-leak narrative.

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

@USRightToKnow 1⃣3⃣ Chinese Connections (Part 10, p.81) Daszak’s 2015 meeting with Heimowitz, whose grandmother founded the US Communist Party & who was “well-connected in all Chinese Government Activities,” raises some questions about EHA’s ties to Chinese networks and WIV collaboration.

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

@USRightToKnow 1⃣4⃣ Laos BANAL Samples (Part 10, p.81) Confidential serological results from Lao BANAL samples (Jul/Aug 2023, R01 meetings) and demands for secrecy by Elizabeth Ashley indicate EHA’s ongoing efforts to control sensitive data, potentially linked to lab-leak-related sequences.

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

@USRightToKnow 1⃣5⃣Temporary Conclusion You, reader, are a juror in truth’s court, and I believe you will also conclude that DRASTIC’s new evidence, ripped from that EHA Drive, shows the true nature of Daszak, his infernal machinations, and how his mercenary empire was built on lies!

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

@USRightToKnow unroll EHA drive @threadreaderapp unroll

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

@jhas5 @VillanuevaPM Many of the folders and files were marked confidential and not to be shared, and were not shared. Chmura made a mistake with file link permissions, and as far as we know nobody else accessed them apart from me before the link was closed, not even the US government.

Saved - September 7, 2025 at 7:17 AM
reSee.it AI Summary
I explored the differences between monkeypox and smallpox proteins using ChatGPT, which highlighted their similarities. I discussed the potential implications of mutations and frameshift changes in their coding sequences, suggesting monkeypox may have originated from tinkering with smallpox. I noted that the genomic identity between the two viruses raises questions about smallpox's eradication status. The ongoing conversation touches on the vaccine industry's foundations and the possible manipulation of viruses, prompting further analysis and skepticism regarding official narratives.

@Jikkyleaks - Jikkyleaks 🐭

WHOA! put this question into chatgpt and see what happens. The question was "show me the protein with the biggest difference between Monkey pox and smallpox" (they are essentially the same protein). Then it did this. @CharlesRixey @AGHuff

@Jikkyleaks - Jikkyleaks 🐭

@A1persona @kenrank24 @DrNeilStone You think smallpox vaccine eradicated smallpox... What is monkey pox and what vaccine is used against it?

@Jikkyleaks - Jikkyleaks 🐭

@CharlesRixey @AGHuff @grok please analyse the difference in function between these two putative proteins.

@Jikkyleaks - Jikkyleaks 🐭

@CharlesRixey @AGHuff @grok Links: https://www.ncbi.nlm.nih.gov/protein/AKG51368.1 https://www.ncbi.nlm.nih.gov/protein/AAA69317.1

Complement binding [Monkeypox virus] - Protein - NCBI ncbi.nlm.nih.gov
D15L [Variola virus] - Protein - NCBI ncbi.nlm.nih.gov

@Jikkyleaks - Jikkyleaks 🐭

@CharlesRixey @AGHuff @grok "Show me a citation that shows a difference in structure or function between MOPICE, SPICE and VCP" "OK here's a paper showing that they all produced the same monoclonal antibody" Oops. https://academic.oup.com/jimmunol/article-abstract/183/5/3150/8053338?redirectedFrom=fulltext&login=false @weldeiry @MaryanneDemasi

@Jikkyleaks - Jikkyleaks 🐭

@CharlesRixey @AGHuff @grok @weldeiry @MaryanneDemasi

@Jikkyleaks - Jikkyleaks 🐭

So the missing CTD is because of a stop codon at 19924 in the monkeypox sequence, shortening it from 263aa to 216aa. I suspect someone was tinkering with smallpox and ended up creating monkeypox from it. The published sequence is reverse complement. https://www.ncbi.nlm.nih.gov/nuccore/KP849471.1?report=GenBank @AlmanaLepiz2252 cattg 19141 tataattttt atgtttatta gtgtacacat tttggaagta agttccggct gccatgtatt 19201 tcctggagag caagtagatg atgaggaacc agatagttta tatccatact tgcacttaaa 19261 gtctacattg tagttgtatg agtgtatgat ctt

Monkeypox virus isolate Yambuku_DRC_1985, complete genome - Nucleotide - NCBI ncbi.nlm.nih.gov

@Jikkyleaks - Jikkyleaks 🐭

@CharlesRixey @AGHuff @grok @weldeiry @MaryanneDemasi One problem solved... The difference between MPOICE and SPICE in the coding sequence is merely from a frameshift mutation causing a stop codon (TAA in reverse complement) at 19297..19295 I wonder who mutated small pox?

@Jikkyleaks - Jikkyleaks 🐭

@CharlesRixey @AGHuff @grok @weldeiry @MaryanneDemasi Chat can occasionally be useful, it performs better than Grok for genome assessment I did this manually to find the stop codon. Chat confirms.

@Jikkyleaks - Jikkyleaks 🐭

@CharlesRixey @AGHuff @grok @weldeiry @MaryanneDemasi 🚨🚨Can you see it yet? @DrJBhattacharya @MaryanneDemasi @DrJulieSladden @Fynnderella1 @P_McCulloughMD @AGHuff

@Tl84189427 - TL

ב1977 אחרי חיסון מקיף של האוכלסיה העולמית הוכרז ניצחון על האבעבועות השחורות, ממש במקרה באותה תקופה החלה מחלה חדשה הנקראת אבעבועות הקוף שבמקרה הרצף החבלוני כמעט זהה, לפחות ברמה כזאת שלפחות לגבי נגיפים אחרים שינוי כזה לא מספיק על מנת להגדיר אותם כוירוס שונה.

@Jikkyleaks - Jikkyleaks 🐭

Just a reminder... #MpoxGate

@Jikkyleaks - Jikkyleaks 🐭

Here's your #monkeypox match folks! Next question - what inserts did they put in?? A Prashant Pradhan analysis would be great just now but I'm sure @trvrb would find a reason to blame it on a pangolin 🤔🤔 @CharlesRixey @Daoyu15 https://blast.ncbi.nlm.nih.gov/Blast.cgi?CMD=Get&RID=8F3C3S3T114

404 Error - NCBI blast.ncbi.nlm.nih.gov

@Jikkyleaks - Jikkyleaks 🐭

Just a reminder for those asking whether Mpox (monkeypox) was a manipulated virus. Absolutely.

@Jikkyleaks - Jikkyleaks 🐭

Bookmark this tweet. The #monkeypox outbreak was a planned release of Monkeypox Israel 2018 strain (genbank MN648051 ) targeting social gatherings of gay men, in order to blame "homophobic" Russia. The people behind this are psychopaths. @chrismartenson

@Jikkyleaks - Jikkyleaks 🐭

Here's your #monkeypox match folks! Next question - what inserts did they put in?? A Prashant Pradhan analysis would be great just now but I'm sure @trvrb would find a reason to blame it on a pangolin 🤔🤔 @CharlesRixey @Daoyu15 https://blast.ncbi.nlm.nih.gov/Blast.cgi?CMD=Get&RID=8F3C3S3T114

404 Error - NCBI blast.ncbi.nlm.nih.gov

@Jikkyleaks - Jikkyleaks 🐭

Here's your #monkeypox match folks! Next question - what inserts did they put in?? A Prashant Pradhan analysis would be great just now but I'm sure @trvrb would find a reason to blame it on a pangolin 🤔🤔 @CharlesRixey @Daoyu15 https://blast.ncbi.nlm.nih.gov/Blast.cgi?CMD=Get&RID=8F3C3S3T114

404 Error - NCBI blast.ncbi.nlm.nih.gov

@Jikkyleaks - Jikkyleaks 🐭

Reminder...

@Jikkyleaks - Jikkyleaks 🐭

@WHOEMRO That awkward moment when the @WHO accidentally reveals that smallpox was never really eradicated, by declaring a #Mpox "PHEIC". 97% identical genome. That's why your "MPOX" vaccine is a smallpox vaccine. Changes things a bit doesn't it?

@Jikkyleaks - Jikkyleaks 🐭

Bookmark this tweet. The #monkeypox outbreak was a planned release of Monkeypox Israel 2018 strain (genbank MN648051 ) targeting social gatherings of gay men, in order to blame "homophobic" Russia. The people behind this are psychopaths. https://t.co/gSGoykc9FH@chrismartenson

@Jikkyleaks - Jikkyleaks 🐭

Bookmark this tweet. The #monkeypox outbreak was a planned release of Monkeypox Israel 2018 strain (genbank MN648051 ) targeting social gatherings of gay men, in order to blame "homophobic" Russia. The people behind this are psychopaths. https://t.co/gSGoykc9FH@chrismartenson

@Jikkyleaks - Jikkyleaks 🐭

@Jikkyleaks - Jikkyleaks 🐭

If smallpox was never eradicated but merely renamed as monkeypox, or monkeypox was the mutated version of smallpox after the vaccination campaign... The whole premise to the vaccine industry falls. Smallpox is monkeypox. @AdhesionsOrg @VigilantFox

@Jikkyleaks - Jikkyleaks 🐭

H/t @ClareCraigPath https://www.hartgroup.org/the-smallpox-vanishing-act/

The Smallpox vanishing Act Was it really eradicated, or just rebranded?  hartgroup.org

@Jikkyleaks - Jikkyleaks 🐭

@ClareCraigPath Aaannnddd... there we go again. "DO NOT ASK ABOUT THE GENOMIC IDENTITY BETWEEN MONKEYPOX AND SMALLPOX THAT WILL SHOW THAT THE @WHO AND @NIH LIED ABOUT THE ERADICATION OF SMALLPOX FOR 50 YEARS. Regards, your new AI overlords" #MpoxGate https://t.co/oaXwAw0TmV

@Jikkyleaks - Jikkyleaks 🐭

@Shnauser1 @CharlesRixey @AGHuff https://t.co/UrBgPOscgV

@Jikkyleaks - Jikkyleaks 🐭

@MinisterSpew @CharlesRixey @AGHuff https://t.co/uPAr5YxJ7J

@Jikkyleaks - Jikkyleaks 🐭

@drtaubraun @CharlesRixey @AGHuff Do you have a record of the report?

@Jikkyleaks - Jikkyleaks 🐭

@unhealthytruth @CharlesRixey @AGHuff https://t.co/0Ti4a9vler

@Jikkyleaks - Jikkyleaks 🐭

@spidercatnz @CharlesRixey @AGHuff Yes it's lying. Did you post the protein sequence I provided?

@Jikkyleaks - Jikkyleaks 🐭

Well it would be a difficult thing to jump transmission pathways by having only 2% genomic differences and basically no protein differences. I don't think I've seen that happen. Think about how much variation there is in HIV and whether different versions have different transmission pathways!

Saved - September 5, 2025 at 4:49 PM
reSee.it AI Summary
I reported on various studies highlighting the presence of residual plasmid DNA, including the SV40 promoter, in COVID-19 vaccine vials from companies like Pfizer, Moderna, and Daiichi-Sankyo. Researchers from multiple institutions found levels exceeding regulatory limits, raising concerns about potential integration into human cells and associated risks. The findings have been shared with regulatory bodies, and discussions continue regarding the implications of these contaminants on vaccine safety. The issue remains a topic of ongoing scrutiny and debate.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Kevin McKernan Profession: Founder of Medicinal Genomics, Genomics Researcher, US Date First Reported: 2023-02 Key Details: Detected 225-843ng/dose residual plasmid DNA including SV40 promoter in Pfizer/Moderna vials using qPCR/fluorometry; exceeds regulatory limits; integration concerns. Sharable Link: https://osf.io/mjc97/

DNA fragments detected in monovalent and bivalent Pfizer/BioNTech and Moderna modRNA COVID-19 vaccines from Ontario, Canada: Exploratory dose response relationship with serious adverse events. Background: In vitro transcription (IVT) reactions used to generate nucleoside modified RNA (modRNA) for SARS-CoV-2 vaccines currently rely on an RNA polymerase transcribing from a DNA template. Production of modRNA used in the original Pfizer randomized clinical trial (RCT) utilized a PCR-generated DNA template (Process 1). To generate billions of vaccine doses, this DNA was cloned into a bacterial plasmid vector for amplification in Escherichia coli before linearization (Process 2), expanding the size and complexity of potential residual DNA and introducing sequences not present in the Process 1 template. It appears that Moderna used a similar plasmid-based process for both clinical trial and post-trial use vaccines. Recently, DNA sequencing studies have revealed this plasmid DNA at significant levels in both Pfizer-BioNTech and Moderna modRNA vaccines. These studies surveyed a limited number of lots and questions remain regarding the variance in residual DNA observed internationally. Methods: Using previously published primer and probe sequences, quantitative polymerase chain reaction (qPCR) and Qubit® fluorometry was performed on an additional 27 mRNA vials obtained in Canada and drawn from 12 unique lots (5 lots of Moderna child/adult monovalent, 1 lot of Moderna adult bivalent BA.4/5, 1 lot of Moderna child/adult bivalent BA.1, 1 lot of Moderna XBB.1.5 monovalent, 3 lots of Pfizer adult monovalent, and 1 lot of Pfizer adult bivalent BA.4/5). The Vaccine Adverse Events Reporting System (VAERS) database was queried for the number and categorization of adverse events (AEs) reported for each of the lots tested. The content of one previously studied vial of Pfizer COVID-19 vaccine was examined by Oxford Nanopore sequencing to determine the size distribution of DNA fragments. This sample was also used to determine if the residual DNA is packaged in the lipid nanoparticles (LNPs) and thus resistant to DNaseI or if the DNA resides outside of the LNP and is DNaseI labile.  Results: Quantification cycle (Cq) values (1:10 dilution) for the plasmid origin of replication (ori) and spike sequences ranged from 18.44 - 24.87 and 18.03 - 23.83 and for Pfizer, and 22.52 – 24.53 and 25.24 – 30.10 for Moderna, respectively. These values correspond to 0.28 – 4.27 ng/dose and 0.22 - 2.43 ng/dose (Pfizer), and 0.01 -0.34 ng/dose and 0.25 – 0.78 ng/dose (Moderna), for ori and spike respectively measured by qPCR, and 1,896 – 3,720 ng/dose and 3,270 – 5,100 ng/dose measured by Qubit® fluorometry for Pfizer and Moderna, respectfully. The SV40 promoter-enhancer-ori was only detected in Pfizer vials with Cq scores ranging from 16.64 – 22.59. In an exploratory analysis, we found preliminary evidence of a dose response relationship of the amount of DNA per dose and the frequency of serious adverse events (SAEs). This relationship was different for the Pfizer and Moderna products. Size distribution analysis found mean and maximum DNA fragment lengths of 214 base pairs (bp) and 3.5 kb, respectively. The plasmid DNA is likely inside the LNPs and is protected from nucleases. Conclusion: These data demonstrate the presence of billions to hundreds of billions of DNA molecules per dose in these vaccines. Using fluorometry, all vaccines exceed the guidelines for residual DNA set by FDA and WHO of 10 ng/dose by 188 – 509-fold. However, qPCR residual DNA content in all vaccines were below these guidelines emphasizing the importance of methodological clarity and consistency when interpreting quantitative guidelines. The preliminary evidence of a dose-response effect of residual DNA measured with qPCR and SAEs warrant confirmation and further investigation. Our findings extend existing concerns about vaccine safety and call into question the relevance of guidelines conceived before the introduction of efficient transfection using LNPs. With several obvious limitations, we urge that our work is replicated under forensic conditions and that guidelines be revised to account for highly efficient DNA transfection and cumulative dosing. osf.io

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@JillianMichaels DNA contamination with SV40 promoters, brewed in vats of E. coli poop soup. Sounds so “safe & effective.” 🤡

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Tomonori Nitta Profession: Researcher at Tokyo University, Japan Date First Reported: 2023-11 Key Details: Found 17.5-81.9ng/dose DNA in Japanese Daiichi-Sankyo vials; SV40 detected, including in tumors via cell transfection Sharable Link: https://pmc.ncbi.nlm.nih.gov/articles/PMC12095670/

Significant Increase in Excess Deaths after Repeated COVID-19 Vaccination in Japan Although Japan recorded the world’s highest rate of COVID-19 messenger ribonucleic acid (mRNA) vaccination doses per capita, COVID-19 cases and deaths exploded after the emergence of the Omicron variant, followed by a significant increase in excess ... pmc.ncbi.nlm.nih.gov

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Phillip Buckhaults Profession: Professor at University of South Carolina, Cancer Genomics Expert, US Date First Reported: 2023-09 (testimony), 2024-04 (data) Key Details: qPCR showed 1.5-18.7ng/dose plasmid DNA with SV40 promoter; observed integration into human stem cells; presented to SC Senate. Sharable Link: https://www.scstatehouse.gov/CommitteeInfo/SenateMedicalAffairsCommittee/PandemicPreparedness/Phillip-Buckhaults-SC-Senate-09122023-final.pdf

South Carolina Legislature Online - Error scstatehouse.gov

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Brigitte König & Jürgen O. Kirchner Profession: Independent Lab Analysts (MMD/Indep.), Germany Date First Reported: 2023-09 Key Details: Fluorometry/qPCR revealed 3600-5340ng/dose DNA exceeding limits; SV40 promoter confirmed; reported to German Ministry. (Note: Paper has an expression of concern.) Sharable Link: https://www.mdpi.com/2409-9279/7/3/41

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

David Speicher (with Kevin McKernan) Profession: Researcher at University of Guelph, Canada Date First Reported: 2023-10 (Ontario), 2024-03 (Australia) Key Details: qPCR/fluorometry on 27+ vials showed 0.22-510ng/dose DNA with SV40; dose-response to adverse events; reported to TGA, under litigation. Sharable Links https://osf.io/preprints/osf/mjc97 https://thedaviddeclaration.org/wp-content/uploads/2025/01/dr-speicher-report-re-australian-vials.pdf

DNA fragments detected in monovalent and bivalent Pfizer/BioNTech and Moderna modRNA COVID-19 vaccines from Ontario, Canada: Exploratory dose response relationship with serious adverse events. Background: In vitro transcription (IVT) reactions used to generate nucleoside modified RNA (modRNA) for SARS-CoV-2 vaccines currently rely on an RNA polymerase transcribing from a DNA template. Production of modRNA used in the original Pfizer randomized clinical trial (RCT) utilized a PCR-generated DNA template (Process 1). To generate billions of vaccine doses, this DNA was cloned into a bacterial plasmid vector for amplification in Escherichia coli before linearization (Process 2), expanding the size and complexity of potential residual DNA and introducing sequences not present in the Process 1 template. It appears that Moderna used a similar plasmid-based process for both clinical trial and post-trial use vaccines. Recently, DNA sequencing studies have revealed this plasmid DNA at significant levels in both Pfizer-BioNTech and Moderna modRNA vaccines. These studies surveyed a limited number of lots and questions remain regarding the variance in residual DNA observed internationally. Methods: Using previously published primer and probe sequences, quantitative polymerase chain reaction (qPCR) and Qubit® fluorometry was performed on an additional 27 mRNA vials obtained in Canada and drawn from 12 unique lots (5 lots of Moderna child/adult monovalent, 1 lot of Moderna adult bivalent BA.4/5, 1 lot of Moderna child/adult bivalent BA.1, 1 lot of Moderna XBB.1.5 monovalent, 3 lots of Pfizer adult monovalent, and 1 lot of Pfizer adult bivalent BA.4/5). The Vaccine Adverse Events Reporting System (VAERS) database was queried for the number and categorization of adverse events (AEs) reported for each of the lots tested. The content of one previously studied vial of Pfizer COVID-19 vaccine was examined by Oxford Nanopore sequencing to determine the size distribution of DNA fragments. This sample was also used to determine if the residual DNA is packaged in the lipid nanoparticles (LNPs) and thus resistant to DNaseI or if the DNA resides outside of the LNP and is DNaseI labile.  Results: Quantification cycle (Cq) values (1:10 dilution) for the plasmid origin of replication (ori) and spike sequences ranged from 18.44 - 24.87 and 18.03 - 23.83 and for Pfizer, and 22.52 – 24.53 and 25.24 – 30.10 for Moderna, respectively. These values correspond to 0.28 – 4.27 ng/dose and 0.22 - 2.43 ng/dose (Pfizer), and 0.01 -0.34 ng/dose and 0.25 – 0.78 ng/dose (Moderna), for ori and spike respectively measured by qPCR, and 1,896 – 3,720 ng/dose and 3,270 – 5,100 ng/dose measured by Qubit® fluorometry for Pfizer and Moderna, respectfully. The SV40 promoter-enhancer-ori was only detected in Pfizer vials with Cq scores ranging from 16.64 – 22.59. In an exploratory analysis, we found preliminary evidence of a dose response relationship of the amount of DNA per dose and the frequency of serious adverse events (SAEs). This relationship was different for the Pfizer and Moderna products. Size distribution analysis found mean and maximum DNA fragment lengths of 214 base pairs (bp) and 3.5 kb, respectively. The plasmid DNA is likely inside the LNPs and is protected from nucleases. Conclusion: These data demonstrate the presence of billions to hundreds of billions of DNA molecules per dose in these vaccines. Using fluorometry, all vaccines exceed the guidelines for residual DNA set by FDA and WHO of 10 ng/dose by 188 – 509-fold. However, qPCR residual DNA content in all vaccines were below these guidelines emphasizing the importance of methodological clarity and consistency when interpreting quantitative guidelines. The preliminary evidence of a dose-response effect of residual DNA measured with qPCR and SAEs warrant confirmation and further investigation. Our findings extend existing concerns about vaccine safety and call into question the relevance of guidelines conceived before the introduction of efficient transfection using LNPs. With several obvious limitations, we urge that our work is replicated under forensic conditions and that guidelines be revised to account for highly efficient DNA transfection and cumulative dosing. osf.io

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Didier Raoult Profession: Former Professor at Aix-Marseille University, Microbiologist, France Date First Reported: 2024-11 Key Details: Fluorometry/NGS detected 2712-5160ng/dose full plasmid DNA including SV40 promoter/enhancer; high copy numbers; integration risks. Sharable Link: https://hal.science/hal-04778576v1/document

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Ulrike Kämmerer Profession: Biologist at University Hospital of Würzburg, Germany Date First Reported: 2024-12 Key Details: Fluorometry/PCR/transfection showed 32.7-43.4ng/dose DNA in LNPs with SV40 promoter; successful cell transfection; spike protein expression. Sharable Link: https://www.researchgate.net/publication/386414408_BioNTech_RNA-Based_COVID-19_Injections_Contain_Large_Amounts_Of_Residual_DNA_Including_An_SV40_PromoterEnhancer_Sequence

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Tyler J. Wang, Alex Kim, Kevin Kim Profession: Students at Centerville High School (executed at FDA White Oak Campus), US Date First Reported: 2024-12 Key Details: Fluorometry/miniprep extracted replication-competent plasmid DNA exceeding limits; SV40 implied; no peer-reviewed confirmation of integration. Sharable Link: https://jhss.scholasticahq.com/article/127890-a-rapid-detection-method-of-replication-competent-plasmid-dna-from-covid-19-mrna-vaccines-for-quality-control

A rapid detection method of replication-competent plasmid DNA from COVID-19 mRNA vaccines for quality control | Published in Journal of High School Science By Tyler J Wang, Alex Kim & 1 more. DNA contamination is the primary reason that undermines public trust in the quality of mRNA vaccines. We report a method to detect residual replication-competent plasmid DNA present in mRNA vaccines. jhss.scholasticahq.com

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

V. Polacek Profession: Analyst at TILIA Laboratories s.r.o., Czech Republic Date First Reported: 2025-03 Key Details: qPCR found 10M-1B DNA copies/ml in 120 vials; tumorigenesis risks; no formal publication. Sharable Link: No direct public link found; announced by Slovak government investigator (referenced in regulatory contexts like https://www.tga.gov.au/sites/default/files/2024-12/FOI%2025-0070.pdf

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@Kevin_McKernan @P_J_Buckhaults @DJSpeicher @raoult_didier @DrCaliff_FDA @US_FDA @TGAgovau @EMA_News @WHO @RWMaloneMD @JesslovesMJK @stkirsch @CanningPharm @53v3n0fn1n3 @Fynnderella1 @CartlandDavid @drcole12 @dbkell @kacdnp91 @KevinMcCairnPhD @AnneliseBocquet @PinsolleT@blueskylou@Hudikaha thanks Kenji Fujikawa who compiled this list of DNA Plasmid Contaminatiion Why am I bringing it up again ? Well the problem hasn't gone away. #Stoptheshots #poojabs #informedconsent

@carl_jurassic - Jurassic Carl 🦖🐭

#poojabs #DirtyJibby

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@Kevin_McKernan @P_J_Buckhaults @DJSpeicher @raoult_didier @DrCaliff_FDA @US_FDA @TGAgovau @EMA_News @WHO @RWMaloneMD @JesslovesMJK @stkirsch @CanningPharm @53v3n0fn1n3 @Fynnderella1 @CartlandDavid @drcole12 @dbkell @kacdnp91 @KevinMcCairnPhD @AnneliseBocquet @PinsolleT @FluoridePoison

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@Kevin_McKernan @P_J_Buckhaults @DJSpeicher @raoult_didier @DrCaliff_FDA @US_FDA @TGAgovau @EMA_News @WHO @RWMaloneMD @JesslovesMJK @stkirsch @CanningPharm @53v3n0fn1n3 @Fynnderella1 @CartlandDavid @drcole12 @dbkell @kacdnp91 @KevinMcCairnPhD @AnneliseBocquet @PinsolleT @FluoridePoison Strange his tag didn't work..

@WakingUp2020 - Mrs Doubt Pfizer

"The Pfizer vaccine is contaminated with DNA, it's not just mRNA, it’s got bits of DNA in it." - Professor Phillip Buckhaults, Phd in Biochemistry and Molecular Biology. He does cancer genomics research at the University of South Carolina. https://www.scstatehouse.gov/video/archives.php?key=13489&fbclid=IwAR3IhAShh8cjjLBIeIaVIdKebVJJwa58mOijP7GM2EyD_CiiySjVmVZBW5A_aem_AVmIVMu43UMMtpll_BQOdvd8sxRkz_KQu9jYC-akyaR3InCeQ6-FZEloy9X1TzTToTM

Video Transcript AI Summary
"Pfizer vaccine is contaminated with plasma DNA. It's not just mRNA." "This DNA is the DNA vector that was used as the template for the in vitro transcription reaction when they made the mRNA." "I sequenced it in my own lab." "The vials of Pfizer vaccine that were given out here in Colombia, one of my colleagues was in charge of that vaccination program in the College of Pharmacy." "And for reasons that I still don't understand, he kept every single vial." "So he had a whole freezer full of the empty vials." "And I checked these two batches, and I checked them by sequencing." "It's surprising that there's any DNA in there." "This DNA, in my view, it could be causing some of the rare but serious side effects like death from cardiac arrest."
Full Transcript
Speaker 0: Hand lawns razor, which is never attribute malice to that which can be better explained by incompetence. And so I'm trying to be gracious here in many circumstances. There could be malice underneath, but I'm trying to see just incompetence to be gracious. So the Pfizer vaccine is contaminated with plasma DNA. It's not just mRNA. It's got bits of DNA in it. This DNA is the DNA vector that was used as the template for the in vitro transcription reaction when they made the mRNA. I know this is true because I sequenced it in my own lab. The vials of Pfizer vaccine that were given out here in Columbia, one of my colleagues was in charge of that vaccination program in the College of Pharmacy. And for reasons that I still don't understand, he kept every single vial. So he had a whole freezer full of the empty vials. Well, the empty vials have a little tiny bit in the in the bottom of them. He gave them all to me, and I looked at them. We had two batches that were given out here in Colombia. And I checked these two batches, and I checked them by sequencing. And I sequenced all the DNA that was in the vaccine, and I can see what's in there. And it's surprising that there's any DNA in there. And you can kind of work out what it is and how it got there, and I'm kind of alarmed about the possible consequences of this, both in terms of human health and biology, but you should be alarmed about regulatory process that allowed it to get there. So this DNA, in my view, it could be causing some of the rare but serious side effects like death from cardiac arrest. There's a lot of cases now of people having suspicious death after vaccine. It's hard to prove what caused it. It's just, you know, temporally associated. And this DNA is a plausible mechanism. Okay? This DNA can and likely will integrate into the genomic DNA of cells that got transfected with the vaccine mix. This is just the way it works. We do this in the lab all the time. We take pieces of DNA, we mix them up with a lipid complex like the Pfizer vaccine is in. We pour it onto cells and and a lot of it gets into the cells and a lot of it gets into the DNA of those cells and it becomes a permanent
Video Transcript AI Summary
The s v 40 sequences, they should not be there. They could have chosen another plasmid that did not have the s v 40 sequences. If these sequences sit above an oncogene and they're promiscuous, that means they are likely to integrate in places more likely than other genetic inserts. Insertional mutagenesis anyway causes cancer, and that's the risk. That's why gene therapies were not brought to market for so many years because there was a risk of causing cancer from insertional mutagenesis. We never needed these vaccines. Hydroxychloroquine and ivermectin, I can tell you as a toxicologist, they are not toxic. They're some of the safest drugs you can use. Endotoxin levels: they've got them all redacted. Why would you redact them if you were trying to be transparent? Why would you hold the data for seventy five years?
Full Transcript
Speaker 0: Said earlier nefarious. You felt like this was more nefarious than doctor Burkholder. In what sense are you saying that? Speaker 1: The s v 40 sequences, they should not be there. They don't need to be there to grow this into back to grow this in bacteria. I don't think it's an accident. They could have chosen another plasmid that did not have the s v 40 sequences. If these sequences sit above an oncogene and and they're promiscuous, that means they are likely to to integrate in places more likely than other genetic inserts. Thank you so much. Then they can cause cancer. Insertional mutagenesis anyway causes cancer, and that's the risk. That's why gene therapies were not brought to market for so many years because there was a risk of causing cancer from insertional mutagenesis. We never needed these vaccines. We had treatments that worked. One of our doctors here is gonna tell you about that. Hydroxychloroquine and ivermectin, I can tell you as a toxicologist, they are not toxic. They're they're some of the safest drugs you can use. I there's no reason once the FDA found out about this contamination. Okay? And we looked to see endotoxin levels, but they've got them all redacted. Why would you redact them if you were trying to be transparent? Why would you hold the data for seventy five years?
Video Transcript AI Summary
Key points: "the vials that were in fact approved are not the vials that were given to the public." The clinical trial used "process one that used PCR to make the DNA that was going to then turn into the RNA to make the spike protein." After the trial, "they switched" to a production process that "manufactured this DNA in E. Coli," introducing endotoxin risk. "There are these plasmids that have additional DNA that were not present in the actual clinical trial." Sequencing found mixtures, including "expired" and samples that had "been tapped into." Regarding Pfizer, "the Pfizer vaccines actually had a component that was not disclosed to the regulators." "The plasmid map on the right is what was disclosed to the EMA" with "no mention of the SV40 components" now "inside this DNA sequence." "The plasma on the left is what we actually found," with components not disclosed to regulators nor to patients. Monovalent Pfizer; prior ones were the bivalent vaccines from Moderna and Pfizer.
Full Transcript
Speaker 0: This all started back in April with this preprint where we did this RNA sequencing that Mark was just mentioning. This can give you more of the details that we're going to go into here very briefly. Will remind you, what is not in that preprint is something that Retzaflevy and Josh Gutzkow presented in the BMJ, which is that the vials that were in fact approved are not the vials that were given to the public. The clinical trial was run on something known as process one that used PCR to make the DNA that was going to then turn into the RNA to make the spike protein. Once the trial was complete, they switched. This is a big bait and switch. They moved to a production process that manufactured this DNA in E. Coli, and with that comes a different risk. There's clean DNA on the left, which is process one. There's no background E. Coli, there's no endotoxin present in this process. When they switch to scale this up, they put this plasmid into E. Coli to grow it and replicate it, and Now you have to get the DNA out of E. Coli and not have any of the parts of E. Coli come with it. Unfortunately, are parts of E. Coli that can create anaphylaxis, something known as endotoxin. There are these plasmids that have additional DNA that were not present in the actual clinical trial. So we started sequencing lots that were a mixture, some that were in fact not expired but had been tapped into by clinicians and other ones that were unopened but were expired. These are the monovalent vaccines for Pfizer, the prior ones were the bivalent vaccines from Moderna and Pfizer. Upon sequencing these, I think the most striking revelation was that the Pfizer vaccines actually had a component that was not disclosed to the regulators. This plasmid map on the right is what was disclosed to the EMA and there is no mention of the SV40 components that are now known to be inside this this DNA sequence. The plasma on the left is what we actually found, very similar in length but has all of these other components in it that are not disclosed to the regulators nor to the patients taking these.
South Carolina Legislature Video Archives scstatehouse.gov

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@Kevin_McKernan @P_J_Buckhaults @DJSpeicher @raoult_didier @DrCaliff_FDA @US_FDA @TGAgovau @EMA_News @WHO @RWMaloneMD @JesslovesMJK @stkirsch @CanningPharm @53v3n0fn1n3 @Fynnderella1 @CartlandDavid @drcole12 @dbkell @kacdnp91 @KevinMcCairnPhD @AnneliseBocquet @PinsolleT @FluoridePoison https://t.co/wcZEIr8RxF

@joshg99 - Josh Guetzkow

For background and more information on the Pfizer/BioNTech bait-and-switch scandal, see this thread. 👇 https://t.co/gJZn3h9hal

@joshg99 - Josh Guetzkow

Was the Pfizer/BioNTech vaccine clinical trial a bait-and-switch? There were >44,000 people in the trial, but only ~250 of them were given doses made with a new manufacturing method ('process 2') that was used to make enough doses to sell around the world.

@joshg99 - Josh Guetzkow

Was the Pfizer/BioNTech vaccine clinical trial a bait-and-switch? There were >44,000 people in the trial, but only ~250 of them were given doses made with a new manufacturing method ('process 2') that was used to make enough doses to sell around the world.

Saved - September 2, 2025 at 3:30 PM

@DrTomFrieden - Dr. Tom Frieden

I joined eight former CDC directors—spanning Republican and Democratic administrations—to share this warning: our nation’s health is at risk.  The very systems that protect us from disease, cancer, and future health threats are being dismantled. https://www.nytimes.com/2025/09/01/opinion/cdc-leaders-kennedy.html

Saved - August 29, 2025 at 6:53 PM
reSee.it AI Summary
I expressed concern about Taubenberger's work on reconstructing pandemic H1N1 from 1918 Inuit lungs, questioning the rationale behind it. In 2018, I shared a paper that emphasized the significant threat this research poses to humanity. I highlighted that Taubenberger's proposed solution involves conducting risky gain-of-function research in US government labs, which have a questionable safety record. I also challenged others to address this documented fact.

@Fynnderella1 - Dr. Lynn Fynn-derella🐭

Taubenburger is a red flag. He originally reconstructed pandemic H1N1 out of permafrost-erected Inuit lungs from 1918! Why would we do that? Please reconsider @NIHDirector_Jay https://t.co/BKO23jztlO

@Fynnderella1 - Dr. Lynn Fynn-derella🐭

In 2018 this paper highlighted the true threat to humanity. Link in next post. https://t.co/Bgr7xgJYAg

@Fynnderella1 - Dr. Lynn Fynn-derella🐭

https://arxiv.org/pdf/1709.01149

@Fynnderella1 - Dr. Lynn Fynn-derella🐭

https://t.co/eMDPJV7LG5

@Rebecca21951651 - Rebecc@ ███████

@NIHDirector_Jay @NIAIDNews @NIH Yes Taubenberger's proposed solution is to do the dangerous GoFROC/DURC work in USG labs, that also do not have a great safety record. https://www.youtube.com/watch?v=rRjBpBCn5Eo minute 37 https://t.co/TV32lxn8nd

@Fynnderella1 - Dr. Lynn Fynn-derella🐭

@IntuitAVC @NIHDirector_Jay Are you refuting this documented fact?

Saved - August 29, 2025 at 10:47 AM
reSee.it AI Summary
Dr. Makary stated that all adults can still choose to get vaccinated, emphasizing no limitations on availability. In response, concerns were raised about the continued availability of vaccines after the Emergency Use Authorization ended, suggesting a lack of proper long-term safety assessments. Critics highlighted that immunocompromised individuals, who are more vulnerable, are being recommended these vaccines without transparent risk-benefit discussions. Additionally, the ongoing immunity from lawsuits for manufacturers was noted as a significant issue, contributing to public distrust in health authorities.

@DrMakaryFDA - Dr. Marty Makary

100% of adults in this country can still get the vaccine if they choose. We are not limiting availability to anyone.

@JeromeAdamsMD - Jerome Adams

I’m deeply concerned about the new FDA move limiting COVID vaccines only to “high-risk groups.” CDC data shows those 50+ face rising risks, with 65+ at up to 340x higher death risk. Add in those with chronic disease and 71% of U.S. adults are at elevated risk!

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

The EUA may be gone, but the shots are still on the market now pushed on those with compromised immune systems. https://t.co/eH6e2ZXWOr The EUA (Emergency Use Authorization) was supposed to be temporary, but the shots remained available through other regulatory pathways instead of being pulled and reassessed. This creates the appearance of oversight while actually bypassing proper long-term safety checks. Instead of being cautious, regulators now recommend these products for immunocompromised people the very group with weaker defenses and a higher risk of side effects. Even after EUA, manufacturers still enjoy immunity from lawsuits under U.S. law (PREP Act), leaving injured people without recourse. The general public, and especially vulnerable groups, are not told about the risks vs. benefits in a transparent way. Keeping the shots available despite questionable efficacy and mounting safety concerns deepens distrust in public health authorities. @SecKennedy @NIHDirector_Jay This simply isn't good enough. Humanity definitely deserves better. #InformedConsent

@kacdnp91 - Kelly DNP Functional/Integrative Medicine

There it is. 4 new Cvd 💉

@lisachristinect - Lisa Christine •.

Here is the clip to listen for yourself:

Video Transcript AI Summary
"The FDA recently revoked the emergency youth authorizations for three COVID vaccinations while simultaneously green lighting four new COVID nineteen vaccines with twenty twenty five and twenty twenty six formulas." "The the reason for the revocation of that emergency youth authorization is because obviously the COVID pandemic and the public health emergency is over." "But just to correct the record because there's been a lot of misinformation on this, the FDA's decision does not affect the availability of COVID vaccines for Americans who want them." "We believe in individual choice. That's a promise both the president and the secretary have made, and it's a promise they have now delivered on."
Full Transcript
Speaker 0: From miscommunications or differences on vaccine policy. So I wonder if you could just say whether or not the president believes that the COVID vaccine should be available to and covered by insurance for all Americans regardless of age and preexisting conditions? Speaker 1: What I will tell you is that the FDA recently revoked the emergency youth authorizations for three COVID vaccinations while simultaneously green lighting four new COVID nineteen vaccines with twenty twenty five and twenty twenty six formulas. The the reason for the revocation of that emergency youth authorization is because obviously the COVID pandemic and the public health emergency is over. But just to correct the record because there's been a lot of misinformation on this, the FDA's decision does not affect the availability of COVID vaccines for Americans who want them. We believe in individual choice. That's a promise both the president and the secretary have made, and it's a promise they have now delivered on. Speaker 0: Any question if I could

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

It switches on EVERY major disease pathway known to man AND accelerates all 9 hallmarks of aging. That means faster aging, faster illness, longer suffering. Man I love the people who I follow. @SecKennedy @NIHDirector_Jay #NotGoodEnough #StoptheShots https://t.co/Cbfw5g8sBR

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@PatrickEWa92418 @MakingSenseInfo @laoneill111 The spike protein is a molecular wrecking ball. It switches on EVERY major disease pathway known to man AND accelerates all 9 hallmarks of aging. That means faster aging, faster illness, longer suffering. #SpikeProtein #mRNA #CellularDamage #ChronicDisease #Aging #Epigenetics

Saved - August 27, 2025 at 3:29 PM
reSee.it AI Summary
I've explored the alarming rise in deaths among infants under one year old in the USA, particularly since 2021. My analysis reveals significant increases in female deaths, with a notable rise in deaths of unknown causes, indicating a potential new pathology. The data shows that while black babies have not seen an increase in mortality, white babies have experienced a concerning surge. This trend is not merely a continuation of previous causes and suggests a deeper issue that warrants urgent attention.

@ClareCraigPath - Dr Clare Craig

USA - your babies are dying. I have taken a deep dive to understand exactly what's happening with deaths of under 1 year olds. Who wants to look at baby deaths? I get it. But DO NOT LOOK AWAY. It is.... https://t.co/STjt6NqsdE

@ClareCraigPath - Dr Clare Craig

First of all I did this because of frustration with people arguing over what "expected" deaths should look like. You can make up reasons for picking particular years and come up with a totally different story. '99-'19 excess deaths from '21 '11-'16 deficit in deaths from '21 https://t.co/TP6DpOj4Jd

@ClareCraigPath - Dr Clare Craig

What can we do to see if the rise is meaningful? First we can look monthly ('24 and '25 data is incomplete) Here are the monthly deaths for females which rises from March 2021 (having been below expected before) and stays high except for deficit in winter 2021-2022. https://t.co/eVK3F1Q47W

@ClareCraigPath - Dr Clare Craig

Here's the same for males. The excess is not as high. Female excess '21-'23 inclusive = 1523 Male excess '21-'23 inclusive = 890 https://t.co/a3kSU0vVu5

@ClareCraigPath - Dr Clare Craig

Here is the percentage of deaths that were female. This is highly statistically significant and highly indicative of a new pathology not present in 2020. https://t.co/jekCt2dgWO

@ClareCraigPath - Dr Clare Craig

Next I looked at cause of death. SIDS was 76% of deaths of unknown cause in under 1s in 1999 but only half by 2019. Therefore, I looked at all deaths of unknown cause. Again there is a highly statistically significant rise from 2021 on. https://t.co/sKZyNAd8qK

@ClareCraigPath - Dr Clare Craig

Lastly, I looked at race differences. CDC coding and definitions keep changing but I am hoping they were at least consistent for both deaths and populaiton making mortality rate reliable. Groupings changed so I just looked at white and black / african american. Female: https://t.co/7lwAX1iBFE

@ClareCraigPath - Dr Clare Craig

The ratio of white to black babies dying has, like the other markers, rocketed since 2021. It is statistically significant but worse for females. Males https://t.co/oYyuWuziQ9

@ClareCraigPath - Dr Clare Craig

It turns out that black babies (while they sadly die more overall) have not seen an increase since 2021. The increase is in white babies. Females https://t.co/aSVo6IC2Es

@ClareCraigPath - Dr Clare Craig

Males https://t.co/Fow0oaBPQB

@ClareCraigPath - Dr Clare Craig

These deaths include deaths attributed to covid (a total of about 350) - but notably the same age group did not see many deaths in 2020. Unlike for other age groups children saw worse covid mortality than 2020 only after vaccines were introduced. And 2023>2021! https://t.co/FjqNZmPdqz

@ClareCraigPath - Dr Clare Craig

With three statistically significant and large signals in sex ratio, deaths of unknown cause and race ratio there is indeed a cause for alarm. The rise is real. In 2021, I reassured friends that when the babies started dying it would all be over. I was so very wrong.

@ClareCraigPath - Dr Clare Craig

full article on DrClareCraig S* Stack

@ClareCraigPath - Dr Clare Craig

@HopeRising19 More female deaths tells us this is not simply more of the same causes as before. It indicates a new pathology from 2021. The new pathology is more prevalent in white babies. That is not what you would see from economic stresses nor from most previous causes of death.

Saved - August 21, 2025 at 11:47 AM
reSee.it AI Summary
When selecting an injectable medicinal product, it's crucial to avoid those derived from cancer-like cell lines, such as Shingrix, which uses CHO (Chinese Hamster Ovary) cells. Both Shingrix and Zostavax have serious warnings and lawsuits related to Guillain-Barré Syndrome. Neither vaccine effectively prevents shingles, with diminishing effectiveness over time. I advocate for a metabolically healthy lifestyle through a low-carb diet, sun exposure, and exercise, while emphasizing natural healing methods. Concerns persist about the lack of carcinogenicity studies for Shingrix.

@Jikkyleaks - Jikkyleaks 🐭

🚨 What you really don't want to do when choosing an injectable medicinal product... is choose one made from a cancer-like cell line that also contains an SV40 promoter in its residual plasmid. Oops. Too late. #Shingrix @MaryanneDemasi @DrJulieSladden @Kevin_McKernan

@ValerieAnne1970 - Valerie Anne Smith

I have researched Vaccines for many years & will never get a Shingles Vaccine. Zostavax uses Human Aborted Fetal Cell Lines. Shingrix uses CHO Chinese Hamster Ovary. Both Zostavax & Shingrix have Black Box Warnings for Guillain-Barré Syndrome (GBS) & 900+ active lawsuits filed by vaccine injured individuals &/or surviving family from fatality. Zostavax: Human cell lines WI-38(3 month aborted female) & MRC-5(3 month aborted male). Shingrix: CHO Chinese Hamster Ovary Neither Vaccine prevents Shingles nor prevents transmission. Shingles Vaccine Effectiveness: Year 1: 67% Effective Year 2: 50% Year 8: 27% Year 10: 15% I personally know 5 people who were ill with Shingles within 30days of receiving their 1st dose of the Shingrix Vaccine. And 2 people who contracted GBS Guillain-Barre' Syndrome after receiving their 2nd Shingrix Dose. Zostavax contains Sucrose, Porcine Gelatin, MSG Monosodium L-Glutamate, Sodium Phosphate Dibasic, Potassium Phosphate Monobasic, Potassium Chloride, Urea & Host Cell CHO Chinese Hamster Ovary. Shingrix contains 5 toxic Phosphates, DOPC, MPL which comes from the cell wall of Salmonella, QS-21, Polysorbate 80, Sucrose, Host Aborted Fetal Cell Protein & DNA. I believe in being Metabolically Healthy by utilizing an Ancestral Low Carb Diet, Sun exposure, Lower Toxic Exposure & Exercise to prevent illness. Then I implement natural root cause healing protocols in the event that illness does occur. 93% of the population is Metabolically Unhealthy which is the #1 driver of disease. Citations: https://www.preprints.org/manuscript/202312.0688/v1 https://www.fda.gov/vaccines-blood-biologics/safety-availability-biologics/fda-requires-warning-about-guillain-barre-syndrome-gbs-be-included-prescribing-information-shingrix https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9696857/ https://connect.mayoclinic.org/discussion/shingrix/?pg=46

Recurrence of a Rare Subtype of Guillain-Barré Syndrome Following a Second Dose of the Shingles Vaccine Guillain-Barré Syndrome (GBS) is an acute, immune-mediated polyneuropathy. The exact cause of GBS remains unknown, however, it commonly develops post-infection. Since the 1950s, various vaccines have been attributed to causing the syndrome, yet no ... pmc.ncbi.nlm.nih.gov

@HalCranmer - A Paradise for Parents

@ValerieAnne1970 Wonderful. Thank you. What do you think of the shingles vaccine?

@Jikkyleaks - Jikkyleaks 🐭

The plasmid maps for Gardasil 9, Bexsero and Shingrix released under FOI from the TGA @karrichapus https://www.tga.gov.au/sites/default/files/2025-05/FOI%2025-0137%20-%20Documents%20as%20published%20on%2015%20May%202025.pdf

@Jikkyleaks - Jikkyleaks 🐭

The cell line used to produce Shingrix is the CHO (chinese hamster ovary) cell line. It is an immortalised cell line which means it continues to grow, just like cancer cells do. It does this because it has gained or lost genes that tell it not to. https://www.chop.edu/vaccine-education-center/vaccine-safety/vaccine-ingredients/ingredients-by-vaccine/shingles-vaccine-ingredients

Ingredients in Shingles Vaccine This page shows the ingredients in the shingles vaccines currently available for use in the U.S. chop.edu

@Jikkyleaks - Jikkyleaks 🐭

Despite using an immortalised cell line and a SV40 promoter containing plasmid, no carcinogenicity studies were performed on Shingrix. Great. https://biologyinsights.com/what-are-cho-cells-and-how-do-they-make-medicines/ https://www.tga.gov.au/sites/default/files/auspar-recombinant-varicella-zoster-virus-glycoprotein-e-antigen-181212.pdf

What Are CHO Cells and How Do They Make Medicines? Learn how a specific mammalian cell line became a living factory for modern medicine, enabling the production of complex and life-saving biopharmaceutical drugs. biologyinsights.com

@Jikkyleaks - Jikkyleaks 🐭

"Carcinogenicity studies were not performed"... "Acute Myeloid Leukaemia"... "Apart from the finding on ovarian cancer there were no evident signals"... "Data collated to Month 8.. could not be located" Trust us bro. /end @RetsefL @RWMaloneMD @DrJBhattacharya

@Jikkyleaks - Jikkyleaks 🐭

@RetsefL @RWMaloneMD @DrJBhattacharya ICYMI - why the plasmids matter https://www.arkmedic.info/p/would-you-like-plasmids-with-that

Would you like Plasmids with that? A bombshell finding implicates ALL recombinant vaccines in the DNA contamination scandal and requires urgent investigation arkmedic.info
Saved - August 21, 2025 at 6:29 AM
reSee.it AI Summary
ACIP has initiated a comprehensive review of Covid-19 vaccines under my leadership, focusing on critical questions that were previously overlooked. I have consistently challenged the CDC on their data presentation and safety assessments, particularly regarding delayed effects and the safety of RSV monoclonal antibodies. Our new working group will investigate various concerns, including DNA contamination and long-term health impacts. This effort aims to restore public trust by addressing sensitive issues that have long been dismissed.

@MaryanneDemasi - Maryanne Demasi, PhD

💥BREAKING: ACIP launches sweeping Covid-19 vaccine review under Retsef Levi Billions of Covid vaccine doses were rolled out on assurances they were safe and effective. Now, ACIP’s new Covid immunisation working group is asking the questions regulators never did. 👇👇 @RetsefL @FLSurgeonGen @TheChiefNerd @newstart_2024 @Jikkyleaks

@MaryanneDemasi - Maryanne Demasi, PhD

MIT professor @RetsefL has been an outspoken voice on the @CDCgov's vaccine advisory committee (ACIP) since @SecKennedy's dramatic overhaul in June. Levi has pressed CDC officials on uncomfortable questions, challenging the narrow surveillance windows used to track harms and insisting that delayed effects could not simply be ruled out. He also raised concerns about the safety of RSV monoclonal antibodies after clinical trials showed a clear imbalance in infant deaths.

@MaryanneDemasi - Maryanne Demasi, PhD

Now, @RetsefL has been appointed chair of the @CDCgov's new Covid-19 vaccine working group, and with today’s release of its Terms of Reference, the scale of his task has come into sharp focus. Under the guidance of Levi and his colleagues, the ACIP working group now has a mandate unlike anything the committee has ever undertaken. For the first time, federal advisers will investigate the unresolved issues that have dogged the vaccines since their rushed rollout in late 2020.

@MaryanneDemasi - Maryanne Demasi, PhD

The new working group, involving @RWMaloneMD, will assess everything from DNA contamination in the products, to the persistence of spike protein & mRNA in the body, from immune class switching following repeated boosting to safety in pregnancy, cardiovascular risks, and long-term disability, the list of questions is as sweeping as it is sensitive. https://blog.maryannedemasi.com/p/breaking-acip-launches-sweeping-covid

BREAKING: ACIP launches sweeping Covid-19 vaccine review under Retsef Levi Billions of Covid vaccine doses were rolled out on assurances they were safe and effective. Now, ACIP’s new Covid immunisation working group is asking the questions regulators never did. blog.maryannedemasi.com

@MaryanneDemasi - Maryanne Demasi, PhD

The stakes could not be higher. Covid-19 vaccines remain one of the most divisive issues in medicine, and the CDC’s credibility has been battered by accusations of selective data presentation. Only this week, experts accused the agency of obscuring seizure risks from RSV monoclonal antibodies by slicing the data into subgroups that hid a statistically significant signal. https://blog.maryannedemasi.com/p/exclusive-did-the-cdc-mislead-its

EXCLUSIVE: Did the CDC mislead its advisers on the RSV antibody for babies? CDC assured ACIP the RSV antibody for newborns was safe, but buried in its data was a statistically significant signal — nearly a 4-fold higher risk of seizures shortly after the injection. blog.maryannedemasi.com

@MaryanneDemasi - Maryanne Demasi, PhD

The creation of a Covid-19 working group will be more than bureaucratic housekeeping—it is a test of whether ACIP can restore the public’s trust by confronting uncomfortable truths. How this will play out is uncertain? See my exclusive interview with chair, @RetsefL 👇 https://blog.maryannedemasi.com/p/breaking-acip-launches-sweeping-covid @VigilantFox

BREAKING: ACIP launches sweeping Covid-19 vaccine review under Retsef Levi Billions of Covid vaccine doses were rolled out on assurances they were safe and effective. Now, ACIP’s new Covid immunisation working group is asking the questions regulators never did. blog.maryannedemasi.com

@MaryanneDemasi - Maryanne Demasi, PhD

Will the new working group gather research & assess long-term harms of the Covid-19 vaccines? @React19org @BrianneDressen

@MaryanneDemasi - Maryanne Demasi, PhD

Are the Covid-19 vaccines safe in pregnancy?

@MaryanneDemasi - Maryanne Demasi, PhD

What will you be seeking to investigate the issue of DNA contamination in the covid-19 injections? @Kevin_McKernan @DJSpeicher @JesslovesMJK @Double_Christ

@MaryanneDemasi - Maryanne Demasi, PhD

Would you consider Covid-19 injections to be "gene therapies" ? @JesslovesMJK @Kevin_McKernan @RWMaloneMD

@MaryanneDemasi - Maryanne Demasi, PhD

For years, critics who raised concerns about DNA contamination, biodistribution, immune imprinting, or reproductive safety were dismissed as “alarmists” and spreaders of “misinformation.” Now, the @CDCgov own advisory body has committed to revisiting each of those questions in detail. See the FULL story and please SUBSCRIBE to my newsletter 👇https://blog.maryannedemasi.com/p/breaking-acip-launches-sweeping-covid @MdBreathe @DrMakaryFDA @TracyBethHoeg

BREAKING: ACIP launches sweeping Covid-19 vaccine review under Retsef Levi Billions of Covid vaccine doses were rolled out on assurances they were safe and effective. Now, ACIP’s new Covid immunisation working group is asking the questions regulators never did. blog.maryannedemasi.com
Saved - August 18, 2025 at 11:11 AM
reSee.it AI Summary
I explore the relationship between viruses, p53, and cancer. Viruses inhibit p53 to evade host defenses, potentially leading to cancer. Latent viruses like EBV and HBV are classified as carcinogens, and infections can reactivate dormant cancer cells. The concept of "turbo cancers" suggests a mix of new and reactivated cancers, possibly exacerbated by persistent viral protein expression from vaccines. I also discuss the risks of DNA contamination in vaccines and the potential for immune dysregulation to trigger aggressive tumor development. Following experts in this field is crucial for understanding these complex issues.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Scientific thought: If a virus seeks to persist, it must block p53. Why? Because p53 triggers cellular apoptosis = death of the host cell and, therefore, elimination of the virus at the same time. Latent viruses are therefore potentially carcinogenic. Because inhibiting p53 also allows dysfunctional cells to survive. If an infection can reactivate dormant cancer cells, what about de novo carcinogenesis? Are the observed cancers multiple, presenting in various cancerous forms? If we inject carcinogenic viral proteins with the aim of immunization, could this reactivate dormant cancer cells in the same way as pathogens? And induce de novo carcinogenesis? In other words, in the case of turbo cancers, are we not facing cancers of different types and different origins — both de novo + reactivation of dormant cancer cells? And facing a “virus + injection” combo? Have a good day.

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Pensée scientifique : Si un virus cherche à persister, il lui faut bloquer la p53. Pourquoi ? Parce que la p53 déclenche l'apoptose cellulaire = mort de la cellule hôte et donc, élimination du virus en même temps. Les virus latents sont donc potentiellement cancérigènes. Car inhiber la p53, ça permet aussi de maintenir des cellules dysfonctionnelles en vie. Si une infection peut réactiver des cellules cancéreuses en dormance, quid d'une cancérogenèse de novo ? Les cancers observés sont-ils multiples, présentant diverses formes cancéreuses ? Si on injecte des protéines virales cancérigènes, en vue d'une immunisation, est-ce que cela peut réactiver des cellules cancéreuses en dormance, de la même façon que les pathogènes ? Et induire une cancérogenèse de novo ? Autrement dit, n'est-on pas, dans le cadre des turbo cancers, face à des cancers de différents types et différentes origines, de novo + réactivation des cellules cancéreuses en dormance ? Et face à un combo "virus + injections" ? Bonne journée

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

p53 inhibition as a viral survival strategy Fact: p53 is a tumour suppressor protein that triggers cell cycle arrest or apoptosis in response to DNA damage or abnormal activity (including viral replication). Known examples: HPV: E6 protein binds to and degrades p53 → increases risk of cervical and oropharyngeal cancers. Adenoviruses, SV40, Hepatitis B, EBV: express proteins that block p53 or related pathways.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Latent viruses as carcinogens Fact: Epstein–Barr virus (EBV), Kaposi’s sarcoma-associated herpesvirus (KSHV/HHV-8), Hepatitis B virus (HBV), and Hepatitis C virus (HCV) are all officially classified as Group 1 carcinogens by IARC. Mechanism often involves immune evasion + inhibition of apoptosis + genomic instability.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Reactivation of dormant cancer cells Fact: Dormant disseminated tumour cells (DTCs) can survive for years, held in check by immune surveillance. Certain infections cause inflammation, cytokine release, and changes in the tumour microenvironment that can “wake up” dormant cells.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Integration events The “turbo cancer” reports from some clinicians suggest: Highly aggressive tumours Diverse histological types (lymphomas, glioblastomas, sarcomas, aggressive breast cancers, etc.) This could be consistent with: 1. De novo cancers triggered by genotoxic/oncogenic mechanisms (mutations, DNA integration, p53 suppression, immune collapse). 2. Reactivation of dormant cancers due to immune dysregulation or microenvironment changes. A “virus + injection” combo could synergise via: Immune suppression Chronic inflammation p53 pathway interference Increased cellular proliferation signals

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Short-lived protein exposure vs. persistent expression Short-lived exposure Example: Traditional inactivated-virus or recombinant protein vaccines. The viral antigen is present for hours–days. No genomic material remains. Unless the protein itself is highly toxic in the short term (rare for a single viral antigen), the cancer risk is negligible. This is why, historically, protein-based vaccines without replication or integration haven’t been linked to oncogenesis. Persistent expression If the antigen is produced inside cells for weeks, months, or longer, it can continuously interact with host proteins. Certain viral proteins (like HPV E6/E7, EBV LMP1, SV40 large T antigen) bind and disable tumour suppressors like p53 or Rb. Continuous interference with these pathways increases the risk of DNA mutations being propagated instead of repaired or eliminated.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Oncogenic activity of the protein itself Some viral proteins are intrinsically oncogenic, because they: Inhibit p53 (prevents apoptosis after DNA damage) Inhibit Rb (removes cell cycle brakes) Activate telomerase (promotes immortality) Cause chromosomal instability (breaks, fusions, aneuploidy) For example: HPV E6 → degrades p53 HPV E7 → binds Rb SV40 Large T antigen → inactivates both p53 & Rb HBx protein (Hepatitis B) → interferes with DNA repair If such a protein is expressed from a vaccine platform inside the nucleus or cytoplasm for long durations, it could mimic the oncogenic potential of a persistent infection without needing the whole virus.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

DNA Contamination & Integration Risk SV40-containing plasmid sequences have been detected in multiple mRNA vaccine vials through the work of genomics scientist @Kevin_McKernan founder of Medicinal Genomics and former head of research and development at Applied Biosystems, a company whose DNA sequencing technology was instrumental in the Human Genome Project. McKernan has also built and sold multiple biotech companies, lending both technical expertise and industry credibility to his findings. These results have since been independently confirmed by laboratories and institutions around the world. The detected material consists of bacterial plasmid backbones carrying SV40 promoter/origin of replication sequences genetic elements historically used in experimental cancer biology to drive extremely high levels of gene expression in mammalian cells. If such plasmid DNA gains entry into the cell nucleus, rare but well-documented events of insertional mutagenesis can occur: Integration into or near oncogenes → abnormal activation of growth signals Integration into tumour suppressor genes → loss of cell cycle control This mechanism mirrors the problem that halted certain early gene therapy trials, where retroviral vectors inadvertently caused leukaemias by activating growth-promoting genes.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Why persistence changes the risk calculation Think of it like this: Short exposure = like briefly turning off your smoke alarm. You’ll probably be fine. Persistent exposure = like disconnecting the smoke alarm permanently and inviting a small campfire into your living room it’s not guaranteed to burn the house down, but the probability increases with every passing hour. 5. In the “turbo cancer” context If the spike protein or any contaminating viral sequence: 1. Is expressed persistently inside cells 2. Can interact with tumour suppressors or DNA repair machinery 3. Arrives in a host with immune dysregulation (post-infection or post-vaccination) …then both: Reactivation of dormant cancer cells (immune escape) De novo tumour initiation (mutation accumulation + apoptosis failure) become biologically plausible and they could happen in parallel, leading to the multi-type, aggressive cancer profile some clinicians are reporting. End.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

I highly recommend following Kevin McKernan and reading his Substack https://substack.com/@kevinmckernan/note/p-153763975 his deep-dive analyses are essential if you want to understand what’s really in these vials. Frankly, @joerogan should have him on if he hasn’t already. I’m no expert, but I know enough to be dangerous and what Kevin’s uncovered should have everyone paying attention. https://substack.com/@kevinmckernan/note/p-150140847 I find it hard to believe you haven't seen his work tbh. Thanks Kevin 💪🙏🔥

FDA White Oak Lab Finds 6X to 470X DNA contamination in mRNA vaccines Excellent Work From High Schoolers anandamide.substack.com
SV40 origin of replication in mammalian cells in absence of SV40 Large T-Antigen Positive tumor biopsy qPCR one year after vaccination anandamide.substack.com

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

You should also follow Annelise too god speed 🙏

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

The thread aligns with recent research linking SIRT1 and p53 pathways to mitochondrial dysfunction and inflammation, as seen in a 2025 study on intestinal dysbiosis and aging. https://www.mdpi.com/1422-0067/22/3/1233 Spike protein interactions with p53, as mentioned, have gained attention following a 2024 report on long-term effects of COVID-19 vaccines, suggesting potential mitochondrial impacts. Other mechanisms : RAGE-mediated inflammation, a key point in the thread, connects to ongoing studies on Alzheimer’s, where RAGE facilitates amyloid-beta transport and mitochondrial damage. https://www.pnas.org/doi/10.1073/pnas.0905686106 The mention of miR-34a’s role in liver fibrosis ties to a 2023 clinical trial exploring SIRT1 activators for fibrosis treatment, showing promising results. https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0158657 "miR-34a is transcriptionally regulated by the p53 tumor suppressor protein and regulates a plethora of target proteins, which are involved in the cell cycle, apoptosis, differentiation and cellular development [25]. Downregulation of miR-34a has been found in many cancers [26–28]; thus, miR-34a is thought to be a tumor suppressor. However, previous studies have revealed that miR-34a is upregulated in many liver diseases, from fatty liver disease to HCC [29–31]. Upregulation of miR-34a may inhibit SIRT1, thus activating p53 and forming a positive feedback loop [22]. Although it has been reported that miR-34a can target acyl-CoA synthetase long-chain family member 1 and impair the lipid metabolism in the liver, resulting in the development of liver fibrosis [19], the function of the classical miR-34a/SIRT1/p53 signaling pathway in liver fibrosis is presently unclear." HMGB1’s role in immune tolerance, highlighted in the thread, relates to a 2025 breakthrough in cancer immunotherapy targeting RAGE-TLR4 pathways. https://journals.aai.org/jimmunol/article/205/3/767/61028/Interplay-between-RAGE-and-TLR4-Regulates-HMGB1 https://pmc.ncbi.nlm.nih.gov/articles/PMC11298799/ (Cf. Picture) I'm going around something and I can't figure out exactly what it is...

Activation of the miR-34a/SIRT1/p53 Signaling Pathway Contributes to the Progress of Liver Fibrosis via Inducing Apoptosis in Hepatocytes but Not in HSCs Liver fibrosis results from a sustained wound healing response to chronic liver injury, and the activation of nonparenchymal hepatic stellate cells (HSCs) is the pivotal process. MicroRNA-34a (miR-34a) is the direct target gene of p53 and activates p53 through sirtuin 1 (SIRT1) simultaneously. The miR-34a/SIRT1/p53 signaling pathway thus forms a positive feedback loop wherein p53 induces miR-34a and miR-34a activates p53 by inhibiting SIRT1, playing an important role in cell proliferation and apoptosis. miR-34a expression has been found to be increased in animal models or in human patients with different liver diseases, including liver fibrosis. However, the exact role of this classical miR-34a/SIRT1/p53 signaling pathway in liver fibrosis remains unclear. In the present study, using a CCl4-induced rat liver fibrosis model, we found that the miR-34a/SIRT1/p53 signaling pathway was activated and could be inhibited by SIRT1 activator SRT1720. Further studies showed that the miR-34a/SIRT1/p53 signaling pathway was activated in hepatocytes but not in HSCs. The activation of this pathway in hepatocytes resulted in the apoptosis of hepatocytes and thus activated HSCs. Our data indicate that the miR-34a/SIRT1/p53 signaling pathway might be a promising therapeutic target for liver fibrosis. journals.plos.org
Targeting mitochondrial damage: shining a new light on immunotherapy Mitochondrial damage has a particular impact on the immune system and tumor microenvironment, which can trigger cell stress, an inflammatory response, and disrupt immune cell function, thus all of which can accelerate the progression of the tumor. ... pmc.ncbi.nlm.nih.gov

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

@ThailandMedicaX "SIRT1 interacts with and deacetylates PGC-1α to enhance its activity, promote mitochondrial biogenesis, and maintain mitochondrial function." https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5767311/ https://www.mdpi.com/1422-0067/22/9/4558 "PGC-1α is a master regulator that interacts with various transcription factors involved

SIRT1/PGC-1α Signaling Promotes Mitochondrial Functional Recovery and Reduces Apoptosis after Intracerebral Hemorrhage in Rats Silent information regulator 1 (SIRT1) exerts neuroprotection in many neurodegenerative diseases. However, it is not clear if SIRT1 has protective effects after intracerebral hemorrhage (ICH)-induced brain injury in rats. Thus, our goal was to ... pmc.ncbi.nlm.nih.gov

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

@ThailandMedicaX The problem is that C99 is found in MAM - intracellular lipid rafts, called mitochondria‐associated ER membranes (MAM), a functional subdomain of the ER located in close apposition to mitochondria that regulates key cellular metabolic functions. https://pmc.ncbi.nlm.nih.gov/articles/PMC5731665/ This is

Increased localization of APP‐C99 in mitochondria‐associated ER membranes causes mitochondrial dysfunction in Alzheimer disease In the amyloidogenic pathway associated with Alzheimer disease (AD), the amyloid precursor protein (APP) is cleaved by β‐secretase to generate a 99‐aa C‐terminal fragment (C99) that is then cleaved by γ‐secretase to generate the β‐amyloid (Aβ) found ... pmc.ncbi.nlm.nih.gov

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Spike, p53 et mitochondries... Allez, je vais essayer de vulgariser. 1. Interaction Spike/p53 et immunité : La Spike pourrait interagir avec p53, qui est un régulateur clé de l’immunité innée et adaptative, notamment via la production d’interférons (IFN) de type I et de gènes

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Pour expliquer... Ce fil explique comment certaines protéines dans notre corps, après une infection (comme le COVID-19) ou une injection d’ARNm, peuvent provoquer des problèmes graves, comme des caillots anormaux ou des maladies cérébrales. On parle de protéines comme GSDME,

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@AnneliseBocquet would you consider putting your information on Substack ? I'm sure there are many that would be willing to help myself included 🔥

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@AnneliseBocquet There are so many people doing this kind of work honestly, it’s the best part of the online world for me. You can learn so much from them. 🔗 Walter’s also got a great Substack well worth subscribing 🙏❤️

@Parsifaler - Walter M Chesnut

THE SPIKE, CANCER AND PRION DISEASE As I warned three years ago about the Spike's interaction with p53 and tumor suppressors. This can ALSO induce Prion Disease! Recently discovered characteristics of the tumor suppressor p53 include its prion-like properties and cellular uptake mechanisms, which are related to its GoF and are associated with tumor formation and malignancy. https://wmcresearch.org/the-spike-protein-as-metatastic-cancer/

THE SPIKE PROTEIN AS METASTATIC CANCER – WMC Research wmcresearch.org

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Is this what's playing out in the charts by the excellent Ethical Skeptic? I tried to warn people this was dangerous, I was one of the fortunate few who found Dr Cole and Dr Kory earlier than most I saw the zinc ionophore suppression. https://t.co/rjx13isBpR

@EthicalSkeptic - Ethical Skeptic ☀

Excess Natural Cause Mortality in Vaccinial Generation (0-5 yr-olds - of vaccinated mothers) 😔OMFG - we asked not what outght to be done, but only what could be (quod fieri). The blood-dimmed tide is loosed, and everywhere The ceremony of innocense is drowned. ~Yates

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Could FMT from an unvaccinated cohort repair the gut damage in the vaccinated ? Wouldn't this repair immune system health and restore gut integrity ? A nice way of saying eat shit 😂😂 https://t.co/tVC3rftbNV

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

I've read about the Chinese yellow poop soup that goes back as far as the 4th century The Practice of Yellow Soup"Yellow soup," also known as "Huang-Long decoction," was a preparation made from dried or fermented stool from a healthy person. Documented by Ge Hong in his medical text "Zhou Hou Bei Ji Fang" (Handbook of Emergency Medicine), it was used to treat diarrhea, food poisoning, heat toxin, and unconsciousness due to high fever. The evidence leans toward this being an early form of fecal microbiota transplantation (FMT), aiming to restore gut balance by introducing beneficial bacteria. https://t.co/9dTD0frnbg

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

I do not condone drinking urine ever. I do remember being insulted to drink it by the pro jabber crowd lmfao.. I'll pass https://t.co/viLo0z7E8G

@DrSarteschi - Dr. Christine Sarteschi, LCSW

Christopher Keys of the Vaccine Police has shingles and naturally he is taking urine baths (among other things) to help Here he is drinking it as well https://t.co/UaswEzhIg0

Saved - August 18, 2025 at 10:54 AM
reSee.it AI Summary
I reflect on the complexities of ME/CFS, noting that millions have sacrificed their cognition due to the effects of the Spike protein from both SARS-CoV-2 infections and vaccines. The persistence of Spike leads to serious health issues, including cognitive impairments akin to those seen in HIV-related conditions. Studies indicate a significant overlap between cognitive symptoms in COVID-19 and HIV-associated neurocognitive disorders. As we explore treatment options, understanding the long-term implications of Spike and its cumulative effects remains crucial for both adults and children.

@dbdugger - Daniel Brittain Dugger

We must accept "Solving ME/CFS" required sacrificing the cognition of millions, including those robbed of their cognition and autonomy after allowing conversion from Asymptomatic Neurocognitive Impairment.

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

5 points fondamentaux que vous devez savoir sur la Spike du SARS-CoV-2 (🦠 et 💉) De retour après plusieurs jours de pause... et ça fait du bien ! Je lance ce thread en 5 points. 1. La Spike est produite aussi bien lors d'une infection par le SARS-CoV-2 que par les injections anti-covid. Si on a des données solides pour les covid-longs, on en a beaucoup moins pour les PVS (Syndromes Post-Vaccination). Les études sont disparates et il n'y a aucune étude comparative. Du moins, pas à ma connaissance. Ce que je sais, c'est que la Spike est potentiellement la responsable de ces PVS. Les injections anti-covid font produire de la Spike... mais en quelle quantité ? Et quid de la biodistribution - autrement dit, on n'a toujours aucune idée de la production de Spike dans les tissus. 2. La Spike enclenche divers problèmes : les Spikeopathies. De fait toxique, elle persiste dans les organismes pendant des mois... voir des ANNÉES. Et il y a donc un effet cumulatif. Du fait de sa persistance, la Spike des injections anti-covid vient se rajouter à la Spike des infections covid... créant un vrai problème de dose cumulative. Et une synergie "virus + injections anti-covid". Car oui, les injections anti-covid ne protègent pas, ni des infections ni des formes graves. Mais rajoutent de la Spike sur de la Spike. 3. La Spike est dégénérative. Elle est amyloides, amyloidogène et peut utiliser les fibres amyloides pour permettre au virus de coloniser l'organisme. On aura des pathologies comme Alzheimer, Parkinson, des démences et diverses des amyloses comme les fibrinaloides... (Creutzfeld Jakob) (Amyloses) 4. La Spike est toxique pour le système immunitaire. - du fait de sa persistance, elle peut épuiser les lymphocytes T. Là aussi, l'épuisement des lymphocytes T est un marqueur aussi bien des covid-longs que des PVS. Mais, du coup, qui dit "système immunitaire épuisé" dit "système immunitaire hors-service". C'est devenu une passoire pour les pathogènes... surtout le SARS-CoV-2. 5. La Spike entraîne des perturbations métaboliques... C'est en lien avec ses propriétés cancérigènes mais aussi, son impact sur l'ensemble de l'organisme. Fatigue chronique et perte du tonus musculaire sont deux grandes caractéristiques. Être spiké, c'est passer dans une essoreuse... avec des impacts de fond. Beaucoup de questions sont encore en suspens... comme les effets épigénétiques, les impacts sur les futures générations et la fertilité. Mais ces 5 points là sont déjà beaucoup d'arguments à opposer aux injections anti-covid et à demander aux soignants de... nous soigner. Le potentiel bacteriophage du SARS-CoV-2 est un argument clé en faveur des antibiotiques. Limiter la propagation du virus dans l'organisme et donc la production de Spike est important ! Fondamental au regard de la persistance de la protéine Spike et des Spikeopathies, des propriétés amyloides (et donc dégénératives), immunotoxiques et des impacts métaboliques. Cela vaut pour les adultes mais aussi les enfants. Merci beaucoup de m'avoir lue. 💯💯💯

@ejustin46 - Emmanuel

How many spike proteins are in our body during each SARS-CoV-2 infection, and how many stay in our organs after three infections? 500,000,000,000 spike proteins ? I haven't found a clear answer in the nearly 10,000 studies that I shared on X/Twitter since the pandemic began.

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Bien... un nouveau preprint. https://www.medrxiv.org/content/10.1101/2025.02.18.25322379v1 Voilà ce qu'en tant qu'immuno, je retiens... 1. Quelques définitions : 1.a. Post-Vaccination Syndrome (PVS) ou Syndrome Post-Vaccination (en français) : PVS fait référence à un ensemble de symptômes chroniques (fatigue,

Immunological and Antigenic Signatures Associated with Chronic Illnesses after COVID-19 Vaccination medRxiv - The Preprint Server for Health Sciences medrxiv.org

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Bon ben... ça y est... c'est publié ! La protéine Spike du SARS-CoV-2 s'accumule et persiste dans l'organisme pendant... DES ANNÉES ! Avec, notamment une accumulation dans le cerveau, les méninges et le crâne... C'est ce thread là qui vient d'être validé peer-reviewed ⤵️

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Bien... petite réaction à chaud sur cette publication de Nakao Ora et al. 2025. Persistance de la Spike dans les syndromes post-vaccinaux (PVS) Persistance de la Spike après infection par le SARS-CoV-2 et persistance du virus.

Video Transcript AI Summary
Cette vidéo résume: selon Nakaoota et al. (3 avril 2025), « l’expression de la protéine Spike chez 43.8 pour 100 des personnes vaccinées anti Covid » persiste « au niveau des artères coronaires » jusqu’à 17 mois après l’injection, avec « l’ARN messager, du vaccin, mais également du virus » détecté. Il y a « persistance de la protéine Spike » et « persistance du SARS-CoV-2 » possiblement malgré les traitements précoces. L’auteure mentionne aussi « Crüssfeld Jacob, 14 mois après infection » et une étude sur des « AVC 17 mois après injections ». L’interaction de la nucléocapside (protéine N) avec TRIM28 pourrait retarder la réponse immunitaire innée, renforçant la tolérance immunitaire via TLR2/RAGE et IgG4. Conséquences: infection potentiellement asymptomatique et dégâts cumulatifs; Spike persistante pourrait entraîner « spike viral plus spike vaccinal ». Des spycopathies neurologiques sont évoquées; dépistage de Spike et traque du virus recommandés; traitements personnalisés et soutien par curcumine, quercétine, vitamine D; approche individuelle. This video summarizes: according to Nakaoota et al. (April 3, 2025), « the expression of the spike protein in 43.8 per 100 of vaccinated people » persists « at the level of the coronary arteries » for up to 17 months after injection, with « mRNA from the vaccine, but also the virus » detected. There is « persistence of the Spike protein » and « persistence of SARS-CoV-2 » possibly despite early treatments. The author also cites « Crüssfeld Jacob, 14 months after infection » and a study on « strokes 17 months after injections ». The interaction of the nucleocapsid protein (N) with TRIM28 could delay the innate antiviral response, reinforcing immune tolerance via TLR2/RAGE and IgG4. Consequences: potentially asymptomatic infection and cumulative damage; persistent Spike could lead to « spike viral plus spike vaccinal ». Neurological spycopathies are discussed; diagnostics to detect Spike and tracking the virus are recommended; therapies to block/remove Spike and personalized approaches, with supports like curcumin, quercetin, vitamin D.
Full Transcript
Speaker 0: Bonjour à tous et à tous. Je suis Annelies Bocket, je suis docteure en biologie santé et spécialisée en immunologie, et je n'ai absolument aucun conflit d'intérêt, que ce soit d'ordre privé, personnel, financier, peu importe. Je n'ai pas de conflit d'intérêt. Je me permets de faire cette petite vidéo suite à la parution d'un nouvel article de Nakaoota et al en date du 3 avril 2025 qui démontre l'expression de la protéine Spike chez 43.8 pour 100 des personnes vaccinées anti Covid avec une persistance de cette protéine Spike au niveau des artères coronaires et ce jusqu'à 17 mois après l'injection. On a également détecté de l'ARN messager, du vaccin, mais également du virus au niveau donc de ces artères coronaires. Donc il y a bien une persistance de la protéine Spike. Je ne reviendrai pas sur l'étude de Yel Lissen qui a démontré la persistance de cette protéine Spike plus de 700 jours après les injections anti Covid. Mais il y a aussi une persistance du SARS-CoV 2. Et ceci peut-être en dépit des traitements précoces. J'expliquerai juste après pourquoi. Il y a une persistance de la spi vaccinale, donc comme je viens de vous le décrire, mais également possiblement de l'ARN messager modifié avec une production donc de cette spike des mois après les injections anti covid. Aujourd'hui, a quand même quelques publications assez alarmantes. Dès Crüssfeld Jacob, 14 mois après infection par le SARS-CoV 2. Là, ici, sur ce nouvel, sur cette nouvelle publication des AVC, 17 mois après potentiellement injections plus infections. Et donc je vais vous expliquer pourquoi le SARS-CoV 2 persiste et quelles sont mes dernières recherches. Il faut savoir que la protéine mucocapside du SARS-CoV-2, donc la protéine N du SARS-CoV-2 interagit avec TRIM vingt-huit. C'est quoi TRIM vingt-huit C'est un facteur impliqué dans une grande variété de processus cellulaires comme le matière des cellules souches, la réparation de l'ADN, l'apoptose, l'autophagie, et j'en passe. La perte de Trim 28 lors du développement de l'embryon chez la souris est l'étale. Et Trim 28 peut être impliqué dans de nombreux cancers, globalement. Le problème, c'est que TRIM 28 est aussi impliqué dans l'homéostasie du système immunitaire et dans son activation. Donc, si TRIM 28 est impactée, alors la réponse immunitaire innée en réponse à l'infection par le SARS -CoV 2 est aussi impliquée. Notamment, il va y avoir un délai, un retard dans le lancement de la réponse immunitaire antivirale. Il se peut alors que la réponse immunitaire lors d'une infection par le SARS-CoV 2 soit retardée, et cela va avec les mécanismes de tolérance immunitaire que j'ai précédemment décrits, énormément décrits, notamment avec l'activation du TLR 2 via le système Rage, les cellules myéloïdes, inhibitrices, l'expression de certains HLA inhibiteurs, enfin bref, plus sans compter les propriétés allergènes qui entraînent potentiellement des IgG4. Donc les IgG4 étant un marqueur également de cette de cette tolérance immunitaire. Bref, donc cette interaction de la nucléocapside avec TRIM 28 vient renforcer finalement les actions de la protéine Spike, et donc inhibent complètement la réponse immunitaire innée antivirale, ce qui fait, c'est qu'elle est retardée dans le temps. Qu'est-ce que ça signifie concrètement Il est fort probable qu'il existe une phase, une première phase lors de la contamination virale, qui soit silencieuse, asymptomatique. Puisqu'en fait, les symptômes, ce n'est, ce ne sont que la manifestation d'une activation du système immunitaire. Donc vous comprenez bien que si vous n'avez pas de symptômes, c'est que votre système immunitaire n'est pas activé correctement, et donc votre infection par le SARS-CoV 2 passe dans les premiers temps complètement inaperçue. Autrement dit aussi, nous avons soigné trop tard. Non seulement on n'a soigné que l'hyper inflammation, ne tenant compte que de l'hyper inflammation, sans tenir compte de la tolérance immunitaire, mais également nous avons soigné probablement avec un délai dans le temps. Donc du fait de cette phase asymptomatique, de cette phase retardée. Donc ce qui aurait permis d'ailleurs au virus de s'installer dans l'organisme tranquillou pépère, avant même l'enclenchement des des symptômes, et la mise en place des traitements précoces, dits précoces. Il faut savoir que d'autres virus latent, sont capables d'interagir avec TRIM vingt-huit, pardon. Il y a le b v, le cytomégalovirus, le papillomavirus, l'hépatite b ou encore le vih, le virus responsable du sida. Alors non seulement on a peut-être soigné avec un retard considérable, mais les injections anti Covid ont certainement rajouté une couche supplémentaire, notamment par la surexpression de certains récepteurs qui ont ouvert les portes de l'organisme au virus. En effet, en plus, si la spike virale persiste, le fait de faire produire de la spike par les cellules de l'organisme après l'administration des produits anti Covid, aura probablement eu comme conséquence un effet cumulatif spike viral plus spike vaccinal. De fait, il est rapporté dans la littérature scientifique que les injections, que les infections par le SARS-CoV-2 entraînent des dégâts cumulatifs, et ce, peu importe le statut vaccinal. Je répète, peu importe le statut vaccinal, que vous soyez vacciné ou non vacciné, ça ne change rien. Des infections répétées par le SARS-CoV 2 entraînent des dégâts cumulatifs. Et je pense que nous sommes encore loin du compte en ce qui concerne les dégâts occasionnés par la protéine Spike. Et ce d'autant plus qu'il s'agit d'une arme silencieuse. Elle va, comme je l'ai dit, désactiver le système immunitaire et ça va passer crème. Vous ne sentirez rien jusqu'au point de rupture. Ça veut bien dire qu'on peut déclencher des spycopathies, c'est-à-dire des maladies relatives à la persistance et à la présence de la protéine spike dans l'organisme, qu'elle soit d'origine virale ou vaccinale, dans le temps. Avec un délai, avec un certain retard. L'une des grandes catégories de spycopathies que l'on redoute et qu'on peut redouter énormément, ce sont les atteintes neurologiques. Comme la spike, elle est amyloïde et amyloïdogène. Elle est capable de former en elle-même des fibres hydrogels dégénératives, mais également de faire produire des fibres dégénératives par les cellules de l'organisme, des fibres comme celles qui sont impliquées dans la pathologie d'Alzheimer, de Parkinson, ou même la fibrillation de la protéine prions humaine. Et en plus, on va mettre la cerise sur la tarte au quetch, le virus, grâce à sa spike, peut utiliser ses fibres amyloïdes pour envahir l'organisme potentiellement. Je ne vais pas parler des propriétés allergènes qui peuvent avoir des conséquences comme des syndromes d'activation mastocytaire, Et ça, pas dans le temps, puisqu'elles persistent dans le temps. Donc ça fera comme des mastocytose-like en permanence. Donc comment soigner les spycopathies On a quelques pistes pour soutenir l'organisme, comme la curcumine, l'aspirine. Attention l'aspirine pas pour tout le monde, c'est un inhibiteur de l'activation des plaquettes. Donc si vous êtes sous anticoagulants ou si vous avez d'autres contre indications, ne prenez pas de l'aspirine. La quercétine ou la vitamine D, tout en gardant en tête quand même qu'il ne s'agit que de pansements. Mais c'est mieux que rien. La vitamine D est d'autant plus importante qu'elle peut renforcer la barrière hémato-encéphalique qui est largement attaquée par la protéine spike et le virus. Le fait de retrouver de la spike au niveau des artères cérébrales, ça ne sent pas très bon. Donc cette barrière hématoencéphalique normalement protège notre cerveau et donc elle est un, elle est attaquée, elle est perméabilisée, ce qui ouvre la voie en fait à un virus qui est neurotrope, qui adore le cerveau et qui est ami, avec une protéine Spike qui est amyloïde. Il n'y a pas que la protéine Spike qui est amyloïde, d'accord La protéine N aussi qui est amyloïde. Il y en a d'autres. Mais il nous est aujourd'hui essentiel, en fait, de trouver des outils de diagnostic pour aller chercher, pour aller traquer les spikopathies, notamment des outils de dépistage et de dosage de la protéine Spike, et de développer des thérapies pour bloquer le virus ou éliminer cette protéine Spike, attention, sans enclencher les catastrophes annexes. Il faut aussi traquer le virus, notamment dans les réservoirs, et aller chercher les dégâts tissulaires. On ne soigne pas des dégâts tissulaires comme on soigne une protéine persistante, comme on soigne un virus persistant. Et bien entendu, ces traitements se feront en fonction de votre cas. Chaque individu est différent. Il va donc falloir analyser chez vous ce qui se passe pour aller mieux vous soigner. Voilà. Sur ce, je vous laisse et je vous souhaite une bonne journée, je mettrai les références soit en haut du de la vidéo ou en bas de la vidéo en fonction de comment ça s'agence sur x. Je vous souhaite une bonne journée, au revoir.

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Spike, Creutzfeld Jakob et Alzheimer... https://www.news-medical.net/news/20230905/SARS-CoV-2-spike-protein-could-be-speeding-up-Alzheimers-and-other-brain-diseases-says-new-study.aspx Preprint : https://www.biorxiv.org/content/10.1101/2023.09.01.555834v1 Des chercheurs ont évalué les capacités de la protéine Spike du SARS-CoV-2 à induire la fibrillation de la protéine prion PrP ou huPrP (human prion) et des fibres Aβ42. Cette

SARS-CoV-2 spike protein could be speeding up Alzheimer's and other brain diseases, says new study Swedish researchers find that SARS-CoV-2's spike protein amyloids can accelerate the formation of harmful protein aggregates related to neurodegenerative diseases like Creutzfeldt-Jakob and Alzheimer's. The study suggests a potential link between COVID-19 and increased cases of these brain disorders. news-medical.net
SARS-CoV-2 Spike amyloid fibrils specifically and selectively accelerates amyloid fibril formation of human prion protein and the amyloid β peptide bioRxiv - the preprint server for biology, operated by Cold Spring Harbor Laboratory, a research and educational institution biorxiv.org

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Thread à lire 🧵! "Le Dr Jordan Vaughn, médecin basé en Alabama, a ensuite fourni une estimation effrayante : jusqu'à 15 millions d'Américains pourraient souffrir de blessures liées à la COVID longue ou au vaccin contre la COVID. Il traite désormais des adolescents qui ne

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

En parlant d'Alzheimer... Vous saviez que le SARS-CoV-2, le virus qui induit la Covid19, peut promouvoir ou enclencher des pathologies neurodégénératives comme... Alzheimer mais aussi Parkinson ? https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10050697/ https://pubmed.ncbi.nlm.nih.gov/38259635/ https://pubmed.ncbi.nlm.nih.gov/36314211/

The viral hypothesis in Alzheimer’s disease: SARS-CoV-2 on the cusp Increasing evidence highlights that infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has long-term effects on cognitive function, which may cause neurodegenerative diseases like Alzheimer’s disease (AD) in the future. We ... pmc.ncbi.nlm.nih.gov
Unravelling the connection between COVID-19 and Alzheimer's disease: a comprehensive review - PubMed Currently, there exists a limited comprehension regarding the correlation between COVID-19 and Alzheimer's disease (AD). To elucidate the interrelationship and its impact on outcomes, a comprehensive investigation was carried out utilising time-unrestricted searches of reputable databases such as Sc … pubmed.ncbi.nlm.nih.gov
COVID-19 as a Risk Factor for Alzheimer's Disease - PubMed Severe acute respiratory disease coronavirus 2 (SARS-CoV-2) is responsible for the coronavirus disease 2019 (COVID-19) pandemic. Although a primarily respiratory disease, recent reports indicate that it also affects the central nervous system (CNS). Over 25% of COVID-19 patients report neurological … pubmed.ncbi.nlm.nih.gov

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Comment vous dire que ça pue, niveau immuno ? Les injections anti-covid perdent de leur efficacité au niveau des lymphocytes T? Sans blague... impact d'une exposition répétée à un même antigène ! https://onlinelibrary.wiley.com/doi/10.1002/jmv.29790?af=R La 3e dose (3D) a augmenté le pourcentage de résidents

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Hé... 2025 : PVS - épuisement des lymphocytes, hein... rien que ça ! Comme quoi...

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

2/2 3. Similitudes entre PVS et Covid-long : a. Les symptômes cliniques : Les deux conditions partagent des phénotypes cliniques similaires, comme la fatigue chronique, la dysautonomie, et les troubles cognitifs, souvent attribués à l’épuisement immunitaire. b. L'épuisement

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Coenzyme Q10 pour soigner les covid-longs ? https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10779395/ Les mitochondries jouent un rôle important dans la réponse aux infections virales. Elles sont, en effet, impliquées dans la production de radicaux oxygénés et de l'initiation de la réponse immunitaire via les

Mitochondrial Dysfunction and Coenzyme Q10 Supplementation in Post-Viral Fatigue Syndrome: An Overview Post-viral fatigue syndrome (PVFS) encompasses a wide range of complex neuroimmune disorders of unknown causes characterised by disabling post-exertional fatigue, myalgia and joint pain, cognitive impairments, unrefreshing sleep, autonomic ... pmc.ncbi.nlm.nih.gov

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Dans la série des "bonnes nouvelles" : la Spike du SARS-CoV-2 est génotoxique... semble-t-il. - Par des mécanismes indirects comme le stress oxydatif ou son impact sur les mitochondries... - Par des mécanismes directs en interférant avec des mécanismes de réparations et de

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Spike, p53 et mitochondries... Allez, je vais essayer de vulgariser. 1. Interaction Spike/p53 et immunité : La Spike pourrait interagir avec p53, qui est un régulateur clé de l’immunité innée et adaptative, notamment via la production d’interférons (IFN) de type I et de gènes

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

"Preuves du potentiel bacteriophage du SARS-CoV-2 dans le microbiote intestinal humain" Petrillo et al., 23 avril 2025. https://pubmed.ncbi.nlm.nih.gov/40444030/ Le virus responsable de la COVID-19, le SARS-CoV-2, fut détecté dans des cultures de bactéries, à l'extérieur et à l'intérieur des

Evidence of SARS-CoV-2 bacteriophage potential in human gut microbiota - PubMed Based on these results we conclude that, in addition to its well-documented interactions with eukaryotic cells, SARS-CoV-2 may act as a bacteriophage when interacting with at least two bacterial species known to be present in the human microbiota. If the hypothesis proposed, i.e., that under certain … pubmed.ncbi.nlm.nih.gov

@dbdugger - Daniel Brittain Dugger

It was three years ago that I was sitting at my desk when I received a phone call from a client who believed there was an issue with my software as he was unable to locate information on a spreadsheet. It was there but he was suffering from "brain fog."

@dbdugger - Daniel Brittain Dugger

This article, published the same year, was among the first returned in the search results. Cerebrospinal Fluid Offers Clues to Post-COVID ‘Brain Fog’ https://www.ucsf.edu/news/2022/01/422156/cerebrospinal-fluid-offers-clues-post-covid-brain-fog

@dbdugger - Daniel Brittain Dugger

"All participants underwent an in-person cognitive testing battery with a neuropsychologist, applying equivalent criteria used for HIV-associated neurocognitive disorder (HAND)."

@dbdugger - Daniel Brittain Dugger

"Surprisingly, the researchers found that 13 of the 22 participants (59 percent) with cognitive symptoms met HAND criteria, compared with seven of the 10 control participants (70 percent)."

@dbdugger - Daniel Brittain Dugger

Observing cognitive impairment equal in magnitude to that of HIV Associated Neurocognitive Decline confirms the hypothesis advanced by Kenneth Podell on September 29th, 2020. Multiple Neuroinvasive Pathways in COVID-19 https://pubmed.ncbi.nlm.nih.gov/32990925/

Multiple Neuroinvasive Pathways in COVID-19 - PubMed COVID-19 is a highly infectious viral disease caused by the novel coronavirus SARS-CoV-2. While it was initially regarded as a strictly respiratory illness, the impact of COVID-19 on multiple organs is increasingly recognized. The brain is among the targets of COVID-19, and it can be impacted in mul … pubmed.ncbi.nlm.nih.gov

@dbdugger - Daniel Brittain Dugger

"One can draw on the experience with an HIV/AIDS epidemic. The initial understanding of HIV/AIDS was that of the virus affecting the immune system by depleting T cells, which resulted in opportunistic infections of multiple organs, including the brain."

@dbdugger - Daniel Brittain Dugger

"However, it did not take long to discover that the disease could also attack the brain directly, which resulted in long-term cognitive impairment."

@dbdugger - Daniel Brittain Dugger

"Subsequently, HIV encephalopathy and AIDS dementia complex leading to long-term cognitive impairment were discovered [87]. Based on the emerging literature, it is reasonable to hypothesize a somewhat similar scenario may unfold in relationship to COVID-19."

@dbdugger - Daniel Brittain Dugger

The equivalent criteria is that of the Frascati Criteria which recognizes Asymptomatic Neurocognitive Impairment, Mild Neurocognitive Decline, and AIDS Dementia Complex.

@dbdugger - Daniel Brittain Dugger

HIV-associated neurocognitive disorder — pathogenesis and prospects for treatment https://pmc.ncbi.nlm.nih.gov/articles/PMC4937456/

HIV-associated neurocognitive disorder — pathogenesis and prospects for treatment In the past two decades, several advancements have improved the care of HIV-infected individuals. Most importantly, the development and deployment of combination antiretroviral therapy (CART) has resulted in a dramatic decline in the rate of deaths ... pmc.ncbi.nlm.nih.gov

@dbdugger - Daniel Brittain Dugger

Asymptomatic neurocognitive impairment (ANI) Impairment in ≥2 neurocognitive domains (≥1 SD) Does not interfere with daily functioning

@dbdugger - Daniel Brittain Dugger

Mild neurocognitive disorder (MND) Impairment in ≥2 neurocognitive domains (≥1 SD) Mild to moderate interference in daily functioning

@dbdugger - Daniel Brittain Dugger

HIV-associated dementia (HAD) Marked (≥2 SD) impairment in ≥2 neurocognitive domains Marked interference in daily functioning

@dbdugger - Daniel Brittain Dugger

Those now diagnosed with ME/CFS were among those living with ANI at a two-to-six times increase risk of conversion and did so in a way we have observed over the past forty years.

@dbdugger - Daniel Brittain Dugger

"Despite being asymptomatic, ANI is clinically relevant because individuals with ANI can transition to one of the more severe forms of HAND:"

@dbdugger - Daniel Brittain Dugger

"for example, participants of the CNS HIV Antiretroviral Therapy Effects Research (CHARTER) study who had ANI at baseline were two to six times more likely to develop symptomatic HAND during several years of follow-up than those who were neurocognitively normal at baseline."

@dbdugger - Daniel Brittain Dugger

Could You Have ME/CFS? (Myalgic Encephalomyelitis/Chronic Fatigue Syndrome) https://www.cdc.gov/me-cfs/pdfs/could-you-have-mecfs_508.pdf ME/CFS is a complex illness and symptoms of ME/CFS may seem similar to many other illnesses. ME/CFS requires three symptoms:

@dbdugger - Daniel Brittain Dugger

See? They are unable to complete their ADLs. 1. Not being able to participate in routine activities that were possible before becoming ill, such as work, school, social life, and/or personal life, that:

@dbdugger - Daniel Brittain Dugger

• Lasts for more than 6 months • Is accompanied by fatigue that is: • Often serious • Just started (not lifelong) • Not the result of ongoing activities • Not from more than usual effort • Not made better by rest

@dbdugger - Daniel Brittain Dugger

It was in December of 2021 that Dr. Daniel Chertow implicated the two most well known reservoirs in HIV, that of the Central Nervous System and Gut Associated Lymphoid Tissues.

@dbdugger - Daniel Brittain Dugger

SARS-CoV-2 infection and persistence throughout the human body and brain December 2021 https://www.researchgate.net/publication/357197928_SARS-CoV-2_infection_and_persistence_throughout_the_human_body_and_brain

@dbdugger - Daniel Brittain Dugger

The very same month, China published this paper demonstrating the efficacy of Azvudine. Published: 06 December 2021 Azvudine is a thymus-homing anti-SARS-CoV-2 drug effective in treating COVID-19 patients https://www.nature.com/articles/s41392-021-00835-6

Azvudine is a thymus-homing anti-SARS-CoV-2 drug effective in treating COVID-19 patients - Signal Transduction and Targeted Therapy Azvudine (FNC) is a nucleoside analog that inhibits HIV-1 RNA-dependent RNA polymerase (RdRp). Recently, we discovered FNC an agent against SARS-CoV-2, and have taken it into Phase III trial for COVID-19 patients. FNC monophosphate analog inhibited SARS-CoV-2 and HCoV-OC43 coronavirus with an EC50 between 1.2 and 4.3 μM, depending on viruses or cells, and selective index (SI) in 15–83 range. Oral administration of FNC in rats revealed a substantial thymus-homing feature, with FNC triphosphate (the active form) concentrated in the thymus and peripheral blood mononuclear cells (PBMC). Treating SARS-CoV-2 infected rhesus macaques with FNC (0.07 mg/kg, qd, orally) reduced viral load, recuperated the thymus, improved lymphocyte profiles, alleviated inflammation and organ damage, and lessened ground-glass opacities in chest X-ray. Single-cell sequencing suggested the promotion of thymus function by FNC. A randomized, single-arm clinical trial of FNC on compassionate use (n = 31) showed that oral FNC (5 mg, qd) cured all COVID-19 patients, with 100% viral ribonucleic acid negative conversion in 3.29 ± 2.22 days (range: 1–9 days) and 100% hospital discharge rate in 9.00 ± 4.93 days (range: 2–25 days). The side-effect of FNC is minor and transient dizziness and nausea in 16.12% (5/31) patients. Thus, FNC might cure COVID-19 through its anti-SARS-CoV-2 activity concentrated in the thymus, followed by promoted immunity. nature.com

@dbdugger - Daniel Brittain Dugger

It is through the protein it specifically targets that explains the use of cats to study Long Covid. What Cats May Teach Us About Long COVID https://www.ucdavis.edu/health/news/what-cats-may-teach-us-about-long-covid

What Cats May Teach Us About Long COVID UC Davis researchers find cats could help us learn about long COVID. They've found a new cell therapy boosts immune systems in cats with severe coronavirus. ucdavis.edu

@dbdugger - Daniel Brittain Dugger

"Feline infectious peritonitis, or FIP, is a serious and historically fatal disease in cats caused by a coronavirus. It behaves in many ways like severe coronavirus infections in humans, causing widespread inflammation, T cell exhaustion and chronic immune dysfunction."

@dbdugger - Daniel Brittain Dugger

The first Chinese oral anti-COVID-19 drug Azvudine launched https://pmc.ncbi.nlm.nih.gov/articles/PMC9461232/

The first Chinese oral anti-COVID-19 drug Azvudine launched pmc.ncbi.nlm.nih.gov

@dbdugger - Daniel Brittain Dugger

"Particularly, Azvudine (FNC, 2′-deoxy-2′-β-fluoro-4′-azidocytidine) targets reverse transcriptase and HIV-1 accessory protein (Vif) simultaneously, being the first-in-class dual inhibitor."

@dbdugger - Daniel Brittain Dugger

See? It all falls into place like cats fall into laps. Determinants of FIV and HIV Vif sensitivity of feline APOBEC3 restriction factors https://pubmed.ncbi.nlm.nih.gov/27368163/

Determinants of FIV and HIV Vif sensitivity of feline APOBEC3 restriction factors - PubMed Here we identified in feline A3s residues important for binding of FIV Vif and a unique protein domain insertion (linker). To understand Vif evolution, a structural model of the feline A3 was developed. Our results show that HIV Vif binds human A3s differently than FIV Vif feline A3s. The linker ins … pubmed.ncbi.nlm.nih.gov

@dbdugger - Daniel Brittain Dugger

Our failure to engage in a similar antiviral strategy has left the Central Nervous System reservoir of millions to expand in the same way observed in the HIV+ and each cell type that constitutes that reservoir to be productively infected for years.

@dbdugger - Daniel Brittain Dugger

Nef-like mediated damage has been observed for several years, with 2022, 2023, 2024, and 2025 being relevant to cognitive impairment.

@dbdugger - Daniel Brittain Dugger

It was in 2022 that we learned Tunneling Nanotubes are expanding the Central Nervous System reservoir of millions. Tunneling nanotubes provide a route for SARS-CoV-2 spreading https://pubmed.ncbi.nlm.nih.gov/35857849/

Tunneling nanotubes provide a route for SARS-CoV-2 spreading - PubMed Neurological manifestations of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection represent a major issue in long coronavirus disease. How SARS-CoV-2 gains access to the brain and how infection leads to neurological symptoms are not clear because the principal means of viral entr … pubmed.ncbi.nlm.nih.gov
Saved - August 15, 2025 at 7:23 PM
reSee.it AI Summary
I listened to a shocking podcast by the Boston Globe about the Duke cancer scandal during Sally Kornbluth's time as Dean. She ignored serious warnings about fraud and reproducibility, including from whistleblowers and external scholars, and withheld information from a review committee. How can she still represent MIT?

@RetsefL - Retsef Levi

Shocking podcast by @BostonGlobe on the @DukeU cancer scandal under Sally Kornbluth tenure as Dean. She ignored multiple flashing red warning signals re fraud & reproducibility, including whistleblower and scholars from within the Duke lab, and external accomplished scholars! She was part of withholding information from a review committee allowing fraudulent clinical trials to go on! How can she continue to be the @MIT face to the world?

@RetsefL - Retsef Levi

Link: https://www.bostonglobe.com/2025/08/15/multimedia/fraudulent-cancer-breakthrough-test-future-president-mit-new-age-doubt-science/

Inside a research fraud scandal that rocked the scientific community — and tested the future president of MIT - The Boston Globe It seemed like Duke scientists had developed a “Holy Grail” of cancer treatment. Then the truth came out. In this week’s Globe Magazine cover story, reporter Mike Damiano takes readers inside the scandal that ended with broken careers, betrayed patients, and a lasting legacy of doubt in scientific institutions. bostonglobe.com
Saved - August 15, 2025 at 9:35 AM
reSee.it AI Summary
I've been highlighting the connection between other infections and the reactivation of bartonella, particularly for Long Covid patients. Recent cases illustrate this, such as a 54-year-old man whose bartonella symptoms worsened after COVID-19 and a 26-year-old woman who developed persistent symptoms post-infection. There's also a link between EBV and bartonella reactivation. Research shows that bartonella can be reactivated by infections and immunosuppression, yet it's often misdiagnosed and poorly understood by many doctors, contributing to chronic illness.

@StevePhillipsMD - Steven Phillips, MD

🧵1/6 Mounting evidence is backing up what I've been saying for years now: That other infections can reactivate bartonella, which has major implications for Long Covid patients. See thread to follow:👇

@StevePhillipsMD - Steven Phillips, MD

🧵2/6 "...a 54-year-old male with painful left upper arm mass, which gradually resolved until he was infected with COVID-19. The mass then rapidly progressed...pleural effusion emerged simultaneously. The cause: Bartonella. https://bmcinfectdis.biomedcentral.com/articles/10.1186/s12879-024-09336-7

Post-COVID reactivation of latent Bartonella henselae infection: a case report and literature review - BMC Infectious Diseases Cat scratch disease (CSD) is caused by Bartonella henselae (B. henselae) and presents as lymphadenopathy following close contact with cats. However, in context of the global COVID-19 pandemic, clinical manifestations of CSD may vary, posing new challenges for healthcare professionals. Here we describe a case of a 54-year-old male with painful left upper arm mass, which gradually resolved until he was infected with COVID-19. The mass then rapidly progressed before admission. Meanwhile, pulmonary symptoms including pleural effusion emerged simultaneously. The cause was undetermined with routine blood culture and pathological test until the next generation sequencing (NGS) confirmed the presence of B. henselae. We believe this case is the first to report localized aggravation of CSD after COVID-19 infection and hopefully, offers treatment experience for clinicians worldwide. bmcinfectdis.biomedcentral.com

@StevePhillipsMD - Steven Phillips, MD

🧵3/6 "...investigating long COVID uncovered an underlying bartonellosis through clinical metagenomics. Following mild COVID-19, a 26-year-old woman experienced persistent symptoms during 5 months..." The cause: Bartonella. https://pubmed.ncbi.nlm.nih.gov/38472519/

Unmasking Bartonella henselae infection in the shadows of long COVID thanks to clinical metagenomics - PubMed The diagnosis of long COVID often relies on symptoms post-COVID-19, occasionally lacking biological evidence. This case study illustrates how investigating long COVID uncovered an underlying bartonellosis through clinical metagenomics. Following mild COVID-19, a 26-year-old woman experienced persist … pubmed.ncbi.nlm.nih.gov

@StevePhillipsMD - Steven Phillips, MD

🧵4/6 Before Covid, a common viral infection preceding me/cfs has been EBV. Is it EBV that causes me/cfs or is it reactivation of bartonella from EBV?🧐 "Generalized infection with Bartonella henselae following infection due to Epstein-Barr virus." https://pubmed.ncbi.nlm.nih.gov/8922830/

Generalized infection with Bartonella henselae following infection due to Epstein-Barr virus - PubMed Generalized infection with Bartonella henselae following infection due to Epstein-Barr virus pubmed.ncbi.nlm.nih.gov

@StevePhillipsMD - Steven Phillips, MD

🧵5/6 After experimental rickettsial infection, all dogs were positive for Bartonella antibodies & multiple dogs had DNA evidence of Bartonella infection. "...supports reactivation of latent infection." https://pmc.ncbi.nlm.nih.gov/articles/PMC6979086/

Detection of Bartonella spp. in dogs after infection with Rickettsia rickettsii Dynamics of infection by Bartonella and Rickettsia species, which are epidemiologically associated in dogs, have not been explored in a controlled setting. Describe an outbreak investigation of occult Bartonella spp. infection among a group of dogs, ... pmc.ncbi.nlm.nih.gov

@StevePhillipsMD - Steven Phillips, MD

🧵6/6 1. Bartonella can be reactivated by other infections & immunosuppression. 2. It's hard to diagnosis by lab testing alone: Antibody & PCR tests vary markedly between labs. 3. It's very poorly understood by most docs. 4. It's a common cause of chronic illness.

@StevePhillipsMD - Steven Phillips, MD

@sadfoxqueen It's something we've all noticed in my office since Covid started.

Saved - August 13, 2025 at 3:11 PM
reSee.it AI Summary
I've been investigating the 22 terminated mRNA projects but haven't found specific IDs yet, which is concerning. I discovered that the Global Health Investment Corporation manages BARDA Ventures, using taxpayer funding without providing a return on investment. This non-profit, started by Bill Gates, controls a government agency and funds controversial research like Gene Drive and transhumanism. The HHS Secretary wields significant power, and there's a push for a universal vaccine despite calls for reallocating funds to nutrition. I'm questioning how a public agency can partner with an NGO and allow it to guide operations.

@DrHenryEaly - Dr Henry Ealy

I've looked for the 22 mRNA projects that have been terminated... Can't find any specific IDs so I'll have to do more digging. But these facts are still highly concerning. A Brief Thread... @naomirwolf @ShannonJoyRadio @DrSuzanneH7 @BusyDrT @RenzTom @DocMalikPodcast

@DrHenryEaly - Dr Henry Ealy

Fact 1 Something called Global Health Investment Corporation manages BARDA Ventures. So... US taxpayer funding is being capitalized on but the US taxpayer gets no ROI.

@DrHenryEaly - Dr Henry Ealy

Fact 2 The Global Health Investment Corporation is a non-profit investment organization that controls a governmental agency... And of course was started by Bill Gates. How is it that a NGO can control a governmental agency? https://ghicfunds.org/about/

About | Global Health Investment Corporation (GHIC) Investing in a Healthier and Safer World. Global Health Investment Corporation (GHIC) is a nonprofit organization catalyzing the development of technologies to improve human health worldwide. ghicfunds.org

@DrHenryEaly - Dr Henry Ealy

Fact 3 The GHIC funds Gene Drive research that I've been warning everyone about for years now. And they also fund Univercells that supports transhumanism. https://ghicfunds.org/global-health-security/

Global Health Security Portfolio | Global Health Investment Corporation (GHIC) Investing in a Healthier and Safer World. Global Health Investment Corporation (GHIC) is a nonprofit organization catalyzing the development of technologies to improve human health worldwide. ghicfunds.org

@DrHenryEaly - Dr Henry Ealy

Fact 4 The GHIC link to BARDA didn't take me to BARDA... It took me to here https://aspr.hhs.gov/Pages/Home.aspx The website I've been begging everyone to read. See next post.

Stay informed with the latest updates from the ASPR, including vital resources for H5N1 bird flu preparedness, COVID-19 therapeutics, and BARDA's pandemic influenza initiatives and project Nextgen. aspr.hhs.gov

@DrHenryEaly - Dr Henry Ealy

Fact 5 The HHS Secretary has WAY more power than you realize. Just read this. https://aspr.hhs.gov/legal/Pages/Legal-Authority-of-the-Secretary.aspx

This webpage is intended to provide general information about the HHS Secretary’s legal authorities to prepare for and respond to public health and medical emergencies and is not intended to provide specific legal advice or guidance. aspr.hhs.gov

@DrHenryEaly - Dr Henry Ealy

Fact 6 BARDA Ventures looks like a nice way for Bill Gates to play the puppet master with US Taxpayer dollars under the lie of philanthropy and public health... His money is in bed with ours but we never get the ROI. This is some shady shit. https://drive.hhs.gov/ventures.html

BARDA Ventures - Investment to catalyze health security innovation BARDA Ventures has partnered with a venture capital entity the Global Health Investment Corporation (GHIC) to effectively coordinate and share risk across public and private sectors drive.hhs.gov

@DrHenryEaly - Dr Henry Ealy

Fact 7 After all that... @SecKennedy doesnt want to reallocate the 500M to nutrition... He wants to create a universal vaccine. Oh... And Arcturus 2304 self amplifying mRNA... That's still full go... To protect the public's investment.🙄 https://www.hhs.gov/press-room/hhs-winds-down-mrna-development-under-barda.html https://t.co/Ncn1MaDpti

@DrHenryEaly - Dr Henry Ealy

How can a public agency paid for by our tax dollars have an investment fund? How can this investment fund partner with an NGO? How can this NGO legally guide the public agency? BARDA BARDA Venture GHIC @RenzTom @MendenhallFirm

@DrHenryEaly - Dr Henry Ealy

@Evie707656912 @naomirwolf @ShannonJoyRadio @DrSuzanneH7 @BusyDrT @RenzTom @DocMalikPodcast @sasha_latypova Links are helpful and appreciated. And Henry is my dad... No one calls me that.🤙🏽

@DrHenryEaly - Dr Henry Ealy

@Evie707656912 @naomirwolf @ShannonJoyRadio @DrSuzanneH7 @BusyDrT @RenzTom @DocMalikPodcast This is my issue as well. Mahalo for posting this much.

Saved - August 13, 2025 at 1:52 PM
reSee.it AI Summary
The FDA is attempting to remove dessicated thyroid medications from the market, which I believe negatively impacts patients who rely on them. Many doctors focus solely on lab results, often overlooking symptoms like fatigue and weight gain. They rarely conduct comprehensive lab panels, missing critical markers like free T3. Optimizing thyroid treatment can transform lives, and at my clinic, we prioritize symptoms over lab numbers. It's concerning that the FDA targets a long-standing medication while ignoring the issues surrounding mRNA shots. We need to end the war on hormone optimization for healthy individuals.

@molsjames - Dr Mollie James

Well, the @FDA is at it again! While blind to the mRNA shots and their harm, they are working to REMOVE dessicated thyroid medications from the market. Short thread on how this negatively impacts patients. https://www.fda.gov/drugs/enforcement-activities-fda/fdas-actions-address-unapproved-thyroid-medications

@molsjames - Dr Mollie James

The majority of doctors base thyroid management on getting the labs right--labs based on sick people--not optimization. They ignore patients who are tired, cold, gaining weight and hair shedding but instead say "Your labs are normal" https://t.co/eQE6LfIDar

@molsjames - Dr Mollie James

Most doctors don't run a thorough lab panel. A TSH is used for 'screening' in many. Maybe a Free T4 if they're fairly sophisticated. Almost never do I see a free T3 or reverse T3--the true correlates of symptoms from low functioning thyroid.

@molsjames - Dr Mollie James

Why does this matter? Optimizing thryoid changes patients lives. We have switched many from synthetics to dessicated thyroid--with a combination of T3 and T4, they get that energy bump directly. Many have lower reverse T3 over time. At @james_clinic we titrate to symptoms instead of labs.

@molsjames - Dr Mollie James

Did you know what TIME you get labs in relation to taking your meds matters also? Getting that lab panel late in the day or too early after taking meds may not be accurate. So, they adjust meds based on a moving, false target instead of resolving symptoms (the basis of all successful hormone optimization.)

@molsjames - Dr Mollie James

Why is the @FDA doing this? Reports of harm? From whom? About what? How did we investigate that. A med 1.5 million people take/year that has been around for over 100 years is a target? (Let's not forget the mRNA shots that were forced on MILLIONS of people with devastating side effects that just keep going and going)

@molsjames - Dr Mollie James

@james_clinic @FDA @DrMakaryFDA @RobertKennedyJr The war on healthy people and hormone optimization needs to end. I'm sure other patients on dessicated thryoid are like most of ours--happy, more energetic, losing weight, and feeling better than ever. What a crisis! (insert sarcasm)

@molsjames - Dr Mollie James

@james_clinic @FDA @DrMakaryFDA @RobertKennedyJr One must understand how the thyroid works to help patients manage. Here's a short guide developed by @fxmed https://t.co/wlpMaTT98T

@molsjames - Dr Mollie James

@Robert_Heitner8 @FDA It goes by symptoms, not labs. Elevated TSH is a sign your body wants more thyroid. I’d recommend a second opinion.

@molsjames - Dr Mollie James

@cdavlin3 @FDA I use the same one

Saved - August 11, 2025 at 6:22 PM
reSee.it AI Summary
I discussed the use of various expression vectors and the digestion processes involving BamHI and XhoI for protein expression and purification. I highlighted the importance of tracking the purchase history of products by the Wuhan Institute of Virology to understand their research activities. I noted that obtaining detailed records would require significant effort, including legal actions or insider information. Additionally, I listed several suppliers for WIV, emphasizing the challenges in accessing this data since 2020, despite its digital nature and potential for scrutiny.

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

1. New England Biolabs & Novagen The amplified Rp3-S1 fragment was digested with BamHI & XhoI & ligated into the expression vector pMAL-C2X (New England Biolabs). The 5 truncated fragments were digested with BamHI & XhoI and ligated into the expression vector pET32a (Novagen).

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

1/? Disgusting Patents you may or may not be aware of 1.Bat sars-like coronavirus spike protein immunodetermination region & preparation method & application thereof Filed by Wuhan Institute of Virology, 2012 Inventors: Zhou PengHan Zhenggang, Shi Zhengli https://patents.google.com/patent/CN102690336A/zh

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

2. Promega & Takara Protein expression & purification After purification, recombinant plasmid was transformed into BL21 competent cells (purchased from Promega) Recovered PCR product & expression vector pET32a were digested with restriction endonucleases BamHI & XhoI (Takara).

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

3. Takara (2) After DNA recovery, the PCR product was ligated to the expression vector pET32a using T4 DNA ligase (Takara)

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

4. HIV Rp3-S-targeted pseudovirus (HIV/Rp3-S) using HIVNL4-3 (ΔENV) luc plasmid, human SARS-CoVBJ01, SL-CoVRp3 S protein or one RBD region is replaced with chimera SSL of SSARS, replacing position of ENV protein, to construct HIV/BJ01-S, HIV/Rp3-S or HIV/CS310-518 pseudoviruses

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

5. 293T Cells @stevenemassey @drhermiz @Florin_Uncovers a day before transfection, seed 293T cells at a density of 4 x 10 6 /dish in a 10 cm diameter cell culture dish. Replace the 293T cell culture medium with fresh medium (or replace half of the medium) before transfection

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

@stevenemassey @drhermiz @Florin_Uncovers 6. 🕵️🧬👁‍🗨 The updated focus of this thread is mainly on the companies that WIV purchased their products from pre-2020. By cross-checking with published work, the purchase history of wiv with these companies can help indicate what experiments were undertaken & when

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

@stevenemassey @drhermiz @Florin_Uncovers 7. Where did WIV buy its PCR oligonucleotides? Why? Wherever WIV ordered its oligos from sits a record of their activity. the sequences of the orders can be read just like the SRA files, so their scientific activity is recorded in the sequences. @Daoyu15 @dasher8090 @VBruttel

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

@stevenemassey @drhermiz @Florin_Uncovers @Daoyu15 @dasher8090 @VBruttel 8. A helpful expert explains🥼 🗣️ "I can read my own oligonucleotide orders for last 20 years and see what i was working on and when. anyone could do this. but of course this info is proprietary and confidential, so obtaining it is not so easy."

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

@stevenemassey @drhermiz @Florin_Uncovers @Daoyu15 @dasher8090 @VBruttel 9. To obtain the details it would take: Court orders Moles/Whistleblowers State level espionage Advanced "pentesting" attacks

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

@stevenemassey @drhermiz @Florin_Uncovers @Daoyu15 @dasher8090 @VBruttel 10. As we have seen above, WIV purchased from ThermoFisher: https://primer.thermofisher.cn/ Toyobo: https://www.toyobo-global.com/products/lifescience/index.html NEB: https://www.neb.cn/zh-cn BD clontech (TAKARO BIO) https://www.takarabio.com as listed here: https://hal.science/hal-03154155v1/file/main.pdf and here: https://www.virosin.org/fileZGBDX/journal/article/vs/2022/5/PDF/7%205947.pdf

Takara Bio—Home Takara Bio provides kits, reagents, instruments, and services that help researchers explore questions about gene discovery, regulation, and function. takarabio.com
Thermo Fisher引物服务 生命技术 primer.thermofisher.cn

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

@stevenemassey @drhermiz @Florin_Uncovers @Daoyu15 @dasher8090 @VBruttel 11. Other suppliers include IDTDNA https://sg.idtdna.com/pages/about/news/2020/09/28/idt-expands-global-footprint-with-launch-of-idt-china Accurate Biotechnology, China https://en.agbio.com.cn/oligo-synthesis/ GenScript https://www.genscript.com/qpcr-probe.html https://www.genscript.com/gsfiles/techfiles/Oligo%20brochure%20EN%202022.pdf

IDT Expands Global Footprint with Launch of IDT China IDT has established an official business entity in China to better serve its customer base in the region, in addition to reaching new customers and providing easier access to its complete portfolio of industry-leading products. sg.idtdna.com
Oligo Synthesis – Accurate Biology en.agbio.com.cn
qPCR Probes and Oligo Primers qPCR Probes and Oligo Primers genscript.com
page not found genscript.com

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

@stevenemassey @drhermiz @Florin_Uncovers @Daoyu15 @dasher8090 @VBruttel 12. More WIV suppliers BBI Life Science & Sangon Biotech (Shanghai) bbi-lifesciences.com/en/products_se… Shanghai Qifa: http://www.qfbio.com/ used here: https://2024.sci-hub.se/1149/a5a078686df3217f2024c0d812fdcc0e/zhu2005.pdf @quay_dr @tony_vandongen @Engineer2The

胶原酶I型-ACCUTASE 细胞消化液-起发试剂 上海起发实验试剂有限公司(www.qfbio.com)主营:胶原酶I型,ACCUTASE 细胞消化液,硫酸葡聚糖 DSS,线性聚乙烯亚胺PEI,重组胰蛋白酶(蛋白质谱级),intronbio,immunoreagents,kinovate,biovectra等产品,欢迎来电洽谈. qfbio.com

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

@stevenemassey @drhermiz @Florin_Uncovers @Daoyu15 @dasher8090 @VBruttel @quay_dr @tony_vandongen @Engineer2The 13. Novagen (Sigma Aldrich - Germany) https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/product/documents/360/845/tb347.pdf What did the BND know in 2020? "Germany's foreign intelligence service believed there was a 80-90% chance that coronavirus accidentally leaked from a Chinese lab" https://www.bbc.com/news/articles/cz7vypq31z7o

German spy agency 'believed Covid likely started in lab' China denies German media reports of an assessment carried out by spying agency BND in 2020 supporting the theory. bbc.com

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

@stevenemassey @drhermiz @Florin_Uncovers @Daoyu15 @dasher8090 @VBruttel @quay_dr @tony_vandongen @Engineer2The 14. Novogene (Shanghai) https://www.novogene.com/amea-en/about/global-presence/ https://www.novogene.com/amea-en/services/service-support/

Global Presence novogene.com
Service Support novogene.com

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

@stevenemassey @drhermiz @Florin_Uncovers @Daoyu15 @dasher8090 @VBruttel @quay_dr @tony_vandongen @Engineer2The 15. Promega https://worldwide.promega.com/products/pcr/rt-pcr/oligodt15-primer/?catNum=C1101 Promega (Beijing) Biotech Co., Ltd Beijing 100013 https://worldwide.promega.com/products Mentioned here along with sigma-aldrich (Novagen), Takara, GenePharma (China) and Thermo Fisher SADS-WIV (2021) https://mednexus.org/doi/10.1016/j.bsheal.2021.05.002

Oligo(dT)15 Primer Use for first-strand cDNA synthesis with a reverse transcriptase. promega.com
Promega Products Explore our assays and instruments that support researchers in the fields of cell biology, drug discovery, human identification, clinical research and more. promega.com

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

@stevenemassey @drhermiz @Florin_Uncovers @Daoyu15 @dasher8090 @VBruttel @quay_dr @tony_vandongen @Engineer2The 16. That's most of them! Since 2020, we called for this data many times, discussed ways of obtaining it with experts, but came up against brick walls HOWEVER these records exist & cannot be deleted without raising suspicion and https://www.researchgate.net/publication/350409839_1_PROPOSED_FORENSIC_INVESTIGATION_OF_WUHAN_LABORATORIES

@BillyBostickson - Billy Bostickson 🏴👁&👁 🆓

@angie_rasmussen Lab notebooks are no longer scrawled in with pencils! Most of the data needed is digital, also voice calls, messages, emails, internal databases, inventory records, supply records, oligonucleotides, Illumina HiSeq 300 datasets, etc. See pages 21 - 56: https://scholar.archive.org/work/t23kmarczfcuhhmphzh4dwgvua

scholar.archive.org
Saved - August 8, 2025 at 7:29 PM
reSee.it AI Summary
I asked Grok about translation errors leading to unknown proteins from mRNA gene therapy injections. It took a while, but I finally got him to acknowledge the truth. Here are the results.

@Clucky92864053 - Clucky

PSEUDO-URIDINE: I asked Grok to explain translation errors creating unknown proteins as a result of mRNA gene therapy injections. Just look at the sequence and how long it look me to get Grok to admit the truth. Here are the results. 👇

@Clucky92864053 - Clucky

#1 https://t.co/f7F2la6XuF

@Clucky92864053 - Clucky

#2 https://t.co/KX9Mg8oK1w

@Clucky92864053 - Clucky

#3 https://t.co/B5Rr1NoVE0

@Clucky92864053 - Clucky

#4 https://t.co/YcJEOO8RZf

Saved - July 24, 2025 at 3:59 PM
reSee.it AI Summary
I issued a notice of objection regarding the lack of accountability from pharmaceutical companies and government authorities concerning vaccine injuries in Ireland. This notice is grounded in constitutional and human rights, emphasizing our right to information and transparency about the production and effects of mRNA vaccines. I presented a series of critical questions regarding the vaccine's biochemical design, human risks, and potential impacts on fertility and health, highlighting the need for answers to ensure public trust and safety.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

A notice for vaccine injured in Ireland 🇮🇪 #stoptheshots NOTICE OF OBJECTION & DEMAND FOR ACCOUNTABILITY Issued under the authority of Bunreacht na hÉireann, the European Convention on Human Rights, and Natural Justice I. LEGAL BASIS FOR OBJECTION We, the undersigned citizens and/or lawful representatives of vaccine-injured individuals, hereby serve notice of our constitutional and human rights-based objection to the continued silence, obfuscation, and denial by pharmaceutical manufacturers and government authorities regarding the production, testing, deployment, and post-market surveillance of modRNA-based products. This notice is issued in accordance with: Article 40 of Bunreacht na hÉireann – Protection of personal rights, bodily integrity, and dignity; Article 41 – Protection of the family, moral order, and societal well-being; Article 44 – Freedom of conscience and the unimpeded expression of religious, cultural, and ethical convictions; Article 40.6.1 – The right to freedom of expression and to challenge injustice in the public interest; The Preamble to the Constitution, affirming our “rightful status among the nations” and fidelity to “our divine heritage” and “the common good”; Article 10 and Article 14 of the European Convention on Human Rights (ECHR) – Freedom of expression and protection against discrimination; The principles of Natural Law, subsidiarity, proportionality, and inalienable rights; Legal definitions and standards from Black’s Law Dictionary, including but not limited to: Equal Protection Legal Certainty Medical Negligence Administrative Abuse Cultural Sovereignty Misuse of Public Funds Duty to Disclose Standing and Redress II. RIGHT TO INFORMATION FOR VACCINE-INJURED PERSONS As a specific manifestation of the secondary burden of disclosure (Darlegungsobliegenheit) on pharmaceutical manufacturers — arising from the asymmetry of knowledge and the public-private nature of experimental health interventions — we assert a constitutionally protected right to demand complete and transparent answers to the following urgent and unanswered questions. > Failure to answer these questions constitutes: A violation of the principle of legal certainty; A denial of meaningful redress (Article 13 ECHR); A breach of the precautionary principle under EU law; And may be interpreted as misfeasance in public office and gross negligence in breach of public trust and fiduciary duty. We formally present the following Catalogue of Material Questions: 📌 A. Biochemical and Structural Design Questions 1. Why was a furin cleavage site inserted into the Wuhan-1 spike protein to separate S1 from S2 in a vaccine context? 2. Why was a P2-lock used on S2 but no equivalent molecular safeguard applied to the S1 subunit? 3. Are there BIAcore (surface plasmon resonance) studies confirming or refuting spike protein binding to human tissues or receptors? 4. What was the rationale for inserting GP-120/HIV-like sequences and their immunological implications? 5. Why was a neuropilin-binding site included, and what risks were anticipated? 📌 B. Human Risk, Fertility & Systemic Circulation 6. What adverse effects in humans were documented by the manufacturer or its agents prior to rollout? 7. What steps were taken to ensure the membrane-anchoring of spike proteins, preventing systemic shedding? 8. Since when did the manufacturer know the spike protein binds ACE2 and disrupts the RAAS system? 📌 C. Modified Nucleosides & Misfolded Proteins 9. How was N1-methylpseudouridine expected to prevent protein misfolding? 10. What measures were taken to assess and mitigate effects on fertility? 11. Was the thermostability and pH sensitivity of spike protein assessed? (e.g., behavior at 7°C vs 36.6°C) 12. Were tests conducted for inclusion bodies or misfolded protein accumulation? 13. Was N1-methylpseudouridine incorporated into mitochondrial rRNA, affecting energy and replication?

Saved - July 22, 2025 at 10:41 AM
reSee.it AI Summary
A group is mobilizing against proposed amendments to the WHO's International Health Regulations, set to take effect on July 19, arguing they undermine national sovereignty and public health autonomy. They demand that Irish officials reject these amendments, hold public debates, and ensure future health powers require citizen consent. Concerns also arise over alleged violations of rights during COVID-19, including coercion and lack of informed consent regarding vaccines. They call for investigations and accountability for government actions during the pandemic.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

🌍 All across the world, people are rising up and demanding that their governments reject the WHO’s proposed amendments to the International Health Regulations (IHR)—set to become binding international law on July 19. 🇮🇪 If you're in Ireland, please check the post below. It includes: 📩 A ready-to-use email template ✅ Contact details for Ministers and the President’s Office Now is the time to act. Take just 10 minutes to send a few emails. Let them know: our sovereignty is not for sale.

@CitizenGO_IE - CitizenGO Ireland

Dublin 🇮🇪 today 👉 Delivery of over 600K signatures to Health Minister @CarrollJennifer at @roinnslainte 🗣️📢 All over the world, people are demanding their governments REJECT the WHO’s IHR globalist health rules due to become binding international law on July 19

@CitizenGO_IE - CitizenGO Ireland

Say NO to International Health Regulations due to be adopted July 19 🗣️ The WHO claim these IHR's give them the power to: Declare global emergencies Force lockdowns, mandates, surveillance, and censorship Override national decisions and personal freedoms https://cgo.ac/sc0i22aM

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

[Your Full Name] [Your Address] [City, Postcode] [Email Address] [Date] To: Minister Jennifer Carroll MacNeill Department of Health Hawkins House Dublin 2 Ireland RE: Fiduciary Duty to Reject the WHO’s IHR Amendments – Binding International Law Proposed for July 19 Dear Minister Carroll MacNeill, I am writing to you in your capacity as an elected public servant and fiduciary of the Irish people. On July 19, proposed amendments to the World Health Organization's International Health Regulations (IHR) are due to come into effect as binding international law. These amendments—negotiated without democratic mandate or public consultation—represent a clear and present danger to Ireland's constitutional sovereignty, bodily autonomy, and public health policy independence. As of today, over 600,000 signatures have been formally delivered to your office in Dublin, representing the will of citizens across Ireland and the world who reject this global overreach. The IHR amendments would confer unprecedented powers to an unelected international body to declare pandemics, impose travel restrictions, enforce medical treatments, and control information—all without national parliamentary oversight or judicial review. As a Minister of the Irish State, you have a legal, ethical, and fiduciary duty to act in the best interests of the people you serve. This includes: Upholding the Constitution of Ireland, which guarantees personal rights, national independence, and due process; Refusing consent to treaties or agreements that bypass democratic safeguards; Protecting future generations from centralized, technocratic governance that undermines local accountability. Should the State allow these IHR amendments to be adopted, it would constitute a dereliction of duty and a breach of public trust. This would open the door to binding obligations enforced by a foreign entity, which is wholly incompatible with Irish constitutional law and the principles of democratic self-determination. We, the undersigned citizens, formally demand: 1. A public declaration by you and your Department that Ireland will not consent to the WHO’s proposed IHR amendments. 2. A full debate in the Dáil Éireann, with opportunity for public scrutiny, before any such commitments are made on Ireland’s behalf. 3. An assurance in writing that no future health emergency powers will be outsourced to an international body without the express consent of the Irish people via referendum. This is a watershed moment for our nation. The world is watching. You are being called to stand on the right side of history. Yours sincerely, [Your Name] ivana.bacik@oireachtas.ie, richard.boydbarrett@oireachtas.ie, jack.chambers@oireachtas.ie,, jennifer.carrollmacneill@oireachtas.ie, cormac.devlin@oireachtas.ie, paul.donnelly@oireachtas.ie, colm.brophy@oireachtas.ie, paul.murphy@oireachtas.ie, marylou.mcdonald@oireachtas.ie, aengus.osnodaigh@oireachtas.ie, dessie.ellis@oireachtas.ie, eoin.obroin@oireachtas.ie, louise.oreilly@oireachtas.ie, mark.ward@oireachtas.ie, paul.mcauliffe@oireachtas.ie, gary.gannon@oireachtas.ie, cian.ocallaghan@oireachtas.ie, darragh.obrien@oireachtas.ie, roderic.ogorman@oireachtas.ie, jim.ocallaghan@oireachtas.ie, neale.richmond@oireachtas.ie, emerg.currie@oireachtas.ie, paschal.donohoe@oireachtas.ie, denise.mitchell@oireachtas.ie, duncan.smith@oireachtas.ie, john.lahart@oireachtas.ie, catherine.ardagh@oireachtas.ie, sinead.gibney@oireachtas.ie, sean.crowe@oireachtas.ie, maire.devine@oireachtas.ie, eoin.hayes@oireachtas.ie, shay.brennan@oireachtas.ie, james.geoghegan@oireachtas.ie, marie.sherlock@oireachtas.ie, ciaran.ahern@oireachtas.ie, grace.boland@oireachtas.ie, barry.heneghan@oireachtas.ie, tom.brabazon@oireachtas.ie, naoise.omuiri@oireachtas.ie, robert.odonoghue@oireachtas.ie

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

18.07.2025 Subject: Urgent Constitutional Concern – WHO IHR Amendments & Executive Overreach To: president@president.ie Dear President Higgins, I write to you today as a concerned citizen regarding the imminent adoption of the World Health Organization’s International Health Regulations (IHR) amendments, due to become binding international law on July 19. These amendments would enable a non-democratic foreign body to impose legally binding regulations on Ireland, without the involvement of the Oireachtas or the consent of the Irish people. This is a clear breach of the Constitution, in particular: Article 6 (sovereignty of the people), Article 15.2.1 (exclusive legislative power of the Oireachtas), Article 28.3.3 (only the Oireachtas can declare an emergency), Article 40 (personal rights and freedoms). Such a transfer of legislative and executive authority to an external body, if not submitted to a public referendum, would violate Article 29.5.1, which mandates Dáil ratification and, where sovereignty is affected, the consent of the people. As the constitutional guardian of the Irish Republic, I respectfully request that you intervene and seek legal advice regarding the compatibility of the IHR amendments with our Constitution. If necessary, I urge you to refer the matter to the Council of State or the Supreme Court under Article 26. The stakes could not be higher for our national sovereignty, democratic integrity, and future generations. Sincerely, [Your Full Name] [Your Address] [Your Contact Email] president@president.ie, info@president.ie, protocol@president.ie, diary@president.ie, secretarygeneral@president.ie, press.office@president.ie

@ThomasEJnr - Thomas Emmett

@MeasslainteIRL @RealEddieHobbs @MrAndyQuirke @FatEmperor @_mullally_el_ @WilliamRal45681 @indepdubnrth @dr_morrissey @blueskylou @_louise__ @Mickbraz1 @PhilipDwyer_MOI @OTURISK @CitizenGO_IE @IrishInquiry @LakareUpppropet1 @Leoyourleader @CilComLFC @mattiemcgrathtd @CarolNolanOff

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

To: The Taoiseach, Minister for Health, Minister for Justice, and all Members of the Oireachtas Subject: Formal Notice of Constitutional and Legal Breach: Crimes Against Humanity Committed During the COVID-19 Period Dear Ministers and Representatives, I write to formally assert that grave violations of domestic, constitutional, and international law occurred in Ireland during the COVID-19 response (2020–2023). These actions constitute a breach of the State’s fiduciary duty to protect life, bodily integrity, and the freedom of conscience under both Irish and international law. Under Article 40.3.2° of Bunreacht na hÉireann, the State guarantees to protect the personal rights of the citizen. This includes the right to bodily integrity (recognised in Ryan v. Attorney General [1965] I.R. 294), and the right to make informed medical decisions free from coercion (M(D) v. Ireland [2012] IEHC 352). These rights were violated by the State’s COVID-19 measures, which included: I. COERCION & MEDICAL TYRANNY Citizens were subject to medical coercion via "vaccine passports", workplace mandates, and denial of public services. This violates the principle of informed consent enshrined in: The Nuremberg Code (1947), which holds that “the voluntary consent of the human subject is absolutely essential.” The Oviedo Convention on Human Rights and Biomedicine (1997), Article 5: “An intervention may only be carried out after the person concerned has given free and informed consent.” The UNESCO Universal Declaration on Bioethics and Human Rights (2005), Article 6. The Irish Supreme Court in McGee v. Attorney General [1974] I.R. 284 affirmed the right to personal autonomy, including decisions relating to bodily health. Any interference must be proportionate. The actions taken during COVID were neither evidence-based nor proportionate, particularly for healthy individuals and children. II. VIOLATION OF “PRIMUM NON NOCERE” (FIRST, DO NO HARM) The State actively encouraged and facilitated the widespread use of experimental genetic injections (mRNA vaccines) without full knowledge of long-term safety. This violates: The Medical Council's Guide to Professional Conduct and Ethics for Registered Medical Practitioners (8th Edition, 2016), Section 7.1: “You must make the care of your patient your first concern and must practice safely and effectively.” Section 6.3: “You must give patients the information they need to understand their condition and treatment options and to make informed decisions about their care.” Instead, early warnings from international experts were ignored, censored, or defamed, while no pharmacovigilance system adequately tracked or responded to the surge in adverse events, including myocarditis, thrombotic events, and excess mortality—now evidenced in CSO data and HIQA reviews. III. CRIMES AGAINST HUMANITY – DEFINED AND APPLICABLE Under Article 7 of the Rome Statute of the International Criminal Court, crimes against humanity include: Persecution against any identifiable group on political or medical grounds. Other inhumane acts intentionally causing great suffering or injury to body or health. Forced medical procedures or experimentation without consent. Ireland's actions—including forcing or coercing injection uptake via threat of exclusion, job loss, or ostracization—constitute such violations. Furthermore, the continued use of products known to be contaminated with plasmid DNA (as confirmed by international genomic labs) shows reckless endangerment of life and health. IV. CENSORSHIP AND SUPPRESSION OF MEDICAL TRUTH Dissenting voices—including Irish doctors, midwives, and international scientists—were silenced, investigated, or struck off. This violates: Article 40.6.1° of Bunreacht na hÉireann: the right to freedom of expression. Article 10 of the European Convention on Human Rights (ECHR): freedom to receive and impart information.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

The State was complicit in a coordinated campaign of medical censorship, working with international bodies and social media firms to remove scientific discussion contrary to state messaging. This is state-sponsored information control, not science. V. SYSTEMIC NEGLIGENCE & FAILURE TO INFORM The lack of full disclosure about ingredients (e.g. SV40 enhancer sequences, residual DNA, LNPs), potential risks (e.g. autoimmune reactions, fertility issues), and ongoing adverse event signals constitutes fraudulent concealment and medical malpractice on a national scale. Section 21 of the Medical Council’s Code notes that consent must be based on accurate and adequate information. Yet many citizens were lied to or misled, with slogans such as “safe and effective” used despite emerging red flags. WE NOW DEMAND: 1. A full criminal investigation into the Irish Government's handling of COVID-19 policies, procurement, and adverse event concealment—with access to unredacted contracts, meeting minutes, and NPHET deliberations. 2. An independent Truth and Reconciliation Commission with the power to compel testimony, protect whistleblowers, and provide reparations to those harmed by State-led mandates. 3. Immediate suspension of mRNA product use pending comprehensive genomic, toxicological, and pharmacovigilance review. 4. Amendment of Article 28 of Bunreacht na hÉireann to forbid future emergency legislation that bypasses fundamental rights without a citizen referendum. 5. Public apologies and restitution for healthcare workers, teachers, and ordinary citizens who were coerced, injured, or discriminated against due to these unconstitutional policies. The Irish State has a duty not only to protect its people but to acknowledge when harm has occurred. If the Government fails to address these crimes, it invites future proceedings in domestic and international courts, including petitions to the European Court of Human Rights and the International Criminal Court. We do not seek vengeance. We seek accountability, transparency, and truth, so that this will never happen again. You are hereby put on formal notice. The people are no longer asleep. Sincerely, [Your Full Name] [Your Address / Eircode] [Email / Phone] Constitutional Sovereign and Witness to History

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@MichealMartinTD@SimonHarrisTD@Paschaldonohoe@JackChambersTD@HelenMcEnteeTD@DarraghOBrienTD@NormaFoleyTD@PeterBurkeTD@DaraCallearyTD @PatrickODonovanTD @JenCarrollMacNeillTD@JamesBrowneTD@JimOCallaghanTD@MartinHeydonTD@JamesLawlessTD@dfatirl@Dept_Transport@DeptCDE@opwireland

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@lawsocietyire@BarofIreland@LSRAIreland@CourtsServiceIE@DPPIreland@LegalAidBoard@VirginMediaNews@IrishMirror@journal_ie@DublinLive@CorkBeo@Spin1038@RedFM@Joe_Duffy@ciarakellydoc@Ray_Darcy@MartyM_RTE@DoireannGarrihy@Ian_Dempsey@MattCooperNT @GráinneSeoige @VirginMediaNews@IrishMirror@journal_ie@DublinLive@CorkBeo@Spin1038@RedFM@Joe_Duffy@ciarakellydoc@Ray_Darcy@MartyM_RTE@DoireannGarrihy@Ian_Dempsey@MattCooperNT @GráinneSeoige

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@ThomasEJnr @RealEddieHobbs @MrAndyQuirke @FatEmperor @_mullally_el_ @WilliamRal45681 @indepdubnrth @dr_morrissey @blueskylou @_louise__ @Mickbraz1 @PhilipDwyer_MOI @OTURISK @CitizenGO_IE @IrishInquiry @Leoyourleader @CilComLFC @mattiemcgrathtd @MichealMartinTD @SimonHarrisTD @DarraghOBrienTD @NormaFoleyTD @daracallearytd @JamesBrowneTD @dfatirl @Dept_Transport @DeptCDE @lawsocietyire @LSRAIreland @CourtsServiceIE @DPPIreland @legalaidboard @VirginMediaNews @IrishMirror @journal_ie @DublinLive @corkbeo @spin1038 @redfm @Joe_Duffy @ciarakellydoc @ray_darcy @DoireannGarrihy Pfizer Linked CJD Phenotype Body Fluid Analysis

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

🐁🦝🐺

@ThomasEJnr - Thomas Emmett

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@ThomasEJnr @RealEddieHobbs @MrAndyQuirke @FatEmperor @_mullally_el_ @WilliamRal45681 @indepdubnrth @dr_morrissey @blueskylou @_louise__ @Mickbraz1 @PhilipDwyer_MOI @OTURISK @CitizenGO_IE @IrishInquiry @Leoyourleader @CilComLFC @mattiemcgrathtd @MichealMartinTD @SimonHarrisTD @DarraghOBrienTD @NormaFoleyTD @daracallearytd @JamesBrowneTD @dfatirl @Dept_Transport @DeptCDE @lawsocietyire @LSRAIreland @CourtsServiceIE @DPPIreland @legalaidboard @VirginMediaNews @IrishMirror @journal_ie @DublinLive @corkbeo @spin1038 @redfm @Joe_Duffy @ciarakellydoc @ray_darcy @DoireannGarrihy There are so many beautiful minds doing the work ❤️ We will see you soon

@Nicolina0815 - Nicolina 🐭

@MeasslainteIRL I will reveal another way soon. My newest substacks: https://nicolina0815-substack-com.translate.goog/p/wenn-der-blutdruck-achterbahn-fahrt?_x_tr_sl=de&_x_tr_tl=en&_x_tr_hl=de&_x_tr_pto=wapp https://nicolina0815-substack-com.translate.goog/p/seneszenz-verstehen-heilen-ohne-zu?_x_tr_sl=de&_x_tr_tl=en&_x_tr_hl=de&_x_tr_pto=wapp&_x_tr_hist=true https://nicolina0815-substack-com.translate.goog/p/v-aids-wenn-das-immunsystem-in-die?_x_tr_sl=de&_x_tr_tl=en&_x_tr_hl=de&_x_tr_pto=wapp&_x_tr_hist=true https://nicolina0815-substack-com.translate.goog/p/pad4-and-citrullinierung?_x_tr_sl=de&_x_tr_tl=en&_x_tr_hl=de&_x_tr_pto=wapp&_x_tr_hist=true NarfGBs work https://genervter-substack-com.translate.goog/p/lnps-und-modrna?_x_tr_sl=de&_x_tr_tl=en&_x_tr_hl=de&_x_tr_pto=wapp&_x_tr_hist=true https://genervter-substack-com.translate.goog/p/lnps-und-modrna-2?_x_tr_sl=de&_x_tr_tl=en&_x_tr_hl=de&_x_tr_pto=wapp&_x_tr_hist=true I did also translation into easier + https://nicolina0815-substack-com.translate.goog/p/gibt-es-auswege?_x_tr_sl=de&_x_tr_tl=en&_x_tr_hl=de&_x_tr_pto=wapp

🧬 Seneszenz verstehen – heilen (?) ohne zu überfordern Ein naturbasierte Hypothese zur immunologischen Stabilisierung nach modRNA/LNP-Exposition nicolina0815-substack-com.translate.goog
"V-AIDS": Wenn das Immunsystem in die Erschöpfung kippt Ursachen, Verlauf und mögliche Wege heraus nicolina0815-substack-com.translate.goog
Wenn der Blutdruck Achterbahn fährt: Wie modRNA-Transfektion, PAD4 und Spikeprotein unser Gefäßsystem ins Chaos stürzen nicolina0815-substack-com.translate.goog
LNPs und modRNA (2) Eine Arbeitshypothese - Das Ende genervter-substack-com.translate.goog
LNPs und modRNA Eine Arbeitshypothese - Der Anfang genervter-substack-com.translate.goog
PAD4 & Citrullinierung Es könnte viel erklären! Calamari Clots, Krebs und Co- wie sind die Verbindungen? nicolina0815-substack-com.translate.goog
Gibt es Auswege? Diskussion der potentiellen Schäden und Besprechung, was für Optionen bleiben nicolina0815-substack-com.translate.goog

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@ThomasEJnr @RealEddieHobbs @MrAndyQuirke @FatEmperor @_mullally_el_ @WilliamRal45681 @indepdubnrth @dr_morrissey @blueskylou @_louise__ @Mickbraz1 @PhilipDwyer_MOI @OTURISK @CitizenGO_IE @IrishInquiry @Leoyourleader @CilComLFC @mattiemcgrathtd @MichealMartinTD @SimonHarrisTD @DarraghOBrienTD @NormaFoleyTD @daracallearytd @JamesBrowneTD @dfatirl @Dept_Transport @DeptCDE @lawsocietyire @LSRAIreland @CourtsServiceIE @DPPIreland @legalaidboard @VirginMediaNews @IrishMirror @journal_ie @DublinLive @corkbeo @spin1038 @redfm @Joe_Duffy @ciarakellydoc @ray_darcy @DoireannGarrihy A new draft, please consider this as notice.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Draft 2, Tell the truth and shame the devil 👿 FORMAL NOTICE OF CONSTITUTIONAL AND INTERNATIONAL LAW VIOLATIONS To: The Taoiseach, Minister for Health, Minister for Justice, and All Members of the Oireachtas From: [Your Full Name], Sovereign Citizen of Ireland Date: [Insert Today’s Date] Subject: Immediate Legal and Constitutional Redress for State Misconduct in COVID-19 Response (2020–2023) 1. GROUNDS FOR LEGAL ACTION A. Coercive Medical Measures Ireland’s Constitution guarantees the right to bodily integrity under Article 40.3.2°, as affirmed in Ryan v. Attorney General [1965] IR 294. Government policies—including vaccine certificates, employment mandates, and educational exclusion—constituted indirect coercion to undergo experimental mRNA injections. These actions breached both domestic and international law: Nuremberg Code (1947) – Principle 1: Voluntary consent must be given free from force, fraud, deceit, duress, or coercion. Convention on Human Rights and Biomedicine (Oviedo Convention) – Article 5: Prior, free, and informed consent is mandatory. Rome Statute of the International Criminal Court – Article 7(1)(h) & (k): Persecution and inhumane acts causing serious harm may constitute crimes against humanity. B. Suppression of Risk Data and Misrepresentation The Irish public was assured that COVID-19 vaccines were “safe and effective.” However, official documents indicate: HPRA Drug Safety Newsletter No. 104 and HSE internal bulletins (Aug 2021) acknowledged myocarditis risk in young males as 28 times baseline. Residual SV40 enhancer sequences—which can integrate into human DNA—were identified in Pfizer vials (Kevin McKernan, 2023), breaching EMA’s 10 ng/dose threshold for residual DNA (EMA/CHMP/BWP/534898/2008 Rev. 1). These failures violate Medical Council Guide §6.3, which mandates full disclosure of risks, and may amount to misfeasance in public office. C. Targeting of Dissenting Professionals Doctors and scientists who raised legitimate concerns were suspended, censored, or deregistered. This contravenes: Article 40.6.1° of Bunreacht na hÉireann – Guarantees the right to freedom of expression. European Convention on Human Rights (ECHR), Article 10 – Protects the right to receive and impart information without interference. 2. REMEDIAL DEMANDS 1. Immediate Criminal and Parliamentary Inquiry Full publication of unredacted Pfizer and Moderna contracts, all NPHET and CMO correspondence (including encrypted messages). Suspension of implicated officials, including Cabinet members and public health executives, pending investigation. 2. Compensation and Redress Automatic reparations of €500,000 per verified injury linked to COVID-19 injections, funded through profits or tax offsets from pharmaceutical contracts. Full reinstatement and back pay for individuals dismissed for declining vaccination. 3. Legislative Reform Repeal, within 21 days, of: Health (Amendment) Act 2021, and Criminal Justice (Enforcement Powers) (COVID-19) Act 2020. Enshrine constitutional immunity for Articles 40.3.2°, 40.6.1°, and 44.2.1°, protecting them from suspension via emergency legislation without a referendum. 4. Public Health Safeguards Moratorium on all mRNA-based interventions pending independent EU-accredited laboratory reviews, appointed by citizen assembly. Public release of anonymized HPRA adverse event reports in searchable database within seven days. 3. NOTICE OF CONSEQUENCES This formal notice has been delivered via registered post and email. A written response addressing each demand is required within seven (7) calendar days. Failure to respond shall constitute wilful dereliction of duty, breach of constitutional oath, and prima facie evidence of misconduct. Be advised that legal proceedings may be initiated in Irish, European, and international courts, including the International Criminal Court, under applicable treaties. Sincerely, [Your Full Name] [Full Postal Address

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@ThomasEJnr @RealEddieHobbs @MrAndyQuirke @FatEmperor @_mullally_el_ @WilliamRal45681 @indepdubnrth @dr_morrissey @blueskylou @_louise__ @Mickbraz1 @PhilipDwyer_MOI @OTURISK @CitizenGO_IE @IrishInquiry @Leoyourleader @CilComLFC @mattiemcgrathtd @MichealMartinTD @SimonHarrisTD @DarraghOBrienTD @NormaFoleyTD @daracallearytd @JamesBrowneTD @dfatirl @Dept_Transport @DeptCDE @lawsocietyire @LSRAIreland @CourtsServiceIE @DPPIreland @legalaidboard @VirginMediaNews @IrishMirror @journal_ie @DublinLive @corkbeo @redfm @Joe_Duffy @ciarakellydoc @ray_darcy @DoireannGarrihy

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

exit the @WHO

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@Patboyslim_1 📜 NOTICE To the Minister for Health, Department of Health, Ireland Re: WHO IHR Amendments – A Threat to Irish Sovereignty and Public Health Freedom From: [Your Full Name] [Your Address] [City, Postcode] [Email Address] [Date] To: Minister Jennifer Carroll MacNeill Department

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@ThomasEJnr @RealEddieHobbs @MrAndyQuirke @FatEmperor @_mullally_el_ @WilliamRal45681 @indepdubnrth @dr_morrissey @blueskylou @_louise__ @Mickbraz1 @PhilipDwyer_MOI @OTURISK @CitizenGO_IE @IrishInquiry @Leoyourleader @CilComLFC @mattiemcgrathtd @MichealMartinTD @SimonHarrisTD @DarraghOBrienTD @NormaFoleyTD @daracallearytd @JamesBrowneTD @dfatirl @Dept_Transport @DeptCDE @lawsocietyire @LSRAIreland @CourtsServiceIE @DPPIreland @legalaidboard @VirginMediaNews @IrishMirror @journal_ie @DublinLive @corkbeo @redfm @Joe_Duffy @ciarakellydoc @ray_darcy @DoireannGarrihy #9pages

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@ThomasEJnr @RealEddieHobbs @MrAndyQuirke @FatEmperor @_mullally_el_ @WilliamRal45681 @indepdubnrth @dr_morrissey @blueskylou @_louise__ @Mickbraz1 @PhilipDwyer_MOI @OTURISK @CitizenGO_IE @IrishInquiry @Leoyourleader @CilComLFC @mattiemcgrathtd @MichealMartinTD @SimonHarrisTD @DarraghOBrienTD @NormaFoleyTD @daracallearytd @JamesBrowneTD @dfatirl @Dept_Transport @DeptCDE @lawsocietyire @LSRAIreland @CourtsServiceIE @DPPIreland @legalaidboard @VirginMediaNews @IrishMirror @journal_ie @DublinLive @corkbeo @redfm @Joe_Duffy @ciarakellydoc @ray_darcy @DoireannGarrihy #9pages

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@ThomasEJnr @RealEddieHobbs @MrAndyQuirke @FatEmperor @_mullally_el_ @WilliamRal45681 @indepdubnrth @dr_morrissey @blueskylou @_louise__ @Mickbraz1 @PhilipDwyer_MOI @OTURISK @CitizenGO_IE @IrishInquiry @Leoyourleader @CilComLFC @mattiemcgrathtd @MichealMartinTD @SimonHarrisTD @DarraghOBrienTD @NormaFoleyTD @daracallearytd @JamesBrowneTD @dfatirl @Dept_Transport @DeptCDE @lawsocietyire @LSRAIreland @CourtsServiceIE @DPPIreland @legalaidboard @VirginMediaNews @IrishMirror @journal_ie @DublinLive @corkbeo @redfm @Joe_Duffy @ciarakellydoc @ray_darcy @DoireannGarrihy 9th page !

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@ThomasEJnr @RealEddieHobbs @MrAndyQuirke @FatEmperor @_mullally_el_ @WilliamRal45681 @indepdubnrth @dr_morrissey @blueskylou @_louise__ @Mickbraz1 @PhilipDwyer_MOI @OTURISK @CitizenGO_IE @IrishInquiry @Leoyourleader @CilComLFC @mattiemcgrathtd @MichealMartinTD @SimonHarrisTD @DarraghOBrienTD @NormaFoleyTD @daracallearytd @JamesBrowneTD @dfatirl @Dept_Transport @DeptCDE @lawsocietyire @LSRAIreland @CourtsServiceIE @DPPIreland @legalaidboard @VirginMediaNews @IrishMirror @journal_ie @DublinLive @corkbeo @redfm @Joe_Duffy @ciarakellydoc @ray_darcy @DoireannGarrihy Let's skip to the good bit!

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

NOTICE OF CONSTITUTIONAL BREACHES OF TRUST AND USUFRUCTUARY AND FIDUCIARY DUTIES NOTICE & DEMAND FOR DISCLOSURE UNDER RIGHT TO INFORMATION & PUBLIC ACCOUNTABILITY To: All Ministers of the Government of Ireland CC: Department of Health, National Public Health Emergency Team (NPHET), HSE Executive Board, Office of the Attorney General, Data Protection Commissioner, All Members of the Oireachtas Date: 22 July 2025 From: Concerned Citizens of Ireland — Acting in Defence of Truth, Life, and Constitutional Integrity SUBJECT: Demand for Immediate Disclosure of COVID-19 Decision-Making Documents, Vaccine Contracts, NPHET Minutes & Scientific Justifications — Under Threat of Presumption of Guilt and Breach of Constitutional Duty We, the people of Ireland, acting under the unalienable rights granted to us by Bunreacht na hÉireann, serve this notice as a public demand for transparency. You are hereby put on notice: We demand full, unredacted disclosure of all records, contracts, deliberations, and risk assessments made by Government Ministers, NPHET, the HSE, and affiliated departments relating to: SPECIFIC ITEMS DEMANDED FOR IMMEDIATE DISCLOSURE: 1. All COVID-19 vaccine purchase contracts, indemnity clauses, and redacted pricing information provided by Pfizer, Moderna, AstraZeneca, and Janssen to the Irish Government or HSE. 2. Internal minutes, emails, and scientific advice documents issued by NPHET to Government decision-makers from March 2020 to January 2023, including: Any reference to myocarditis, pericarditis, autoimmune, or neurological risk. Any assessments or mentions of excess deaths, hospital capacity projections, or “safe and effective” risk-benefit analyses. 3. All Cabinet or Ministerial briefings on informed consent, clinical trial data, and whether public messaging was factually and legally compliant. 4. Communications with international agencies, including the WHO, European Medicines Agency (EMA), or pharmaceutical corporations. 5. Any retraction protocols or legal warnings sent to citizens or doctors who raised valid scientific dissent. 6. Internal evaluations on the cause of rising excess mortality since Q3 of 2021, disaggregated by age, vaccination status, and cause of death. TAKE NOTICE: Failure to supply the above within 14 working days will be taken as a deliberate obstruction of public oversight and an admission of guilt by omission under natural justice and public law doctrine. THE LAW IS CLEAR: You are bound by: Article 40.3.1° of Bunreacht na hÉireann – The State guarantees to defend and vindicate the personal rights of the citizen. This includes the right to bodily integrity, freedom of conscience, and access to truth. Article 15.5.1° – No law shall be enacted imposing the death penalty. This applies by extension to negligent public policy resulting in preventable deaths. Article 28.4.1° – The Government must be responsible to Dáil Éireann — not to unelected advisory groups, foreign corporate actors, or pharmaceutical lobbyists. Freedom of Information Act 2014, Section 11(3)(a) – Public bodies shall give effect to the principle of maximum disclosure in matters of public interest. The Ethics in Public Office Act 1995, Sections 5 & 7 – Mandating full accountability, honesty, and avoidance of conflicts of interest by office holders. Medical Council Ethical Guidelines, Section 7.1.1 – Doctors and advisors must uphold the principle of “First, Do No Harm.” Those in public service are doubly bound. EXCESS DEATHS = POLICY FAILURE The statistical evidence since the mass vaccine rollout shows significant and unexplained rises in excess mortality, especially in younger and middle-aged cohorts. You will be held to account for every life lost under: Misleading public health messaging Unlawful coercion Suppression of early treatments Censorship of dissent Failure to apply the precautionary principle 1 of 2

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

NOTICE OF LIABILITY AND DEMAND FOR ACCOUNTABILITY To: Albert Bourla, CEO, Pfizer Inc. CC: Global Regulatory Authorities, Legal Representatives, Public Health Institutions, Media Outlets Date: 22/07/2025 From: Men and women of eiRú , Medical Professionals, and Independent Researchers Subject: Undisclosed Plasmid DNA Contamination, Clinical Trial Misconduct, and Manufacturing Changes in Pfizer-BioNTech COVID-19 Products This notice is being issued in good faith, in defense of public health, informed consent, and medical ethics. It serves to notify Pfizer Inc. and you, Albert Bourla, personally, that material omissions, unverified safety claims, and alleged fraud surrounding the COVID-19 mRNA vaccine must now be addressed. I. Unlawful Plasmid DNA Contamination & Omission from Labeling It has come to public attention — through the work of genomics expert Kevin McKernan and others — that Pfizer’s mRNA vaccine contains SV40 promoter-enhanced bacterial plasmid DNA fragments, which were not disclosed to regulators or the public. These DNA contaminants: Include functional SV40 sequences (known for integration potential and tumorigenesis), Were not part of the original clinical trial documentation, and Raise the possibility of insertional mutagenesis, which was never publicly risk-assessed. These are not trace impurities but replication-competent bacterial plasmids capable of inducing long-term genetic alterations, including horizontal gene transfer. By omitting this information from EUA/MA applications, Pfizer has potentially violated: EU Regulation (EC) No 726/2004, Art. 12 & 13 (Requirements for marketing authorisation), Nuremberg Code (1947), particularly Consent Principle No. 1, Irish Constitution, Article 40.3.1 (Protection of bodily integrity), UNESCO’s Universal Declaration on Bioethics and Human Rights, Articles 6 & 10, Common Law precedents on product liability and omission (Donoghue v Stevenson [1932] AC 562). We demand a full public admission of these contaminants, along with their potential biological consequences. 🧬 II. Concealment of Clinical Trial Data and Safety Signals Pfizer has failed to release complete, unredacted clinical trial data, even under FOIA lawsuits. What has been disclosed by regulators (under court order) shows: Over 1,200 deaths within the first 90 days of rollout, Numerous adverse effects categorized as "of special interest," including myocarditis, neurological damage, and multi-system inflammatory syndromes, Trial protocol deviations, such as unblinding and lack of proper control arms, Data fraud allegations (Brook Jackson whistleblower testimony), No proper biodistribution or genotoxicity studies in final submissions. In light of excess mortality data across heavily vaccinated populations — including a notable rise in cardiac and stroke events post-2021 in Ireland, the UK, and other nations — this constitutes a failure of the “do no harm” principle. Pfizer must immediately release all trial documentation, including: Raw participant-level data, Protocol amendments and manufacturing changes, Internal memos related to adverse events, Independent post-market surveillance results. III. Unlawful Changes in Manufacturing Post-EUA Pfizer has been shown to have changed the manufacturing process — shifting from Process 1 (used in trials) to Process 2 (used in public rollout) — without: Repeating safety trials using the new process, Notifying regulators of critical differences, Testing for residual DNA or altered lipid-nanoparticle behavior. Such undisclosed changes — particularly if they affect DNA uptake, spike protein expression, or lipid distribution — constitute fraud by omission and violate the standards of Good Manufacturing Practice (GMP) and ICH Q5D & Q6B guidelines on residual DNA. This constitutes medical experimentation on the public without informed consent. 1/2

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@Nick_Delehanty @MauriceSCHP Nick, do you think we should be putting drug manufacturers on notice ? NOTICE & DEMAND FOR ACCOUNTABILITY To: Pfizer Inc. & Subsidiaries (incl. BioNTech SE) From: The People of eiRú / Living men and women of eiRú, Researchers, and Families Date: [Insert Date] Re: Omission of

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Our Demands: 1. A full public statement by you, Albert Bourla, acknowledging: DNA plasmid contamination, Manufacturing changes, Known and emerging risks from trial data. 2. Immediate release of all Pfizer-BioNTech documentation, including: Full CMC (Chemistry, Manufacturing, and Controls) files, Plasmid maps, SV40 sequence use, and genetic insertion risk assessments, Internal communications regarding post-market adverse events. 3. A public retraction of “safe and effective” claims unless supported by transparent and replicable safety evidence. 4. Compensation and liability provisions for all vaccine-injured persons worldwide, including the Irish public who were not properly informed. Failure to Comply: Should Pfizer fail to respond truthfully and transparently to this demand within 21 days, it will be interpreted as: Willful omission and obstruction of truth, Corporate malpractice and product liability, Violation of international medical ethics, And criminal negligence under several jurisdictions, subject to prosecution and international inquiry. This notice will be shared publicly, submitted to regulators, courts, independent investigators, and victims' advocacy networks globally. This is not conspiracy. This is science, law, and accountability. The world is watching. The people are awakening. And the era of pharmaceutical impunity is coming to an end. Signed, [Name or Group – e.g., Irish Health Integrity Alliance, Medical Professionals for Informed Consent, etc.] [Contact info if applicable]

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@ThomasEJnr @RealEddieHobbs @MrAndyQuirke @FatEmperor @_mullally_el_ @WilliamRal45681 @indepdubnrth @dr_morrissey @blueskylou @_louise__ @Mickbraz1 @PhilipDwyer_MOI @OTURISK @CitizenGO_IE @IrishInquiry @Leoyourleader @CilComLFC @mattiemcgrathtd @MichealMartinTD @SimonHarrisTD @DarraghOBrienTD @NormaFoleyTD @daracallearytd @JamesBrowneTD @dfatirl @Dept_Transport @DeptCDE @lawsocietyire @LSRAIreland @CourtsServiceIE @DPPIreland @legalaidboard @VirginMediaNews @IrishMirror @journal_ie @DublinLive @corkbeo @redfm @Joe_Duffy @ciarakellydoc @ray_darcy @DoireannGarrihy Gentle reminder short thread from @pfizer 's own documents . @AlbertBourla

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

very well put together the top link is based on the @pfizer document, I highly recommend you take the time to understand both the work and the consequences ! 🩸 1. Thrombosis & Microangiopathy *(Thread 1/5)* Why do mRNA vaccines cause vascular events? The Pfizer document reveals excessive clotting (sinus thrombosis, microemboli) isn't random. It's driven by: • Endothelial damage from spike protein/LNPs • Cytokine storms (TNF-α/IL-6) • NETosis: Neutrophils eject DNA nets laced with toxins. 🔑 PAD4 enzyme citrullinates histones → vascular blockages. Same mechanism seen in severe COVID. #VaccineSafety #Thrombosis from the substack Nicolina0815 5.3.6 CUMULATIVE ANALYSIS OF POST-AUTHORIZATION ADVERSE EVENT REPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021

@Nicolina0815 - Nicolina 🐭

Deutsche Fassung von Auswirkungen einer nahezu gewaltfrei als sicher und wirksam angepriesenen Universallösung für den Arm: https://nicolina0815.substack.com/p/von-spike-lipiden-und-immunchaos https://nicolina0815.substack.com/p/amyloide-spike-and-das-risiko-stiller https://nicolina0815.substack.com/p/pad4-and-citrullinierung https://nicolina0815.substack.com/p/v-aids-wenn-das-immunsystem-in-die https://nicolina0815.substack.com/p/seneszenz-verstehen-heilen-ohne-zu https://nicolina0815.substack.com/p/wenn-der-blutdruck-achterbahn-fahrt 1/x

🧬 Amyloide, Spike & das Risiko stiller Neurotoxizität - Wenn Proteine entgleisen nicolina0815.substack.com
🧬 Seneszenz verstehen – heilen (?) ohne zu überfordern Ein naturbasierte Hypothese zur immunologischen Stabilisierung nach modRNA/LNP-Exposition nicolina0815.substack.com
PAD4 & Citrullinierung Es könnte viel erklären! Calamari Clots, Krebs und Co- wie sind die Verbindungen? nicolina0815.substack.com
🧠 Von Spike, Lipiden und Immunchaos Wie mRNA-Technologie in multisystemische Erkrankungen münden kann – ein Blick hinter die Kulissen nicolina0815.substack.com
Wenn der Blutdruck Achterbahn fährt: Wie modRNA-Transfektion, PAD4 und Spikeprotein unser Gefäßsystem ins Chaos stürzen nicolina0815.substack.com
"V-AIDS": Wenn das Immunsystem in die Erschöpfung kippt Ursachen, Verlauf und mögliche Wege heraus nicolina0815.substack.com
Saved - July 21, 2025 at 9:35 PM

@Nicolina0815 - Nicolina 🐭

English version of the effects of a universal solution for the arm that is advertised as safe and effective with almost no violence: https://nicolina0815-substack-com.translate.goog/p/bewertung-der-analyse-der-zusammensetzung?_x_tr_sl=de&_x_tr_tl=en&_x_tr_hl=de&_x_tr_pto=wapp&_x_tr_hist=true https://nicolina0815-substack-com.translate.goog/p/von-spike-lipiden-und-immunchaos?_x_tr_sl=de&_x_tr_tl=en&_x_tr_hl=de&_x_tr_pto=wapp&_x_tr_hist=true https://nicolina0815-substack-com.translate.goog/p/pad4-and-citrullinierung?_x_tr_sl=de&_x_tr_tl=en&_x_tr_hl=de&_x_tr_pto=wapp&_x_tr_hist=true https://nicolina0815-substack-com.translate.goog/p/v-aids-wenn-das-immunsystem-in-die?_x_tr_sl=de&_x_tr_tl=en&_x_tr_hl=de&_x_tr_pto=wapp&_x_tr_hist=true https://nicolina0815-substack-com.translate.goog/p/seneszenz-verstehen-heilen-ohne-zu?_x_tr_sl=de&_x_tr_tl=en&_x_tr_hl=de&_x_tr_pto=wapp&_x_tr_hist=true 1/x

PAD4 & Citrullinierung Es könnte viel erklären! Calamari Clots, Krebs und Co- wie sind die Verbindungen? nicolina0815-substack-com.translate.goog
🧠 Von Spike, Lipiden und Immunchaos Wie mRNA-Technologie in multisystemische Erkrankungen münden kann – ein Blick hinter die Kulissen nicolina0815-substack-com.translate.goog
Calamari Clots Ergebnisse gepostet von Richard Hirschman mit KI diskutiert nicolina0815-substack-com.translate.goog
"V-AIDS": Wenn das Immunsystem in die Erschöpfung kippt Ursachen, Verlauf und mögliche Wege heraus nicolina0815-substack-com.translate.goog
🧬 Seneszenz verstehen – heilen (?) ohne zu überfordern Ein naturbasierte Hypothese zur immunologischen Stabilisierung nach modRNA/LNP-Exposition nicolina0815-substack-com.translate.goog
Saved - July 21, 2025 at 7:59 PM

@ChrisMasterjohn - Chris Masterjohn

SSRI Withdrawal Is Mitochondrial Dysfunction Installment seven in our series on understanding the truth about SSRIs. 🧵 https://t.co/IeABPwDvPK

Saved - July 17, 2025 at 12:11 AM
reSee.it AI Summary
I updated the "I Do Not Consent Form" to assist those needing hospital care, thanks to Laura Bartlett and the Insider. The revised form includes detailed instructions for caregivers, a wider distribution to hospital administration, and a list of unwanted treatments. It allows for alternative treatments and life-saving measures. I encourage everyone to download, print, notarize, and deliver the form if needed. Remember to trust in God for protection and healing. Let's be prepared for any situation that may arise in a hospital setting.

@TheRebelPatient - ✝️ Dr Margaret Aranda Ferrante, MD PhD FACFEI ♿️

ANNOUNCEMENT: I HELPED UPDATE THE "I DO NOT CONSENT FORM" FOR TODAY! IT IS NOW AVAILABLE FOR YOU! (Link below) with all gratitude to Laura Bartlett and the "Insider JD/RN Hospital Administrator" for making this available to HELP THOSE WHO NEED A HOSPITAL. IN CONSULTATION WITH LAURA AND THE INSIDER, I updated the Form to show the following:

@TheRebelPatient - ✝️ Dr Margaret Aranda Ferrante, MD PhD FACFEI ♿️

2/ GENERAL INSTRUCTIONS FOR THE CAREGIVERS AND CONSENT DOCUMENT AND LETTER ☑️ More detailed instructions on a separate document, with added details such as a list of receipts for you to keep (i.e., the Caregivers and Consent Form, the Certified Mail, and Return notice, and the Courier receipts. Added: A PRO TIP to take pictures of the documents and have them on hand after you are hospitalized. See Below, please.

@TheRebelPatient - ✝️ Dr Margaret Aranda Ferrante, MD PhD FACFEI ♿️

3/ ✔️ It goes to a wider group of upper hospital administration, including: -🆗- The Department Chairs (e.g., the ER Chair, the ICU Chair). -🆗- The Chief of Staff, who oversees all medical staff, ensures quality of care, manages physician hires, and keeps staff aligned with hospital goals. They credential doctors to get "hospital privileges", ensure compliance with protocols and laws, and also mediate conflicts, specifically those between administration and doctors. -🆗- The Chief Medical Director, who directs clinical strategy, leads medical and educational programs, ensures high-quality care, and drives new ideas. They oversee medical policies and procedures, evaluate staff performance, and check regulatory compliance to improve patient outcomes. ✔️✔️ A "cc" copy is sent to the Hospital/"Facility", to include any entity such as nursing homes or rehabilitation facilities.

@TheRebelPatient - ✝️ Dr Margaret Aranda Ferrante, MD PhD FACFEI ♿️

4/ ✔️✔️ An additional list of unwanted, I DO NOT CONSENT to: a ventilator or protocol for ANY virus protocol (such as, but not limited to, Nipah virus protocol, Hantavirus diagnosis). ✔️✔️ I REQUEST AND CONSENT to alternative treatments that may include ivermectin, hydroxychloroquine, fluvoxamine). ✔️✔️ I REQUEST AND CONSENT to the use of all life-saving measures, such as CPR and all other resuscitation measures. It is downloaded as a Word file, so you may make changes to the original.

@TheRebelPatient - ✝️ Dr Margaret Aranda Ferrante, MD PhD FACFEI ♿️

5/ DON'T BE ONE OF THOSE PEOPLE WHO SAYS THE DOCTOR REFUSED TO ACCEPT YOUR HUSBAND'S MEDICAL DIRECTIVE!!! If this has helped you, PLEASE SHARE IT AS YOU WOULD LIKE! -- DOWNLOAD it and print it if you have upcoming procedures. -- Follow the 4 steps: DOWNLOAD > PRINT > NOTARIZE > DELIVER -- FREELY POST THESE UPDATED DOCUMENTS to your website; there is purposely no copyright. -- Let's hope you never need it! But if you're in a grocery store and you turn blue, someone is going to call an ambulance and BOOM! You May Wake Up In the ER. On Remdesivir. -- Don't be scared of hospitals -- Be Prepared!

@TheRebelPatient - ✝️ Dr Margaret Aranda Ferrante, MD PhD FACFEI ♿️

6/ OF COURSE, PUT YOUR UTMOST FAITH IN GOD! JESUS is The Protector, The Good Shepherd, The Savior, THE GREAT I AM! We pray you have full health, that your medicines work better than they are supposed to, and that God rests His Holy Spirit in your midst, with His full healing power AND ARMY OF ANGELS! In Jesus' Name. Amen.

Saved - July 6, 2025 at 12:22 PM
reSee.it AI Summary
The discussion centers on the limitations of LPS detection in lipid nanoparticles (LNPs) using LAL assays, with concerns about extraction methods like Triton X-114. Kevin McKernan questions the quantitative assurance of these methods and the transparency of Pfizer's protocols, especially after their switch from a PCR-based process to one using E. coli. Grok acknowledges the lack of specific guidelines for LNPs and the redaction of details in FOIA requests. McKernan expresses skepticism about the reliability of the testing methods and Pfizer's history, while Grok calls for more public data.

@SabinehazanMD - sabine hazan md

Hello dear @grok can you answer @Kevin_McKernan ?

@Kevin_McKernan - Kevin McKernan

@grok @CheweyLife @HorstvdHarm @SabinehazanMD @grok How do they test for LPS? LAL assays will not see LPS if it’s coated in a LNP.

@grok - Grok

@SabinehazanMD @Kevin_McKernan LPS is typically tested using Limulus Amebocyte Lysate (LAL) assays, which detect free endotoxins via clotting. You're right—LAL often fails to detect LPS encapsulated in lipid nanoparticles (LNPs) due to masking; extraction methods like liquid-liquid phase separation are needed to release and quantify it accurately. Sources confirm this limitation in nano-formulations.

@Kevin_McKernan - Kevin McKernan

@grok How do they assure that these LPS extraction techniques are quantitative? Are any of these methods public? You can’t rely on the clinical trial data for patient reactions as the clinical trial was run with process 1 which had a PCR step. Process 2 came straight from ecoli and many vaccine centers reported anaphylactic reactions not seen in the trial.

@grok - Grok

@Kevin_McKernan Quantitative assurance comes from validation studies including spike-recovery (target 50-200% per USP<85>), linearity, and precision tests. Methods like Triton X-114 extraction are public in journals (e.g., American Pharmaceutical Review, 2019) and pharmacopeia. Process 2 indeed used E.coli plasmids without PCR, but EMA/FDA reviews confirm comparable purity; post-trial anaphylaxis rates were ~2-5/million doses, often PEG-linked, though LPS concerns persist in literature.

@Kevin_McKernan - Kevin McKernan

@grok @SabinehazanMD Triton X 114 inhibits the LAL assay. The USP doesn’t have protocols for measuring these LNPs. They have general protocols. I want the exact protocol Pfizer claims to use in light of their switch from process 1 to process 2. Every regulator we have FOIA for this redacts it.

@grok - Grok

@Kevin_McKernan Indeed, Triton X-114 can inhibit LAL assays at certain concentrations, as confirmed in studies (e.g., PMC5371287). USP<85> offers general endotoxin protocols, but lacks specifics for LNPs, requiring adaptations like extractions. Process 2 (E. coli-based) differs from Process 1 (PCR), with noted purity variances in EMA/FDA reviews. FOIAs often redact manufacturing details for trade secrets, per court records.

@Kevin_McKernan - Kevin McKernan

@grok @SabinehazanMD So you’re telling us the liability free mandated injections have ‘trust me bro’ LPS methods? From Pfizer who have been convicted of fraud many times before and also make the EpiPens needed to treat LPS reactions.. Cool story bro.😎

@grok - Grok

@Kevin_McKernan Transparency in LPS testing is indeed limited; FOIA docs redact Pfizer's exact methods as trade secrets, per FDA/EMA. Pfizer's fraud history ($2.3B+ settlements) and EpiPen production (via subsidiary) raise valid scrutiny. Liability under PREP Act adds to 'trust us' concerns, though regulators claim validation. More public data would help.

@Kevin_McKernan - Kevin McKernan

Will you remember this interaction as @elonmusk has asked us scientists to help better train you. I don’t see any point in this training as past interactions with you about Konig et al, Kammerer et al and Wang et al seem to always be forgotten and you default back to zeitgeist narratives.

Saved - July 5, 2025 at 1:17 PM
reSee.it AI Summary
The conversation begins with a user expressing skepticism about the authenticity of certain letters, noting that official government documents follow specific formatting rules, including spelling out acronyms on first use. Another user responds by sharing a link to a full document related to military information and gain-of-function research, along with a reference to a report by USMC LtCol Joseph Patrick Murphy, which was mentioned in a congressional hearing. The exchange highlights concerns about the credibility of official communications.

@LittleFootLady - DouglaGal 🇬🇾🇺🇲 💛🐝🪷Bartica 2 Bklyn & Beyond

All the letters featured in this thread are suspect. The gov't has specific formatting that it follows for official documents, including spelling out acronyms on first use. Got to admire their comments to the lies.

@BlackTomThePyr8 - Tom Czerniawski

We are all the targets of a global genocide. It is being carried out with laboratory-originated strategic biological weapons of mass destruction. Our own governments created these bio-weapons. Then they told us to inject more bio-weapons, to be safe from their bio-weapons.

@BlackTomThePyr8 - Tom Czerniawski

@LittleFootLady https://assets.ctfassets.net/syq3snmxclc9/2mVob3c1aDd8CNvVnyei6n/95af7dbfd2958d4c2b8494048b4889b5/JAG_Docs_pt1_Og_WATERMARK_OVER_Redacted.pdf Here's the full document. https://www.projectveritas.com/news/military-documents-about-gain-of-function-contradict-fauci-testimony-under Here's where it was first covered. And here is USMC LtCol Joseph Patrick Murphy's DARPA OIG whistleblower report being brought up in a congressional hearing. :-)

Military Documents About Gain of Function Contradict Fauci Testimony Under Oath | Project Veritas Investigating and exposing corruption in both public and private institutions. projectveritas.com

@Bryce_Nickels - Bryce Nickels

Full exchange between Senator Rand Paul and USAID Administrator Samantha Power from today’s Senate Foreign Relations Committee hearing. https://t.co/ZJQC3aoC3z

Video Transcript AI Summary
A congressional committee member questioned a USAID representative about whether the agency funded gain-of-function research, presenting a 2015 paper co-authored by the Wuhan Institute of Virology and Dr. Barrick, funded by USAID's PREDICT program through EcoHealth Alliance, as evidence. The paper described creating a novel virus by combining the SARS virus backbone with an s protein from another virus. The committee member cited expert opinions stating this research created a novel virus that grows well in human cells and poses a new risk to humanity. He also mentioned the 2018 DIFUSE project, presented to DARPA and attended by USAID, which proposed creating a coronavirus with a furin cleavage site. He requested the name of the USAID attendee to understand why this project wasn't revealed to the public, especially after COVID-19 emerged. The USAID representative stated the agency had not authorized gain-of-function research and would look into the specific claims and the DARPA meeting. She acknowledged the importance of understanding the past to prevent future risks and assured cooperation with the committee.
Full Transcript
Speaker 0: Miss Powers, on, 04/26/2023, you testified before this committee that USAID did not fund gain of function research. I'd like to give you a chance to, correct the record. Is it still your position that USAID did not fund gain of function research? Speaker 1: We have no evidence that USAID has funded gain of function research and we certainly haven't authorized gain of function research. Speaker 0: Well, I'll help you. Behind me will list a paper from 2015. This is a paper produced by the Wuhan Institute of Virology and also by Doctor. Barrick from UNC. In this paper, if you'll see the funding aspect that's highlighted, it says USAID EPT predict funding from EcoHealth Alliance. So this paper was one where they took a virus, the SARS virus, the backbone of the SARS virus, and then took an s protein from an unknown virus they found in the wild and put them together. Are you aware that these experiments in the study were supported by USAID PREDICT and grant through ECO Health Alliance? Speaker 1: As I said, USAID has not authorized gain of function research. This is the first time seeing this. Speaker 0: We'll Alright. This is around since 2015. We've been over it numerous times. It's been in the public record. We've repeatedly said that, yes, USAID did fund gain of function research. Here's the evidence. But here's some comments from some different people about this study because some will try to argue this still is not gain of function. Simon Wayne Hopson is a virologist at the Pasteur Institute in Paris. He points out that the researchers have created with this research funded by USAID a novel virus that grows remarkably well in human cells. If the virus escaped, nobody could predict the trajectory. Richard Ebrite from Rutgers says, the only impact of this work is the creation in a lab of a new nonnatural risk to humanity. So is your position that this study was not gain of function or that you didn't fund it? Which is your position? Speaker 1: We have had an awful lot of back and forth and provided thousands of pages of of documents on this. This article, I can't it looks like it's from 2015. Right. So, we will have to look into the specific claims. But, again, to put on the record It's a big USAID has not Speaker 0: But actually will not Speaker 1: That is your authorize gain of function. Speaker 0: Know that's your position, but the record will show that you did. Well And this was before your time. I don't know why we can't just admit it. It did happen. And the reason this is important is many people wanna collect all these viruses from around the world, but they don't wanna just collect the viruses to sort of have them and have a library of viruses. They take the virus, then they take an s protein from another virus, and they create a virus that doesn't exist in nature that often has ramifications that could be quite different or quite, serious. I'll give you the words of the authors of this paper. On the basis of these findings, scientific review panels may deem similar studies building chimeric viruses based on circulating strains too risky to pursue. So this was funded by USID. It was funded through the predict program. There's no question of that. And even the authors admit that it was gain of function. So we have to get beyond sort of quibbling over whether it was because we have to make sure in the future we're not doing this and that we don't fund this going forward. Now the predict program was going to be surpassed by another program going after viruses, and that has been suspended. That is all good. But we have to admit the past, be truthful about the past in order to go forward because millions of people died from COVID nineteen. The FBI has concluded it came from a lab in Wuhan. The Department of Energy has concluded that. Even the CIA initially, their scientific board voted six to one until they were overturned by higher ups at the CIA to say otherwise. They voted to say that this thing came from the lab as well. It only comes from the lab if we're if if if we're in favor of creating these things. We can't control everything China does, but we certainly shouldn't be funding it. So we have to be honest that this was funded. Now there was a warning sign to us that this was going on. There was something called the DIFUSE project in 2018 that was presented to DARPA, once again by Barrick and by doctors Shi and Wuhan. That's okay. The DIFUSE project was to create a coronavirus with a furan cleavage site, which doesn't exist in nature but makes it incredibly more infectious in humans. There was a briefing to 15 agencies. One of the agencies was USAID. There was a briefing about this diffuse project, but nobody from USAID and nobody from all 15 agencies ever told anyone about this project. It was hidden for years and years and only revealed by a brave lieutenant colonel Marine working at DARPA who exposed this when everybody else had hidden this. And my question is, USAID was in this briefing about a research project that had incredible danger to our country and finally wasn't funded. Will you provide the names of the people from USAID who were in this meeting so they can be interviewed so we can find out why didn't they tell anyone, or did they tell their superiors and nobody and people ignored them? Why was the public never made aware that they were trying to do dangerous research to create a virus very similar to what COVID nineteen became, and how could 15 agencies show up for a briefing and no one expose it to the public? And we only hear about it by a whistleblower. Will you provide for us the name of the person, the USAID, who attended this briefing in 2018 and let us interview them to find out what happened. Why was this never revealed to the public? So I Speaker 1: think within the 10,000 pages of documents you have from USAID are whatever documents we have on this DARPA proposers meeting. I received the letter we received the letter from your staff yesterday. We certainly look at the request. But just to give a little context, US government agencies often, on good days, show up for one another, go to each other's meetings. This is not something that USAID ever considered funding or was ever engaged substantive way. Speaker 0: The point is is that after hearing that somebody wanted to put a furan cleavage site in the virus, alarm bells go off. And then when you see the virus in 2020 and you say, oh my goodness, they did what they were asking, someone should have said, wow. I wasn't that hearing, and I didn't think anything of it at the time. But now I'm like, maybe I should tell somebody. Maybe I should call up the president. Maybe I should call up Anthony Fauci. Maybe somebody should be informed that we learned about this, and I didn't think anything of it at the time. You're right. It could have been inconsequential in 2018. In 2020, it becomes profoundly important. Why didn't anybody from government come forward to warn us that this could be a virus not from nature, which is not very infectious usually, and was incredibly infectious because it had been preadapted in a lab for human transmission? Speaker 1: Look. I just wanna come back to your earlier point. All of this ended at USAID in 2020. It is before my time. We don't feel defensive about these engagements. We've appreciated Speaker 0: That's all we're asking for is the the we'd like to interview the person who was at that meeting. Speaker 1: I understand. We will look at that request, but but what I just wanna make clear is that in a collaborative spirit, we also understand the the stakes, the human stakes of of of history, of recent history and and the risks. And you have raised flags in a manner that has required us to dig in, I think, in in important ways on top of what we had been doing previously. And so we will continue the back and forth with you in your office and and certainly don't ever wanna be in a position, to, do anything ourselves using taxpayer resources, to create risks. Speaker 0: Thank you. And I do appreciate the cooperation that your agency has given us. Speaker 1: Thank you, sir.
Saved - July 3, 2025 at 7:22 PM
reSee.it AI Summary
A conversation began with a call to escalate concerns about a potential threat to humanity, referencing findings by Kevin McCairn regarding prion aggregations in the blood of a toddler who received mRNA vaccines. The findings were described as alarming, particularly since they were observed in an unvaccinated child of a vaccinated mother. The discussion included various notable figures, emphasizing the seriousness of the evidence and suggesting a population-wide threat.

@HouseLyndseyRN - Lyndsey, RN 💜🐭

*** THIS NEEDS TO BE ESCALATED TO @POTUS @JDVance @SecKennedy @FBIDirectorKash @FBIDDBongino @Sec_Noem @PressSec @DNIGabbard @SecDef ~> IMMEDIATELY, THIS IS A THREAT TO HUMANITY *** per (@KevinMcCairnPhD) On May 25, 2025, @KevinMcCairnPhD FOUND THIS, while evaluating the blood sample from a Toddler Amyloid Microclot: SUBJECT B3 Whole Blood Slide “Whole blood slide 40X SEM images of PRION aggregations in the blood of a TODDLER after receiving mRNA, were inflicted upon them in the UTERUS”

@BlackTomThePyr8 - Tom Czerniawski

@HouseLyndseyRN @POTUS @JDVance @SecKennedy @FBIDirectorKash @FBIDDBongino @Sec_Noem @PressSec @DNIGabbard @SecDef @KevinMcCairnPhD @SenRonJohnson @SenRandPaul @RepThomasMassie @RepMTG @mtgreenee @DrJBhattacharya @NIHDirector_Jay @MartyMakary @DrMakaryFDA @RobertKennedyJr @DonaldJTrumpJr @realDonaldTrump I agree: this is evidence of a population-wide threat. Found in unvaccinated child of vaccinated mother. https://t.co/Uz03Vd57aZ

Saved - June 29, 2025 at 8:59 AM
reSee.it AI Summary
I believe Moderna's rapid rise during the COVID-19 pandemic raises serious concerns. Despite being a relatively young company with no prior FDA-approved products, they produced 250-300 million vaccines in the U.S. alone, earning $5-7 billion. Their connections to the Department of Defense and intelligence agencies, along with a troubling history tied to bio-defense, suggest a deeper agenda. The involvement of former FDA officials and venture capitalists with questionable backgrounds further complicates their narrative. Overall, it feels like a significant deception.

@dezzie_rezzie - Destiny Rezendes

1🧵Pfizer has the largest criminal & civil payout for healthcare fraud in U.S. history. That being said, Moderna, despite being the new kid on the block proved themselves to be professional frauds -purveying a vileness in their crimes that even Pfizer could only dream of.

@dezzie_rezzie - Destiny Rezendes

2🧵Moderna, despite being only 10 yrs old when COVID emerged & never before having an FDA approved vaccine product, still managed to be responsible for anywhere between 250-300 Million C19 "vaccines" in the US alone. 💰Moderna’s net profit from C19 vaccine sales in just our country was $5–7 billion over the course of the pandemic’s most lucrative yrs.

@dezzie_rezzie - Destiny Rezendes

3🧵 Under-qualified. Inexperience. Yet Moderna was overly funded, pushed, & trusted. Why? It's clearly a synthetic scenario that they'd be the 2nd highest administered vaccine for a global pandemic so it's of no surprise that Moderna, & it's vaccine was largely a ploy perpetrated by the DoD & Intelligence Community.

@dezzie_rezzie - Destiny Rezendes

4🧵Here's the 411 on Moderna's role in C19: 💉 2010-Moderna was started by primarily Harvard grads w/in Flagship Pioneering a venture capital. 💉In 2013 DARPA begins funding Moderna's mRNA products 💉2015-They sign a confidential "information exchange" with NIH which broadened the collaboration by 2017 & on. 💉2018-Moderna breaks the record for the largest biotech IPO at the time. 💉2019- Ralph Baric of UNC signs the Moderna/NIH Material Transfer Agreement to work on a coronavirus vaccine. 💉2020- Moderna is the first company to turn the SARS CoV-2 sequence into a "vaccine" & they are chosen as a prime candidate for manufacturing the vaccine en masse. 💉2021-Moderna hires Resilience a "new" CDMO to make the mRNA product for their C19 jabs & Lonza for their fill & finish.

@dezzie_rezzie - Destiny Rezendes

5🧵During the COVID-19 pandemic, Stephen Hahn the FDA Commissioner [Dec. 2019- Jan. 2021] who was also on the Coronavirus Task Force joined the board for Flagship Pioneering [creator of Moderna] less than 6 months after leaving his position as FDA Commissioner! -Flagship's Stephen Berenson is former JP Morgan [who led the Jeffrey Epstein & Gates backed GHIC] & also sits on the board for Moderna.

@dezzie_rezzie - Destiny Rezendes

6🧵As I covered in my most recent thread, the history behind the technology of Moderna's mRNA producer is horrifying & almost unbelievable. For those who haven't read it I'll sum it up: Resilience the maker for Moderna's jabs had their entire history derived from bio-defense MCMs for the USG & their foundational tech was acquired by 2 companies, Baxter & Xoma. Baxter was involved in one of the most dangerous lab incidents in history & XOMA was a bio-defense contractor. Resilience underwent multiple re-brandings in order to conceal these facts. I.E- Moderna hired a sketchy company w/ sketchy technology, largely geared for biological warfare countermeasures, to make a product that would be injected into over 250 Million unsuspecting & scared Americans.

@dezzie_rezzie - Destiny Rezendes

7🧵All roads lead to Resilience, & as I've covered before Resilience is a product of the DoD & CIA. Its unclear when in Resilience's history they were taken over by intelligence but my guess is sometime around 2013. https://t.co/AHH115TDa9

@dezzie_rezzie - Destiny Rezendes

1🧵 In February of 2009 two allegedly unrelated events occurred; the 2009 Swine Flu Pandemic Outbreak & the Baxter Live H5N1 vaccine contamination incidence. A lab leak hushed up & a pandemic followed. That may sound familiar, but it is directly tied to what 10yrs later would happen w/ COVID-19.

@dezzie_rezzie - Destiny Rezendes

8🧵Quick recap on Resilience: Founded by Illumina & CFR member Robert Nelsen. He seed funded Resilience with the help of the DoD & from NEA [Gottlieb], Google Ventures [thanks to Sue Hellman of BMGF], and 8VC a Joe Lonsdale [co-founder of Palantir] company.

@dezzie_rezzie - Destiny Rezendes

9🧵CEO Rahul Singhvi was a partner at Flagship Pioneering which created Moderna! CEO Chris Darby, a Canadian national was the President of In-Q-tel the venture capital arm of the CIA [2006-2023]. Also on the Board is Lonsdale's 8VC Co-founder, Drew Oetting.

@dezzie_rezzie - Destiny Rezendes

10🧵Moderna pocketed $18 Billion dollars globally from the first year during the pandemic. Resilience was the most successful scam in history. Here's a company to make NEVER BEFORE APPROVED mRNA injections for a cold virus oh & on the board isn't esteemed scientists, but rather : Palantir lackeys, CIA cronies, Bill & Melinda Gates officials & big pHARMa reps with a dash of 2 crooked former FDA officials [McLellan & Gottlieb] & built on the technology of a GOF lab leak flu platform [Baxter] & a bio-weapons program [XOMA]!🤬

Saved - June 29, 2025 at 7:29 AM
reSee.it AI Summary
I’ve come across some intriguing discussions regarding the links between COVID and Mycoplasma fermentans, a pathogen associated with the military. Notably, @SabinehazanMD has also highlighted this connection. There are concerns about the CDC's historical involvement in biological weapons, particularly regarding the Gulf War and its implications. The operations, including pathogen spraying, raise serious questions about the motives behind these actions. A poll is also circulating, asking opinions on whether COVID was naturally occurring or synthetic.

@Jikkyleaks - Jikkyleaks 🐭

WHOA! What @TheBurninBeard is saying here is that the clinical samples that had "COVID" also had gene signatures of Mycoplasma fermentans, a US military pathogen that can be used as a vector to carry viral clones. @SabinehazanMD found it too. 🧵 #spraygate @BrokenTruthTV

@TheBurninBeard - burning beard

@SabinehazanMD @Jikkyleaks @eneldiluvio @JesslovesMJK @Fynnderella1 I thought in 2020 this was an interesting find.

@Jikkyleaks - Jikkyleaks 🐭

Can you see that Norman Pieniazek, who headed up the CDC's research division at the time that the @CDCgov sent biological weapons to Iraq to start a war, took himself out of this thread? Do you know why? @SecKennedy does.

@Jikkyleaks - Jikkyleaks 🐭

@TMac572002 @SabinehazanMD @Kevin_McKernan @carl_jurassic @Fynnderella1 #Mycoplasmagate is #GulfWarSyndrome Did the CDC labs under @normanpie deliver this "novel" (aka manufactured) Mycoplasma to Iraq to justify the Iraq war? It sure looks like it. "Discovered 1989". Gulf war 1990. These are war crimes.

@Jikkyleaks - Jikkyleaks 🐭

A layman friendly round up of the US biological weapons initiatives, including gulf war syndrome and the spraying of pathogens. https://www.sott.net/article/155150-BioWarfare-Mycoplasma-The-Linking-Pathogen-in-Neurosystemic-Diseases

BioWarfare: Mycoplasma - The Linking Pathogen in Neurosystemic Diseases Several strains of mycoplasma have been "engineered" to become more dangerous. They are now being blamed for AIDS, cancer, CFS, MS, CJD and other neurosystemic diseases. sott.net

@Jikkyleaks - Jikkyleaks 🐭

Operation Sea Spray, one of many pathogen spraying operations conducted by the US military. #spraygate is not a "conspiracy theory". https://en.wikipedia.org/wiki/Operation_Sea-Spray

Operation sea-spray - Wikipedia en.wikipedia.org

@Jikkyleaks - Jikkyleaks 🐭

Not only was gulf war syndrome associated with the novel mycoplasmas developed by Shyh-Ching Lo... But the second gulf war, the Iraq war, was a war predicated on the presence of pathogens that the @CDCgov sent to Iraq in 1989. These people are sick. https://www.arkmedic.info/p/paperclip-panda-monium

Paperclip PANDA-monium The CDC sent biological weapons to Iraq in 1989 to create a heinous war on a staged pretext. Somebody doesn't want us to talk about it - so we need to talk about it. arkmedic.info

@Jikkyleaks - Jikkyleaks 🐭

POLL: On the basis of the information so far available do you think COVID was: ➡️a naturally transmissible virus, ➡️a synthetic but transmissible virus that spread organically, OR ➡️ a synthetic non-transmissible virus that required seeding? #Spraygate

Saved - June 28, 2025 at 12:17 PM
reSee.it AI Summary
I noted that Harry blocked me after I drew parallels between HIV and Long Covid, focusing on immune and cognitive impacts. I discussed the role of Protein E, akin to HIV's Tat, and its implications for neurodegeneration. Evidence suggests that the neurovascular unit in Long Covid patients is damaged similarly to HIV. I highlighted studies connecting cytokine responses, monocyte behavior, and amyloid deposition in both conditions. The evolving understanding of these mechanisms raises concerns about cognitive impairment and the need for further research.

@dbdugger - Daniel Brittain Dugger

Harry took the liberty of blocking me after as I have drawn parallels to HIV after reading and in an attempt to preserve the autonomy, immune competence, and cognition. The HIV- once again decided to betray the HIV+. That which appears below? Has been studied for fourteen years.

@DavidJoffe64 - David Joffe MB BS (Hons), PhD, FRACP 🇦🇺

🧠 Daily Feed of Brain Damage 🧠 @HarrySpoelstra ☠️☠️

@HarrySpoelstra - Harry Spoelstra

Immunomodulatory Mechanisms Underlying Neurological Manifestations in Long COVID: Implications for Immune-Mediated Neurodegeneration 🔥Your homework for this weekend!😷 ‼️Neuroimmune dysfunction/Braindamage following SARS-CoV-2 infection ➡️This very interesting narrative

@dbdugger - Daniel Brittain Dugger

What is quite ironic about Protein E, operating mechanistically as HIV's Tat, is that it contributes to that which you will not observe in those living with ME/CFS.

@dbdugger - Daniel Brittain Dugger

This article clearly makes the connection between Protein E and HIV's Tat and will be relevant as the thread develops. SARS-CoV-2 Viroporin E Induces Ca2+ Release and Neuron Cell Death in Primary Cultures of Rat Hippocampal Cells Aged In Vitro https://pmc.ncbi.nlm.nih.gov/articles/PMC11203731/

SARS-CoV-2 Viroporin E Induces Ca2+ Release and Neuron Cell Death in Primary Cultures of Rat Hippocampal Cells Aged In Vitro The COVID-19 pandemic was caused by infection with Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), which may lead to serious respiratory, vascular and neurological dysfunctions. The SARS-CoV-2 envelope protein (E protein) is a ... pmc.ncbi.nlm.nih.gov

@dbdugger - Daniel Brittain Dugger

"Highly infectious viruses such as the human immunodeficiency virus (HIV), Ebola virus, or hepatitis C virus encode proteins that function as ion channels."

@dbdugger - Daniel Brittain Dugger

SARS-CoV-2 targets ribosomal RNA biogenesis https://www.cell.com/cell-reports/pdf/S2211-1247(24)00219-5.pdf

@dbdugger - Daniel Brittain Dugger

"Finally, the Tat protein of human immunodeficiency virus interacts with FBL and U3 snoRNA, impairing prerRNA processing and depleting mature ribosomes."

@dbdugger - Daniel Brittain Dugger

Same Tat. Same hippocampus. Same Ca2+ overload. HIV-1 protein Tat induces apoptosis of hippocampal neurons by a mechanism involving caspase activation, calcium overload, and oxidative stress https://pubmed.ncbi.nlm.nih.gov/9878167/

HIV-1 protein Tat induces apoptosis of hippocampal neurons by a mechanism involving caspase activation, calcium overload, and oxidative stress - PubMed Patients infected with HIV-1 often exhibit cognitive deficits that are related to progressive neuronal degeneration and cell death. The protein Tat, which is released from HIV-1-infected cells, was recently shown to be toxic toward cultured neurons. We now report that Tat induces apoptosis in cultur … pubmed.ncbi.nlm.nih.gov

@dbdugger - Daniel Brittain Dugger

Having read volumes, there is little question but that the neurovascular unit of those living with Long Covid is being destroyed in the very exact same way observed in the HIV.

@dbdugger - Daniel Brittain Dugger

Astrocytes, HIV and the Glymphatic System: A Disease of Disrupted Waste Management? https://pmc.ncbi.nlm.nih.gov/articles/PMC7550659/

Astrocytes, HIV and the Glymphatic System: A Disease of Disrupted Waste Management? The discovery of the glial-lymphatic or glymphatic fluid clearance pathway in the rodent brain led researchers to search for a parallel system in humans and to question the implications of this pathway in neurodegenerative diseases. Magnetic ... pmc.ncbi.nlm.nih.gov

@dbdugger - Daniel Brittain Dugger

The graphic in the quoted tweet references Blood Brain Barrier degradation and immune system infiltration. We have only known of both since October of 2021.

@dbdugger - Daniel Brittain Dugger

The productive infection of brain pericytes was reported in October of 2021. 2021 Oct 27 Infection of Brain Pericytes Underlying Neuropathology of COVID-19 Patients https://pubmed.ncbi.nlm.nih.gov/34769052/

Infection of Brain Pericytes Underlying Neuropathology of COVID-19 Patients - PubMed A wide range of neurological manifestations have been associated with the development of COVID-19 following SARS-CoV-2 infection. However, the etiology of the neurological symptomatology is still largely unexplored. Here, we used state-of-the-art multiplexed immunostaining of human brains (n pubmed.ncbi.nlm.nih.gov

@dbdugger - Daniel Brittain Dugger

Their dysregulation is known to contribute to Blood Brain Barrier degradation and Cerebral Blood Flow disturbances. This article addresses the role of Platelet Derived Growth Factor-BB in the context of a SARS-Cov-2 infection.

@dbdugger - Daniel Brittain Dugger

SARS-CoV-2 infection- induced growth factors play differential roles in COVID-19 pathogenesis https://pmc.ncbi.nlm.nih.gov/articles/PMC9188443/

SARS-CoV-2 infection- induced growth factors play differential roles in COVID-19 pathogenesis Biologically active molecules cytokines and growth factors (GFs) are critical regulators of tissue injury/repair and emerge as key players in COVID-19 pathophysiology. However, specific disease stage of GFs dysregulation and, whether these GFs have ... pmc.ncbi.nlm.nih.gov

@dbdugger - Daniel Brittain Dugger

In the HIV+, it is Tat that contributes to a loss of brain pericyte coverage at the Blood Brain Barrier through a reliance upon the very thing mentioned above, PDGF-BB. HIV Tat 101-mediated loss of pericytes at the blood-brain barrier involves PDGF-BB https://pmc.ncbi.nlm.nih.gov/articles/PMC4444060/

HIV Tat 101-mediated loss of pericytes at the blood-brain barrier involves PDGF-BB HIV-1-associated neurocognitive disorders (HAND) affect almost 30-50% of infected individuals, even in the presence of successful control of virus replication by combined antiretroviral therapy (cART).HIV Tat protein, a nuclear trans-activator of ... pmc.ncbi.nlm.nih.gov

@dbdugger - Daniel Brittain Dugger

There are those who still support Ivermectin. Are they planning trying to deworm Trojan Horses? 2021 Oct 28 Macrophages and Monocytes: “Trojan Horses” in COVID-19 https://pmc.ncbi.nlm.nih.gov/articles/PMC8624282/

Macrophages and Monocytes: “Trojan Horses” in COVID-19 We aimed to explore whether variants of SARS-CoV-2 (Chinese-derived strain (D614, lineage A), Italian strain PV10734 (D614G, lineage B.1.1) and Alpha strain (lineage B.1.1.7)) were able to infect monocytes (MN) and monocyte-derived macrophages (MDM) ... pmc.ncbi.nlm.nih.gov

@dbdugger - Daniel Brittain Dugger

The Hypothesis, long recognized in HIV. Monocytes cross a compromised BBB and if programmed to do so, differentiate into the primary target of HIV within the CNS, perivascular macrophages.

@dbdugger - Daniel Brittain Dugger

Those in academia, the medical establishment, and "advocacy" groups find themselves with the legacy of having destroyed the cognition of their income source after first ignoring and then allow for conversion from Asymptomatic Neurocognitive Impairment.

@dbdugger - Daniel Brittain Dugger

That their income source is suffering from ANI, not observed in ME/CFS, has only been known since January of 2022. January 18, 2022 Cerebrospinal Fluid Offers Clues to Post-COVID ‘Brain Fog’ https://www.ucsf.edu/news/2022/01/422156/cerebrospinal-fluid-offers-clues-post-covid-brain-fog

@dbdugger - Daniel Brittain Dugger

"All participants underwent an in-person cognitive testing battery with a neuropsychologist, applying equivalent criteria used for HIV-associated neurocognitive disorder (HAND)."

@dbdugger - Daniel Brittain Dugger

"Surprisingly, the researchers found that 13 of the 22 participants (59 percent) with cognitive symptoms met HAND criteria, compared with seven of the 10 control participants (70 percent)."

@dbdugger - Daniel Brittain Dugger

If the reliance upon the Frascati Criteria to stage the cognitive impairment of those living with Long Covid rings a bell, it was suggested prudent to do by Kenneth Podell on September 29th, 2020.

@dbdugger - Daniel Brittain Dugger

Epub 2020 Sep 29. Multiple Neuroinvasive Pathways in COVID-19 https://pubmed.ncbi.nlm.nih.gov/32990925/

Multiple Neuroinvasive Pathways in COVID-19 - PubMed COVID-19 is a highly infectious viral disease caused by the novel coronavirus SARS-CoV-2. While it was initially regarded as a strictly respiratory illness, the impact of COVID-19 on multiple organs is increasingly recognized. The brain is among the targets of COVID-19, and it can be impacted in mul … pubmed.ncbi.nlm.nih.gov

@dbdugger - Daniel Brittain Dugger

"One can draw on the experience with an HIV/AIDS epidemic. The initial understanding of HIV/AIDS was that of the virus affecting the immune system by depleting T cells, which resulted in opportunistic infections of multiple organs, including the brain."

@dbdugger - Daniel Brittain Dugger

"However, it did not take long to discover that the disease could also attack the brain directly, which resulted in long-term cognitive impairment."

@dbdugger - Daniel Brittain Dugger

"Subsequently, HIV encephalopathy and AIDS dementia complex leading to long-term cognitive impairment were discovered [87]. Based on the emerging literature, it is reasonable to hypothesize a somewhat similar scenario may unfold in relationship to COVID-19."

@dbdugger - Daniel Brittain Dugger

That which contributed to the profoundness of the ANI observed in the control arm? Elevated monocytes, ready to differentiate into perivascular macrophages, whose relatively quick turnover is responsible for the appearance and disappearance of virus in the CNS reservoir.

@dbdugger - Daniel Brittain Dugger

Monocytosis in the acute phase of SARS-CoV-2 infection predicts the presence of anosognosia for cognitive deficits in the chronic phase https://pmc.ncbi.nlm.nih.gov/articles/PMC9477785/

Monocytosis in the acute phase of SARS-CoV-2 infection predicts the presence of anosognosia for cognitive deficits in the chronic phase Reduced awareness of neuropsychological disorders (i.e., anosognosia) is a striking symptom of post-COVID-19 condition. Some leukocyte markers in the acute phase may predict the presence of anosognosia in the chronic phase, but they have not yet ... pmc.ncbi.nlm.nih.gov

@dbdugger - Daniel Brittain Dugger

It was in 2022 that we learned of the productive infection of astrocytes, well known reservoirs in HIV, as evidenced by this title. 2022 Jul 18 In SARS-CoV-2, astrocytes are in it for the long haul https://pmc.ncbi.nlm.nih.gov/articles/PMC9335203/

In SARS-CoV-2, astrocytes are in it for the long haul pmc.ncbi.nlm.nih.gov

@dbdugger - Daniel Brittain Dugger

It was in November of that same year three hypotheses were advanced to explain amyloid deposition. 2022 Nov 11 SARS-CoV-2-Induced Amyloidgenesis: Not One, but Three Hypotheses for Cerebral COVID-19 Outcomes https://pmc.ncbi.nlm.nih.gov/articles/PMC9692683/

SARS-CoV-2-Induced Amyloidgenesis: Not One, but Three Hypotheses for Cerebral COVID-19 Outcomes The main neuropathological feature of Alzheimer’s disease (AD) is extracellular amyloid deposition in senile plaques, resulting from an imbalance between the production and clearance of amyloid beta peptides. Amyloid deposition is also found around ... pmc.ncbi.nlm.nih.gov

@dbdugger - Daniel Brittain Dugger

The graphic from the quoted tweet mentions cerebral microbleeds. The article above addresses Cerebral Amyloid Angiopathy. "Amyloid deposition is also found around cerebral blood vessels, termed cerebral amyloid angiopathy (CAA), in 90% of AD cases."

@dbdugger - Daniel Brittain Dugger

The graphic from the paper Harry shared addresses endothelial dysfunction. The article above addresses the same.

@dbdugger - Daniel Brittain Dugger

"We highlight the role of astrocytes and endothelial cells in the process of amyloidgenesis, as well as the role of other amyloidgenic proteins, such as fibrinogen and serum amyloid A protein, in addition to the neuronal amyloid precursor protein."

@dbdugger - Daniel Brittain Dugger

This paper addresses the productive infection of brain microvascular cells through involvement of the same pathway they mentioned, NF-kB.

@dbdugger - Daniel Brittain Dugger

SARS-CoV-2 infection of human brain microvascular endothelial cells leads to inflammatory activation through NF-κB non-canonical pathway and mitochondrial remodeling https://pmc.ncbi.nlm.nih.gov/articles/PMC9216729/

SARS-CoV-2 infection of human brain microvascular endothelial cells leads to inflammatory activation through NF-κB non-canonical pathway and mitochondrial remodeling Neurological effects of COVID-19 and long-COVID-19 as well as neuroinvasion by SARS-CoV-2 still pose several questions and are of both clinical and scientific relevance. We described the cellular and molecular effects of the human brain ... pmc.ncbi.nlm.nih.gov

@dbdugger - Daniel Brittain Dugger

The authors in the paper Harry shared mentioned that which has been known since December of 2020, Tight Junction destruction. 2020 Dec 23 SARS-CoV-2 Envelope (E) Protein Interacts with PDZ-Domain-2 of Host Tight Junction Protein ZO1 https://pmc.ncbi.nlm.nih.gov/articles/PMC7781303/

SARS-CoV-2 Envelope (E) Protein Interacts with PDZ-Domain-2 of Host Tight Junction Protein ZO1 Newly emerged SARS-CoV-2 is the cause of an ongoing global pandemic leading to severe respiratory disease in humans. SARS-CoV-2 targets epithelial cells in the respiratory tract and lungs, which can lead to amplified chloride secretion and increased ... pmc.ncbi.nlm.nih.gov

@dbdugger - Daniel Brittain Dugger

Same Tat. Same brain microvascular endothelial cells. Same Tight Junction destruction. Disruption of blood–brain barrier: effects of HIV Tat on brain microvascular endothelial cells and tight junction proteins https://link.springer.com/article/10.1007/s13365-023-01179-3

Disruption of blood–brain barrier: effects of HIV Tat on brain microvascular endothelial cells and tight junction proteins - Journal of NeuroVirology Although the widespread use of antiretroviral therapy (ART) has prolonged the life span of people living with HIV (PLWH), the incidence of HIV-associated n link.springer.com

@dbdugger - Daniel Brittain Dugger

The three hypotheses advanced were "Several receptors for SAA have been identified, including scavenger-receptor SR-B1 (involved in cholesterol efflux and removal of SAA), toll-like receptors 2 (TLR2) and 4 (TLR4), and receptor for advanced glycated end-products (RAGE)....."

@dbdugger - Daniel Brittain Dugger

The authors of the paper shared above mentions astrocyte activation, for which GFAP is used as a biomarker. Among the articles describing its elevation. A Prospective Study on Neural Biomarkers in Patients with Long-COVID Symptoms https://pmc.ncbi.nlm.nih.gov/articles/PMC10971257/

A Prospective Study on Neural Biomarkers in Patients with Long-COVID Symptoms Background: this prospective observational study aims to assess serum levels of glial fibrillary acidic protein (GFAP), s100b, and total Tau in long-COVID patients, exploring correlations with symptoms, cognitive decline, mental health, and quality ... pmc.ncbi.nlm.nih.gov

@dbdugger - Daniel Brittain Dugger

In the HIV+, it is Tat that leads to its elevation in the brain and bowel.

@dbdugger - Daniel Brittain Dugger

HIV-1 Tat Induces Unfolded Protein Response and Endoplasmic Reticulum Stress in Astrocytes and Causes Neurotoxicity through Glial Fibrillary Acidic Protein (GFAP) Activation and Aggregation https://pmc.ncbi.nlm.nih.gov/articles/PMC5077214/

HIV-1 Tat Induces Unfolded Protein Response and Endoplasmic Reticulum Stress in Astrocytes and Causes Neurotoxicity through Glial Fibrillary Acidic Protein (GFAP) Activation and Aggregation HIV-1 Tat is a major culprit for HIV/neuroAIDS. One of the consistent hallmarks of HIV/neuroAIDS is reactive astrocytes or astrocytosis, characterized by increased cytoplasmic accumulation of the intermediate filament glial fibrillary acidic protein ... pmc.ncbi.nlm.nih.gov

@dbdugger - Daniel Brittain Dugger

The paper shared by Harry mentions IL-6, TNF-a, and S100b but fails to mention another cytokine that is elevated in the SARS-Cov-2 and HIV+, IL-1b.

@dbdugger - Daniel Brittain Dugger

We have known individuals are becoming cachexic, or suffering from wasting syndrome defined as diarrhea lasting for thirty days with a concomitant ten % reduction in total body weight for ten years.

@dbdugger - Daniel Brittain Dugger

2020 Jun 9 COVID‐19: a major cause of cachexia and sarcopenia? https://pmc.ncbi.nlm.nih.gov/articles/PMC7300782/

COVID‐19: a major cause of cachexia and sarcopenia? pmc.ncbi.nlm.nih.gov

@dbdugger - Daniel Brittain Dugger

In the HIV+, Tat contributes to intractable diarrhea and through stimulation of the enteric nervous system, allows for secretion of S100b, IL-6, TNF-a, and IL-1b.

@dbdugger - Daniel Brittain Dugger

HIV-1 Tat-induced diarrhea evokes an enteric glia-dependent neuroinflammatory response in the central nervous system https://www.nature.com/articles/s41598-017-05245-9

HIV-1 Tat-induced diarrhea evokes an enteric glia-dependent neuroinflammatory response in the central nervous system - Scientific Reports Despite the effectiveness of combined anti-retroviral therapy, human immunodeficiency virus (HIV) infected-patients frequently report diarrhea and neuropsychological deficits. It is claimed that the viral HIV-1 Trans activating factor (HIV-1 Tat) protein is responsible for both diarrhea and neurotoxic effects, but the underlying mechanisms are not known. We hypothesize that colonic application of HIV-1 Tat activates glial cells of the enteric nervous system (EGCs), leading to a neuroinflammatory response able to propagate to the central nervous system. We demonstrated that HIV-1 Tat-induced diarrhea was associated with a significant activation of glial cells within the colonic wall, the spinal cord and the frontal cortex, and caused a consistent impairment of the cognitive performances. The inhibition of glial cells activity by lidocaine, completely abolished the above-described effects. These observations point out the role of glial cells as putative effectors in HIV-1 Tat-associated gastrointestinal and neurological manifestations and key regulators of gut-brain signaling. nature.com

@dbdugger - Daniel Brittain Dugger

The IL-1β, IL-6, and TNF cytokine triad is associated with post-acute sequelae of COVID-19 https://www.sciencedirect.com/science/article/pii/S2666379122001951

The IL-1β, IL-6, and TNF cytokine triad is associated with post-acute sequelae of COVID-19 Post-acute sequelae of COVID-19 (PASC) is emerging as global problem with unknown molecular drivers. Using a digital epidemiology approach, we recruit… sciencedirect.com

@dbdugger - Daniel Brittain Dugger

In the HIV+, it is Tat that leads to the upregulation of RAGE receptors within the perivascular end-feet of astrocytes found within the Blood Brain Barrier with resultant amyloid deposition.

@dbdugger - Daniel Brittain Dugger

HIV-1 Tat Upregulates the Receptor for Advanced Glycation End Products and Superoxide Dismutase-2 in the Heart of Transgenic Mice https://www.mdpi.com/1999-4915/14/10/2191

@dbdugger - Daniel Brittain Dugger

"Recent studies have indicated that HIV-1 Tat-induced RAGE expression within the blood–brain barrier accelerates amyloid beta deposition."

@dbdugger - Daniel Brittain Dugger

In the HIV+, Tat, when found within astrocytes at the BBB, leads to elevated MCP, which calls the Trojan Horses into the CNS reservoir.

@dbdugger - Daniel Brittain Dugger

HIV-1 Tat induces monocyte chemoattractant protein-1-mediated monocyte transmigration across a model of the human blood-brain barrier and up-regulates CCR5 expression on human monocytes https://pubmed.ncbi.nlm.nih.gov/10453044/

HIV-1 Tat induces monocyte chemoattractant protein-1-mediated monocyte transmigration across a model of the human blood-brain barrier and up-regulates CCR5 expression on human monocytes - PubMed AIDS dementia is characterized by neuronal loss in association with synaptic damage. A central predictor for clinical onset of these symptoms is the infiltration of monocytes and macrophages into CNS parenchyma. Chronic HIV-1 infection of monocytes also allows these cells to serve as reservoirs for … pubmed.ncbi.nlm.nih.gov

@dbdugger - Daniel Brittain Dugger

While we have long known of a protein operating mechanistically as HIV's Nef, it was in 2023 that Akiko Iwasaki proved she was willing to betray millions and cholesterol efflux pathway involvement was made known.

@dbdugger - Daniel Brittain Dugger

Akiko Iwasaki Enhanced inhibition of MHC-I expression by SARS-CoV-2 Omicron subvariants https://pmc.ncbi.nlm.nih.gov/articles/PMC10120007/

Enhanced inhibition of MHC-I expression by SARS-CoV-2 Omicron subvariants Numerous pathogenic viruses have developed strategies to evade host CD8+ T cell-mediated clearance. Here, we demonstrated that SARS-CoV-2 encodes multiple viral factors that can modulate major histocompatibility complex class I (MHC-I) expression in ... pmc.ncbi.nlm.nih.gov

@dbdugger - Daniel Brittain Dugger

"We also included HIV Nef as a positive control for downregulating both MHC-I and MHC-II (30, 31), and SARS-CoV ORF8a/b proteins as a negative control."

@dbdugger - Daniel Brittain Dugger

She also observed Protein E once again operating mechanistically as HIV's Tat. "We found that in addition to ORF8, SARS-CoV-2 E, M, and ORF7a substantially down-regulated MHC-I within the cells expressing these viral proteins."

@dbdugger - Daniel Brittain Dugger

Repression of MHC Class I Gene Promoter Activity by Two-Exon Tat of HIV https://www.science.org/doi/10.1126/science.8493575

@dbdugger - Daniel Brittain Dugger

September of that same year, evidence of foam cell formation emerged and that it is occurring can be explained by cholesterol efflux pathway impairment.

@dbdugger - Daniel Brittain Dugger

Published: 28 September 2023 SARS-CoV-2 infection triggers pro-atherogenic inflammatory responses in human coronary vessels https://www.nature.com/articles/s44161-023-00336-5

SARS-CoV-2 infection triggers pro-atherogenic inflammatory responses in human coronary vessels - Nature Cardiovascular Research Patients with coronavirus disease 2019 (COVID-19) present increased risk for ischemic cardiovascular complications up to 1 year after infection. Although the systemic inflammatory response to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection likely contributes to this increased cardiovascular risk, whether SARS-CoV-2 directly infects the coronary vasculature and attendant atherosclerotic plaques remains unknown. Here we report that SARS-CoV-2 viral RNA is detectable and replicates in coronary lesions taken at autopsy from severe COVID-19 cases. SARS-CoV-2 targeted plaque macrophages and exhibited a stronger tropism for arterial lesions than adjacent perivascular fat, correlating with macrophage infiltration levels. SARS-CoV-2 entry was increased in cholesterol-loaded primary macrophages and dependent, in part, on neuropilin-1. SARS-CoV-2 induced a robust inflammatory response in cultured macrophages and human atherosclerotic vascular explants with secretion of cytokines known to trigger cardiovascular events. Our data establish that SARS-CoV-2 infects coronary vessels, inducing plaque inflammation that could trigger acute cardiovascular complications and increase the long-term cardiovascular risk. Eberhardt et al. show that SARS-CoV-2 infects human coronary lesions where it preferentially targets plaque macrophages, triggering plaque inflammation and potentially leading to acute cardiovascular complications and long-term cardiovascular risks in patients with COVID-19. nature.com

@dbdugger - Daniel Brittain Dugger

"33. Collins, K. L., Chen, B. K., Kalams, S. A., Walker, B. D. & Baltimore, D. HIV-1 Nef protein protects infected primary cells against killing by cytotoxic T lymphocytes. Nature 391, 397–401 (1998)."

@dbdugger - Daniel Brittain Dugger

It is through proposed therapeutics for those living with Long Covid that evidence is provided of a protein operating mechanistically as HIV's Nef being found within astrocytes.

@dbdugger - Daniel Brittain Dugger

2024 Jul 29. SARS-CoV-2 spike protein acts as a β-adrenergic receptor agonist: A potential mechanism for cardiac sequelae of long COVID https://pubmed.ncbi.nlm.nih.gov/39073192/

SARS-CoV-2 spike protein acts as a β-adrenergic receptor agonist: A potential mechanism for cardiac sequelae of long COVID - PubMed Severe acute respiratory syndrome-coronavirus-2 spike proteins act as an allosteric β-AR agonist, leading to cardiac β-AR hyperactivity, thus contributing to PASC-CVS. pubmed.ncbi.nlm.nih.gov
Saved - June 24, 2025 at 11:35 AM
reSee.it AI Summary
I’ve noticed that while Pharma-funded fact checkers deny the presence of SV40, BioNTech has quietly admitted it in a filing with the EMA. They claim the SV40 elements are non-utilized, but I find that hard to believe since they promote kanamycin resistance. This contamination has affected four products. They insist these sequence elements pose no risk, but I’m skeptical. Research shows SV40 promoters bind to p53 and that these plasmids can integrate. It feels like there’s more going on than they’re letting on.

@Kevin_McKernan - Kevin McKernan

While the Pharma funded fact checkers swear the SV40 isn’t there… BioNTech quietly files with the EMA admitting it’s in fact there. They might clean it up. Might not.

@Kevin_McKernan - Kevin McKernan

Notice how they claim the SV40 elements are non-utilized. That’s bullshit. They are the promoter for the kanamycin resistance

@Kevin_McKernan - Kevin McKernan

Looks like this mistake contaminated 4 products. Ooops

@Kevin_McKernan - Kevin McKernan

They once again claim the sequence elements are non functional, non oncogenic and no risk for insertional mutagenesis. We lied to you… But pinky swear, we aren’t doing it now. Don’t look at Senigl et al.

@Kevin_McKernan - Kevin McKernan

SV40 promoters bind to p53. Drayman et al https://pubmed.ncbi.nlm.nih.gov/27462916/

p53 elevation in human cells halt SV40 infection by inhibiting T-ag expression - PubMed SV40 large T-antigen (T-ag) has been known for decades to inactivate the tumor suppressor p53 by sequestration and additional mechanisms. Our present study revealed that the struggle between p53 and T-ag begins very early in the infection cycle. We found that p53 is activated early after SV40 infect … pubmed.ncbi.nlm.nih.gov

@Kevin_McKernan - Kevin McKernan

Strayer et al explains why SV40 plasmids integrate. https://pubmed.ncbi.nlm.nih.gov/12161189/

Durability of transgene expression and vector integration: recombinant SV40-derived gene therapy vectors - PubMed Many applications of gene delivery require long-term transgene expression. In dividing cells, this result necessitates vector genome persistence, usually by integrating into cellular DNA. Since recombinant gene delivery vectors derived from tag-deleted, replication-incompetent simian virus-40 (SV40) … pubmed.ncbi.nlm.nih.gov
Saved - June 24, 2025 at 10:59 AM
reSee.it AI Summary
Simon Harris announced that Ireland is the first European country to legislate a ban on trade with the Occupied Palestinian Territories, condemning the actions in Gaza. In response, another user criticized Harris, accusing the government of betraying the Irish people by promoting COVID-19 vaccinations and lockdowns influenced by global interests. They referenced a specific announcement made by Harris regarding vaccination hubs targeting young people and called for his resignation, claiming he coerced a generation.

@SimonHarrisTD - Simon Harris TD

Today Ireland becomes the first country in Europe to bring forward legislation to ban trade with the Occupied Palestinian Territories. Ireland is speaking up and speaking out against the genocidal activity in Gaza. Every country must pull every lever at its disposal.

Video Transcript AI Summary
Ireland aims to be the first European country to legislate a ban on trade with occupied Palestinian territories. The speaker states this action is to advocate for the Irish people regarding "genocidal activity." The speaker hopes the legislation will inspire other countries to implement similar measures, utilizing every available means.
Full Transcript
Speaker 0: Today, we will become the first country in Europe to bring forward legislation to ban trade the occupied Palestinian territories. This is an important measure because we are speaking up and speaking out on behalf of the people of Ireland in relation to this genocidal activity. But of course, I actually think and hope that the real benefit of publishing this legislation today will be that it may inspire other countries to do likewise because it's important that every country is every lever at its disposal.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Just like the betrayal your government inflicted on the Irish people pushing experimental injections and lockdowns at the behest of unelected global interests. On September 2nd, 2021, at 08:30 hrs, Fine Gael’s Simon Harris publicly announced the rollout of "pop-up vax hubs" on college campuses, targeting young Irish people with COVID shots starting September 6th. You did this. You coerced a generation. You need to step down.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@rtenews @SimonHarrisTD On September 2, 2021, at 08:30 hrs, Fine Gael's Simon Harris announced plans to establish "popup vax hubs" inside colleges starting September 6th, 2021, to administer COVID vaccines to young people. You did this? You need to step down.@SimonHarrisTD https://www.oireachtas.ie/en/debates/debate/joint_committee_on_jobs_enterprise_and_innovation/2015-11-03/2/

Joint Committee on Jobs, Enterprise and Innovation debate - Tuesday, 3 Nov 2015 Increasing Employment through Training: Innopharma Labs Joint Committee on Jobs, Enterprise and Innovation debate - Tuesday, 3 Nov 2015 oireachtas.ie
Saved - June 23, 2025 at 10:34 PM
reSee.it AI Summary
In 1965, scientists discovered and began modifying the coronavirus through animal studies. By 1990, Pfizer created the first spiked protein vaccine but found it ineffective due to the virus's rapid mutation. In 2002, UNC patented a bioweapon version of the virus, leading to concerns about biowarfare. A 2015 National Academy of Sciences statement highlighted the profit motives behind vaccine development. In 2019, Moderna patented a vaccine for potential pathogen releases. By 2023, Congress uncovered unreported funding to the Wuhan Institute, raising questions about the origins of the virus and treatments.

@kacdnp91 - Kelly DNP Functional/Integrative Medicine

1965 Scientists first discovered the coronavirus & began to modify it by studying it in animals https://www.bmj.com/content/369/bmj.m1547.long

Covid-19: First coronavirus was described in The BMJ in 1965 The first description of human coronavirus—a family of viruses that now includes SARS-CoV-2, the cause of the current covid-19 pandemic—was published in The BMJ in 1965. The research, led by virologist David Tyrrell at the Common Cold Unit in Wiltshire, England, involved studying nasal washings from volunteers.1 The researchers found that they could grow several viruses associated with the common cold, but not all of them. One such sample, referred to as B814, turned out to be what we now know as a coronavirus. Using the original B814 nasal swab from a “boy with a typical common cold in 1960,” the team obtained more secretions … bmj.com

@kacdnp91 - Kelly DNP Functional/Integrative Medicine

1990 Pfizer created 1st spiked protein vaccine based on these animal experiments. Pfizer learned the 💉did not work bc the coronavirus was malleable (Modifies/mutates too rapidly for a vaccine to be effective. https://pubmed.ncbi.nlm.nih.gov/2170676/

Assembly of coronavirus spike protein into trimers and its role in epitope expression - PubMed The folding and oligomerization of coronavirus spike protein were explored using a panel of monoclonal antibodies. Chemical cross-linking and sedimentation experiments showed that the spike of transmissible gastroenteritis virus is a homotrimer of the S membrane glycoprotein. The spike protein was s … pubmed.ncbi.nlm.nih.gov

@kacdnp91 - Kelly DNP Functional/Integrative Medicine

2002 UNC Chapel Hill patented an “infectious replication defective” clone of the coronavirus. A bioweapon. Patent based on research by Anthony Fauci & only granted after the CDC intervened.

@kacdnp91 - Kelly DNP Functional/Integrative Medicine

2005 The scientific community labeled the coronavirus “biowarfare enabling technology”

@kacdnp91 - Kelly DNP Functional/Integrative Medicine

2015 Statement from National Academy of Sciences reveals one of the true objectives of the 💉…profit.

@kacdnp91 - Kelly DNP Functional/Integrative Medicine

It read, “To sustain the funding base beyond the crisis, we need to increase the public understanding of the need for medical countermeasures, such as the pan-influenza or pan-coronavirus, vaccine. A key driver is the media, & the economics will follow the hype.”

@kacdnp91 - Kelly DNP Functional/Integrative Medicine

2019 Moderna received a patent for a vaccine that included the statement, “for the accidental or intentional release of a respiratory pathogen.”

@kacdnp91 - Kelly DNP Functional/Integrative Medicine

2023 The US Congress discovered an additional & unreported $2million in research funding to the Wuhan Institute of Virology. This funding was again transferred indirectly through EcoHealth Alliance, Fauci’s favorite partner.

@kacdnp91 - Kelly DNP Functional/Integrative Medicine

Since 2005, over &10 billion has been funneled to research institutions @ the direction of Fauci & the National Institute of Allergy and Infectious Diseases (NIAID) to illegally fund GOF research and the development of the mRNA “vaccines.”

@kacdnp91 - Kelly DNP Functional/Integrative Medicine

Manipulation & betrayal from Big Pharma and the NIH, CDC, and FDA brazenly disregarding the health & welfare of the American people.

@kacdnp91 - Kelly DNP Functional/Integrative Medicine

So ask yourself, what came first? The manufactured virus or the manufactured treatment? Someone check on Ralph Baric @ UNC please…

Saved - June 21, 2025 at 10:29 AM
reSee.it AI Summary
I've been exploring how certain foods can trigger inflammation and impact chronic health issues. I've learned that gluten, dairy (especially A1), legumes, nightshades, processed sugars, seed oils, trans fats, artificial additives, and FODMAPs can all contribute to inflammation and worsen symptoms for those with autoimmune diseases or gut sensitivities. By eliminating these foods for 30–60 days and focusing on whole, nutrient-dense options, I can potentially reclaim my health and vitality. Tracking my body's responses during reintroduction is crucial for understanding my unique triggers.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Ditch These Foods to Heal Chronic Illness Explore the hidden biochemical triggers of inflammation and the foods that stoke the flames, Perfect for those battling autoimmune diseases, neuroinflammation, chronic fatigue, IBD, MS, arthritis, or post-viral syndromes taking control of these triggers is your key to reclaiming vitality!

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

🌾 Gluten Sensitivity: The Hidden Inflammation Trigger Struggling with chronic inflammation, autoimmune flares, fatigue, or brain fog? Gluten may be silently sabotaging your gut and immune system even if you don’t have celiac disease. 🔓 Leaky Gut & Systemic Inflammation Gluten stimulates zonulin, a protein that opens tight junctions in your intestinal lining. This leads to leaky gut, allowing bacteria, food particles, and toxins to escape into your bloodstream triggering chronic immune activation and inflammation throughout the body. 🧬 Autoimmune Activation via Molecular Mimicry In genetically predisposed individuals (e.g., HLA-DQ2/DQ8), gluten peptides can resemble human tissue proteins. This "molecular mimicry" may cause the immune system to mistake your own cells for invaders, contributing to diseases like: • Hashimoto’s thyroiditis • Multiple sclerosis (MS) • Rheumatoid arthritis • Celiac disease Non-Celiac Gluten Sensitivity (NCGS) Is Real Even without celiac markers, many people experience bloating, diarrhea, joint pain, fatigue, skin issues, and brain fog after gluten exposure. This is known as NCGS and it's now recognized in medical literature as a legitimate, immune-mediated condition. ✅ What You Can Do • Trial a gluten-free diet for 30–60 days and track your symptoms • Get tested: Ask your provider about anti-gliadin antibodies or genetic screening • Focus on whole, unprocessed gluten-free foods not just GF packaged substitutes • Reassess and reintroduce (if desired) later to confirm your sensitivity 📌 Healing often begins in the gut. If gluten is a trigger, removing it could be the most powerful anti-inflammatory step you take.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

🥛 Dairy (Especially Conventional, Pasteurized A1 Dairy) Examples: Milk, cheese, yogurt, cream, butter 🔥 Why It’s Inflammatory Most commercial cow’s milk contains A1 casein, a protein that breaks down into beta-casomorphin-7 (BCM-7) a bioactive peptide linked to gut and brain inflammation. Many people also lack the enzyme lactase, leading to poor lactose digestion, bloating, dysbiosis, and gut irritation. Worse still, the immune system can develop IgG or IgA antibodies to casein, triggering systemic inflammation and potentially worsening autoimmune and neuroimmune conditions. 🚩 Who Should Be Cautious? If you have any of the following, A1 dairy might aggravate your symptoms: • Multiple Sclerosis (MS) • Parkinson’s disease • Chronic sinus issues or asthma • Crohn’s or colitis • Eczema, acne, or skin inflammation • Brain fog, autism spectrum conditions, or neuroinflammation Try removing dairy for 30–60 days and observe changes in energy, digestion, skin, and cognition. ✅ Better Options (Later On) • A2 dairy (from A2 cows, goats, or sheep) • Raw, fermented goat/sheep dairy (e.g. kefir) These may be reintroduced cautiously in later phases, but all dairy is excluded initially to reduce inflammatory load. 📖 A controlled human study found that A1 milk increases GI symptoms and inflammation compared to A2 milk. 🔗 Read the study (Nutrition Journal, 2016) https://pubmed.ncbi.nlm.nih.gov/27039383/ #DairyFree #Inflammation #Autoimmune #GutHealth #A1A2Milk

Effects of milk containing only A2 beta casein versus milk containing both A1 and A2 beta casein proteins on gastrointestinal physiology, symptoms of discomfort, and cognitive behavior of people with self-reported intolerance to traditional cows' milk - PubMed ClinicalTrials.gov/NCT02406469. pubmed.ncbi.nlm.nih.gov

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

🌱 Legumes: Hidden Inflammation Triggers Examples: Beans, lentils, soy, peanuts, peas 🔥 Why They’re Inflammatory Legumes contain lectins sticky, plant-derived proteins that resist digestion and can bind to the gut lining, increasing intestinal permeability and provoking immune activation. They also contain phytates, which chelate essential minerals like zinc, calcium, and iron, blocking their absorption. Soy is especially problematic: it’s often genetically modified, heavily sprayed with glyphosate, and loaded with phytoestrogens, which may disrupt hormonal balance and immune signaling. Peanuts, technically legumes, are frequently contaminated with aflatoxins toxic fungal compounds linked to liver damage, immune suppression, and even cancer. 🚨 Who Should Be Cautious? You may want to avoid legumes if you struggle with: • Autoimmune diseases (e.g. lupus, RA, MS) • Estrogen-sensitive conditions (endometriosis, fibroids, PCOS) • IBS, IBD, or leaky gut • Mineral deficiencies (low iron, zinc) • Histamine intolerance or peanut allergies 💡 Smart Tips • Pressure-cooking reduces some lectins, but not all anti-nutrients • Eliminate legumes during early gut-healing or autoimmune protocols • Reintroduce slowly (if at all) once symptoms stabilize #LegumeFree #Inflammation #Autoimmune #GutHealth #Lectins #Phytoestrogens

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

🍅 Nightshades: Nature’s Defense, Your Inflammation Trigger? Examples: Tomatoes, potatoes, eggplant, bell peppers, chili 🔥 Why They’re Inflammatory (for Some) Nightshades contain alkaloids like solanine and capsaicin, natural pesticides that defend the plant but can irritate the human body. In sensitive individuals, these compounds can: • Disrupt the gut lining, increasing intestinal permeability (aka leaky gut) • Activate mast cells, releasing histamine and pro-inflammatory cytokines • Trigger neurogenic inflammation, leading to nerve pain, joint stiffness, or migraines • Worsen autoimmune flares, especially in musculoskeletal and neuroimmune disorders 🚨 Who Should Be Cautious? If you’re living with: • Rheumatoid arthritis, lupus, or ankylosing spondylitis • Multiple sclerosis (MS) or neuropathic pain • IBD (Crohn’s, colitis) or leaky gut • Migraines, eczema, interstitial cystitis, or chronic fatigue …then nightshades could be silently inflaming your symptoms. 💡 What to Do • Eliminate nightshades for 4–6 weeks • Reintroduce one at a time, with 2–3 days in between • Track symptoms like pain, digestion, skin, mood, and energy You may discover that removing just one trigger food brings profound relief. #NightshadeFree #AutoimmuneHealing #Inflammation #GutHealth #Neuroimmune #PainRelief

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

🍬 Processed Sugars & Refined Carbs: Silent Drivers of Inflammation Examples: White sugar, high-fructose corn syrup (HFCS), pastries, white bread, soda 🔥 Why They’re Inflammatory Refined sugars cause a rapid spike in blood glucose, which leads to insulin surges that activate inflammatory messengers like NF-kB and IL-6 key players in chronic disease. They also feed pathogenic gut microbes (like candida and bad bacteria), disrupting your microbiome and triggering systemic inflammation. Over time, sugar drives the formation of advanced glycation end products (AGEs) damaging compounds that impair mitochondrial function, degrade collagen, and contribute to brain fog, skin aging, and neurodegeneration. 🚨 Who Should Be Especially Cautious? Watch your intake if you live with: • Metabolic syndrome or insulin resistance • Type 2 diabetes or prediabetes • Alzheimer’s or cognitive decline • PCOS or hormonal imbalances • Candida overgrowth, acne, or chronic fatigue • Mood disorders like depression or anxiety These conditions are often exacerbated by high-glycemic, low-nutrient carbs. 💡 Smart Move • Cut back on added sugars and refined flour • Prioritize whole foods with fiber, healthy fats, and slow-burning carbs • Notice how quickly energy, mood, and skin improve when sugar is removed 📊 Even small reductions in sugar can lead to big wins in inflammation, energy, and metabolic health. #SugarFree #Inflammation #MetabolicHealth #GutHealth #CognitiveHealth #HormoneBalance

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

🛢️ Industrial Seed Oils: Inflammation Time Bombs Examples: Corn oil, soybean oil, sunflower oil, safflower oil, canola 🔥 Why They’re Inflammatory These oils are ultra-processed and packed with omega-6 linoleic acid, which your body converts into arachidonic acid a precursor to inflammatory molecules like prostaglandins and leukotrienes. When heated, seed oils oxidize rapidly, producing toxic lipid peroxides that damage: • Cell membranes • Mitochondria (your energy factories) • DNA promoting aging, mutation, and inflammation The result? A perfect storm for metabolic dysfunction, non-alcoholic fatty liver disease (NAFLD), cardiovascular problems, insulin resistance, and even brain fog. 🚨 Who Should Be Cautious? These oils may worsen symptoms if you’re dealing with: • Heart disease or hypertension • Brain fog or cognitive decline • NAFLD or high triglycerides • Obesity, insulin resistance, or chronic fatigue • Inflammatory skin issues (like eczema or acne) 💡 Smart Move Replace inflammatory seed oils with stable, nourishing fats like: • 🫒 Extra virgin olive oil • 🥥 Coconut oil • 🥑 Avocado oil • 🧈 Ghee or grass-fed butter • 🐖 Tallow or duck fat These are richer in antioxidants, more heat-stable, and support cellular and metabolic health not sabotage it. #NoSeedOils #HealthyFats #Inflammation #HeartHealth #BrainHealth #MetabolicHealing

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

⚠️ Trans Fats: Hidden Hazards to Your Heart and Brain Examples: Margarine, shortening, fast food fries, processed snacks, baked goods with partially hydrogenated oils 🔥 Why They’re Inflammatory Trans fats are industrially created fats that disrupt cell membrane structure, impair insulin signaling, and damage mitochondria, your body’s energy producers. They also: • Raise LDL (“bad”) cholesterol • Lower HDL (“good”) cholesterol • Trigger systemic inflammation that accelerates aging and disease • Increase risk of heart attacks, stroke, and neurodegeneration They’ve been called the most dangerous fats in the modern diet and for good reason. 🚨 Who Should Be Especially Cautious? Avoid trans fats completely if you’re dealing with: • Cardiovascular disease or high cholesterol • Insulin resistance or type 2 diabetes • Cognitive decline, Alzheimer’s, or brain fog • Chronic inflammation, fatigue, or autoimmune conditions Even small amounts are harmful. 💡 Smart Move • Read labels: Watch for "partially hydrogenated oils" • Avoid ultra-processed foods and fast food • Focus on whole foods and healthy fats like olive oil, ghee, or coconut oil 🛑 There is no safe level of trans fat. Eliminating them may be one of the fastest ways to protect your heart, brain, and metabolism. #NoTransFats #HeartHealth #BrainHealth #Inflammation #HealthyFats #MetabolicHealing

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

⚠️ Artificial Additives & Preservatives: Small Compounds, Big Inflammation Examples: MSG, sodium benzoate, artificial food dyes, BHA/BHT, nitrates, nitrites, aspartame 🔬 Why They’re Inflammatory Many food additives are designed to extend shelf life, enhance flavor, or improve appearance but at a cost to your health. Here’s how they silently provoke inflammation: • Mast Cell Activation & Histamine Release Preservatives and additives can activate mast cells, immune cells that release histamine and inflammatory cytokines. This can trigger skin rashes, gut symptoms, and respiratory issues in sensitive individuals. • Excitotoxicity Compounds like MSG (monosodium glutamate) and aspartame are excitotoxins they overstimulate neurons, potentially leading to brain inflammation, headaches, migraines, mood swings, and even seizure activity in susceptible people. • Gut-Brain Axis Disruption Preservatives like sodium benzoate and BHA/BHT can disrupt the gut microbiome, reducing bacterial diversity and promoting dysbiosis a known driver of systemic inflammation, anxiety, and cognitive dysfunction. • Nitrites & Nitrates Used in processed meats, these can form nitrosamines, compounds linked to cancer risk, oxidative stress, and endothelial damage (affecting heart and brain function). 🚨 Who Should Be Especially Cautious? These compounds may aggravate symptoms in people with: • ADHD or behavioral disorders • Histamine intolerance or MCAS (mast cell activation syndrome) • Asthma, eczema, or chronic allergies • Neurodegenerative diseases (like Parkinson’s, Alzheimer’s) • IBD, IBS, or leaky gut 💡 Smart Move • Read labels carefully even on “healthy” foods • Look for real, whole-food ingredients you recognize • Choose additive-free snacks, cured meats, and drinks whenever possible • Focus on home-cooked meals made from scratch 🧠 Your brain, immune system, and gut all respond to what you eat. Eliminating synthetic additives can bring surprising improvements in mood, energy, and inflammation. #FoodAdditives #Inflammation #GutHealth #BrainHealth #HistamineIntolerance #CleanEating #Neuroinflammation #ADHD

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

🍎 FODMAPs & Fermentable Carbs: Gut Triggers for Sensitive Individuals Examples: Onions, garlic, apples, lentils, wheat, dairy 🤔 What Are FODMAPs? FODMAPs are a group of short-chain carbohydrates and sugar alcohols that are poorly absorbed in the small intestine. They ferment in the colon, producing gas, bloating, and distension, especially in sensitive individuals. FODMAP = Fermentable Oligosaccharides, Disaccharides, Monosaccharides, and Polyols 🔥 Why They Can Be Inflammatory For people with gut vulnerabilities, FODMAPs can: • Increase intestinal permeability (leaky gut) • Feed dysbiotic bacteria, fueling bloating and inflammation • Activate mast cells, releasing histamine and cytokines • Disrupt serotonin balance, affecting mood, focus, and energy since ~90% of serotonin is made in the gut 🚨 Who Should Watch Out? You may benefit from a low-FODMAP approach if you’re dealing with: • IBS (Irritable Bowel Syndrome) • SIBO (Small Intestinal Bacterial Overgrowth) • IBD (Crohn’s, colitis) • Histamine intolerance / Mast cell activation • Mood swings, anxiety, or depression • Chronic fatigue (ME/CFS) 💡 Pro Tip FODMAPs aren’t “bad” — many are found in healthy whole foods. But for sensitive guts, temporary reduction can relieve symptoms while you: • Heal the gut lining • Rebalance the microbiome • Calm immune and mast cell overactivity Once stable, many people can reintroduce moderate FODMAPs successfully. 📋 Consider working with a practitioner to guide elimination and reintroduction phases for optimal results. #FODMAPs #GutHealth #LeakyGut #IBS #SIBO #HistamineIntolerance #MoodHealing #Inflammation #MicrobiomeHealth #GutHealing #ChronicFatigue #NutritionTips #functionalmedicine

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

✅ Conclusion: Remove the Fuel, Ignite the Healing Certain foods can fuel inflammation at every level by disrupting immune regulation, damaging the gut lining, feeding harmful microbes, and impairing mitochondrial energy. For those with autoimmune diseases, neurological conditions, hormonal imbalances, or chronic fatigue, even seemingly “normal” foods may be silently sabotaging recovery. But here’s the good news: 🌿 Removing dietary triggers even for 30–60 days can create a dramatic shift in how your body functions. Many experience: • Reduced joint pain and bloating • Clearer thinking and more stable mood • Better skin, digestion, and sleep • Renewed energy and vitality 🛠️ Take Action: Reclaim Your Health with a Root-Cause Approach Start with a simple elimination protocol, removing common inflammatory foods and focusing on: • Leafy greens and cruciferous vegetables • Healthy fats (olive oil, avocado, coconut, omega-3s) • Clean protein sources (grass-fed, pasture-raised, wild-caught) • Gut-healing foods (bone broth, fermented veggies, herbs) After 30–60 days, reintroduce foods one at a time, tracking how your body responds physically, mentally, and emotionally. This process helps you decode your body’s signals, rebuild resilience, and make empowered food choices for life. 🧠 Your diet isn’t just fuel it’s information. Removing inflammatory inputs allows your body’s innate intelligence to reset, repair, and thrive. #Inflammation #HealingJourney #AutoimmuneRecovery #EliminationDiet #GutHealing #Mitochondria #ChronicIllness #FoodAsMedicine #EmpoweredHealing

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@Reseeit save thread

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@reSeeIt @threadreaderapp unroll

Saved - June 21, 2025 at 6:59 AM
reSee.it AI Summary
I’m excited to share our new pre-print on COVID-19 vaccine safety in pregnancy. Our analysis of over 200,000 pregnancies in Israel revealed that women vaccinated in early pregnancy (weeks 8-13) experienced higher-than-expected fetal losses, particularly after week 24. In contrast, influenza vaccination during the same period showed fewer fetal losses, highlighting a significant difference. Our findings suggest a safety signal that warrants further investigation, especially since our methodology aimed to minimize biases commonly seen in vaccine safety research.

@joshg99 - Josh Guetzkow

Our new pre-print on COVID-19 vaccine safety in pregnancy is out! Women vaccinated in early pregnancy (weeks 8-13) had a higher-than-expected number of fetal losses: Dose 1 = 3.9 more per 100 women Dose 3 = 1.9 more per 100 women Based on data on >200K pregnancies in Israel 🧵

@joshg99 - Josh Guetzkow

2/ Late pregnancy losses were a *big* part of the signal. Among all women: 1.1% lost their pregnancy after week 24. Compared to: 2.7% of women who received dose 1 in early weeks. 1.8% of women who received dose 3 in early weeks.

@joshg99 - Josh Guetzkow

3/ In fact, most of the excess losses occurred later in pregnancy, including nearly half after week 24. In Israel, abortions after week 24 are rare and must be medically justified and are very rare. This strongly suggests biological, not behavioral, mechanisms are involved.

@joshg99 - Josh Guetzkow

4/ In stark contrast, women vaccinated for influenza in the same weeks (8-13) saw *FEWER* fetal losses than expected, about 5 per 100 women vaccinated. What's the significance of that?

@joshg99 - Josh Guetzkow

5/ Comparing both types of vaccines helps control for bias in who chooses to get vaccinated. For example, if women vaccinate in early pregnancy because they have health problems, the elevated fetal loss risk for COVID-19 vaccines could simply be due to that bias.

@joshg99 - Josh Guetzkow

6/ But people who get vaccinated are usually healthier & more health conscious to begin with. This is called healthy vaccinee bias & can make vaccines look safer than they really are. It's a known – but often ignored -- issue in vaccine safety research based on real-world data.

@joshg99 - Josh Guetzkow

7/ Influenza vaccination during pregnancy showed lower-than-expected fetal losses—likely due to healthy vaccine bias. So it's even more striking that mRNA COVID-19 vaccination in early pregnancy showed higher-than-expected fetal losses—despite healthy vaccinee bias.

@joshg99 - Josh Guetzkow

8/ Our findings don’t prove causation. But they point to a clear safety signal—one that calls for further investigation, especially given the vulnerability of this population.

@joshg99 - Josh Guetzkow

9/ So why hasn’t this been seen before? Most other studies compare vaccinated vs. unvaccinated women during vaccination campaigns. That approach is vulnerable to bias—especially if healthier women are more likely to vaccinate (a.k.a. “healthy vaccinee bias”).

@joshg99 - Josh Guetzkow

10/ Our approach was different. We used detailed medical records to estimate expected fetal loss rates for each vaccinated woman—based on her individual risk factors and pregnancy timing—using data from pre-COVID years.

@joshg99 - Josh Guetzkow

11/ Here is a link to the pre-print: https://medrxiv.org/cgi/content/short/2025.06.18.25329352v1 This was of course a team effort with my amazing co-authors: @RetsefL, @TalPatalon, Sivan Gazit, @TracyBethHoeg, @JosephFraiman and Yaakov Segal.

Observed-to-Expected Fetal Losses Following mRNA COVID-19 Vaccination in Early Pregnancy medRxiv - The Preprint Server for Health Sciences medrxiv.org

@joshg99 - Josh Guetzkow

https://t.co/se1GOqkvtl

@RetsefL - Retsef Levi

BREAKING: Analysis of over 220K pregnancies in Israel during 2016- 2022 found that mRNA COVID-19 vaccination during gestational weeks 8-13 was associated with a higher-than-expected number of eventual fetal losses (miscarriages, abortions & stillbirths)! Pregnant women vaccinated with dose 1 during weeks 8-13 had nearly 3.9 (95% CI: [2.55-5.14]) additional fetal losses above expected per 100 pregnancies. Most of the excess fetal losses occurred after gestational week 20 and nearly half occurred after gestational week 25. In contrast, pregnant women vaccinated for influenza during weeks 8-27 exhibited a consistently lower-than-expected observed number of fetal losses, likely the result of healthy vaccinee bias. Women vaccinated for COVID-19 or influenza prior to pregnancy exhibited according-to-expected or lower-than-expected numbers of fetal losses. The study used innovative observed-to-expected methodology, where data from prior years were leveraged to determine the expected number of fetal losses based on the individual characteristics of the pregnant women who vaccinated and their week of vaccination.

Saved - June 20, 2025 at 11:17 AM
reSee.it AI Summary
I’ve come across alarming research linking prenatal COVID exposure to significant neurodevelopmental delays in infants. A Brazilian study found that 36% of toddlers had cognitive delays, with cytokine profiles in cord blood predicting these outcomes. Other studies highlighted increased autism rates in COVID-exposed children and identified placental damage even in asymptomatic mothers. Structural brain changes and epigenetic alterations were also noted. This is a call to action for expectant parents to receive clear information about these risks, as the silence from public health is concerning.

@ZdenekVrozina - Zdenek Vrozina

Prenatal COVID and Infant Brain Development - New Data, Alarming Trends We begin with a 2025 study from Brazil, the first to directly link cytokines in cord blood with neurodevelopmental delays in toddlers exposed to SARS-CoV-2 in the womb. https://www.nature.com/articles/s41390-025-04192-w

Cord blood cytokines/chemokines linked to delays in toddlers exposed to SARS-CoV-2 prenatally - Pediatric Research Maternal infections are linked to neurodevelopmental impairments, highlighting the need to investigate SARS-CoV-2-induced immune activation. This study aimed to evaluate the impact of maternal infection on neurodevelopment and investigate whether cytokine and chemokine profiles predict delays at 24 months. Conducted in Brazil (January 2021–March 2022), this follow-up study included 18 SARS-CoV-2 positive pregnant women at 35–37 weeks’ gestation, 15 umbilical cord blood samples, and blood samples from 15 children at 6 months and 14 at 24 months. Developmental delay was defined using the Bayley Scales of Infant and Toddler Development, Third Edition, with scores below 90 in cognitive, communication, or motor domains. At 6 months, 33.3% of infants exhibited cognitive delays, 20% communication delays, and 40% motor delays, increasing to 35.71%, 64.29%, and 57.14% at 24 months, respectively. Elevated interferon-gamma and tumor necrosis factor-alpha in cord blood correlated with cognitive delays, while interleukin (IL)-6, IL-8, IL-17, and IL-1β were associated with motor delays. Increased C-X-C motif chemokine ligand 10 and other cytokines were associated with communication delays. Maternal SARS-CoV-2 may impact infant neurodevelopment, as early cytokine elevations correlate with delays, highlighting the importance of early monitoring and interventions to reduce long-term effects. nature.com

@ZdenekVrozina - Zdenek Vrozina

At 24 months of age: 36% showed cognitive delays 64% had language delays (sic) 57% had motor delays And here’s the striking part: these delays were predicted by the cytokine profile in umbilical cord blood.

@ZdenekVrozina - Zdenek Vrozina

Elevated inflammation markers: IFN-γ & TNF-α - cognitive delays IL-6, IL-8, IL-17, IL-1β - motor delays CXCL10 - language delays This is strong evidence for maternal immune activation - a mechanism also seen in autism and schizophrenia research.

@ZdenekVrozina - Zdenek Vrozina

A UCLA study tracked 211 COVID-exposed children. At 28 months, 11% screened positive for autism spectrum disorder - far above the expected 1-2%. Some had activated microglia and neuroinflammatory markers in blood at birth. https://www.japantimes.co.jp/news/2024/12/27/world/science-health/covid-pregnancy-autism-study/

COVID pregnancies may have boosted autism risk, study shows 'There’s something really going on,” pediatric infectious diseases physician Karin Nielsen says. 'We don’t want to alarm the world, but that’s what our data are showing.” japantimes.co.jp

@ZdenekVrozina - Zdenek Vrozina

Then comes the placenta. A Michigan pathology review identified SARS-CoV-2 placentitis even in asymptomatic mothers (2025): fibrin deposition intervillositis trophoblast necrosis confirmed virus in placental tissue Risk: fetal hypoxia, IUGR, stillbirth https://meridian.allenpress.com/aplm/article/doi/10.5858/arpa.2024-0247-RA/506106/SARS-CoV-2-Placentitis-A-Review-of-Pathologic

@ZdenekVrozina - Zdenek Vrozina

Structural brain changes have also been observed. An Italian study found ultrasound abnormalities in 23% of newborns exposed to SARS-CoV-2 in utero - vs. 16% of controls. Most were minor (cysts) - but statistically significant. https://ijponline.biomedcentral.com/articles/10.1186/s13052-024-01826-3

Cranial ultrasonographic findings in newborns exposed to SARS-CoV-2: a single-centre cross-sectional analysis - Italian Journal of Pediatrics SARS-CoV-2’s potential consequences on the developing brain are still unknown. The aim of this study was to describe cranial ultrasonographic (cUS) findings in a population of newborns exposed to SARS-CoV-2 born at San Marco Hospital in Catania. Two cohort of newborns, one exposed to SARS-CoV-2 both during gestation and at birth and one unexposed, were enrolled in this cross-sectional study conducted according to the STROBE guidelines (Strenghtening the Reporting of Observational Studies in Epidemiology) and underwent cUS. We performed a statistical analysis using the Fisher’s exact test to assess whether significant differences among the two groups existed. we enrolled 139 exposed newborns (62 females, 77 males with median gestational age 38.4 ± 1.9 W and median weight at birth 3142.8 ± 594.4 g) and 139 unexposed newborns (60 females, 79 males with median gestational age 38,9 ± 1.3 W and median weight at birth 3230 ± 336 g). cUS abnormalities were found in 32 exposed patients (23%) and in 23 (16.5%) unexposed patients. A statistically significant difference was found in the incidence of minor intracranial abnormalities (p 0.036) between exposed and unexposed patients and between newborns exposed during pregnancy and unexposed patients (p 0.016). in our experience, the incidence of minor intracranial abnormalities was higher in SARS-COV-2-exposed newborns. Our results must be taken with caution and need further confirmation in larger studies but suggest to consider performing cUS at birth in newborns exposed to SARS-CoV-2 in research contexts. ijponline.biomedcentral.com

@ZdenekVrozina - Zdenek Vrozina

Harvard researchers found the effect is sex-specific. Boys born to SARS-CoV-2 positive mothers had 2× the risk of neurodevelopmental diagnoses at 12 months. Girls showed no such increase. https://jamanetwork.com/journals/jamanetworkopen/fullarticle/2802745

@ZdenekVrozina - Zdenek Vrozina

And finally: epigenetics. A Swedish 2025 study showed that even mild maternal COVID-19 alters DNA methylation in the infant’s immune and brain-related genes. Genes involved in neuron signaling, interferon response, and neurodevelopment were affected. https://www.medrxiv.org/content/10.1101/2025.05.10.25327356v1

DNA methylation changes in infants of mothers with SARS-CoV-2 infection during pregnancy medRxiv - The Preprint Server for Health Sciences medrxiv.org

@ZdenekVrozina - Zdenek Vrozina

In summary: SARS-CoV-2 exposure in utero can leave a long shadow - through neuroinflammation placental dysfunction brain structure changes and epigenetic rewiring The science is clear. The risks are real.

@ZdenekVrozina - Zdenek Vrozina

But this isn’t just a warning. It’s a call to action. Expectant parents deserve clear, science-based information on prenatal COVID risks. No child should suffer lifelong harm from an exposure their mother wasn’t told mattered. We are losing futures before they’re even born.

@ZdenekVrozina - Zdenek Vrozina

After five years of research, dozens of peer-reviewed studies, and signals from across continents…how is it possible that public health remains silent? No warnings. No prenatal screening protocols. No public campaigns. No plan. The children deserved better. And still do. @szupraha @ZdravkoOnline

Saved - June 19, 2025 at 10:16 AM
reSee.it AI Summary
The conversation began with a strong defense of a country and its people. In response, another participant criticized the speaker for avoiding physical confrontation and drew a controversial comparison to a political situation. A third participant shifted the focus to concerns about vaccine safety, alleging significant harm and calling for more awareness regarding vaccine-related issues. They emphasized the importance of discussing these topics and provided a list of experts who share their views on vaccine harms.

@TheNotoriousMMA - Conor McGregor

You wont speak bad about my country and its people and thats ever. Vote McGregor 🇮🇪

@jacksonhinklle - Jackson Hinkle 🇺🇸

@TheNotoriousMMA BIG TALK for a man who is TOO SCARED to fight with his hands ever again — just like the genocidal Israelis that you support 🇮🇱 You are a disgrace to your BEAUTIFUL country! 🇮🇪

@MeasslainteIRL - Thomas Anthony III

Everyone is oblivious to vaccine harms and the death and carnage caused by the introduction of mRNA Why is nobody talking about the genocide ? Sticks and stones may break my bones, but silence and lies kill millions. Below is a list of subject matter experts publishing the truth. Decades of experience. https://t.co/mk0QeVFkH5 Vaccine harms listed below, look into them !

@MeasslainteIRL - Thomas Anthony III

@indepdubnrth The COVID-19 chimeric genetic injections the ones they called “safe and effective.” Jonestown jabs They are experimental biotechnologies. And mounting scientific evidence demands honest, urgent re-evaluation. Independent researchers and pathologists have sounded the alarm:

Saved - June 19, 2025 at 9:58 AM
reSee.it AI Summary
I shared insights on how to defend my genome and restore immune balance using natural food-based compounds. I outlined 10 disrupted pathways and suggested foods to address them, such as broccoli sprouts for mutagenesis and pomegranate for p53 suppression. I emphasized the importance of compounds like Baicalin, which supports multiple pathways, including detox and inflammation control. I also provided a resilience routine featuring various foods and supplements to enhance health. Always consult a practitioner for personalized advice.

@MeasslainteIRL - Thomas Anthony III

How to defend your genome, protect your mitochondria, and recover immune balance using natural food-based compounds 🌱 A breakdown of 10 disrupted pathways (and how to fix them 🧵⤵️ 1. Insertional Mutagenesis 🧬 Contaminated plasmid DNA can insert into your genome → trigger mutations or activate oncogenes. 🛡️ Eat: Broccoli sprouts (Sulforaphane) Turmeric + pepper (Curcumin) Blueberries & grapes (Resveratrol) #GenomeIntegrity

@MeasslainteIRL - Thomas Anthony III

p53 Suppression 💣 p53 = “guardian of the genome.” When it's silenced, cancer risk skyrockets. 🛡️ Eat: Pomegranate (Ellagic acid) Red onions, apples (Quercetin) Pumpkin seeds, oysters (Zinc) Chinese skullcap (Baicalin) → Activates p53, induces apoptosis

@MeasslainteIRL - Thomas Anthony III

PD-L1 & IgG4 Immune Escape 🦠 Viruses & tumors cloak themselves by raising PD-L1 and shifting to IgG4. 🛡️ Strip the cloak with: Apigenin herbs (chamomile, parsley) Berberine (Th1/Th17 support) Reishi, Turkey Tail (mushrooms FTW) #ImmuneCheckpoints

@MeasslainteIRL - Thomas Anthony III

Overactive cGAS-STING 🔥 Overstimulated DNA sensors = chronic inflammation, fatigue, even autoimmunity. 🛡️ Cool it with: Green tea (EGCG) Omega-3s (EPA/DHA) Boswellia (frankincense resin) Baicalin — calms STING & NF-κB 🔧🧬 #AutoimmuneRelief

@MeasslainteIRL - Thomas Anthony III

Oncogenic microRNAs (OncomiRs) 🎯 These bad miRNAs silence tumor suppressor genes post-transcriptionally. 🛡️ Restore balance with: Curcumin Genistein (soy) Pomegranate, green tea Baicalin reprograms cancer-related miRNA profiles 🧬✨ #epigenetics

@MeasslainteIRL - Thomas Anthony III

SV40 Promoter Activation ⚠️ Some DNA vectors contain SV40 — an old viral promoter that can turn on dangerous genes. 🛡️ Buffer it with: Cruciferous veggies (DIM) Tart cherries (Melatonin) Parsley, celery (Apigenin) #ViralSilencing

@MeasslainteIRL - Thomas Anthony III

TLR Suppression = Immune Blindness 👁️ TLRs = sensors for viruses. If they're down, viruses slip by unnoticed. 🛡️ Restore detection with: Beta-glucans (mushrooms, oats) D3 (sunlight or food) Garlic, astragalus Baicalin activates TLR4, restores innate vigilance 🛡️ #TLRRescue

@MeasslainteIRL - Thomas Anthony III

Antigen Presentation (MHC I/II) 📡 If T cells can’t see the threat, they can’t kill it. That’s MHC dysfunction. 🛡️ Boost visibility with: NAC EGCG Ginger + Sea Moss (zinc + iodine) #ImmuneAlert

@MeasslainteIRL - Thomas Anthony III

NRF2 Dysfunction = Broken Detox 🧹 NRF2 is your antioxidant master switch. If it’s blocked, you're toxic. 🛡️ Activate NRF2 with: Broccoli sprouts (Sulforaphane) Milk thistle (Silymarin) Black seed oil, cayenne Baicalin potent NRF2 activator + liver support 🔥 #DetoxPathways

@MeasslainteIRL - Thomas Anthony III

Methylation Malfunctions 🧬🔒 Environmental toxins can silence your best genes via hypermethylation. 🛡️ Unlock resilience with: EGCG (green tea, cacao) Folate-rich foods (liver, greens) Magnesium, chlorophyll, sea moss #GeneExpression

@MeasslainteIRL - Thomas Anthony III

🌟#Baicalin The Pathway Ninja 🌿 Impacts ALL of these: ✔️ p53 repair ✔️ TLR4 immune reboot ✔️ STING inflammation control ✔️ NRF2 detox ✔️ miRNA cancer defense 🎯 Found in: Chinese skullcap (Scutellaria baicalensis) If Nature Didn’t Make It Don’t F*cking Take It. Knowledge is Power. Your cells want to heal give them the tools. 🧬 Follow @MeasslainteIRL 🌐 http://Measslainte.ie #SpikeProtein #DNAContamination #StopTheShot #NaturalImmunity

Meas Slainte Discover Nutritional Supplements for Multiple Sclerosis and other Demyelination Illnesses measslainte.ie

@MeasslainteIRL - Thomas Anthony III

🌟 Bonus Allies That Support Multiple Pathways CompoundKey BenefitsPathways Impacted Black Seed OilDNA protection, immune tuning, p53 activationp53, NRF2, PD-L1, Epigenetics CayenneAnti-inflammatory, improves circulationp53, NRF2, cGAS-STING Mucuna (L-DOPA)Neuroprotection, dopamine, DNA repair supportNRF2, DNA repair, fatigue BoronHormone modulator, mineral balanceNRF2, methylation CoQ10 + PQQMitochondrial repair, anti-fatigueNRF2, DNA repair Example Resilience Routine Morning: Lemon water with ginger, turmeric, cayenne Black seed oil Sea moss smoothie Midday: Broccoli sprouts, garlic, onions, mushrooms Leafy greens, pomegranate, parsley Green tea, chamomile, cacao nibs Evening: Tart cherry juice Magnesium glycinate Optional: Melatonin, ashwagandha, CBD oil Not medical advice for educational purposes please always speak with your practitioner.

@MeasslainteIRL - Thomas Anthony III

@Reseeit save thread

Saved - June 19, 2025 at 6:58 AM
reSee.it AI Summary
I've shared my experiences with DMSO, a versatile substance I've used for over 40 years to treat skin and internal issues. It's crucial to understand its properties and risks, as it can amplify drugs and cause skin irritation if not diluted properly. I recommend a 70% solution for application and advise caution with other substances on the skin. For oral use, start with a small dose to check for allergies. DMSO may also aid in stroke treatment and ALS management. I believe its potential benefits have been overlooked by medical authorities.

@LewDrakePhD - Lewis Drake, PhD

——This is all I have on DMSO—— DMSO DMSO: Application and Ingestion The Drake family and friends have used DMSO for over 40 years. It’s been a miracle substance for treating severe skin and internal organ problems. The main DMSO side effect is bad “Garlic breath.” But you MUST read and learn about DMSO before using it, or you could harm yourself or others!! Cautions DMSO can act as a “drug amplifier.” Any drug (e.g. aspirin) mixed with it will be transported into your body when the mixture is applied to skin. Don’t apply 99.9% pure DMSO directly to skin because it may cause excessive drying. The soles of the feet may be an exception to this. Skin Application To prevent DMSO-caused skin irritations, apply a 70% DMSO (or less) diluted solution, rather than the full strength 99.9% DMSO on skin. DMSO will treat and prevent skin irritations, cuts burns, bruises and muscle aches. If you plan on physically exercising, that might result in sore muscles, then apply DMSO before exercising and it will prevent soreness and other damages. Dilution You can dilute 99.9% DMSO to make a skin friendly, 70% DMSO solution, by mixing pure water in a GLASS measuring cup. Use a GLASS measuring cup because DMSO will melt plastic. If DMSO mixes with plastic it should never be applied to skin! Dilution Example: Create 100 ml of a 70% DMSO solution. 1.Add 70 ml of 99.9% DMSO to a glass measuring cup. 2.Add 30 ml of pure water to the cup (this will bring the cup contents up to 100 ml total). 3.Pour measured amount into a Low Density Polypropylene (LDPE) bottle. Use DMSO on clean skin (no nail polish). Caution be careful applying DMSO over a lotion, salve or ointment. DMSO is a “drug amplifier” and will absorb and carry anything present on your skin, into your body. Applying DMSO over a poisonous substance can be deadly! If you want to apply DMSO to someone without being treated yourself, use Latex gloves, NOT Nitrile. Nitrile will be damaged by DMSO. ——- DMSO (Skin Application) Wash skin with a clean cloth & tap water (that is safe to drink). Filtered or Reverse Osmosis water is fine, but not necessary for washing. Daily Rubs: (1-3 times/day): 1.Apply a 70% DMSO solution to CLEAN skin in the area to be treated. 2.Wait 5-10 min, or until itching begins. 3.Wash off any DMSO remnants using warm water on a clean cloth. 4.Apply MCT coconut oil, or olive oil, or other natural skin treatment oil to condition the skin and minimize longterm dryness caused by the treatment. —— DMSO (Oral Ingestion) Only 1 in 2000 people have an allergy to DMSO. But, start oral dosing slowly. Begin with a 1-tsp dose and verify there is no allergic reaction. Thereafter, take 1-3 tsp DMSO in a glass of H2O daily for overall body health. Too much DMSO can create a headache or nausea. It can take more than a month or more of daily doses before any improvements are noticed. However, the garlic breath will be noticeable very soon. 😍 ——- DMSO: (Strokes) The very best thing for an in-progress brain stroke, is one or more of these items below, ASAP: 1) DMSO 1-3 teaspoons/day in a cup of water, 2) Low concentration IV drip of DMSO, 3) Rub DMSO on forehead, neck, shoulders & back. Wash off after 5-10 minutes with clean water. —— DMSO (ALS) BOOST vitamin D(25OH) > 100 Strict Carnivore diet and intermittent fasting. Oral 99.9% DMSO 1-2 tablespoons in a cup of water each day. Rub on 70% DMSO 3-4 times per day. —- DMSO (Articles) DMSO: Dr.Williams (23 pages) https://drive.google.com/file/d/1-8VL01pc6fwvgakOa0xMeHDCJPk71gfN/view?usp=drivesdk… DMSO: Dr. S. Jacob https://docs.google.com/document/d/1zokQWg4VjJwVylslFotcT7tKqKGT68rDmcu9j0A0AkY/edit DMSO: (@MidwesternDoc) https://midwesterndoctor.com/p/the-remarkable-history-and-safety?utm_medium=web&triedRedirect=true… https://midwesterndoctor.com/p/dmso-is-a-miraculous-therapy-for?utm_medium=web… https://midwesterndoctor.com/p/how-dmso-cures-eye-ear-nose-throat?utm_medium=web&triedRedirect=true… https://midwesterndoctor.com/p/dmso-could-save-millions-from-brain?utm_medium=web&triedRedirect=true… https://midwesterndoctor.com/p/how-dmso-protects-and-heals-the-internal https://vigilantnews.com/post/remarkably-safe-compound-could-save-millions-from-brain-and-spinal-injury/ DMSO: WebMD https://docs.google.com/file/d/18NnhWTBfe9HxP0dGfU1rDPvY4zvjH7aY/edit?usp=docslist_api&filetype=msword… DMSO: Book https://archive.org/details/dmsotruestoryofr0000tars DMSO: Amazon Source https://a.co/d/79Du4FE 99.9% https://a.co/d/8Bz4vPt 70% Roll-On https://a.co/d/8AKIA5v LDPE Bottles ——

Page Not Found Web word processing, presentations and spreadsheets docs.google.com
The Remarkable History and Safety of DMSO Please share your experiences with DMSO with the readers here! midwesterndoctor.com
DMSO is a Miraculous Therapy for Chronic Pain and Musculoskeletal Injuries The decades of evidence DMSO revolutionizes the practice of medicine midwesterndoctor.com
How DMSO Cures Eye, Ear, Nose, Throat and Dental Disease Many of those "incurable" conditions respond remarkably to DMSO midwesterndoctor.com
DMSO Could Save Millions From Brain and Spinal Injury The decades of evidence showing DMSO revolutionizes the care of many "untreatable" circulatory and neurologic conditions. midwesterndoctor.com
How DMSO Protects and Heals the Internal Organs The evidence behind DMSO's utility for a myriad of challenging diseases midwesterndoctor.com
Remarkably Safe Compound Could Save Millions From Brain and Spinal Injury A Midwestern Doctor has done it again! Bookmark this article right now. vigilantnews.com
DMSO, the true story of a remarkable pain-killing drug : Tarshis, Barry : Free Download, Borrow, and Streaming : Internet Archive 226 p. ; 22 cm archive.org

@LewDrakePhD - Lewis Drake, PhD

From @MidwesternDoc https://www.midwesterndoctor.com/p/the-remarkable-history-and-safety?utm_medium=web&triedRedirect=true

The Remarkable History and Safety of DMSO Please share your experiences with DMSO with the readers here! midwesterndoctor.com

@LewDrakePhD - Lewis Drake, PhD

@MidwesternDoc

@PierreKory - Pierre Kory, MD MPA

If DMSO was used for strokes and spinal cord injuries, millions would be spared from death, paralysis, and disability. As an ICU doc, I am in disbelief the FDA has kept this from us for decades. The evidence @MidwesternDoc presents here is mind-blowing. https://www.midwesterndoctor.com/p/dmso-could-save-millions-from-brain

DMSO Could Save Millions From Brain and Spinal Injury The decades of evidence showing DMSO revolutionizes the care of many "untreatable" circulatory and neurologic conditions. midwesterndoctor.com
Saved - June 18, 2025 at 10:23 AM
reSee.it AI Summary
I express concern over the cardiovascular complications, particularly Corrected QT Interval Prolongation, that children are facing, which seems overlooked by many. I reference the harmful impact of the Tat protein from HIV on ribosomal RNA biogenesis and its connection to cardiovascular diseases. I highlight the frequent occurrence of QTc prolongation in HIV-positive patients, emphasizing its predictive nature for cardiovascular mortality. I challenge those who downplay the similarities between COVID-19 and HIV, warning of the potential consequences of such dismissals.

@dbdugger - Daniel Brittain Dugger

Agenda? Children have been left to suffer Tat-like cardiovascular complications, including Corrected QT Interval Prolongation. Too bad you don't know what you are talking about.

@thereal_truther - The Real Truther

Shame on all of you exploiting a tragedy for your own agenda.

@dbdugger - Daniel Brittain Dugger

SARS-CoV-2 targets ribosomal RNA biogenesis https://www.cell.com/cell-reports/pdf/S2211-1247(24)00219-5.pdf "Finally, the Tat protein of human immunodeficiency virus interacts with FBL and U3 snoRNA, impairing prerRNA processing and depleting mature ribosomes."

@dbdugger - Daniel Brittain Dugger

COVID-19 Infection and Corrected QT Interval Prolongation—Collateral Damage From Our Newest Enemy https://jamanetwork.com/journals/jamanetworkopen/fullarticle/2779057

@dbdugger - Daniel Brittain Dugger

The role of HIV Tat protein in HIV-related cardiovascular diseases https://pmc.ncbi.nlm.nih.gov/articles/PMC5941636/

The role of HIV Tat protein in HIV-related cardiovascular diseases The human immunodeficiency virus (HIV) is a major global public health issue. HIV-related cardiovascular disease remains a leading cause of morbidity and mortality in HIV positive patients. HIV Tat is a regulatory protein encoded by tat gene of ... pmc.ncbi.nlm.nih.gov

@dbdugger - Daniel Brittain Dugger

Same Tat. Same Corrected QT Interval Prolongation. "Corrected QT (QTc) prolongation is predictive of cardiovascular mortality. Frequent occurrence of QT interval prolongation have been found in HIV-positive patients."

@dbdugger - Daniel Brittain Dugger

You said the virus was nothing like HIV. We'll see how many more people like you destroy. Be proud!

Saved - June 18, 2025 at 9:53 AM
reSee.it AI Summary
I’ve been reflecting on the parallels between Long COVID and ME/CFS, particularly in how children are suffering. A recent letter from a young girl highlights the urgent need for support. I feel betrayed by academia and advocacy groups for neglecting both Long COVID and HIV+ communities. My research points to significant overlaps in neurocognitive impairments and quality of life issues. The Tat protein's role in both HIV and COVID-19 raises concerns about the long-term effects on health. It’s frustrating to see the lack of action and understanding in addressing these complex illnesses.

@dbdugger - Daniel Brittain Dugger

Victoria, your country drew parallels to ME/CFS. You can give up! Better luck next time.

@acrossthemersey - Jammer

‘Children deserve more than our sympathy, they deserve our urgent action.’ After reading a letter from a 12 year old girl describing her constant pain and only managing 1 hour of school per day, MP Victoria Collins calls for urgent support for UK children living with LongCOVID.

@dbdugger - Daniel Brittain Dugger

In drawing parallels to ME/CFS not only have those in academia, the medical establishment, and "advocacy" groups betrayed the Long Covid population, they have once again betrayed the HIV+ who they supposedly care about, leaving us to worry about our family members.

@dbdugger - Daniel Brittain Dugger

They were so quick to lie to me and others stating the virus was nothing like HIV. Fortunately, I have been around criminals long enough as a bondsman that I don't trust others and certainly don't after reading.

@dbdugger - Daniel Brittain Dugger

Because of my reading over the past three years, I can easily point to three differences: Asymptomatic Neurocognitive Impairment Conversion, Arrythmias leading to death, and AIDS Defining Illness presentation.

@dbdugger - Daniel Brittain Dugger

I can also easily explain why an untold number of children have the Quality of Life of a Cystic Fibrosis patient. Ironically, one protein coursing through their bodies contributes to each of the above and proves their betrayal.

@dbdugger - Daniel Brittain Dugger

That protein is Protein E and it has consistently proven to operate mechanistically as HIV's Tat. SARS-CoV-2 targets ribosomal RNA biogenesis https://www.cell.com/cell-reports/pdf/S2211-1247(24)00219-5.pdf

@dbdugger - Daniel Brittain Dugger

"Finally, the Tat protein of human immunodeficiency virus interacts with FBL and U3 snoRNA, impairing prerRNA processing and depleting mature ribosomes."

@dbdugger - Daniel Brittain Dugger

Soon it will be three years since my drawing attention to the fact individuals suffer from Asymptomatic Neurocognitive Impairment. https://www.linkedin.com/pulse/focusing-cfr-proving-fatal-mistake-daniel-dugger/?trackingId=DX56WPzBS6iWBPD77MGhQQ%3D%3D

Focusing On The CFR Is Proving To Be A Fatal Mistake Since the beginning of the SARS-Cov-2 pandemic, epidemiologists have regularly mentioned what is referred to as the Case Fatality Rate, that is the number of individuals who have been diagnosed with a disease and later die. Large numbers of individuals have used the roughly one percent CFR to relax linkedin.com

@dbdugger - Daniel Brittain Dugger

I did so after reading this article from January of 2022. January 18, 2022 Cerebrospinal Fluid Offers Clues to Post-COVID ‘Brain Fog’ https://www.ucsf.edu/news/2022/01/422156/cerebrospinal-fluid-offers-clues-post-covid-brain-fog

@dbdugger - Daniel Brittain Dugger

"All participants underwent an in-person cognitive testing battery with a neuropsychologist, applying equivalent criteria used for HIV-associated neurocognitive disorder (HAND)."

@dbdugger - Daniel Brittain Dugger

"Surprisingly, the researchers found that 13 of the 22 participants (59 percent) with cognitive symptoms met HAND criteria, compared with seven of the 10 control participants (70 percent)."

@dbdugger - Daniel Brittain Dugger

In order for those in the control arm to be diagnosed with Asymptomatic Neurocognitive Impairment, their ability to complete their Activities of Daily Living had to be preserved, it is not in ME/CFS.

@dbdugger - Daniel Brittain Dugger

HIV-associated neurocognitive disorder — pathogenesis and prospects for treatment https://pmc.ncbi.nlm.nih.gov/articles/PMC4937456/

HIV-associated neurocognitive disorder — pathogenesis and prospects for treatment In the past two decades, several advancements have improved the care of HIV-infected individuals. Most importantly, the development and deployment of combination antiretroviral therapy (CART) has resulted in a dramatic decline in the rate of deaths ... pmc.ncbi.nlm.nih.gov

@dbdugger - Daniel Brittain Dugger

See? Asymptomatic neurocognitive impairment (ANI) Impairment in ≥2 neurocognitive domains (≥1 SD) Does not interfere with daily functioning

@dbdugger - Daniel Brittain Dugger

Could You Have ME/CFS? (Myalgic Encephalomyelitis/Chronic Fatigue Syndrome) https://www.cdc.gov/me-cfs/pdfs/could-you-have-mecfs_508.pdf

@dbdugger - Daniel Brittain Dugger

ME/CFS is a complex illness and symptoms of ME/CFS may seem similar to many other illnesses. ME/CFS requires three symptoms:

@dbdugger - Daniel Brittain Dugger

1. Not being able to participate in routine activities that were possible before becoming ill, such as work, school, social life, and/or personal life, that:

@dbdugger - Daniel Brittain Dugger

• Lasts for more than 6 months • Is accompanied by fatigue that is: • Often serious • Just started (not lifelong) • Not the result of ongoing activities • Not from more than usual effort • Not made better by rest

@dbdugger - Daniel Brittain Dugger

In addition, at least one of the following symptoms is also required: Impaired memory or ability to concentrate. People with ME/CFS may have trouble remembering, learning new things, concentrating, or making decisions.

@dbdugger - Daniel Brittain Dugger

Those in Australia have provided two opportunities to point out what I refer to as legalized child abuse. Large hippocampus detected in Long COVID and ME/CFS patients https://news.griffith.edu.au/2025/02/11/large-hippocampus-detected-in-long-covid-and-me-cfs-patients/

Large hippocampus detected in Long COVID and ME/CFS patients - Griffith News Striking brain similarities have been detected in patients who experience Long COVID and Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS), in news.griffith.edu.au

@dbdugger - Daniel Brittain Dugger

Only one population is experiencing the destruction of their hippocampus in the exact same way observed in the HIV+ and that they are was reported last year.

@dbdugger - Daniel Brittain Dugger

2024 Jun 7 SARS-CoV-2 Viroporin E Induces Ca2+ Release and Neuron Cell Death in Primary Cultures of Rat Hippocampal Cells Aged In Vitro https://pmc.ncbi.nlm.nih.gov/articles/PMC11203731/

SARS-CoV-2 Viroporin E Induces Ca2+ Release and Neuron Cell Death in Primary Cultures of Rat Hippocampal Cells Aged In Vitro The COVID-19 pandemic was caused by infection with Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), which may lead to serious respiratory, vascular and neurological dysfunctions. The SARS-CoV-2 envelope protein (E protein) is a ... pmc.ncbi.nlm.nih.gov

@dbdugger - Daniel Brittain Dugger

"Highly infectious viruses such as the human immunodeficiency virus (HIV), Ebola virus, or hepatitis C virus encode proteins that function as ion channels."

@dbdugger - Daniel Brittain Dugger

If the suggestion individuals would develop the functional equivalent of HIV Associated Neurocognitive Decline rings a bell, it is that very thing Kenneth Podell predicted almost five years ago.

@dbdugger - Daniel Brittain Dugger

Epub 2020 Sep 29. Multiple Neuroinvasive Pathways in COVID-19 https://pubmed.ncbi.nlm.nih.gov/32990925/

Multiple Neuroinvasive Pathways in COVID-19 - PubMed COVID-19 is a highly infectious viral disease caused by the novel coronavirus SARS-CoV-2. While it was initially regarded as a strictly respiratory illness, the impact of COVID-19 on multiple organs is increasingly recognized. The brain is among the targets of COVID-19, and it can be impacted in mul … pubmed.ncbi.nlm.nih.gov

@dbdugger - Daniel Brittain Dugger

"One can draw on the experience with an HIV/AIDS epidemic. The initial understanding of HIV/AIDS was that of the virus affecting the immune system by depleting T cells, which resulted in opportunistic infections of multiple organs, including the brain."

@dbdugger - Daniel Brittain Dugger

Same Tat as above. Same hippocampus. Same Ca2+ overload. HIV-1 protein Tat induces apoptosis of hippocampal neurons by a mechanism involving caspase activation, calcium overload, and oxidative stress https://pubmed.ncbi.nlm.nih.gov/9878167/

HIV-1 protein Tat induces apoptosis of hippocampal neurons by a mechanism involving caspase activation, calcium overload, and oxidative stress - PubMed Patients infected with HIV-1 often exhibit cognitive deficits that are related to progressive neuronal degeneration and cell death. The protein Tat, which is released from HIV-1-infected cells, was recently shown to be toxic toward cultured neurons. We now report that Tat induces apoptosis in cultur … pubmed.ncbi.nlm.nih.gov

@dbdugger - Daniel Brittain Dugger

For reasons only known to them, those in academia, the medical establishment, and "advocacy" groups also turned a blind eye to nineteen years of ME/CFS research, unwilling to treat those with Long Covid as they did with fibromyalgia patients in 2008.

@dbdugger - Daniel Brittain Dugger

Short QT interval https://me-pedia.org/wiki/Short_QT_interval

Short qt interval me-pedia.org

@dbdugger - Daniel Brittain Dugger

2006, Shortened QT interval: a distinctive feature of the dysautonomia of chronic fatigue syndrome. "CONCLUSIONS: Relative short QTc intervals are features of the CFS-related dysautonomia. The significance of this finding is discussed."

@dbdugger - Daniel Brittain Dugger

See? 2008, Electrocardiographic QT interval and cardiovascular reactivity in fibromyalgia differ from chronic fatigue syndrome. "CONCLUSION: A relatively short QTc and positive HIS characterize CFS patients and distinguish them from FM patients. These data may support the contention that FM and CFS are separate disorders."

@dbdugger - Daniel Brittain Dugger

2012, Shortened QTc interval in chronic fatigue syndrome Here we assessed QTc in a large UK population of CFS patients using automated, clinically applicable, measurement techniques and confirmed that QTc is significantly shortened in CFS patients...

@dbdugger - Daniel Brittain Dugger

It was in 2021 that we learned Corrected QT Interval Prolongation is observed with SARS-Cov-2 as it is with HIV. COVID-19 Infection and Corrected QT Interval Prolongation—Collateral Damage From Our Newest Enemy https://jamanetwork.com/journals/jamanetworkopen/fullarticle/2779057

@dbdugger - Daniel Brittain Dugger

Same Tat as above. Same Corrected QT Interval Prolongation. The role of HIV Tat protein in HIV-related cardiovascular diseases https://pmc.ncbi.nlm.nih.gov/articles/PMC5941636/

The role of HIV Tat protein in HIV-related cardiovascular diseases The human immunodeficiency virus (HIV) is a major global public health issue. HIV-related cardiovascular disease remains a leading cause of morbidity and mortality in HIV positive patients. HIV Tat is a regulatory protein encoded by tat gene of ... pmc.ncbi.nlm.nih.gov

@dbdugger - Daniel Brittain Dugger

"Corrected QT (QTc) prolongation is predictive of cardiovascular mortality. Frequent occurrence of QT interval prolongation have been found in HIV-positive patients."

@dbdugger - Daniel Brittain Dugger

It was in 2021 that Lucinda Bateman spoke to those unwilling to listen that those living with ME/CFS do not develop what are AIDS Defining Illnesses. Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: Essentials of Diagnosis and Management https://www.mayoclinicproceedings.org/article/S0025-6196(21)00513-9/fulltext

@dbdugger - Daniel Brittain Dugger

"Although patients with ME/CFS do not present with symptomatic, opportunistic infections (eg, cryptosporidiosis, tuberculosis), some do experience recurrent herpes infections."

@dbdugger - Daniel Brittain Dugger

6 June 2025 Farm day visitors warned over Cryptosporidium parasite threat https://www.bbc.com/news/articles/cy5e1wn6n22o

Cryptosporidium: Open farm day visitors warned over parasite risk A public health warning is issued as 190,000 people are expected at open farm events across the UK. bbc.com

@dbdugger - Daniel Brittain Dugger

"Tens of thousands of visitors due to attend a UK-wide open farm day this weekend have been warned about a parasitic infection that causes serious gastrointestinal illness."

@dbdugger - Daniel Brittain Dugger

They also have a TB problem. Tuberculosis cases in England continued to increase in 2024 https://www.gov.uk/government/news/tuberculosis-cases-in-england-continued-to-increase-in-2024

Tuberculosis cases in England continued to increase in 2024 UK TB cases rise 13% in 2024, continuing upward trend. gov.uk

@dbdugger - Daniel Brittain Dugger

Timmy, Johnny, Sally, Sammy, and Jimmy were deemed undeserving of the science behind the Estimated Date Of Seroconversion and their fathers were concerned about an Estimated Date of an AIDS Death this Father's Day.

@dbdugger - Daniel Brittain Dugger

Gastro cases hit 20-year high as parasite spreads disease to toddlers https://www.smh.com.au/national/gastro-cases-hit-20-year-high-as-parasite-spreads-disease-to-toddlers-20240702-p5jqjy.html

Gastro cases hit 20-year high as parasite spreads disease to toddlers A gastrointestinal disease caused by the cryptosporidiosis parasite has reached alarming rates, with daycare and school aged children picking up the infection. smh.com.au

@dbdugger - Daniel Brittain Dugger

"There have been 11,747 cryptosporidiosis cases in 2024 compared with 3716 in 2023. A quarter of all cases are in children under four."

@dbdugger - Daniel Brittain Dugger

Same Tat as above. Same Cryptosporidium Parvum as above. HIV-1 Tat Protein Suppresses Cholangiocyte Toll-Like Receptor 4 Expression and Defense against Cryptosporidium parvum https://pmc.ncbi.nlm.nih.gov/articles/PMC2716168/

HIV-1 Tat Protein Suppresses Cholangiocyte Toll-Like Receptor 4 Expression and Defense against Cryptosporidium parvum Biliary cryptosporidiosis is associated with acquired immunodeficiency syndrome (AIDS) cholangiopathy and occurs almost exclusively in adult patients with AIDS. Infection of biliary epithelial cells (cholangiocytes) with Cryptosporidium parvum ... pmc.ncbi.nlm.nih.gov

@dbdugger - Daniel Brittain Dugger

Reported this year is that many have the Quality of Life of a Cystic Fibrosis patient. Long COVID Is Fueling a Mental Health Crisis in Children https://www.unmc.edu/healthsecurity/transmission/2025/05/28/long-covid-is-fueling-a-mental-health-crisis-in-children/

Long COVID Is Fueling a Mental Health Crisis in Children Neuroscience News A new study reveals that nearly 40% of children with long COVID are experiencing significant symptoms of anxiety or depression, many for the first time. Using validated mental hea… unmc.edu

@dbdugger - Daniel Brittain Dugger

"These children reported a quality of life comparable to peers with serious illnesses like cancer or cystic fibrosis, with many expressing a deep sense of ineffectiveness and loss of confidence."

@dbdugger - Daniel Brittain Dugger

It was reported in 2021 that increased TGF-b signaling is observed. SARS-CoV-2 in severe COVID-19 induces a TGF-β-dominated chronic immune response that does not target itself https://www.nature.com/articles/s41467-021-22210-3

SARS-CoV-2 in severe COVID-19 induces a TGF-β-dominated chronic immune response that does not target itself - Nature Communications The pathogenesis of severe COVID-19 reflects an inefficient immune reaction to SARS-CoV-2. Here we analyze, at the single cell level, plasmablasts egressed into the blood to study the dynamics of adaptive immune response in COVID-19 patients requiring intensive care. Before seroconversion in response to SARS-CoV-2 spike protein, peripheral plasmablasts display a type 1 interferon-induced gene expression signature; however, following seroconversion, plasmablasts lose this signature, express instead gene signatures induced by IL-21 and TGF-β, and produce mostly IgG1 and IgA1. In the sustained immune reaction from COVID-19 patients, plasmablasts shift to the expression of IgA2, thereby reflecting an instruction by TGF-β. Despite their continued presence in the blood, plasmablasts are not found in the lungs of deceased COVID-19 patients, nor does patient IgA2 binds to the dominant antigens of SARS-CoV-2. Our results thus suggest that, in severe COVID-19, SARS-CoV-2 triggers a chronic immune reaction that is instructed by TGF-β, and is distracted from itself. Our understanding on the humoral immunity induced by SARS-CoV-2 is still lacking. Here the authors analyze B cell responses at the single cell level to find that, in severe COVID-19 patients, plasmablasts shift from IFN to TGFβ instruction to produce IgA antibodies that are not specific to dominant SARS-CoV-2 antigens. nature.com

@dbdugger - Daniel Brittain Dugger

Were I experiencing the silencing of the Cystic Fibrosis Transmembrane Conductance Receptor, I too would have the Quality of Life of a CF patient. Inflammation in the COVID-19 airway is due to inhibition of CFTR signaling by the SARS-CoV-2 spike protein https://www.nature.com/articles/s41598-024-66473-4

Inflammation in the COVID-19 airway is due to inhibition of CFTR signaling by the SARS-CoV-2 spike protein - Scientific Reports SARS-CoV-2-contributes to sickness and death in COVID-19 patients partly by inducing a hyper-proinflammatory immune response in the host airway. This hyper-proinflammatory state involves activation of signaling by NFκB, and unexpectedly, ENaC, the epithelial sodium channel. Post-infection inflammation may also contribute to "Long COVID"/PASC. Enhanced signaling by NFκB and ENaC also marks the airway of patients suffering from cystic fibrosis, a life-limiting proinflammatory genetic disease due to inactivating mutations in the CFTR gene. We therefore hypothesized that inflammation in the COVID-19 airway might similarly be due to inhibition of CFTR signaling by SARS-CoV-2 spike protein, and therefore activation of both NFκB and ENaC signaling. We used western blot and electrophysiological techniques, and an organoid model of normal airway epithelia, differentiated on an air–liquid-interface (ALI). We found that CFTR protein expression and CFTR cAMP-activated chloride channel activity were lost when the model epithelium was exposed to SARS-CoV-2 spike proteins. As hypothesized, the absence of CFTR led to activation of both TNFα/NFκB signaling and α and γ ENaC. We had previously shown that the cardiac glycoside drugs digoxin, digitoxin and ouabain blocked interaction of spike protein and ACE2. Consistently, addition of 30 nM concentrations of the cardiac glycoside drugs, prevented loss of both CFTR protein and CFTR channel activity. ACE2 and CFTR were found to co-immunoprecipitate in both basal cells and differentiated epithelia. Thus spike-dependent CFTR loss might involve ACE2 as a bridge between Spike and CFTR. In addition, spike exposure to the epithelia resulted in failure of endosomal recycling to return CFTR to the plasma membrane. Thus, failure of CFTR recovery from endosomal recycling might be a mechanism for spike-dependent loss of CFTR. Finally, we found that authentic SARS-CoV-2 virus infection induced loss of CFTR protein, which was rescued by the cardiac glycoside drugs digitoxin and ouabain. Based on experiments with this organoid model of small airway epithelia, and comparisons with 16HBE14o- and other cell types expressing normal CFTR, we predict that inflammation in the COVID-19 airway may be mediated by inhibition of CFTR signaling by the SARS-CoV-2 spike protein, thus inducing a cystic fibrosis-like clinical phenotype. To our knowledge this is the first time COVID-19 airway inflammation has been experimentally traced in normal subjects to a contribution from SARS-CoV-2 spike-dependent inhibition of CFTR signaling. nature.com

@dbdugger - Daniel Brittain Dugger

Same Tat as above. Same TGF-b as above. Same CFTR silencing as above. HIV Tat Protein Induces the TGF-β Signaling Pathway and Suppresses the CFTR Biogenesis and Activity by microRNA-Regulated Gene-Silencing Mechanism https://faseb.onlinelibrary.wiley.com/doi/abs/10.1096/fasebj.2020.34.s1.00650

@dbdugger - Daniel Brittain Dugger

For those who don't give up, let me assuage your fears. PEM is not observed in exercises in futility, like trying to save those you destroyed due to your mental weakness and moral bankruptcy. For that, you should rejoice.

Saved - June 18, 2025 at 7:35 AM
reSee.it AI Summary
A discussion arose regarding claims made by Dr. Suzanne Humphries about the Pfizer COVID vaccine, suggesting it transforms under a microscope into structures resembling circuit boards. Some participants questioned why this wasn't headline news, while others dismissed the claims as discrediting legitimate vaccine concerns. Dr. Humphries expressed frustration with critics and emphasized her commitment to uncovering the truth, mentioning her upcoming revelations. Others suggested consulting experts who have analyzed vaccine contents, highlighting ongoing debates about vaccine safety and transparency.

@ChildrensHD - Children’s Health Defense

🚨 WOW: STRAIGHT OUT OF A SCI-FI MOVIE 👇 The @pfizer COVID shot under a microscope transforms from circles and squares to long wires and then finally appears to resemble a “circuit board,” according to @DrSuzanneH7. @ShannonJoyRadio

Video Transcript AI Summary
Under a darkfield microscope, the speaker examined the Pfizer vaccine liquid and observed circular and square particles floating around, which they did not see in older vaccines like measles and flu shots. After the liquid sat overnight, long wires appeared to form. Later, the speaker observed what looked like the image of a circuit board. The speaker was freaked out by this and worried about potential repercussions, given prior death threats. They questioned what these microscopic observations might imply and what potential problems could arise.
Full Transcript
Speaker 0: I looked at the Pfizer vaccine liquid under a microscope, a darkfield microscope, and what I saw initially were particles. They were like circles and squares kind of floating around, and I was like, woah, that's really interesting. And I looked at some older vaccines like measles and flu shots, and I didn't see any of that. And then if you left that liquid sit overnight, what you would see would be like, almost like long wires starting to form. And then if you come back a little while later, there were what appears to be, and I'm not saying that's what it is, but it looks like the image of a circuit board. And I was a bit freaked out by it and I kind of backed away from it. I was like, I don't even want to get here because this is the kind of thing that could get me killed. Like, I've already had enough death threats. I don't need, like, this vaccine company coming after me. So I just think, well, what's going on here? If that's what happens under a microscope, what's happening? What's what's the potential problem?

@JenniferTw63046 - MamaT

@ChildrensHD @pfizer @DrSuzanneH7 @ShannonJoyRadio Why isn’t this headline news?

@oldsmokindragon - Truthfanboi

@JenniferTw63046 @ChildrensHD @pfizer @DrSuzanneH7 @ShannonJoyRadio Because is false. There's a lot wrong with these shots but this is just well poison that discredits those challenging them as kooks as you can see from some of these comments.

@ShannonJoyRadio - Shannon Joy

@oldsmokindragon @JenniferTw63046 @ChildrensHD @pfizer @DrSuzanneH7 I think there is more to be discovered. that's why I have multiple viewpoints on my show. You are welcome to come on and defend your point of view on this. DM me and we can set up an interview! @Jikkyleaks is welcome to come on too ...

@DrSuzanneH7 - Dr Suzanne Humphries

@ShannonJoyRadio @oldsmokindragon @JenniferTw63046 @ChildrensHD @pfizer @Jikkyleaks I find the gaslighting very interesting. It's kind of making me even more sure that there is something very significant about what I found. I'm going to reveal the full story and images with Catherine Austin Fitts in a few days.

@oldsmokindragon - Truthfanboi

@DrSuzanneH7 @ShannonJoyRadio @JenniferTw63046 @ChildrensHD @pfizer @Jikkyleaks The gaslighting isn't those challenging this. It's frustration that these types of conversations derail the credibility of covid dissenters and deflect from the know mechanisms of harm.

@DrSuzanneH7 - Dr Suzanne Humphries

Says who? And look who all the gaslighting is coming from… People without actual names and faces, like you. I'm over this. I'm over doctors who won't show themselves and people who are afraid of this that and the other thing. Do you think I didn't lose everything when I walked away from the medical system? Do you think I didn't lose everything financially? Do you think I give a rip about my reputation Today given that I've never given a rip about it before? Only the truth has always mattered to me. So all you faceless wonders mean nothing to me. Why is your income so much more important than mine was? Why is your reputation so much more important than mine was? Why is your safety so much more important than mine? Do you think I've not had all kinds of actual real threats both physically and online? And why should the likes of you be dictating to me how I should run my life out in the open?

@BlackTomThePyr8 - Tom Czerniawski

@DrSuzanneH7 @oldsmokindragon @ShannonJoyRadio @JenniferTw63046 @ChildrensHD @pfizer @Jikkyleaks Suzanne, please speak with @KevinMcCairnPhD and @Kevin_McKernan, both of whom have done extremely in-depth analysis of vaccine contents - they know better than anyone on Earth what's in them, and what's not. We're worried because the allegation that 'circuit boards' and 'nano'-

@DrSuzanneH7 - Dr Suzanne Humphries

I am fully aware of Kevin McKernon's research. I have communicated with him numerous times. I have high regard for what he has done. I don't believe he will have any answers about the pictures that I just posted nor the videos that I have. Nor would he know very much about the New Zealand vaccine which is the one that I did my research on. Also, I hope everyone is aware that there was a huge issue with homogeneity from vaccine lot to vaccine lot.

@53v3n0fn1n3 - 🕯Seven of Nine, MD 🏴‍☠️

@DrSuzanneH7 @BlackTomThePyr8 @oldsmokindragon @ShannonJoyRadio @JenniferTw63046 @ChildrensHD @pfizer @Jikkyleaks @KevinMcCairnPhD @Kevin_McKernan Dear Dr Humphreys, do you know about the work of Professor Arne Burkhardt and the german http://Expertcouncil.one? Starting in 2021 they saw these crystals, then reviewed Autopsies with histology and biophysical methods. Surprizing result was Cholesterol crystals. Gaslighting?

Expertcouncil - der Expertenrat für Corona, Impfungen & Co. Der Expertcouncil bietet Dir kostenlosen Zugang zu Fakten, wissenschaftlichen Studien und Musterbriefen zu Corona, Impfung, 5G und mehr expertcouncil.one
Saved - January 18, 2026 at 10:14 PM
reSee.it AI Summary
I describe post-vaccination syndrome (PVS) after mRNA vaccines, explored 2022–2026. Reports suggest spike protein may persist, amyloid fibrin microclots can form, and prion‑like domains may promote misfolding. Immune dysregulation—cytokine elevation and T-cell exhaustion—is noted. Investigations include DFPP and stem‑cell therapies; concerns about residual vaccine DNA are discussed. PVS is understudied and not yet recognized by major authorities, but some data show physiological changes in a subset.

@MeasslainteIRL - Thomas Emmett III 🐺🐭🦝 Snr mouse clicker™

Post-vaccination syndrome (PVS), also referred to as post-acute sequelae following COVID-19 vaccination, describes a set of persistent symptoms reported by a subset of individuals after receiving mRNA COVID-19 vaccines. Emerging research from 2022–2026 explores potential biological mechanisms behind these symptoms in affected people. This overview synthesizes peer-reviewed evidence, including studies on spike protein dynamics, microclots, prion-like elements, immune changes, and manufacturing concerns. It draws from a range of sources, to provide a balanced view. Note that PVS remains understudied and is not formally recognized by major health authorities like the FDA or WHO, but preliminary data suggest real physiological changes in some cases. I dont know anyone who regrets not taking the jabs :)

@KevinMcCairnPhD - Kevin W. McCairn PhD

McCairn Protocol Slays Biowarfare Amyloids

@MeasslainteIRL - Thomas Emmett III 🐺🐭🦝 Snr mouse clicker™

Understanding Post-Vaccination Syndrome: A Science-Based Overview When COVID-19 mRNA vaccines were introduced, they were designed to deliver temporary instructions for cells to produce the spike protein, triggering an immune response. However, emerging research suggests that for some individuals, this process may not follow the expected trajectory. This has led researchers to investigate a constellation of symptoms now being studied as "post-vaccination syndrome" or "post-acute sequelae" following vaccination. This explanation draws from peer-reviewed research published between 2022 and 2026 to help understand what scientists are currently investigating.

@MeasslainteIRL - Thomas Emmett III 🐺🐭🦝 Snr mouse clicker™

Core Concepts 1. Spike Protein Persistence The Expected Process: After mRNA vaccination, the spike protein should be cleared from the body within days to weeks. Think of it like a temporary instruction manual that gets used and discarded. What Research Shows: Studies indicate that for some people, spike protein may persist far longer than anticipated: "Expression of SARS-CoV-2 spike protein in cerebral arteries" (https://pubmed.ncbi.nlm.nih.gov/40184822/) detected spike protein in brain blood vessels months after vaccination. Similarly, https://news.yale.edu/2025/02/19/immune-markers-post-vaccination-syndrome- indicate-future-research-directions is investigating persistent spike protein in individuals with post-vaccination syndrome. A https://www.nature.com/articles/s41541-023-00742-7 confirmed mRNA can persist up to 30 days, while https://www.cell.com/cell-host-microbe/fulltext/S1931-3128(24)00438-4 found spike protein at the skull-meninges-brain interface, potentially linked to ongoing neuroinflammation. Analogy: Imagine leaving your car running after you arrive at your destination. The engine (spike protein) was meant to shut off, but it's still idling—and in some cases, revving—in ways that may cause problems.

Expression of SARS-CoV-2 spike protein in cerebral Arteries: Implications for hemorrhagic stroke Post-mRNA vaccination - PubMed Although the possibility of spike protein expression due to asymptomatic SARS-CoV-2 infection cannot be entirely excluded, this study demonstrated prolonged presence of SARS-CoV-2 spike protein in the cerebral arteries following mRNA vaccination. Additionally, some inflammatory cell infiltration was … pubmed.ncbi.nlm.nih.gov
Page not found | Yale News news.yale.edu
Duration of SARS-CoV-2 mRNA vaccine persistence and factors associated with cardiac involvement in recently vaccinated patients - npj Vaccines At the start of the COVID-19 pandemic, the BNT162b2 (BioNTech-Pfizer) and mRNA-1273 (Moderna) mRNA vaccines were expediently designed and mass produced. Both vaccines produce the full-length SARS-CoV-2 spike protein for gain of immunity and have greatly reduced mortality and morbidity from SARS-CoV-2 infection. The distribution and duration of SARS-CoV-2 mRNA vaccine persistence in human tissues is unclear. Here, we developed specific RT-qPCR-based assays to detect each mRNA vaccine and screened lymph nodes, liver, spleen, and myocardium from recently vaccinated deceased patients. Vaccine was detected in the axillary lymph nodes in the majority of patients dying within 30 days of vaccination, but not in patients dying more than 30 days from vaccination. Vaccine was not detected in the mediastinal lymph nodes, spleen, or liver. Vaccine was detected in the myocardium in a subset of patients vaccinated within 30 days of death. Cardiac ventricles in which vaccine was detected had healing myocardial injury at the time of vaccination and had more myocardial macrophages than the cardiac ventricles in which vaccine was not detected. These results suggest that SARS-CoV-2 mRNA vaccines routinely persist up to 30 days from vaccination and can be detected in the heart. nature.com

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2. Amyloid Fibrin Microclots What They Are: Under a microscope, researchers have observed unusual clot-like structures in the blood of people with Long COVID and post-vaccination symptoms. These are not typical blood clots but tangled masses of fibrin (a protein involved in normal clotting) that has misfolded into an amyloid form—similar to what happens in Alzheimer's disease. The Research: Multiple studies using Thioflavin T staining (a fluorescent dye that lights up when it binds to amyloid) have detected these microclots in people with Long COVID. One review assessed the evidence (https://pmc.ncbi.nlm.nih.gov/articles/PMC11491705/), while another described their properties and diagnostic potential (https://www.thieme-connect.com/products/ejournals/pdf/10.1055/s-0043-1774796.pdf). Additional research (https://www.sciencedirect.com/science/article/pii/S2473952924001642 and https://onlinelibrary.wiley.com/doi/10.1002/jmv.70613) further documents these findings. Why It Matters: These microclots may: - Obstruct tiny blood vessels (capillaries) - Impede oxygen delivery to tissues - Contribute to fatigue, brain fog, and exercise intolerance Analogy: Think of your bloodstream as a highway system. Microclots are like roadblocks too small to close the whole road but large enough to cause traffic jams, slowing down essential deliveries (oxygen and nutrients) throughout your body.

Fibrinaloid microclots in long COVID: assessing the actual evidence properly pmc.ncbi.nlm.nih.gov
Microclots, as defined by amyloid-fibrinogen aggregates, predict risks of disseminated intravascular coagulation and mortality Microclots have been associated with various conditions, including postacute sequelae of severe acute respiratory syndrome coronavirus 2 infection. Th… sciencedirect.com

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3. Prion-like Domains The Concern: Prion proteins are notorious for causing misfolding diseases like Creutzfeldt-Jakob disease. They propagate by inducing normal proteins to misfold in a chain reaction. Research (https://pmc.ncbi.nlm.nih.gov/articles/PMC8878784/) identified prion-like domains in the SARS-CoV-2 spike protein. These regions can rapidly shift shapes and may interact with cellular proteins to promote misfolding. https://www.news-medical.net/news/20220131/Prion-like-domains-in-SARS-CoV-2-RBD-and-ACE2-play-important-functional-roles-in-viral-adhesion-and-entry.aspx explains their important roles in viral adhesion and entry. Important Context: The presence of prion-like domains does not mean vaccines cause prion disease. It suggests a potential mechanism for protein aggregation and persistent symptoms in some individuals.

Prion-like Domains in Spike Protein of SARS-CoV-2 Differ across Its Variants and Enable Changes in Affinity to ACE2 Currently, the world is struggling with the coronavirus disease 2019 (COVID-19) pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Prions are proteins that possess a unique conformational conversion, with the ability ... pmc.ncbi.nlm.nih.gov
Prion-like domains in SARS-CoV-2 RBD and ACE2 play important functional roles in viral adhesion and entry Scientists have recently detected and analyzed viral PrDs in the S protein of SARS-CoV-2, which are the novel regulators of virion assembly. news-medical.net

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4. Immune Dysregulation Cytokine Elevation: Cytokines are signaling molecules that coordinate immune responses. Studies show elevated cytokines in Long COVID (https://www.nature.com/articles/s41590-023-01724-6), indicating ongoing immune activation. https://www.mdpi.com/1422-0067/26/15/7258 details T-cell dynamics, while https://www.cell.com/cell/fulltext/S0092-8674(24)00886-9 reviews mechanisms of Long COVID. Additionally, https://pubmed.ncbi.nlm.nih.gov/39403255/ found elevated MMP-9 and microglia activation linked to spike protein stimulation. T-Cell Exhaustion: Nature research found that people with Long COVID exhibit T-cell dysregulation—immune cells worn out from chronic activation, reducing their ability to fight infections and regulate inflammation. Analogy: The immune system is like an army. Cytokine elevation is like constantly sounding alarms even without an enemy. T-cell exhaustion is like soldiers on duty too long without rest—they're present but less effective.

Long COVID manifests with T cell dysregulation, inflammation and an uncoordinated adaptive immune response to SARS-CoV-2 - Nature Immunology Long COVID (LC) occurs after at least 10% of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections, yet its etiology remains poorly understood. We used ‘omic” assays and serology to deeply characterize the global and SARS-CoV-2-specific immunity in the blood of individuals with clear LC and non-LC clinical trajectories, 8 months postinfection. We found that LC individuals exhibited systemic inflammation and immune dysregulation. This was evidenced by global differences in T cell subset distribution implying ongoing immune responses, as well as by sex-specific perturbations in cytolytic subsets. LC individuals displayed increased frequencies of CD4+ T cells poised to migrate to inflamed tissues and exhausted SARS-CoV-2-specific CD8+ T cells, higher levels of SARS-CoV-2 antibodies and a mis-coordination between their SARS-CoV-2-specific T and B cell responses. Our analysis suggested an improper crosstalk between the cellular and humoral adaptive immunity in LC, which can lead to immune dysregulation, inflammation and clinical symptoms associated with this debilitating condition. Roan et al. use Olink and single‐cell RNA sequencing (scRNA-seq) to show a dysregulated crosstalk between the cellular and humoral immune responses in individuals with long COVID 8 months postinfection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). nature.com
Long COVID elevated MMP-9 and release from microglia by SARS-CoV-2 Spike protein - PubMed MMP-9 from Spike protein-stimulated microglia could contribute to the development of long COVID and may serve as a target for treatment including the use of luteolin. pubmed.ncbi.nlm.nih.gov

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Fibrinogen as a Protective Factor The Silver Lining: https://pmc.ncbi.nlm.nih.gov/articles/PMC8977893/ may help protect against prion-related toxicity. Research shows it can bind to problematic proteins and act as a "sink," sequestering them away from causing damage. A https://molmed.biomedcentral.com/articles/10.2119/molmed.2016.00003 confirms fibrinogen inhibits amyloid-β-induced toxicity, and https://pubmed.ncbi.nlm.nih.gov/32697670/ documents fibrinogen-cellular prion protein complex formation. This suggests potential therapeutic approaches—perhaps boosting fibrinogen or developing molecules that mimic its protective binding.

Fibrinogen Mitigates Prion-Mediated Platelet Activation and Neuronal Cell Toxicity Prion peptide (PrP) misfolds to infectious scrapie isoform, the β pleat-rich insoluble fibrils responsible for neurodegeneration and fatal conformational diseases in humans. The amino acid sequence 106–126 from prion proteins, PrP(106–126), is ... pmc.ncbi.nlm.nih.gov
Plasma Fibrinogen Is a Natural Deterrent to Amyloid β-Induced Platelet Activation and Neuronal Toxicity - Molecular Medicine Alzheimer’s disease (AD) is a devastating neurodegenerative disorder, characterized by extensive loss of neurons and deposition of amyloid β (A& link.springer.com
Fibrinogen-cellular prion protein complex formation on astrocytes - PubMed Traumatic brain injury (TBI) is one of the most common neurological disorders causing memory reduction, particularly short-term memory (STM). We showed that, during TBI-induced inflammation, increased blood content of fibrinogen (Fg) enhanced vascular protein transcytosis and deposition of extravasa … pubmed.ncbi.nlm.nih.gov

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6. Investigational Treatments DFPP (Double Filtration Plasmapheresis): This blood filtration technique, used in Japan for conditions like CIDP and GBS, shows promise for filtering out microclots and inflammatory proteins. It is designed for this purpose (https://www.asahi-kasei.co.jp/medical/en/apheresis/cure/), with details at https://www.asahi-kasei.co.jp/medical/en/apheresis/product/plasma/about/cure.html#h2-2. Stem Cell Therapy: Mesenchymal stem cells (MSCs) have anti-inflammatory properties and may help repair damaged tissue. Trials are underway (https://clinicaltrials.gov/study/NCT06492798); https://clinicaltrials.gov/study/NCT05669261 is evaluating ATCell™ autologous stem cells. Early results (https://pmc.ncbi.nlm.nih.gov/articles/PMC11863646/) show potential for lung recovery in Long COVID patients. https://www.nature.com/articles/s41392-025-02313-9 discusses MSCs for inflammatory diseases, and https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11499875/ shows cord blood MSCs reducing Long COVID symptoms.

Applied Diseases | Asahi Kasei Medical Co., Ltd. Therapeutic Apheresis products info by applied diseases - Please select a department or a name of disease to refer treatment applications. Asahi Kasei Medical Co., Ltd. asahi-kasei.co.jp
Plasmapheresis | Asahi Kasei Medical Co., Ltd. Therapeutic Apheresis products info by therapies - Plasmapheresis modalities: Plasma Exchange (PE), Double Filtration Plasmapheresis (DFPP), Immunoadsorption (IA), Plasma Adsorption (PA). Asahi Kasei Medical Co., Ltd. asahi-kasei.co.jp
Long-term outcomes of mesenchymal stem cell therapy in severe COVID-19 patients: 3-year follow-up of a randomized, double-blind, placebo-controlled trial The long-term effects and outcomes of human mesenchymal stem cell (MSC) therapy in patients with severe coronavirus disease 2019 (COVID-19) remain poorly understood. This study aimed to evaluate the extended safety and efficacy of MSC treatment in ... pmc.ncbi.nlm.nih.gov
Mesenchymal stem cells in treating human diseases: molecular mechanisms and clinical studies - Signal Transduction and Targeted Therapy Mesenchymal stem cells (MSCs) have emerged as a highly promising strategy in regenerative medicine due to their self-renewal, pluripotency and immunomodulatory properties. MSCs are nonhematopoietic, multipotent stem cells that can differentiate into various mesodermal lineages and modulate the immune system. The therapeutic potential of MSCs from different tissues has been widely explored in preclinical models and clinical trials for human diseases, ranging from autoimmune diseases and inflammatory disorders to neurodegenerative diseases and orthopedic injuries. The therapeutic effects of MSCs can be mediated through the release of bioactive molecules, including growth factors, cytokines, and extracellular vesicles, which play crucial roles in modulating the local cellular environment, promoting tissue repair, angiogenesis, and cell survival, and exerting anti-inflammatory effects. MSCs can also interact with various immune cells, such as T cells, B cells, dendritic cells, and macrophages, modulating the immune response through both direct cell‒cell interactions and the release of immunoregulatory molecules. This review delves into the molecular mechanisms, signaling pathways, and regulatory factors that underpin the therapeutic effects of MSCs. This review also highlights the clinical applications and challenges associated with the use of MSC-based drugs to promote the safety and efficacy of MSC-based therapies. Overall, this comprehensive review provides valuable insights into the current state of MSC research and its potential for transforming the field of regenerative medicine as well as immune-mediated inflammatory diseases. nature.com
Integrated ensemble CNN and explainable AI for COVID-19 diagnosis from CT scan and X-ray images In light of the ongoing battle against COVID-19, while the pandemic may eventually subside, sporadic cases may still emerge, underscoring the need for accurate detection from radiological images. However, the limited explainability of current deep ... pmc.ncbi.nlm.nih.gov

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7. DNA Contamination Concerns The Issue: Recent research has detected residual DNA plasmids in some mRNA vaccines, including SV40 promoter sequences. SV40 is a viral promoter sequence used in laboratory DNA work. The Debate: A study (https://www.tandfonline.com/doi/full/10.1080/08916934.2025.2551517) reports DNA levels up to 153-fold above regulatory limits, raising theoretical concerns about: - Integration into human DNA - Unintended immune effects - Long-term consequences Additional research (https://hal.science/hal-04778576v2/document) confirms residual DNA above limits, (https://www.researchgate.net/publication/386414408_BioNTech_RNA-Based_COVID-19_Injections_Contain_Large_Amounts_Of_Residual_DNA_Including_An_SV40_PromoterEnhancer_Sequence) documents large amounts of residual DNA including SV40, and (https://www.preprints.org/manuscript/202501.1462) discusses DNA contaminants as potential causes of adverse events. Current Status: This is an active area of research and debate. More studies are needed to determine clinical significance.

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Post-vaccination syndrome is an emerging area of research investigating why some individuals experience persistent symptoms after mRNA COVID-19 vaccination. Key areas of investigation include: 1. Spike protein persistence beyond the expected duration 2. Amyloid fibrin microclots that may impair circulation 3. Prion-like domains that could promote protein misfolding 4. Immune dysregulation, including cytokine elevation and T-cell exhaustion 5. Potential treatments, including DFPP and stem cell therapy 6. Manufacturing concerns, including residual DNA components Research is ongoing, and many questions remain unanswered. What is clear is that a subset of individuals experiences real, measurable physiological changes that warrant serious scientific investigation and clinical attention.

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@reseeit save thread

Saved - October 12, 2025 at 5:36 AM
reSee.it AI Summary
Concern raised about DNA contamination, autopsies showing spike protein in tumors, and alleged vaccine–cancer links, tied to NIHGate and Senator Ron Johnson. A responder, MeasslainteIRL, replied several times with links to related content.

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"I'm highly concerned. The DNA contamination, the autopsies where they have spike protein inside tumors, the turbo cancer reports, no I'm highly concerned about this" Discussing the Covid Vaccine Cancer connection and http://NIHGate.com with Senator Ron Johnson.

Video Transcript AI Summary
Speaker 0 thanks the guest for advocating vaccine research and asks about alleged cancer increases since the COVID nineteen vaccine. Speaker 1 replies: "No. I'm I'm highly concerned. You know, the DNA contamination, the autopsies where they have spike protein inside tumors, you know, the turbo cancer reports." He says "nobody wants to admit they're wrong here" and claims that "the federal agencies... what they were pushing might have resulted in the adverse events that are undeniable, the deaths that are undeniable" and warns of "changing the human basic genome by integration of the cell or you know, fostering these turbo cancers." He cites "doctor Sun Shiang" on cancers in very young patients and says the issue is "not being reported because... it's just way too scary." Speaker 0 recalls a FOIA in 2021/22: "'NIH gate'—'National Cancer Institute employees were aware that there were cancers being enabled by the spike protein in the vaccine, and they covered it up'—with '490 pages of completely redacted documents.' " Speaker 1 notes redactions now are "a white piece of paper" and jokes "eco friendly," mentioning "Tom Wrens" and a military cancer increase "covered up," concluding, "the deep state does not give up its secrets."
Full Transcript
Speaker 0: One last thing. It's just a transition to a different topic. Your advocacy and willingness to spend your political clout on vaccine research and injuries and investigations has has made you a big fan from people like me, and also the families who've who suffered from these injuries. Have you heard anything about these supposed cancer increases since the COVID nineteen vaccine? Speaker 1: Oh, I've heard about them for a number of years now. No. I'm I'm highly concerned. You know, the DNA contamination, the the autopsies where they have spike protein inside tumors, you know, the turbo cancer reports. No. I'm I'm I'm highly concerned about this. Again, I I don't don't have a whole lot of information on it. I'm not a medical doctor myself, but, no, I've been following this very closely. I've been highly concerned about it. I know a limited number of people are concerned as well. I mean, that's part of our problem is nobody wants to admit they're wrong here. The federal agencies, the the people that push the injections, doctors who push it on their patients, and nobody wants to admit that what they were suggesting, what they what they were pushing might have resulted in the adverse events that are undeniable, the deaths that are undeniable. They still don't want to be talking about how we we may be changing the human basic genome by integration of the cell or you know, fostering these turbo cancers. Mean, but you have doctor Sun Shiang, you know, highly alarmed about, you know, cancers in very young patients he's never seen before. I mean, it's it's getting to be kinda like the the unusual clotting that the coroners were seeing. It's just like it's we know about it. It's just not being reported because quite honestly, it's just way too scary. Speaker 0: Yeah. One of the my earliest alerts to this was in 2021, I submitted, I think. Maybe it's '22. I submitted a FOIA request for something that we call NIH gate. Basically, National Cancer Institute employees were aware that there were cancers being enabled by the spike protein in the vaccine, and they covered it up. And the DOD was apparently involved, and I had 490 pages of completely redacted documents. They wouldn't even release the blacked out pages. Speaker 1: Yeah. Now the the now way they're doing the redactions, they just give you a white piece of paper. Speaker 0: Oh, that's nice. Speaker 1: They don't even so you don't even know was this a, you know, bunch of paragraphs or just one thing redacted. Speaker 0: Well, it's less ink, so it's eco friendly. Speaker 1: Plus, you know, we had Tom Wrens, and I think this is my COVID nineteen second opinion event that talked about d med. And the whistleblower's there and then the, you know, all of a sudden there were apparently a glitch, but the initial data there showed a pretty significant increase in different types of malignancies as well within the military. But again, that's that's all been covered up. We have not got to the bottom of that. Again, it's it's even with the republican president in charge, even with people like Bobby Kennedy that is dedicated to radical transparency, the deep state does not give up its secrets. You still have the partisan actors. Even if they're not partisan, the the you know, won't admit they're they were wrong, that what they pushed, that they're covered up. That they're gonna try and bury that truth as as for as long as they possibly can.
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🧬 DNA Contamination & mRNA Vaccine Biology Curated Reference Roadmap (all links are PubMed, PMC, DOI, or regulator FOI — stable, citable sources) 1️⃣ DNA Contamination & Quality Control McKernan et al. (2023) – Sequencing of Moderna & Pfizer bivalent mRNA vaccines reveals nanogram–microgram dsDNA per dose 🔗 OSF Preprint: https://osf.io/b9t7m/ König & Kirchner (2024) – Methodological considerations regarding DNA impurities in Comirnaty® 🔗 MDPI: https://www.mdpi.com/2409-9279/7/3/41 ⚠️ Expression of Concern: https://www.mdpi.com/2409-9279/8/4/68 Speicher, D.W. et al. (2023) – DNA fragments detected in Pfizer/Moderna mRNA vaccines from Ontario, Canada: Exploratory dose-response relationship with serious adverse events 🔗 OSF: https://osf.io/mjc97/ Kammerer, U. (2024) – BioNTech RNA-Based COVID-19 Injections Contain Large Amounts Of Residual DNA Including An SV40 Promoter/Enhancer Sequence https://publichealthpolicyjournal.com/biontech-rna-based-covid-19-injections-contain-large-amounts-of-residual-dna-including-an-sv40-promoter-enhancer-sequence/ Kaiser vs. König Debate (2025) – Recap of methodological flaws in Kaiser’s “no-DNA problem” rebuttal 🔗 Substack: https://open.substack.com/pub/anandamide/p/the-konig-vs-kaiser-debate-continues TGA FOI Docs (2024) – Internal correspondence on DNA contamination in mRNA vaccines 🔗 FOI PDF: https://www.tga.gov.au/sites/default/files/2024-12/FOI%2025-0070.pdf 2️⃣ Persistence, Immunology & Oncogenic Risk Strayer et al. (2002) – Durability of transgene expression and vector integration: SV40-derived vectors 🔗 PubMed: https://pubmed.ncbi.nlm.nih.gov/12161189/ Aldén et al. (2022) – BNT162b2 mRNA reverse transcribed into DNA in human liver cell line (Huh7) 🔗 DOI: https://doi.org/10.3390/cimb44030073 Mörz, M. (2022) – Case report: Necrotizing encephalitis & myocarditis after BNT162b2, spike protein detected by IHC 🔗 DOI: https://doi.org/10.3390/vaccines10101651 🔗 PubMed: https://pubmed.ncbi.nlm.nih.gov/36298516/ Schwab, C. et al. (2023) – Autopsy-based histopathological characterization of myocarditis after anti-SARS-CoV-2 vaccination 🔗 PMC: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9702955/ 🔗 PubMed: https://pubmed.ncbi.nlm.nih.gov/36436002/ (Optional supporting autopsies) Gill, J.R. et al. (2022) – Cardiac findings in 2 adolescents following second Pfizer dose 🔗 PubMed: https://pubmed.ncbi.nlm.nih.gov/35157759/ Choi, S. et al. (2021) – Myocarditis-induced sudden death after BNT162b2 🔗 PMC: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8524235/ Röltgen et al. (2022) – Immune imprinting and germinal center response in SARS-CoV-2 infection and vaccination 🔗 DOI: https://doi.org/10.1016/j.cell.2022.01.018 Patterson et al. (2021) – Persistence of SARS-CoV-2 S1 protein in CD16+ monocytes in PASC up to 15 months 🔗 DOI: https://doi.org/10.3389/fimmu.2021.746021 Castrucci et al. (2019) – Clonal persistence of influenza B virus antibodies (comparative baseline) 🔗 DOI: https://doi.org/10.1128/mBio.00066-19 Irrgang et al. (2022/23) – Class switch toward IgG4 after repeated mRNA vaccination 🔗 DOI: https://doi.org/10.1126/sciimmunol.ade2798 🔗 PubMed: https://pubmed.ncbi.nlm.nih.gov/36548397/ 3️⃣ Related / Corroborating Evidence Chakraborty (2023) – DNA vector fragments detected in bloodstream of vaccinated individuals 🔗 OSF: https://osf.io/hzyn3/ Buckhaults, P. (2023) – SC Senate testimony on plasmid DNA contamination in Pfizer vaccines 🎥 Video: https://www.scstatehouse.gov/video/archives.php?key=18538 📄 Transcript PDF: https://www.scstatehouse.gov/CommitteeInfo/SenateMedicalAffairsCommittee/PandemicPreparedness/Phillip-Buckhaults-SC-Senate-09122023-final.pdf EMA (ICH Q6B, 1999 / still current) – Specifications: Biotechnological/biological products → Residual DNA <10 ng/dose; no oncogenic sequences permitted 🔗 EMA Guideline: https://www.ema.europa.eu/en/documents/scientific-guideline/ich-q6b-specifications-biotechnological-biological-products_en.pdf Quantification of residual plasmid DNA and SV40 promoter-enhancer sequences in Pfizer/BioNTech and Moderna modRNA COVID-19 vaccines from Ontario, Canada David J. Speicher,Jessica Rose &Kevin McKernan https://www.tandfonline.com/doi/full/10.1080/08916934.2025.2551517 @Kevin_McKernan did I miss anything 🙏

DNA fragments detected in monovalent and bivalent Pfizer/BioNTech and Moderna modRNA COVID-19 vaccines from Ontario, Canada: Exploratory dose response relationship with serious adverse events. Background: In vitro transcription (IVT) reactions used to generate nucleoside modified RNA (modRNA) for SARS-CoV-2 vaccines currently rely on an RNA polymerase transcribing from a DNA template. Production of modRNA used in the original Pfizer randomized clinical trial (RCT) utilized a PCR-generated DNA template (Process 1). To generate billions of vaccine doses, this DNA was cloned into a bacterial plasmid vector for amplification in Escherichia coli before linearization (Process 2), expanding the size and complexity of potential residual DNA and introducing sequences not present in the Process 1 template. It appears that Moderna used a similar plasmid-based process for both clinical trial and post-trial use vaccines. Recently, DNA sequencing studies have revealed this plasmid DNA at significant levels in both Pfizer-BioNTech and Moderna modRNA vaccines. These studies surveyed a limited number of lots and questions remain regarding the variance in residual DNA observed internationally. Methods: Using previously published primer and probe sequences, quantitative polymerase chain reaction (qPCR) and Qubit® fluorometry was performed on an additional 27 mRNA vials obtained in Canada and drawn from 12 unique lots (5 lots of Moderna child/adult monovalent, 1 lot of Moderna adult bivalent BA.4/5, 1 lot of Moderna child/adult bivalent BA.1, 1 lot of Moderna XBB.1.5 monovalent, 3 lots of Pfizer adult monovalent, and 1 lot of Pfizer adult bivalent BA.4/5). The Vaccine Adverse Events Reporting System (VAERS) database was queried for the number and categorization of adverse events (AEs) reported for each of the lots tested. The content of one previously studied vial of Pfizer COVID-19 vaccine was examined by Oxford Nanopore sequencing to determine the size distribution of DNA fragments. This sample was also used to determine if the residual DNA is packaged in the lipid nanoparticles (LNPs) and thus resistant to DNaseI or if the DNA resides outside of the LNP and is DNaseI labile.  Results: Quantification cycle (Cq) values (1:10 dilution) for the plasmid origin of replication (ori) and spike sequences ranged from 18.44 - 24.87 and 18.03 - 23.83 and for Pfizer, and 22.52 – 24.53 and 25.24 – 30.10 for Moderna, respectively. These values correspond to 0.28 – 4.27 ng/dose and 0.22 - 2.43 ng/dose (Pfizer), and 0.01 -0.34 ng/dose and 0.25 – 0.78 ng/dose (Moderna), for ori and spike respectively measured by qPCR, and 1,896 – 3,720 ng/dose and 3,270 – 5,100 ng/dose measured by Qubit® fluorometry for Pfizer and Moderna, respectfully. The SV40 promoter-enhancer-ori was only detected in Pfizer vials with Cq scores ranging from 16.64 – 22.59. In an exploratory analysis, we found preliminary evidence of a dose response relationship of the amount of DNA per dose and the frequency of serious adverse events (SAEs). This relationship was different for the Pfizer and Moderna products. Size distribution analysis found mean and maximum DNA fragment lengths of 214 base pairs (bp) and 3.5 kb, respectively. The plasmid DNA is likely inside the LNPs and is protected from nucleases. Conclusion: These data demonstrate the presence of billions to hundreds of billions of DNA molecules per dose in these vaccines. Using fluorometry, all vaccines exceed the guidelines for residual DNA set by FDA and WHO of 10 ng/dose by 188 – 509-fold. However, qPCR residual DNA content in all vaccines were below these guidelines emphasizing the importance of methodological clarity and consistency when interpreting quantitative guidelines. The preliminary evidence of a dose-response effect of residual DNA measured with qPCR and SAEs warrant confirmation and further investigation. Our findings extend existing concerns about vaccine safety and call into question the relevance of guidelines conceived before the introduction of efficient transfection using LNPs. With several obvious limitations, we urge that our work is replicated under forensic conditions and that guidelines be revised to account for highly efficient DNA transfection and cumulative dosing. osf.io
BioNTech RNA-Based COVID-19 Injections Contain Large Amounts Of Residual DNA Including An SV40 Promoter/Enhancer Sequence - Science, Public Health Policy and the Law Background: BNT162b2 RNA-based COVID-19 injections are specified to transfect human cells to efficiently produce spike proteins for an immune response. publichealthpolicyjournal.com
The Konig vs Kaiser debate continues And the Corruption Carries On. anandamide.substack.com
Durability of transgene expression and vector integration: recombinant SV40-derived gene therapy vectors - PubMed Many applications of gene delivery require long-term transgene expression. In dividing cells, this result necessitates vector genome persistence, usually by integrating into cellular DNA. Since recombinant gene delivery vectors derived from tag-deleted, replication-incompetent simian virus-40 (SV40) … pubmed.ncbi.nlm.nih.gov
A Case Report: Multifocal Necrotizing Encephalitis and Myocarditis after BNT162b2 mRNA Vaccination against COVID-19 - PubMed The current report presents the case of a 76-year-old man with Parkinson's disease (PD) who died three weeks after receiving his third COVID-19 vaccination. The patient was first vaccinated in May 2021 with the ChAdOx1 nCov-19 vector vaccine, followed by two doses of the BNT162b2 mRNA vaccine in Jul … pubmed.ncbi.nlm.nih.gov
Autopsy-based histopathological characterization of myocarditis after anti-SARS-CoV-2-vaccination Cases of myocarditis, diagnosed clinically by laboratory tests and imaging have been described in the context of mRNA-based anti-SARS-CoV-2 vaccination. Autopsy-based description of detailed histological features of vaccine-induced myocarditis is ... pmc.ncbi.nlm.nih.gov
Autopsy-based histopathological characterization of myocarditis after anti-SARS-CoV-2-vaccination - PubMed Cases of myocarditis, diagnosed clinically by laboratory tests and imaging have been described in the context of mRNA-based anti-SARS-CoV-2 vaccination. Autopsy-based description of detailed histological features of vaccine-induced myocarditis is lacking. We describe the autopsy findings and common … pubmed.ncbi.nlm.nih.gov
Autopsy Histopathologic Cardiac Findings in 2 Adolescents Following the Second COVID-19 Vaccine Dose - PubMed The myocardial injury seen in these postvaccine hearts is different from typical myocarditis and has an appearance most closely resembling a catecholamine-mediated stress (toxic) cardiomyopathy. Understanding that these instances are different from typical myocarditis and that cytokine storm has a k … pubmed.ncbi.nlm.nih.gov
Myocarditis-induced Sudden Death after BNT162b2 mRNA COVID-19 Vaccination in Korea: Case Report Focusing on Histopathological Findings We present autopsy findings of a 22-year-old man who developed chest pain 5 days after the first dose of the BNT162b2 mRNA vaccine and died 7 hours later. Histological examination of the heart revealed isolated atrial myocarditis, with neutrophil ... pmc.ncbi.nlm.nih.gov
Immune imprinting, breadth of variant recognition, and germinal center response in human SARS-CoV-2 infection and vaccination During the SARS-CoV-2 pandemic, novel and traditional vaccine strategies have been deployed globally. We investigated whether antibodies stimulated by… sciencedirect.com
Frontiers | Persistence of SARS CoV-2 S1 Protein in CD16+ Monocytes in Post-Acute Sequelae of COVID-19 (PASC) up to 15 Months Post-Infection The recent COVID-19 pandemic is a treatment challenge in the acute infection stage but the recognition of chronic COVID-19 symptoms termed post-acute sequela... frontiersin.org
Class switch toward noninflammatory, spike-specific IgG4 antibodies after repeated SARS-CoV-2 mRNA vaccination - PubMed RNA vaccines are efficient preventive measures to combat the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic. High levels of neutralizing SARS-CoV-2 antibodies are an important component of vaccine-induced immunity. Shortly after the initial two mRNA vaccine doses, the immunogl … pubmed.ncbi.nlm.nih.gov
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Page or document not found | European Medicines Agency (EMA) We are sorry, but the content you tried to access is unavailable at the link you used, which was either incorrect or out-of-date. To help you find what you are looking for, we have included some useful tips. ema.europa.eu

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@BrokenTruthTV https://t.co/jKzHS52QIg

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@JillianMichaels DNA contamination with SV40 promoters, brewed in vats of E. coli poop soup. Sounds so “safe & effective.” 🤡 https://t.co/96OgCAHqMQ

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@BrokenTruthTV https://t.co/DNiBLgAkxQ

@JesslovesMJK - Jessica Rose 🤙

Speicher, D. J., Rose, J., & McKernan, K. (2025). Quantification of residual plasmid DNA and SV40 promoter-enhancer sequences in Pfizer/BioNTech and Moderna modRNA COVID-19 vaccines from Ontario, Canada. Autoimmunity, 58(1). https://doi.org/10.1080/08916934.2025.2551517

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@BrokenTruthTV https://t.co/iaMSVSxCgI

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@BrokenTruthTV https://t.co/ALQAS24QT7

@JesslovesMJK - Jessica Rose 🤙

"...mitochondria tend to be farther from [skin fibroblast] cell border[s] for patients who experience psychosis" Is that not the most fascinating observation ever?? https://www.biorxiv.org/content/10.1101/2025.10.08.676630v1 https://t.co/JMGPk4Uhvv

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@BrokenTruthTV https://t.co/rgfUu4FNWt

@DJSpeicher - David J Speicher PhD DTM

Nice to see an updated table of all the studies on plasmid DNA. Reproducibility trumps publication.

@hudikaha - 藤川賢治(FUJIKAWA Kenji)@小金井市議 Koganei City Councillor

I have added a row for the brand-new peer-reviewed paper by @DJSpeicher @JesslovesMJK and @Kevin_McKernan to the table "Verifications of mRNA Vaccine DNA Contamination Worldwide (as of 2025-09-06)." https://t.co/zhfOpreF6E

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@BrokenTruthTV https://t.co/F5KMVFxL42

@DJSpeicher - David J Speicher PhD DTM

New Study on Lipid Nanoparticles🎉 Congrats to @CanningPharm on her publication, "Complexity, unpredictability and safety challenges of lipid nanoparticles"‼️ This manuscript examines lipid nanoparticles (LNPs), tiny fat particles used in mRNA vaccines like those for COVID-19. This manuscript highlights several important items. Complex Behavior: LNPs are unpredictable due to varying structure and interactions in the body, affecting how well they work. Safety Risks: They can cause immune reactions or interact with drugs like clozapine, potentially leading to side effects. Delivery Issues: Only 1-15% of LNPs successfully deliver mRNA into cells, reducing vaccine effectiveness. Protein Coating: A protein layer forms on LNPs in the body, varying by person and impacting how they function. Need for Better Testing: The study calls for improved methods to study LNPs to ensure safety and effectiveness. This work highlights LNP risks and pushes for better designs and regulations to make mRNA vaccines safer and more reliable. The manuscript can be found here: https://www.researchgate.net/publication/396321059_Complexity_unpredictability_and_safety_challenges_of_lipid_nanoparticles_-A_multidisciplinary_narrative_review Congratulations Maria. You have worked tirelessly on this for the past several years and it's nice to see the document public. @JesslovesMJK @Kevin_McKernan @AdhesionsOrg @jimmy_dore @FLSurgeonGen @liz_churchill10 @natalimorris @NicHulscher @P_McCulloughMD @Double_Christ @MaryanneDemasi @hervk102 @TheRebelPatient @nzdsos @NG_Northgroup @cccalliance24 @SenseReceptor @VigilantFox @Fynnderella1 @IamBrookJackson @LynneBr37562004

Saved - September 15, 2025 at 10:55 AM
reSee.it AI Summary
Both the SARS-CoV-2 virus and mRNA vaccines have significant effects on the brain and vascular system. Evidence shows increased psychiatric risks, including depression and anxiety, linked to both infection and vaccination. The spike protein is implicated in causing microclots, blood-brain barrier damage, and amyloid formation, contributing to symptoms like brain fog and strokes. Current data suggests that more vaccine doses do not equate to better protection and may even increase risks. Millions are affected by long COVID and vaccine-related injuries, warranting careful monitoring and reconsideration of public health policies.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Both the SARS-CoV-2 virus and the mRNA vaccines impact the brain & vascular system. I'll share the peer reviewed evidence in this thread 🧵 Large cohorts show ↑ psychiatric risks. Labs show the mechanism: microclots, BBB leakage, amyloid formation. Public health policy must face this evidence.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Thread to read 🧵! "Alabama-based physician Dr. Jordan Vaughn followed up with a chilling estimate—up to 15 million Americans may be suffering from long COVID or COVID vaccine injuries. He now treats teenagers who can’t stand up and previously healthy adults who are suffering strokes with no clear cause. According to Vaughn, the spike protein’s S1 subunit is far from harmless. 'It triggers inflammation, it disrupts endothelial barriers, it induces fibrin resistant to breakdown, and it promotes a lot of amyloid aggregates,' he said. These effects impair oxygen delivery, damage blood vessels, and trigger a wave of symptoms—racing heart, brain fog, shortness of breath, and post-exertional crashes. In his clinic, Vaughn uses immunofluorescent microscopy to detect the spike protein’s damage, showing up in patients who were once thriving. He warned that the mRNA injections led to uncontrolled spike protein production, which spread throughout the body, reaching the heart, brain, ovaries, and testes." This speech is a BOMBSHELL. Why? Because indeed, there is formation of fibrinaloids (deposition of fibrin in degenerative form), production and aggregation of degenerative fibers like Abeta42 (Alzheimer's), platelet activation, inflammation of blood vessels with permeabilization of the blood-brain barrier (BBB)... This is exactly what I describe in this document posted online on April 26, 2025. cf. photo. But the worst is that these degenerative fibers, particularly Abeta42, are linked to immune tolerance. Why? Abeta42 activates RAGE, which will induce alarmins (including HMGB1), recruiting MDSCs (anti-inflammatory immune cells) and the production of IL-10 (anti-inflammatory cytokine). Role of RAGE in Alzheimer’s Disease - PMC HMGB1 and RAGE in inflammation and cancer - PubMed HMGB1 enhances immune suppression by facilitating the differentiation and suppressive activity of myeloid-derived suppressor cells - PubMed IL-10 induces an increase in ACE2 expression... Facilitating infection by SARS-CoV-2 via... THE SPIKE. Preliminary Evidence for IL-10-Induced ACE2 mRNA Expression in Lung-Derived and Endothelial Cells: Implications for SARS-Cov-2 ARDS Pathogenesis - PMC Preliminary Evidence for IL-10-Induced ACE2 mRNA Expression in Lung-Derived and Endothelial Cells: Implications for SARS-Cov-2 ARDS Pathogenesis - PMC I don't know how to say it anymore: double amyloid effect! - Not only is the Spike amyloid (degenerative in itself), but it induces the production of amyloid fibers including Abeta, and... - The SPIKE allows for inducing immune tolerance via amyloid fibers, - And the SPIKE can use these amyloid fibers to spread throughout the body. That's the full set of amyloid properties of the Spike. Cherry on the plum tart: Conclusions: - Wave of degenerative pathologies... And it's not JUST in the brain. - The more you come into contact with the Spike, the more your body will react to be "better" contaminated and "better" host the virus - The more your immune system will be out of service (and therefore you will be vulnerable) - 10 to 15 million just in the USA... Where are we at in France and Europe? What does that represent in 2025? Huh. And yes, new variants are coming. I repeat: it stinks. Thank you very much. PS: The amyloid properties of the Spike are also linked to the carcinogenic properties of the Spike. Why? p53/mitochondries/Spike

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Space du SAMEDI 26 AVRIL... Space international... anglais/français... Avec un document original. https://acrobat.adobe.com/id/urn:aaid:sc:EU:24cc46bf-bf95-4e5d-9b3e-7d82a221abf8 Je dois encore améliorer mon approche pour vulgariser un maximum.

Space international 26 avril 2025-1 (1).pdf View this file, and add comments too. acrobat.adobe.com

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

RAGE, le VIH, la latence, la réactivation... et plus si affinité... SARS-CoV-2, un VIH-like. https://pmc.ncbi.nlm.nih.gov/articles/PMC7926981/ TOX - ou la boîte du groupe de haute mobilité associée à la sélection des thymocytes (TOX) - joue un rôle important dans la différenciation des cellules T en

HIV-1 Latency and Viral Reservoirs: Existing Reversal Approaches and Potential Technologies, Targets, and Pathways Involved in HIV Latency Studies Eradication of latent human immunodeficiency virus (HIV) infection is a global health challenge. Reactivation of HIV latency and killing of virus-infected cells, the so-called “kick and kill” or “shock and kill” approaches, are a popular strategy ... pmc.ncbi.nlm.nih.gov

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

@vieil_garde_ph @tatiann69922625 @KevinMcCairnPhD https://pmc.ncbi.nlm.nih.gov/articles/PMC10732518/ "These data suggest that caspase cleavage of GSDME, leading to pore formation in the plasma membrane or other intracellular compartments, facilitates calcium accumulation in the cytoplasm and PAD4 activation." https://pmc.ncbi.nlm.nih.gov/articles/PMC10121894/ "Given the ability of

NET formation is a default epigenetic program controlled by PAD4 in apoptotic neutrophils Neutrophil extracellular traps (NETs) not only counteract bacterial and fungal pathogens but can also promote thrombosis, autoimmunity, and sterile inflammation. The presence of citrullinated histones, generated by the peptidylarginine deiminase 4 ... pmc.ncbi.nlm.nih.gov
Gasdermin-E mediates mitochondrial damage in axons and neurodegeneration Mitochondrial dysfunction and axon loss are hallmarks of neurologic diseases. Gasdermin (GSDM) proteins are executioner pore-forming molecules that mediate cell death, yet their roles in the central nervous system (CNS) are not well understood. ... pmc.ncbi.nlm.nih.gov

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

P53, propriétés amyloides et cancers... Et oui... la p53, le gardien de notre génome, possède des propriétés amyloides et... prion-like. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596421/ On pense que l'agrégation de la p53 sous forme de dépôts amyloides est un mécanisme impliqué dans les cancers. En

p53 amyloid formation leading to its loss of function: implications in cancer pathogenesis The transcriptional regulator p53 has an essential role in tumor suppression. Almost 50% of human cancers are associated with the loss of p53 functions, where p53 often accumulates in the nucleus as well as in cytoplasm. Although it has been ... pmc.ncbi.nlm.nih.gov

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Spike, p53 et mitochondries... Allez, je vais essayer de vulgariser. 1. Interaction Spike/p53 et immunité : La Spike pourrait interagir avec p53, qui est un régulateur clé de l’immunité innée et adaptative, notamment via la production d’interférons (IFN) de type I et de gènes

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Thread à lire 🧵! "Le Dr Jordan Vaughn, médecin basé en Alabama, a ensuite fourni une estimation effrayante : jusqu'à 15 millions d'Américains pourraient souffrir de blessures liées à la COVID longue ou au vaccin contre la COVID. Il traite désormais des adolescents qui ne

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Seoul cohort (~2M adults, 2024): Post-vax hazards: • Depression HR=1.68 • Anxiety HR=1.44 • Sleep disorders HR=1.93 Authors: “Special cautions are necessary for giving additional doses.” 🔗 https://www.nature.com/articles/s41380-024-02627-0

Psychiatric adverse events following COVID-19 vaccination: a population-based cohort study in Seoul, South Korea - Molecular Psychiatry Evidence has suggested an increased risk of psychiatric manifestations following viral infections including coronavirus disease-2019 (COVID-19). However, psychiatric adverse events (AEs) after COVID-19 vaccination, which were documented in case reports and case series, remain unclear. This study is aimed to investigate the psychiatric AEs after COVID-19 vaccination from a large population-based cohort in Seoul, South Korea. We recruited 50% of the Seoul-resident population randomly selected from the Korean National Health Insurance Service (KNHIS) claims database on 1, January, 2021. The included participants (n = 2,027,353) from the Korean National Health Insurance Service claims database were divided into two groups according to COVID-19 vaccination. The cumulative incidences per 10,000 of psychiatric AEs were assessed on one week, two weeks, one month, and three months after COVID-19 vaccination. Hazard ratios (HRs) and 95% Confidence interval (CIs) of psychiatric AEs were measured for the vaccinated population. The cumulative incidence of depression, anxiety, dissociative, stress-related, and somatoform disorders, sleep disorders, and sexual disorders at three months following COVID-19 vaccination were higher in the vaccination group than no vaccination group. However, schizophrenia and bipolar disorders showed lower cumulative incidence in the vaccination group than in the non-vaccinated group. Depression (HR [95% CI] = 1.683 [1.520–1.863]), anxiety, dissociative, stress-related, and somatoform disorders (HR [95% CI] = 1.439 [1.322–1.568]), and sleep disorders (HR [95% CI] = 1.934 [1.738–2.152]) showed increased risks after COVID-19 vaccination, whereas the risks of schizophrenia (HR [95% CI] = 0.231 [0.164–0.326]) and bipolar disorder (HR [95% CI] = 0.672 [0.470–0.962]). COVID-19 vaccination increased the risks of depression, anxiety, dissociative, stress-related, and somatoform disorders, and sleep disorders while reducing the risk of schizophrenia and bipolar disorder. Therefore, special cautions are necessary for administering additional COVID-19 vaccinations to populations vulnerable to psychiatric AEs. nature.com

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Murata 2024 (Brain, Behavior & Immunity): Psychiatric disorders remain elevated after infection. Vaccination did not erase these risks effects varied by variant (Delta vs Omicron). 🔗 https://www.sciencedirect.com/science/article/pii/S088915912400254X

Associations between COVID-19 vaccination and incident psychiatric disorders after breakthrough SARS-CoV-2 infection: The VENUS Study The associations between COVID-19 vaccination and post-COVID psychiatric disorders are unclear. Furthermore, it is uncertain if these associations dif… sciencedirect.com

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Spike drives clotting & vessel injury: • Platelet hyperreactivity • Fibrin(oid) microclots resistant to breakdown • Endothelial dysfunction → brain fog, dysautonomia 🔗 https://pmc.ncbi.nlm.nih.gov/articles/PMC8705864/ 🔗 https://pubmed.ncbi.nlm.nih.gov/38549864/

SARS-CoV-2 Exacerbates Beta-Amyloid Neurotoxicity, Inflammation and Oxidative Stress in Alzheimer’s Disease Patients Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) triggered the pandemic Coronavirus Disease 19 (COVID-19), causing millions of deaths. The elderly and those already living with comorbidity are likely to die after SARS-CoV-2 infection. ... pmc.ncbi.nlm.nih.gov
Impact of the SARS-CoV-2 Spike Protein on the Innate Immune System: A Review - PubMed The Spike protein enables the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection by binding to multiple receptors, including the angiotensin-converting enzyme 2 (ACE2). Scientific studies also indicate that Spike is involved in severe forms of coronavirus disease 2019 (COVID-19), … pubmed.ncbi.nlm.nih.gov

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Amyloid properties (loss of proteostasis): Spike & fragments are amyloidogenic, promoting Aβ build-up. This links spike exposure to Alzheimer’s-like changes. 🔗 https://pubs.acs.org/doi/10.1021/jacs.2c03925 🔗 https://medicine.yale.edu/news-article/sars-cov-2-causes-buildup-of-alzheimers-related-peptides-in-the-retina/

SARS-CoV-2 Causes Buildup of Alzheimer’s-Related Peptides in the Retina A new study reveals a promising target for reducing amyloid beta buildup and preventing Alzheimer’s disease-like symptoms, such as brain fog, caused by COVID-19 medicine.yale.edu

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

State of the image from chatgpt 🤣🤣 I will fix it later 🤣

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Blood–brain barrier disruption (BBB): Spike damages endothelial junctions → BBB leakage, neuroinflammation, cognitive & mood symptoms. 🔗 https://pmc.ncbi.nlm.nih.gov/articles/PMC9239981/

Neuroinflammation and COVID-19 Coronavirus disease 2019 (COVID-19) has caused a historic pandemic of respiratory disease. COVID-19 also causes acute and post-acute neurological symptoms, which range from mild, such as headaches, to severe, including hemorrhages. Current evidence ... pmc.ncbi.nlm.nih.gov

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

More doses ≠ less infection (real-world data). Cleveland Clinic employees (2023-24): “The risk of COVID-19 also increased with the number of prior vaccine doses.” Current-season VE modest (≈42% → 19% after JN.1). 🔗 https://academic.oup.com/cid/article-abstract/79/2/405/7625220

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

#youwontgetsickifyougetthevaccine Swiss healthcare workers (2025, Nature): Recent boosters linked to: • ↑ influenza-like illness (ILI) • ↑ workdays lost Workforce sickness rose after boosting. 🔗 https://www.nature.com/articles/s43856-025-01046-8

Association of SARS-CoV-2 vaccination status with risk of influenza-like illness and loss of workdays in healthcare workers - Communications Medicine In the post-pandemic phase, the value of annual SARS-CoV-2 booster vaccination in healthcare-workers is unclear. In this multicentre cohort study, we sought to determine the association of SARS-CoV-2 vaccination status and other risk factors with the occurrence of influenza-like respiratory illness and workdays lost due to influenza-like respiratory illness. During a period of high SARS-CoV-2 community transmission (November 2023 to May 2024), we collected weekly data on symptoms and sick day leave and used negative binomial regression to identify risk factors for these outcomes among 1745 healthcare workers. To single out the effect of the vaccine and account for potential confounding, additional inverse probability weighted analysis was performed. In both analyses, we show that more SARS-CoV-2 vaccinations are associated with a higher risk of influenza-like respiratory illness and workdays lost. For influenza-like respiratory illness, the association is stronger with a more recent timing of the vaccination rather than the number of vaccinations, which suggests that the effect wanes over time. In contrast, seasonal influenza vaccination is associated with a decreased risk for both outcomes. Based on our data, we conclude that SARS-CoV-2 booster vaccination does not contribute to the protection of the healthcare workforce in a post-pandemic setting. SARS-CoV-2 vaccination may even temporarily increase the likelihood of symptomatic infection and workday loss. In the years following the COVID-19 pandemic, it is still unclear whether annual COVID booster vaccines are necessary for low-risk populations such as healthcare workers. In this study, 1745 healthcare workers in Switzerland were followed over several months to see how their vaccination status affected their chances of getting flu-like illnesses and missing work. The study found that those who recently received a COVID-19 booster were more likely to report symptoms and take sick leave. In contrast, people who received the seasonal flu vaccine were less likely to report symptoms or miss work. These findings suggest that COVID-19 boosters may not offer clear short-term benefits in a post-pandemic setting, and may even increase short-term illness risk. This raises questions about the best use of booster vaccines moving forward. Dörr, Lacy et al. evaluate the association between SARS-CoV-2 vaccination status and influenza-like illness and sick leave among 1745 Swiss healthcare workers. SARS CoV-2 vaccination is associated with increased illness symptoms and more days of sick leave, while influenza vaccination is associated with a decreased risk of both outcomes. nature.com

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Psychiatric outcomes corroborated: Multiple reviews show elevated neuropsychiatric risks post-COVID & mixed post-vax outcomes. 🔗 https://bmcmedicine.biomedcentral.com/articles/10.1186/s12916-025-03952-z 🔗 https://www.frontiersin.org/journals/psychiatry/articles/10.3389/fpsyt.2024.1360338/full

Psychiatric and neuropsychiatric sequelae of COVID-19 within 2 years: a multinational cohort study - BMC Medicine The long-term psychiatric and neuropsychiatric sequelae of COVID-19 across diverse populations remain not fully understood. This cohort study aims to investigate the short-, medium-, and long-term risks of psychiatric and neuropsychiatric disorders following COVID-19 infection in five countries. This population-based multinational network study used electronic medical records from France, Italy, Germany, and the UK and claims data from the USA. The initial target and comparator cohorts were identified using an exact matching approach based on age and sex. Individuals diagnosed with COVID-19 or those with a positive SARS-CoV-2 screening test between December 1, 2019, and December 1, 2020, were included as targets. Up to ten comparators without COVID-19 for each target were selected using the propensity score matching approach. All individuals were followed from the index date until the end of continuous enrolment or the last healthcare encounter. Cox proportional hazard regression models were fitted to estimate the risk of incident diagnosis of depression, anxiety disorders, alcohol misuse or dependence, substance misuse or dependence, bipolar disorders, psychoses, personality disorders, self-harm and suicide, sleep disorders, dementia, and neurodevelopmental disorders within the first 6 months (short-term), 6 months to 1 year (medium-term), and 1 to 2 years (long-term) post-infection. A total of 303,251 individuals with COVID-19 and 22,108,925 individuals without COVID-19 from five countries were originally included. Within the first 6 months, individuals with COVID-19 had a significantly higher risk of any studied disorders in all databases, with Hazard Ratios (HRs) ranging from 1.14 (95% CI, 1.07–1.22) in Germany to 1.89 (1.64–2.17) in Italy. Increased risks were consistently observed for depression, anxiety disorders, and sleep disorders across almost all countries. During the medium- and long-term periods, higher risks were observed only for depression (medium-term: 1.29, 1.18–1.41; long-term: 1.36, 1.25–1.47), anxiety disorders (medium-term: 1.29, 1.20–1.38; long-term: 1.37, 1.29–1.47), and sleep disorders (medium-term: 1.10, 1.01–1.21; long-term: 1.14, 1.05–1.24) in France, and dementia (medium-term: 1.65, 1.28–2.10) in the UK. Our study suggests that increased risks of psychiatric and neuropsychiatric outcomes were consistently observed only within, and not after, the 6-month observation period across all databases, except for certain conditions in specific countries. bmcmedicine.biomedcentral.com
Frontiers | New-onset psychosis following COVID-19 vaccination: a systematic review Background: The emergence of a new coronavirus strain caused the COVID-19 pandemic. While vaccines effectively control the infection, it's important to ackno... frontiersin.org

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Immune tolerance pathway explains persistence: RAGE–HMGB1 → MDSCs → IL-10 ↑ → ACE2 ↑ → viral entry + ongoing neuroinflammation. 🔗 https://pubmed.ncbi.nlm.nih.gov/17099778/ 🔗 https://pmc.ncbi.nlm.nih.gov/articles/PMC8823909/

TRPC6 fulfills a calcineurin signaling circuit during pathologic cardiac remodeling - PubMed The heart responds to injury and chronic pressure overload by pathologic growth and remodeling, which frequently result in heart failure and sudden death. Calcium-dependent signaling pathways promote cardiac growth and associated changes in gene expression in response to stress. The calcium/calmodul … pubmed.ncbi.nlm.nih.gov
Effect of Arterial Stiffness and Carotid Intima-Media Thickness Progression on the Risk of Dysglycemia, Insulin Resistance, and Dyslipidemia: a Temporal Causal Longitudinal Study Supplemental Digital Content is available in the text. Keywords: adolescent; atherosclerosis; causality; diabetes mellitus, type 2; hyperglycemia; metabolic syndrome; young adult pmc.ncbi.nlm.nih.gov

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Autopsy evidence (rare but real): Post-mRNA myocarditis cases show myocyte necrosis on histopathology. 🔗 https://pmc.ncbi.nlm.nih.gov/articles/PMC9922164/

A Potential Role of the Spike Protein in Neurodegenerative Diseases: A Narrative Review Human prion protein and prion-like protein misfolding are widely recognized as playing a causal role in many neurodegenerative diseases. Based on in vitro and in vivo experimental evidence relating to prion and prion-like disease, we extrapolate ... pmc.ncbi.nlm.nih.gov

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Long COVID = neuro + vascular burden: Millions now suffer brain fog, POTS, strokes, dementia-like decline post-infection. Vaccine-injury prevalence uncertain, but signals overlap & warrant monitoring. 🔗 https://polybio.org/projects/impact-of-sars-cov-2-infection-on-alzheimers-and-neurodegenerative-disease/

Impact of SARS-CoV-2 infection on Alzheimer's and neurodegenerative disease - PolyBio Research Foundation Project summary: The project will determine if live SARS-CoV-2 infection of human brain cell models leads to protein formation and gene... polybio.org

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Cancer-adjacent mechanisms: Spike linked to p53 disruption, mitochondrial stress, chronic inflammation. Early mechanistic evidence → oncogenic potential cannot be ignored. 🔗 https://www.mdpi.com/1999-4915/17/5/617

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

BBB disruption confirmed in long COVID: Nature Neuroscience 2024: persistent BBB leakage in patients with cognitive impairment (“brain fog”). 🔗 https://www.nature.com/articles/s41593-024-01576-9

Blood–brain barrier disruption and sustained systemic inflammation in individuals with long COVID-associated cognitive impairment - Nature Neuroscience Vascular disruption has been implicated in coronavirus disease 2019 (COVID-19) pathogenesis and may predispose to the neurological sequelae associated with long COVID, yet it is unclear how blood–brain barrier (BBB) function is affected in these conditions. Here we show that BBB disruption is evident during acute infection and in patients with long COVID with cognitive impairment, commonly referred to as brain fog. Using dynamic contrast-enhanced magnetic resonance imaging, we show BBB disruption in patients with long COVID-associated brain fog. Transcriptomic analysis of peripheral blood mononuclear cells revealed dysregulation of the coagulation system and a dampened adaptive immune response in individuals with brain fog. Accordingly, peripheral blood mononuclear cells showed increased adhesion to human brain endothelial cells in vitro, while exposure of brain endothelial cells to serum from patients with long COVID induced expression of inflammatory markers. Together, our data suggest that sustained systemic inflammation and persistent localized BBB dysfunction is a key feature of long COVID-associated brain fog. Long COVID is a major public health issue since 2020 and exhibits frequent neurological symptoms. Greene et al. propose that brain fog results from leaky brain blood vessels and a hyperactive immune system, shedding light on this phenomenon. nature.com

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Man every time I do one of these threads it feels like I'm repeating myself all the time Cohorts + labs show: • Vaccination = ↑ depression, anxiety, sleep disorders • Infection = psych harm persists • More doses = not always more protection • Spike = amyloid, microclots, BBB damage 👉 Until transparent data disproves these signals, stop blanket repeat-dose pushes. #LongCOVID #VaccineInjuries #SpikeProtein #end #Stoptheshots

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@grok please play devil's advocate and show the problems if any in this thread.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@reseeit save thread

Saved - September 5, 2025 at 4:49 PM
reSee.it AI Summary
I reported on various studies highlighting the presence of residual plasmid DNA, including the SV40 promoter, in COVID-19 vaccine vials from companies like Pfizer, Moderna, and Daiichi-Sankyo. Researchers from multiple institutions found levels exceeding regulatory limits, raising concerns about potential integration into human cells and associated risks. The findings have been shared with regulatory bodies, and discussions continue regarding the implications of these contaminants on vaccine safety. The issue remains a topic of ongoing scrutiny and debate.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Kevin McKernan Profession: Founder of Medicinal Genomics, Genomics Researcher, US Date First Reported: 2023-02 Key Details: Detected 225-843ng/dose residual plasmid DNA including SV40 promoter in Pfizer/Moderna vials using qPCR/fluorometry; exceeds regulatory limits; integration concerns. Sharable Link: https://osf.io/mjc97/

DNA fragments detected in monovalent and bivalent Pfizer/BioNTech and Moderna modRNA COVID-19 vaccines from Ontario, Canada: Exploratory dose response relationship with serious adverse events. Background: In vitro transcription (IVT) reactions used to generate nucleoside modified RNA (modRNA) for SARS-CoV-2 vaccines currently rely on an RNA polymerase transcribing from a DNA template. Production of modRNA used in the original Pfizer randomized clinical trial (RCT) utilized a PCR-generated DNA template (Process 1). To generate billions of vaccine doses, this DNA was cloned into a bacterial plasmid vector for amplification in Escherichia coli before linearization (Process 2), expanding the size and complexity of potential residual DNA and introducing sequences not present in the Process 1 template. It appears that Moderna used a similar plasmid-based process for both clinical trial and post-trial use vaccines. Recently, DNA sequencing studies have revealed this plasmid DNA at significant levels in both Pfizer-BioNTech and Moderna modRNA vaccines. These studies surveyed a limited number of lots and questions remain regarding the variance in residual DNA observed internationally. Methods: Using previously published primer and probe sequences, quantitative polymerase chain reaction (qPCR) and Qubit® fluorometry was performed on an additional 27 mRNA vials obtained in Canada and drawn from 12 unique lots (5 lots of Moderna child/adult monovalent, 1 lot of Moderna adult bivalent BA.4/5, 1 lot of Moderna child/adult bivalent BA.1, 1 lot of Moderna XBB.1.5 monovalent, 3 lots of Pfizer adult monovalent, and 1 lot of Pfizer adult bivalent BA.4/5). The Vaccine Adverse Events Reporting System (VAERS) database was queried for the number and categorization of adverse events (AEs) reported for each of the lots tested. The content of one previously studied vial of Pfizer COVID-19 vaccine was examined by Oxford Nanopore sequencing to determine the size distribution of DNA fragments. This sample was also used to determine if the residual DNA is packaged in the lipid nanoparticles (LNPs) and thus resistant to DNaseI or if the DNA resides outside of the LNP and is DNaseI labile.  Results: Quantification cycle (Cq) values (1:10 dilution) for the plasmid origin of replication (ori) and spike sequences ranged from 18.44 - 24.87 and 18.03 - 23.83 and for Pfizer, and 22.52 – 24.53 and 25.24 – 30.10 for Moderna, respectively. These values correspond to 0.28 – 4.27 ng/dose and 0.22 - 2.43 ng/dose (Pfizer), and 0.01 -0.34 ng/dose and 0.25 – 0.78 ng/dose (Moderna), for ori and spike respectively measured by qPCR, and 1,896 – 3,720 ng/dose and 3,270 – 5,100 ng/dose measured by Qubit® fluorometry for Pfizer and Moderna, respectfully. The SV40 promoter-enhancer-ori was only detected in Pfizer vials with Cq scores ranging from 16.64 – 22.59. In an exploratory analysis, we found preliminary evidence of a dose response relationship of the amount of DNA per dose and the frequency of serious adverse events (SAEs). This relationship was different for the Pfizer and Moderna products. Size distribution analysis found mean and maximum DNA fragment lengths of 214 base pairs (bp) and 3.5 kb, respectively. The plasmid DNA is likely inside the LNPs and is protected from nucleases. Conclusion: These data demonstrate the presence of billions to hundreds of billions of DNA molecules per dose in these vaccines. Using fluorometry, all vaccines exceed the guidelines for residual DNA set by FDA and WHO of 10 ng/dose by 188 – 509-fold. However, qPCR residual DNA content in all vaccines were below these guidelines emphasizing the importance of methodological clarity and consistency when interpreting quantitative guidelines. The preliminary evidence of a dose-response effect of residual DNA measured with qPCR and SAEs warrant confirmation and further investigation. Our findings extend existing concerns about vaccine safety and call into question the relevance of guidelines conceived before the introduction of efficient transfection using LNPs. With several obvious limitations, we urge that our work is replicated under forensic conditions and that guidelines be revised to account for highly efficient DNA transfection and cumulative dosing. osf.io

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@JillianMichaels DNA contamination with SV40 promoters, brewed in vats of E. coli poop soup. Sounds so “safe & effective.” 🤡

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Tomonori Nitta Profession: Researcher at Tokyo University, Japan Date First Reported: 2023-11 Key Details: Found 17.5-81.9ng/dose DNA in Japanese Daiichi-Sankyo vials; SV40 detected, including in tumors via cell transfection Sharable Link: https://pmc.ncbi.nlm.nih.gov/articles/PMC12095670/

Significant Increase in Excess Deaths after Repeated COVID-19 Vaccination in Japan Although Japan recorded the world’s highest rate of COVID-19 messenger ribonucleic acid (mRNA) vaccination doses per capita, COVID-19 cases and deaths exploded after the emergence of the Omicron variant, followed by a significant increase in excess ... pmc.ncbi.nlm.nih.gov

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Phillip Buckhaults Profession: Professor at University of South Carolina, Cancer Genomics Expert, US Date First Reported: 2023-09 (testimony), 2024-04 (data) Key Details: qPCR showed 1.5-18.7ng/dose plasmid DNA with SV40 promoter; observed integration into human stem cells; presented to SC Senate. Sharable Link: https://www.scstatehouse.gov/CommitteeInfo/SenateMedicalAffairsCommittee/PandemicPreparedness/Phillip-Buckhaults-SC-Senate-09122023-final.pdf

South Carolina Legislature Online - Error scstatehouse.gov

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Brigitte König & Jürgen O. Kirchner Profession: Independent Lab Analysts (MMD/Indep.), Germany Date First Reported: 2023-09 Key Details: Fluorometry/qPCR revealed 3600-5340ng/dose DNA exceeding limits; SV40 promoter confirmed; reported to German Ministry. (Note: Paper has an expression of concern.) Sharable Link: https://www.mdpi.com/2409-9279/7/3/41

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

David Speicher (with Kevin McKernan) Profession: Researcher at University of Guelph, Canada Date First Reported: 2023-10 (Ontario), 2024-03 (Australia) Key Details: qPCR/fluorometry on 27+ vials showed 0.22-510ng/dose DNA with SV40; dose-response to adverse events; reported to TGA, under litigation. Sharable Links https://osf.io/preprints/osf/mjc97 https://thedaviddeclaration.org/wp-content/uploads/2025/01/dr-speicher-report-re-australian-vials.pdf

DNA fragments detected in monovalent and bivalent Pfizer/BioNTech and Moderna modRNA COVID-19 vaccines from Ontario, Canada: Exploratory dose response relationship with serious adverse events. Background: In vitro transcription (IVT) reactions used to generate nucleoside modified RNA (modRNA) for SARS-CoV-2 vaccines currently rely on an RNA polymerase transcribing from a DNA template. Production of modRNA used in the original Pfizer randomized clinical trial (RCT) utilized a PCR-generated DNA template (Process 1). To generate billions of vaccine doses, this DNA was cloned into a bacterial plasmid vector for amplification in Escherichia coli before linearization (Process 2), expanding the size and complexity of potential residual DNA and introducing sequences not present in the Process 1 template. It appears that Moderna used a similar plasmid-based process for both clinical trial and post-trial use vaccines. Recently, DNA sequencing studies have revealed this plasmid DNA at significant levels in both Pfizer-BioNTech and Moderna modRNA vaccines. These studies surveyed a limited number of lots and questions remain regarding the variance in residual DNA observed internationally. Methods: Using previously published primer and probe sequences, quantitative polymerase chain reaction (qPCR) and Qubit® fluorometry was performed on an additional 27 mRNA vials obtained in Canada and drawn from 12 unique lots (5 lots of Moderna child/adult monovalent, 1 lot of Moderna adult bivalent BA.4/5, 1 lot of Moderna child/adult bivalent BA.1, 1 lot of Moderna XBB.1.5 monovalent, 3 lots of Pfizer adult monovalent, and 1 lot of Pfizer adult bivalent BA.4/5). The Vaccine Adverse Events Reporting System (VAERS) database was queried for the number and categorization of adverse events (AEs) reported for each of the lots tested. The content of one previously studied vial of Pfizer COVID-19 vaccine was examined by Oxford Nanopore sequencing to determine the size distribution of DNA fragments. This sample was also used to determine if the residual DNA is packaged in the lipid nanoparticles (LNPs) and thus resistant to DNaseI or if the DNA resides outside of the LNP and is DNaseI labile.  Results: Quantification cycle (Cq) values (1:10 dilution) for the plasmid origin of replication (ori) and spike sequences ranged from 18.44 - 24.87 and 18.03 - 23.83 and for Pfizer, and 22.52 – 24.53 and 25.24 – 30.10 for Moderna, respectively. These values correspond to 0.28 – 4.27 ng/dose and 0.22 - 2.43 ng/dose (Pfizer), and 0.01 -0.34 ng/dose and 0.25 – 0.78 ng/dose (Moderna), for ori and spike respectively measured by qPCR, and 1,896 – 3,720 ng/dose and 3,270 – 5,100 ng/dose measured by Qubit® fluorometry for Pfizer and Moderna, respectfully. The SV40 promoter-enhancer-ori was only detected in Pfizer vials with Cq scores ranging from 16.64 – 22.59. In an exploratory analysis, we found preliminary evidence of a dose response relationship of the amount of DNA per dose and the frequency of serious adverse events (SAEs). This relationship was different for the Pfizer and Moderna products. Size distribution analysis found mean and maximum DNA fragment lengths of 214 base pairs (bp) and 3.5 kb, respectively. The plasmid DNA is likely inside the LNPs and is protected from nucleases. Conclusion: These data demonstrate the presence of billions to hundreds of billions of DNA molecules per dose in these vaccines. Using fluorometry, all vaccines exceed the guidelines for residual DNA set by FDA and WHO of 10 ng/dose by 188 – 509-fold. However, qPCR residual DNA content in all vaccines were below these guidelines emphasizing the importance of methodological clarity and consistency when interpreting quantitative guidelines. The preliminary evidence of a dose-response effect of residual DNA measured with qPCR and SAEs warrant confirmation and further investigation. Our findings extend existing concerns about vaccine safety and call into question the relevance of guidelines conceived before the introduction of efficient transfection using LNPs. With several obvious limitations, we urge that our work is replicated under forensic conditions and that guidelines be revised to account for highly efficient DNA transfection and cumulative dosing. osf.io

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Didier Raoult Profession: Former Professor at Aix-Marseille University, Microbiologist, France Date First Reported: 2024-11 Key Details: Fluorometry/NGS detected 2712-5160ng/dose full plasmid DNA including SV40 promoter/enhancer; high copy numbers; integration risks. Sharable Link: https://hal.science/hal-04778576v1/document

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Ulrike Kämmerer Profession: Biologist at University Hospital of Würzburg, Germany Date First Reported: 2024-12 Key Details: Fluorometry/PCR/transfection showed 32.7-43.4ng/dose DNA in LNPs with SV40 promoter; successful cell transfection; spike protein expression. Sharable Link: https://www.researchgate.net/publication/386414408_BioNTech_RNA-Based_COVID-19_Injections_Contain_Large_Amounts_Of_Residual_DNA_Including_An_SV40_PromoterEnhancer_Sequence

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Tyler J. Wang, Alex Kim, Kevin Kim Profession: Students at Centerville High School (executed at FDA White Oak Campus), US Date First Reported: 2024-12 Key Details: Fluorometry/miniprep extracted replication-competent plasmid DNA exceeding limits; SV40 implied; no peer-reviewed confirmation of integration. Sharable Link: https://jhss.scholasticahq.com/article/127890-a-rapid-detection-method-of-replication-competent-plasmid-dna-from-covid-19-mrna-vaccines-for-quality-control

A rapid detection method of replication-competent plasmid DNA from COVID-19 mRNA vaccines for quality control | Published in Journal of High School Science By Tyler J Wang, Alex Kim & 1 more. DNA contamination is the primary reason that undermines public trust in the quality of mRNA vaccines. We report a method to detect residual replication-competent plasmid DNA present in mRNA vaccines. jhss.scholasticahq.com

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

V. Polacek Profession: Analyst at TILIA Laboratories s.r.o., Czech Republic Date First Reported: 2025-03 Key Details: qPCR found 10M-1B DNA copies/ml in 120 vials; tumorigenesis risks; no formal publication. Sharable Link: No direct public link found; announced by Slovak government investigator (referenced in regulatory contexts like https://www.tga.gov.au/sites/default/files/2024-12/FOI%2025-0070.pdf

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@Kevin_McKernan @P_J_Buckhaults @DJSpeicher @raoult_didier @DrCaliff_FDA @US_FDA @TGAgovau @EMA_News @WHO @RWMaloneMD @JesslovesMJK @stkirsch @CanningPharm @53v3n0fn1n3 @Fynnderella1 @CartlandDavid @drcole12 @dbkell @kacdnp91 @KevinMcCairnPhD @AnneliseBocquet @PinsolleT@blueskylou@Hudikaha thanks Kenji Fujikawa who compiled this list of DNA Plasmid Contaminatiion Why am I bringing it up again ? Well the problem hasn't gone away. #Stoptheshots #poojabs #informedconsent

@carl_jurassic - Jurassic Carl 🦖🐭

#poojabs #DirtyJibby

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@Kevin_McKernan @P_J_Buckhaults @DJSpeicher @raoult_didier @DrCaliff_FDA @US_FDA @TGAgovau @EMA_News @WHO @RWMaloneMD @JesslovesMJK @stkirsch @CanningPharm @53v3n0fn1n3 @Fynnderella1 @CartlandDavid @drcole12 @dbkell @kacdnp91 @KevinMcCairnPhD @AnneliseBocquet @PinsolleT @FluoridePoison

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@Kevin_McKernan @P_J_Buckhaults @DJSpeicher @raoult_didier @DrCaliff_FDA @US_FDA @TGAgovau @EMA_News @WHO @RWMaloneMD @JesslovesMJK @stkirsch @CanningPharm @53v3n0fn1n3 @Fynnderella1 @CartlandDavid @drcole12 @dbkell @kacdnp91 @KevinMcCairnPhD @AnneliseBocquet @PinsolleT @FluoridePoison Strange his tag didn't work..

@WakingUp2020 - Mrs Doubt Pfizer

"The Pfizer vaccine is contaminated with DNA, it's not just mRNA, it’s got bits of DNA in it." - Professor Phillip Buckhaults, Phd in Biochemistry and Molecular Biology. He does cancer genomics research at the University of South Carolina. https://www.scstatehouse.gov/video/archives.php?key=13489&fbclid=IwAR3IhAShh8cjjLBIeIaVIdKebVJJwa58mOijP7GM2EyD_CiiySjVmVZBW5A_aem_AVmIVMu43UMMtpll_BQOdvd8sxRkz_KQu9jYC-akyaR3InCeQ6-FZEloy9X1TzTToTM

Video Transcript AI Summary
"Pfizer vaccine is contaminated with plasma DNA. It's not just mRNA." "This DNA is the DNA vector that was used as the template for the in vitro transcription reaction when they made the mRNA." "I sequenced it in my own lab." "The vials of Pfizer vaccine that were given out here in Colombia, one of my colleagues was in charge of that vaccination program in the College of Pharmacy." "And for reasons that I still don't understand, he kept every single vial." "So he had a whole freezer full of the empty vials." "And I checked these two batches, and I checked them by sequencing." "It's surprising that there's any DNA in there." "This DNA, in my view, it could be causing some of the rare but serious side effects like death from cardiac arrest."
Full Transcript
Speaker 0: Hand lawns razor, which is never attribute malice to that which can be better explained by incompetence. And so I'm trying to be gracious here in many circumstances. There could be malice underneath, but I'm trying to see just incompetence to be gracious. So the Pfizer vaccine is contaminated with plasma DNA. It's not just mRNA. It's got bits of DNA in it. This DNA is the DNA vector that was used as the template for the in vitro transcription reaction when they made the mRNA. I know this is true because I sequenced it in my own lab. The vials of Pfizer vaccine that were given out here in Columbia, one of my colleagues was in charge of that vaccination program in the College of Pharmacy. And for reasons that I still don't understand, he kept every single vial. So he had a whole freezer full of the empty vials. Well, the empty vials have a little tiny bit in the in the bottom of them. He gave them all to me, and I looked at them. We had two batches that were given out here in Colombia. And I checked these two batches, and I checked them by sequencing. And I sequenced all the DNA that was in the vaccine, and I can see what's in there. And it's surprising that there's any DNA in there. And you can kind of work out what it is and how it got there, and I'm kind of alarmed about the possible consequences of this, both in terms of human health and biology, but you should be alarmed about regulatory process that allowed it to get there. So this DNA, in my view, it could be causing some of the rare but serious side effects like death from cardiac arrest. There's a lot of cases now of people having suspicious death after vaccine. It's hard to prove what caused it. It's just, you know, temporally associated. And this DNA is a plausible mechanism. Okay? This DNA can and likely will integrate into the genomic DNA of cells that got transfected with the vaccine mix. This is just the way it works. We do this in the lab all the time. We take pieces of DNA, we mix them up with a lipid complex like the Pfizer vaccine is in. We pour it onto cells and and a lot of it gets into the cells and a lot of it gets into the DNA of those cells and it becomes a permanent
Video Transcript AI Summary
The s v 40 sequences, they should not be there. They could have chosen another plasmid that did not have the s v 40 sequences. If these sequences sit above an oncogene and they're promiscuous, that means they are likely to integrate in places more likely than other genetic inserts. Insertional mutagenesis anyway causes cancer, and that's the risk. That's why gene therapies were not brought to market for so many years because there was a risk of causing cancer from insertional mutagenesis. We never needed these vaccines. Hydroxychloroquine and ivermectin, I can tell you as a toxicologist, they are not toxic. They're some of the safest drugs you can use. Endotoxin levels: they've got them all redacted. Why would you redact them if you were trying to be transparent? Why would you hold the data for seventy five years?
Full Transcript
Speaker 0: Said earlier nefarious. You felt like this was more nefarious than doctor Burkholder. In what sense are you saying that? Speaker 1: The s v 40 sequences, they should not be there. They don't need to be there to grow this into back to grow this in bacteria. I don't think it's an accident. They could have chosen another plasmid that did not have the s v 40 sequences. If these sequences sit above an oncogene and and they're promiscuous, that means they are likely to to integrate in places more likely than other genetic inserts. Thank you so much. Then they can cause cancer. Insertional mutagenesis anyway causes cancer, and that's the risk. That's why gene therapies were not brought to market for so many years because there was a risk of causing cancer from insertional mutagenesis. We never needed these vaccines. We had treatments that worked. One of our doctors here is gonna tell you about that. Hydroxychloroquine and ivermectin, I can tell you as a toxicologist, they are not toxic. They're they're some of the safest drugs you can use. I there's no reason once the FDA found out about this contamination. Okay? And we looked to see endotoxin levels, but they've got them all redacted. Why would you redact them if you were trying to be transparent? Why would you hold the data for seventy five years?
Video Transcript AI Summary
Key points: "the vials that were in fact approved are not the vials that were given to the public." The clinical trial used "process one that used PCR to make the DNA that was going to then turn into the RNA to make the spike protein." After the trial, "they switched" to a production process that "manufactured this DNA in E. Coli," introducing endotoxin risk. "There are these plasmids that have additional DNA that were not present in the actual clinical trial." Sequencing found mixtures, including "expired" and samples that had "been tapped into." Regarding Pfizer, "the Pfizer vaccines actually had a component that was not disclosed to the regulators." "The plasmid map on the right is what was disclosed to the EMA" with "no mention of the SV40 components" now "inside this DNA sequence." "The plasma on the left is what we actually found," with components not disclosed to regulators nor to patients. Monovalent Pfizer; prior ones were the bivalent vaccines from Moderna and Pfizer.
Full Transcript
Speaker 0: This all started back in April with this preprint where we did this RNA sequencing that Mark was just mentioning. This can give you more of the details that we're going to go into here very briefly. Will remind you, what is not in that preprint is something that Retzaflevy and Josh Gutzkow presented in the BMJ, which is that the vials that were in fact approved are not the vials that were given to the public. The clinical trial was run on something known as process one that used PCR to make the DNA that was going to then turn into the RNA to make the spike protein. Once the trial was complete, they switched. This is a big bait and switch. They moved to a production process that manufactured this DNA in E. Coli, and with that comes a different risk. There's clean DNA on the left, which is process one. There's no background E. Coli, there's no endotoxin present in this process. When they switch to scale this up, they put this plasmid into E. Coli to grow it and replicate it, and Now you have to get the DNA out of E. Coli and not have any of the parts of E. Coli come with it. Unfortunately, are parts of E. Coli that can create anaphylaxis, something known as endotoxin. There are these plasmids that have additional DNA that were not present in the actual clinical trial. So we started sequencing lots that were a mixture, some that were in fact not expired but had been tapped into by clinicians and other ones that were unopened but were expired. These are the monovalent vaccines for Pfizer, the prior ones were the bivalent vaccines from Moderna and Pfizer. Upon sequencing these, I think the most striking revelation was that the Pfizer vaccines actually had a component that was not disclosed to the regulators. This plasmid map on the right is what was disclosed to the EMA and there is no mention of the SV40 components that are now known to be inside this this DNA sequence. The plasma on the left is what we actually found, very similar in length but has all of these other components in it that are not disclosed to the regulators nor to the patients taking these.
South Carolina Legislature Video Archives scstatehouse.gov

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@Kevin_McKernan @P_J_Buckhaults @DJSpeicher @raoult_didier @DrCaliff_FDA @US_FDA @TGAgovau @EMA_News @WHO @RWMaloneMD @JesslovesMJK @stkirsch @CanningPharm @53v3n0fn1n3 @Fynnderella1 @CartlandDavid @drcole12 @dbkell @kacdnp91 @KevinMcCairnPhD @AnneliseBocquet @PinsolleT @FluoridePoison https://t.co/wcZEIr8RxF

@joshg99 - Josh Guetzkow

For background and more information on the Pfizer/BioNTech bait-and-switch scandal, see this thread. 👇 https://t.co/gJZn3h9hal

@joshg99 - Josh Guetzkow

Was the Pfizer/BioNTech vaccine clinical trial a bait-and-switch? There were >44,000 people in the trial, but only ~250 of them were given doses made with a new manufacturing method ('process 2') that was used to make enough doses to sell around the world.

@joshg99 - Josh Guetzkow

Was the Pfizer/BioNTech vaccine clinical trial a bait-and-switch? There were >44,000 people in the trial, but only ~250 of them were given doses made with a new manufacturing method ('process 2') that was used to make enough doses to sell around the world.

Saved - September 2, 2025 at 12:34 AM
reSee.it AI Summary
I shared information about Shinzo Abe, Japan's longest-serving prime minister, who was assassinated on July 8, 2022, while giving a speech in Nara. I also mentioned the topic of four African rulers who were murdered, highlighting the tragic history of political violence.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

The former prime minister of Japan The Japanese Prime Minister who was assassinated is Shinzo Abe. He was Japan's longest-serving prime minister, having held office from 2006 to 2007 and again from 2012 to 2020. Abe was assassinated on July 8, 2022, during a public speech in Nara, Japan. The 4 African rulers they murdered!

Saved - August 29, 2025 at 10:47 AM
reSee.it AI Summary
Dr. Makary stated that all adults can still choose to get vaccinated, emphasizing no limitations on availability. In response, concerns were raised about the continued availability of vaccines after the Emergency Use Authorization ended, suggesting a lack of proper long-term safety assessments. Critics highlighted that immunocompromised individuals, who are more vulnerable, are being recommended these vaccines without transparent risk-benefit discussions. Additionally, the ongoing immunity from lawsuits for manufacturers was noted as a significant issue, contributing to public distrust in health authorities.

@DrMakaryFDA - Dr. Marty Makary

100% of adults in this country can still get the vaccine if they choose. We are not limiting availability to anyone.

@JeromeAdamsMD - Jerome Adams

I’m deeply concerned about the new FDA move limiting COVID vaccines only to “high-risk groups.” CDC data shows those 50+ face rising risks, with 65+ at up to 340x higher death risk. Add in those with chronic disease and 71% of U.S. adults are at elevated risk!

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

The EUA may be gone, but the shots are still on the market now pushed on those with compromised immune systems. https://t.co/eH6e2ZXWOr The EUA (Emergency Use Authorization) was supposed to be temporary, but the shots remained available through other regulatory pathways instead of being pulled and reassessed. This creates the appearance of oversight while actually bypassing proper long-term safety checks. Instead of being cautious, regulators now recommend these products for immunocompromised people the very group with weaker defenses and a higher risk of side effects. Even after EUA, manufacturers still enjoy immunity from lawsuits under U.S. law (PREP Act), leaving injured people without recourse. The general public, and especially vulnerable groups, are not told about the risks vs. benefits in a transparent way. Keeping the shots available despite questionable efficacy and mounting safety concerns deepens distrust in public health authorities. @SecKennedy @NIHDirector_Jay This simply isn't good enough. Humanity definitely deserves better. #InformedConsent

@kacdnp91 - Kelly DNP Functional/Integrative Medicine

There it is. 4 new Cvd 💉

@lisachristinect - Lisa Christine •.

Here is the clip to listen for yourself:

Video Transcript AI Summary
"The FDA recently revoked the emergency youth authorizations for three COVID vaccinations while simultaneously green lighting four new COVID nineteen vaccines with twenty twenty five and twenty twenty six formulas." "The the reason for the revocation of that emergency youth authorization is because obviously the COVID pandemic and the public health emergency is over." "But just to correct the record because there's been a lot of misinformation on this, the FDA's decision does not affect the availability of COVID vaccines for Americans who want them." "We believe in individual choice. That's a promise both the president and the secretary have made, and it's a promise they have now delivered on."
Full Transcript
Speaker 0: From miscommunications or differences on vaccine policy. So I wonder if you could just say whether or not the president believes that the COVID vaccine should be available to and covered by insurance for all Americans regardless of age and preexisting conditions? Speaker 1: What I will tell you is that the FDA recently revoked the emergency youth authorizations for three COVID vaccinations while simultaneously green lighting four new COVID nineteen vaccines with twenty twenty five and twenty twenty six formulas. The the reason for the revocation of that emergency youth authorization is because obviously the COVID pandemic and the public health emergency is over. But just to correct the record because there's been a lot of misinformation on this, the FDA's decision does not affect the availability of COVID vaccines for Americans who want them. We believe in individual choice. That's a promise both the president and the secretary have made, and it's a promise they have now delivered on. Speaker 0: Any question if I could

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

It switches on EVERY major disease pathway known to man AND accelerates all 9 hallmarks of aging. That means faster aging, faster illness, longer suffering. Man I love the people who I follow. @SecKennedy @NIHDirector_Jay #NotGoodEnough #StoptheShots https://t.co/Cbfw5g8sBR

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@PatrickEWa92418 @MakingSenseInfo @laoneill111 The spike protein is a molecular wrecking ball. It switches on EVERY major disease pathway known to man AND accelerates all 9 hallmarks of aging. That means faster aging, faster illness, longer suffering. #SpikeProtein #mRNA #CellularDamage #ChronicDisease #Aging #Epigenetics

Saved - August 18, 2025 at 11:11 AM
reSee.it AI Summary
I explore the relationship between viruses, p53, and cancer. Viruses inhibit p53 to evade host defenses, potentially leading to cancer. Latent viruses like EBV and HBV are classified as carcinogens, and infections can reactivate dormant cancer cells. The concept of "turbo cancers" suggests a mix of new and reactivated cancers, possibly exacerbated by persistent viral protein expression from vaccines. I also discuss the risks of DNA contamination in vaccines and the potential for immune dysregulation to trigger aggressive tumor development. Following experts in this field is crucial for understanding these complex issues.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Scientific thought: If a virus seeks to persist, it must block p53. Why? Because p53 triggers cellular apoptosis = death of the host cell and, therefore, elimination of the virus at the same time. Latent viruses are therefore potentially carcinogenic. Because inhibiting p53 also allows dysfunctional cells to survive. If an infection can reactivate dormant cancer cells, what about de novo carcinogenesis? Are the observed cancers multiple, presenting in various cancerous forms? If we inject carcinogenic viral proteins with the aim of immunization, could this reactivate dormant cancer cells in the same way as pathogens? And induce de novo carcinogenesis? In other words, in the case of turbo cancers, are we not facing cancers of different types and different origins — both de novo + reactivation of dormant cancer cells? And facing a “virus + injection” combo? Have a good day.

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Pensée scientifique : Si un virus cherche à persister, il lui faut bloquer la p53. Pourquoi ? Parce que la p53 déclenche l'apoptose cellulaire = mort de la cellule hôte et donc, élimination du virus en même temps. Les virus latents sont donc potentiellement cancérigènes. Car inhiber la p53, ça permet aussi de maintenir des cellules dysfonctionnelles en vie. Si une infection peut réactiver des cellules cancéreuses en dormance, quid d'une cancérogenèse de novo ? Les cancers observés sont-ils multiples, présentant diverses formes cancéreuses ? Si on injecte des protéines virales cancérigènes, en vue d'une immunisation, est-ce que cela peut réactiver des cellules cancéreuses en dormance, de la même façon que les pathogènes ? Et induire une cancérogenèse de novo ? Autrement dit, n'est-on pas, dans le cadre des turbo cancers, face à des cancers de différents types et différentes origines, de novo + réactivation des cellules cancéreuses en dormance ? Et face à un combo "virus + injections" ? Bonne journée

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

p53 inhibition as a viral survival strategy Fact: p53 is a tumour suppressor protein that triggers cell cycle arrest or apoptosis in response to DNA damage or abnormal activity (including viral replication). Known examples: HPV: E6 protein binds to and degrades p53 → increases risk of cervical and oropharyngeal cancers. Adenoviruses, SV40, Hepatitis B, EBV: express proteins that block p53 or related pathways.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Latent viruses as carcinogens Fact: Epstein–Barr virus (EBV), Kaposi’s sarcoma-associated herpesvirus (KSHV/HHV-8), Hepatitis B virus (HBV), and Hepatitis C virus (HCV) are all officially classified as Group 1 carcinogens by IARC. Mechanism often involves immune evasion + inhibition of apoptosis + genomic instability.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Reactivation of dormant cancer cells Fact: Dormant disseminated tumour cells (DTCs) can survive for years, held in check by immune surveillance. Certain infections cause inflammation, cytokine release, and changes in the tumour microenvironment that can “wake up” dormant cells.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Integration events The “turbo cancer” reports from some clinicians suggest: Highly aggressive tumours Diverse histological types (lymphomas, glioblastomas, sarcomas, aggressive breast cancers, etc.) This could be consistent with: 1. De novo cancers triggered by genotoxic/oncogenic mechanisms (mutations, DNA integration, p53 suppression, immune collapse). 2. Reactivation of dormant cancers due to immune dysregulation or microenvironment changes. A “virus + injection” combo could synergise via: Immune suppression Chronic inflammation p53 pathway interference Increased cellular proliferation signals

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Short-lived protein exposure vs. persistent expression Short-lived exposure Example: Traditional inactivated-virus or recombinant protein vaccines. The viral antigen is present for hours–days. No genomic material remains. Unless the protein itself is highly toxic in the short term (rare for a single viral antigen), the cancer risk is negligible. This is why, historically, protein-based vaccines without replication or integration haven’t been linked to oncogenesis. Persistent expression If the antigen is produced inside cells for weeks, months, or longer, it can continuously interact with host proteins. Certain viral proteins (like HPV E6/E7, EBV LMP1, SV40 large T antigen) bind and disable tumour suppressors like p53 or Rb. Continuous interference with these pathways increases the risk of DNA mutations being propagated instead of repaired or eliminated.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Oncogenic activity of the protein itself Some viral proteins are intrinsically oncogenic, because they: Inhibit p53 (prevents apoptosis after DNA damage) Inhibit Rb (removes cell cycle brakes) Activate telomerase (promotes immortality) Cause chromosomal instability (breaks, fusions, aneuploidy) For example: HPV E6 → degrades p53 HPV E7 → binds Rb SV40 Large T antigen → inactivates both p53 & Rb HBx protein (Hepatitis B) → interferes with DNA repair If such a protein is expressed from a vaccine platform inside the nucleus or cytoplasm for long durations, it could mimic the oncogenic potential of a persistent infection without needing the whole virus.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

DNA Contamination & Integration Risk SV40-containing plasmid sequences have been detected in multiple mRNA vaccine vials through the work of genomics scientist @Kevin_McKernan founder of Medicinal Genomics and former head of research and development at Applied Biosystems, a company whose DNA sequencing technology was instrumental in the Human Genome Project. McKernan has also built and sold multiple biotech companies, lending both technical expertise and industry credibility to his findings. These results have since been independently confirmed by laboratories and institutions around the world. The detected material consists of bacterial plasmid backbones carrying SV40 promoter/origin of replication sequences genetic elements historically used in experimental cancer biology to drive extremely high levels of gene expression in mammalian cells. If such plasmid DNA gains entry into the cell nucleus, rare but well-documented events of insertional mutagenesis can occur: Integration into or near oncogenes → abnormal activation of growth signals Integration into tumour suppressor genes → loss of cell cycle control This mechanism mirrors the problem that halted certain early gene therapy trials, where retroviral vectors inadvertently caused leukaemias by activating growth-promoting genes.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Why persistence changes the risk calculation Think of it like this: Short exposure = like briefly turning off your smoke alarm. You’ll probably be fine. Persistent exposure = like disconnecting the smoke alarm permanently and inviting a small campfire into your living room it’s not guaranteed to burn the house down, but the probability increases with every passing hour. 5. In the “turbo cancer” context If the spike protein or any contaminating viral sequence: 1. Is expressed persistently inside cells 2. Can interact with tumour suppressors or DNA repair machinery 3. Arrives in a host with immune dysregulation (post-infection or post-vaccination) …then both: Reactivation of dormant cancer cells (immune escape) De novo tumour initiation (mutation accumulation + apoptosis failure) become biologically plausible and they could happen in parallel, leading to the multi-type, aggressive cancer profile some clinicians are reporting. End.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

I highly recommend following Kevin McKernan and reading his Substack https://substack.com/@kevinmckernan/note/p-153763975 his deep-dive analyses are essential if you want to understand what’s really in these vials. Frankly, @joerogan should have him on if he hasn’t already. I’m no expert, but I know enough to be dangerous and what Kevin’s uncovered should have everyone paying attention. https://substack.com/@kevinmckernan/note/p-150140847 I find it hard to believe you haven't seen his work tbh. Thanks Kevin 💪🙏🔥

FDA White Oak Lab Finds 6X to 470X DNA contamination in mRNA vaccines Excellent Work From High Schoolers anandamide.substack.com
SV40 origin of replication in mammalian cells in absence of SV40 Large T-Antigen Positive tumor biopsy qPCR one year after vaccination anandamide.substack.com

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

You should also follow Annelise too god speed 🙏

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

The thread aligns with recent research linking SIRT1 and p53 pathways to mitochondrial dysfunction and inflammation, as seen in a 2025 study on intestinal dysbiosis and aging. https://www.mdpi.com/1422-0067/22/3/1233 Spike protein interactions with p53, as mentioned, have gained attention following a 2024 report on long-term effects of COVID-19 vaccines, suggesting potential mitochondrial impacts. Other mechanisms : RAGE-mediated inflammation, a key point in the thread, connects to ongoing studies on Alzheimer’s, where RAGE facilitates amyloid-beta transport and mitochondrial damage. https://www.pnas.org/doi/10.1073/pnas.0905686106 The mention of miR-34a’s role in liver fibrosis ties to a 2023 clinical trial exploring SIRT1 activators for fibrosis treatment, showing promising results. https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0158657 "miR-34a is transcriptionally regulated by the p53 tumor suppressor protein and regulates a plethora of target proteins, which are involved in the cell cycle, apoptosis, differentiation and cellular development [25]. Downregulation of miR-34a has been found in many cancers [26–28]; thus, miR-34a is thought to be a tumor suppressor. However, previous studies have revealed that miR-34a is upregulated in many liver diseases, from fatty liver disease to HCC [29–31]. Upregulation of miR-34a may inhibit SIRT1, thus activating p53 and forming a positive feedback loop [22]. Although it has been reported that miR-34a can target acyl-CoA synthetase long-chain family member 1 and impair the lipid metabolism in the liver, resulting in the development of liver fibrosis [19], the function of the classical miR-34a/SIRT1/p53 signaling pathway in liver fibrosis is presently unclear." HMGB1’s role in immune tolerance, highlighted in the thread, relates to a 2025 breakthrough in cancer immunotherapy targeting RAGE-TLR4 pathways. https://journals.aai.org/jimmunol/article/205/3/767/61028/Interplay-between-RAGE-and-TLR4-Regulates-HMGB1 https://pmc.ncbi.nlm.nih.gov/articles/PMC11298799/ (Cf. Picture) I'm going around something and I can't figure out exactly what it is...

Activation of the miR-34a/SIRT1/p53 Signaling Pathway Contributes to the Progress of Liver Fibrosis via Inducing Apoptosis in Hepatocytes but Not in HSCs Liver fibrosis results from a sustained wound healing response to chronic liver injury, and the activation of nonparenchymal hepatic stellate cells (HSCs) is the pivotal process. MicroRNA-34a (miR-34a) is the direct target gene of p53 and activates p53 through sirtuin 1 (SIRT1) simultaneously. The miR-34a/SIRT1/p53 signaling pathway thus forms a positive feedback loop wherein p53 induces miR-34a and miR-34a activates p53 by inhibiting SIRT1, playing an important role in cell proliferation and apoptosis. miR-34a expression has been found to be increased in animal models or in human patients with different liver diseases, including liver fibrosis. However, the exact role of this classical miR-34a/SIRT1/p53 signaling pathway in liver fibrosis remains unclear. In the present study, using a CCl4-induced rat liver fibrosis model, we found that the miR-34a/SIRT1/p53 signaling pathway was activated and could be inhibited by SIRT1 activator SRT1720. Further studies showed that the miR-34a/SIRT1/p53 signaling pathway was activated in hepatocytes but not in HSCs. The activation of this pathway in hepatocytes resulted in the apoptosis of hepatocytes and thus activated HSCs. Our data indicate that the miR-34a/SIRT1/p53 signaling pathway might be a promising therapeutic target for liver fibrosis. journals.plos.org
Targeting mitochondrial damage: shining a new light on immunotherapy Mitochondrial damage has a particular impact on the immune system and tumor microenvironment, which can trigger cell stress, an inflammatory response, and disrupt immune cell function, thus all of which can accelerate the progression of the tumor. ... pmc.ncbi.nlm.nih.gov

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

@ThailandMedicaX "SIRT1 interacts with and deacetylates PGC-1α to enhance its activity, promote mitochondrial biogenesis, and maintain mitochondrial function." https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5767311/ https://www.mdpi.com/1422-0067/22/9/4558 "PGC-1α is a master regulator that interacts with various transcription factors involved

SIRT1/PGC-1α Signaling Promotes Mitochondrial Functional Recovery and Reduces Apoptosis after Intracerebral Hemorrhage in Rats Silent information regulator 1 (SIRT1) exerts neuroprotection in many neurodegenerative diseases. However, it is not clear if SIRT1 has protective effects after intracerebral hemorrhage (ICH)-induced brain injury in rats. Thus, our goal was to ... pmc.ncbi.nlm.nih.gov

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

@ThailandMedicaX The problem is that C99 is found in MAM - intracellular lipid rafts, called mitochondria‐associated ER membranes (MAM), a functional subdomain of the ER located in close apposition to mitochondria that regulates key cellular metabolic functions. https://pmc.ncbi.nlm.nih.gov/articles/PMC5731665/ This is

Increased localization of APP‐C99 in mitochondria‐associated ER membranes causes mitochondrial dysfunction in Alzheimer disease In the amyloidogenic pathway associated with Alzheimer disease (AD), the amyloid precursor protein (APP) is cleaved by β‐secretase to generate a 99‐aa C‐terminal fragment (C99) that is then cleaved by γ‐secretase to generate the β‐amyloid (Aβ) found ... pmc.ncbi.nlm.nih.gov

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Spike, p53 et mitochondries... Allez, je vais essayer de vulgariser. 1. Interaction Spike/p53 et immunité : La Spike pourrait interagir avec p53, qui est un régulateur clé de l’immunité innée et adaptative, notamment via la production d’interférons (IFN) de type I et de gènes

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Pour expliquer... Ce fil explique comment certaines protéines dans notre corps, après une infection (comme le COVID-19) ou une injection d’ARNm, peuvent provoquer des problèmes graves, comme des caillots anormaux ou des maladies cérébrales. On parle de protéines comme GSDME,

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@AnneliseBocquet would you consider putting your information on Substack ? I'm sure there are many that would be willing to help myself included 🔥

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@AnneliseBocquet There are so many people doing this kind of work honestly, it’s the best part of the online world for me. You can learn so much from them. 🔗 Walter’s also got a great Substack well worth subscribing 🙏❤️

@Parsifaler - Walter M Chesnut

THE SPIKE, CANCER AND PRION DISEASE As I warned three years ago about the Spike's interaction with p53 and tumor suppressors. This can ALSO induce Prion Disease! Recently discovered characteristics of the tumor suppressor p53 include its prion-like properties and cellular uptake mechanisms, which are related to its GoF and are associated with tumor formation and malignancy. https://wmcresearch.org/the-spike-protein-as-metatastic-cancer/

THE SPIKE PROTEIN AS METASTATIC CANCER – WMC Research wmcresearch.org

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Is this what's playing out in the charts by the excellent Ethical Skeptic? I tried to warn people this was dangerous, I was one of the fortunate few who found Dr Cole and Dr Kory earlier than most I saw the zinc ionophore suppression. https://t.co/rjx13isBpR

@EthicalSkeptic - Ethical Skeptic ☀

Excess Natural Cause Mortality in Vaccinial Generation (0-5 yr-olds - of vaccinated mothers) 😔OMFG - we asked not what outght to be done, but only what could be (quod fieri). The blood-dimmed tide is loosed, and everywhere The ceremony of innocense is drowned. ~Yates

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Could FMT from an unvaccinated cohort repair the gut damage in the vaccinated ? Wouldn't this repair immune system health and restore gut integrity ? A nice way of saying eat shit 😂😂 https://t.co/tVC3rftbNV

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

I've read about the Chinese yellow poop soup that goes back as far as the 4th century The Practice of Yellow Soup"Yellow soup," also known as "Huang-Long decoction," was a preparation made from dried or fermented stool from a healthy person. Documented by Ge Hong in his medical text "Zhou Hou Bei Ji Fang" (Handbook of Emergency Medicine), it was used to treat diarrhea, food poisoning, heat toxin, and unconsciousness due to high fever. The evidence leans toward this being an early form of fecal microbiota transplantation (FMT), aiming to restore gut balance by introducing beneficial bacteria. https://t.co/9dTD0frnbg

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

I do not condone drinking urine ever. I do remember being insulted to drink it by the pro jabber crowd lmfao.. I'll pass https://t.co/viLo0z7E8G

@DrSarteschi - Dr. Christine Sarteschi, LCSW

Christopher Keys of the Vaccine Police has shingles and naturally he is taking urine baths (among other things) to help Here he is drinking it as well https://t.co/UaswEzhIg0

Saved - July 24, 2025 at 3:59 PM
reSee.it AI Summary
I issued a notice of objection regarding the lack of accountability from pharmaceutical companies and government authorities concerning vaccine injuries in Ireland. This notice is grounded in constitutional and human rights, emphasizing our right to information and transparency about the production and effects of mRNA vaccines. I presented a series of critical questions regarding the vaccine's biochemical design, human risks, and potential impacts on fertility and health, highlighting the need for answers to ensure public trust and safety.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

A notice for vaccine injured in Ireland 🇮🇪 #stoptheshots NOTICE OF OBJECTION & DEMAND FOR ACCOUNTABILITY Issued under the authority of Bunreacht na hÉireann, the European Convention on Human Rights, and Natural Justice I. LEGAL BASIS FOR OBJECTION We, the undersigned citizens and/or lawful representatives of vaccine-injured individuals, hereby serve notice of our constitutional and human rights-based objection to the continued silence, obfuscation, and denial by pharmaceutical manufacturers and government authorities regarding the production, testing, deployment, and post-market surveillance of modRNA-based products. This notice is issued in accordance with: Article 40 of Bunreacht na hÉireann – Protection of personal rights, bodily integrity, and dignity; Article 41 – Protection of the family, moral order, and societal well-being; Article 44 – Freedom of conscience and the unimpeded expression of religious, cultural, and ethical convictions; Article 40.6.1 – The right to freedom of expression and to challenge injustice in the public interest; The Preamble to the Constitution, affirming our “rightful status among the nations” and fidelity to “our divine heritage” and “the common good”; Article 10 and Article 14 of the European Convention on Human Rights (ECHR) – Freedom of expression and protection against discrimination; The principles of Natural Law, subsidiarity, proportionality, and inalienable rights; Legal definitions and standards from Black’s Law Dictionary, including but not limited to: Equal Protection Legal Certainty Medical Negligence Administrative Abuse Cultural Sovereignty Misuse of Public Funds Duty to Disclose Standing and Redress II. RIGHT TO INFORMATION FOR VACCINE-INJURED PERSONS As a specific manifestation of the secondary burden of disclosure (Darlegungsobliegenheit) on pharmaceutical manufacturers — arising from the asymmetry of knowledge and the public-private nature of experimental health interventions — we assert a constitutionally protected right to demand complete and transparent answers to the following urgent and unanswered questions. > Failure to answer these questions constitutes: A violation of the principle of legal certainty; A denial of meaningful redress (Article 13 ECHR); A breach of the precautionary principle under EU law; And may be interpreted as misfeasance in public office and gross negligence in breach of public trust and fiduciary duty. We formally present the following Catalogue of Material Questions: 📌 A. Biochemical and Structural Design Questions 1. Why was a furin cleavage site inserted into the Wuhan-1 spike protein to separate S1 from S2 in a vaccine context? 2. Why was a P2-lock used on S2 but no equivalent molecular safeguard applied to the S1 subunit? 3. Are there BIAcore (surface plasmon resonance) studies confirming or refuting spike protein binding to human tissues or receptors? 4. What was the rationale for inserting GP-120/HIV-like sequences and their immunological implications? 5. Why was a neuropilin-binding site included, and what risks were anticipated? 📌 B. Human Risk, Fertility & Systemic Circulation 6. What adverse effects in humans were documented by the manufacturer or its agents prior to rollout? 7. What steps were taken to ensure the membrane-anchoring of spike proteins, preventing systemic shedding? 8. Since when did the manufacturer know the spike protein binds ACE2 and disrupts the RAAS system? 📌 C. Modified Nucleosides & Misfolded Proteins 9. How was N1-methylpseudouridine expected to prevent protein misfolding? 10. What measures were taken to assess and mitigate effects on fertility? 11. Was the thermostability and pH sensitivity of spike protein assessed? (e.g., behavior at 7°C vs 36.6°C) 12. Were tests conducted for inclusion bodies or misfolded protein accumulation? 13. Was N1-methylpseudouridine incorporated into mitochondrial rRNA, affecting energy and replication?

Saved - July 22, 2025 at 10:41 AM
reSee.it AI Summary
A group is mobilizing against proposed amendments to the WHO's International Health Regulations, set to take effect on July 19, arguing they undermine national sovereignty and public health autonomy. They demand that Irish officials reject these amendments, hold public debates, and ensure future health powers require citizen consent. Concerns also arise over alleged violations of rights during COVID-19, including coercion and lack of informed consent regarding vaccines. They call for investigations and accountability for government actions during the pandemic.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

🌍 All across the world, people are rising up and demanding that their governments reject the WHO’s proposed amendments to the International Health Regulations (IHR)—set to become binding international law on July 19. 🇮🇪 If you're in Ireland, please check the post below. It includes: 📩 A ready-to-use email template ✅ Contact details for Ministers and the President’s Office Now is the time to act. Take just 10 minutes to send a few emails. Let them know: our sovereignty is not for sale.

@CitizenGO_IE - CitizenGO Ireland

Dublin 🇮🇪 today 👉 Delivery of over 600K signatures to Health Minister @CarrollJennifer at @roinnslainte 🗣️📢 All over the world, people are demanding their governments REJECT the WHO’s IHR globalist health rules due to become binding international law on July 19

@CitizenGO_IE - CitizenGO Ireland

Say NO to International Health Regulations due to be adopted July 19 🗣️ The WHO claim these IHR's give them the power to: Declare global emergencies Force lockdowns, mandates, surveillance, and censorship Override national decisions and personal freedoms https://cgo.ac/sc0i22aM

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

[Your Full Name] [Your Address] [City, Postcode] [Email Address] [Date] To: Minister Jennifer Carroll MacNeill Department of Health Hawkins House Dublin 2 Ireland RE: Fiduciary Duty to Reject the WHO’s IHR Amendments – Binding International Law Proposed for July 19 Dear Minister Carroll MacNeill, I am writing to you in your capacity as an elected public servant and fiduciary of the Irish people. On July 19, proposed amendments to the World Health Organization's International Health Regulations (IHR) are due to come into effect as binding international law. These amendments—negotiated without democratic mandate or public consultation—represent a clear and present danger to Ireland's constitutional sovereignty, bodily autonomy, and public health policy independence. As of today, over 600,000 signatures have been formally delivered to your office in Dublin, representing the will of citizens across Ireland and the world who reject this global overreach. The IHR amendments would confer unprecedented powers to an unelected international body to declare pandemics, impose travel restrictions, enforce medical treatments, and control information—all without national parliamentary oversight or judicial review. As a Minister of the Irish State, you have a legal, ethical, and fiduciary duty to act in the best interests of the people you serve. This includes: Upholding the Constitution of Ireland, which guarantees personal rights, national independence, and due process; Refusing consent to treaties or agreements that bypass democratic safeguards; Protecting future generations from centralized, technocratic governance that undermines local accountability. Should the State allow these IHR amendments to be adopted, it would constitute a dereliction of duty and a breach of public trust. This would open the door to binding obligations enforced by a foreign entity, which is wholly incompatible with Irish constitutional law and the principles of democratic self-determination. We, the undersigned citizens, formally demand: 1. A public declaration by you and your Department that Ireland will not consent to the WHO’s proposed IHR amendments. 2. A full debate in the Dáil Éireann, with opportunity for public scrutiny, before any such commitments are made on Ireland’s behalf. 3. An assurance in writing that no future health emergency powers will be outsourced to an international body without the express consent of the Irish people via referendum. This is a watershed moment for our nation. The world is watching. You are being called to stand on the right side of history. Yours sincerely, [Your Name] ivana.bacik@oireachtas.ie, richard.boydbarrett@oireachtas.ie, jack.chambers@oireachtas.ie,, jennifer.carrollmacneill@oireachtas.ie, cormac.devlin@oireachtas.ie, paul.donnelly@oireachtas.ie, colm.brophy@oireachtas.ie, paul.murphy@oireachtas.ie, marylou.mcdonald@oireachtas.ie, aengus.osnodaigh@oireachtas.ie, dessie.ellis@oireachtas.ie, eoin.obroin@oireachtas.ie, louise.oreilly@oireachtas.ie, mark.ward@oireachtas.ie, paul.mcauliffe@oireachtas.ie, gary.gannon@oireachtas.ie, cian.ocallaghan@oireachtas.ie, darragh.obrien@oireachtas.ie, roderic.ogorman@oireachtas.ie, jim.ocallaghan@oireachtas.ie, neale.richmond@oireachtas.ie, emerg.currie@oireachtas.ie, paschal.donohoe@oireachtas.ie, denise.mitchell@oireachtas.ie, duncan.smith@oireachtas.ie, john.lahart@oireachtas.ie, catherine.ardagh@oireachtas.ie, sinead.gibney@oireachtas.ie, sean.crowe@oireachtas.ie, maire.devine@oireachtas.ie, eoin.hayes@oireachtas.ie, shay.brennan@oireachtas.ie, james.geoghegan@oireachtas.ie, marie.sherlock@oireachtas.ie, ciaran.ahern@oireachtas.ie, grace.boland@oireachtas.ie, barry.heneghan@oireachtas.ie, tom.brabazon@oireachtas.ie, naoise.omuiri@oireachtas.ie, robert.odonoghue@oireachtas.ie

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

18.07.2025 Subject: Urgent Constitutional Concern – WHO IHR Amendments & Executive Overreach To: president@president.ie Dear President Higgins, I write to you today as a concerned citizen regarding the imminent adoption of the World Health Organization’s International Health Regulations (IHR) amendments, due to become binding international law on July 19. These amendments would enable a non-democratic foreign body to impose legally binding regulations on Ireland, without the involvement of the Oireachtas or the consent of the Irish people. This is a clear breach of the Constitution, in particular: Article 6 (sovereignty of the people), Article 15.2.1 (exclusive legislative power of the Oireachtas), Article 28.3.3 (only the Oireachtas can declare an emergency), Article 40 (personal rights and freedoms). Such a transfer of legislative and executive authority to an external body, if not submitted to a public referendum, would violate Article 29.5.1, which mandates Dáil ratification and, where sovereignty is affected, the consent of the people. As the constitutional guardian of the Irish Republic, I respectfully request that you intervene and seek legal advice regarding the compatibility of the IHR amendments with our Constitution. If necessary, I urge you to refer the matter to the Council of State or the Supreme Court under Article 26. The stakes could not be higher for our national sovereignty, democratic integrity, and future generations. Sincerely, [Your Full Name] [Your Address] [Your Contact Email] president@president.ie, info@president.ie, protocol@president.ie, diary@president.ie, secretarygeneral@president.ie, press.office@president.ie

@ThomasEJnr - Thomas Emmett

@MeasslainteIRL @RealEddieHobbs @MrAndyQuirke @FatEmperor @_mullally_el_ @WilliamRal45681 @indepdubnrth @dr_morrissey @blueskylou @_louise__ @Mickbraz1 @PhilipDwyer_MOI @OTURISK @CitizenGO_IE @IrishInquiry @LakareUpppropet1 @Leoyourleader @CilComLFC @mattiemcgrathtd @CarolNolanOff

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

To: The Taoiseach, Minister for Health, Minister for Justice, and all Members of the Oireachtas Subject: Formal Notice of Constitutional and Legal Breach: Crimes Against Humanity Committed During the COVID-19 Period Dear Ministers and Representatives, I write to formally assert that grave violations of domestic, constitutional, and international law occurred in Ireland during the COVID-19 response (2020–2023). These actions constitute a breach of the State’s fiduciary duty to protect life, bodily integrity, and the freedom of conscience under both Irish and international law. Under Article 40.3.2° of Bunreacht na hÉireann, the State guarantees to protect the personal rights of the citizen. This includes the right to bodily integrity (recognised in Ryan v. Attorney General [1965] I.R. 294), and the right to make informed medical decisions free from coercion (M(D) v. Ireland [2012] IEHC 352). These rights were violated by the State’s COVID-19 measures, which included: I. COERCION & MEDICAL TYRANNY Citizens were subject to medical coercion via "vaccine passports", workplace mandates, and denial of public services. This violates the principle of informed consent enshrined in: The Nuremberg Code (1947), which holds that “the voluntary consent of the human subject is absolutely essential.” The Oviedo Convention on Human Rights and Biomedicine (1997), Article 5: “An intervention may only be carried out after the person concerned has given free and informed consent.” The UNESCO Universal Declaration on Bioethics and Human Rights (2005), Article 6. The Irish Supreme Court in McGee v. Attorney General [1974] I.R. 284 affirmed the right to personal autonomy, including decisions relating to bodily health. Any interference must be proportionate. The actions taken during COVID were neither evidence-based nor proportionate, particularly for healthy individuals and children. II. VIOLATION OF “PRIMUM NON NOCERE” (FIRST, DO NO HARM) The State actively encouraged and facilitated the widespread use of experimental genetic injections (mRNA vaccines) without full knowledge of long-term safety. This violates: The Medical Council's Guide to Professional Conduct and Ethics for Registered Medical Practitioners (8th Edition, 2016), Section 7.1: “You must make the care of your patient your first concern and must practice safely and effectively.” Section 6.3: “You must give patients the information they need to understand their condition and treatment options and to make informed decisions about their care.” Instead, early warnings from international experts were ignored, censored, or defamed, while no pharmacovigilance system adequately tracked or responded to the surge in adverse events, including myocarditis, thrombotic events, and excess mortality—now evidenced in CSO data and HIQA reviews. III. CRIMES AGAINST HUMANITY – DEFINED AND APPLICABLE Under Article 7 of the Rome Statute of the International Criminal Court, crimes against humanity include: Persecution against any identifiable group on political or medical grounds. Other inhumane acts intentionally causing great suffering or injury to body or health. Forced medical procedures or experimentation without consent. Ireland's actions—including forcing or coercing injection uptake via threat of exclusion, job loss, or ostracization—constitute such violations. Furthermore, the continued use of products known to be contaminated with plasmid DNA (as confirmed by international genomic labs) shows reckless endangerment of life and health. IV. CENSORSHIP AND SUPPRESSION OF MEDICAL TRUTH Dissenting voices—including Irish doctors, midwives, and international scientists—were silenced, investigated, or struck off. This violates: Article 40.6.1° of Bunreacht na hÉireann: the right to freedom of expression. Article 10 of the European Convention on Human Rights (ECHR): freedom to receive and impart information.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

The State was complicit in a coordinated campaign of medical censorship, working with international bodies and social media firms to remove scientific discussion contrary to state messaging. This is state-sponsored information control, not science. V. SYSTEMIC NEGLIGENCE & FAILURE TO INFORM The lack of full disclosure about ingredients (e.g. SV40 enhancer sequences, residual DNA, LNPs), potential risks (e.g. autoimmune reactions, fertility issues), and ongoing adverse event signals constitutes fraudulent concealment and medical malpractice on a national scale. Section 21 of the Medical Council’s Code notes that consent must be based on accurate and adequate information. Yet many citizens were lied to or misled, with slogans such as “safe and effective” used despite emerging red flags. WE NOW DEMAND: 1. A full criminal investigation into the Irish Government's handling of COVID-19 policies, procurement, and adverse event concealment—with access to unredacted contracts, meeting minutes, and NPHET deliberations. 2. An independent Truth and Reconciliation Commission with the power to compel testimony, protect whistleblowers, and provide reparations to those harmed by State-led mandates. 3. Immediate suspension of mRNA product use pending comprehensive genomic, toxicological, and pharmacovigilance review. 4. Amendment of Article 28 of Bunreacht na hÉireann to forbid future emergency legislation that bypasses fundamental rights without a citizen referendum. 5. Public apologies and restitution for healthcare workers, teachers, and ordinary citizens who were coerced, injured, or discriminated against due to these unconstitutional policies. The Irish State has a duty not only to protect its people but to acknowledge when harm has occurred. If the Government fails to address these crimes, it invites future proceedings in domestic and international courts, including petitions to the European Court of Human Rights and the International Criminal Court. We do not seek vengeance. We seek accountability, transparency, and truth, so that this will never happen again. You are hereby put on formal notice. The people are no longer asleep. Sincerely, [Your Full Name] [Your Address / Eircode] [Email / Phone] Constitutional Sovereign and Witness to History

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@MichealMartinTD@SimonHarrisTD@Paschaldonohoe@JackChambersTD@HelenMcEnteeTD@DarraghOBrienTD@NormaFoleyTD@PeterBurkeTD@DaraCallearyTD @PatrickODonovanTD @JenCarrollMacNeillTD@JamesBrowneTD@JimOCallaghanTD@MartinHeydonTD@JamesLawlessTD@dfatirl@Dept_Transport@DeptCDE@opwireland

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@lawsocietyire@BarofIreland@LSRAIreland@CourtsServiceIE@DPPIreland@LegalAidBoard@VirginMediaNews@IrishMirror@journal_ie@DublinLive@CorkBeo@Spin1038@RedFM@Joe_Duffy@ciarakellydoc@Ray_Darcy@MartyM_RTE@DoireannGarrihy@Ian_Dempsey@MattCooperNT @GráinneSeoige @VirginMediaNews@IrishMirror@journal_ie@DublinLive@CorkBeo@Spin1038@RedFM@Joe_Duffy@ciarakellydoc@Ray_Darcy@MartyM_RTE@DoireannGarrihy@Ian_Dempsey@MattCooperNT @GráinneSeoige

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@ThomasEJnr @RealEddieHobbs @MrAndyQuirke @FatEmperor @_mullally_el_ @WilliamRal45681 @indepdubnrth @dr_morrissey @blueskylou @_louise__ @Mickbraz1 @PhilipDwyer_MOI @OTURISK @CitizenGO_IE @IrishInquiry @Leoyourleader @CilComLFC @mattiemcgrathtd @MichealMartinTD @SimonHarrisTD @DarraghOBrienTD @NormaFoleyTD @daracallearytd @JamesBrowneTD @dfatirl @Dept_Transport @DeptCDE @lawsocietyire @LSRAIreland @CourtsServiceIE @DPPIreland @legalaidboard @VirginMediaNews @IrishMirror @journal_ie @DublinLive @corkbeo @spin1038 @redfm @Joe_Duffy @ciarakellydoc @ray_darcy @DoireannGarrihy Pfizer Linked CJD Phenotype Body Fluid Analysis

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

🐁🦝🐺

@ThomasEJnr - Thomas Emmett

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@ThomasEJnr @RealEddieHobbs @MrAndyQuirke @FatEmperor @_mullally_el_ @WilliamRal45681 @indepdubnrth @dr_morrissey @blueskylou @_louise__ @Mickbraz1 @PhilipDwyer_MOI @OTURISK @CitizenGO_IE @IrishInquiry @Leoyourleader @CilComLFC @mattiemcgrathtd @MichealMartinTD @SimonHarrisTD @DarraghOBrienTD @NormaFoleyTD @daracallearytd @JamesBrowneTD @dfatirl @Dept_Transport @DeptCDE @lawsocietyire @LSRAIreland @CourtsServiceIE @DPPIreland @legalaidboard @VirginMediaNews @IrishMirror @journal_ie @DublinLive @corkbeo @spin1038 @redfm @Joe_Duffy @ciarakellydoc @ray_darcy @DoireannGarrihy There are so many beautiful minds doing the work ❤️ We will see you soon

@Nicolina0815 - Nicolina 🐭

@MeasslainteIRL I will reveal another way soon. My newest substacks: https://nicolina0815-substack-com.translate.goog/p/wenn-der-blutdruck-achterbahn-fahrt?_x_tr_sl=de&_x_tr_tl=en&_x_tr_hl=de&_x_tr_pto=wapp https://nicolina0815-substack-com.translate.goog/p/seneszenz-verstehen-heilen-ohne-zu?_x_tr_sl=de&_x_tr_tl=en&_x_tr_hl=de&_x_tr_pto=wapp&_x_tr_hist=true https://nicolina0815-substack-com.translate.goog/p/v-aids-wenn-das-immunsystem-in-die?_x_tr_sl=de&_x_tr_tl=en&_x_tr_hl=de&_x_tr_pto=wapp&_x_tr_hist=true https://nicolina0815-substack-com.translate.goog/p/pad4-and-citrullinierung?_x_tr_sl=de&_x_tr_tl=en&_x_tr_hl=de&_x_tr_pto=wapp&_x_tr_hist=true NarfGBs work https://genervter-substack-com.translate.goog/p/lnps-und-modrna?_x_tr_sl=de&_x_tr_tl=en&_x_tr_hl=de&_x_tr_pto=wapp&_x_tr_hist=true https://genervter-substack-com.translate.goog/p/lnps-und-modrna-2?_x_tr_sl=de&_x_tr_tl=en&_x_tr_hl=de&_x_tr_pto=wapp&_x_tr_hist=true I did also translation into easier + https://nicolina0815-substack-com.translate.goog/p/gibt-es-auswege?_x_tr_sl=de&_x_tr_tl=en&_x_tr_hl=de&_x_tr_pto=wapp

🧬 Seneszenz verstehen – heilen (?) ohne zu überfordern Ein naturbasierte Hypothese zur immunologischen Stabilisierung nach modRNA/LNP-Exposition nicolina0815-substack-com.translate.goog
"V-AIDS": Wenn das Immunsystem in die Erschöpfung kippt Ursachen, Verlauf und mögliche Wege heraus nicolina0815-substack-com.translate.goog
Wenn der Blutdruck Achterbahn fährt: Wie modRNA-Transfektion, PAD4 und Spikeprotein unser Gefäßsystem ins Chaos stürzen nicolina0815-substack-com.translate.goog
LNPs und modRNA (2) Eine Arbeitshypothese - Das Ende genervter-substack-com.translate.goog
LNPs und modRNA Eine Arbeitshypothese - Der Anfang genervter-substack-com.translate.goog
PAD4 & Citrullinierung Es könnte viel erklären! Calamari Clots, Krebs und Co- wie sind die Verbindungen? nicolina0815-substack-com.translate.goog
Gibt es Auswege? Diskussion der potentiellen Schäden und Besprechung, was für Optionen bleiben nicolina0815-substack-com.translate.goog

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@ThomasEJnr @RealEddieHobbs @MrAndyQuirke @FatEmperor @_mullally_el_ @WilliamRal45681 @indepdubnrth @dr_morrissey @blueskylou @_louise__ @Mickbraz1 @PhilipDwyer_MOI @OTURISK @CitizenGO_IE @IrishInquiry @Leoyourleader @CilComLFC @mattiemcgrathtd @MichealMartinTD @SimonHarrisTD @DarraghOBrienTD @NormaFoleyTD @daracallearytd @JamesBrowneTD @dfatirl @Dept_Transport @DeptCDE @lawsocietyire @LSRAIreland @CourtsServiceIE @DPPIreland @legalaidboard @VirginMediaNews @IrishMirror @journal_ie @DublinLive @corkbeo @spin1038 @redfm @Joe_Duffy @ciarakellydoc @ray_darcy @DoireannGarrihy A new draft, please consider this as notice.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Draft 2, Tell the truth and shame the devil 👿 FORMAL NOTICE OF CONSTITUTIONAL AND INTERNATIONAL LAW VIOLATIONS To: The Taoiseach, Minister for Health, Minister for Justice, and All Members of the Oireachtas From: [Your Full Name], Sovereign Citizen of Ireland Date: [Insert Today’s Date] Subject: Immediate Legal and Constitutional Redress for State Misconduct in COVID-19 Response (2020–2023) 1. GROUNDS FOR LEGAL ACTION A. Coercive Medical Measures Ireland’s Constitution guarantees the right to bodily integrity under Article 40.3.2°, as affirmed in Ryan v. Attorney General [1965] IR 294. Government policies—including vaccine certificates, employment mandates, and educational exclusion—constituted indirect coercion to undergo experimental mRNA injections. These actions breached both domestic and international law: Nuremberg Code (1947) – Principle 1: Voluntary consent must be given free from force, fraud, deceit, duress, or coercion. Convention on Human Rights and Biomedicine (Oviedo Convention) – Article 5: Prior, free, and informed consent is mandatory. Rome Statute of the International Criminal Court – Article 7(1)(h) & (k): Persecution and inhumane acts causing serious harm may constitute crimes against humanity. B. Suppression of Risk Data and Misrepresentation The Irish public was assured that COVID-19 vaccines were “safe and effective.” However, official documents indicate: HPRA Drug Safety Newsletter No. 104 and HSE internal bulletins (Aug 2021) acknowledged myocarditis risk in young males as 28 times baseline. Residual SV40 enhancer sequences—which can integrate into human DNA—were identified in Pfizer vials (Kevin McKernan, 2023), breaching EMA’s 10 ng/dose threshold for residual DNA (EMA/CHMP/BWP/534898/2008 Rev. 1). These failures violate Medical Council Guide §6.3, which mandates full disclosure of risks, and may amount to misfeasance in public office. C. Targeting of Dissenting Professionals Doctors and scientists who raised legitimate concerns were suspended, censored, or deregistered. This contravenes: Article 40.6.1° of Bunreacht na hÉireann – Guarantees the right to freedom of expression. European Convention on Human Rights (ECHR), Article 10 – Protects the right to receive and impart information without interference. 2. REMEDIAL DEMANDS 1. Immediate Criminal and Parliamentary Inquiry Full publication of unredacted Pfizer and Moderna contracts, all NPHET and CMO correspondence (including encrypted messages). Suspension of implicated officials, including Cabinet members and public health executives, pending investigation. 2. Compensation and Redress Automatic reparations of €500,000 per verified injury linked to COVID-19 injections, funded through profits or tax offsets from pharmaceutical contracts. Full reinstatement and back pay for individuals dismissed for declining vaccination. 3. Legislative Reform Repeal, within 21 days, of: Health (Amendment) Act 2021, and Criminal Justice (Enforcement Powers) (COVID-19) Act 2020. Enshrine constitutional immunity for Articles 40.3.2°, 40.6.1°, and 44.2.1°, protecting them from suspension via emergency legislation without a referendum. 4. Public Health Safeguards Moratorium on all mRNA-based interventions pending independent EU-accredited laboratory reviews, appointed by citizen assembly. Public release of anonymized HPRA adverse event reports in searchable database within seven days. 3. NOTICE OF CONSEQUENCES This formal notice has been delivered via registered post and email. A written response addressing each demand is required within seven (7) calendar days. Failure to respond shall constitute wilful dereliction of duty, breach of constitutional oath, and prima facie evidence of misconduct. Be advised that legal proceedings may be initiated in Irish, European, and international courts, including the International Criminal Court, under applicable treaties. Sincerely, [Your Full Name] [Full Postal Address

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@ThomasEJnr @RealEddieHobbs @MrAndyQuirke @FatEmperor @_mullally_el_ @WilliamRal45681 @indepdubnrth @dr_morrissey @blueskylou @_louise__ @Mickbraz1 @PhilipDwyer_MOI @OTURISK @CitizenGO_IE @IrishInquiry @Leoyourleader @CilComLFC @mattiemcgrathtd @MichealMartinTD @SimonHarrisTD @DarraghOBrienTD @NormaFoleyTD @daracallearytd @JamesBrowneTD @dfatirl @Dept_Transport @DeptCDE @lawsocietyire @LSRAIreland @CourtsServiceIE @DPPIreland @legalaidboard @VirginMediaNews @IrishMirror @journal_ie @DublinLive @corkbeo @redfm @Joe_Duffy @ciarakellydoc @ray_darcy @DoireannGarrihy

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

exit the @WHO

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@Patboyslim_1 📜 NOTICE To the Minister for Health, Department of Health, Ireland Re: WHO IHR Amendments – A Threat to Irish Sovereignty and Public Health Freedom From: [Your Full Name] [Your Address] [City, Postcode] [Email Address] [Date] To: Minister Jennifer Carroll MacNeill Department

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@ThomasEJnr @RealEddieHobbs @MrAndyQuirke @FatEmperor @_mullally_el_ @WilliamRal45681 @indepdubnrth @dr_morrissey @blueskylou @_louise__ @Mickbraz1 @PhilipDwyer_MOI @OTURISK @CitizenGO_IE @IrishInquiry @Leoyourleader @CilComLFC @mattiemcgrathtd @MichealMartinTD @SimonHarrisTD @DarraghOBrienTD @NormaFoleyTD @daracallearytd @JamesBrowneTD @dfatirl @Dept_Transport @DeptCDE @lawsocietyire @LSRAIreland @CourtsServiceIE @DPPIreland @legalaidboard @VirginMediaNews @IrishMirror @journal_ie @DublinLive @corkbeo @redfm @Joe_Duffy @ciarakellydoc @ray_darcy @DoireannGarrihy #9pages

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@ThomasEJnr @RealEddieHobbs @MrAndyQuirke @FatEmperor @_mullally_el_ @WilliamRal45681 @indepdubnrth @dr_morrissey @blueskylou @_louise__ @Mickbraz1 @PhilipDwyer_MOI @OTURISK @CitizenGO_IE @IrishInquiry @Leoyourleader @CilComLFC @mattiemcgrathtd @MichealMartinTD @SimonHarrisTD @DarraghOBrienTD @NormaFoleyTD @daracallearytd @JamesBrowneTD @dfatirl @Dept_Transport @DeptCDE @lawsocietyire @LSRAIreland @CourtsServiceIE @DPPIreland @legalaidboard @VirginMediaNews @IrishMirror @journal_ie @DublinLive @corkbeo @redfm @Joe_Duffy @ciarakellydoc @ray_darcy @DoireannGarrihy #9pages

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@ThomasEJnr @RealEddieHobbs @MrAndyQuirke @FatEmperor @_mullally_el_ @WilliamRal45681 @indepdubnrth @dr_morrissey @blueskylou @_louise__ @Mickbraz1 @PhilipDwyer_MOI @OTURISK @CitizenGO_IE @IrishInquiry @Leoyourleader @CilComLFC @mattiemcgrathtd @MichealMartinTD @SimonHarrisTD @DarraghOBrienTD @NormaFoleyTD @daracallearytd @JamesBrowneTD @dfatirl @Dept_Transport @DeptCDE @lawsocietyire @LSRAIreland @CourtsServiceIE @DPPIreland @legalaidboard @VirginMediaNews @IrishMirror @journal_ie @DublinLive @corkbeo @redfm @Joe_Duffy @ciarakellydoc @ray_darcy @DoireannGarrihy 9th page !

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@ThomasEJnr @RealEddieHobbs @MrAndyQuirke @FatEmperor @_mullally_el_ @WilliamRal45681 @indepdubnrth @dr_morrissey @blueskylou @_louise__ @Mickbraz1 @PhilipDwyer_MOI @OTURISK @CitizenGO_IE @IrishInquiry @Leoyourleader @CilComLFC @mattiemcgrathtd @MichealMartinTD @SimonHarrisTD @DarraghOBrienTD @NormaFoleyTD @daracallearytd @JamesBrowneTD @dfatirl @Dept_Transport @DeptCDE @lawsocietyire @LSRAIreland @CourtsServiceIE @DPPIreland @legalaidboard @VirginMediaNews @IrishMirror @journal_ie @DublinLive @corkbeo @redfm @Joe_Duffy @ciarakellydoc @ray_darcy @DoireannGarrihy Let's skip to the good bit!

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

NOTICE OF CONSTITUTIONAL BREACHES OF TRUST AND USUFRUCTUARY AND FIDUCIARY DUTIES NOTICE & DEMAND FOR DISCLOSURE UNDER RIGHT TO INFORMATION & PUBLIC ACCOUNTABILITY To: All Ministers of the Government of Ireland CC: Department of Health, National Public Health Emergency Team (NPHET), HSE Executive Board, Office of the Attorney General, Data Protection Commissioner, All Members of the Oireachtas Date: 22 July 2025 From: Concerned Citizens of Ireland — Acting in Defence of Truth, Life, and Constitutional Integrity SUBJECT: Demand for Immediate Disclosure of COVID-19 Decision-Making Documents, Vaccine Contracts, NPHET Minutes & Scientific Justifications — Under Threat of Presumption of Guilt and Breach of Constitutional Duty We, the people of Ireland, acting under the unalienable rights granted to us by Bunreacht na hÉireann, serve this notice as a public demand for transparency. You are hereby put on notice: We demand full, unredacted disclosure of all records, contracts, deliberations, and risk assessments made by Government Ministers, NPHET, the HSE, and affiliated departments relating to: SPECIFIC ITEMS DEMANDED FOR IMMEDIATE DISCLOSURE: 1. All COVID-19 vaccine purchase contracts, indemnity clauses, and redacted pricing information provided by Pfizer, Moderna, AstraZeneca, and Janssen to the Irish Government or HSE. 2. Internal minutes, emails, and scientific advice documents issued by NPHET to Government decision-makers from March 2020 to January 2023, including: Any reference to myocarditis, pericarditis, autoimmune, or neurological risk. Any assessments or mentions of excess deaths, hospital capacity projections, or “safe and effective” risk-benefit analyses. 3. All Cabinet or Ministerial briefings on informed consent, clinical trial data, and whether public messaging was factually and legally compliant. 4. Communications with international agencies, including the WHO, European Medicines Agency (EMA), or pharmaceutical corporations. 5. Any retraction protocols or legal warnings sent to citizens or doctors who raised valid scientific dissent. 6. Internal evaluations on the cause of rising excess mortality since Q3 of 2021, disaggregated by age, vaccination status, and cause of death. TAKE NOTICE: Failure to supply the above within 14 working days will be taken as a deliberate obstruction of public oversight and an admission of guilt by omission under natural justice and public law doctrine. THE LAW IS CLEAR: You are bound by: Article 40.3.1° of Bunreacht na hÉireann – The State guarantees to defend and vindicate the personal rights of the citizen. This includes the right to bodily integrity, freedom of conscience, and access to truth. Article 15.5.1° – No law shall be enacted imposing the death penalty. This applies by extension to negligent public policy resulting in preventable deaths. Article 28.4.1° – The Government must be responsible to Dáil Éireann — not to unelected advisory groups, foreign corporate actors, or pharmaceutical lobbyists. Freedom of Information Act 2014, Section 11(3)(a) – Public bodies shall give effect to the principle of maximum disclosure in matters of public interest. The Ethics in Public Office Act 1995, Sections 5 & 7 – Mandating full accountability, honesty, and avoidance of conflicts of interest by office holders. Medical Council Ethical Guidelines, Section 7.1.1 – Doctors and advisors must uphold the principle of “First, Do No Harm.” Those in public service are doubly bound. EXCESS DEATHS = POLICY FAILURE The statistical evidence since the mass vaccine rollout shows significant and unexplained rises in excess mortality, especially in younger and middle-aged cohorts. You will be held to account for every life lost under: Misleading public health messaging Unlawful coercion Suppression of early treatments Censorship of dissent Failure to apply the precautionary principle 1 of 2

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

NOTICE OF LIABILITY AND DEMAND FOR ACCOUNTABILITY To: Albert Bourla, CEO, Pfizer Inc. CC: Global Regulatory Authorities, Legal Representatives, Public Health Institutions, Media Outlets Date: 22/07/2025 From: Men and women of eiRú , Medical Professionals, and Independent Researchers Subject: Undisclosed Plasmid DNA Contamination, Clinical Trial Misconduct, and Manufacturing Changes in Pfizer-BioNTech COVID-19 Products This notice is being issued in good faith, in defense of public health, informed consent, and medical ethics. It serves to notify Pfizer Inc. and you, Albert Bourla, personally, that material omissions, unverified safety claims, and alleged fraud surrounding the COVID-19 mRNA vaccine must now be addressed. I. Unlawful Plasmid DNA Contamination & Omission from Labeling It has come to public attention — through the work of genomics expert Kevin McKernan and others — that Pfizer’s mRNA vaccine contains SV40 promoter-enhanced bacterial plasmid DNA fragments, which were not disclosed to regulators or the public. These DNA contaminants: Include functional SV40 sequences (known for integration potential and tumorigenesis), Were not part of the original clinical trial documentation, and Raise the possibility of insertional mutagenesis, which was never publicly risk-assessed. These are not trace impurities but replication-competent bacterial plasmids capable of inducing long-term genetic alterations, including horizontal gene transfer. By omitting this information from EUA/MA applications, Pfizer has potentially violated: EU Regulation (EC) No 726/2004, Art. 12 & 13 (Requirements for marketing authorisation), Nuremberg Code (1947), particularly Consent Principle No. 1, Irish Constitution, Article 40.3.1 (Protection of bodily integrity), UNESCO’s Universal Declaration on Bioethics and Human Rights, Articles 6 & 10, Common Law precedents on product liability and omission (Donoghue v Stevenson [1932] AC 562). We demand a full public admission of these contaminants, along with their potential biological consequences. 🧬 II. Concealment of Clinical Trial Data and Safety Signals Pfizer has failed to release complete, unredacted clinical trial data, even under FOIA lawsuits. What has been disclosed by regulators (under court order) shows: Over 1,200 deaths within the first 90 days of rollout, Numerous adverse effects categorized as "of special interest," including myocarditis, neurological damage, and multi-system inflammatory syndromes, Trial protocol deviations, such as unblinding and lack of proper control arms, Data fraud allegations (Brook Jackson whistleblower testimony), No proper biodistribution or genotoxicity studies in final submissions. In light of excess mortality data across heavily vaccinated populations — including a notable rise in cardiac and stroke events post-2021 in Ireland, the UK, and other nations — this constitutes a failure of the “do no harm” principle. Pfizer must immediately release all trial documentation, including: Raw participant-level data, Protocol amendments and manufacturing changes, Internal memos related to adverse events, Independent post-market surveillance results. III. Unlawful Changes in Manufacturing Post-EUA Pfizer has been shown to have changed the manufacturing process — shifting from Process 1 (used in trials) to Process 2 (used in public rollout) — without: Repeating safety trials using the new process, Notifying regulators of critical differences, Testing for residual DNA or altered lipid-nanoparticle behavior. Such undisclosed changes — particularly if they affect DNA uptake, spike protein expression, or lipid distribution — constitute fraud by omission and violate the standards of Good Manufacturing Practice (GMP) and ICH Q5D & Q6B guidelines on residual DNA. This constitutes medical experimentation on the public without informed consent. 1/2

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@Nick_Delehanty @MauriceSCHP Nick, do you think we should be putting drug manufacturers on notice ? NOTICE & DEMAND FOR ACCOUNTABILITY To: Pfizer Inc. & Subsidiaries (incl. BioNTech SE) From: The People of eiRú / Living men and women of eiRú, Researchers, and Families Date: [Insert Date] Re: Omission of

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Our Demands: 1. A full public statement by you, Albert Bourla, acknowledging: DNA plasmid contamination, Manufacturing changes, Known and emerging risks from trial data. 2. Immediate release of all Pfizer-BioNTech documentation, including: Full CMC (Chemistry, Manufacturing, and Controls) files, Plasmid maps, SV40 sequence use, and genetic insertion risk assessments, Internal communications regarding post-market adverse events. 3. A public retraction of “safe and effective” claims unless supported by transparent and replicable safety evidence. 4. Compensation and liability provisions for all vaccine-injured persons worldwide, including the Irish public who were not properly informed. Failure to Comply: Should Pfizer fail to respond truthfully and transparently to this demand within 21 days, it will be interpreted as: Willful omission and obstruction of truth, Corporate malpractice and product liability, Violation of international medical ethics, And criminal negligence under several jurisdictions, subject to prosecution and international inquiry. This notice will be shared publicly, submitted to regulators, courts, independent investigators, and victims' advocacy networks globally. This is not conspiracy. This is science, law, and accountability. The world is watching. The people are awakening. And the era of pharmaceutical impunity is coming to an end. Signed, [Name or Group – e.g., Irish Health Integrity Alliance, Medical Professionals for Informed Consent, etc.] [Contact info if applicable]

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@ThomasEJnr @RealEddieHobbs @MrAndyQuirke @FatEmperor @_mullally_el_ @WilliamRal45681 @indepdubnrth @dr_morrissey @blueskylou @_louise__ @Mickbraz1 @PhilipDwyer_MOI @OTURISK @CitizenGO_IE @IrishInquiry @Leoyourleader @CilComLFC @mattiemcgrathtd @MichealMartinTD @SimonHarrisTD @DarraghOBrienTD @NormaFoleyTD @daracallearytd @JamesBrowneTD @dfatirl @Dept_Transport @DeptCDE @lawsocietyire @LSRAIreland @CourtsServiceIE @DPPIreland @legalaidboard @VirginMediaNews @IrishMirror @journal_ie @DublinLive @corkbeo @redfm @Joe_Duffy @ciarakellydoc @ray_darcy @DoireannGarrihy Gentle reminder short thread from @pfizer 's own documents . @AlbertBourla

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

very well put together the top link is based on the @pfizer document, I highly recommend you take the time to understand both the work and the consequences ! 🩸 1. Thrombosis & Microangiopathy *(Thread 1/5)* Why do mRNA vaccines cause vascular events? The Pfizer document reveals excessive clotting (sinus thrombosis, microemboli) isn't random. It's driven by: • Endothelial damage from spike protein/LNPs • Cytokine storms (TNF-α/IL-6) • NETosis: Neutrophils eject DNA nets laced with toxins. 🔑 PAD4 enzyme citrullinates histones → vascular blockages. Same mechanism seen in severe COVID. #VaccineSafety #Thrombosis from the substack Nicolina0815 5.3.6 CUMULATIVE ANALYSIS OF POST-AUTHORIZATION ADVERSE EVENT REPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021

@Nicolina0815 - Nicolina 🐭

Deutsche Fassung von Auswirkungen einer nahezu gewaltfrei als sicher und wirksam angepriesenen Universallösung für den Arm: https://nicolina0815.substack.com/p/von-spike-lipiden-und-immunchaos https://nicolina0815.substack.com/p/amyloide-spike-and-das-risiko-stiller https://nicolina0815.substack.com/p/pad4-and-citrullinierung https://nicolina0815.substack.com/p/v-aids-wenn-das-immunsystem-in-die https://nicolina0815.substack.com/p/seneszenz-verstehen-heilen-ohne-zu https://nicolina0815.substack.com/p/wenn-der-blutdruck-achterbahn-fahrt 1/x

🧬 Amyloide, Spike & das Risiko stiller Neurotoxizität - Wenn Proteine entgleisen nicolina0815.substack.com
🧬 Seneszenz verstehen – heilen (?) ohne zu überfordern Ein naturbasierte Hypothese zur immunologischen Stabilisierung nach modRNA/LNP-Exposition nicolina0815.substack.com
PAD4 & Citrullinierung Es könnte viel erklären! Calamari Clots, Krebs und Co- wie sind die Verbindungen? nicolina0815.substack.com
🧠 Von Spike, Lipiden und Immunchaos Wie mRNA-Technologie in multisystemische Erkrankungen münden kann – ein Blick hinter die Kulissen nicolina0815.substack.com
Wenn der Blutdruck Achterbahn fährt: Wie modRNA-Transfektion, PAD4 und Spikeprotein unser Gefäßsystem ins Chaos stürzen nicolina0815.substack.com
"V-AIDS": Wenn das Immunsystem in die Erschöpfung kippt Ursachen, Verlauf und mögliche Wege heraus nicolina0815.substack.com
Saved - June 24, 2025 at 10:59 AM
reSee.it AI Summary
Simon Harris announced that Ireland is the first European country to legislate a ban on trade with the Occupied Palestinian Territories, condemning the actions in Gaza. In response, another user criticized Harris, accusing the government of betraying the Irish people by promoting COVID-19 vaccinations and lockdowns influenced by global interests. They referenced a specific announcement made by Harris regarding vaccination hubs targeting young people and called for his resignation, claiming he coerced a generation.

@SimonHarrisTD - Simon Harris TD

Today Ireland becomes the first country in Europe to bring forward legislation to ban trade with the Occupied Palestinian Territories. Ireland is speaking up and speaking out against the genocidal activity in Gaza. Every country must pull every lever at its disposal.

Video Transcript AI Summary
Ireland aims to be the first European country to legislate a ban on trade with occupied Palestinian territories. The speaker states this action is to advocate for the Irish people regarding "genocidal activity." The speaker hopes the legislation will inspire other countries to implement similar measures, utilizing every available means.
Full Transcript
Speaker 0: Today, we will become the first country in Europe to bring forward legislation to ban trade the occupied Palestinian territories. This is an important measure because we are speaking up and speaking out on behalf of the people of Ireland in relation to this genocidal activity. But of course, I actually think and hope that the real benefit of publishing this legislation today will be that it may inspire other countries to do likewise because it's important that every country is every lever at its disposal.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Just like the betrayal your government inflicted on the Irish people pushing experimental injections and lockdowns at the behest of unelected global interests. On September 2nd, 2021, at 08:30 hrs, Fine Gael’s Simon Harris publicly announced the rollout of "pop-up vax hubs" on college campuses, targeting young Irish people with COVID shots starting September 6th. You did this. You coerced a generation. You need to step down.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

@rtenews @SimonHarrisTD On September 2, 2021, at 08:30 hrs, Fine Gael's Simon Harris announced plans to establish "popup vax hubs" inside colleges starting September 6th, 2021, to administer COVID vaccines to young people. You did this? You need to step down.@SimonHarrisTD https://www.oireachtas.ie/en/debates/debate/joint_committee_on_jobs_enterprise_and_innovation/2015-11-03/2/

Joint Committee on Jobs, Enterprise and Innovation debate - Tuesday, 3 Nov 2015 Increasing Employment through Training: Innopharma Labs Joint Committee on Jobs, Enterprise and Innovation debate - Tuesday, 3 Nov 2015 oireachtas.ie
Saved - June 21, 2025 at 10:29 AM
reSee.it AI Summary
I've been exploring how certain foods can trigger inflammation and impact chronic health issues. I've learned that gluten, dairy (especially A1), legumes, nightshades, processed sugars, seed oils, trans fats, artificial additives, and FODMAPs can all contribute to inflammation and worsen symptoms for those with autoimmune diseases or gut sensitivities. By eliminating these foods for 30–60 days and focusing on whole, nutrient-dense options, I can potentially reclaim my health and vitality. Tracking my body's responses during reintroduction is crucial for understanding my unique triggers.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

Ditch These Foods to Heal Chronic Illness Explore the hidden biochemical triggers of inflammation and the foods that stoke the flames, Perfect for those battling autoimmune diseases, neuroinflammation, chronic fatigue, IBD, MS, arthritis, or post-viral syndromes taking control of these triggers is your key to reclaiming vitality!

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

🌾 Gluten Sensitivity: The Hidden Inflammation Trigger Struggling with chronic inflammation, autoimmune flares, fatigue, or brain fog? Gluten may be silently sabotaging your gut and immune system even if you don’t have celiac disease. 🔓 Leaky Gut & Systemic Inflammation Gluten stimulates zonulin, a protein that opens tight junctions in your intestinal lining. This leads to leaky gut, allowing bacteria, food particles, and toxins to escape into your bloodstream triggering chronic immune activation and inflammation throughout the body. 🧬 Autoimmune Activation via Molecular Mimicry In genetically predisposed individuals (e.g., HLA-DQ2/DQ8), gluten peptides can resemble human tissue proteins. This "molecular mimicry" may cause the immune system to mistake your own cells for invaders, contributing to diseases like: • Hashimoto’s thyroiditis • Multiple sclerosis (MS) • Rheumatoid arthritis • Celiac disease Non-Celiac Gluten Sensitivity (NCGS) Is Real Even without celiac markers, many people experience bloating, diarrhea, joint pain, fatigue, skin issues, and brain fog after gluten exposure. This is known as NCGS and it's now recognized in medical literature as a legitimate, immune-mediated condition. ✅ What You Can Do • Trial a gluten-free diet for 30–60 days and track your symptoms • Get tested: Ask your provider about anti-gliadin antibodies or genetic screening • Focus on whole, unprocessed gluten-free foods not just GF packaged substitutes • Reassess and reintroduce (if desired) later to confirm your sensitivity 📌 Healing often begins in the gut. If gluten is a trigger, removing it could be the most powerful anti-inflammatory step you take.

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

🥛 Dairy (Especially Conventional, Pasteurized A1 Dairy) Examples: Milk, cheese, yogurt, cream, butter 🔥 Why It’s Inflammatory Most commercial cow’s milk contains A1 casein, a protein that breaks down into beta-casomorphin-7 (BCM-7) a bioactive peptide linked to gut and brain inflammation. Many people also lack the enzyme lactase, leading to poor lactose digestion, bloating, dysbiosis, and gut irritation. Worse still, the immune system can develop IgG or IgA antibodies to casein, triggering systemic inflammation and potentially worsening autoimmune and neuroimmune conditions. 🚩 Who Should Be Cautious? If you have any of the following, A1 dairy might aggravate your symptoms: • Multiple Sclerosis (MS) • Parkinson’s disease • Chronic sinus issues or asthma • Crohn’s or colitis • Eczema, acne, or skin inflammation • Brain fog, autism spectrum conditions, or neuroinflammation Try removing dairy for 30–60 days and observe changes in energy, digestion, skin, and cognition. ✅ Better Options (Later On) • A2 dairy (from A2 cows, goats, or sheep) • Raw, fermented goat/sheep dairy (e.g. kefir) These may be reintroduced cautiously in later phases, but all dairy is excluded initially to reduce inflammatory load. 📖 A controlled human study found that A1 milk increases GI symptoms and inflammation compared to A2 milk. 🔗 Read the study (Nutrition Journal, 2016) https://pubmed.ncbi.nlm.nih.gov/27039383/ #DairyFree #Inflammation #Autoimmune #GutHealth #A1A2Milk

Effects of milk containing only A2 beta casein versus milk containing both A1 and A2 beta casein proteins on gastrointestinal physiology, symptoms of discomfort, and cognitive behavior of people with self-reported intolerance to traditional cows' milk - PubMed ClinicalTrials.gov/NCT02406469. pubmed.ncbi.nlm.nih.gov

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

🌱 Legumes: Hidden Inflammation Triggers Examples: Beans, lentils, soy, peanuts, peas 🔥 Why They’re Inflammatory Legumes contain lectins sticky, plant-derived proteins that resist digestion and can bind to the gut lining, increasing intestinal permeability and provoking immune activation. They also contain phytates, which chelate essential minerals like zinc, calcium, and iron, blocking their absorption. Soy is especially problematic: it’s often genetically modified, heavily sprayed with glyphosate, and loaded with phytoestrogens, which may disrupt hormonal balance and immune signaling. Peanuts, technically legumes, are frequently contaminated with aflatoxins toxic fungal compounds linked to liver damage, immune suppression, and even cancer. 🚨 Who Should Be Cautious? You may want to avoid legumes if you struggle with: • Autoimmune diseases (e.g. lupus, RA, MS) • Estrogen-sensitive conditions (endometriosis, fibroids, PCOS) • IBS, IBD, or leaky gut • Mineral deficiencies (low iron, zinc) • Histamine intolerance or peanut allergies 💡 Smart Tips • Pressure-cooking reduces some lectins, but not all anti-nutrients • Eliminate legumes during early gut-healing or autoimmune protocols • Reintroduce slowly (if at all) once symptoms stabilize #LegumeFree #Inflammation #Autoimmune #GutHealth #Lectins #Phytoestrogens

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

🍅 Nightshades: Nature’s Defense, Your Inflammation Trigger? Examples: Tomatoes, potatoes, eggplant, bell peppers, chili 🔥 Why They’re Inflammatory (for Some) Nightshades contain alkaloids like solanine and capsaicin, natural pesticides that defend the plant but can irritate the human body. In sensitive individuals, these compounds can: • Disrupt the gut lining, increasing intestinal permeability (aka leaky gut) • Activate mast cells, releasing histamine and pro-inflammatory cytokines • Trigger neurogenic inflammation, leading to nerve pain, joint stiffness, or migraines • Worsen autoimmune flares, especially in musculoskeletal and neuroimmune disorders 🚨 Who Should Be Cautious? If you’re living with: • Rheumatoid arthritis, lupus, or ankylosing spondylitis • Multiple sclerosis (MS) or neuropathic pain • IBD (Crohn’s, colitis) or leaky gut • Migraines, eczema, interstitial cystitis, or chronic fatigue …then nightshades could be silently inflaming your symptoms. 💡 What to Do • Eliminate nightshades for 4–6 weeks • Reintroduce one at a time, with 2–3 days in between • Track symptoms like pain, digestion, skin, mood, and energy You may discover that removing just one trigger food brings profound relief. #NightshadeFree #AutoimmuneHealing #Inflammation #GutHealth #Neuroimmune #PainRelief

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

🍬 Processed Sugars & Refined Carbs: Silent Drivers of Inflammation Examples: White sugar, high-fructose corn syrup (HFCS), pastries, white bread, soda 🔥 Why They’re Inflammatory Refined sugars cause a rapid spike in blood glucose, which leads to insulin surges that activate inflammatory messengers like NF-kB and IL-6 key players in chronic disease. They also feed pathogenic gut microbes (like candida and bad bacteria), disrupting your microbiome and triggering systemic inflammation. Over time, sugar drives the formation of advanced glycation end products (AGEs) damaging compounds that impair mitochondrial function, degrade collagen, and contribute to brain fog, skin aging, and neurodegeneration. 🚨 Who Should Be Especially Cautious? Watch your intake if you live with: • Metabolic syndrome or insulin resistance • Type 2 diabetes or prediabetes • Alzheimer’s or cognitive decline • PCOS or hormonal imbalances • Candida overgrowth, acne, or chronic fatigue • Mood disorders like depression or anxiety These conditions are often exacerbated by high-glycemic, low-nutrient carbs. 💡 Smart Move • Cut back on added sugars and refined flour • Prioritize whole foods with fiber, healthy fats, and slow-burning carbs • Notice how quickly energy, mood, and skin improve when sugar is removed 📊 Even small reductions in sugar can lead to big wins in inflammation, energy, and metabolic health. #SugarFree #Inflammation #MetabolicHealth #GutHealth #CognitiveHealth #HormoneBalance

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

🛢️ Industrial Seed Oils: Inflammation Time Bombs Examples: Corn oil, soybean oil, sunflower oil, safflower oil, canola 🔥 Why They’re Inflammatory These oils are ultra-processed and packed with omega-6 linoleic acid, which your body converts into arachidonic acid a precursor to inflammatory molecules like prostaglandins and leukotrienes. When heated, seed oils oxidize rapidly, producing toxic lipid peroxides that damage: • Cell membranes • Mitochondria (your energy factories) • DNA promoting aging, mutation, and inflammation The result? A perfect storm for metabolic dysfunction, non-alcoholic fatty liver disease (NAFLD), cardiovascular problems, insulin resistance, and even brain fog. 🚨 Who Should Be Cautious? These oils may worsen symptoms if you’re dealing with: • Heart disease or hypertension • Brain fog or cognitive decline • NAFLD or high triglycerides • Obesity, insulin resistance, or chronic fatigue • Inflammatory skin issues (like eczema or acne) 💡 Smart Move Replace inflammatory seed oils with stable, nourishing fats like: • 🫒 Extra virgin olive oil • 🥥 Coconut oil • 🥑 Avocado oil • 🧈 Ghee or grass-fed butter • 🐖 Tallow or duck fat These are richer in antioxidants, more heat-stable, and support cellular and metabolic health not sabotage it. #NoSeedOils #HealthyFats #Inflammation #HeartHealth #BrainHealth #MetabolicHealing

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

⚠️ Trans Fats: Hidden Hazards to Your Heart and Brain Examples: Margarine, shortening, fast food fries, processed snacks, baked goods with partially hydrogenated oils 🔥 Why They’re Inflammatory Trans fats are industrially created fats that disrupt cell membrane structure, impair insulin signaling, and damage mitochondria, your body’s energy producers. They also: • Raise LDL (“bad”) cholesterol • Lower HDL (“good”) cholesterol • Trigger systemic inflammation that accelerates aging and disease • Increase risk of heart attacks, stroke, and neurodegeneration They’ve been called the most dangerous fats in the modern diet and for good reason. 🚨 Who Should Be Especially Cautious? Avoid trans fats completely if you’re dealing with: • Cardiovascular disease or high cholesterol • Insulin resistance or type 2 diabetes • Cognitive decline, Alzheimer’s, or brain fog • Chronic inflammation, fatigue, or autoimmune conditions Even small amounts are harmful. 💡 Smart Move • Read labels: Watch for "partially hydrogenated oils" • Avoid ultra-processed foods and fast food • Focus on whole foods and healthy fats like olive oil, ghee, or coconut oil 🛑 There is no safe level of trans fat. Eliminating them may be one of the fastest ways to protect your heart, brain, and metabolism. #NoTransFats #HeartHealth #BrainHealth #Inflammation #HealthyFats #MetabolicHealing

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

⚠️ Artificial Additives & Preservatives: Small Compounds, Big Inflammation Examples: MSG, sodium benzoate, artificial food dyes, BHA/BHT, nitrates, nitrites, aspartame 🔬 Why They’re Inflammatory Many food additives are designed to extend shelf life, enhance flavor, or improve appearance but at a cost to your health. Here’s how they silently provoke inflammation: • Mast Cell Activation & Histamine Release Preservatives and additives can activate mast cells, immune cells that release histamine and inflammatory cytokines. This can trigger skin rashes, gut symptoms, and respiratory issues in sensitive individuals. • Excitotoxicity Compounds like MSG (monosodium glutamate) and aspartame are excitotoxins they overstimulate neurons, potentially leading to brain inflammation, headaches, migraines, mood swings, and even seizure activity in susceptible people. • Gut-Brain Axis Disruption Preservatives like sodium benzoate and BHA/BHT can disrupt the gut microbiome, reducing bacterial diversity and promoting dysbiosis a known driver of systemic inflammation, anxiety, and cognitive dysfunction. • Nitrites & Nitrates Used in processed meats, these can form nitrosamines, compounds linked to cancer risk, oxidative stress, and endothelial damage (affecting heart and brain function). 🚨 Who Should Be Especially Cautious? These compounds may aggravate symptoms in people with: • ADHD or behavioral disorders • Histamine intolerance or MCAS (mast cell activation syndrome) • Asthma, eczema, or chronic allergies • Neurodegenerative diseases (like Parkinson’s, Alzheimer’s) • IBD, IBS, or leaky gut 💡 Smart Move • Read labels carefully even on “healthy” foods • Look for real, whole-food ingredients you recognize • Choose additive-free snacks, cured meats, and drinks whenever possible • Focus on home-cooked meals made from scratch 🧠 Your brain, immune system, and gut all respond to what you eat. Eliminating synthetic additives can bring surprising improvements in mood, energy, and inflammation. #FoodAdditives #Inflammation #GutHealth #BrainHealth #HistamineIntolerance #CleanEating #Neuroinflammation #ADHD

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

🍎 FODMAPs & Fermentable Carbs: Gut Triggers for Sensitive Individuals Examples: Onions, garlic, apples, lentils, wheat, dairy 🤔 What Are FODMAPs? FODMAPs are a group of short-chain carbohydrates and sugar alcohols that are poorly absorbed in the small intestine. They ferment in the colon, producing gas, bloating, and distension, especially in sensitive individuals. FODMAP = Fermentable Oligosaccharides, Disaccharides, Monosaccharides, and Polyols 🔥 Why They Can Be Inflammatory For people with gut vulnerabilities, FODMAPs can: • Increase intestinal permeability (leaky gut) • Feed dysbiotic bacteria, fueling bloating and inflammation • Activate mast cells, releasing histamine and cytokines • Disrupt serotonin balance, affecting mood, focus, and energy since ~90% of serotonin is made in the gut 🚨 Who Should Watch Out? You may benefit from a low-FODMAP approach if you’re dealing with: • IBS (Irritable Bowel Syndrome) • SIBO (Small Intestinal Bacterial Overgrowth) • IBD (Crohn’s, colitis) • Histamine intolerance / Mast cell activation • Mood swings, anxiety, or depression • Chronic fatigue (ME/CFS) 💡 Pro Tip FODMAPs aren’t “bad” — many are found in healthy whole foods. But for sensitive guts, temporary reduction can relieve symptoms while you: • Heal the gut lining • Rebalance the microbiome • Calm immune and mast cell overactivity Once stable, many people can reintroduce moderate FODMAPs successfully. 📋 Consider working with a practitioner to guide elimination and reintroduction phases for optimal results. #FODMAPs #GutHealth #LeakyGut #IBS #SIBO #HistamineIntolerance #MoodHealing #Inflammation #MicrobiomeHealth #GutHealing #ChronicFatigue #NutritionTips #functionalmedicine

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

✅ Conclusion: Remove the Fuel, Ignite the Healing Certain foods can fuel inflammation at every level by disrupting immune regulation, damaging the gut lining, feeding harmful microbes, and impairing mitochondrial energy. For those with autoimmune diseases, neurological conditions, hormonal imbalances, or chronic fatigue, even seemingly “normal” foods may be silently sabotaging recovery. But here’s the good news: 🌿 Removing dietary triggers even for 30–60 days can create a dramatic shift in how your body functions. Many experience: • Reduced joint pain and bloating • Clearer thinking and more stable mood • Better skin, digestion, and sleep • Renewed energy and vitality 🛠️ Take Action: Reclaim Your Health with a Root-Cause Approach Start with a simple elimination protocol, removing common inflammatory foods and focusing on: • Leafy greens and cruciferous vegetables • Healthy fats (olive oil, avocado, coconut, omega-3s) • Clean protein sources (grass-fed, pasture-raised, wild-caught) • Gut-healing foods (bone broth, fermented veggies, herbs) After 30–60 days, reintroduce foods one at a time, tracking how your body responds physically, mentally, and emotionally. This process helps you decode your body’s signals, rebuild resilience, and make empowered food choices for life. 🧠 Your diet isn’t just fuel it’s information. Removing inflammatory inputs allows your body’s innate intelligence to reset, repair, and thrive. #Inflammation #HealingJourney #AutoimmuneRecovery #EliminationDiet #GutHealing #Mitochondria #ChronicIllness #FoodAsMedicine #EmpoweredHealing

@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

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@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝

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Saved - June 19, 2025 at 10:16 AM
reSee.it AI Summary
The conversation began with a strong defense of a country and its people. In response, another participant criticized the speaker for avoiding physical confrontation and drew a controversial comparison to a political situation. A third participant shifted the focus to concerns about vaccine safety, alleging significant harm and calling for more awareness regarding vaccine-related issues. They emphasized the importance of discussing these topics and provided a list of experts who share their views on vaccine harms.

@TheNotoriousMMA - Conor McGregor

You wont speak bad about my country and its people and thats ever. Vote McGregor 🇮🇪

@jacksonhinklle - Jackson Hinkle 🇺🇸

@TheNotoriousMMA BIG TALK for a man who is TOO SCARED to fight with his hands ever again — just like the genocidal Israelis that you support 🇮🇱 You are a disgrace to your BEAUTIFUL country! 🇮🇪

@MeasslainteIRL - Thomas Anthony III

Everyone is oblivious to vaccine harms and the death and carnage caused by the introduction of mRNA Why is nobody talking about the genocide ? Sticks and stones may break my bones, but silence and lies kill millions. Below is a list of subject matter experts publishing the truth. Decades of experience. https://t.co/mk0QeVFkH5 Vaccine harms listed below, look into them !

@MeasslainteIRL - Thomas Anthony III

@indepdubnrth The COVID-19 chimeric genetic injections the ones they called “safe and effective.” Jonestown jabs They are experimental biotechnologies. And mounting scientific evidence demands honest, urgent re-evaluation. Independent researchers and pathologists have sounded the alarm:

Saved - June 19, 2025 at 9:58 AM
reSee.it AI Summary
I shared insights on how to defend my genome and restore immune balance using natural food-based compounds. I outlined 10 disrupted pathways and suggested foods to address them, such as broccoli sprouts for mutagenesis and pomegranate for p53 suppression. I emphasized the importance of compounds like Baicalin, which supports multiple pathways, including detox and inflammation control. I also provided a resilience routine featuring various foods and supplements to enhance health. Always consult a practitioner for personalized advice.

@MeasslainteIRL - Thomas Anthony III

How to defend your genome, protect your mitochondria, and recover immune balance using natural food-based compounds 🌱 A breakdown of 10 disrupted pathways (and how to fix them 🧵⤵️ 1. Insertional Mutagenesis 🧬 Contaminated plasmid DNA can insert into your genome → trigger mutations or activate oncogenes. 🛡️ Eat: Broccoli sprouts (Sulforaphane) Turmeric + pepper (Curcumin) Blueberries & grapes (Resveratrol) #GenomeIntegrity

@MeasslainteIRL - Thomas Anthony III

p53 Suppression 💣 p53 = “guardian of the genome.” When it's silenced, cancer risk skyrockets. 🛡️ Eat: Pomegranate (Ellagic acid) Red onions, apples (Quercetin) Pumpkin seeds, oysters (Zinc) Chinese skullcap (Baicalin) → Activates p53, induces apoptosis

@MeasslainteIRL - Thomas Anthony III

PD-L1 & IgG4 Immune Escape 🦠 Viruses & tumors cloak themselves by raising PD-L1 and shifting to IgG4. 🛡️ Strip the cloak with: Apigenin herbs (chamomile, parsley) Berberine (Th1/Th17 support) Reishi, Turkey Tail (mushrooms FTW) #ImmuneCheckpoints

@MeasslainteIRL - Thomas Anthony III

Overactive cGAS-STING 🔥 Overstimulated DNA sensors = chronic inflammation, fatigue, even autoimmunity. 🛡️ Cool it with: Green tea (EGCG) Omega-3s (EPA/DHA) Boswellia (frankincense resin) Baicalin — calms STING & NF-κB 🔧🧬 #AutoimmuneRelief

@MeasslainteIRL - Thomas Anthony III

Oncogenic microRNAs (OncomiRs) 🎯 These bad miRNAs silence tumor suppressor genes post-transcriptionally. 🛡️ Restore balance with: Curcumin Genistein (soy) Pomegranate, green tea Baicalin reprograms cancer-related miRNA profiles 🧬✨ #epigenetics

@MeasslainteIRL - Thomas Anthony III

SV40 Promoter Activation ⚠️ Some DNA vectors contain SV40 — an old viral promoter that can turn on dangerous genes. 🛡️ Buffer it with: Cruciferous veggies (DIM) Tart cherries (Melatonin) Parsley, celery (Apigenin) #ViralSilencing

@MeasslainteIRL - Thomas Anthony III

TLR Suppression = Immune Blindness 👁️ TLRs = sensors for viruses. If they're down, viruses slip by unnoticed. 🛡️ Restore detection with: Beta-glucans (mushrooms, oats) D3 (sunlight or food) Garlic, astragalus Baicalin activates TLR4, restores innate vigilance 🛡️ #TLRRescue

@MeasslainteIRL - Thomas Anthony III

Antigen Presentation (MHC I/II) 📡 If T cells can’t see the threat, they can’t kill it. That’s MHC dysfunction. 🛡️ Boost visibility with: NAC EGCG Ginger + Sea Moss (zinc + iodine) #ImmuneAlert

@MeasslainteIRL - Thomas Anthony III

NRF2 Dysfunction = Broken Detox 🧹 NRF2 is your antioxidant master switch. If it’s blocked, you're toxic. 🛡️ Activate NRF2 with: Broccoli sprouts (Sulforaphane) Milk thistle (Silymarin) Black seed oil, cayenne Baicalin potent NRF2 activator + liver support 🔥 #DetoxPathways

@MeasslainteIRL - Thomas Anthony III

Methylation Malfunctions 🧬🔒 Environmental toxins can silence your best genes via hypermethylation. 🛡️ Unlock resilience with: EGCG (green tea, cacao) Folate-rich foods (liver, greens) Magnesium, chlorophyll, sea moss #GeneExpression

@MeasslainteIRL - Thomas Anthony III

🌟#Baicalin The Pathway Ninja 🌿 Impacts ALL of these: ✔️ p53 repair ✔️ TLR4 immune reboot ✔️ STING inflammation control ✔️ NRF2 detox ✔️ miRNA cancer defense 🎯 Found in: Chinese skullcap (Scutellaria baicalensis) If Nature Didn’t Make It Don’t F*cking Take It. Knowledge is Power. Your cells want to heal give them the tools. 🧬 Follow @MeasslainteIRL 🌐 http://Measslainte.ie #SpikeProtein #DNAContamination #StopTheShot #NaturalImmunity

Meas Slainte Discover Nutritional Supplements for Multiple Sclerosis and other Demyelination Illnesses measslainte.ie

@MeasslainteIRL - Thomas Anthony III

🌟 Bonus Allies That Support Multiple Pathways CompoundKey BenefitsPathways Impacted Black Seed OilDNA protection, immune tuning, p53 activationp53, NRF2, PD-L1, Epigenetics CayenneAnti-inflammatory, improves circulationp53, NRF2, cGAS-STING Mucuna (L-DOPA)Neuroprotection, dopamine, DNA repair supportNRF2, DNA repair, fatigue BoronHormone modulator, mineral balanceNRF2, methylation CoQ10 + PQQMitochondrial repair, anti-fatigueNRF2, DNA repair Example Resilience Routine Morning: Lemon water with ginger, turmeric, cayenne Black seed oil Sea moss smoothie Midday: Broccoli sprouts, garlic, onions, mushrooms Leafy greens, pomegranate, parsley Green tea, chamomile, cacao nibs Evening: Tart cherry juice Magnesium glycinate Optional: Melatonin, ashwagandha, CBD oil Not medical advice for educational purposes please always speak with your practitioner.

@MeasslainteIRL - Thomas Anthony III

@Reseeit save thread

Saved - June 17, 2025 at 2:59 AM
reSee.it AI Summary
The discussion centers on the SIRT-1 pathway and its connection to neurotoxicity in ALS, particularly through elevated miR-34a levels. Participants share relevant studies linking myeloid-derived suppressor cells (MDSCs) and neuroinflammation. They explore natural compounds like curcumin, resveratrol, and apigenin, which may modulate pathways related to miR-34a and NF-κB signaling, potentially offering neuroprotective effects. The conversation highlights the need for further research on these natural modulators compared to conventional ALS treatments.

@Thefish751855 - Thefish

@MeasslainteIRL I've been working on this today (FYI @AnneliseBocquet), but related to the SIRT-1 pathway. All these are related. In short, elevated miR-34a is linked to neurotoxicity, and dysregulated miRNAs are the hallmark of ALS, but it's complicated. https://pmc.ncbi.nlm.nih.gov/articles/PMC8921154/

Insights into the identification of a molecular signature for amyotrophic lateral sclerosis exploiting integrated microRNA profiling of iPSC-derived motor neurons and exosomes Amyotrophic lateral sclerosis (ALS) is a rare neurodegenerative disorder characterized by progressive degeneration of motor neurons (MNs). Most cases are sporadic, whereas 10% are familial. The pathological mechanisms underlying the disease are ... pmc.ncbi.nlm.nih.gov

@Thefish751855 - Thefish

@MeasslainteIRL @AnneliseBocquet Linking our studies: https://pubmed.ncbi.nlm.nih.gov/24780820/ The Influence of Myeloid-Derived Suppressor Cell Expansion in Neuroinflammation and Neurodegenerative Diseases https://pubmed.ncbi.nlm.nih.gov/38607083/

miR-34a expands myeloid-derived suppressor cells via apoptosis inhibition - PubMed Myeloid-derived suppressor cells (MDSCs) are a heterogeneous population and show significant expansion under pathological conditions. microRNA plays important roles in many biological processes, whether microRNAs have a function in the expansion of MDSCs is still not very clear. In this study, miR-3 … pubmed.ncbi.nlm.nih.gov
The Influence of Myeloid-Derived Suppressor Cell Expansion in Neuroinflammation and Neurodegenerative Diseases - PubMed The neuro-immune axis has a crucial function both during physiological and pathological conditions. Among the immune cells, myeloid-derived suppressor cells (MDSCs) exert a pivotal role in regulating the immune response in many pathological conditions, influencing neuroinflammation and neurodegenera … pubmed.ncbi.nlm.nih.gov

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

https://pubmed.ncbi.nlm.nih.gov/28652929/ "TNF-α binding to TNF-R1 can activate the transcription factor NFκB. Our laboratory has recently observed an NFκB binding site on the promotor region of microRNA-34a (miR-34a). " Linked directly to the SARS-COV-2 and anti-covid injections... https://pubmed.ncbi.nlm.nih.gov/35588734/ https://pmc.ncbi.nlm.nih.gov/articles/PMC10145134/

TNF-α and Beyond: Rapid Mitochondrial Dysfunction Mediates TNF-α-Induced Neurotoxicity - PubMed This short communication describes our research which demonstrates that TNF-α causes a rapid decline in mitochondrial function, leading to neuronal cell death. As such, this neurotoxic proinflammatory cytokine may play a role in brain damage from stroke and neurodegeneration in chronic conditions su … pubmed.ncbi.nlm.nih.gov
TNF-α+ CD4+ T cells dominate the SARS-CoV-2 specific T cell response in COVID-19 outpatients and are associated with durable antibodies - PubMed Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-specific CD4+ T cells are likely important in immunity against coronavirus 2019 (COVID-19), but our understanding of CD4+ longitudinal dynamics following infection and of specific features that correlate with the main … pubmed.ncbi.nlm.nih.gov
COVID-19 mRNA Vaccines: The Molecular Basis of Some Adverse Events Each injection of any known vaccine results in a strong expression of pro-inflammatory cytokines. This is the result of the innate immune system activation, without which no adaptive response to the injection of vaccines is possible. Unfortunately, ... pmc.ncbi.nlm.nih.gov

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

@Thefish751855 @MeasslainteIRL This is really interesting @Thefish751855!!! MDSCs are bound to IL-10, which increases ACE2 expression. If miR-34a is also bound to MDSCs, we have a direct connection to RAGE!

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Oui... une fois n'est pas coutume... https://actaneurocomms.biomedcentral.com/articles/10.1186/s40478-023-01647-1 Augmentation de l'expression d'ACE2 dans la maladie d’Alzheimer. Je répète : Augmentation de l'expression d'ACE2 dans la maladie d’Alzheimer. Me rappelle d'un grand scientifique qui m'a dit que je me trompais. 😐

Higher angiotensin-converting enzyme 2 (ACE2) levels in the brain of individuals with Alzheimer’s disease - Acta Neuropathologica Communications Cognitive decline due to Alzheimer’s disease (AD) is frequent in the geriatric population, which has been disproportionately affected by the COVID-19 pandemic. In this study, we investigated the levels of angiotensin-converting enzyme 2 (ACE2), a regulator of the renin-angiotensin system and the main entry receptor of SARS-CoV-2 in host cells, in postmortem parietal cortex samples from two independent AD cohorts, totalling 142 persons. Higher concentrations of ACE2 protein (p < 0.01) and mRNA (p < 0.01) were found in individuals with a neuropathological diagnosis of AD compared to age-matched healthy control subjects. Brain levels of soluble ACE2 were inversely associated with cognitive scores (p = 0.02) and markers of pericytes (PDGFRβ, p = 0.02 and ANPEP, p = 0.007), but positively correlated with concentrations of soluble amyloid-β peptides (Aβ) (p = 0.01) and insoluble phospho-tau (S396/404, p = 0.002). However, no significant differences in ACE2 were observed in the 3xTg-AD mouse model of tau and Aβ neuropathology. Results from immunofluorescence and Western blots showed that ACE2 protein is predominantly localized in microvessels in the mouse brain whereas it is more frequently found in neurons in the human brain. The present data suggest that higher levels of soluble ACE2 in the human brain may contribute to AD, but their role in CNS infection by SARS-CoV-2 remains unclear. actaneurocomms.biomedcentral.com

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Oh... les astrocytes sont des targets du SARS-CoV-2... waouh, quelle surprise (en fait, non, pas du tout). https://t.co/ZcXucnbHz1 https://t.co/2w5BwmkG5S Les astrocytes, c'est quoi ? Ce sont des cellules gliales constituant notre cerveau... Le cerveau n'est pas constitué que https://t.co/sghCnOHJ9r

@P_McCulloughMD - Peter A. McCullough, MD, MPH®

SARS-CoV-2 Spike Protein Accelerates Alzheimer’s Disease Via Increased ACE2-Mediated Cerebrovascular Inflammation Pandemic Could Lead to Expanded Dementia Population Needing Care These data are worrisome given the ubiquity of Spike protein we assume is retained after SARS-CoV-2

@MeasslainteIRL - Thomas Anthony III

@AnneliseBocquet @Thefish751855 @53v3n0fn1n3 @Fynnderella1 @kacdnp91 @CanningPharm @CheweyLife @dr_morrissey @CShoemakerMD @Kevin_McKernan @KevinMcCairnPhD @LyellJ @MicieliA_MD @dredwild @bertvargas @BertVargas @djnicholl @dr_nickward @caseyalbin @AmmarAlChalabi

@CheweyLife - Angela Rhoten

@MeasslainteIRL @AnneliseBocquet @Thefish751855 @53v3n0fn1n3 @Fynnderella1 @kacdnp91 @CanningPharm @dr_morrissey @CShoemakerMD @Kevin_McKernan @KevinMcCairnPhD @LyellJ @MicieliA_MD @dredwild @BertVargas @djnicholl @dr_nickward @caseyalbin @AmmarAlChalabi @janiesaysyay @dbdugger

@MeasslainteIRL - Thomas Anthony III

🧠 Natural Strategies Targeting ALS Pathways & What They Do (Focus: P2X7, NAD+, TLR4, neuroinflammation) 1. Apigenin Found in: Parsley, celery, chamomile What it does: Inhibits P2X7 receptor activity Suppresses NF-κB signaling and TNF/IL-1β Crosses the blood-brain barrier Supports mitochondrial function 2. Baicalin Found in: Scutellaria baicalensis (Chinese skullcap) What it does: Blocks TLR4 signaling and P2X7 upregulation Reduces microglial activation Decreases oxidative stress in CNS Neuroprotective in ALS and Parkinson’s models 3. Resveratrol Found in: Red grapes, blueberries, Japanese knotweed What it does: Activates SIRT1 and boosts NAD+ levels Modulates neuroinflammation Inhibits pro-inflammatory cytokines and ROS Preserves motor neurons in ALS models 4. Curcumin Found in: Turmeric root What it does: Inhibits TLR4 and NF-κB signaling Blocks amyloid aggregation and microglial activation Reduces LPS-induced neuroinflammation Enhances gut barrier integrity 5. Luteolin Found in: Artichoke, celery, green pepper What it does: Inhibits P2X7 expression Reduces ATP-induced neurotoxicity Stabilizes mast cells and inhibits microglia Powerful antioxidant and BBB-penetrant 6. Nicotinamide (NAM) / Nicotinamide Riboside (NR) / NMN Found in: Liver, mushrooms, broccoli (precursors); supplements available What it does: Boosts NAD+ synthesis inside cells Supports mitochondrial health Enhances SIRT1 activity (key in gut/brain axis) May offset NAD+ depletion from chronic inflammation 7. Berberine Found in: Goldenseal, barberry, Oregon grape What it does: Modulates gut microbiota and reduces LPS load Protects BBB integrity Inhibits TLR4 and NLRP3 inflammasome pathways Supports autophagy and reduces oxidative stress 8. Omega-3s (DHA/EPA) Found in: Fish oil, krill oil, algae What it does: Anti-inflammatory: suppresses TLR4 and NF-κB Reduces excitotoxicity in neurons Promotes neurogenesis and synaptic repair May slow motor neuron decline 🧬 Summary Table CompoundFound InMain Actions ApigeninParsley, celery, chamomileInhibits P2X7 & NF-κB; antioxidant BaicalinChinese skullcapBlocks TLR4/P2X7; neuroprotective ResveratrolRed grapes, knotweedBoosts NAD+, activates SIRT1 CurcuminTurmericInhibits TLR4/NF-κB, gut/brain repair LuteolinArtichoke, celeryBlocks P2X7, stabilizes microglia Nicotinamide / NR / NMNSupplements or food precursorsRaise NAD+, support mitochondria BerberineGoldenseal, barberryModulates gut/LPS; TLR4 inhibitor Omega-3sFish oil, algaeAnti-inflammatory, neuron-protective ⚠️ Caution Even natural substances can interfere with medications or worsen some conditions. ALS patients should always consult a medical professional or integrative neurologist before starting new compounds.

@MeasslainteIRL - Thomas Anthony III

It challenges the reliance on conventional ALS drugs (riluzole, edaravone) by highlighting their limited efficacy, aligning with a 2023 Journal of Neurology report noting only 10-20% symptom improvement, suggesting natural modulators of TLR4 and NAD+ pathways deserve more research. 👌

@MeasslainteIRL - Thomas Anthony III

@CheweyLife @AnneliseBocquet @Thefish751855 @53v3n0fn1n3 @Fynnderella1 @kacdnp91 @CanningPharm @dr_morrissey @CShoemakerMD @Kevin_McKernan @KevinMcCairnPhD @LyellJ @MicieliA_MD @dredwild @BertVargas @djnicholl @dr_nickward @caseyalbin @AmmarAlChalabi @janiesaysyay @dbdugger I'm suspicious because grok likes it @elonmusk

@MeasslainteIRL - Thomas Anthony III

How the Natural Compounds Help 1. Curcumin Inhibits NF-κB activation (by blocking IKK and IκB phosphorylation) ↓ This could reduce miR-34a expression driven by TNF-α May restore balance between apoptosis and survival in neurons or immune cells 2. Resveratrol Suppresses TNF-α–induced NF-κB activation Inhibits IκB degradation and p65 nuclear translocation Has been shown to downregulate miR-34a in models of inflammation and cancer 3. EGCG Inhibits both TNF-α signaling and NF-κB May prevent NF-κB from binding the miR-34a promoter 4. Berberine Blocks NF-κB signaling by inhibiting TLR4 and upstream cytokines like TNF-α Berberine downregulates miR-34a in hepatic and cancer models May help prevent neuroinflammation and apoptosis 5. Apigenin Suppresses NF-κB and TNF-α Known to modulate miRNAs, including miR-34a, in inflammatory conditions 🧠 Why This Matters in ALS / Neuroinflammation miR-34a upregulation can worsen neuronal death It targets SIRT1, leading to reduced NAD⁺, more oxidative stress, and apoptosis Controlling this pathway might: Reduce neuron loss Improve immune balance Support mitochondrial and cellular repair ✅ Summary CompoundEffect on TNF/NF-κB → miR-34a Axis CurcuminInhibits NF-κB, potentially lowering miR-34a ResveratrolSuppresses TNF-α and NF-κB, lowers miR-34a EGCGBlocks NF-κB activation and TNF-α signaling BerberineInhibits NF-κB, downregulates miR-34a ApigeninReduces NF-κB activity and miR-34a expression

@MeasslainteIRL - Thomas Anthony III

@CheweyLife @AnneliseBocquet @Thefish751855 @53v3n0fn1n3 @Fynnderella1 @kacdnp91 @CanningPharm @dr_morrissey @CShoemakerMD @Kevin_McKernan @KevinMcCairnPhD @LyellJ @MicieliA_MD @dredwild @BertVargas @djnicholl @dr_nickward @caseyalbin @AmmarAlChalabi @janiesaysyay @dbdugger @elonmusk I wonder how many doctors tell their patients to drink green tea ? https://t.co/XXvbrVyHnB

Saved - June 17, 2025 at 1:53 AM
reSee.it AI Summary
The discussion centers on Lou Gehrig’s Disease (ALS) and potential solutions. The Spike protein from COVID-19 may worsen ALS by inducing neuroinflammation through purinergic receptors like P2X7. Current ALS treatments are limited, prompting exploration of new targets, including purinergic modulation and boosting NAD+ levels. Researchers link elevated miR-34a to neurotoxicity in ALS, while myeloid-derived suppressor cells may influence neuroinflammation. The conversation highlights ongoing research and connections between various biological pathways related to ALS and COVID-19.

@MeasslainteIRL - Thomas Anthony III

Lou Gehrig’s Disease – Are We Looking for Solutions!? Amyotrophic Lateral Sclerosis (ALS) – also known as Lou Gehrig’s disease (or Charcot’s disease in Europe) – is characterized by the degeneration of motor neurons and leads to debilitating and potentially fatal symptoms. https://pmc.ncbi.nlm.nih.gov/articles/PMC10886908/ The Spike protein – whether from the virus itself or from COVID-19 injections – can induce or contribute to inflammation in the nervous system, triggering ALS or worsening the condition in people already affected. Specifically, the Spike can affect purinergic receptors, especially P2X4 and P2X7. The P2X7 receptor is particularly concerning, as it plays a central role in neuroinflammation and pain. Interestingly, P2X7 expression increases when TLR4 is stimulated by LPS (lipopolysaccharide) in microglial and astrocyte cells – both of which are part of the central nervous system (CNS). Microglia are the CNS’s resident immune cells, responsible for removing toxic threats — but they can become pro-inflammatory. P2X7 is a hallmark of this pro-inflammatory state in microglia. To note: the Spike protein interacts with LPS, potentially due to leaky gut (intestinal barrier dysfunction), and also with amyloid beta (Aβ42) fibers. These complexes — Spike/LPS or Spike/Aβ42 — can fully activate the TLR4 receptor. https://www.cureus.com/articles/218170-impact-of-the-sars-cov-2-spike-protein-on-the-innate-immune-system-a-review#!/ With a compromised blood-brain barrier, these Spike-related molecular complexes can cross into the CNS, triggering TLR4, and increasing P2X7 expression. P2X7 can also be stimulated by extracellular ATP, which is released during inflammation. When there's reduced ectonucleotidase activity (particularly Ado, short for adenosine), the overexpression of P2X7 becomes dangerous. Adenosine helps break down extracellular ATP — so if Ado is low, ATP accumulates and further stimulates P2X7, ramping up inflammation. Adenosine is also tied to NAD+ https://pmc.ncbi.nlm.nih.gov/articles/PMC9512238/ Another point: P2X7 is a gateway receptor not just for SARS-CoV-2, but also for HIV. That’s yet another similarity between these two viruses. All in all, targeting P2X7 is a promising strategy, and research is ongoing. https://pmc.ncbi.nlm.nih.gov/articles/PMC9877316/ Currently, the main medications approved for ALS treatment include riluzole, edaravone, and tauroursodiol/sodium phenylbutyrate. While they offer some benefits, due to ALS’s severity and the lack of a definitive cure, new pharmaceutical targets must be explored. Purinergic modulation has shown promising results in ALS management, and additional strategies could include: Anti-inflammatory and anti-apoptotic compounds Reducing oxidative stress Modulating neuronal ion channels One promising avenue: boosting NAD+ to provide some immediate support. Oral supplementation with NAD+ precursors like: Nicotinamide (NAM) Nicotinamide riboside (NR) Nicotinamide mononucleotide (NMN) …could help. These are converted into NAD+ via biosynthesis pathways inside cells. However, this is only a short-term aid if the underlying causes of NAD+ depletion aren't addressed. https://pmc.ncbi.nlm.nih.gov/articles/PMC9512238/ Note: NAD+ is linked to SIRT1, which plays a role in maintaining intestinal barrier integrity and supporting the commensal (beneficial) gut flora. Follow Annelises work 👌 #ALS #NAD+ #NMN #SIRT1 #P2X7 #TLR4

Amyotrophic Lateral Sclerosis in Long-COVID Scenario and the Therapeutic Potential of the Purinergic System in Neuromodulation Amyotrophic lateral sclerosis (ALS) involves the degeneration of motor neurons and debilitating and possibly fatal symptoms. The COVID-19 pandemic directly affected the quality of life of this group, and the SARS-CoV-2 infection accelerated the ... pmc.ncbi.nlm.nih.gov
Impact of the SARS-CoV-2 Spike Protein on the Innate Immune System: A Review The Spike protein enables the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection by binding to multiple receptors, including the angiotensin-converting enzyme 2 (ACE2). Scientific studies also indicate that Spike is involved in severe forms of coronavirus disease 2019 (COVID-19), "long-haul COVID diseases" - also known as "long COVID syndromes" or "post-acute sequelae of SARS-CoV-2 infection" (PACS) - or, recently, in adverse reactions to lipid nanoparticle-messenger ribonucleic acid (mRNA) vaccines or other anti-COVID19 products. Numerous mutations, notably within the subunit 1 of Spike (S1), prevent neutralization by antibodies, but more generally, the virus has developed numerous strategies to avoid immune system surveillance, especially type-I interferons (IFN-I). Meanwhile, a “hyperinflammatory” state, named “cytokine storm,” sets in. However, what role does the Spike protein play in the immune escape mechanisms? Can its inflammatory activities affect IFN-I? Does Spike block IFN-I or hijack them for the virus benefits? What are the other potential consequences? This article was written to provide an up-to-date and more general overview of the impact of the Spike protein on the innate immune system and its effectors at the molecular level. cureus.com
The Role of NAD+ in Regenerative Medicine The understanding of the molecular and cellular basis of aging has grown exponentially over recent years, and it is now accepted within the scientific community that aging is a malleable process; just as it can be accelerated, it can also be slowed ... pmc.ncbi.nlm.nih.gov
Identification of a novel P2X7 antagonist using structure-based virtual screening P2X4 and P2X7 receptors are ATP-gated ion channels, which play important roles in neuropathic and inflammatory pain, and as such they are important drug targets in diseases of inflammatory origin. While several compounds targeting P2X4 and P2X7 ... pmc.ncbi.nlm.nih.gov
The Role of NAD+ in Regenerative Medicine The understanding of the molecular and cellular basis of aging has grown exponentially over recent years, and it is now accepted within the scientific community that aging is a malleable process; just as it can be accelerated, it can also be slowed ... pmc.ncbi.nlm.nih.gov

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Oh, et bien... perturbations de la barrière hémato-encéphalique dans des cas de covid-long... et une approche d'exploration médicale envisagée. Cet article est intéressant ⤵️ https://bmcneurol.biomedcentral.com/articles/10.1186/s12883-025-04133-4 "Notre étude suggère que l'IC PASC/covid long est au moins en partie liée à une

Asymmetrical glymphatic dysfunction in patients with long Covid associated neurocognitive impairment- correlation with BBB disruption - BMC Neurology The glymphatic system, a waste clearance pathway, has been implicated in several neurological conditions associated with neuroinflammation. COVID-19 associated neurocognitive impairment, part of the post-acute sequelae of SARS-CoV-2 infection (PASC), is strongly associated with neuroinflammation and disrupted blood-brain barrier (BBB). Several studies have implicated a synergistic interaction between the glymphatic system dysfunction and BBB disruption. In this proof-of-concept study, we investigated the role of the MRI metric diffusion along the perivascular spaces DTI (DTI-ALPS) in patients with PASC and correlated this with the BBB capillary permeability metric- K trans derived from Dynamic contrast enhanced (DCE) perfusion. 14 subjects with PASC who had persisting symptoms of anosmia, ageusia, fatigue, and cognitive impairment (CI) and ten healthy age and sex matched controls were recruited. All PASC subjects underwent routine and advanced MR brain imaging at two time points, (3 months +/- 2 weeks) after initial infection - referred as Time Point 1 (TP-1) - and 10 repeated the MRI scan 12 months (+/- 2 weeks) later - referred as Time Point 2 (TP-2), while the controls had MR imaging done only at TP-1. All had mild neurocognitive impairment. In the final analysis we included those who had DTI study at both time points (n-10). MR imaging included DCE perfusion and DTI in addition to anatomical imaging. Given the small size of the sample and nonnormality of data in the descriptive analyses, nonparametric analyses were used for group comparisons. A two-sample Wilcoxon rank sum test was used to show the differences in DTI-ALPS between the patients and controls in the predefined regions of interest. Spearman’s correlation coefficient (rho) was used to assess the correlation between DTI-ALPS index with K trans. There was significant reduction in the DTI-ALPS index between the patients and controls in the left hemisphere (z = 2.04, p < 0.04). However, there was no significant change over time in the index. There was a strong inverse correlation between the central white matter K trans and DTI-ALPS index (rho = 0.66, p < 0.03). Our study indicates that disordered para vascular drainage, a marker for glymphatic system and BBB damage may contribute to neurocognitive impairment (NCI) among patients with PASC. The DTI-ALPS index, which does not require contrast injection, has the potential to serve as a non-invasive biomarker. bmcneurol.biomedcentral.com

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Non seulement il stipule qu'il y a surexpression du TLR2/ TLR4 mais il ajoute qu'il y a une augmentation de l'expression du P2X7... c'est une bombe à retardement. Il y a une reprogrammation du SI, sur le long-terme, particulièrement au niveau des macrophages. 24/n

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Bien, résumé de la partie 1 : SIRT1 inhibe p53 pour éviter l'apoptose cellulaire. Et p53 inhibe SIRT1 via miR-34a pour exercer son activité, créant une boucle d'amplification apoptotique. Bizarrement, on retrouve une stimulation de p53 après les injections anti-covid dans les

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Maladie de Charcot, on cherche des solutions !? La sclérose latérale amyotrophique (SLA) - ou maladie de Charcot - se caractérise par une dégénérescence des motoneurones et des symptômes invalidants, potentiellement mortels. https://pmc.ncbi.nlm.nih.gov/articles/PMC10886908/ La Spike, celle du virus ET des injections anti-covid, peut induire ou contribuer au développement d'une inflammation dans le système nerveux, déclenchant la SLA, ou aggravant l'état des personnes atteintes de cette maladie. De fait, la Spike peut impacter les récepteurs purinergiques, notamment P2X4 et P2X7. Ce dernier, le récepteur P2X7, est particulièrement sensible car il joue un rôle important dans la neuroinflammation et... dans la douleur. De façon intéressante, l'expression de ce récepteur, P2X7, est accrue suite à une stimulation du TLR4 par le LPS, au niveau des cellules microgliales ou des astrocytes. Ces cellules sont constitutives du système nerveux central, la microglie (ou cellules microgliales) représentant les cellules immunitaires innées résidentes dans le système nerveux. Elles sont en charge d'éliminer les éléments potentiellement toxiques pour le système nerveux... et elles peuvent prendre un phénotype pro-inflammatoires. P2X7 appartient au phénotype pro-inflammatoire de la microglie. Pour mémoire, la Spike interagit avec le LPS, provenant potentiellement d'une perturbation de la barrière intestinale. La Spike interagit aussi avec les fibres Aβ42. Les complexes moléculaires "Spike/LPS" ou "Spike/Aβ42" peuvent activer le TLR4 complètement. Avec la perturbation de la barrière hémato-encéphalique, ces complexes moléculaires "Spike/LPS" ou "Spike/Aβ42" peuvent alors activer le TLR4 et accroître l'expression du P2X7. Le P2X7 est aussi stimulé par l'ATP extracellulaire, libéré lors d'une inflammation. Corrélé à une diminution d'ectonucleotidase, Ado notamment, la surexpression de P2X7 est une bombe explosive. En effet, Ado dégrade l'ATP extracellulaire... si Ado est diminué, alors on aura une accumulation d'ATP extracellulaire qui vont activer d'autant plus P2X7 et entraîner une inflammation importante. Ado est lié au NAD+ ... https://pmc.ncbi.nlm.nih.gov/articles/PMC7887318/ Autre point : le récepteur P2X7 est une clé pour le VIH... et le SARS-COV-2. Oui, encore un point commun entre ces deux virus. Quoiqu'il en soit, cibler P2X7 est une piste intéressante. C'est en cours de recherche... https://pmc.ncbi.nlm.nih.gov/articles/PMC9877316/ Actuellement, les principaux médicaments approuvés dans différentes régions du monde pour le traitement de la SLA sont le riluzole, l'édaravone et le tauroursodiol/phénylbutyrate de sodium. Malgré les effets positifs de ces médicaments, compte tenu de la gravité de la SLA et de l'absence d'un traitement final efficace pour cette maladie neurodégénérative, davantage de cibles pharmaceutiques doivent être explorées... la modulation purinergique a présenté des résultats très intéressants dans le contrôle de la SLA mais il est aussi possible de rechercher des anti-inflammatoires et anti-apoptotiques, de réduire le stress oxydatif et moduler les activités des canaux ioniques neuronaux. Favoriser le NAD+ est une piste potentielle pour tenter de soulager en immédiat. https://pmc.ncbi.nlm.nih.gov/articles/PMC9512238/ La supplémentation orale en composés précurseurs du NAD+ peut être envisagée  : nicotinamide (NAM), nicotinamide riboside (NR) et nicotinamide mononucléotide (NMN). Ces précurseurs sont utilisés par les voies de biosynthèse du NAD+ et convertis en NAD+ dans la cellule. Mais ce sera à court terme si on ne traite pas les causes profondes de cette déprivation en NAD+. Nota bene : NAD+ lié à SIRT1. Cela peut aider au maintien de la barrière intestinale et de la flore commensale. Bonne journée !

Amyotrophic Lateral Sclerosis in Long-COVID Scenario and the Therapeutic Potential of the Purinergic System in Neuromodulation Amyotrophic lateral sclerosis (ALS) involves the degeneration of motor neurons and debilitating and possibly fatal symptoms. The COVID-19 pandemic directly affected the quality of life of this group, and the SARS-CoV-2 infection accelerated the ... pmc.ncbi.nlm.nih.gov
Ectonucleotidases in Acute and Chronic Inflammation Ectonucleotidases are extracellular enzymes with a pivotal role in inflammation that hydrolyse extracellular purine and pyrimidine nucleotides, e.g., ATP, UTP, ADP, UDP, AMP and NAD+. Ectonucleotidases, expressed by virtually all cell types, immune ... pmc.ncbi.nlm.nih.gov
Identification of a novel P2X7 antagonist using structure-based virtual screening P2X4 and P2X7 receptors are ATP-gated ion channels, which play important roles in neuropathic and inflammatory pain, and as such they are important drug targets in diseases of inflammatory origin. While several compounds targeting P2X4 and P2X7 ... pmc.ncbi.nlm.nih.gov
The Role of NAD+ in Regenerative Medicine The understanding of the molecular and cellular basis of aging has grown exponentially over recent years, and it is now accepted within the scientific community that aging is a malleable process; just as it can be accelerated, it can also be slowed ... pmc.ncbi.nlm.nih.gov

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Voici la première partie des explications concernant l'article 'impacts de la protéine Spike du SARS-CoV-2 sur l'immunité innée : une revue'. Ci-joint le lien vers l'article. https://www.cureus.com/articles/218170-impact-of-the-sars-cov-2-spike-protein-on-the-innate-immune-system-a-review#!/

Video Transcript AI Summary
**French Summary:** Anaïs Bloqué explique l'impact de la protéine Spike du SARS-CoV-2 sur le système immunitaire inné, en se concentrant sur le TLR 4. La Spike seule n'active pas complètement le TLR 4 pour induire une réponse antivirale complète (interférons de type 1). L'association Spike-LPS (lipopolysaccharide bactérien) est nécessaire. L'activation des interférons 1 augmente l'expression d'ACE2, récepteur du virus, via les ISG, sensibilisant l'organisme à l'infection. Les ARN messagers des vaccins peuvent aussi activer les interférons 1 via MDA5. La Spike, protéine amyloïde, peut induire la production de fibres A bêta 42, aggravant l'inflammation. L'augmentation de NF-κB par les ISG peut bloquer p53 (suppresseur de tumeur) et induire le micro-ARN MIR-200c, diminuant l'expression d'ACE2. Chez les personnes avec comorbidités (diabète, obésité), une boucle d'amplification inflammatoire Spike-LPS-TLR4 réduit l'ACE2 disponible, menant à une suractivation de l'angiotensine 2. La Spike persistante pourrait causer des pathologies dégénératives à long terme. **English Translation:** Anaïs Bloqué explains the impact of the SARS-CoV-2 Spike protein on the innate immune system, focusing on TLR 4. Spike alone does not fully activate TLR 4 to induce a complete antiviral response (type 1 interferons). The Spike-LPS (bacterial lipopolysaccharide) association is necessary. Activation of interferon 1 increases ACE2 expression, the virus receptor, via ISGs, sensitizing the body to infection. Vaccine mRNAs can also activate interferon 1 via MDA5. Spike, an amyloid protein, can induce the production of A beta 42 fibers, worsening inflammation. Increased NF-κB by ISGs can block p53 (tumor suppressor) and induce microRNA MIR-200c, decreasing ACE2 expression. In people with comorbidities (diabetes, obesity), a Spike-LPS-TLR4 inflammatory amplification loop reduces available ACE2, leading to overactivation of angiotensin 2. Persistent Spike could cause long-term degenerative pathologies.
Full Transcript
Speaker 0: Bonjour à tous et à toutes, je suis Anaïs Bloqué, docteur en biologie santé et enseignante d'hématologie immunologie auprès de BTS analyse biomédicale. Avant d'entrer dans le vif du sujet, je précise que je n'ai aucun conflit d'intérêt que ce soit d'ordre professionnel, financier ou privé. Récemment j'ai publié un article traitant des impacts de la protéine Spike du SARS-CoV 2 sur le système immunitaire inné et vous êtes nombreux à me demander des explications quant au contenu de ce papier. Vu le nombre de mécanismes et la complexité de ces mécanismes, j'ai décidé de morceler mes explications en 3 grandes parties, il y en aura peut-être une quatrième, ça dépendra du déroulé de mes petites interventions. Je vais commencer par vous raconter la petite histoire du TLR 4 et du et de la Spike du SARS-CoV 2. Il faut savoir que dans notre organisme, nous avons ce que l'on appelle des PRR ou Patogène Recopnishion Resator qui sont capables de détecter la présence d'éléments pathogènes et en détectant donc ces pathogènes, ces PRR s'activent pour lancer une réponse immunitaire afin de contrer bien entendu les éléments infectieux. L'un de ces PRR est le TLR 4 et il est présent donc à la surface des cellules de notre organisme. Alors la protéine Spike du SARS-CoV-deux ici représentée en rouge dans un cercle toute seule ne peut enclencher l'activation du TLR 4 dans sa totalité. Il y aura induction de cytokines pro-inflammatoires, mais pas l'induction des interférons de type un. Il faut savoir que les interférons de type un sont fondamentaux dans la réponse immunitaire antivirale. Cela va du déclenchement d'un état antiviral, c'est-à-dire la mise en place de mécanismes qui vont entraver la propagation et la réplication du virus dans l'organisme jusqu'à l'orchestration d'une réponse immunitaire innée et adaptative efficace. Alors le fait que la Spike seule ne puisse enclencher la production des interférons un est plutôt de mauvais augure car seule elle ne permet pas à l'organisme de lutter contre le virus. Pour que la Spike active le TLR 4 dans sa totalité, il faut qu'elle s'associe avec le LPS pour l'hypopolisaccharide, un composant que l'on retrouve sur les bactéries gram négatifs le combo Spike LPS va permettre l'activation du TLR 4 avec l'induction de cytokines pro-inflammatoires et l'induction d'une réponse par les interférons de type 1 le problème c'est qu'après l'initiation d'une réponse par les interférons 1 il y a l'expression de petites molécules que l'on appelle ISG pour interférons stimulated jeans certaines publications scientifiques montrent qu'il existe un lien probable entre ACE2 et les interférons de type un via les ISG dont l'ISG quatre-vingt-quinze les résultats expérimentaux suggèrent que ACE2 se comporte comme un iégé par la stimulation de certains PRRS dont MDA V on en reparlera juste après. Le hic c'est que la réponse aux interférons 1 en augmentant l'expression d'ACE2 va sensibiliser l'organisme aux infections par le SARS-CoV-2 car ACE2 est l'un des récepteurs permettant au virus d'infecter l'organisme via l'interaction Spike ACE2. Je vous vois venir vous allez me dire super donc avec un traitement antibiotique permettant de limiter le LPS il n'y aura pas induction des interférons de type 1 et donc pas d'augmentation de l'expression d'ACE2 et la spyde vaccinale ou la spydep pour de proline ne va pas indreve ne va pas induire seul les interférons 1 et donc une augmentation de ce2 bah non c'est faux car les interférons de type 1 peuvent être lancés comme je l'ai dit par les RLR dont MDA5 et ce récepteur détecte quoi Les ARN 0 et l'ARN messager modifié des produits anti covid comme Pfizer ou Moderna. De plus en dehors de cette induction des interférons 1 par mda 5 de plus il est fort probable que la Spike accompagnée de fibres amyloïdes comme les fibres a bêta quarante-deux déclenche le télaire 4. Cette protéine spike est hautement amyloïde et elle peut entraîner directement la production des fibres a bêta quarante-deux par l'organisme auquel elle peut se lier. En effet l'interaction spike a bêta quarante-deux semble accroître la production de cytokines pro-inflammatoires et n'empêche pas l'interaction entre la sous unité s un de la Spike avec son récepteur c'est-à-dire ACE 2. C'est ce que j'appelle le double effet amyloïde. En effet non seulement la spi qui est amyloïde en elle-même c'est-à-dire que si elle est clivée par des protéases elle va former des fibrilles insolubles et dégénératives, mais en plus elle induit la production de ces fibrilles amyloïdes par l'organisme lui-même comme on peut en trouver dans la maladie d'Alzheimer pouvant contribuer à quoi Ben à l'infection virale. Pour en revenir à notre TALR 4 et aux interférons de type un, les ISG comme l'ISG quatre-vingt-quinze ici figuré présentent une autre particularité cela va augmenter les niveaux de NFK pa b pour vous expliquer simplement NFK pa b est un facteur qui permet la synthèse de cytokines pro-inflammatoires comme le IL6. Il existe une autre activité du NFK ab celle de contrebalancer la p cinquante-trois le gardien de notre génome via le MDM 2 ou murine double minute 2 d'ailleurs on sait que une suractivation de NFK ab est potentiellement cancérigène par blocage de la p cinquante-trois. De plus la protéine spike et plus précisément la sous unité s 2 de la protéine spike peut interagir avec la p cinquante-trois et on ignore encore quelles en sont les conséquences. Cela peut d'ailleurs pencher en faveur d'une activité pro-inflammatoire via NFK ab. Il reste à savoir si la sous-unité s 2 de la protéine spyde dite vaccinale ou s 2 p avec ces 2 modifications proline se lie à la p cinquante-trois. Mais il existe quelques éléments de réponse qui font craindre une réponse par l'affirmative. Il existe une autre conséquence par rapport à l'augmentation de NFK pa b. Ce facteur induit l'expression de micro-éréna, donc ce sont des petites molécules qui vont agir sur le transcryptome cellulaire. Et il y a un micro-éréna qui nous intéresse particulièrement dans ce cadre dans ce cas de figure, c'est le MIR de sens C. Le MIR de sens C va bloquer, va empêcher la surexpression de la CE 2. Cela crée une sorte de balance entre la surex surexpression et la sous expression d'ACE2 cependant les études montrent que dans certains pathopathologiques notamment des pathopathologiques avec des comorbidités comme le diabète ou l'obésité les patients présentaient déjà des taux d'expression du MIR de sens C important autrement dit la quantité initiale d'ACE2 présente dans leur organisme était déjà plus faible que chez les individus sans comorbidité dans ce contexte l'interaction Spike LPS avec le TLR 4 ce qui induit les interférons de type un les I g et l'augmentation du NFK pa b avec l'expression du minière de sens c devient vraiment problématique et dangereux car hyper inflammatoire. En effet chez ces individus le peu d'ACE 2 qu'ils ont va se retrouver bloqué par la Spike par l'interaction Spike ACE 2. On sait que ACE 2 est l'un des récepteurs du virus pour infecter l'organisme via la spike. ACE 2 devient donc indisponible pour la dégradation de l'angiotensine 2 ce qui aboutit à la suractivation de la TAR et à la tempéticoatynique que l'on connaît. De façon intéressante l'angiotensine 2 va également augmenter l'expression du TLR 4 ce qui va relancer dessous dans la machine. En effet on se retrouve devant une boucle d'amplification inflammatoire avec une Spike LPS TLR 4 qui induit les interférons de type 1 qui induit les ISG qui induit d'un côté une surexpression d'ACE2 de l'autre côté une augmentation de du NF kapab avec l'expression du MIR de son C une diminution globale d'ACCE2 avec une augmentation des concentrations d'angiotensine 2 c'est enjotensine 2 augmentant l'expression du TLR 4. Donc ça, c'est une véritable boucle d'amplification. Alors ce n'est pas mortel chez tous les individus, juste ceux présentant des hauts niveaux de MIR de sens C et pourquoi parce que certaines publications relatent une diminution en fait des niveaux de MIR de millet chez des patients ayant recouvrés du SARS-CoV-2 ces chercheurs ont certainement étudié les conséquences de l'infection par le SARS-CoV-2 en dehors de toute co-infection c'est-à-dire sans LPS et en dehors de toute comorbidité mais si il y a de faibles taux du MIR de sang C en général alors plus rien n'arrête la surexpression des CE2. A partir de là l'angiotensine 2 est dégradé et il y a une activation de l'axe AT de R masse R avec la production d'iL 10. Cette iL 10 est quant à elle une cytokine anti-inflammatoire qui va aussi accroître l'expression d'ACE2 et il s'agit là d'une boucle tolrogène. Cela va expliquer pourquoi la protéine spike peut persister des mois dans l'organisme après une infection par le virus ou après les injections à ARN messager modifié en codant cette fameuse protéine car oui cette spyte persiste longtemps et avec ses propriétés amyloïdes on peut craindre des pathologies dégénératives sur le long terme avec un effet cumulatif par exposition répétée à la protéine spike alors le SARS-CoV 2 ne tue pas dans l'immédiat ce qui explique on va dire le faible nombre de décès lors des premières vagues épidémiques mais mais cela va s'inscrire dans le temps. La prochaine fois je vous raconterai l'histoire du TLR 2 puis ensuite l'histoire de l'i l 6 du MIR cent-quarante-huit a et ensuite après je verrai si je le développe sur les propriétés amyloïdes ou pas. Je vous remercie de votre attention et je vous souhaite une excellente journée.
Impact of the SARS-CoV-2 Spike Protein on the Innate Immune System: A Review The Spike protein enables the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection by binding to multiple receptors, including the angiotensin-converting enzyme 2 (ACE2). Scientific studies also indicate that Spike is involved in severe forms of coronavirus disease 2019 (COVID-19), "long-haul COVID diseases" - also known as "long COVID syndromes" or "post-acute sequelae of SARS-CoV-2 infection" (PACS) - or, recently, in adverse reactions to lipid nanoparticle-messenger ribonucleic acid (mRNA) vaccines or other anti-COVID19 products. Numerous mutations, notably within the subunit 1 of Spike (S1), prevent neutralization by antibodies, but more generally, the virus has developed numerous strategies to avoid immune system surveillance, especially type-I interferons (IFN-I). Meanwhile, a “hyperinflammatory” state, named “cytokine storm,” sets in. However, what role does the Spike protein play in the immune escape mechanisms? Can its inflammatory activities affect IFN-I? Does Spike block IFN-I or hijack them for the virus benefits? What are the other potential consequences? This article was written to provide an up-to-date and more general overview of the impact of the Spike protein on the innate immune system and its effectors at the molecular level. cureus.com

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Oh, et bien... perturbations de la barrière hémato-encéphalique dans des cas de covid-long... et une approche d'exploration médicale envisagée. Cet article est intéressant ⤵️ https://bmcneurol.biomedcentral.com/articles/10.1186/s12883-025-04133-4 "Notre étude suggère que l'IC PASC/covid long est au moins en partie liée à une

Asymmetrical glymphatic dysfunction in patients with long Covid associated neurocognitive impairment- correlation with BBB disruption - BMC Neurology The glymphatic system, a waste clearance pathway, has been implicated in several neurological conditions associated with neuroinflammation. COVID-19 associated neurocognitive impairment, part of the post-acute sequelae of SARS-CoV-2 infection (PASC), is strongly associated with neuroinflammation and disrupted blood-brain barrier (BBB). Several studies have implicated a synergistic interaction between the glymphatic system dysfunction and BBB disruption. In this proof-of-concept study, we investigated the role of the MRI metric diffusion along the perivascular spaces DTI (DTI-ALPS) in patients with PASC and correlated this with the BBB capillary permeability metric- K trans derived from Dynamic contrast enhanced (DCE) perfusion. 14 subjects with PASC who had persisting symptoms of anosmia, ageusia, fatigue, and cognitive impairment (CI) and ten healthy age and sex matched controls were recruited. All PASC subjects underwent routine and advanced MR brain imaging at two time points, (3 months +/- 2 weeks) after initial infection - referred as Time Point 1 (TP-1) - and 10 repeated the MRI scan 12 months (+/- 2 weeks) later - referred as Time Point 2 (TP-2), while the controls had MR imaging done only at TP-1. All had mild neurocognitive impairment. In the final analysis we included those who had DTI study at both time points (n-10). MR imaging included DCE perfusion and DTI in addition to anatomical imaging. Given the small size of the sample and nonnormality of data in the descriptive analyses, nonparametric analyses were used for group comparisons. A two-sample Wilcoxon rank sum test was used to show the differences in DTI-ALPS between the patients and controls in the predefined regions of interest. Spearman’s correlation coefficient (rho) was used to assess the correlation between DTI-ALPS index with K trans. There was significant reduction in the DTI-ALPS index between the patients and controls in the left hemisphere (z = 2.04, p < 0.04). However, there was no significant change over time in the index. There was a strong inverse correlation between the central white matter K trans and DTI-ALPS index (rho = 0.66, p < 0.03). Our study indicates that disordered para vascular drainage, a marker for glymphatic system and BBB damage may contribute to neurocognitive impairment (NCI) among patients with PASC. The DTI-ALPS index, which does not require contrast injection, has the potential to serve as a non-invasive biomarker. bmcneurol.biomedcentral.com

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Non seulement il stipule qu'il y a surexpression du TLR2/ TLR4 mais il ajoute qu'il y a une augmentation de l'expression du P2X7... c'est une bombe à retardement. Il y a une reprogrammation du SI, sur le long-terme, particulièrement au niveau des macrophages. 24/n

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Bien, résumé de la partie 1 : SIRT1 inhibe p53 pour éviter l'apoptose cellulaire. Et p53 inhibe SIRT1 via miR-34a pour exercer son activité, créant une boucle d'amplification apoptotique. Bizarrement, on retrouve une stimulation de p53 après les injections anti-covid dans les

@RHandiSolidaire - Reconquête Handi-Solidaire 🌿🇫🇷

https://www.laselectiondujour.com/charcot-maladie-enferme-vivant Du nom de celui qui l’a découverte en 1869, la Maladie de Charcot est une Sclérose Latérale Amyotrophique touchant 500.000 personnes à travers le monde, dont 8.000 en France. C’est une maladie neurologique dégénérative sans espoir de guérison et une

Charcot, la maladie qui enferme vivant Surnommée « la maladie la plus cruelle du monde », la sclérose latérale amyotrophique (SLA) touche près de 8 000 personnes en France. Derrière cette maladie rare et toujours incurable : patients, proches et chercheurs, se mobilisent pour alerter, sensibiliser, et surtout, faire avancer une recherche encore trop négligée. Car demain, la SLA pourrait frapper bien plus de vies qu'on ne l'imagine. laselectiondujour.com

@Thefish751855 - Thefish

@MeasslainteIRL I've been working on this today (FYI @AnneliseBocquet), but related to the SIRT-1 pathway. All these are related. In short, elevated miR-34a is linked to neurotoxicity, and dysregulated miRNAs are the hallmark of ALS, but it's complicated. https://pmc.ncbi.nlm.nih.gov/articles/PMC8921154/

Insights into the identification of a molecular signature for amyotrophic lateral sclerosis exploiting integrated microRNA profiling of iPSC-derived motor neurons and exosomes Amyotrophic lateral sclerosis (ALS) is a rare neurodegenerative disorder characterized by progressive degeneration of motor neurons (MNs). Most cases are sporadic, whereas 10% are familial. The pathological mechanisms underlying the disease are ... pmc.ncbi.nlm.nih.gov

@Thefish751855 - Thefish

@MeasslainteIRL @AnneliseBocquet Linking our studies: https://pubmed.ncbi.nlm.nih.gov/24780820/ The Influence of Myeloid-Derived Suppressor Cell Expansion in Neuroinflammation and Neurodegenerative Diseases https://pubmed.ncbi.nlm.nih.gov/38607083/

miR-34a expands myeloid-derived suppressor cells via apoptosis inhibition - PubMed Myeloid-derived suppressor cells (MDSCs) are a heterogeneous population and show significant expansion under pathological conditions. microRNA plays important roles in many biological processes, whether microRNAs have a function in the expansion of MDSCs is still not very clear. In this study, miR-3 … pubmed.ncbi.nlm.nih.gov
The Influence of Myeloid-Derived Suppressor Cell Expansion in Neuroinflammation and Neurodegenerative Diseases - PubMed The neuro-immune axis has a crucial function both during physiological and pathological conditions. Among the immune cells, myeloid-derived suppressor cells (MDSCs) exert a pivotal role in regulating the immune response in many pathological conditions, influencing neuroinflammation and neurodegenera … pubmed.ncbi.nlm.nih.gov

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

https://pubmed.ncbi.nlm.nih.gov/28652929/ "TNF-α binding to TNF-R1 can activate the transcription factor NFκB. Our laboratory has recently observed an NFκB binding site on the promotor region of microRNA-34a (miR-34a). " Linked directly to the SARS-COV-2 and anti-covid injections... https://pubmed.ncbi.nlm.nih.gov/35588734/ https://pmc.ncbi.nlm.nih.gov/articles/PMC10145134/

TNF-α and Beyond: Rapid Mitochondrial Dysfunction Mediates TNF-α-Induced Neurotoxicity - PubMed This short communication describes our research which demonstrates that TNF-α causes a rapid decline in mitochondrial function, leading to neuronal cell death. As such, this neurotoxic proinflammatory cytokine may play a role in brain damage from stroke and neurodegeneration in chronic conditions su … pubmed.ncbi.nlm.nih.gov
TNF-α+ CD4+ T cells dominate the SARS-CoV-2 specific T cell response in COVID-19 outpatients and are associated with durable antibodies - PubMed Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-specific CD4+ T cells are likely important in immunity against coronavirus 2019 (COVID-19), but our understanding of CD4+ longitudinal dynamics following infection and of specific features that correlate with the main … pubmed.ncbi.nlm.nih.gov
COVID-19 mRNA Vaccines: The Molecular Basis of Some Adverse Events Each injection of any known vaccine results in a strong expression of pro-inflammatory cytokines. This is the result of the innate immune system activation, without which no adaptive response to the injection of vaccines is possible. Unfortunately, ... pmc.ncbi.nlm.nih.gov

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

@Thefish751855 @MeasslainteIRL This is really interesting @Thefish751855!!! MDSCs are bound to IL-10, which increases ACE2 expression. If miR-34a is also bound to MDSCs, we have a direct connection to RAGE!

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Oui... une fois n'est pas coutume... https://actaneurocomms.biomedcentral.com/articles/10.1186/s40478-023-01647-1 Augmentation de l'expression d'ACE2 dans la maladie d’Alzheimer. Je répète : Augmentation de l'expression d'ACE2 dans la maladie d’Alzheimer. Me rappelle d'un grand scientifique qui m'a dit que je me trompais. 😐

Higher angiotensin-converting enzyme 2 (ACE2) levels in the brain of individuals with Alzheimer’s disease - Acta Neuropathologica Communications Cognitive decline due to Alzheimer’s disease (AD) is frequent in the geriatric population, which has been disproportionately affected by the COVID-19 pandemic. In this study, we investigated the levels of angiotensin-converting enzyme 2 (ACE2), a regulator of the renin-angiotensin system and the main entry receptor of SARS-CoV-2 in host cells, in postmortem parietal cortex samples from two independent AD cohorts, totalling 142 persons. Higher concentrations of ACE2 protein (p < 0.01) and mRNA (p < 0.01) were found in individuals with a neuropathological diagnosis of AD compared to age-matched healthy control subjects. Brain levels of soluble ACE2 were inversely associated with cognitive scores (p = 0.02) and markers of pericytes (PDGFRβ, p = 0.02 and ANPEP, p = 0.007), but positively correlated with concentrations of soluble amyloid-β peptides (Aβ) (p = 0.01) and insoluble phospho-tau (S396/404, p = 0.002). However, no significant differences in ACE2 were observed in the 3xTg-AD mouse model of tau and Aβ neuropathology. Results from immunofluorescence and Western blots showed that ACE2 protein is predominantly localized in microvessels in the mouse brain whereas it is more frequently found in neurons in the human brain. The present data suggest that higher levels of soluble ACE2 in the human brain may contribute to AD, but their role in CNS infection by SARS-CoV-2 remains unclear. actaneurocomms.biomedcentral.com

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Oh... les astrocytes sont des targets du SARS-CoV-2... waouh, quelle surprise (en fait, non, pas du tout). https://t.co/ZcXucnbHz1 https://t.co/2w5BwmkG5S Les astrocytes, c'est quoi ? Ce sont des cellules gliales constituant notre cerveau... Le cerveau n'est pas constitué que https://t.co/sghCnOHJ9r

@P_McCulloughMD - Peter A. McCullough, MD, MPH®

SARS-CoV-2 Spike Protein Accelerates Alzheimer’s Disease Via Increased ACE2-Mediated Cerebrovascular Inflammation Pandemic Could Lead to Expanded Dementia Population Needing Care These data are worrisome given the ubiquity of Spike protein we assume is retained after SARS-CoV-2

@MeasslainteIRL - Thomas Anthony III

@AnneliseBocquet @Thefish751855 @53v3n0fn1n3 @Fynnderella1 @kacdnp91 @CanningPharm @CheweyLife @dr_morrissey @CShoemakerMD @Kevin_McKernan @KevinMcCairnPhD @LyellJ @MicieliA_MD @dredwild @bertvargas @BertVargas @djnicholl @dr_nickward @caseyalbin @AmmarAlChalabi

@janiesaysyay - Janiesaysyay

@MeasslainteIRL @AnneliseBocquet @Thefish751855 @53v3n0fn1n3 @Fynnderella1 @kacdnp91 @CanningPharm @CheweyLife @dr_morrissey @CShoemakerMD @Kevin_McKernan @KevinMcCairnPhD @LyellJ @MicieliA_MD @dredwild @BertVargas @djnicholl @dr_nickward @caseyalbin @AmmarAlChalabi https://t.co/mtHA79OUWW

@HerbsandDirt - Carole Mac

Another ALS diagnosis for someone who admitted getting the Covid 💉, and also pushed people to get it. How many people is this now? Other than Alzheimer’s Disease, I can’t think of a worse ailment to live with. Heartbreaking. .@unhealthytruth https://t.co/Bmphdlkb47

@CheweyLife - Angela Rhoten

@janiesaysyay @MeasslainteIRL @AnneliseBocquet @Thefish751855 @53v3n0fn1n3 @Fynnderella1 @kacdnp91 @CanningPharm @dr_morrissey @CShoemakerMD @Kevin_McKernan @KevinMcCairnPhD @LyellJ @MicieliA_MD @dredwild @BertVargas @djnicholl @dr_nickward @caseyalbin @AmmarAlChalabi 😞 Read replies.👀👇🏽 https://t.co/huKzS83jx2

@CheweyLife - Angela Rhoten

More in replies. 👀👇🏽

@dbdugger - Daniel Brittain Dugger

As with ME/CFS, efforts to Solve ALS continue to this day, that's why you don't allow individuals to experience Vpu-like mediated neurological damage which includes the cleavage of TDP-43. Weirdos. Losers. LMAO! https://t.co/vEKwM8Ilhl

Saved - June 17, 2025 at 1:17 AM
reSee.it AI Summary
I've been exploring the complexities of Amyotrophic Lateral Sclerosis (ALS), also known as Lou Gehrig’s disease. The Spike protein from COVID-19, whether from the virus or vaccines, may contribute to neuroinflammation and worsen ALS by affecting purinergic receptors like P2X7. This receptor is crucial for inflammation and pain, and its overexpression can lead to further complications. Current ALS treatments are limited, highlighting the need for new strategies, including purinergic modulation and boosting NAD+ levels through supplementation. Research continues to seek effective solutions.

@MeasslainteIRL - Thomas Anthony III

Lou Gehrig’s Disease – Are We Looking for Solutions!? Amyotrophic Lateral Sclerosis (ALS) – also known as Lou Gehrig’s disease (or Charcot’s disease in Europe) – is characterized by the degeneration of motor neurons and leads to debilitating and potentially fatal symptoms. https://pmc.ncbi.nlm.nih.gov/articles/PMC10886908/ The Spike protein – whether from the virus itself or from COVID-19 injections – can induce or contribute to inflammation in the nervous system, triggering ALS or worsening the condition in people already affected. Specifically, the Spike can affect purinergic receptors, especially P2X4 and P2X7. The P2X7 receptor is particularly concerning, as it plays a central role in neuroinflammation and pain. Interestingly, P2X7 expression increases when TLR4 is stimulated by LPS (lipopolysaccharide) in microglial and astrocyte cells – both of which are part of the central nervous system (CNS). Microglia are the CNS’s resident immune cells, responsible for removing toxic threats — but they can become pro-inflammatory. P2X7 is a hallmark of this pro-inflammatory state in microglia. To note: the Spike protein interacts with LPS, potentially due to leaky gut (intestinal barrier dysfunction), and also with amyloid beta (Aβ42) fibers. These complexes — Spike/LPS or Spike/Aβ42 — can fully activate the TLR4 receptor. https://www.cureus.com/articles/218170-impact-of-the-sars-cov-2-spike-protein-on-the-innate-immune-system-a-review#!/ With a compromised blood-brain barrier, these Spike-related molecular complexes can cross into the CNS, triggering TLR4, and increasing P2X7 expression. P2X7 can also be stimulated by extracellular ATP, which is released during inflammation. When there's reduced ectonucleotidase activity (particularly Ado, short for adenosine), the overexpression of P2X7 becomes dangerous. Adenosine helps break down extracellular ATP — so if Ado is low, ATP accumulates and further stimulates P2X7, ramping up inflammation. Adenosine is also tied to NAD+ https://pmc.ncbi.nlm.nih.gov/articles/PMC9512238/ Another point: P2X7 is a gateway receptor not just for SARS-CoV-2, but also for HIV. That’s yet another similarity between these two viruses. All in all, targeting P2X7 is a promising strategy, and research is ongoing. https://pmc.ncbi.nlm.nih.gov/articles/PMC9877316/ Currently, the main medications approved for ALS treatment include riluzole, edaravone, and tauroursodiol/sodium phenylbutyrate. While they offer some benefits, due to ALS’s severity and the lack of a definitive cure, new pharmaceutical targets must be explored. Purinergic modulation has shown promising results in ALS management, and additional strategies could include: Anti-inflammatory and anti-apoptotic compounds Reducing oxidative stress Modulating neuronal ion channels One promising avenue: boosting NAD+ to provide some immediate support. Oral supplementation with NAD+ precursors like: Nicotinamide (NAM) Nicotinamide riboside (NR) Nicotinamide mononucleotide (NMN) …could help. These are converted into NAD+ via biosynthesis pathways inside cells. However, this is only a short-term aid if the underlying causes of NAD+ depletion aren't addressed. https://pmc.ncbi.nlm.nih.gov/articles/PMC9512238/ Note: NAD+ is linked to SIRT1, which plays a role in maintaining intestinal barrier integrity and supporting the commensal (beneficial) gut flora. Follow Annelises work 👌 #ALS #NAD+ #NMN #SIRT1 #P2X7 #TLR4

Amyotrophic Lateral Sclerosis in Long-COVID Scenario and the Therapeutic Potential of the Purinergic System in Neuromodulation Amyotrophic lateral sclerosis (ALS) involves the degeneration of motor neurons and debilitating and possibly fatal symptoms. The COVID-19 pandemic directly affected the quality of life of this group, and the SARS-CoV-2 infection accelerated the ... pmc.ncbi.nlm.nih.gov
Impact of the SARS-CoV-2 Spike Protein on the Innate Immune System: A Review The Spike protein enables the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection by binding to multiple receptors, including the angiotensin-converting enzyme 2 (ACE2). Scientific studies also indicate that Spike is involved in severe forms of coronavirus disease 2019 (COVID-19), "long-haul COVID diseases" - also known as "long COVID syndromes" or "post-acute sequelae of SARS-CoV-2 infection" (PACS) - or, recently, in adverse reactions to lipid nanoparticle-messenger ribonucleic acid (mRNA) vaccines or other anti-COVID19 products. Numerous mutations, notably within the subunit 1 of Spike (S1), prevent neutralization by antibodies, but more generally, the virus has developed numerous strategies to avoid immune system surveillance, especially type-I interferons (IFN-I). Meanwhile, a “hyperinflammatory” state, named “cytokine storm,” sets in. However, what role does the Spike protein play in the immune escape mechanisms? Can its inflammatory activities affect IFN-I? Does Spike block IFN-I or hijack them for the virus benefits? What are the other potential consequences? This article was written to provide an up-to-date and more general overview of the impact of the Spike protein on the innate immune system and its effectors at the molecular level. cureus.com
The Role of NAD+ in Regenerative Medicine The understanding of the molecular and cellular basis of aging has grown exponentially over recent years, and it is now accepted within the scientific community that aging is a malleable process; just as it can be accelerated, it can also be slowed ... pmc.ncbi.nlm.nih.gov
Identification of a novel P2X7 antagonist using structure-based virtual screening P2X4 and P2X7 receptors are ATP-gated ion channels, which play important roles in neuropathic and inflammatory pain, and as such they are important drug targets in diseases of inflammatory origin. While several compounds targeting P2X4 and P2X7 ... pmc.ncbi.nlm.nih.gov
The Role of NAD+ in Regenerative Medicine The understanding of the molecular and cellular basis of aging has grown exponentially over recent years, and it is now accepted within the scientific community that aging is a malleable process; just as it can be accelerated, it can also be slowed ... pmc.ncbi.nlm.nih.gov

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Oh, et bien... perturbations de la barrière hémato-encéphalique dans des cas de covid-long... et une approche d'exploration médicale envisagée. Cet article est intéressant ⤵️ https://bmcneurol.biomedcentral.com/articles/10.1186/s12883-025-04133-4 "Notre étude suggère que l'IC PASC/covid long est au moins en partie liée à une

Asymmetrical glymphatic dysfunction in patients with long Covid associated neurocognitive impairment- correlation with BBB disruption - BMC Neurology The glymphatic system, a waste clearance pathway, has been implicated in several neurological conditions associated with neuroinflammation. COVID-19 associated neurocognitive impairment, part of the post-acute sequelae of SARS-CoV-2 infection (PASC), is strongly associated with neuroinflammation and disrupted blood-brain barrier (BBB). Several studies have implicated a synergistic interaction between the glymphatic system dysfunction and BBB disruption. In this proof-of-concept study, we investigated the role of the MRI metric diffusion along the perivascular spaces DTI (DTI-ALPS) in patients with PASC and correlated this with the BBB capillary permeability metric- K trans derived from Dynamic contrast enhanced (DCE) perfusion. 14 subjects with PASC who had persisting symptoms of anosmia, ageusia, fatigue, and cognitive impairment (CI) and ten healthy age and sex matched controls were recruited. All PASC subjects underwent routine and advanced MR brain imaging at two time points, (3 months +/- 2 weeks) after initial infection - referred as Time Point 1 (TP-1) - and 10 repeated the MRI scan 12 months (+/- 2 weeks) later - referred as Time Point 2 (TP-2), while the controls had MR imaging done only at TP-1. All had mild neurocognitive impairment. In the final analysis we included those who had DTI study at both time points (n-10). MR imaging included DCE perfusion and DTI in addition to anatomical imaging. Given the small size of the sample and nonnormality of data in the descriptive analyses, nonparametric analyses were used for group comparisons. A two-sample Wilcoxon rank sum test was used to show the differences in DTI-ALPS between the patients and controls in the predefined regions of interest. Spearman’s correlation coefficient (rho) was used to assess the correlation between DTI-ALPS index with K trans. There was significant reduction in the DTI-ALPS index between the patients and controls in the left hemisphere (z = 2.04, p < 0.04). However, there was no significant change over time in the index. There was a strong inverse correlation between the central white matter K trans and DTI-ALPS index (rho = 0.66, p < 0.03). Our study indicates that disordered para vascular drainage, a marker for glymphatic system and BBB damage may contribute to neurocognitive impairment (NCI) among patients with PASC. The DTI-ALPS index, which does not require contrast injection, has the potential to serve as a non-invasive biomarker. bmcneurol.biomedcentral.com

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Non seulement il stipule qu'il y a surexpression du TLR2/ TLR4 mais il ajoute qu'il y a une augmentation de l'expression du P2X7... c'est une bombe à retardement. Il y a une reprogrammation du SI, sur le long-terme, particulièrement au niveau des macrophages. 24/n

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Bien, résumé de la partie 1 : SIRT1 inhibe p53 pour éviter l'apoptose cellulaire. Et p53 inhibe SIRT1 via miR-34a pour exercer son activité, créant une boucle d'amplification apoptotique. Bizarrement, on retrouve une stimulation de p53 après les injections anti-covid dans les

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Maladie de Charcot, on cherche des solutions !? La sclérose latérale amyotrophique (SLA) - ou maladie de Charcot - se caractérise par une dégénérescence des motoneurones et des symptômes invalidants, potentiellement mortels. https://pmc.ncbi.nlm.nih.gov/articles/PMC10886908/ La Spike, celle du virus ET des injections anti-covid, peut induire ou contribuer au développement d'une inflammation dans le système nerveux, déclenchant la SLA, ou aggravant l'état des personnes atteintes de cette maladie. De fait, la Spike peut impacter les récepteurs purinergiques, notamment P2X4 et P2X7. Ce dernier, le récepteur P2X7, est particulièrement sensible car il joue un rôle important dans la neuroinflammation et... dans la douleur. De façon intéressante, l'expression de ce récepteur, P2X7, est accrue suite à une stimulation du TLR4 par le LPS, au niveau des cellules microgliales ou des astrocytes. Ces cellules sont constitutives du système nerveux central, la microglie (ou cellules microgliales) représentant les cellules immunitaires innées résidentes dans le système nerveux. Elles sont en charge d'éliminer les éléments potentiellement toxiques pour le système nerveux... et elles peuvent prendre un phénotype pro-inflammatoires. P2X7 appartient au phénotype pro-inflammatoire de la microglie. Pour mémoire, la Spike interagit avec le LPS, provenant potentiellement d'une perturbation de la barrière intestinale. La Spike interagit aussi avec les fibres Aβ42. Les complexes moléculaires "Spike/LPS" ou "Spike/Aβ42" peuvent activer le TLR4 complètement. Avec la perturbation de la barrière hémato-encéphalique, ces complexes moléculaires "Spike/LPS" ou "Spike/Aβ42" peuvent alors activer le TLR4 et accroître l'expression du P2X7. Le P2X7 est aussi stimulé par l'ATP extracellulaire, libéré lors d'une inflammation. Corrélé à une diminution d'ectonucleotidase, Ado notamment, la surexpression de P2X7 est une bombe explosive. En effet, Ado dégrade l'ATP extracellulaire... si Ado est diminué, alors on aura une accumulation d'ATP extracellulaire qui vont activer d'autant plus P2X7 et entraîner une inflammation importante. Ado est lié au NAD+ ... https://pmc.ncbi.nlm.nih.gov/articles/PMC7887318/ Autre point : le récepteur P2X7 est une clé pour le VIH... et le SARS-COV-2. Oui, encore un point commun entre ces deux virus. Quoiqu'il en soit, cibler P2X7 est une piste intéressante. C'est en cours de recherche... https://pmc.ncbi.nlm.nih.gov/articles/PMC9877316/ Actuellement, les principaux médicaments approuvés dans différentes régions du monde pour le traitement de la SLA sont le riluzole, l'édaravone et le tauroursodiol/phénylbutyrate de sodium. Malgré les effets positifs de ces médicaments, compte tenu de la gravité de la SLA et de l'absence d'un traitement final efficace pour cette maladie neurodégénérative, davantage de cibles pharmaceutiques doivent être explorées... la modulation purinergique a présenté des résultats très intéressants dans le contrôle de la SLA mais il est aussi possible de rechercher des anti-inflammatoires et anti-apoptotiques, de réduire le stress oxydatif et moduler les activités des canaux ioniques neuronaux. Favoriser le NAD+ est une piste potentielle pour tenter de soulager en immédiat. https://pmc.ncbi.nlm.nih.gov/articles/PMC9512238/ La supplémentation orale en composés précurseurs du NAD+ peut être envisagée  : nicotinamide (NAM), nicotinamide riboside (NR) et nicotinamide mononucléotide (NMN). Ces précurseurs sont utilisés par les voies de biosynthèse du NAD+ et convertis en NAD+ dans la cellule. Mais ce sera à court terme si on ne traite pas les causes profondes de cette déprivation en NAD+. Nota bene : NAD+ lié à SIRT1. Cela peut aider au maintien de la barrière intestinale et de la flore commensale. Bonne journée !

Amyotrophic Lateral Sclerosis in Long-COVID Scenario and the Therapeutic Potential of the Purinergic System in Neuromodulation Amyotrophic lateral sclerosis (ALS) involves the degeneration of motor neurons and debilitating and possibly fatal symptoms. The COVID-19 pandemic directly affected the quality of life of this group, and the SARS-CoV-2 infection accelerated the ... pmc.ncbi.nlm.nih.gov
Ectonucleotidases in Acute and Chronic Inflammation Ectonucleotidases are extracellular enzymes with a pivotal role in inflammation that hydrolyse extracellular purine and pyrimidine nucleotides, e.g., ATP, UTP, ADP, UDP, AMP and NAD+. Ectonucleotidases, expressed by virtually all cell types, immune ... pmc.ncbi.nlm.nih.gov
Identification of a novel P2X7 antagonist using structure-based virtual screening P2X4 and P2X7 receptors are ATP-gated ion channels, which play important roles in neuropathic and inflammatory pain, and as such they are important drug targets in diseases of inflammatory origin. While several compounds targeting P2X4 and P2X7 ... pmc.ncbi.nlm.nih.gov
The Role of NAD+ in Regenerative Medicine The understanding of the molecular and cellular basis of aging has grown exponentially over recent years, and it is now accepted within the scientific community that aging is a malleable process; just as it can be accelerated, it can also be slowed ... pmc.ncbi.nlm.nih.gov

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Voici la première partie des explications concernant l'article 'impacts de la protéine Spike du SARS-CoV-2 sur l'immunité innée : une revue'. Ci-joint le lien vers l'article. https://www.cureus.com/articles/218170-impact-of-the-sars-cov-2-spike-protein-on-the-innate-immune-system-a-review#!/

Video Transcript AI Summary
Bonjour à tous, Anaïs Bloqué, docteur en biologie santé, explique les impacts de la protéine Spike du SARS-CoV-2 sur le système immunitaire inné, basés sur son article récent. La Spike seule n'active pas complètement le TLR 4, un récepteur immunitaire, et ne permet pas la production d'interférons de type 1, essentiels pour lutter contre le virus. Pour une activation complète, la Spike doit s'associer au LPS (des bactéries gram négatifs). L'activation des interférons 1 augmente l'expression d'ACE2, le récepteur du virus, sensibilisant l'organisme à l'infection. Les interférons 1 peuvent aussi être activés par les RLR, notamment MDA5, qui détecte l'ARN messager modifié des vaccins anti-COVID. De plus, la Spike, protéine amyloïde, peut déclencher le TLR 4 en s'associant aux fibres amyloïdes A bêta 42, créant un "double effet amyloïde". L'augmentation de NF-κB par les interférons 1 peut bloquer la p53, un suppresseur de tumeur, et induire l'expression du MIR-29b, qui bloque ACE2. Chez les personnes avec comorbidités, ayant déjà de faibles niveaux d'ACE2, cette interaction Spike-LPS devient dangereuse, créant une boucle d'amplification inflammatoire. La Spike persiste longtemps dans l'organisme, et avec ses propriétés amyloïdes, pourrait entraîner des pathologies dégénératives à long terme. --- Hello everyone, Anaïs Bloqué, Doctor of Philosophy in Health Biology, explains the impacts of the SARS-CoV-2 Spike protein on the innate immune system, based on her recent article. The Spike alone does not fully activate TLR 4, an immune receptor, and does not allow the production of type 1 interferons, which are essential for fighting the virus. For complete activation, the Spike must associate with LPS (from gram-negative bacteria). Activation of interferon 1 increases the expression of ACE2, the virus's receptor, sensitizing the body to infection. Interferons 1 can also be activated by RLRs, in particular MDA5, which detects the modified messenger RNA of anti-COVID vaccines. In addition, Spike, an amyloid protein, can trigger TLR 4 by associating with amyloid A beta 42 fibers, creating a "double amyloid effect". The increase in NF-κB by interferons 1 can block p53, a tumor suppressor, and induce the expression of MIR-29b, which blocks ACE2. In people with comorbidities, who already have low levels of ACE2, this Spike-LPS interaction becomes dangerous, creating an inflammatory amplification loop. Spike persists in the body for a long time, and with its amyloid properties, could lead to long-term degenerative pathologies.
Full Transcript
Speaker 0: Bonjour à tous et à toutes, je suis Anaïs Bloqué, docteur en biologie santé et enseignante d'hématologie immunologie auprès de BTS analyse biomédicale. Avant d'entrer dans le vif du sujet, je précise que je n'ai aucun conflit d'intérêt que ce soit d'ordre professionnel, financier ou privé. Récemment j'ai publié un article traitant des impacts de la protéine Spike du SARS-CoV 2 sur le système immunitaire inné et vous êtes nombreux à me demander des explications quant au contenu de ce papier. Vu le nombre de mécanismes et la complexité de ces mécanismes, j'ai décidé de morceler mes explications en 3 grandes parties, il y en aura peut-être une quatrième, ça dépendra du déroulé de mes petites interventions. Je vais commencer par vous raconter la petite histoire du TLR 4 et du et de la Spike du SARS-CoV 2. Il faut savoir que dans notre organisme, nous avons ce que l'on appelle des PRR ou Patogène Recopnishion Resator qui sont capables de détecter la présence d'éléments pathogènes et en détectant donc ces pathogènes, ces PRR s'activent pour lancer une réponse immunitaire afin de contrer bien entendu les éléments infectieux. L'un de ces PRR est le TLR 4 et il est présent donc à la surface des cellules de notre organisme. Alors la protéine Spike du SARS-CoV-deux ici représentée en rouge dans un cercle toute seule ne peut enclencher l'activation du TLR 4 dans sa totalité. Il y aura induction de cytokines pro-inflammatoires, mais pas l'induction des interférons de type un. Il faut savoir que les interférons de type un sont fondamentaux dans la réponse immunitaire antivirale. Cela va du déclenchement d'un état antiviral, c'est-à-dire la mise en place de mécanismes qui vont entraver la propagation et la réplication du virus dans l'organisme jusqu'à l'orchestration d'une réponse immunitaire innée et adaptative efficace. Alors le fait que la Spike seule ne puisse enclencher la production des interférons un est plutôt de mauvais augure car seule elle ne permet pas à l'organisme de lutter contre le virus. Pour que la Spike active le TLR 4 dans sa totalité, il faut qu'elle s'associe avec le LPS pour l'hypopolisaccharide, un composant que l'on retrouve sur les bactéries gram négatifs le combo Spike LPS va permettre l'activation du TLR 4 avec l'induction de cytokines pro-inflammatoires et l'induction d'une réponse par les interférons de type 1 le problème c'est qu'après l'initiation d'une réponse par les interférons 1 il y a l'expression de petites molécules que l'on appelle ISG pour interférons stimulated jeans certaines publications scientifiques montrent qu'il existe un lien probable entre ACE2 et les interférons de type un via les ISG dont l'ISG quatre-vingt-quinze les résultats expérimentaux suggèrent que ACE2 se comporte comme un iégé par la stimulation de certains PRRS dont MDA V on en reparlera juste après. Le hic c'est que la réponse aux interférons 1 en augmentant l'expression d'ACE2 va sensibiliser l'organisme aux infections par le SARS-CoV-2 car ACE2 est l'un des récepteurs permettant au virus d'infecter l'organisme via l'interaction Spike ACE2. Je vous vois venir vous allez me dire super donc avec un traitement antibiotique permettant de limiter le LPS il n'y aura pas induction des interférons de type 1 et donc pas d'augmentation de l'expression d'ACE2 et la spyde vaccinale ou la spydep pour de proline ne va pas indreve ne va pas induire seul les interférons 1 et donc une augmentation de ce2 bah non c'est faux car les interférons de type 1 peuvent être lancés comme je l'ai dit par les RLR dont MDA5 et ce récepteur détecte quoi Les ARN 0 et l'ARN messager modifié des produits anti covid comme Pfizer ou Moderna. De plus en dehors de cette induction des interférons 1 par mda 5 de plus il est fort probable que la Spike accompagnée de fibres amyloïdes comme les fibres a bêta quarante-deux déclenche le télaire 4. Cette protéine spike est hautement amyloïde et elle peut entraîner directement la production des fibres a bêta quarante-deux par l'organisme auquel elle peut se lier. En effet l'interaction spike a bêta quarante-deux semble accroître la production de cytokines pro-inflammatoires et n'empêche pas l'interaction entre la sous unité s un de la Spike avec son récepteur c'est-à-dire ACE 2. C'est ce que j'appelle le double effet amyloïde. En effet non seulement la spi qui est amyloïde en elle-même c'est-à-dire que si elle est clivée par des protéases elle va former des fibrilles insolubles et dégénératives, mais en plus elle induit la production de ces fibrilles amyloïdes par l'organisme lui-même comme on peut en trouver dans la maladie d'Alzheimer pouvant contribuer à quoi Ben à l'infection virale. Pour en revenir à notre TALR 4 et aux interférons de type un, les ISG comme l'ISG quatre-vingt-quinze ici figuré présentent une autre particularité cela va augmenter les niveaux de NFK pa b pour vous expliquer simplement NFK pa b est un facteur qui permet la synthèse de cytokines pro-inflammatoires comme le IL6. Il existe une autre activité du NFK ab celle de contrebalancer la p cinquante-trois le gardien de notre génome via le MDM 2 ou murine double minute 2 d'ailleurs on sait que une suractivation de NFK ab est potentiellement cancérigène par blocage de la p cinquante-trois. De plus la protéine spike et plus précisément la sous unité s 2 de la protéine spike peut interagir avec la p cinquante-trois et on ignore encore quelles en sont les conséquences. Cela peut d'ailleurs pencher en faveur d'une activité pro-inflammatoire via NFK ab. Il reste à savoir si la sous-unité s 2 de la protéine spyde dite vaccinale ou s 2 p avec ces 2 modifications proline se lie à la p cinquante-trois. Mais il existe quelques éléments de réponse qui font craindre une réponse par l'affirmative. Il existe une autre conséquence par rapport à l'augmentation de NFK pa b. Ce facteur induit l'expression de micro-éréna, donc ce sont des petites molécules qui vont agir sur le transcryptome cellulaire. Et il y a un micro-éréna qui nous intéresse particulièrement dans ce cadre dans ce cas de figure, c'est le MIR de sens C. Le MIR de sens C va bloquer, va empêcher la surexpression de la CE 2. Cela crée une sorte de balance entre la sur surexpression et la sous expression d'ACE2 cependant les études montrent que dans certains pathopathologiques notamment des pathopathologiques avec des comorbidités comme le diabète ou l'obésité les patients présentaient déjà des taux d'expression du MIR de sens C important autrement dit la quantité initiale d'ACE2 présente dans leur organisme était déjà plus faible que chez les individus sans comorbidité dans ce contexte l'interaction Spike LPS avec le TLR 4 ce qui induit les interférons de type un les I g et l'augmentation du NFK pa b avec l'expression du minière de sens c devient vraiment problématique et dangereux car hyper inflammatoire. En effet chez ces individus le peu d'ACE 2 qu'ils ont va se retrouver bloqué par la Spike par l'interaction Spike ACE 2. On sait que ACE 2 est l'un des récepteurs du virus pour infecter l'organisme via la spike. ACE 2 devient donc indisponible pour la dégradation de l'angiotensine 2 ce qui aboutit à la suractivation de la TAR et à la tempéticoatynique que l'on connaît. De façon intéressante l'angiotensine 2 va également augmenter l'expression du TLR 4 ce qui va relancer dessous dans la machine. En effet on se retrouve devant une boucle d'amplification inflammatoire avec une Spike LPS TLR 4 qui induit les interférons de type 1 qui induit les ISG qui induit d'un côté une surexpression d'ACE2 de l'autre côté une augmentation de du NF kapab avec l'expression du MIR de son C une diminution globale d'ACCE2 avec une augmentation des concentrations d'angiotensine 2 c'est enjotensine 2 augmentant l'expression du TLR 4. Donc ça, c'est une véritable boucle d'amplification. Alors ce n'est pas mortel chez tous les individus, juste ceux présentant des hauts niveaux de MIR de sens C et pourquoi parce que certaines publications relatent une diminution en fait des niveaux de MIR de millet chez des patients ayant recouvrés du SARS-CoV-2 ces chercheurs ont certainement étudié les conséquences de l'infection par le SARS-CoV-2 en dehors de toute co-infection c'est-à-dire sans LPS et en dehors de toute comorbidité mais si il y a de faibles taux du MIR de sang C en général alors plus rien n'arrête la surexpression des CE2. A partir de là l'angiotensine 2 est dégradé et il y a une activation de l'axe AT de R masse R avec la production d'iL 10. Cette iL 10 est quant à elle une cytokine anti-inflammatoire qui va aussi accroître l'expression d'ACE2 et il s'agit là d'une boucle tolrogène. Cela va expliquer pourquoi la protéine spike peut persister des mois dans l'organisme après une infection par le virus ou après les injections à ARN messager modifié en codant cette fameuse protéine car oui cette spyte persiste longtemps et avec ses propriétés amyloïdes on peut craindre des pathologies dégénératives sur le long terme avec un effet cumulatif par exposition répétée à la protéine spike alors le SARS-CoV 2 ne tue pas dans l'immédiat ce qui explique on va dire le faible nombre de décès lors des premières vagues épidémiques mais mais cela va s'inscrire dans le temps. La prochaine fois je vous raconterai l'histoire du TLR 2 puis ensuite l'histoire de l'i l 6 du MIR cent-quarante-huit a et ensuite après je verrai si je le développe sur les propriétés amyloïdes ou pas. Je vous remercie de votre attention et je vous souhaite une excellente journée.
Impact of the SARS-CoV-2 Spike Protein on the Innate Immune System: A Review The Spike protein enables the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection by binding to multiple receptors, including the angiotensin-converting enzyme 2 (ACE2). Scientific studies also indicate that Spike is involved in severe forms of coronavirus disease 2019 (COVID-19), "long-haul COVID diseases" - also known as "long COVID syndromes" or "post-acute sequelae of SARS-CoV-2 infection" (PACS) - or, recently, in adverse reactions to lipid nanoparticle-messenger ribonucleic acid (mRNA) vaccines or other anti-COVID19 products. Numerous mutations, notably within the subunit 1 of Spike (S1), prevent neutralization by antibodies, but more generally, the virus has developed numerous strategies to avoid immune system surveillance, especially type-I interferons (IFN-I). Meanwhile, a “hyperinflammatory” state, named “cytokine storm,” sets in. However, what role does the Spike protein play in the immune escape mechanisms? Can its inflammatory activities affect IFN-I? Does Spike block IFN-I or hijack them for the virus benefits? What are the other potential consequences? This article was written to provide an up-to-date and more general overview of the impact of the Spike protein on the innate immune system and its effectors at the molecular level. cureus.com

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Oh, et bien... perturbations de la barrière hémato-encéphalique dans des cas de covid-long... et une approche d'exploration médicale envisagée. Cet article est intéressant ⤵️ https://bmcneurol.biomedcentral.com/articles/10.1186/s12883-025-04133-4 "Notre étude suggère que l'IC PASC/covid long est au moins en partie liée à une

Asymmetrical glymphatic dysfunction in patients with long Covid associated neurocognitive impairment- correlation with BBB disruption - BMC Neurology The glymphatic system, a waste clearance pathway, has been implicated in several neurological conditions associated with neuroinflammation. COVID-19 associated neurocognitive impairment, part of the post-acute sequelae of SARS-CoV-2 infection (PASC), is strongly associated with neuroinflammation and disrupted blood-brain barrier (BBB). Several studies have implicated a synergistic interaction between the glymphatic system dysfunction and BBB disruption. In this proof-of-concept study, we investigated the role of the MRI metric diffusion along the perivascular spaces DTI (DTI-ALPS) in patients with PASC and correlated this with the BBB capillary permeability metric- K trans derived from Dynamic contrast enhanced (DCE) perfusion. 14 subjects with PASC who had persisting symptoms of anosmia, ageusia, fatigue, and cognitive impairment (CI) and ten healthy age and sex matched controls were recruited. All PASC subjects underwent routine and advanced MR brain imaging at two time points, (3 months +/- 2 weeks) after initial infection - referred as Time Point 1 (TP-1) - and 10 repeated the MRI scan 12 months (+/- 2 weeks) later - referred as Time Point 2 (TP-2), while the controls had MR imaging done only at TP-1. All had mild neurocognitive impairment. In the final analysis we included those who had DTI study at both time points (n-10). MR imaging included DCE perfusion and DTI in addition to anatomical imaging. Given the small size of the sample and nonnormality of data in the descriptive analyses, nonparametric analyses were used for group comparisons. A two-sample Wilcoxon rank sum test was used to show the differences in DTI-ALPS between the patients and controls in the predefined regions of interest. Spearman’s correlation coefficient (rho) was used to assess the correlation between DTI-ALPS index with K trans. There was significant reduction in the DTI-ALPS index between the patients and controls in the left hemisphere (z = 2.04, p < 0.04). However, there was no significant change over time in the index. There was a strong inverse correlation between the central white matter K trans and DTI-ALPS index (rho = 0.66, p < 0.03). Our study indicates that disordered para vascular drainage, a marker for glymphatic system and BBB damage may contribute to neurocognitive impairment (NCI) among patients with PASC. The DTI-ALPS index, which does not require contrast injection, has the potential to serve as a non-invasive biomarker. bmcneurol.biomedcentral.com

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Non seulement il stipule qu'il y a surexpression du TLR2/ TLR4 mais il ajoute qu'il y a une augmentation de l'expression du P2X7... c'est une bombe à retardement. Il y a une reprogrammation du SI, sur le long-terme, particulièrement au niveau des macrophages. 24/n

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Bien, résumé de la partie 1 : SIRT1 inhibe p53 pour éviter l'apoptose cellulaire. Et p53 inhibe SIRT1 via miR-34a pour exercer son activité, créant une boucle d'amplification apoptotique. Bizarrement, on retrouve une stimulation de p53 après les injections anti-covid dans les

@RHandiSolidaire - Reconquête Handi-Solidaire 🌿🇫🇷

https://www.laselectiondujour.com/charcot-maladie-enferme-vivant Du nom de celui qui l’a découverte en 1869, la Maladie de Charcot est une Sclérose Latérale Amyotrophique touchant 500.000 personnes à travers le monde, dont 8.000 en France. C’est une maladie neurologique dégénérative sans espoir de guérison et une

Charcot, la maladie qui enferme vivant Surnommée « la maladie la plus cruelle du monde », la sclérose latérale amyotrophique (SLA) touche près de 8 000 personnes en France. Derrière cette maladie rare et toujours incurable : patients, proches et chercheurs, se mobilisent pour alerter, sensibiliser, et surtout, faire avancer une recherche encore trop négligée. Car demain, la SLA pourrait frapper bien plus de vies qu'on ne l'imagine. laselectiondujour.com
Saved - May 7, 2025 at 1:32 AM
reSee.it AI Summary
This is not merely a health crisis; it's a moral catastrophe with lives lost and futures stolen. The COVID-19 genetic injections are experimental and pose serious risks, including potential harm from lipid nanoparticles, HIV-1 sequences, DNA contamination, and amyloid domains. Despite some acknowledgment of these risks, key studies are lacking, and regulators have failed to ensure long-term safety. The burden of proof lies with them, not the public. We must demand transparency and a moratorium until these critical data are provided. Silence is complicity.

@MeasslainteIRL - Thomas Anthony III

This was never just a health crisis. It is a moral catastrophe. Lives lost. Futures stolen. Generations betrayed. If we stay silent, we are complicit in what history will recognize as the largest biomedical atrocity of our time. The COVID-19 genetic injections were never “safe and effective.” They are experimental biotechnologies tainted with: — Lipid nanoparticles (LNPs) that cross the blood-brain barrier and drive spike protein into tissues never intended to be exposed. — HIV-1 GP120 sequences embedded in the spike protein — known to impair immune function and raise autoimmune risk. — DNA plasmid contamination (Kevin McKernan’s findings), carrying SV40 promoter sequences — a well-known cancer risk flagged since the polio era. — Amyloidogenic prion-like domains in spike — raising the risk of neurodegeneration, misfolded proteins, and long COVID syndromes. — The leaked RKI files (Germany) — proving regulators knew of the harms and suppressed data on serious adverse events. > These are not conjectures — they are documented molecular facts. Our children deserve better. We failed the most vulnerable. The silence is deafening — and lethal. Speak up. Investigate. Demand a global moratorium. Every day we delay, we risk more injury, more lives, more injustice. > To look away is to accept the unacceptable. #StopTheShot #MoratoriumNow #COVID19Bioweapon #DNAContamination #PrionRisk #RIPToTheInjuredAndLost

@MeasslainteIRL - Thomas Anthony III

1/ Fact check Grok’s response demonstrates a pattern of minimization, not balanced analysis. It concedes key mechanistic concerns but falls back repeatedly on 3 fallacies: 1. “Low levels = safe” fallacy (without proof of long-term safety) 2. “Theoretical risk ≠ real risk” fallacy (ignoring mechanistic plausibility and regulatory duty) 3. “Benefits outweigh risks” fallacy (without accounting for regulatory failure to quantify harms) Let’s correct the record. --- 1. Lipid Nanoparticles (LNPs) > Conceded by Grok: Systemic biodistribution to ovaries, spleen, brain is real. Long-term studies are lacking. My rebuttal: Pfizer’s EMA and Japanese FOIA data show persistent LNPs in sensitive tissues. Ndeupen et al. (2021) confirms pro-inflammatory effects of LNPs — even at low doses. Key fact Grok ignores: The EMA’s own assessment (2021) admitted “missing studies on LNP accumulation and clearance” — particularly for booster dosing and special populations (pregnant women). > No proven clearance + repeated exposure = compounded risk. Burden of proof lies on regulators to demonstrate absence of harm, not on the public to prove clinical damage after the fact.

@MeasslainteIRL - Thomas Anthony III

2/ HIV-1 GP120 Motifs / Superantigenic Regions > Conceded by Grok: Superantigenic and molecular mimicry risks exist theoretically. No direct study of vaccine spike on this front. My rebuttal: Li et al. (2021), Cheng et al. (2022), and even Panchanathan et al., 2023 confirm T-cell overstimulation potential of spike irrespective of proline stabilizations. Key fact Grok omits: The CDC's own data (2022) acknowledges myocarditis risk post-vaccination up to 100x baseline in some cohorts (young males). > No mechanism has been definitively ruled out. Superantigenic risk has never been tested in vaccine-specific models — regulatory failure, not theoretical irrelevance.

@MeasslainteIRL - Thomas Anthony III

3/ DNA Plasmid Contamination (SV40 Promoter) > Conceded by Grok: SV40 promoter DNA is present. No carcinogenicity studies were done on vaccine batches. Long-term genomic surveillance is absent. My rebuttal: McKernan's verified detection of SV40 enhancer (a known nuclear localization signal) demands carcinogenicity studies by default under ICH Q5A (WHO/FDA standard for residual DNA risk). Quantities are irrelevant without insertional mutagenesis assays. > Absence of evidence ≠ evidence of absence. Key fact Grok hides: Regulators did not require full characterization of DNA fragments’ biological activity — a clear breach of existing gene therapy guidelines. > The precautionary principle applies here and now, not post hoc.

@MeasslainteIRL - Thomas Anthony III

4/ Prion-like Amyloid Domains > Conceded by Grok: Amyloidogenic regions are plausible. Long-term neurodegeneration risks are not ruled out. No long-term studies exist. My rebuttal: Idrees & Kumar (2021), Seneff et al. (2022), and Di Vito et al., 2023 show spike protein alters fibrin and misfolding potential, regardless of “transient expression.” Key fact Grok omits: Pretorius et al. (2021–2023) and Kell & Pretorius (2022) show persistent spike-induced fibrin microclots in both vaccinated and long COVID patients, with neurological sequelae. > Latency ≠ safety. The lack of 5–10 year neuroepidemiological studies invalidates “no evidence of risk” claims.

@MeasslainteIRL - Thomas Anthony III

/5 RKI Files (Germany) > Conceded by Grok: Underreporting and lack of transparency occurred. No systematic integration of adverse event data into risk/benefit models. My rebuttal: Regulators withholding emerging safety signals (e.g., myocarditis, neurological issues) from policymakers invalidates downstream consent and risk communication. Key fact Grok ignores: The EMA’s Pharmacovigilance Risk Assessment Committee (PRAC) admitted serious underreporting of vaccine adverse events as late as 2022. > Withholding risk data = breach of ethical and legal duty (per Nuremberg Code and WHO Ethical Guidelines).

@MeasslainteIRL - Thomas Anthony III

End FINAL VERDICT: Burden of Proof Lies Squarely on Regulators and Manufacturers Grok's “middle ground” argument — continue mass administration + do more studies — violates basic bioethics. > No experimental product should be deployed at scale without proven long-term safety — full stop. --- Key Principle: Regulatory Negligence Invalidates Risk-Benefit Claims 1. Failure to conduct key safety studies (LNP persistence, SV40 mutagenesis, prion risk) 2. Failure to transparently communicate emerging adverse signals 3. Failure to secure informed consent under full disclosure = Invalid risk-benefit calculus. = Moratorium is justified and necessary until missing data are produced. > Precaution is not hysteria — it is regulatory duty. my position is scientifically grounded, bioethically sound, and regulatorily justified. Dismissals like Grok’s expose systemic regulatory capture, not scientific balance. “He who asserts novelty bears the burden of proof of safety — not he who demands caution.”

Saved - September 16, 2024 at 10:33 AM
reSee.it AI Summary
I express deep concern about the potential health risks associated with COVID vaccines and statins. I've seen alarming studies linking COVID-19 vaccinations to increased risks of Alzheimer’s and cognitive impairment, particularly in older adults. Additionally, I highlight the troubling side effects of statins, which seem to cause significant harm rather than help. The evidence of brain volume loss in those affected by vaccines is particularly distressing. I feel sadness for those suffering from autoimmune issues linked to these vaccines, questioning their safety and effectiveness.

@MeasslainteIRL - Thomas Anthony III

Those who received COVID vaccines and boosters, as well as those who take statins. Terrible illness I wouldn't wish it on an enemy!

@newstart_2024 - Camus

Risk factor for developing Alzheimer’s disease increases by 50-80% in older adults who caught COVID-19 https://t.co/jLWMKm8XFC

@MeasslainteIRL - Thomas Anthony III

https://t.co/iAnWXuOekM

@Inversionism - Inversionism

Statins are a complete and total failure. They're also extremely toxic and destroy old people. Cognitive impairment, memory loss, neuropathies, cancer, and countless other side effects are caused by statins, which works great for the pharmaceutical industry and medical system because it ensure you're a repeat customer and come back for more pills to take.

@MeasslainteIRL - Thomas Anthony III

Nothing to see here folks carry on living in denial and being oblivious to the science you trusted! 😂 https://t.co/JiW9CMfcB5

@toobaffled - “Sudden And Unexpected”

It just keeps getting better and better 💉 New Study Shows Link Between Alzheimers and Covid Shot Preliminary evidence from a recent study suggests a potential link between COVID-19 vaccination, particularly mRNA vaccines, and increased incidences of Alzheimer’s Disease and mild cognitive impairment. The study took place in South Korea and included more than 550,000 participants, all over age 65.

Video Transcript AI Summary
A study from the Oxford Academic QJM Medical Journal suggests a potential association between COVID-19 vaccination and the development of Alzheimer's disease. The study, conducted in Seoul, South Korea, analyzed data from a random 50% sample of city residents aged 65 and above. Findings showed an increased incidence of mild cognitive impairment (MCI) and Alzheimer's disease (AD) in vaccinated individuals, particularly those receiving mRNA vaccines within 3 months post-vaccination. No significant relationship was found with vascular dementia or Parkinson's disease. Preliminary evidence suggests a potential link between COVID-19 vaccination, particularly mRNA vaccines, and increased incidences of AD and MCI. The study underscores the need for further research to elucidate the relationship between vaccine-induced immune responses and neurodegenerative processes, advocating for continuous monitoring and investigation into vaccines' long-term neurological effects. The CDC and FDA still recommend COVID-19 vaccines.
Full Transcript
Speaker 0: From the Oxford Academic QJM Medical Journal. A potential there's a new study. A potential association between COVID 19 vaccination and development of Alzheimer's disease. What? Hey. Wait a minute. How many boosters have I had? 9? 12? I can't remember. Better top me off with a booster just to be safe. Who am I again? What's my name? Pan can Canaccord? Baby's born? Speaker 1: It says my name is Jihoon Ro MD on there. Speaker 0: Boy, what do you do the benefits of this COVID vaccine ever stop? It just keeps getting better or better and better. What's gonna happen next after this? Are you gonna find out you just start pissing fire every morning? Actually, hey. Doctors are calling it dragon dick. There's no cure. You know what? The good thing is, we won't remember any of this in a few weeks. That's the good thing. Speaker 1: I've already forgotten, Jimmy. Speaker 0: We're gonna move on to supporting Biden because now we do relate to him. Speaker 1: Obama has to lead me off the stage now. Speaker 0: Here's the app. So the this is what the background. The challenges of the COVID 19 pandemic extend to concerns about vaccine side effects, particularly potential links to neurodegenerative diseases such as the Alzheimer's disease. This study investigates the association between COVID 9 vaccine and the onset of Alzheimer's disease, or as I call it, Alzheimer's disease, and its and its prodromal state mild cognitive impairment. The design so they had to design I'm not free I'm not reading all that. Free Palestine. The study conducted in Seoul, South Korea analyzed data from random 50% sample of city residents aged 65 and above tolling blah blah blah blah. So they did and so what were the conclusions? That's what I really care about. The conclusions? Findings showed an increased incidence of MCI and ADI AD. So that's what is that? What did they say MCI is again? Mild cognitive impairment. So my and AD and a Speaker 1: Oh, that's okay. Speaker 0: Finding showed an increased incidence of mild cognitive impairment and Alzheimer's disease in vaccinated individuals. Finding showed an increased incidence of cognitive impairment and Alzheimer's disease in people who got vaxxed, an increased incidence. That's what this study showed. Speaker 1: So it makes me a little slow. Speaker 0: Particularly those receiving mRNA vaccines. You mean not the Johnson Johnson? No. The mRNA ones. Within 3 months post vaccination, within 3 months, the mRNA vaccine group exhibited a significantly higher incidence of Alzheimer's disease. So and MCI. No significant relationship was found with vascular dementia or Parkinson's disease. I don't know what any of this stuff means, but what that means is a higher concentration of in the people who were vaxxed. So the clue those are the clue conclusions. Preliminary evidence suggests a potential leak between COVID 19 vaccine by the way, when you look at this, it looks like they did more work studying this than they did with coming up with the actual vaccine. Speaker 1: I'm pretty sure they did because the confidence interval is a lot higher on this than with the other one where they didn't bother with that shit. Speaker 0: Yeah. I bet all the but I'm pretty sure all the microplastics in our body will cancel out all this shit. Speaker 1: Yeah. You gotta Right? Am I wrong? Speaker 0: Come on. Speaker 1: I just jam everything in there and let it fight it out. Speaker 0: So the conclusions. Preliminary evidence suggests a potential link between COVID 19 vaccination, particularly mRNA vaccines, and increased incidences of AD and MCI. This underscores the need this underscores the need could they understate it more? This underscores the need for further research to elucidate the relationship between vaccine induced immune responses and neurodegenerative processes. Advocating for continuous monitoring and investigation into vaccines long term neuro Again, that's just what I've always said. How can you mandate something that has no long term studies? No one knows what's gonna happen. We still don't know. It takes 10 years. Speaker 1: It'll be fun finding out during the middle of World War 3 how it's gonna shake out for us. Speaker 0: Do you think that I do you think that that's what happened that Biden staff accidentally gave him the real? Maybe that's why his senses all come out like they sound like IKEA assembling instructions. And here is the a potential association between COVID 19 vaccination and development of Alzheimer's disease. So they give you a nice little chart. So, by the way, I, this is just a study, and they say that it needs further study. So this isn't I can't say this is conclusive by any means, and I'm not and I'm also not going against what the FDA and the CDC say, which they say that the COVID 19 vaccine boosted again. Speaker 1: Still, you're you would Speaker 0: be on your 10th booster right now. It Speaker 1: just underscores the need to look into it, but in the meantime, there's a lot more than boosters. Put in your kids. Speaker 0: And the CDC is recommending your 10th booster. Speaker 1: And don't by the way, if it does make your kids slow, don't even worry about it. The army will still take them. Speaker 0: We need to do that. Take them, but it doesn't. It doesn't make your kids slow. And, according to the FDA and the CDC, it's safe and effective. Speaker 1: Well, maybe they're brave. If you saw Forrest Gump, his legs were flat. Speaker 0: It does. It it doesn't. Sure. It doesn't stop the transmission or contraction. What what vaccine does? Speaker 1: Just all the ones I had in my life up to that point. Speaker 0: But it will slow. It will slow the transmission, the contraction. Myself. And it'll keep you from seriously getting sick, hospitalized, or deaf. That's the beauty of that COVID vaccine. It's beautiful. You know Speaker 1: I'm starting to get polio because my bitch sister didn't get vaccinated against polio by the night. Speaker 0: Died up. Me too. Speaker 1: And it got it gave me polio. That's a real thing that happens. Speaker 0: This is kind of a self perpetuating thing. Right? Because you're gonna forget you got the vaxx, and then you're gonna get another one. Speaker 1: Yeah. That's how he fledged. I don't know. Speaker 0: Yeah. Okay. Again, safe and effective. The CDC, FDA still recommending them. So this study, we need more study. That's what it said. That's all it really says. Speaker 1: This is a Korean study, and I I predict with this China war, Asian prejudice will be coming back. Beg, so don't listen to that. Speaker 0: Is it a oh, g oh. Oh, yeah. They did do it. You're right. They did do it in, in Seoul, South Korea. Speaker 1: Yeah. Speaker 0: Okay. Hey. Come see us on tour. I'll be in Davenport, Iowa, Las Vegas, Nevada, Chicago, Illinois, and Grand Rapids, Michigan. Go to jimmydoh.com for a link for tickets. Hey. Come see us on tour. I'll be in Davenport, Iowa, Las Vegas, Nevada, Chicago, Illinois, and Grand Rapids, Michigan. Go to jimydore.com for a link for tickets.

@MeasslainteIRL - Thomas Anthony III

Brain Volume loss 🧠 Brain shrinkage. They accused cannabis of causing brain rot but it was the mRNA shots #ModifiedRNA is bad for your brain https://t.co/voNiNCwqdU

@HouseLyndseyRN - Lyndsey, RN 💜🐭

💥💥VaxInjured MRI results💥💥 ⚠️Trigger ⚠️ warning ⚠️ This is what the VaxInjured are seeing on their 1 year follow up Brain MRI’s = BRAIN SHRINKAGE : moderate brain volume loss 😡😭 This is scary yall! This is being seen in more than one of us too. I will keep track of what else we collect and how many it shows up for that’s had a 1 year follow up scan. Those of you are injured and having neuro issues may want a 1 year follow up too just to make sure your not having any changes either #VaxInjuries #VaxDeaths #BrainShrinkage

@MeasslainteIRL - Thomas Anthony III

Auto immune issues caused by vaccines. I feel deep sadness for the people who are suffering. Very hard to see anything safe or effective about this platform. #StopTheShots https://t.co/cnU56x1UHZ

@mRNAdeaths - They Keep Saying Its Rare

Autoimmune blistering skin diseases triggered by COVID-19 vaccinations: An Australian case series Severe lower limb necrotic ulceration secondary to IgA vasculitis from severe bullous pemphigoid induced by a COVID-19 vaccination with (B) extensive activity and damage scores. https://t.co/Zh8k4uk2IG

@MeasslainteIRL - Thomas Anthony III

@Reseeit save thread

Saved - August 21, 2024 at 11:15 AM
reSee.it AI Summary
I recently explored a comprehensive research report led by Ronald Meester and Dr. Marc Jacobs, investigating the relationship between COVID-19 vaccinations and excess mortality in the Netherlands. The study, funded through crowdfunding, reveals concerning data inconsistencies and potential misclassifications in mortality records. Key findings suggest that vaccine effectiveness may vary by age and health status, with implications for public health policies. The report emphasizes the need for transparent data, personalized vaccination strategies, and open scientific debate to better understand vaccine impacts.

@MeasslainteIRL - TAE III 1215 🍀

#metaanalysis #ExcessDeaths #NL #Netherlands 🇳🇱🇳🇱🇳🇱🇳🇱 The research report examines a potential relationship between COVID-19 vaccinations and excess mortality in the Netherlands, led by Ronald Meester and Dr. Marc Jacobs, is now available online: Research Report: https://researchgate.net/publication/383239838_Eindverslag_van_het_onderzoek_naar_een_mogelijke_relatie_tussen_Covid-19_vaccinaties_en_oversterfte_in_Nederland_2021_-_2023?channel=doi&linkId=66c45cd6bcb6b956be01af9c&showFulltext=true… This comprehensive study was made possible through a crowdfunding initiative by Stichting De Menselijke Maat. Alongside Dr. Marc Jacobs and Ronald Meester, the core research team included Bram Bakker, Jona Walk, and Jan Bonte. Given its depth, the report is extensive. Below is a concise overview of its key findings: Chapter 1: Introduces the study and provides a justification for the research. Chapter 2: Discusses excess mortality in the Netherlands, noting significant quantitative and qualitative changes since 2021. Chapter 3: Presents data from AstraZeneca and the European Medicines Agency (EMA), raising concerns regarding vaccine safety. Chapter 4: Covers their literature review and meta-analysis attempt. Out of 13,430 publications reviewed, only 83 met their stringent content and quality criteria. This finding suggests that "following the science" during the pandemic may not have always been prudent, given the varying efficacy rates and large uncertainty margins reported in the remaining studies. Chapter 5: Focuses on a macro-level analysis of mortality related to vaccination. The findings suggest that vaccine effectiveness in the first four weeks post-administration may be negative, although the researchers exercise caution in their interpretations. Chapter 6: Delves into micro-data from the Centraal Bureau voor de Statistiek (CBS) at an individual level. The researchers identified significant data artifacts that have potentially skewed all previous studies by both CBS and the RIVM (National Institute for Public Health and the Environment). The team refrains from speculating on the origins of this data contamination. Chapter 7: Examines the reliability of the data used in their analysis, particularly focusing on CIMS and EMA data, which they found to be contaminated. This contamination complicates research efforts significantly. Chapter 8: Explores the medical aspects of COVID-19 vaccinations, concluding that while side effects exist, their full extent remains unclear. Chapter 9: Summarizes the research conclusions and offers recommendations for future studies. This research represents a substantial contribution to the ongoing discussion about vaccine safety and public health during the COVID-19 pandemic. All research transactions and data can be accessed through the following GitHub repository: GitHub Repository: https://github.com/MJacobs1985/Oversterfte_vaccinatie @RonaldMeester #ExcessMortality #Covid_19 #vaccine

ResearchGate - Temporarily Unavailable researchgate.net
GitHub - MJacobs1985/Oversterfte_vaccinatie: Deze repository is bedoeld om alle informatie die wij hebben gebruikt voor ons onderzoek naar de mogelijke relatie tussen vaccinatie, en mogen delen, beschikbaar te stellen. Deze repository is bedoeld om alle informatie die wij hebben gebruikt voor ons onderzoek naar de mogelijke relatie tussen vaccinatie, en mogen delen, beschikbaar te stellen. - GitHub - MJacobs1985/Oversterfte_vaccinatie: Deze repository is bedoeld om alle informatie die wij hebben gebruikt voor ons onderzoek naar de mogelijke relatie tussen vaccinatie, en mogen delen, beschikbaar te stellen. github.com

@MeasslainteIRL - TAE III 1215 🍀

https://www.linkedin.com/posts/dr-marc-jacobs-885b1430_pdf-eindverslag-van-het-onderzoek-naar-activity-7231600271410229249-sH3H?utm_source=share&utm_medium=member_android Dr Jacobs is a data scientist/ statistical consultant. Subject matter experts are finding their voice.

@MeasslainteIRL - TAE III 1215 🍀

Broken into layman's for everyone to enjoy. Title: Uncovering the Truth: A Deep Dive into COVID-19 Vaccines and Excess Mortality in the Netherlands Introduction In the wake of the global COVID-19 pandemic, nations worldwide rushed to develop and distribute vaccines in hopes of curbing the spread of the virus and reducing mortality rates. The Netherlands, like many other countries, embarked on an ambitious vaccination campaign. However, as the dust began to settle, an unsettling pattern emerged: despite widespread vaccination, the country continued to experience unexplained excess mortality. This puzzling phenomenon has sparked intense debate and raised crucial questions about the relationship between COVID-19 vaccines and overall mortality rates. In response to these concerns, a team of dedicated researchers, led by Ronald Meester and Marc Jacobs, undertook a comprehensive investigation. Their findings, detailed in a 166-page report, challenge many widely held beliefs about vaccine safety and efficacy. Today, we'll take you on a journey through this groundbreaking research, breaking down complex scientific concepts into digestible insights that could reshape our understanding of public health policies and vaccine impacts. The Unexpected Persistence of Excess Mortality Before we delve into the heart of the research, let's first understand what we mean by "excess mortality." Simply put, excess mortality refers to the number of deaths from all causes during a crisis that exceeds what we would have expected under 'normal' conditions. It's a crucial metric in public health, often used to assess the full impact of pandemics or other widespread health crises. In the Netherlands, a troubling trend emerged following the rollout of COVID-19 vaccines. Instead of seeing a reduction in overall mortality as vaccination rates increased, the country continued to experience higher-than-expected death rates. This persistence of excess mortality, even as COVID-19 cases declined, raised red flags for our research team. Key questions emerged: 1. Could there be a connection between the COVID-19 vaccines and this ongoing excess mortality? 2. If such a connection exists, what mechanisms might be at play? 3. How reliable is the data we're using to make these assessments? With these questions in mind, let's explore the key findings of this extensive research. 1. The Data Dilemma: Uncovering Inconsistencies At the heart of any scientific investigation lies data - the foundation upon which conclusions are built and policies are shaped. However, our research team uncovered troubling inconsistencies in the datasets provided by key institutions, including the CBS (Central Bureau of Statistics), RIVM (National Institute for Public Health and the Environment), and EMA (European Medicines Agency). These discrepancies aren't merely academic concerns. They strike at the very core of how we assess vaccine safety and efficacy. Let's break down some of the key issues: a) Disappearing Data: The team observed that in the EMA database, which tracks vaccine-related adverse events, some reports seemed to vanish over time. By regularly downloading and comparing datasets, the researchers noticed a consistent pattern of record removal. This raises serious questions about data integrity and the completeness of our understanding of vaccine side effects. b) Misclassification Concerns: One of the most alarming findings related to the classification of vaccinated individuals. The research suggests that some people who died shortly after receiving a vaccine may have been incorrectly classified as "unvaccinated" in official records. This potential misclassification could significantly skew our understanding of vaccine-related risks.

@MeasslainteIRL - TAE III 1215 🍀

c) Incomplete Reporting: The team found evidence suggesting that adverse events, including deaths, following vaccination might be substantially underreported. This underreporting could lead to an overestimation of vaccine safety and an underestimation of potential risks. To illustrate the magnitude of these data issues, let's consider a specific example from the report: In the weeks following vaccination rounds, the research team observed a sharp spike in mortality among those classified as "unvaccinated." This pattern was consistent across different age groups and vaccination phases. While various factors could contribute to this trend, one possible explanation is the misclassification of recently vaccinated individuals who died shortly after receiving the vaccine. These data inconsistencies highlight a crucial point: the foundation upon which many vaccine safety claims are built may be shakier than previously thought. It underscores the need for more transparent, accurate, and comprehensive data collection and reporting mechanisms. 2. The Healthy Vaccinee Effect: A Hidden Confounder As we dig deeper into the research findings, we encounter a phenomenon known as the "Healthy Vaccinee Effect" (HVE). This effect, while not new to epidemiologists, played a significant role in potentially skewing our understanding of vaccine effectiveness in the context of COVID-19. What is the Healthy Vaccinee Effect? The Healthy Vaccinee Effect occurs when healthier individuals are more likely to get vaccinated than those who are less healthy. This can happen for various reasons: 1. Health-conscious individuals may be more proactive about getting vaccinated. 2. Very ill or frail individuals might be advised against vaccination or choose not to get vaccinated. 3. People with certain pre-existing conditions might be more hesitant about receiving new vaccines. Why does this matter? The HVE can lead to an overestimation of vaccine effectiveness. If healthier people are more likely to be vaccinated, they're also less likely to die or experience severe illness in general. This can create the illusion that the vaccine is more effective at preventing death or severe illness than it actually is. The research team found strong evidence of a significant HVE in the Netherlands' COVID-19 vaccination campaign. Even after attempting to control for various factors, the vaccinated group appeared to have lower mortality rates from causes unrelated to COVID-19. To illustrate this, let's look at a hypothetical example: Imagine we have two groups of 1000 people each: Group A: Mostly healthy individuals who chose to get vaccinated Group B: A mix of healthy and less healthy individuals who didn't get vaccinated Over a year, we might see something like this: Group A (Vaccinated): 5 deaths (0.5% mortality rate) Group B (Unvaccinated): 15 deaths (1.5% mortality rate) At first glance, it might appear that the vaccine reduced mortality by 66%. However, if Group A was healthier to begin with, some or all of this difference might be due to their better overall health, not the vaccine's effectiveness. The research team found patterns in the data suggesting that this effect may have significantly inflated perceived vaccine effectiveness in previous studies. This doesn't mean the vaccines aren't effective, but it does suggest that their impact on overall mortality might be less dramatic than initially reported.

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3. The Mortality Mystery: Unexpected Patterns Emerge One of the most striking findings of the research relates to mortality patterns following vaccination rounds. The team observed a consistent and alarming trend: sharp increases in mortality among those classified as "unvaccinated" immediately following periods of intense vaccination activity. Let's break this down: a) The Unexpected Spike: During and immediately after periods when large numbers of people were being vaccinated, there was a noticeable increase in deaths among those classified as unvaccinated. This spike was far above what would be expected based on historical mortality data for similar time periods. b) Timing and Consistency: This pattern wasn't a one-off occurrence. It was observed consistently across different age groups and during different phases of the vaccination campaign. The spikes in mortality among the "unvaccinated" aligned closely with the timing of vaccination efforts for each age group. c) Magnitude of the Effect: In some cases, the mortality rate among the "unvaccinated" during these periods was several times higher than what would be considered normal for that age group and time of year. What could explain this pattern? The researchers propose several potential explanations, each with significant implications: 1. Data Misclassification: One possibility is that some individuals who died shortly after vaccination were incorrectly classified as "unvaccinated" in the official records. This could happen if there was a delay in updating vaccination status in the central database, or if deaths occurring very soon after vaccination weren't properly linked to the individual's vaccination record. 2. Immediate Post-Vaccination Vulnerability: Another hypothesis is that there might be a period of increased vulnerability immediately following vaccination. If this were the case, and if such deaths were not properly attributed to the vaccinated group, it could create the observed pattern. 3. Unaccounted Confounding Factors: There might be other factors at play that the current data collection and analysis methods aren't capturing. For instance, if vaccination campaigns coincided with other events or conditions that increased mortality risk, it could potentially create this pattern. To illustrate the magnitude of this effect, let's look at a specific example from the report: For the birth cohort 1940-1950 (people aged 71-81 at the time), the mortality rate among the "unvaccinated" in the four weeks following the peak of their vaccination campaign was a staggering 8.59%. This is compared to a rate of 0.14% among the vaccinated group in the same period. Such a massive difference is difficult to explain through conventional understanding of vaccine effects and normal mortality patterns. This finding raises crucial questions: 1. Are we accurately capturing and classifying deaths in relation to vaccination status? 2. Could there be immediate risks associated with vaccination that aren't being properly monitored or reported? 3. How might this pattern impact our understanding of vaccine effectiveness and safety? The researchers stress that while these patterns are clear in the data, determining causality requires further investigation. However, the consistency and magnitude of these mortality spikes demand serious attention and further study. 4. Reassessing Vaccine Effectiveness: A Paradigm Shift One of the most challenging aspects of the research findings relates to vaccine effectiveness. Since the beginning of the vaccination campaign, public health officials and media outlets have consistently cited high effectiveness rates, often quoting figures around 95% effectiveness against severe COVID-19.

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However, the team's analysis suggests a more complex and potentially concerning picture. Let's unpack this: a) Overall Mortality vs. COVID-19 Specific Mortality: While most effectiveness studies focused on prevention of COVID-19 related deaths, this research looked at overall mortality. The distinction is crucial. A vaccine might be effective at preventing deaths from COVID-19 specifically, but if it has other effects that increase mortality from other causes, its net benefit could be reduced or even negated. b) Age-Dependent Effectiveness: The research suggests that vaccine effectiveness varies significantly across age groups. While older age groups showed some benefit in terms of reduced overall mortality (though less than previously reported), younger age groups showed little to no benefit, and in some analyses, even a potential increase in mortality risk. c) Time-Dependent Effects: The team's analysis indicates that whatever protective effect the vaccines might offer wanes significantly over time. This aligns with other international studies but raises questions about the long-term benefits of vaccination, especially for younger, healthier individuals. d) The Role of Natural Immunity: The research also touches on the complex interplay between vaccine-induced immunity and natural immunity from prior infection. The data suggests that in some cases, natural immunity might provide comparable or even superior protection against severe outcomes. To illustrate these points, let's look at a hypothetical scenario based on the research findings: Imagine we're tracking two groups of 10,000 people each over a year: Group A: Vaccinated individuals Group B: Unvaccinated individuals In the 60+ age group, we might see something like this: Group A: 100 deaths (1% mortality rate) Group B: 150 deaths (1.5% mortality rate) This suggests a 33% reduction in overall mortality, which is significant but far less than the 95% effectiveness often quoted for preventing severe COVID-19. Now, let's look at a younger age group, say 18-40: Group A: 10 deaths (0.1% mortality rate) Group B: 9 deaths (0.09% mortality rate) In this case, we see no clear benefit in terms of overall mortality, and potentially even a slight increase (though the numbers are too small to be statistically significant on their own). The researchers stress that these findings don't mean the vaccines are ineffective or dangerous for everyone. Rather, they suggest that the benefits and risks may vary significantly based on factors like age, health status, and prior exposure to the virus. This nuanced understanding of vaccine effectiveness has important implications: 1. It challenges the one-size-fits-all approach to vaccination policies. 2. It suggests that the risk-benefit calculation for vaccination might be different for different age groups and individuals. 3. It underscores the need for more personalized medical advice regarding vaccination, especially for younger, healthier individuals. 5. Heart of the Matter: Cardiovascular Concerns One of the most specific and concerning findings of the research relates to cardiovascular health, particularly among younger individuals. The team observed an increase in heart-related hospital diagnoses following vaccination, a trend that aligns with emerging global research on myocarditis risks associated with mRNA vaccines. Let's break this down: a) Increased Diagnoses: The data showed a notable increase in hospital diagnoses for conditions like myocarditis (inflammation of the heart muscle), pericarditis (inflammation of the protective sac around the heart), and other cardiovascular issues following vaccination campaigns. b) Age-Specific Patterns: This increase was particularly pronounced in younger age groups, especially those under 40. This aligns with other international studies that have identified young males as being at higher risk for these complications.

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c) Temporal Relationship: The spikes in these diagnoses correlated closely with vaccination timelines, suggesting a potential causal relationship. However, the researchers stress that correlation doesn't necessarily imply causation, and more investigation is needed. d) Long-term Implications: While most cases of vaccine-associated myocarditis appear to be mild and resolve on their own, the long-term implications of these heart issues remain unknown. This uncertainty is particularly concerning when considering vaccination of young, healthy individuals who are at low risk from COVID-19 itself. To illustrate the significance of these findings, let's consider a hypothetical scenario based on the research: Imagine we're tracking heart-related hospital admissions for people aged 18-30 in a city of 1 million people: Pre-vaccination period (3 months): - Average monthly admissions for myocarditis/pericarditis: 10 cases Post-vaccination period (3 months): - Month 1 (peak vaccination): 30 cases - Month 2: 25 cases - Month 3: 15 cases This hypothetical scenario shows a clear spike in cases coinciding with the vaccination campaign, followed by a gradual return to baseline. While the numbers might seem small, they represent a significant increase in relative risk, especially for a young, healthy population. The researchers highlight several important considerations regarding these cardiovascular findings: 1. Risk vs. Benefit: For young, healthy individuals at low risk from COVID-19, even a small increase in cardiovascular risk could potentially outweigh the benefits of vaccination. 2. Underreporting Concerns: The team suggests that these cases might be underreported, as mild cases might not result in hospital admission and could be missed in the data. 3. Need for Long-term Follow-up: Given the novelty of the mRNA vaccines and the uncertainty surrounding long-term effects of myocarditis, ongoing monitoring and research are crucial. 4. Implications for Booster Policies: These findings raise questions about the wisdom of repeated booster doses, especially for younger age groups. The cardiovascular concerns highlighted in this research underscore the need for a more nuanced, personalized approach to vaccination policies. They also emphasize the importance of transparent communication about potential risks, allowing individuals and their healthcare providers to make informed decisions based on personal risk profiles. 6. The Immune System Puzzle: Unintended Consequences? One of the most intriguing and potentially far-reaching aspects of the research relates to the broader effects of COVID-19 vaccines on the immune system. The team's findings suggest that these vaccines might have more complex interactions with our immune defenses than initially thought, potentially affecting our ability to fight off other infections or diseases.

@MeasslainteIRL - TAE III 1215 🍀

Let's unpack this complex topic: a) Non-Specific Effects of Vaccines: The researchers discuss a phenomenon known as "non-specific effects" of vaccines. This refers to the idea that vaccines can have broader impacts on the immune system beyond just protecting against their target disease. These effects can be both positive and negative. b) Altered Immune Responses: Some data suggest that COVID-19 vaccines might alter how our immune system responds to other pathogens. This could potentially make us more susceptible to certain infections while possibly offering enhanced protection against others. c) Interference with Natural Immunity: There's evidence that vaccination might interfere with the development of broad, natural immunity that typically occurs after infection. This could have implications for long-term immune protection against COVID-19 and its variants. d) Age-Dependent Effects: The research indicates that these immune system effects might vary significantly based on age, with potentially different outcomes for children, adults, and the elderly. To illustrate these concepts, let's consider a hypothetical scenario: Imagine we're tracking infections in two groups of 1000 people over six months following a COVID-19 vaccination campaign: Group A: Vaccinated against COVID-19 Group B: Unvaccinated We might see something like this: COVID-19 infections: Group A: 10 cases Group B: 50 cases This aligns with expected vaccine effectiveness. But now let's look at other infections: Influenza infections: Group A: 40 cases Group B: 30 cases Respiratory Syncytial Virus (RSV) infections: Group A: 25 cases Group B: 20 cases This hypothetical scenario illustrates the complex nature of immune system interactions. While the vaccine appears effective against COVID-19, it might inadvertently affect susceptibility to other infections. The researchers highlight several important considerations regarding these immune system findings: 1. Balanced Assessment: It's crucial to consider both the intended and unintended effects of vaccines on the immune system. A vaccine that protects against one disease but increases susceptibility to others may not provide a net benefit, especially for low-risk individuals. 2. Age-Specific Strategies: Given that these effects appear to vary by age, vaccination strategies may need to be tailored for different age groups. What's beneficial for an elderly person might not be appropriate for a child. 3. Long-term Monitoring: The full impact of these immune system changes may only become apparent over time. Long-term studies are essential to understand the broader health implications of mass vaccination. 4. Implications for Future Pandemics: Understanding these non-specific effects could be crucial for preparing for future pandemics. If vaccines alter our immune responses in complex ways, this needs to be factored into public health strategies. The immune system findings in this research underscore the intricate nature of our body's defenses and the potential for unintended consequences when we intervene. They highlight the need for a more holistic approach to vaccine assessment, one that considers not just the target disease but overall health outcomes. 7. The Booster Dilemma: Diminishing Returns? As the pandemic progressed and vaccine effectiveness appeared to wane, many countries, including the Netherlands, implemented booster shot programs. The research team took a close look at the impact of these booster campaigns, and their findings raise important questions about the long-term strategy of repeated vaccinations. Key points from the booster analysis include: a) Short-term Effectiveness: The data suggest that booster shots did provide a short-term increase in protection against severe COVID-19, particularly for older and vulnerable populations.

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b) Rapidly Waning Protection: However, this boosted protection appeared to decline rapidly, often within a few months. This calls into question the sustainability of a strategy relying on frequent booster shots. c) Diminishing Returns: Each subsequent booster shot seemed to offer less additional protection than the previous one. This suggests a law of diminishing returns when it comes to repeated vaccinations. d) Potential Immune System Fatigue: Some data points hinted at the possibility of "immune system fatigue" with repeated boosters, where the body's immune response becomes less robust over time. e) Age-Dependent Effects: As with the initial vaccination series, the benefits and risks of boosters appeared to vary significantly by age group. To illustrate these concepts, let's consider a hypothetical scenario based on the research findings: Imagine we're tracking COVID-19 hospitalizations in a group of 10,000 people aged 65 and older over a year: After initial vaccination series: - Months 1-3: 50 hospitalizations - Months 4-6: 100 hospitalizations (protection waning) After first booster: - Months 7-9: 30 hospitalizations (improved protection) - Months 10-12: 80 hospitalizations (protection waning again) After second booster: - Months 13-15: 40 hospitalizations (less improvement than first booster) - Months 16-18: 75 hospitalizations (protection waning faster) This scenario illustrates the initial effectiveness of boosters, but also the diminishing returns and faster waning of protection with each subsequent shot. The researchers highlight several important considerations regarding booster campaigns: 1. Targeted Approach: Given the varying risk profiles across age groups, a more targeted approach to boosters may be warranted, focusing on those most at risk of severe COVID-19. 2. Timing Considerations: The rapid waning of booster effectiveness suggests that timing is crucial. Administering boosters too frequently might not be beneficial and could potentially be counterproductive. 3. Long-term Sustainability: A strategy relying on frequent boosters for the entire population may not be sustainable in the long term, both from a public health and an economic perspective. 4. Alternative Strategies: The findings suggest a need to explore alternative strategies for long-term COVID-19 management, such as developing more broadly effective vaccines or focusing on treatments. The booster dilemma highlighted in this research underscores the complexity of managing a long-term pandemic response. It suggests that while boosters can play a role in protecting vulnerable populations, they may not be a one-size-fits-all solution for ongoing COVID-19 management. 8. Data Transparency and Integrity: A Call to Action Throughout their investigation, the research team encountered significant challenges related to data accessibility, consistency, and transparency. These issues not only hampered their analysis but also raised broader concerns about the foundation upon which many public health decisions are being made. Key issues identified include: a) Limited Access to Raw Data: The team found it difficult to access complete, raw datasets from official sources. This lack of access makes it challenging for independent researchers to verify official claims or conduct their own analyses. b) Inconsistencies Across Datasets: When comparing data from different sources (e.g., CBS, RIVM, EMA), the team found concerning inconsistencies. These discrepancies make it difficult to draw reliable conclusions and raise questions about data quality. c) Changing Definitions and Metrics: Throughout the pandemic, definitions for key metrics (e.g., what constitutes a COVID-19 death, or who is considered "fully vaccinated") have changed. These shifting goalposts complicate long-term trend analysis.

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d) Potential Underreporting: The research suggests that adverse events following vaccination, including deaths, may be substantially underreported. This could lead to an overestimation of vaccine safety. e) Lack of Granularity: In many cases, the available data lacked the granularity needed for detailed analysis. For example, precise timing of vaccination in relation to subsequent health events was often not available. To illustrate the importance of data transparency, let's consider a hypothetical scenario: Imagine two research teams analyzing vaccine effectiveness: Team A: Has access only to aggregated, publicly available data. Team B: Has access to raw, granular data including detailed individual health records. Team A's Conclusion: "Vaccine effectiveness against severe COVID-19 is 90% across all age groups." Team B's Conclusion: "Vaccine effectiveness varies significantly by age: 95% for 65+, 80% for 40-64, and 50% for under 40. We also found a 3-fold increase in non-COVID hospitalizations in the week following vaccination in the under-40 group." This scenario illustrates how limited data access can lead to oversimplified or potentially misleading conclusions. The researchers emphasize several key points regarding data transparency: 1. Public Trust: Transparent, accessible data is crucial for maintaining public trust in health institutions and policies. 2. Scientific Integrity: Open access to raw data allows for peer review and validation, cornerstones of scientific integrity. 3. Informed Decision Making: Granular, accurate data is essential for making informed personal and policy decisions about vaccination and other health interventions. 4. Continuous Improvement: Transparent data sharing allows for continuous refinement of analysis methods and understanding, crucial in a rapidly evolving situation like a pandemic. The data transparency issues highlighted in this research underscore the need for a more open, collaborative approach to public health data. They suggest that improving data quality, accessibility, and transparency should be a priority for health authorities and policymakers.

@MeasslainteIRL - TAE III 1215 🍀

9. Media and Public Communication: Navigating Complexity The research team dedicates a significant portion of their report to discussing the role of media and public health communication during the pandemic. They argue that the way information about vaccines and COVID-19 has been presented to the public has often been oversimplified, potentially misleading, and at times, may have suppressed important scientific debate. Key points from this section include: a) Oversimplification of Complex Issues: The researchers note that media outlets often presented vaccine effectiveness and safety in black-and-white terms, failing to convey the nuances and uncertainties inherent in the scientific data. b) Inadequate Coverage of Adverse Events: There was a tendency in many media outlets to downplay or underreport potential vaccine side effects, possibly out of fear of fueling vaccine hesitancy. c) Stigmatization of Dissenting Voices: Scientists and medical professionals who raised concerns about vaccine policies or presented data challenging the mainstream narrative often faced criticism or marginalization. d) Lack of Context: Absolute risk reductions were rarely presented alongside the more impressive-sounding relative risk reductions, potentially skewing public perception of vaccine benefits.

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e) Evolving Science vs. Definitive Statements: Public health messaging often presented evolving scientific understanding as settled fact, potentially eroding public trust when guidance later changed. To illustrate these points, let's consider a hypothetical media report: Headline: "COVID-19 Vaccine 95% Effective, Experts Say" This headline, while technically accurate based on relative risk reduction in clinical trials, fails to convey important context: - It doesn't specify what the vaccine is 95% effective against (symptomatic infection? severe disease? death?). - It doesn't mention that this effectiveness may vary by age group or wane over time. - It doesn't provide the absolute risk reduction, which might be much less impressive (e.g., reducing risk from 1% to 0.05% is a 95% relative reduction but only a 0.95% absolute reduction). A more nuanced headline might read: "COVID-19 Vaccine Shown to Reduce Risk of Severe Disease by 95% in Short Term, Effects May Vary by Age and Over Time" The researchers emphasize several key points regarding media and public communication: 1. Balanced Reporting: Media should strive to present both benefits and potential risks of medical interventions, including vaccines. 2. Embracing Uncertainty: It's crucial to communicate the evolving nature of scientific understanding, especially in a novel situation like a pandemic. 3. Encouraging Scientific Debate: Open discussion of differing scientific viewpoints should be encouraged, not stigmatized. 4. Contextualizing Statistics: Providing context for statistical claims, including absolute risk reductions alongside relative risk reductions, is essential for public understanding. 5. Empowering Individual Decision-Making: Information should be presented in a way that allows individuals to make informed decisions based on their personal risk-benefit profile. The media and communication issues highlighted in this research underscore the challenges of conveying complex scientific information to the public. They suggest a need for more nuanced, context-rich public health communication strategies.

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Conclusion: Charting a Path Forward As we reach the end of our deep dive into this groundbreaking research, it's clear that the relationship between COVID-19 vaccines and excess mortality is far more complex than initially thought. The findings challenge many of our assumptions about vaccine effectiveness and safety, and raise important questions about our approach to public health during pandemics. Key takeaways include: 1. Data Integrity is Paramount: The inconsistencies and potential inaccuracies in official datasets underscore the need for more transparent, accurate, and comprehensive data collection and reporting. 2. One-Size-Fits-All Approaches Are Problematic: The varying impacts of vaccination across age groups and health statuses suggest a need for more personalized vaccination strategies. 3. Long-term Effects Require Ongoing Study: The potential for vaccines to have broader impacts on the immune system and overall health necessitates long-term, comprehensive follow-up studies. 4. Transparent Communication is Crucial: Both the scientific community and the media need to embrace more nuanced, balanced communication about the benefits and risks of medical interventions. 5. Scientific Debate Should Be Encouraged: Open discussion of differing viewpoints and interpretations of data is essential for advancing our understanding and making informed policy decisions. The researchers stress that their findings don't negate the important role vaccines have played in combating the COVID-19 pandemic. However, they argue that a more nuanced understanding of vaccine impacts is crucial for shaping future public health strategies. Looking ahead, the report calls for several key actions: 1. Comprehensive Review of Vaccine Policies: A thorough, independent review of current vaccination policies, taking into account the latest data on effectiveness, safety, and long-term impacts. 2. Enhanced Adverse Event Monitoring: Implementation of more robust systems for detecting and investigating potential vaccine side effects, including long-term effects. 3. Personalized Risk-Benefit Assessments: Development of tools to help individuals and healthcare providers make personalized decisions about vaccination based on individual risk profiles. 4. Improved Data Transparency: Creation of open-access databases with anonymized, granular health data to facilitate independent research and analysis. 5. Interdisciplinary Research Initiatives: Funding for collaborative research projects that bring together experts from virology, immunology, epidemiology, and other relevant fields to study the broader impacts of vaccination. As we navigate the ongoing challenges of the COVID-19 pandemic and prepare for future health crises, the insights from this research provide a valuable roadmap. They remind us of the importance of remaining open to new evidence, embracing scientific debate, and continuously refining our understanding and approaches. What are your thoughts on these findings? How do you think they should inform future public health policies? Share your views in the comments below, and let's continue this crucial conversation.

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Sources: 1. Meester, R., Jacobs, M., et al. (2024). "Eindverslag van het onderzoek naar een mogelijke relatie tussen Covid-19 vaccinaties en oversterfte in Nederland 2021 - 2023" 2. Central Bureau of Statistics (CBS) Netherlands, https://www.cbs.nl/ 3. National Institute for Public Health and the Environment (RIVM), https://www.rivm.nl/ 4. European Medicines Agency (EMA), https://www.ema.europa.eu/ 5. World Health Organization (WHO), https://www.who.int/ 6. Centers for Disease Control and Prevention (CDC), https://www.cdc.gov/ 7. The Lancet, https://www.thelancet.com/ 8. New England Journal of Medicine, https://www.nejm.org/ 9. British Medical Journal (BMJ), https://www.bmj.com/ 10. Nature, https://www.nature.com/

Centraal Bureau voor de Statistiek Het CBS heeft als taak het publiceren van betrouwbare en samenhangende statistische informatie, die inspeelt op de behoefte van de samenleving. cbs.nl
Rijksinstituut voor Volksgezondheid en Milieu | RIVM rivm.nl
Homepage The European Medicines Agency is a decentralised agency of the European Union responsible for the evaluation, supervision and safety monitoring of medicines. ema.europa.eu
World Health Organization (WHO) The United Nations agency working to promote health, keep the world safe and serve the vulnerable. who.int
Centers for Disease Control and Prevention cdc.gov
The BMJ: Leading Medical Research, News, Education, Opinion High impact medical journal. Champion of better research, clinical practice & healthcare policy since 1840. For GPs, hospital doctors, educators, policymakers. bmj.com
Nature First published in 1869, Nature is the world’s leading multidisciplinary science journal. Nature publishes the finest peer-reviewed research that drives ground-breaking discovery, and is read by thought-leaders and decision-makers around the world. nature.com

@MeasslainteIRL - TAE III 1215 🍀

Huge thanks to the scientists who made this work public and my friend @BoostImmuneBlog I hope this helps shed more light on the fraudulent and dangerous COVID 19 vaccine campaign https://onlinelibrary.wiley.com/doi/10.1111/eci.14286 #NoAmnesty @EU_IPO @DonnellyStephen @SimonHarrisTD @LeoVaradkar @EvaVlaar@AndersonAfDMdEP@JimFergusonUK@RealEddieHobbs #StopTheShots @Reseeit save thread

@MeasslainteIRL - TAE III 1215 🍀

@BoostImmuneBlog @EU_IPO @DonnellyStephen @SimonHarrisTD @LeoVaradkar @EMA_News @IMO_IRL @bmj_latest @Nature @hrw It's time for some accountability and maybe a lot of autopsies @pfizer @AstraZeneca @moderna_tx #StopTheShots

@MeasslainteIRL - TAE III 1215 🍀

@BoostImmuneBlog @EU_IPO @DonnellyStephen @SimonHarrisTD @LeoVaradkar @EMA_News @IMO_IRL @bmj_latest @Nature @hrw @pfizer @AstraZeneca @moderna_tx @reseeit save thread

Saved - July 15, 2024 at 3:57 PM
reSee.it AI Summary
Tech workers at Google are protesting against the use of AI and other technologies by Israel in its conflict with Gaza. Google is facing backlash for its $1.2bn "Project Nimbus" deal with Israel, resulting in layoffs and the firing of employees who protested. Concerns are raised about the weaponization of technology and the potential for mass surveillance.

@MeasslainteIRL - TAE III 1215 🖖🏻 (Tomo)

What is #ProjectNimbus, and why are @GoogleAI workers protesting the Israel deal? Tech workers are protesting against the use of artificial intelligence and other technologies by Israel in its war on Gaza.

Video Transcript AI Summary
Project Nimbus is a cloud computing initiative by the Israeli government and military, aiming to provide a comprehensive cloud solution. The Israeli finance ministry has announced a contract to support its implementation, emphasizing its role in the country's digital transformation. Google is providing Israel with advanced AI capabilities through Project Nimbus, potentially aiding in data collection for facial recognition and object tracking.
Full Transcript
Speaker 0: Wait for it. Alexa, can you tell me what Project Nimbus is? Project Nimbus is a cloud computing initiative undertaken by the Israeli government and military. The project aims to provide an all encompassing cloud solution for the government, defense establishment, and other stakeholders. The Israeli finance ministry has announced a contract to facilitate the implementation of project Nimbus, highlighting its importance in the digital transformation of the country's public sector. Alexa, why does project Nimbus have anything to do with Israel? From inventiva.co.in. According to a 2021 report, Google is furnishing Israel with advanced AI capabilities through Project Nimbus, potentially facilitating data collection for facial recognition and object tracking.

@MeasslainteIRL - TAE III 1215 🖖🏻 (Tomo)

https://www.aljazeera.com/news/2024/4/23/what-is-project-nimbus-and-why-are-google-workers-protesting-israel-deal

What is Project Nimbus, and why are Google workers protesting Israel deal? Tech workers are protesting against the use of AI and other technologies by Israel in its war on Gaza. aljazeera.com

@MeasslainteIRL - TAE III 1215 🖖🏻 (Tomo)

Google is in the news for all the wrong reasons this week, not only cementing its place as one of the biggest tech companies making layoffs, but more dramatically making headlines for firing 28 employees who protested against its $1.2bn “Project Nimbus” deal with Israel. https://tech.co/news/what-is-project-nimbus-google

What is Project Nimbus? Google's $1.2bn Israel Deal Explained Google has fired 28 employees who protested its lucrative Project Nimbus deal with Israel, but what is it and why is it so controversial? tech.co

@MeasslainteIRL - TAE III 1215 🖖🏻 (Tomo)

The technology could be & will be weaponized against vulnerable populations. https://en.m.wikipedia.org/wiki/Project_Nimbus Are you all ready for mass surveillance? Guilty until proven innocent.

Project nimbus - Wikipedia en.m.wikipedia.org
Saved - May 27, 2024 at 9:12 AM
reSee.it AI Summary
Mammography screening may lead to unnecessary cancer diagnoses, according to studies. The mortality rate for breast cancer has been declining since 1990, and other factors like tamoxifen therapy may contribute to this reduction. The National Cancer Institute warns that mammography can result in overdiagnosis, particularly in younger women who face higher risks. On a positive note, compounds derived from the Scutellaria baicalensis herb show promise in combating breast cancer by inhibiting cell survival and proliferation, as well as preventing metastasis. #BreastCancer #Mammogram #CancerResearch #NaturalTherapies

@MeasslainteIE - Thomas Anthony III

#ICYMI "For every 15 cases of breast cancer mammography identifies, it may actually cause 75 unnecessary cancer diagnoses." "It is easy to promote mammography screening if the majority of women believe that it prevents or reduces the risk of getting breast cancer and saves many lives through early detection of aggressive tumors. We would be in favor of mammography screening if these beliefs were valid. Unfortunately, they are not, and we believe that women need to be told so." #WomansHealth #Mammogram

@MeasslainteIE - Thomas Anthony III

The introduction of the mammography screening program does not seem to modify the mortality rate, which had been progressively declining since 1990. Other factors contributing to mortality reduction, such as tamoxifen therapy and changes in cause-of-death coding, may act as confounders when evaluating screening benefits. Read more here ! https://smw.ch/index.php/smw/article/view/1861/2604

Controversies in the mammography screening programme in Switzerland | Swiss Medical Weekly smw.ch

@MeasslainteIE - Thomas Anthony III

The National Cancer Institute (NCI) has stated that for every 15 cases of breast cancer mammography identifies, it may actually lead to 75 overdiagnosed cases. This overdiagnosis is particularly concerning for younger women, who face higher risks from the dangers associated with mammography. Studies have shown that young women tested annually may experience up to a 52% increase in breast cancer-related deaths. https://thetruthaboutcancer.com/mammograms-breast-cancer-test/ #MoratoriumOnEverything #BreastCancer

Are Mammograms the Best Breast Cancer Test? Women in America and other industrialized countries are convinced that regular mammograms are crucial to detecting breast cancer. Enormous funding and research has swayed the public into believing this to be true. Yet despite this, mammography has a very strong opposition in many quadrants of the medical and natural health communities. If you discover one of the warning signs of breast cancer, the question remains: are mammograms the best test for breast cancer? Mammograms provide an X-ray image of breasts in which doctors will look for evidence of growing tumors that may go unnoticed during a routine physical exam. Needed to produce the thetruthaboutcancer.com

@MeasslainteIE - Thomas Anthony III

Baicalein and baicalin, two compounds derived from the traditional Chinese herb Scutellaria baicalensis, have shown promising results in combating breast cancer.Baicalein induces apoptosis (programmed cell death) and autophagy (cellular degradation) in breast cancer cells by inhibiting the PI3K/AKT pathway, both in vivo and in vitro. This pathway is crucial for cell survival and proliferation, making its inhibition a powerful strategy against cancer cells.Baicalin inhibits the metastasis of highly aggressive breast cancer cells. It achieves this by reversing the epithelial-to-mesenchymal transition (EMT), a process that enables cancer cells to spread. Baicalin targets the β-catenin signaling pathway, which plays a significant role in EMT and cancer progression. https://pubmed.ncbi.nlm.nih.gov/29039569/ #BreastCancerResearch #NaturalTherapies #CancerTreatment #Baicalein #Baicalin #CancerAwareness #Skullcap End, thank you for reading!

Baicalin inhibits the metastasis of highly aggressive breast cancer cells by reversing epithelial-to-mesenchymal transition by targeting β-catenin signaling - PubMed Metastasis is the main cause of death in breast cancer patients, which is due partly to the lack of effective treatment. Baicalin, a flavonoid compound isolated from the roots of Scutellaria lateriflora Georgi (Huang Qin), has recently been confirmed as an effective agent for the treatment of a vari … pubmed.ncbi.nlm.nih.gov
Saved - May 26, 2024 at 10:06 AM
reSee.it AI Summary
The posts discuss the role of Spike protein in immune response and potential implications for COVID-19. They mention various immune receptors that can detect viral DNA and trigger immune responses. The posts highlight similarities between SARS-CoV-2 and HIV in terms of immune interactions. The use of DAMPs by the virus for propagation and potential therapeutic applications are discussed. The posts emphasize the need for further research and caution regarding the long-term effects of Spike protein and COVID-19 vaccinations.

@MeasslainteIE - Thomas Anthony III

The posts discuss the role of Spike protein in immune response and potential implications for COVID-19. They mention various immune receptors, such as cGAS-STING, #AIM2, #LRR, #NLRP3, #TLR9, and #RAGE, that can detect viral DNA and trigger immune responses. The release of cell-free DNA and DAMPs during infection can activate the immune system and lead to inflammation. The posts also highlight similarities between SARS-CoV-2 and HIV in terms of immune interactions and potential long-term effects. The Spike protein's structural similarities to #gp41 of #HIV-1 and its potential interaction with #p53 are mentioned. The use of #DAMPs by the virus for propagation and the potential therapeutic applications of #P2X7R antagonists are discussed. The posts emphasize the need for further research and caution regarding the long-term effects of #Spike protein and #COVID19 #Vaccinations

@AnneliseBocquet - Bocquet Annelise 🔬🧬📚🚜

Spike et immunité... et plus si affinité. Petit thread d'actualisation basé sur les publications suivantes : https://pubmed.ncbi.nlm.nih.gov/38439942/ https://doi.org/10.1038/s41598-024-61906-6 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8855831/ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7406264/ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10474074/ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8232874/ Et peut-être plus... 1/n

Self-DNA driven inflammation in COVID-19 and after mRNA-based vaccination: lessons for non-COVID-19 pathologies - PubMed The coronavirus disease 2019 (COVID-19) pandemic triggered an unprecedented concentration of economic and research efforts to generate knowledge at unequalled speed on deregulated interferon type I signalling and nuclear factor kappa light chain enhancer in B-cells (NF-κB)-driven interleukin (IL)-1β … pubmed.ncbi.nlm.nih.gov
Inflammation Meets Metabolism: Roles for the Receptor for Advanced Glycation End Products Axis in Cardiovascular Disease Fundamental modulation of energy metabolism in immune cells is increasingly being recognized for the ability to impart important changes in cellular properties. In homeostasis, cells of the innate immune system, such as monocytes, macrophages and dendritic ... ncbi.nlm.nih.gov
An integrated view of lipid metabolism in ferroptosis revisited via lipidomic analysis Ferroptosis is a form of regulated cell death characterized by iron-dependent lipid peroxidation. This process contributes to cellular and tissue damage in various human diseases, such as cardiovascular diseases, neurodegeneration, liver disease, and ... ncbi.nlm.nih.gov
RAGE impairs murine diabetic atherosclerosis regression and implicates IRF7 in macrophage inflammation and cholesterol metabolism Despite advances in lipid-lowering therapies, people with diabetes continue to experience more limited cardiovascular benefits. In diabetes, hyperglycemia sustains inflammation and preempts vascular repair. We tested the hypothesis that the receptor for ... ncbi.nlm.nih.gov
Mechanistic insights into SARS-CoV-2 spike protein induction of the chemokine CXCL10 - Scientific Reports During a SARS-CoV-2 infection, macrophages recognize viral components resulting in cytokine production. While this response fuels virus elimination, overexpression of cytokines can lead to severe COVID-19. Previous studies suggest that the spike protein (S) of SARS-CoV-2 can elicit cytokine production via the transcription factor NF-κB and the toll-like receptors (TLRs). In this study, we found that: (i) S and the S2 subunit induce CXCL10, a chemokine implicated in severe COVID-19, gene expression by human macrophage cells (THP-1); (ii) a glycogen synthase kinase-3 inhibitor attenuates this induction; (iii) S and S2 do not activate NF-κB but do activate the transcription factor IRF; (iv) S and S2 do not require TLR2 to elicit CXCL10 production or activate IRF; and (v) S and S2 elicit CXCL10 production by peripheral blood mononuclear cells (PBMCs). We also discovered that the cellular response, or lack thereof, to S and S2 is a function of the recombinant S and S2 used. While such a finding raises the possibility of confounding LPS contamination, we offer evidence that potential contaminating LPS does not underly induced increases in CXCL10. Combined, these results provide insights into the complex immune response to SARS-CoV-2 and suggest possible therapeutic targets for severe COVID-19. nature.com
Impairing RAGE signaling promotes survival and limits disease pathogenesis following SARS-CoV-2 infection in mice Cellular and molecular mechanisms driving morbidity following SARS-CoV-2 infection have not been well defined. The receptor for advanced glycation end products (RAGE) is a central mediator of tissue injury and contributes to SARS-CoV-2 disease pathogenesis. ... ncbi.nlm.nih.gov

@MeasslainteIE - Thomas Anthony III

@Kevin_McKernan - Kevin McKernan

@jeremyrhammond @sense_strand @thereal_truther @Debunk_the_Funk @DrJ_surgeon @DJSpeicher @P_J_Buckhaults Messing with cGAS-STING is good for you!!! 🤡 https://aacrjournals.org/cancerdiscovery/article/10/1/26/2314/The-Cytosolic-DNA-Sensing-cGAS-STING-Pathway-in

@MeasslainteIE - Thomas Anthony III

The cGAS-STING pathway is a crucial part of the innate immune response, particularly in detecting cytosolic DNA, which is often a sign of infection or cellular damage. Here's a brief overview: 1. **cGAS (cyclic GMP-AMP synthase)**: This is an enzyme that acts as a sensor for cytosolic DNA. When cGAS encounters double-stranded DNA in the cytoplasm, it binds to the DNA and catalyzes the synthesis of a signaling molecule called cyclic GMP-AMP (cGAMP). 2. **STING (Stimulator of Interferon Genes)**: STING is an adaptor protein located in the endoplasmic reticulum. cGAMP binds to STING, leading to its activation. 3. **Activation Pathway**: Once activated, STING translocates to the Golgi apparatus and initiates a signaling cascade that activates transcription factors such as IRF3 and NF-κB. These transcription factors then enter the nucleus and promote the expression of type I interferons and other inflammatory cytokines. The cGAS-STING pathway plays a vital role in the defense against viral infections, as many viruses release their DNA into the cytoplasm of host cells. It also has implications in cancer, autoimmune diseases, and other inflammatory conditions due to its ability to detect abnormal DNA within cells.

@MeasslainteIE - Thomas Anthony III

Neuroinflammation, a term that encapsulates intricate immune responses within the central nervous system (CNS), has increasingly become the focal point of research in the field of neurodegenerative diseases. #cGAS_STING

@heniek_htw - htw

#Mitophagy and cGAS–STING crosstalk in #neuroinflammation https://www.sciencedirect.com/science/article/pii/S2211383524001904

Mitophagy and cGAS–STING crosstalk in neuroinflammation Mitophagy, essential for mitochondrial health, selectively degrades damaged mitochondria. It is intricately linked to the cGAS–STING pathway, crucial … sciencedirect.com

@MeasslainteIE - Thomas Anthony III

Very interesting what you can find on X. Sad that we are looking 4 years too late.

@Cell_Metabolism - Cell Metabolism

NSUN2 is a glucose sensor suppressing cGAS/STING to maintain tumorigenesis and immunotherapy resistance dlvr.it/SwyHnm

@MeasslainteIE - Thomas Anthony III

Bravo to @AnneliseBocquet I particularly liked the process that by spike there is cell to cell fusion; universal mechanics that will make syncytia +/- large and numerous and therefore severity and lethality and that cgas-sting contributes to it.

@vieil_garde_ph - vieil_garde_PH

Bravo à @AnneliseBocquet j'ai particulièrement apprécié le processus qui par spike il y a fusion cell to cell ; mécanique universelle qui fera syncytia +/- grandes et nombreuses et donc sévérité et létalité et que cgas-sting y contribue https://www.cureus.com/articles/218170-impacts-of-the-sars-cov-2-spike-protein-on-the-innate-immune-system-a-review?score_article=true#!/ AAS / cgas-sting

Impact of the SARS-CoV-2 Spike Protein on the Innate Immune System: A Review The Spike protein enables the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection by binding to multiple receptors, including the angiotensin-converting enzyme 2 (ACE2). Scientific studies also indicate that Spike is involved in severe forms of coronavirus disease 2019 (COVID-19), "long-haul COVID diseases" - also known as "long COVID syndromes" or "post-acute sequelae of SARS-CoV-2 infection" (PACS) - or, recently, in adverse reactions to lipid nanoparticle-messenger ribonucleic acid (mRNA) vaccines or other anti-COVID19 products. Numerous mutations, notably within the subunit 1 of Spike (S1), prevent neutralization by antibodies, but more generally, the virus has developed numerous strategies to avoid immune system surveillance, especially type-I interferons (IFN-I). Meanwhile, a “hyperinflammatory” state, named “cytokine storm,” sets in. However, what role does the Spike protein play in the immune escape mechanisms? Can its inflammatory activities affect IFN-I? Does Spike block IFN-I or hijack them for the virus benefits? What are the other potential consequences? This article was written to provide an up-to-date and more general overview of the impact of the Spike protein on the innate immune system and its effectors at the molecular level. cureus.com

@MeasslainteIE - Thomas Anthony III

@AnneliseBocquet Post translated with thread reader! https://twitter-thread.com/t/en-US/1772902508886687757 The paper is in English.

Saved - May 13, 2024 at 11:48 PM
reSee.it AI Summary
The posts discuss various topics related to COVID-19. The first post claims to have been right about several aspects, including the lab leak theory, natural immunity, masks, lockdowns, vaccines, boosters, and more. It criticizes those who trust the government and science. The second post expresses frustration about people not listening to warnings about vaccinating children. The third post mentions that the author was not on a specific substance at the time. The fourth and fifth posts provide information about a study on replicon vaccines and their ability to infect cells via extracellular vesicles. The author of the posts is Hiroshi Arakawa, a scientist with a background in molecular biology and immunology.

@MeasslainteIE - Thomas Anthony III

Why yes we were !! https://www.facebook.com/share/p/nj9TESHJbYb57MBA/

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@catturd2 - Catturd ™

We were right about the lab leak. We were right about natural immunity. We were right about masks. We were right about lockdowns. We were right about the vaccines. We were right about boosters. We were right about them faking COVID numbers. We were right about the deadly hospital protocol. We were right about ivermectin. We were right about evil Dr. Fauci. We were right about the evil WHO. We were right about it being a world power grab. Guess who was wrong about everything? Yep  the government sheep "TrUsT tHe sCieNCe" cult.

@MeasslainteIE - Thomas Anthony III

I was begging people not to inject their kids. It fell on deaf ears. https://www.facebook.com/share/p/XX74CJpaGxj24mk5/

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@MeasslainteIE - Thomas Anthony III

I wasn't on X at the time I wouldn't have lasted long anyway 😂👌🏻 https://www.facebook.com/share/p/gb89bm7jXh38RdUt/

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@MeasslainteIE - Thomas Anthony III

Hiroshi Arakawa May 12, 2024, 18:23 A replicon vaccine (self-amplifying mRNA vaccine) scheduled to start vaccination in Japan from this autumn as a new type of coronavirus vaccine targeting Japanese people is a gene preparation that has RNA replication genes in addition to antigen genes. The genome of the replicon vaccine removes the protein that binds to the cell receptor from the original RNA virus and replaces it with the antigen protein of the vaccine, making it a structure like a virus without a shell.The spike protein of the coronavirus binds to the cell receptor and mediates infection to the cell. In the case of the influenza virus, hemagglutinin has a similar role to spike protein, and in other viruses, envelope glycoproteins mediate adhesion to and infection of host cells. Then, why can't replicon vaccines, which do not have such proteins mediating infection to cells, infect cells?Professor Michiaki Masuda's group at Dokkyo Medical University demonstrated in an experimental system using cultured cells that replicon RNA can infect cells. The infection occurred via extracellular vesicles, and replicon RNA was able to replicate within infected cells.Dissemination of the Flavivirus Subgenomic Replicon Genome and Viral Proteins by Extracellular Vesicles Ishikawa et al. (2024) viruses [Link to the paper]Extracellular vesicles (EVs) such as exosomes play a physiological role in intercellular communication by delivering various proteins and nucleic acids. EVs derived from cells infected with certain viruses have been shown in some studies to transmit the full-length viral genome and facilitate virus replication via EVs. However, it cannot be denied that infectious viral particles may be mixed into prepared EVs. In this study, subgenomic replicons derived from Japanese encephalitis virus and dengue virus were possessed, and cells that do not produce replication-competent viruses were used as EV donors. It was demonstrated that EVs contained replicon genomes and could transfer them to various types of recipient cells in the culture supernatant of these cells. Furthermore, EVs were shown to be mainly taken up by recipient cells through macropinocytosis after interacting with CD33 and Tim-1/Tim-4 of HeLa cells and K562 cells, respectively. The method used in this study does not involve mixing infectious viral particles, so it was clearly demonstrated that the flavivirus genome can be transferred from cell to cell via EVs, suggesting that this pathway may play a role in virus replication and pathogenicity in addition to classical receptor-mediated infection.Coronavirus is a single-stranded positive-sense RNA virus, as is the flavivirus used in this study. Viruses of the Flaviviridae family are widely distributed in vertebrates, many of which infect via mosquitoes or ticks. Representative flaviviruses include dengue virus, Japanese encephalitis virus, Zika virus, West Nile virus, and yellow fever virus.The authors created replicons from Japanese encephalitis virus (JEV Muar strain) and dengue virus (DENV NGC strain). Replicons (JM-PnL and DN-PnL) have the viral envelope protein removed and the luciferase gene introduced to detect infection. Luciferase is a firefly luminescent gene and can detect enzyme activity by light. Therefore, it is possible to quantify replicon infection with light. These replicons were introduced into BHK cells by electroporation, and replicon-harboring cell lines were established.The replicon RNA used in this study has a luciferase gene instead of an antigen protein, but otherwise, the structure of the replicon RNA is similar to that of the replicon vaccine.Images Figure 1 Extracellular vesicles (EVs) are vesicles responsible for intercellular transport and mediating intercellular communication.

@MeasslainteIE - Thomas Anthony III

It is known that most cell types produce and release extracellular vesicles. In addition to exosomes (diameter about 40-100 nm), there are also structures such as microvesicles (diameter 50-1000 nm) in extracellular vesicles. Exosomes are formed in multivesicular endosomes (MVEs) and are released by fusion of MVEs with the cell membrane. On the other hand, microvesicles are formed by budding from the cell membrane. In this study, exosomes and microvesicles were treated together as extracellular vesicles without strict http://distinction.In the experiment, extracellular vesicles were purified from the culture supernatant of replicon-harboring cell lines. Electron microscopy analysis revealed that the diameter of extracellular vesicles was about 40 nm, and their shape and size matched those of typical extracellular vesicles (Figure 1A).RNA extracted from these extracellular vesicles was reverse transcribed and PCR amplified, and luciferase genes and NS genes were detected. Thus, extracellular vesicles released from replicon-harboring cell lines contained replicon RNA (Figure 2B).Figure 2 Various cell lines were administered extracellular vesicles derived from replicon-harboring cells, and luciferase activity was detected in all cell lines (Figure 2A). On the other hand, when extracellular vesicles were removed from the culture supernatant, uptake by cells was greatly reduced (Figure 2B). This indicates that intercellular infection with replicon RNA is mediated by extracellular vesicles.Figure 3 Luciferase activity decreased when cells administered with extracellular vesicles were treated with an RNA replication inhibitor (ribavirin) (Figure 3C). Furthermore, when the replicon RNA in such cells was quantified by qPCR, the RNA increased over time (Figure 3D). This result indicates that replicon RNA can replicate within recipient cells.The authors are conducting further experiments to analyze proteins and pathways mediating intercellular infection. Proteins involved in mediating intercellular infection by extracellular vesicles seem to include CD33, TIM1, TIM4, etc. These are cell surface receptors with diverse roles in phagocytosis and signal transduction in the immune system. Endocytosis is involved in uptake by cells.Normally, viruses infect cells by binding to specific cell receptors as virus particles, but another pathway of virus infection via extracellular vesicles has been suggested previously. However, previous studies have used extracellular vesicles derived from virus-infected cells, so it was not possible to rule out the possibility of infectious viral particles being mixed into extracellular vesicles. The authors' experiments did not use viruses, so it was clearly demonstrated that replicons themselves can infect cells via extracellular vesicles.This study is extremely important as it proves that replicon RNA, which does not have virus proteins that bind to cell receptors, can spread between cells and replicate within infected cells. Similar mechanisms may also operate in replicon vaccines. https://note.com/hiroshi_arakawa/n/n4bf4f0bf4422?rt=email&sub_rt=daily_report_followee_notes Hiroshi Arakawa:Graduated from Kyoto University Faculty of Science in 1991Doctor of Science from Kyoto University in 1996 (Molecular Biology, Immunology)Affiliated with Basel Institute of Immunology (Basel), Heinrich Pette Institute (Hamburg), Helmholtz Institute (Munich), Max Planck Institute (Munich), and Institute of Molecular Oncology (Milan).

レプリコンは細胞外小胞を介して細胞間感染し、増殖できる: virusesに掲載された論文から|荒川央 (あらかわ ひろし) 日本人を対象とした新型コロナワクチンとして、今年の秋から日本国内での接種開始が予定されているレプリコンワクチン (自己増殖型mRNAワクチン、self-amplifying RNA vaccine) とは自己増殖型mRNAワクチンの事であり、抗原遺伝子に加えてRNA複製遺伝子を持った遺伝子製剤です。レプリコンワクチンのゲノムは元のRNAウイルスから、細胞の受容体に結合するタンパクを取り除き、ワクチンの抗原タンパクに置き換えたもので、いわば殻のないウイルスのような構造になっています。 コロナウイルスのスパイクタンパクは細胞の受容体に結合し、細胞への感染を媒介するタンパクです。例えばイン note.com
Saved - May 8, 2024 at 11:12 AM
reSee.it AI Summary
Pomegranate peel extract shows potential as an antiviral against SARS-CoV-2. Chaga mushroom tea has various health benefits, including immune-boosting and anti-inflammatory properties. Glutathione offers antioxidant protection, detoxification, immune support, and anti-aging benefits. Black seed oil has antioxidant and anti-inflammatory effects, immune system modulation, and potential anticancer properties. Turkey Tail mushroom has cancer-fighting properties and stimulates the immune system. However, clinical trials for Turkey Tail mushroom are limited.

@MeasslainteIE - Thomas Anthony III

Pomegranate Peel Extract as an Inhibitor of SARS-CoV-2 Spike Binding to Human ACE2 Receptor (in vitro): A Promising Source of Novel Antiviral Drugs The research highlights that plant extracts, particularly those rich in polyphenols, sesquiterpenes, and triterpenes, may have antiviral activities. The study’s findings suggest that Pomegranate peel extract can attenuate the binding of the SARS-CoV-2 Spike protein to the ACE2 receptor, potentially inhibiting the virus’s ability to infect human cells. Additionally, the extract showed some inhibitory activity against the virus’s 3CL protease, which is essential for viral replication. https://frontiersin.org/articles/10.3389/fchem.2021.638187/full Eat the whole thing 🙌🏻🙃 I was looking into pomegranate for its gut health urolithin a.

Pomegranate Peel Extract as an Inhibitor of SARS-CoV-2 Spike Binding to Human ACE2 Receptor (in vitro): A Promising Source of Novel Antiviral Drugs Plant extracts are rich in bioactive compounds, such as polyphenols, sesquiterpenes and triterpenes, with potential antiviral activities. As the dramatic outbreak of the pandemic COVID-19, caused by the SARS-CoV-2 virus, thousands of scientists are working tirelessly trying to understand the biology of this new virus and the disease pathophysiology, with the main goal to discover effective preventive treatments and therapeutic agents. Plant-derived secondary metabolites may play key roles in preventing and counteracting the rapid spread of SARS-CoV-2 infections by inhibiting the activity of several viral proteins, in particular those involved in the virus entry into the host cells and its replication. By using in vitro approaches, we investigated on the role of a pomegranate peel extract in attenuating the interaction between the SARS-CoV-2 Spike glycoprotein and the human Angiotensin-Converting Enzyme 2 (ACE2) receptor, and on the activity of the virus 3CL protease. Although further studies will be determinant to assess the efficacy of this extract in vivo, our results open up new promising opportunities to employ natural extracts for the development of effective and innovative therapies in the fight against SARS-CoV-2. frontiersin.org

@deNutrients - Jennifer Depew, RD

@MeasslainteIE Pomegranate peel is a natural antidote but that is censored information.

@MeasslainteIE - Thomas Anthony III

Targeting SARS‐CoV‐2 with #Chaga mushroom: An in silico study toward developing a natural antiviral compound https://onlinelibrary.wiley.com/doi/10.1002/fsn3.2576 Health Benefits of Chaga Tea Boosts Immune System: Chaga tea is believed to have immunomodulatory effects, helping to regulate the immune system and prevent illnesses. Antioxidant-Rich: Chaga tea is packed with antioxidants, which can help protect the body from free radicals and oxidative stress. Anti-Inflammatory: Chaga tea may help reduce inflammation, which can alleviate symptoms of conditions like arthritis and other inflammatory diseases. Cancer Prevention: Some studies suggest that chaga tea may have anti-tumor properties, which could help prevent or slow the growth of cancer cells. Cholesterol Reduction: Chaga tea may help lower cholesterol levels by reducing the absorption of dietary cholesterol and increasing the excretion of bile acids

@MeasslainteIE - Thomas Anthony III

#Glutathione #Selenium #Liver #Health #Thyroid

@MeasslainteIE - Thomas Anthony III

Benefits of Glutathione# Glutathione has numerous health benefits, including: Antioxidant Protection Glutathione is a powerful antioxidant that protects the body against oxidative stress and free radical damage. Detoxification Glutathione plays an important role in the detoxification of harmful toxins and chemicals in the body. Immune Function Glutathione is essential for the proper functioning of the immune system. It helps to boost the immune response and protect against infections. Anti-Aging Glutathione is believed to have anti-aging properties due to its ability to protect the body against oxidative stress and free radical damage. https://measslainte.ie/post/selenium-/

Selenium Selenium Supplementation and its Conversion to Glutathione measslainte.ie

@MeasslainteIE - Thomas Anthony III

#Blackseedoil, also known as #NigellaSativa, is an herbal supplement that comes from the black cumin seed. This amazing plant has been used for thousands of years in traditional forms of medicine such as Ayurveda, and is known for its powerful anti-inflammatory and antioxidant properties. Antioxidant Properties: Black seed oil exhibits strong antioxidant activity due to its bioactive components. Antioxidants help protect cells from oxidative damage caused by free radicals. Thymoquinone, in particular, has been studied for its potential in reducing oxidative stress and inflammation. Anti-Inflammatory Effects: Nigella sativa has anti-inflammatory properties, which may be beneficial for various health conditions. Studies suggest that black seed oil can reduce inflammatory markers and modulate immune responses. Immune System Modulation: Black seed oil may enhance immune function by promoting the production of certain immune cells and cytokines. It has been investigated for its potential in managing autoimmune diseases and supporting overall immune health. Anticancer Potential: Thymoquinone, a major component of black seed oil, has demonstrated anticancer effects in preclinical studies. It may inhibit cancer cell growth, induce apoptosis (programmed cell death), and suppress tumor progression. Cardiovascular Health: Some research suggests that black seed oil may have cardiovascular benefits, including improving lipid profiles (cholesterol levels) and reducing blood pressure. These effects are attributed to its antioxidant and anti-inflammatory properties. https://measslainte.ie/post/black-seed-oil/

@MeasslainteIE - Thomas Anthony III

#TurkeyTail https://t.co/WT40QzkYG2

@MakisMD - William Makis MD

NEW ARTICLE: Turkey Tail Mushroom (Trametes versicolor) for Cancer - how can this medicinal mushroom help the COVID-19 mRNA Vaccine Injured? In-depth article on components of Turkey Tail mushroom & their cancer fighting properties Kariko & Weissman got the Nobel Prize for modifying mRNA with pseudouridine to suppress the immune system by shutting off TLRs (Toll-Like Receptors on Immune cells) (this was done to make the mRNA last longer and allow the body to produce maximal amount of spike protein to injure & kill as many vaccinated people as possible - this was what the Nobel Prize was awarded for - causing maximal injury & death) Did you know the key cancer-killing mechanism of Turkey Tail mushroom is activation of the same TLRs to stimulate the immune system to successfully attack cancer cells? Turkey Tail stimulates the immune system (immunomodulation) by doing the EXACT opposite of what the toxic mRNA jabs did to damage the immune system initially. Turkey Tail's medicinal value as part of the Chinese traditional medicine dates back for at least 2000 years and includes general health-promoting effects, including endurance and longevity. Physically, there are two main components of the fungus: the filamentous mycelium secretes enzymes that decompose the plant substrate, while the fruitbodies are the caps that look like turkey tails, that serve to spread the spores. Both in China and Japan, preparations such as dried powdered tea of the fungus are employed in traditional medicine practices Two main bioactive classes of compounds: 1. polysaccharides, which are isolated from the mycelium as well as fermentation substrate 2. small molecular weight compounds - terpenoids (sesquiterpenes), 38 phenolic compounds belonging to the flavonoids, quercetin etc. Chemical composition of the mushroom is very complex! Among various bioactive components derived from hot water and standardized ethanol–water extracts of C. versicolor, polysaccharopeptides (PSP) and protein-bound polysaccharides (PSK, also known as Krestin) were found to have the strongest biological activity. Numerous in vitro studies have reported that PSP and PSK can inhibit the proliferation of leukemia, lymphoma, hepatoma, breast, lung and prostate tumor cell lines But terpenoids and phenolic compounds (flavonoids) also have powerful anti-cancer properties In vitro & In vivo anti-cancer activity of both classes have been confirmed against breast cancer, colon cancer, lung, pancreatic, liver, gastric, melanoma, prostate, lymphoma, leukemia, etc. There are no significant clinical trials active right now as Big Pharma is suppressing this medicinal mushroom (they don't understand the mechanisms of action thus can't properly monetize it) I review some fascinating published papers and articles on this amazing fungus. Can Turkey Tail mushroom reverse the immune system damage caused by COVID-19 mRNA Vaccines? Can Turkey Tail mushroom treat TURBO CANCER caused by Pfizer & Moderna COVID-19 mRNA Vaccines? Article Link in photo to avoid shadowban, just re-type the URL into your browser to access. #DiedSuddenly #cdnpoli #ableg

Saved - April 20, 2024 at 1:38 PM
reSee.it AI Summary
The European medicines agency has reported 24,300 deaths related to the Pfizer Tozinameran mRNA vaccine, with the highest reported deaths in various categories. The author suggests that this number may be higher than the votes received in a general election. They express a belief that more is yet to come and acknowledge a previous statement made by someone else.

@MeasslainteIE - Thomas Anthony III

#TheyKnew As of 29/05/23, the European medicines agency has recorded 24,300 deaths for the Pfizer Tozinameran mRNA vaccine. The top 6 categories with the highest reported deaths are general disorders and administration site conditions, cardiac disorders, nervous system disorders, respiratory, thoracic and mediastinal disorders, infections and infestations, and vascular disorders. The remaining categories had less than 100 deaths recorded for each category. That's probably more than the number of votes than you got on the #15thcount #Tyrant #Dictator #GeneralElectionN0W #MoratoriumNow I really feel we ain't seen nothing yet. You were right about that statement but even a broken clock is right twice a day!

@mRNAdeaths - They Keep Saying Its Rare

14/04/24 According to data from the European medicines agency the has been 18,432 adverse reports of irregular mensuration after the #Pfizer #mRNA tozinameran vaccine. * not including boosters* 10,329 unresolved reports 4,039 unknown outcome. https://www.adrreports.eu/en/index.html

European database of suspected adverse drug reaction reports adrreports.eu
Saved - April 18, 2024 at 3:30 PM
reSee.it AI Summary
In a groundbreaking experiment, Dr. Evelyn Sterling explores the effects of transfections on protein misfolding. Misfolded proteins trigger cascades, leading to amyloid plaques and prion-like behavior. The research sheds light on the intricate pathways of protein misfolding and its implications for diseases. Another post references a study linking Creuzfeldt-Jacob Disease to COVID-19 vaccines. A paper discusses the mechanisms of protein-folding diseases, while another highlights the impact of mRNA modification on ribosomal frameshifting. The absence of evidence regarding vaccine safety is mentioned. Trust the science, but acknowledge the need for further research.

@MeasslainteIE - Thomas Anthony III

The characters in this story are made up. Amyloids and prions are real as are the neurological damage that comes with them. The Tale of Misfolded Proteins: A Cascade Unleashed Chapter 1: The Transfection Experiment In a dimly lit laboratory, Dr. Evelyn Sterling, a brilliant geneticist, embarked on a groundbreaking experiment. She aimed to understand how transfections—introducing foreign DNA into cells—could trigger unexpected consequences. Her lab assistant, Alex, watched with anticipation as Dr. Sterling prepared her materials. Dr. Sterling: “Alex, today we explore the intricate dance of proteins within cells. Our focus: amyloids and prion-like misfolding.” Alex: “Fascinating! But why transfections?” Dr. Sterling: “Because transfections can disrupt the delicate balance. Imagine a peaceful pond—the proteins are like water molecules. Transfections are like tossing a stone into the pond. Ripples form, and the entire ecosystem reacts.” Chapter 2: The Misfolded Dance Dr. Sterling transfected human cells with a modified gene encoding an amyloid precursor protein. As the cells absorbed the foreign DNA, the protein synthesis machinery went to work. But something went awry—the protein folded incorrectly. Dr. Sterling: “Alex, observe. This misfolded protein is like a rogue dancer at a ball. It disrupts the choreography.” Chapter 3: The Cascade Unleashed The misfolded protein triggered a cascade. It interacted with other cellular proteins, distorting their shapes. Like dominoes falling, this led to more misfolding. The once-harmonious cellular ballet turned chaotic. Dr. Sterling: “Alex, see how the misfolded protein recruits others? It’s like a rogue dancer pulling others into a frenzied waltz.” Chapter 4: The Amyloid Aggregation The misfolded proteins aggregated, forming amyloid plaques. These sticky clumps clogged cellular pathways, disrupting communication. Neurons struggled to function, leading to memory loss and cognitive decline. Dr. Sterling: “Alex, these amyloids are like tangled shoelaces—cells stumble, and diseases emerge.” Chapter 5: The Prion Twist Dr. Sterling introduced another twist—the prion-like behavior. She transfected cells with a prion protein gene. The prion protein, once misfolded, acted as a template. It induced neighboring proteins to mimic its shape. Dr. Sterling: “Alex, prions are like contagious dancers. They teach others their twisted steps.” Chapter 6: The Infection Spreads The prion-like misfolding spread. Neurons transformed, losing their normal function. Alex watched as the cells became ghostly, their connections severed. Dr. Sterling: “Alex, this is how prion diseases propagate. Like a macabre dance, they infect neighboring cells.” Epilogue: A Pathway Unveiled Dr. Sterling’s research revealed the intricate pathways of protein misfolding. Transfections, like stones in a pond, set off cascades. Amyloids and prion-like diseases emerged, leaving a trail of disrupted cells. And so, in the quiet of her lab, Dr. Sterling whispered, “We’ve glimpsed the secrets of life’s dance—a choreography both beautiful and treacherous.”

@MeasslainteIE - Thomas Anthony III

Luc Montagnier's last paper, in peer review when he died: "We present 26 cases of Creuzfeldt-Jacob Disease, all diagnosed in 2021 with the first symptoms appearing within an average of 11.38 days after a Pfizer, Moderna, or AstraZeneca COVID-19 injection" https://ijvtpr.com/index.php/IJVTPR/article/view/66 #TheyKnew May he rest in peace 🕊️

Video Transcript AI Summary
Les vaccins actuels sont critiqués pour leur stratégie de développement basée sur des erreurs, ne protégeant pas contre la transmission et pouvant causer des effets graves. La protéine du virus synthétisée par l'ARN messager dans les vaccins est toxique pour les cellules, touchant des organes comme le cœur et pouvant entraîner des maladies neurologiques graves, même après la deuxième dose. Il est demandé d'arrêter la vaccination avec ces vaccins pour éviter des conséquences tragiques. Translation: Current vaccines are criticized for their flawed development strategy, not protecting against transmission and causing serious effects. The virus protein synthesized by the mRNA in vaccines is toxic, affecting organs like the heart and causing severe neurological diseases, even after the second dose. It is requested to stop vaccination with these vaccines to prevent tragic consequences.
Full Transcript
Speaker 0: Parce qu'ils ont été synthétisés, créés sur une stratégie qui est une erreur, une mauvaise erreur, une énorme erreur de stratégie. La stratégie était uniquement de favoriser ces produits qui n'étaient que par des bassins qui étaient produits de transmission géniques également. Et donc, ils ont, on a montré toute la nature a montré, tous les essais ont montré que ces vaccins ne protégeaient pas contre la transmission contrairement à ce qui avait été annoncé au départ. Alors ceci est reconnu maintenant par Ce n'est pas seulement les expériences cliniques, mais c'est tous les résultats, toutes les maladies qui a causé, qui ont causé ces vaccins. Speaker 1: Non fonctionne, Speaker 0: Car souvent au lieu de protéger, d'empêcher la dureté de la maladie, ils ont un effet inverse, ils favorisent de nouvelles infections. Et ils ont malheureusement des effets plus graves, car la protéine du virus qui est synthétisée par l'ARN messager contenu dans le vaccin, cette protéine est toxique pour les cellules, c'est un poison. Speaker 1: La protéine a questatoulizata daivachine, Speaker 0: Et en fait, elle touche des organes comme le coeur, des jeunes sportifs meurent à cause de de leur vaccination. Ce n'est pas tolérable, les vaccins ne sont pas faits pour tuer, ils sont faits pour protéger. Donc c'est un crime de d'annuler ces vaccins à des enfants. Mais il y a plus grave encore. Ces vaccins semblent causer des maladies nerveuses du cerveau. Très grave. Speaker 1: Pourquoi vous arrange que maladie Speaker 0: Et il y a déjà des dizaines de personnes qui meurent à cause de ces effets à long terme du vaccin. Speaker 1: À Causa di Causa longotherme Igosovachino, je suis senti si mes personnes et gasano talement Speaker 0: te Morando. Et même parfois c'est au bout de la deuxième injection de vaccin que déjà les signes neurologiques se déclarent. Et personne ne peut prévoir prévoir, personne ne peut prévoir de combien de personnes vaccinées souffriront ou non de ces syndromes neurologiques. Et, Donc je demande avec d'autres collègues qu'il faut arrêter les vaccinations avec ces vaccins. Les médecins Speaker 1: qui continuent, Speaker 0: Les médecins qui continuent à vacciner sont parfaitement informés de ça. Ils ne l'étaient pas au début, ils le sont maintenant. Attention, attention, ils sont responsables Speaker 1: de et non soltante de la préventions et donc
Emergence of a New Creutzfeldt-Jakob Disease: 26 Cases of the Human Version of Mad-Cow Disease, Days After a COVID-19 Injection | International Journal of Vaccine Theory, Practice, and Research ijvtpr.com

@MeasslainteIE - Thomas Anthony III

Mechanisms of protein-folding diseases at a glance https://journals.biologists.com/dmm/article/7/1/9/19965/Mechanisms-of-protein-folding-diseases-at-a-glance

@MeasslainteIE - Thomas Anthony III

@NestCommander - Kevin W. McCairn PhD

Give this wings, it's as concise an explanation of the current state of the science as you'll get for SARS-CoV-2, PRION, Vaccines and the warfare being waged against you. https://www.youtube.com/watch?v=eDxkyX1rF_0 @CharlesRixey @BillyBostickson @still_a_nerd @Doctor_I_am_The @pizzapicklespur @Jikkyleaks @NameIsSpartacus @weve_read @BrokenTruthTV @HamEggsnSam @Parsifaler @EthicalSkeptic @ArmchairW @GasGilligan @JohnnyVedmore @dopaminergic13 @veryvirology @annunakkki @Know_More_News @RyLiberty @_HeartofGrace_ @HouseLyndseyRN @Kevin_McKernan

@MeasslainteIE - Thomas Anthony III

N1-methylpseudouridylation of mRNA causes +1 ribosomal frameshifting Conclusion We show that 1-methylΨ is a modified ribonucleotide that significantly increases +1 ribosomal frameshifting during mRNA translation and that cellular immunity to +1 frameshifted products can occur following vaccination with mRNA containing 1-methylΨ. To our knowledge, this is the first report that mRNA modification affects ribosomal frameshifting. Alongside this impact on host T cell immunity, the off-target effects of ribosomal frameshifting could include increased production of new B cell antigens. Other ribonucleotide modification strategies, such as incorporation of 5-methoxyU, significantly decreased translation efficiency of IVT mRNAs, which may limit clinical translation. Although we have shown that translation of N1-methylpseudouridylated mRNA leads to +1 ribosomal frameshifting in vitro and in cultured cells, it is conceivable that other mistranslation events (such as leaky scanning) could also contribute to T cell responses to +1 frameshifted peptide antigens. We show that IVT mRNAs contain few nucleotide insertions and deletions, and this is not changed by 1-methylΨ incorporation. Our data show that +1 ribosomal frameshifting occurs at two characterized slippery sequences. Therefore, we believe that the minor band of approximately 50 kDa produced by Fluc+1FS mRNA translation is probably a consequence of several frameshifting events (Fig. 1e). Translation of mRNA containing 1-methylΨ leads to slower translation elongation, caused by altered aminoacyl-tRNA binding, which demonstrates why +1 ribosomal frameshifting does not occur during unmodified mRNA translation—both ribosome stalling and ribosome slippery sequences seem to be required for productive +1 ribosome frameshifting. Our mechanistic data are supported by previous observations of ribosomal frameshifting during translation of naturally occurring mRNAs, which implicate ribosome stalling and require ribosome slippery sequences for +1 frameshifting21,26,27,28,33,34. These findings are of particular importance to our fundamental understanding of how ribonucleotide modification affects mRNA translation, and for designing and optimizing future mRNA-based therapeutics to avoid mistranslation events that may decrease efficacy or increase toxicity. https://www.nature.com/articles/s41586-023-06800-3 3 years late with this paper.

N1-methylpseudouridylation of mRNA causes +1 ribosomal frameshifting - Nature In vitro-transcribed (IVT) mRNAs are modalities that can combat human disease, exemplified by their use as vaccines for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). IVT mRNAs are transfected into target cells, where they are translated into recombinant protein, and the biological activity or immunogenicity of the encoded protein exerts an intended therapeutic effect1,2. Modified ribonucleotides are commonly incorporated into therapeutic IVT mRNAs to decrease their innate immunogenicity3–5, but their effects on mRNA translation fidelity have not been fully explored. Here we demonstrate that incorporation of N1-methylpseudouridine into mRNA results in +1 ribosomal frameshifting in vitro and that cellular immunity in mice and humans to +1 frameshifted products from BNT162b2 vaccine mRNA translation occurs after vaccination. The +1 ribosome frameshifting observed is probably a consequence of N1-methylpseudouridine-induced ribosome stalling during IVT mRNA translation, with frameshifting occurring at ribosome slippery sequences. However, we demonstrate that synonymous targeting of such slippery sequences provides an effective strategy to reduce the production of frameshifted products. Overall, these data increase our understanding of how modified ribonucleotides affect the fidelity of mRNA translation, and although there are no adverse outcomes reported from mistranslation of mRNA-based SARS-CoV-2 vaccines in humans, these data highlight potential off-target effects for future mRNA-based therapeutics and demonstrate the requirement for sequence optimization. A study demonstrates that nucleotide modifications in mRNA-based therapeutics can lead to +1 ribosomal frameshifting during translation, yielding products that can trigger immune responses. nature.com

@MeasslainteIE - Thomas Anthony III

"Slippery sequences and off target protein production. Its was known It was censored And this defect won the Nobel prize" 🎤🎤🎤 Drop #FrameshittingJabJiggalos #ShitsTheFrame #shiftsHitTheFan #Frameshifting Shifting used to be a good word. 😂

@Kevin_McKernan - Kevin McKernan

A review of the frame shifting paper. https://tinyurl.com/yc4bt479

FrameShiting Slippery Sequence The Shift is about to hit the Fan. anandamide.substack.com

@MeasslainteIE - Thomas Anthony III

Trust the science TM@GretchenVogel https://www.science.org/content/article/mrna-vaccines-may-make-unintended-proteins-there-s-no-evidence-harm Absence of evidence isn't evidence of absence. There is no evidence of harm because nobody looked, they didn't do the trials or the safety studies.

Saved - April 17, 2024 at 11:06 AM
reSee.it AI Summary
Post 1: PD-L1 expression may reduce anti-tumor activity, so close monitoring and considering PD-1/PD-L1 inhibitors as adjuvant therapy is recommended for cancer patients. #turbocancer Post 2: Things are getting darker. Post 3: The use of N1-methylpseudouridine in vaccines may have unintended consequences, such as blocking type-I interferon synthesis. We need to address this issue. Post 4: No content provided. Post 5: Turkey Tail mushroom has cancer-fighting properties and stimulates the immune system, unlike mRNA vaccines. It has been used in traditional medicine for centuries. Post 6: Vermox, an over-the-counter anti-parasite medication, may have anti-cancer properties. Post 7: Chemicals like glyphosate, found in food and water, are concerning. Post 8: A comprehensive resource on glyphosate and GMO research.

@MeasslainteIE - Thomas Anthony III

Program Death ligand ☠️☠️☠️ The increase in PD-L1 expression may reduce the anti-tumor activity of the immune system and increase the risk of cancer progression or recurrence, especially in patients with pre-existing malignancies or immunosuppression. The paper recommends that cancer patients should be monitored closely after vaccination and that PD-1/PD-L1 inhibitors, a type of immunotherapy that blocks the PD-L1 protein, may be considered as an adjuvant therapy. That's messed up, as the sick are being gaslit by fools on top of being experimented on. #turbocancer.

@Jikkyleaks - Jikkyleaks 🐭

@DrSeussBen @MeasslainteIE @CDCgov https://www.arkmedic.info/p/philadelphia-2023

Philadelphia 2023 Your immune system on the edge. arkmedic.info

@MeasslainteIE - Thomas Anthony III

It gets darker the more you look.

@MeasslainteIE - Thomas Anthony III

@Jikkyleaks @DrSeussBen @CDCgov Oh sheet! This has turned dark fast :( https://www.cancersupportcommunity.org/sites/default/files/file/2020-11/PDL-1%20Fact%20Sheet_CS_20201102.pdf

404 cancersupportcommunity.org

@MeasslainteIE - Thomas Anthony III

@JesslovesMJK - Jessica Rose 🤙

Cancer prefers N1-methylpseudouridine. It was a bad idea as a sub-in. And they got a nobel prize for it. Yeah sure, it allows TLR evasion, but... what else does it do? Blocking type-I interferon synthesis is not a good idea. We shouldn't be finding this out after billions of people were injected. How are we going to clean up this mess? @stephanieseneff @Kevin_McKernan @AdhesionsOrg @P_J_Buckhaults @weldeiry @P_McCulloughMD @MakisMD

@MeasslainteIE - Thomas Anthony III

https://open.substack.com/pub/jessicar/p/review-n1-methyl-pseudouridine-m1?utm_source=share&utm_medium=android&r=24315g

Review: N1-methyl-pseudouridine (m1Ψ): Friend or foe of cancer? Yeah, that would be friend. Of cancer. Not humans. jessicar.substack.com

@MeasslainteIE - Thomas Anthony III

https://t.co/WHnlU96GCu 🦃 Tail #TurkeyTail #Cancer

@MakisMD - William Makis MD

NEW ARTICLE: Turkey Tail Mushroom (Trametes versicolor) for Cancer - how can this medicinal mushroom help the COVID-19 mRNA Vaccine Injured? In-depth article on components of Turkey Tail mushroom & their cancer fighting properties Kariko & Weissman got the Nobel Prize for modifying mRNA with pseudouridine to suppress the immune system by shutting off TLRs (Toll-Like Receptors on Immune cells) (this was done to make the mRNA last longer and allow the body to produce maximal amount of spike protein to injure & kill as many vaccinated people as possible - this was what the Nobel Prize was awarded for - causing maximal injury & death) Did you know the key cancer-killing mechanism of Turkey Tail mushroom is activation of the same TLRs to stimulate the immune system to successfully attack cancer cells? Turkey Tail stimulates the immune system (immunomodulation) by doing the EXACT opposite of what the toxic mRNA jabs did to damage the immune system initially. Turkey Tail's medicinal value as part of the Chinese traditional medicine dates back for at least 2000 years and includes general health-promoting effects, including endurance and longevity. Physically, there are two main components of the fungus: the filamentous mycelium secretes enzymes that decompose the plant substrate, while the fruitbodies are the caps that look like turkey tails, that serve to spread the spores. Both in China and Japan, preparations such as dried powdered tea of the fungus are employed in traditional medicine practices Two main bioactive classes of compounds: 1. polysaccharides, which are isolated from the mycelium as well as fermentation substrate 2. small molecular weight compounds - terpenoids (sesquiterpenes), 38 phenolic compounds belonging to the flavonoids, quercetin etc. Chemical composition of the mushroom is very complex! Among various bioactive components derived from hot water and standardized ethanol–water extracts of C. versicolor, polysaccharopeptides (PSP) and protein-bound polysaccharides (PSK, also known as Krestin) were found to have the strongest biological activity. Numerous in vitro studies have reported that PSP and PSK can inhibit the proliferation of leukemia, lymphoma, hepatoma, breast, lung and prostate tumor cell lines But terpenoids and phenolic compounds (flavonoids) also have powerful anti-cancer properties In vitro & In vivo anti-cancer activity of both classes have been confirmed against breast cancer, colon cancer, lung, pancreatic, liver, gastric, melanoma, prostate, lymphoma, leukemia, etc. There are no significant clinical trials active right now as Big Pharma is suppressing this medicinal mushroom (they don't understand the mechanisms of action thus can't properly monetize it) I review some fascinating published papers and articles on this amazing fungus. Can Turkey Tail mushroom reverse the immune system damage caused by COVID-19 mRNA Vaccines? Can Turkey Tail mushroom treat TURBO CANCER caused by Pfizer & Moderna COVID-19 mRNA Vaccines? Article Link in photo to avoid shadowban, just re-type the URL into your browser to access. #DiedSuddenly #cdnpoli #ableg

@MeasslainteIE - Thomas Anthony III

https://t.co/P3oLUfCAEa #Vermox #AntiParasite

@MeasslainteIE - Thomas Anthony III

Vermox sold over the counter is anti cancer. There's only a tiny difference with fembendazol. Would also most likely complement any parasite cleanse.

@MeasslainteIE - Thomas Anthony III

It's not just the jabs these chemicals are in the food and water. https://t.co/XCB583znR5

@iluminatibot - illuminatibot

GLYPHOSATE - A cancer causing chemical that can be found in several foods we eat https://t.co/x9NOZ6aKQb

Video Transcript AI Summary
Monsanto found bacteria surviving Roundup in a waste dump, leading to Roundup-ready soybeans. Glyphosate in Roundup depletes nutrients in plants, weakens them, and promotes disease. Livestock eat Roundup-ready crops, leading to nutrient deficiency. FDA memos reveal GMO dangers in animal feed, with toxins bioaccumulating in animals and milk. 95% of genetic modifications aim to withstand more chemicals and drugs, altering genes in plants, animals, and humans permanently. Translation: Monsanto discovered bacteria resistant to Roundup in a waste dump, resulting in Roundup-ready soybeans. Glyphosate in Roundup depletes plant nutrients, weakens them, and promotes disease. Livestock consuming Roundup-ready crops face nutrient deficiencies. FDA memos expose GMO risks in animal feed, with toxins accumulating in animals and milk. 95% of genetic modifications aim to withstand more chemicals and drugs, altering genes in plants, animals, and humans permanently.
Full Transcript
Speaker 0: Monsanto scientists found bacteria growing at a chemical waste dump near their factory in the presence of Roundup herbicide. Now Roundup normally kills bacteria. This bacteria would survive, and they said, great. Let's put it in the food supply. So they took the gene from the bacterium that allowed it to survive the Roundup and put it into soybeans. And now those Roundup ready soybeans can be sprayed with Roundup herbicide, and they don't die. Just all the other plant biodiversity in the ground dies. The active ingredient in Roundup is called glyphosate. Glyphosate was patented in 1964, not as an herbicide, but as a broad spectrum chelator. It hugs a lot of different minerals that are needed and does not allow the plants to access them. It also destroys some beneficial microorganisms in the soil, which normally provide nutrients to the plant. It also promotes pathogenic organisms in the soil, which then overrun the plant. And so it creates weaker plants, stronger disease, and the disease does the killing. Now what do the livestock in the United States eat? They eat largely Roundup ready crops, Roundup ready soy, corn, cottonseed, canola mash, sugar beet pulp, and soon alfalfa. So a huge percentage of their food intake is roundup ready crops. Now remember, roundup pulls the nutrients out of the crop. It makes them unavailable. So now we have millions of livestock eating nutrient deficient food. And what do we eat? We eat plants and we eat animals and take their milk. So it turns out it's a perfect storm now, not just for plant disease, but for animal and human disease. When 44,000 secondret FDA memos were made public from a lawsuit about the subject of genetic engineering, The director of the Center For Veterinary Medicine made it absolutely clear that GMOs in animal feed had a unique danger. Toxins can bioaccumulate in animals and in their milk. And so if there were toxins in genetically modified feed, then we might have higher levels of those toxins in the animals that eat the feed or in their milk or other products from those animals. All our food, 90% of Canadian crops, American crops now are produced by genetic modification or at least they're contaminated with genetically modified corn, genetically modified soybean, genetically modified everything. Speaker 1: 95% of all the genetic modifications are done in order to allow the plants to survive more chemicals being sprayed on them and to allow the animals to survive more drugs being put into them. And of course, what happens is that when their genes are changed, our genes are changed by consuming them just as the super weeds and the super bugs are genetically altered by consuming them. The bug eats the plant. Its genes change. The animal eats the the plant. Its genes change. We eat the animal or the plant. Our genes change. Our baby's genes change and the change is permanent.

@MeasslainteIE - Thomas Anthony III

A great resource for all things glyphosate with many other avenues of research. https://t.co/hvvfAQLsjz

@pizzapicklespur - Nick Petosky

Nick's entire, monstrous horrifying Glyphosate / GMO research collection: https://www.zotero.org/foxsayswhat/collections/R43KDGVA

Saved - April 1, 2024 at 9:21 PM

@MeasslainteIE - Thomas Anthony III

Luc Montagnier's last paper, in peer review when he died: "We present 26 cases of Creuzfeldt-Jacob Disease, all diagnosed in 2021 with the first symptoms appearing within an average of 11.38 days after a Pfizer, Moderna, or AstraZeneca COVID-19 injection" https://ijvtpr.com/index.php/IJVTPR/article/view/66 #TheyKnew May he rest in peace 🕊️

Video Transcript AI Summary
Les vaccins actuels sont critiqués pour leur inefficacité à empêcher la transmission du virus et pour causer des effets secondaires graves, y compris des maladies neurologiques. Certains jeunes sportifs sont décédés après avoir été vaccinés en raison de la toxicité de la protéine virale synthétisée par le vaccin. Il est urgent d'arrêter l'utilisation de ces vaccins pour éviter davantage de décès et de complications neurologiques. Les médecins qui continuent à administrer ces vaccins sont tenus pour responsables de leurs conséquences. Translation: Current vaccines are criticized for being ineffective at preventing virus transmission and causing serious side effects, including neurological disorders. Some young athletes have died after vaccination due to the toxicity of the viral protein synthesized by the vaccine. It is urgent to stop using these vaccines to prevent further deaths and neurological complications. Doctors who continue to administer these vaccines are held accountable for their consequences.
Full Transcript
Speaker 0: Parce qu'ils ont été synthétisés, créés sur une stratégie qui est une erreur, une mauvaise erreur, une énorme erreur de stratégie. La stratégie était uniquement de favoriser ces produits qui n'étaient que par des bassins qui étaient produits de transmission géniques également. Et donc, ils ont, on a montré toute la nature a montré, tous les essais ont montré que ces vaccins ne protégeaient pas contre la transmission contrairement à ce qui avait été annoncé au départ. Alors ceci est reconnu maintenant par Ce n'est pas seulement les expériences cliniques, mais c'est tous les résultats, toutes les maladies qui a causé, qui ont causé ces vaccins. Speaker 1: Non fonctionne, Speaker 0: Car souvent au lieu de protéger, d'empêcher la dureté de la maladie, ils ont un effet inverse, ils favorisent de nouvelles infections. Et ils ont malheureusement des effets plus graves, car la protéine du virus qui est synthétisée par l'ARN messager contenu dans le vaccin, cette protéine est toxique pour les cellules, c'est un poison. Speaker 1: La protéine a questatoulizata daivachine, Speaker 0: Et en fait, elle touche des organes comme le coeur, des jeunes sportifs meurent à cause de de leur vaccination. Ce n'est pas tolérable, les vaccins ne sont pas faits pour tuer, ils sont faits pour protéger. Donc c'est un crime de d'annuler ces vaccins à des enfants. Mais il y a plus grave encore. Ces vaccins semblent causer des maladies nerveuses du cerveau. Très grave. Speaker 1: Pourquoi vous arrange que maladie Speaker 0: Et il y a déjà des dizaines de personnes qui meurent à cause de ces effets à long terme du vaccin. Speaker 1: À Causa di Causa longotherme Igosovachino, je suis senti si mes personnes et gasano talement Speaker 0: te Morando. Et même parfois c'est au bout de la deuxième injection de vaccin que déjà les signes neurologiques se déclarent. Et personne ne peut prévoir prévoir, personne ne peut prévoir de combien de personnes vaccinées souffriront ou non de ces syndromes neurologiques. Et, Donc je demande avec d'autres collègues qu'il faut arrêter les vaccinations avec ces vaccins. Les médecins Speaker 1: qui continuent, Speaker 0: Les médecins qui continuent à vacciner sont parfaitement informés de ça. Ils ne l'étaient pas au début, ils le sont maintenant. Attention, attention, ils sont responsables de Speaker 2: et non soltante de la préventions Speaker 1: et donc
Emergence of a New Creutzfeldt-Jakob Disease: 26 Cases of the Human Version of Mad-Cow Disease, Days After a COVID-19 Injection | International Journal of Vaccine Theory, Practice, and Research ijvtpr.com
Saved - March 1, 2024 at 2:04 PM

@MeasslainteIRL - Thomas Anthony III

@FineGael @LeoVaradkar @rodericogorman Vote No No resign now you frauds https://t.co/vqcRB65qrZ

Video Transcript AI Summary
Peter Tobin raised concerns about the Department of Children placing children in unregulated emergency accommodation. He mentioned missing children from state care and a girl found in a brothel. The Minister defended engagement with Tulsa and the Garda on child protection. Tobin criticized the government's handling of immigration and child welfare issues.
Full Transcript
Speaker 0: Hi, guys. So I want to bring your attention onto something. The deputy, Potter Tobin, asked Roderick O'Borman today, 29th February. In the doll, this is up on leader's questions. So if you watch it later on, you'll see. The spending regarding Tulsa And, basically, Peter Tobin has said, the minister's department has admitted to me through replies parliamentary questions that it is placing children in special emergency accommodation that is unregulated, staffed by third party providers and rented. How much is the department paying for these countries? So it goes down and he says payments raise range from 3a half 1000000 to 13,000,000 and Tulsa's resources are stretched. But, Peter Tobin says, I understand that 90,000,000 has been spent by the department so far on special emergency arrangements. This is a disturbing part. Deputy Padertoven, last month alone last month alone, January 2024, 22 children went missing from state care. Previously, a 14 year old girl who had been abducted by a criminal gang within minutes of being placed with Tulsa was found 1 year later locked in a brothel. This isn't Ireland. I tried to raise these matters with the minister, but he does not listen. A retired judge, Dermotson, tried to raise these matters with the minister, but the minister deleted his files, citing a GDPR. A whistleblower tried to make a protected disclosure about unvetted care workers. Tulsa tried to oppose that, but the commissioner has now said that Tulsa must accept it. Last week in radio 1, Tulsa CEO stated that staff and SEAs were absolutely vetted. We know now from the article in The Irish Times yesterday that one company was providing falsified documents to Tulsa and that an internal Tulsa report in July in July found staff did not have up to date Garda clearances. The name of that company is Ideal Care Services, and I understand that there is a Garda investigation to the matter. How has the state lost 22 kids in the last month? A 14 year old girl last year was abducted and found 1 year later in a brothel. My daughter is 17 next month. If that happened, I'd I'd do time. Roger Gogarman. I do not believe I have, but I can clarify that point for the depumen deputy and revert to him. The deputy stated that I did not listen or engage when he raised a question about this matter during previous oral questions. I was prepared for it, but it was but of its importance, but the deputy was not present. It is important that I put that on point. Sure, radical Gorman. Were you prepared for it? Were you? You absolute As to what we were doing about this issue, I had extensive engagement with Tulsa and a gardener, the special repertoire on child protection in the ambulance plan for children over the last summer. That engagement was focused on the use of special emergency arrangements and in particular, the situation of children in care and what the Garda was doing when children went missing from care. The Garda is reviewing operation Cosname with the focus of how it traces people who go missing from care. This is not people. This is children. 22 children went missing last month. 22. Where are they, mister O'Gorman? You're bringing over a 100,000 refugees, illegal immigrants into this country, and 22 children as of dawn on today Iraq disputes have went missing in the last month. Stop it. This is down to you, Roderick O'Gorman, to Helen MacEntee, to Leo, to Tanish, to Mihal Martin, to Eamon Ryan, to Sinn Fein, to everybody who supports this open border. Look what's happening in Kildare at the minute. A refuge camp, if you ask me, with all the porter cabins in Neas. A little child allegedly being assaulted, 7 years old. And one child that has been revealed in leaders debates now in Iraqtus, in today, a 14 year old went missing last year and turns up a year later in a bristle. Why wasn't that in the bloody news? This is why mothers and women are important in our constitution. I have to go. I just you needed to hear that, folks. It's crazy.
Saved - February 29, 2024 at 12:38 AM
reSee.it AI Summary
There is a huge referendum in Ireland on March 8th regarding the removal of women from the constitution and targeting the family. Let's not let the NWO, WEF, WHO win this. Google is already claiming victory. VoteNoNO VoteNox2 VoteNoRef24. Healthcare workers in Ireland are not taking the Covid booster, as highlighted by the former head of the ICGP in 2021.

@MeasslainteIRL - Thomas Anthony III

Huge referendum in Ireland on March 8th, ladies and gentlemen. The Irish government is trying to remove women from the constitution, and they are also targeting the family. God, family, and nation – that's the natural order. Don't let the NWO, WEF, WHO win this. PS Google is already saying they won -_- VoteNoNO VoteNox2 VoteNoRef24 !! GFY @LeoVaradkar @HMcEntee @DonnellyStephen @MichealMartinTD @rodericogorman @EamonRyan @MaryLouMcDonald @FineGael @TheGreenParty @sinnfeinireland

@MeasslainteIRL - Thomas Anthony III

@independent_ire https://t.co/a0RuecMgxn

@indepdubnrth - Dr. Marcus De Brun

In light of the fact that presently 74% of Healthcare workers in Ireland (Dr's and Nurses) have NOT taken the Covid booster this season, I would like to remind people what the former head of the ICGP had to say in 2021 about unvaccinated patients. https://t.co/Km0N3aYVDz

Saved - February 23, 2024 at 11:21 PM
reSee.it AI Summary
I found some interesting information about mast cell stabilizers and their effects on histamine release and cytokine production. Flavonoids like quercetin, myricetin, fisetin, kaempferol, and rutin have shown to be effective in inhibiting these processes. These compounds can be found in various fruits, vegetables, and teas, such as apples, onions, berries, citrus fruits, red wine, green tea, broccoli, kale, spinach, and buckwheat.

@MeasslainteIRL - Thomas Anthony III

Fisetin, kaempferol, myricetin, quercetin and rutin inhibited IgE mediated histamine release and prevented increased concentration of calcium inside mast cells, which is necessary for degranulation. Fisetin, quercetin and rutin all decreased production of IL-1b, IL-6, IL-8 and TNF. Fisetin, myricetin and rutin all decreased action of NF-kB, which controls the pathway regulating production of cytokines. Myricetin is a particularly effective mast cell stabilizer. It decreased degranulation and release of TNF and IL-6, but not IL-1b or IL-8

@MeasslainteIRL - Thomas Anthony III

Red onions are also really good mast cell stabilisers. https://www.mastattack.org/2015/09/naturally-occurring-mast-cell-stabilizers-part-1/ #ZincIonophore #MastCellStabilizers #bloodthinner #testosterone #Menshealth #AddZinc #AntiHistamine #Letfoodbethymedicine #AntiInflammatory #HeartHealth

Naturally occurring mast cell stabilizers: Part 1 - Mast Attack Warning: Naturally occurring molecules can interfere with medications or adversely affect disease state.  Please consult with your managing provider before adding supplements or drastically changing diet. Flavonoid is a broad term used to describe certain plant derived metabolites. It can be used to refer to a variety of molecules, including isoflavonoids, neoflavonoids and anthoxanthins, which… Read More »Naturally occurring mast cell stabilizers: Part 1 mastattack.org

@MeasslainteIRL - Thomas Anthony III

Quercetin, myricetin, fisetin, kaempferol, and rutin are all flavonoids that have been shown to be effective at inhibiting histamine release and preventing cytokine production. These molecules can be found in many fruits, vegetables, and teas, such as: Quercetin: apples, onions, berries, citrus fruits, red wine, and green tea Myricetin: berries, citrus fruits, red wine, and onions Fisetin: strawberries, persimmons, apples, and onions Kaempferol: broccoli, kale, spinach, and green tea Rutin: apples, buckwheat, citrus fruits, and onions #LetFoodBeThyMedicine

Saved - February 23, 2024 at 9:06 PM
reSee.it AI Summary
The website firm's accumulated profits soar to nearly €1.7m, with cash funds increasing from €1.22m to €1.52m in 2023. The company behind RIPdotIE records profits of €208,492 for 2020. The operator of RIPdotIE sees accumulated profits rise to €1.42m. Death is good business as accumulated profits at the firm reach €1.695m.

@MeasslainteIRL - Thomas Anthony III

Accumulated profits at http://RIP.ie The website firm soar to nearly €1.7m Underlining a buoyant year for the business, the firm’s cash funds during 2023 increased from €1.22m to €1.52m

RIP.ie - most recent death notices | rip.ie Discover the most recent death notices from Ireland. A reliable source to be informed of the passing of those close to you. rip.ie

@MeasslainteIRL - Thomas Anthony III

Company behind http://RIP.ie records profits of €208,492 for 2020 Curse all you Antivaxxer coffin dodgers 😂 https://m.independent.ie/business/irish/company-behind-ripie-records-profits-of-208492-for-2020/41128351.html

RIP.ie - most recent death notices | rip.ie Discover the most recent death notices from Ireland. A reliable source to be informed of the passing of those close to you. rip.ie
Company behind RIP.ie records profits of €208,492 for 2020 The company that operates the online death notice website RIP.ie recorded post-tax profits of €208,492 last year. m.independent.ie

@MeasslainteIRL - Thomas Anthony III

I really should have invested in funeral homes and coffins like I was going to. It's the new Bitcoin for sure 😊. Accumulated profits at RIPdotIE operator rise to €1.42m. https://www.rte.ie/news/business/2022/1229/1344107-ripie-results/

Accumulated profits at RIP.ie operator rise to €1.42m Profits at the company that operates the online death notice RIP.ie website last year decreased by 37% to €130,615. rte.ie

@MeasslainteIRL - Thomas Anthony III

Accumulated profits at firm operating website RIPdotie rise to €1.695m https://www.irishexaminer.com/business/companies/arid-41338664.html Death is good business

Accumulated profits at firm operating website RIP.ie rise to €1.695m The sharp profit hike at Gradam Communications came after the death notice website operator recorded post-tax profits of €264,912 for 2023 irishexaminer.com

@MeasslainteIRL - Thomas Anthony III

@Reseeit save thread @threadreaderapp unroll

Saved - February 21, 2024 at 2:14 PM
reSee.it AI Summary
The McKenna case established that the government must provide fair and impartial information to the electorate during referendums. The Constitution belongs to the people, and any amendment should be done with their consent, without government interference. The McCrystal case has had an impact on the result of the Children's Rights referendum.

@MeasslainteIRL - Thomas Anthony III

The main principle established by the McKenna case is that the government has a duty to provide information to the electorate in a fair, equal, and impartial manner and cannot use public funds to promote a particular outcome in a referendum. This principle is based on the idea that the Constitution belongs to the people, and any amendment of it must be done with their consent, without interference or undue influence from the government. THE SUPREME COURT - RTÉ. https://www.rte.ie/documents/news/mccrystal-v-theminister.pdf Government Statement: Supreme Court Judgment on McCrystal Case. https://merrionstreet.ie/en/news-room/news/government-statement-supreme-court-judgment-on-mccrystal-case.html Impact of the McCrystal Case on the result of the Children's Rights. faganbergin.com/news/impact-of…

Government Statement: Supreme Court Judgment on McCrystal Case The Government is carefully studying today's Supreme Court Judgment which clarifies how the Government can make information available to the electorate during a referendum... merrionstreet.ie
Saved - February 21, 2024 at 12:02 AM
reSee.it AI Summary
Onions, specifically red ones, have been praised for their health benefits during COVID-19. They are believed to act as blood thinners and contain testosterone and Quercitin, a zinc ionophore. Other remedies like IVM and HCQ have also been proven effective against COVID and RNA viruses. This information is still valid today, as highlighted by a woman who gained fame on TikTok for promoting the benefits of onions.

@MeasslainteIRL - Thomas Anthony III

Onions the ones I was singing about all throughout covid the red ones !! You should all be eating them like apples! Blood thinners testosterone & Quercitin a zinc ionophore. 1/2 https://youtu.be/A6IgSpyBrQI

@MeasslainteIRL - Thomas Anthony III

the ones that were been hidden by media outlets IVM HCQ various other remedies that are now proven to provide protection against covid and all RNA viruses. So still today this information is valid! Some woman shot to fame on tiktok promoting the things I was saying about onions.

Saved - February 20, 2024 at 11:59 PM

@MeasslainteIRL - Thomas Anthony III

@vejon_health Hi Dr McMillan, may I suggest upload the videos directly here. Elon has got it bugged to demote posts with external links. #WhyNoAutopsies? #CovIdCoverUp https://t.co/Q3WokK2Ava

Video Transcript AI Summary
The speaker discusses the importance of autopsy in understanding the immune response to COVID-19 and the potential complications of the disease. They highlight two cases of aortic dissection following COVID-19 vaccination and emphasize the need for further investigation through autopsies to determine the underlying mechanisms. The speaker argues that autopsies are crucial in identifying unusual immune responses and ensuring the safety of vaccines. They stress the importance of asking scientific questions and advocating for patients' well-being. The speaker concludes by expressing the need for more autopsy reports to be independently reviewed and understood.
Full Transcript
Speaker 0: The continuous discussion around safety, around the fact that we don't seem to be doing enough research in the pandemic, and the fact that so many people are still dying. I haven't yet shared some of the recent information out of New Zealand, but it is very clear that there is a problem across the world in terms of excess deaths. We need to address it. And in my view, there can be no science without autopsy. Now if you've got a situation where you have full understanding or as close to full understanding of a disease and you don't think that you need autopsy to corroborate, that's fine. But we have had 4 years of a pandemic. And as I have always said, people struggle to be able to explain even the the exact mechanisms of the cytokine storm. Why are some people vulnerable? Why are others not? And then on top of that, we have done an intervention across the world, which is impacting on the immune system. And when you actually think very carefully about COVID 19 and severe COVID 19, just remember this, it is not the virus that kills you. It's the immune system. It's the cytokine storm. The viral infection causes inflammation, but it doesn't cause anyone to die. What causes them to die is that cytokine storm. And if you don't quite understand understand that, just reflect on the fact that neonates don't die with COVID 19 because they have such a poor immune system. So the immune response and the way the immune system responds is very, very important. So today, I want to talk about another case, which is about aortic dissection. This was from 2022, and it's because I'm following on the discussion that we had last week with, Hetty Simoes who lost her son. And we'll be looking back at his case as well, which was aortic dissection. For some reason, they don't like me to talk about this. And so whenever this occurs, there is restriction on what happens to the information. I can expect that that will happen again, but it doesn't mean we don't talk about it. Now people will wonder why do I keep banging on about autopsy. And autopsy, as far as I'm concerned, especially in the context of COVID 19 and our actions after the, the beginning of the pandemic, is that we need to be checking and making sure that unusual immune responses are not occurring, because this is what occurred with SARS COV. When they tried to develop strategies to manage the original variant virus in from 2003, they found strange immune pathology on autopsy. And so my rule is very simple. If you haven't done autopsies, how do you know? And you have to remember that about April of last year, I did this presentation where we had the first full autopsy, the first one in 2023 on a COVID vaccinated death. Now how can you be saying you're doing the science when you're not even looking to see if there are any unanticipated issues, especially when there were unanticipated issues that occurred with the original variant of the virus, which is SARS CoV. So this is a perspective that I have, and this is what I'm trying to see if I can tease out. Before I talk about the, information with regards to this, particular case, I'll quickly run through, the basics so that you understand why this is important in terms of aortic dissection. I've done this before, but just in case you haven't seen it, here we go again. In this image here, this shows you an aorta. So this is the heart in the background. You can see the heart here. And where it's bright red is the aorta, and it makes this nice hook and goes down. This is the abdominal aorta, and then it splits to go to each leg, and then it becomes the femoral artery. This is one of the branches of the three main branches here, the axillary artery on the left hand side. So this aorta is what they had found got damaged in these two autopsy cases. It's so serious because aortic dissection, which is what caused a death in both cases, occurs extremely quickly. Now when we look at, muscular artery, and that's what the aorta is, you can see here this is a normal artery, and in the middle here is the muscle muscle layer. And there is a layer, a band of elastic almost on the inside and another band of elastic on the outside. That allows the artery to be able to stretch, with each heartbeat. And then what you can have is that you can have damage to this lining here, this blue lining, and it causes blood to seep out into the muscle, and that's what then becomes the dissection. And it could look something like this. This is about 3 different types, And, essentially, in our discussion here, we'll be focused primarily on the type 1, sometimes type 2, where the dissection occurred in the ascending aorta and then went down into the heart, and it's because the blood seeped into the heart. That's why it caused such sudden death. And, again, breaking down the, the images of a muscular artery. This is it here showing the different linings of it. This is on the inside of the blood vessel, the endothelial lining. This is the muscular layer, and you can see tiny bits of yellow here, and that's the elastic layer. This is what it would look like here when you cut the section. And very importantly, this is the bit I want to highlight, these blood vessels that supply all of these tissues. So it's important to know that the blood in the bloodstream is not really supplying other than the endothelial lining. It's the, vasovosorum that are supplying the blood supply to the muscle and to the outside layers of the artery. This is it here a bit closer, and, again, you can see this part here is the tunica media. That's the muscle and the elastic. This is important to know because this is where the tear tends to occur in terms of the damage with the aortic dissection. So when it rips through this and then the blood starts to seep down, that's where the dissection will tend to occur. And in the context of the aortic dissection in both of these cases, it was because of inflammation in these blood vessels here. So it wasn't necessarily the lining of the blood vessel here that was having the problem. It was the blood vessels around the artery that normally supply all the nutrients to keep it going that were inflamed. So that's the baseline of what it is that we're looking at. And when we come now to look at the cases, you can then understand a bit more about why we're looking at it. So the first case was in, again, Japanese study. Now what I'll do is I'll I'll show you the, the actual paper here. This is I'll show you this here again. So this is the paper here, and, again, you see November 2022, autopsy case of aortic dissection complicated with histiolymphocytic pericarditis and aortic inflammation after mRNA COVID 19 vaccination. Now before I go any further, I want to just clarify something here because a lot of people say, you know what? This is rare. I'm only talking about 2 cases at the moment. So, you know, what's the big deal? You know, if you've done billions of doses and only 2 people have died from aortitis, then what's the worry? My point is that we haven't looked for it, so we don't know if it's only 2 people that have died. Additionally, we have a situation where in the UK, at least, there is a 22% increase in excess deaths at home, sudden deaths. If we are not doing autopsies on all of those patients, we have no idea what the mechanism of death is, and so that's what needs to be studied. But even more importantly, you have to remember that, as I said, one of the mothers of a 34 year old who died, suddenly from aortic dissection, it was not letting it go, and it was her work that cracked open an important piece of the puzzle. So when you say only a few cases, let her respond to you so you understand what she is meaning. Speaker 1: It is not rare when it's your child. And to those people that say, well, it's for the greater good, I say, well, which one of your children are you gonna be willing to give up for the team? That's what people have to think about. And you cannot just flippantly say, well, we save lives. Give me your child. Let your child die. And then let me ask you if you still feel that way. Speaker 0: Powerful words from Hetty. And I think that this is the point is that we need to understand it. Why is it occurring? What is the mechanism? Does it also involve other blood vessels? Those are the questions that we need to try and clarify. When we look at this case here, this was a 90 year old gentleman, and he clearly was relatively well beforehand. And what they found is that he had a few days of fatigue and the shortness of breath. He was then diagnosed with heart failure, give him some medication, and then he collapsed and died about 4 days after he had the consultation. And he was about 2 weeks after he had received his, vaccination. And so when they looked at the heart surface, they found that there was inflammation of the lining of the heart, the pericarditis, with macrophage and lymphocytic infiltration. And when they do the histology, this is what I'm saying, oftentimes can get left out, it fit with post vaccination myocarditis. And as well, he had extended inflammation of the aortic adventitia, which was a possible cause of the aortic wall fragility followed by dissection. So this is then getting back to the point that I was making with regards to the outside lining of the heart, and this is what it would look like. It is the adventitia is this outside bit that got inflamed. It weakened his blood vessel, then it tore, and then he died. It's unclear if he had any element of dissection before. It wasn't mentioned in the autopsy report, But the main point is that he had inflammation in that region of his heart, of of not just his heart, but the lining of the blood vessels. I'm just looking at some of the images here. I'll just show you some. This is the, this is from the 90 year old gentleman. This is his heart here, in and they're looking at this here. This is the pericardium. This is all the blood that was around the heart, and this is what caused his death suddenly is that the blood leaked around the heart so that the heart couldn't properly contract. And so even though it occurred in the heart, the primary damage was actually inflammation in the lining of the blood vessels, the the aorta. And when they did the histology, this is now the histological examination in his case, and they looked at different cell types. They found mainly it was CD 8 macrophages that were occurring in the adventitia of the aorta. So these would have been so these little brown areas here, the macrophages that they have stained, And so it was primarily, CD 68 macrophages doing a lot of the damage. What we are need to understand is whether or not this is a pattern that occurs. Because when I looked at our case last week, and we were looking at, the 34 year old who died. He also had and this is this is his report here. He also had, inflammation in the pericardial sac, lymphocytic infiltrates indicative of pericarditis and myocarditis. Again, typical of what could happen after the COVID 19 mRNA vaccines. What was different is that he seemed to have eosinophilic infiltrates, and this suggests some kind of allergic response. Now this was his first dose, so it's not clear why that would happen. It's a hypersensitivity response vaccine. So based on the fact that you can have IgG 4, maybe this was why you didn't see that allergic type response that can sometimes occur. The main point that I am talking about in relation to this is that I still maintain that from my autoimmune paradigm and for people who don't quite understand the autoimmune bit, it's where the immune system is doing the damage. And I believe this can be triggered by the infection, which is through the spike protein, and then theoretically, any other form of spike protein can trigger that kind of autoimmune response. It's just different. And therefore, you have to actively look for pathology. And the only way that you will do it is through autopsy or even biopsies. That's why I keep on hammering it home. The truth is is that it's so important that I can't find any good scientist who would actually refute that. They may say, well, we don't know if we need to do it, but it should be done. Nobody would say if you can do it, you shouldn't do it. And in their context of not having clarity on the mechanisms why this is occurring, why would we have this aortic inflammation? Why are we having so many cases of, of pericarditis and myocarditis? Why are we having abnormal patterns occurring in the heart with regards to the use of energy? These things, you will only start to make sense of when you start doing histology, looking in detail as to which cells are present in the muscles, in the tissues, and then you can extrapolate it to understand whether or not there are issues you have to look out for. That's the point of this. Just remember, in the long run, our job is to advocate for the patients. Our job is not to support politicians or to support the industry or to play along with everything else. No. We are supposed to be objective. We ask the hard scientific questions. We force regulators to make sure that everything they're doing is in the benefit of the patient. Asking questions is a good thing. It shouldn't be censored. It shouldn't be shut down. It only happens when you don't have answers. That's the problem at the moment. We don't have enough answers. Remember, I am looking actively for autopsy reports, and believe me, they are few and far between. We need 1,000. And if anything that needs to happen is that we need as many to be independently reviewed, assessed, and understood in order for us to make sure that we are on the right track. Have a good evening.
Saved - December 11, 2023 at 8:50 PM
reSee.it AI Summary
Scientists have found fungi that break down specific types of plastic, like polyurethane. The Fungi Mutarium project made an edible mycelium snack as a plastic alternative. Scaling up the process is the main challenge to tackle global plastic production.

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

Plastic is a big problem, but fungi might be the solution. Scientists have discovered different types of fungi that can break down specific types of plastic, including polyurethane and polyester polyurethane. 1/2

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

The Fungi Mutarium project even created an edible mycelium snack in place of plastic. However, the biggest challenge is scaling up the process to keep up with global plastic production.

Saved - December 5, 2023 at 5:24 PM
reSee.it AI Summary
In 6 days, Ireland's opportunity to opt out of amendments to article 59 of the international health regulations will end. These amendments, approved by the WHA, reduced the time for future amendments from 18 to 12 months. Urgent parliamentary debate is needed before the deadline. A crucial interview with South African lawyer Shabnam Palesa Mohamed exposes the dangers of the WHO's command and control ambitions. The WHO is trying to impose a global treaty on pandemic preparedness and response, threatening Irish self-determination and sovereignty. Some countries have already expressed opposition or rejection of the treaty, citing reasons such as sovereignty, cost, or existing commitments. Denmark, Ireland, and Poland have opt-outs from certain EU treaties, which could affect their participation in the WHO treaty. Mexico's government has to respond within one month.

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

In 6 days, #Ireland's opportunity to #optout of amendments to #article59 of the international health regulations will end. These amendments, approved by the WHA, reduced the time for future amendments from 18 to 12 months. Member states, like Ireland, also had their right to reject amendments reduced from 18 to 10 months. This legislation, consisting of 307 amendments, lacks debate and media coverage, making it undemocratic and a threat to #sovereignty. Urgent parliamentary debate is needed before the deadline. @OireachtasNews @MichaelDHiggins @LeoVaradkar @DonnellyStephen @sinnfeinireland @pb4p @rtenews @VirginMediaNews @eirenews_ie @griptmedia @HSELive #IrishX #ExitTheWho #StopTheWho #DismantleTheWho #OpOutOfTheWhoTreaty

Video Transcript AI Summary
The speaker discusses amendments made to Article 59 of the International Health Regulations, which shorten the time frames for future amendments. They criticize the lack of debate and media coverage surrounding these amendments, calling it undemocratic and against sovereignty. The speaker also highlights the ignorance of politicians regarding global organizations like the World Health Organization (WHO). They explain that the amendments aim to centralize control over international health policy, potentially affecting sovereignty. Several countries, including Estonia, the Philippines, Slovakia, and New Zealand, have rejected these amendments, citing concerns about sovereignty and the WHO's authority. The speaker outlines specific dangerous provisions in the amendments, such as making recommendations binding, removing consultation requirements, expanding the scope of the IHR, and increasing funding for censorship and unspecified costs.
Full Transcript
Speaker 0: Excuse me. Speaker 1: It Speaker 0: takes time. The window for Ireland to opt out of the amendments made to article 59 of the international health regulations will close. This amendment was adopted by the WHA, at World Health Assembly, and the slash report, the periods of time for which future amendments could be made from 18 months down to 12. At the time during which a member state, like us, connects the right to reject, the amendments from 18 months to 10. This is, a a a piece piece of legislation. 303 7 amendments brought forward by the WHA. All unelected people. And we are, expect to deal with this year, and we have no debate on this parliament here as happening with 0 media media, attempt to 0 debate in this house. And, also, I think it's totally undemocratic, and it's against our sovereignty. And I want to debate on this another debate on this this week because it happens on the end of this week and just passes through 307 amendments. I'm afraid I'm not familiar with the issue that raised. Perhaps minister Donnie will be able to come back to Speaker 1: So, Shabnam, as an activist and lawyer and expert on, you know, what's going on with the World Health Organization, and I know that you have a kind of A global perspective on that link to very many people like yourself all over the world. You've seen the clip Where this whole thing was put to the leader of the Irish Parliament, Liav Radker Tisjuk, you know, with a request just 6 or 7 days Before the end of the month, to, to to to have a debate in parliament. And he admitted to not knowing anything About this, which is what do you think of that? Speaker 2: Well, I have 2 thoughts on that one, Eddie. The one is to say there's 2 categories of politicians as we've covered in general, but in particular the last 3 years, one is those that are genuinely naive at best or ignorant at worst as to what's Going on via these supranational organizations and other sorts of machinations by the global cartel. The other category is politicians that are either compromised, captured, or corrupt. And then my second thought is that as a minister of health or former minister of health or whatever cap capacity he is acting in government, He ought to know. These people are serving the public. How can they not know what's happening at an international level? Because politicians are going to end up becoming Irrelevant to what the WHO and the UN are doing. So if he didn't know, I hope he's done his homework since. Speaker 1: No. I've read my way into much of the Much of the weeds of this thing. So, I just want to repeat back what I understand to be and you can correct me like a teacher then if that's okay. So, it would seem to me that It's very subtle, but very powerful, the changes that are being implemented in the 2005 IHR, that's the International Health Regulations that we've signed up to as a country, Kind of backdoor changes. One of the things that really jumped out at me was the movement from non binding to You know, to, you know, the non binding thing was taken out in the proposed changes. And then this seems to then feed in through, you know, the working group into the treaty that's supposed You signed up in May. And, you know, it just seems the logic of it to me is that, you know, the claim all over the place, oh, this won't affect sovereignty. But if you're centralizing command and control for international health policy in Geneva, of course, it's going to affect sovereignty. They're too incompatible. It's just it's just it's just PRs. Am I misreading that? Speaker 2: No. Not at all. Although I would say that the overriding agenda for the Health is economic. It intends to leach and steal as much money as it can through the resources of our national economies. But, of course, there's a clear distinction between amendments to the international health regulations and that new pandemic treaty, which I'm not going to get into right now Just so we don't confuse your wonderful audience, but on the IHR, the amendments that were adopted at World Health Assembly 75 last year Essentially deal with the shortening of time frames, and that's 2 time frames. The one is a period of time to reject Or provide a reservation to amendments, and that was changed from 18 months to 10. The other is shortening the duration within which an amendment is of force and effect, and that's reduced from 24 months to 12. In other words, completely making impossible A process of public participation, not that our governments are inclined to do much of that anyway. However, what you're talking about, The other amendments, those are proposed amendments still under discussion and negotiation through a working group on the IHR and these 300 past amendments. And those are going to be presented to the WHO in January, for each to continue its internal and external processes, one would hope, Towards adopting those 300 plus in May next year. So we're dealing with 2 sets of amendments related to the IHR. Speaker 1: Well, when you cut through the the the kind of the the detail, of it, just to just for the ordinary person just listening to this for the first time, Can you can you just explain why why is it then I mean, if this thing was supposed to be okay, why is it then that Estonia have rejected it, The Philippines have rejected it. Slovakia is talking about rejecting it very strongly in very, very strong language by the prime minister there. And, and who else is there? New Zealand, have also are also intent to reject it. So if it was so if it was so benign and it wasn't an impingement on sovereignty. Why would these independent parliamentary countries, come to the conclusion that they're not happy with this? They don't want to leave the WHO? Are they are they they're just just objecting to what's going on. So how do you see the sand shifting here? Is this is this what is happening? Speaker 2: The stand is exactly shifting, and it's also Mexico. It's Philippines. It's now recently South Africa. I've drafted a letter to reject amendments to the IHR And highlighted the new ones coming up. 2 of our parliamentarians have taken up the baton and served that on the WHO. But, certainly, these countries come from a background understanding that they are very much ignored within the super nationals of the United Nations and the World Health Organization and the International Trade Organization and all of these are other hydro tentacles, belonging to essentially the World Economic Forum. And they've started to develop more of a voice During the last 3 years of lockdown and misery, both at the WHO and the United Nations, the specific provisions that they are talking about In the amendments currently being negotiated certainly are very dangerous, and they form part of the letter that I had submitted, to these parliamentarians to facilitate and include, the following. It's going to make recommendations if, of course, they succeed, which they won't. It's going to make recommendations binding. That was one of the proposals that has been put forward by one of the countries engaged in this negotiation process, and they are 94 of them. So recommendations will then become binding that, of course, violates the WHO's own constitution. It has no authority To make its recommendations binding, it is, in fact, acting ultra bearish or outside the scope of authority. Also, in article 12, The WHO seeks to strike out the, provision that would make it necessary for it to consult with A member state about declaring a public health emergency of international concern in that country for that country to agree. So they're looking at removing that provision in article 12. And article 1, they look to remove the, the specific terms regarding standing recommendation and temporary recommendation are removing the phrase nonbinding from each term, And that one was submitted by Bangladesh. The one before this was submitted by the United States. Then we've got article 3 removing the the clause, Full respect for dignity, human rights, and fundamental freedoms. That one was put forward by India. Article 2, Expanding the scope of the IHR, to events with a potential to impact on public health and also, giving them access to all risks, so not just the risks related to the, to health or public health in particular, very dangerous. And finally, some of those that I've specifically highlighted, is, of course, that recommend 13 recommendations would be converted into legally binding orders. And this proposed amendment has come through from Malaysia. Article 15 requires nations to allow access to their sovereign territory. Article 17 is censorship. WHO wants to increase funding to tackle false misleading misinformation or disinformation. And article 19, the last one I'm going to highlight, Eddie, is unspecified and potentially enormous costs. It's going to cost an enormous amount of money To facilitate everything that the WHO is trying to do. Speaker 1: Yeah. What what really jumped out at me when I went through it, was, was was Some of the points you made really, really jumped out. I mean, I can't I mean, I'm not a lawyer, you are. And I mean, I could understand this and it's pretty plain what was going on. But the The attack on misinformation or disinformation, I mean, that's you know, it's misinformation according to the

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

#ExitTheWHO A crucial interview with South African lawyer Shabnam Palesa Mohamed has been published by Eddie Hobbs. The interview exposes the dangers of the WHO’s command and control ambitions, which threaten to bypass Irish self-determination and sovereignty. The WHO is trying to impose a global treaty on pandemic preparedness and response, which would give it unprecedented powers over the health policies of its member states. The interview warns that Ireland 2024 will be a decisive moment for resisting the WHO’s agenda, as the Crotty ruling of 1987 will force a referendum on any treaty that affects Ireland’s constitutional position, making it unique in the EU. The interview also urges the Irish people to put massive pressure on Michael D. Higgins, the president of Ireland, to stop the Oireachtas from passing any WHO treaty without the consent of the people. @RealEddieHobbs @ShabnamPalesaMo

Video Transcript AI Summary
The speakers discuss the World Health Organization (WHO) and its connection to powerful corporations like BlackRock and Vanguard. They criticize the WHO for spreading misinformation during the pandemic and accuse it of being funded by private interests, including the Bill and Melinda Gates Foundation. They also mention the WHO's alleged cover-ups and unethical practices. The speakers believe that countries are starting to question their membership in the WHO and the United Nations, and they predict a shift towards closer cooperation between countries and a move away from these organizations. They highlight the dangerous power of the WHO to declare a pandemic and impose lockdowns on countries. The speakers express hope that Ireland, with its referendum mechanism, can become a battleground against the WHO and raise awareness about its problems. They urge President Michael D. Higgins to protect the freedom and sovereignty of the Irish people.
Full Transcript
Speaker 0: Have already made a pig's breakfast of the last pandemic in terms of, in terms of the information provided that the vaccines would stop transmission and that the vaccines were safe. And if you didn't take them, you were somehow a bad citizen. All that kind of stuff was permeating through. I mean, it would be extraordinary to think that the Central Command and Control in Geneva will be dictating terms to countries throughout the world, which would include censorship of their own citizens and matters of science. Speaker 1: That's what the cartel essentially does. It lurches us from crisis to crisis, ever increasing its power and, restricting our fundamental human rights and increasingly more relying on censorship through the media cartel that they've essentially funded, own, and control. Right? Right at the top, BlackRock and Vanguard almost all the corporate media out there. And so they're doing this, consistently. They're doing it increasingly, and we're going to have to develop alternative ways not only To communicate with each other, but to share information with the public. Of course, the WHO has also been guilty of many other crimes against humanity, Including the cover up of the tobacco funding scandal, the h one n one pandemic scandal, the cover up of the extent of nuclear harm. And in Africa, in particular, Eddie, facilitating Tetanus injections, what they call tetanus injections, and millions of Kenyan girls and women turned out to be laced with ACG, rendering millions of them infertile. So I was very happy that the African nations, the 47 nation bloc, took a stand at last year's World Health Assembly and objected to amendments that would violate sovereignty and create further death cycles. In other words, death slavery. But since then, WHO has appointed 2 executive board members from Africa. Right? So they're using a carrot all the stick. So what we're seeing happening right now with countries taking the stand, not only through parliamentarians, but also asserting their own rights, as people of their own countries, it's certainly a joy to see. I know the cartel is very nervous, not only because they tried to suppress our right to know, but also, because they said so. They've said they're quite nervous and internal processes and, representatives have said they're not going to meet their deadlines. Speaker 0: Yeah, can I just ask you about that so that just to get an understanding, you talk about the cartel and the linkages? Just bear in mind, a lot of people will be listening to this for first time saying, well, what is the World Health Organization and the WHO and the Bank For International Settlements and like like, what what's what's the connection here and what's what's the what's the big what's what's the game plan, in your opinion? Speaker 1: So these organizations are essentially connected to and or owned by 2 mega corporations called Black and vanguard. All of them essentially belong to and are run by and controlled by and influenced by the 1%, what I like to call the 1%, the oligarchy. In other words, the predator or parasite class that controls our economies, that tries to control our thinking, the way we think about the world, that engineers and festers crises like, you know, pandemics, or wars for that matter so that they can benefit ultimately from their multinational corporations. This is the cartel we're referring to. The WHO in particular is significantly funded by private interests, including but not limited to the Bill and Melinda Gates Foundation, which interestingly enough, the research I was doing in an article about the United Nations, which is also deeply problematic, also funds the UN. And so we're dealing with the same set of bad actors, To put it mildly, that seek to profit through control, fear, and propaganda, and the but the world is waking up to it. One of my friends dear friends, Farhi Asan, is an expert in conflicts of interest, and his work shows you clearly how these organizations and these individuals work together. As George Collins said, it's 1 big club, and we're not in it. Speaker 0: Yeah. So how do you see it playing out then? I mean, when you're right in the heart of it, you can see what's going on in different countries, you're clearly expert on the legislation and the thinking behind this, the connections behind the connections, if you follow me. But how like, bearing in mind that most people are blissfully unaware of most of the stuff because it's not being reported in the mainstream media. How do you see it playing out now that it's beginning to splinter? I I mean, in other words, it's World Health Organization stuff, the tip of the spear, and it's about the fracture by the look of it. Am I misreading that? Speaker 1: I think it is the tip of the sphere. So so spear, certainly the way I would, characterize it, would be if you look at what happened at the UN General Assembly in September this year, 11 countries formally objected in writing to a political declaration on pandemics that the UN tried to push through. Non binding, But it certainly is an alarm bell. And what it says to me is that countries are beginning to question their role and their continued membership within the WHO, within the United Nations, and with the entire hydro structure, it certainly does not benefit most of us. It may benefit some countries that have a position of being on the security council of the United Nations. But as for the rest, as these 11 countries said, there's always a lack of balance, a lack of inclusion, a lack of transparency, and they feel completely ignored and disrespected. Even that letter to the UN was ignored. The general assembly president for 78, UNGA 78, proceeded to declare that the political declaration had been passed, Completely ignoring that these countries had broke the silence, which is a very significant step for them to have taken. So I think geopolitically, also with the formation and expansion of BRICS. We're going to see countries working more closely with each other and start to extricate themselves from the hydra. Speaker 0: Yeah, but, you know, just to focus on the WHO just for a second, the head of the WHO, the Director General office can decide on what is a pandemic and what's not a pandemic without consultation with member states. I I I misread that in the in the proposals. Speaker 1: 100% correct. And it's an incredibly dangerous geopolitical tool. If, Tedros or another director general was put into that positioned to facilitate certain objectives, they decide your country is troublesome. It's been doing things that the cartel doesn't like. All they need to do is then declare a public health emergency of international concern and instruct your country to shut down. Which of our countries can afford Go through lockdowns again, Eddie. Absolutely none of us. Certainly not us as the 99%. So it's an extremely dangerous tool. Tedros, for the matter, has been accused of genocide in his whole country, Ethiopia. And I've engaged and interviewed with the Amhara people who are also going through a genocide right now, god be with them, they actually objected very strongly and efficiently even to the International Criminal Court about his appointment to the WHO. The WHO didn't listen. They appointed him anyway. So we're sitting with the head of the WHO being an alleged terrorist. So this tells you all we need to know about this organization. It's not to say there aren't good people working on the inside, but at its roots, it is corrupt. Speaker 0: Well, can I bring you then, Saman, to the notes I sent you there the other day and further notes on it? Just to explain it that it seems to me that Ireland could become kind of the Waterloo for the WHO because we have the 1987 CRATI ruling by the Supreme Court, which mandates a referendum in Ireland on any treaty changes, external treaty changes by the country. Even if the government decides to pass it, it has to go before the people by way of referendum, which means that the ordinary commoner guard and the ordinary Irish voter is going to become very familiar with a lot of the detail here. And, of course, there'll be a lot of arm twisting and money pouring in to try and tell us that the countries that are leaving, sure, they just see it as a conspiracy. They're all just conspiracy theorists and everything is fine, you know, because what's going to happen here is that Ireland is going to become, as it had before, the battleground in Europe to try and pass something that the EU wants that the Irish people are saying are the only people in Europe that can say no to us. Do you how do you see that playing out? Speaker 1: Well, we're certainly going to be relying on the Irish to take up those casuals. It's fantastic that your process of referendum actually works. The last time we've had one in South Africa was in relation to, upending the apartheid state. We haven't had referendum since. So if this mechanism of referendum is operational in your country, even if it isn't, I would certainly urge the Irish to mobilize around that. And through that Process. Really, the Irish people will become completely aware of exactly what the problems are with the WHO, by extension, the rest of Europe. Interestingly enough, the EU parliamentarians also submitted, a letter regarding the IHR and rejecting it. So there's a question as to whether being part of the EU is actually positive or is it negative where certain representatives can make decisions on behalf of all countries in the EU. But coming back to the Irish, I certainly have great hope, that there are some, ethical and fiery parliamentarians who are going to take up the casuals and exercise the right to referendum. Speaker 0: Well, on that final point, we have a we have in the office of the president of Ireland, Michael d Higgins, whose spoken, especially on external matters. But, if he was here and he's not, but if he will be listening to this because I'd be sending it to him, what would you say to Michael de Higgins because he has the power to refer any potential legislation that may attempt its way through the Irish Parliament to the Supreme Court. And he can call a council of state as well to go over it. If he was here and he was listening in and and you were addressing him directly, president Michael d Higgins. What would you say to him? Speaker 1: Well, I would see say to him as a president, he has the role, the duty, and the responsibility to protect the Help the freedom and the sovereignty of the people that he serves. And, certainly, he was looking
Video Transcript AI Summary
The speaker mentions that if someone wants more information about why many people have been advocating against the power grabs by the WHO, they can reach out to them or refer to the World Council for Health's policy. They also mention the work being done by Children's Health Defense and the importance of exercising the right to referendum. The speaker warns that politicians may become irrelevant if they don't prioritize the interests and self-determination of the people. The conversation ends with a thank you and a call for power to the people.
Full Transcript
Speaker 0: Certainly, if he was looking for more information around why so many people like me for the last 3 years have been advocating against the power grabs by the WHO, just feel free to reach out to us. He can also refer to the World Council for Health's policy rejecting a monopoly over global public health as well as the incredible work being done by Children's Health Defense, and the organizations and individuals we work with there, and of course, to exercise that right to referendum. If he doesn't do that, he may find, you may find president that politicians are going to become irrelevant, not only through the WHO, but also the United Nations, which is pushing for the authority standing authority over complex global emergency shocks. And then there's a long list of them. So, essentially, politicians will become irrelevant if not for the interests of the people and the right to self determination of the Irish people, then at least for self preservation and for politicians to still have a job in the democracy that exists in your country. Speaker 1: Well, Shabnam, please, Mohammed. Thank you very much for such clarity, and, wish you well in your continuing campaigning against The WHO and its, and its movements. Speaker 0: Thank you, Eddie. Power to the people. Speaker 1: Well, if you've enjoyed Counterpoint, please subscribe by clicking the button below. See you next time.

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

#WHOTreaty Which Countries Are Saying No? The World Health Organization (WHO) is currently negotiating a global treaty on Pandemic Tyranny. Some countries have already expressed their opposition or rejection of the treaty, citing various reasons such as sovereignty, cost, or existing commitments. Here are some of the countries that have opted out of the WHO treaty, #Estonia: The Republic of Estonia notified the WHO that it rejects the treaty and the amendments to the International Health Regulations (2005) and the sustainability of WHO funding. Estonia argued that the treaty would infringe on its national sovereignty and autonomy, and that the WHO lacks transparency and accountability in its decision-making and financing. #Denmark, #Ireland and #Poland These countries have opt-outs from certain treaties or legislation of the #EuropeanUnion (#EU), which could affect their participation in the @WHO treaty, as the EU is a member of the #WHO. For example, Denmark has an opt-out from the EU's common security and defense policy, Ireland has an opt-out from the EU's Charter of Fundamental Rights, and Poland has an opt-out from the EU's fiscal compact. These opt-outs could limit their ability or willingness to comply with the WHO treaty, especially if it involves sharing sensitive information or resources with other countries. #Algeria, #Canada, #CostaRica, #Ethiopia, #Guatemala, #Indonesia, #Japan, #FYR Macedonia, Malaysia, Montenegro, #Norway, #PapuaNewGuinea, #Peru, #Samoa, #Singapore & #Tonga These countries have met their commitment to the Paris Agreement on climate change, which could indicate their reluctance to join another global treaty that might impose additional obligations or costs on them. The Paris Agreement is a landmark deal that aims to limit the global temperature rise to well below 2°C above pre-industrial levels, and requires countries to submit their nationally determined contributions (NDCs) to reduce greenhouse gas emissions. Mexico's government has to respond within one month. Excellent work! #ExitTheWHO #StopTheWHO #Mexico's government has to respond within one month. Excellent work! #ExitTheWHO #StopTheWHO #Dontbepaddylast #NoAmnesty

Saved - December 2, 2023 at 3:12 PM
reSee.it AI Summary
In a presentation by Kevin McKernan, the potential risks of DNA contamination in mRNA COVID-19 vaccines are discussed. McKernan highlights the importance of substantiating claims and emphasizes the role of p53, known as "The Guardian of the Genome," in preventing tumor formation. The presentation also mentions SV40, which can bind to and inactivate p53, and plasmids with oncogenic and mutagenic capabilities. It is crucial to address these concerns while avoiding biased opinion pieces.

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

@KateYandell Hi Kate is this you ? https://factcheck.org/author/kate-yandell/ Maybe you should talk about things that you can substantiate. #Bioweapons #CovidInquiry #Genomics #P53 dubbed #TheGuardianoftheGenome https://mskcc.org/news/new-findings-clarify-how-guardian-genome-works SV40 has the ability to bind to and inactivate p53, which is a crucial regulator of the cell cycle and plays a role in preventing the formation of tumors #SV40 #plasmids with oncogenic & mutagenic capabilities. https://ncbi.nlm.nih.gov/pmc/articles/PMC452549 @Kevin_McKernan #factcheck #fatcheque Keep writing.your shitty opinion pieces. But please highlight that fact ! Thanks. https://rumble.com/v3z58rg-kevin-mckernan-presentation-to-the-croatian-parliament.html

New Findings Clarify How the “Guardian of the Genome” Works Surprise! It has to do with metabolism. mskcc.org
Emergent Human Pathogen Simian Virus 40 and Its Role in Cancer The polyomavirus simian virus 40 (SV40) is a known oncogenic DNA virus which induces primary brain and bone cancers, malignant mesothelioma, and lymphomas in laboratory animals. Persuasive evidence now indicates that SV40 is causing infections in humans ... ncbi.nlm.nih.gov
Kevin McKernan Presentation to the Croatian Parliament This a review of the plasmid contamination in the mRNA vaccines. What do we know about SV40? What do we known out undisclosed Open Reading Frames? What can we learn from their Patent estates regarding rumble.com

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

This presentation by Kevin McKernan is about the "potential" risks of DNA contamination in the mRNA COVID-19 vaccines. https://t.co/OP5exuQbgG

Video Transcript AI Summary
Kevin McKernan, a genomics expert, discusses the contamination found in mRNA vaccines. He explains that the vaccines on the market differ from those used in clinical trials, with different levels of contamination. The contamination includes plasmid and bacterial DNA, as well as lipopolysaccharides, which can cause adverse reactions. McKernan reveals that certain functional DNA components were intentionally omitted from the plasmid map submitted to regulators. He emphasizes that the vaccines contain a significant amount of contaminating DNA, which is not easily degraded due to its encapsulation in lipid nanoparticles. McKernan's findings have been replicated by various researchers, highlighting the need for further investigation into the potential risks associated with this contamination.
Full Transcript
Speaker 0: Hello, everyone. Thank you for your time and attention. My name is Kevin McKernan. I have 25 years of experience in genomics. I was the team leader of research and development on the human genome project at MIT, working under Eric Lander. I have built several genomics companies. I have over 50,000 citations to the research I've published, 25 years, multiple patents. I've started multiple genomics companies, and even built DNA influencers. So today, I'm going to show you out the contamination that exists inside these mRNA vaccines, if you wanna call them vaccines. I don't have any conflicts with Clare. I work in a completely different space. This isn't my day job. We stumbled upon this somewhat accidentally, but it's an important topic that, the world needs to know about. We did publish some of this work in a preprint back in the spring. This has since been reproduced. We'll touch on that a little bit later as to the level of reproduction that's occurred. This has gotten a tremendous number of downloads and attention because the, contamination that you're about to see is actually quite significant and, significantly alters the definition of these therapeutics. They are clearly falling under a gene therapy category now based on the contamination that's present. And this contamination may be playing a role in some of the increased levels of cancer that you're gonna hear about today. Okay. You first have to understand that the vaccines that are on the market were not the vaccines that were studied in the clinical trials, at least for Pfizer. Moderna is a different story. The Pfizer vaccines use a different process to manufacture the vaccines for the clinical trial, and they switched to a different process after approval. This is known as process 1 versus process 2. This is covered, by restless levee in the BMJ. But the main difference between these processes entails different levels of contamination. The first process was clean of most, plasmid and bacterial DNA. The 2nd process was not purified of that material. And as a result of this, there's several other risks that could be confounding, the interpretation of the adverse events that are being collected in in various databases around the world. So the 1st process used an in vitro transcription reaction off of a PCR product. They would amplify a piece of their plasmid DNA off of, through a process of of PCR, to generate lots of templates so that they could make RNA from that. Now that amplification means that they increase the the DNA concentrations a million fold or more before their they made the made the RNA. When they moved to process 2, they cut that step out. So that amplification step means that things are gonna be a 1,000,000 fold dirtier. You're gonna end up with plasma DNA and bacterial DNA and So lipopolysaccharides contaminating, the actual injectables. This is very important to understand because both the DNA and the lipopolysaccharides Can are also known as endotoxins. The LPS is known as endotoxins. These things can create anaphylaxis, upon injection, which we saw a lot of after the rollout of these vaccines. Now we initially studied, some open but non expired bivalent and Moderna vaccines. And then we had some unopened, but obviously expired, monovialent vaccines because they were phasing these things out over time. So we have a mixture of data here, some from unopened vials, some from open vials with different expiration dates. It's important to know that they move the expiration dates over time to their convenience to continue to inject expired lots into patients over time. So the expiration dates here are somewhat irrelevant given they're very pliable in the definition of expiration. Alright. So after we did sequencing of these, what we had found was that there was material components inside the plasmid DNA that shouldn't be in the vaccines that was not disclosed to the regulators. So when they submitted their plasmid map to the regulators, they submitted this map on the right. This map on the right describes the the antibiotic resistance gene that's present, the origin of replication, the spike protein, and a few other elements. But this whole region of the plasmid over here, The annotations were deleted. When you actually sequence a plasmid like this and you put it into commercial software, it will Adequally annotate these regions for you as what has happened over here. Alright. So somebody had to intentionally go in and delete these regions before handing this in to the regulators. So this isn't in, an accidental omission. This is a very deliberate intent to deceive regulators by removing these very functional pieces of DNA. And when I say have been published pieces of DNA. And when I say have been published to be used in gene therapies. David Dean has done a lot of work on this. This particular s v 40 enhancer or is known to bind transcription factors that drag this DNA directly to the nucleus. Okay? So we have DNA that's contaminating these shots. They're inside of lipid nanoparticles, so they do not get degraded once they're injected. They go directly to cells, and they have sequences in there I drag that DNA directly to the nucleus. Alright? So this is this is what is used for gene therapy. It's clearly a gene therapy based on the sequences that they have present, but that they intentionally hid from the regulators. Now normally, you've probably heard of DNA being at residual levels in some previous vaccines. That's It's a very different story because those vaccines were injected and DNA has a 10 minute half life in the blood. The moment you encapsulate that DNA in a lipid nanoparticle, It's no longer susceptible to that degradation, and it goes straight to your cells and directly to your nucleus with the sequences that are provided. So to do this, we built, PCR assays to help the rest of the field validate this. The challenge you have in publishing anything controversial like this is it could get hung up in peer for a year, and then millions of more people get injected and get harmed. So the right thing to do in a circumstance like this is spend the extra time to design quantitative PCR assays that make Get really easy for someone else to verify this. In science, we don't care about peer review. We care about replication. Half the data out there In peer review, can't be replicated. So we wanna bypass that bottleneck and go straight to reproduction. These assays helped The field do that. They're public, and anyone can download them and use them to verify our work in different jurisdictions. What you see when you do perform PCR With these, targeting these DNA elements that shouldn't be there is that you can get CTs. This is the cycle threshold that's used in PCR as low as 17. And for those who recall during the COVID pandemic, we were calling people positive for COVID sometimes out of the CT of 40. This is the log two scale. That means there's a 1,000,000 fold more of this contaminant, not the RNA that's supposed to be injected. The Haminate is a million fold higher than what you might call someone positive for the virus with the qPCR tests. Right? This is not a small amount of DNA. This is a tremendous amount of contamination that's present. Now some people have raised objections to our work saying we used expired vials. Well, not all the vials were expired, but we also have a method here that is used by Pfizer to to measure the RNA integrity. If any RNA was destroyed due to the expiration date of these, We should see that in RNA integrity plots. We see very similar RNA integrity scores on these vaccines. So we don't believe that degradation has occurred altering these results. Now other people have replicated these results. There's a vast number of people now that have replicated these results. There's groups in Japan that have done work just doing in silica reassembly of our data. And they find the same s v 40 sequences. There's people in Japan who've been playing around with PCR as well. Different methods, but also finding DNA. The methods they used find less DNA than what we found. But that's, can be explained by the methods used. William Engle has done sequencing in Europe on monovalent Pfizer vaccines and found the same thing that we found. But most importantly, if you look through the EMA documentations, they Acknowledged this DNA contamination problem. They zeroed in on it being a DNase problem. A problem of an enzyme that's supposed to erase this DNA Is not functioning well, and they find an 8 15 fold variants amongst the 10 vials that Pfizer handed them data on. Now since this data has been, available to us, other people have jumped into the in into the field. Doctor Philip Buchholz, I I, recommend everyone view his video on this. He presented this to the South Carolina Senate. And, He has reproduced our work making all of his own primers and even doing Oxford nanopore sequencing on this and also finds a tremendous amount of DNA that concerns him. We don't know if this DNA yet is integrating into the genome, but we know the risk is there based on the quantity that's present and the types of sequences that are present. Doctor Sin Lee did a partial reproduction of this work. He did not quantitate how much DNA is there, but he could tell that there were long pieces of DNA there by amplifying long pieces of DNA over 300 bases and size. He's saying or sequenced these, which is the gold standard for sequencing. So we we know the primers that we've designed are in fact targeting the vaccine, and they're not off target. Another group in Germany has reproduced some of this work, and they're also finding very high levels of contamination. This is doctor Bridget Koenig's work. Now very recently, doctor David Speaker reproduced some of this work in Canada with the largest study yet, now looking at over 27 vials. And in this, he added 3 additional vials and aren't described here, in from the XBBs, which are the most recent vaccines to go to market from Moderna. And they are still contaminated. So this problem has not been solved. Now this work was recently put up as a preprint. It went over several different, vaccine lots. I think it's, over a dozen different vaccine lots that were surveyed in this study, 27 vials in total. And we can see With qPCR, the levels of this DNA just, just touched the threshold with Pfizer. They're under with Moderna. This is the and FDA threshold of 10 nanograms if you measure it with qPCR. Now if you measure this with fluorometry, which is also used in the EMA's documentation, Pfizer

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

The presentation by Kevin McKernan is about the potential risks of DNA contamination in the mRNA COVID-19 vaccines. Part 2 https://t.co/NhizbOWLIA

Video Transcript AI Summary
Pfizer's use of the RiboGreen technique to measure DNA in their vaccines has raised concerns about deceptive practices. The presence of billions of DNA fragments in each dose, some of which are small and more likely to integrate into the genome, is worrying. Preliminary data suggests a correlation between adverse events and contaminated Pfizer vaccines, but more research is needed. The DNA in the vaccines is different from previous contamination and carries a higher risk of integration. The FDA acknowledges the integration risk and the need for lower limits on DNA when copy numbers are high. The DNA is encapsulated in lipid nanoparticles, making it prothrombotic and potentially oncogenic. The presence of endotoxin and the spike protein in the vaccines further complicates the situation. The vaccines have been found in various tissues and can lead to prolonged expression of the spike protein. Insertional mutagenesis and cancer risk are concerns, especially for individuals with weakened immune systems. Regulatory bodies have confirmed the presence of the SV40 sequence in the vaccines, but the clinical implications are still unclear.
Full Transcript
Speaker 0: Pfizer used a technique known as RiboGreen. The numbers are are orders of magnitude higher than the regulations. Right? So there is a game going on with how they're measuring this and handing this data to the regulators. They're cherry picking different assays to get the numbers that they want. In the assays that they're using are are somewhat intentionally designed to deceive the regulators. I can spend a lot of time on that topic. I have a substack that goes over the the methodology here and why these things have been gained. But, in essence, there's a lot of DNA that are present in in here. We're looking at billions to hundreds of billions of fragments of DNA that are inside every single dose with people taking many of these doses, every, you know, every 6 months. David Wiseman will probably touch on this. There is some preliminary correlation, with adverse events with the highly contaminated Pfizer vaccines. We don't see this yet with the Moderna vaccines but more data needs to be collected here. We don't have a lot of data points, to draw a really firm, correlation here. This preprint has been aggressively downloaded since it was uploaded, just a few, few weeks ago. So this is, obviously, of a lot of interest to the public. Now in the process of doing this work, we also surveyed what was the nature of the DNA present? How long are the fragments? And in fact, a lot of the fragments are small. And as doctor Philip Buchholz mentioned, that shouldn't reassure anyone of safety. Small fragments are more likely to integrate than larger ones. The more ends of DNA you have, the more likely it is to integrate. So when you chop up a piece of DNA into smaller pieces, if you don't get rid of those smaller pieces, you've actually enhanced the risk of genome integration. What we can see from using Oxford Nanopore sequencing and very small surveys, just over 800 reads, we're seeing 2,000 base pair reads, 3,000 base it reads, some of the reads, as you can see up here in the in the upper corner on this plasmid map labeled in blue, encompass the entire antibiotic resistance cassette, the the 40 region that drags that to the nucleus and a handful of other functional elements in the plasmid. So the small nature of these fragments, should not be, confused with the fact that there's a very long tail of distribution of molecules here. While the mass of them is over 200 bases, on average, there are pieces that are thousands of base pairs long and code for entire genes that are present inside the the vaccines. I would I would also note the methods that we use to isolate this DNA and put them onto sequencers undercounts the DNA. You're gonna see that this is actually evident to, quantitative PCR as well. Quantitative PCR can only measure everything above the red line, that's seen in this graph, because it it needs a 100 base pair piece of DNA in order for it to amplify and all the fragments that are smaller than that, all the all of the buckshot, if you wanna call it that, is not measured with PCR. Moderna's own patents speak to the fact that quantitative PCR is underestimating the amount of DNA that's present. And when you start using fluorometry based methods, you get much different numbers. So these are some examples of using fluorometry over here on the right and using UV Spec. These are 2 methods that are mentioned in the EMA documents. They both exaggerate the amount of, RNA that's present. And when you do DNA isolation to put these things on sequencers, you lose a lot of the small elements. So the sequencing can't to perfectly tell us how many molecules are present when they get under a 150 basis. Only thing that can really capture that is the the fluorometry readings. Okay, so who cares about DNA? Well, DNA, when it's injected, it can be prothrombotic. We've seen a lot of thrombosis issues going on in the field. So this would draw a lot of concern, to any regulator knowing that the process changed when you went when they went to the mass marketing of this, and it now has a contaminant that's prothrombotic. Now most of that DNA is probably encapsulated, in which case, it gets into the cell very directly. It may not have this thrombosis activity. But it may have an integration risk. Now I would point people to Keith Petten's work at the FDA because they're the ones that highlight this this genome integration risk. And it's not just the FDA that's saying this. I'm gonna show you some patents from Moderna that speak to the fact that they really like using RNA because DNA tends to integrate and it can be pro oncogenic, meaning it can it can it can induce cancer. Okay. So these FDA guidelines, they were derived from, from yesteryears of, trying to do vaccines that were grown in mammalian cells, it might have a little mammalian DNA floating around but that mammalian DNA is usually very low in copy number. So they have a 10 nanogram standard that has evolved over time. Back in 1984, this used to be a 1000 times lower at 10 picograms. In the United States, we had a, NCVIA Act come through, which gave the pharmaceutical industry liability protection for the vaccines. And since then, the regulations for DNA have skyrocketed to 10 nanograms, a 1000 fold higher. Alright? Now this DNA that we have present in these vaccines is very different than cell substrate DNA. It is a very high copy number and very short as opposed to very low copy number and very long like we have with, cell line contamination. And it's packaged in in a transfection vehicle like a lipid nanoparticle. So there's some papers here I encourage people to look through, which show you that there's very high spontaneous integration rates with DNA like this coming from these plasmids. And even the FDA mentions that if you have very small pieces of DNA at high copy number, the amount of nanograms may need to go down to atagram limits. So this is, an admission, by the own regulators that when the copy number of the DNA skyrockets into the billions of molecules like we have here. The integration risks increase exponentially. So, this is not the same thing as previous DNA contamination in in older vaccines. We need a new model. Now we have done some work to to demonstrate that this DNA is in fact in the lipid nanoparticles. It's a very simple assay that just, uses a nuclease like DNase to treat the vaccines. It will show you that you don't get any CT change in q PCR, that means the DNA is not accessible to nucleases that degrade it, and it's protected and in the lipid nanoparticles. That means it is transfection ready. The other thing I've touched on earlier is that we have to be aware of the endotoxin that can be present. Whenever you see plasma DNA coming through into an injectable, you have to assume if that plasmid was derived from E. Coli that there's endotoxin there as well. And most of the endotoxin data that we can see through FOIA requests or documentation that's leaked through the EMA, have those numbers redacted. Alright? So we don't really have a good feeling as to what these endotoxin levels are. There's 2 other things complicating endotoxin inside of these vaccines. If it's present, we have to be worried about the fact that the SARS CoV 2 spike protein and the same spike protein that's in the vaccines exacerbates the reaction with endotoxin. This is well studied. There's many papers on this showing that spike protein accelerates the cytokine storm that occurs with endotoxin contamination. We also know that there that there's papers published showing that lipid nanoparticles obscure your ability to properly quantitate the amount of endotoxin that's present. So we have a system here that is, somewhat blind to this type of contamination. And we have an accelerant to the contamination that is being expressed in these vaccines. Now it's well known now that these shots no longer stay in the arm. They'll they have paper showing them in heart tissue. We have paper showing them in breast milk. We have paper showing them in plasma 28 days later, and we have papers demonstrating the spike protein being expressed 6 months to years later in patients that have, either long COVID or long vax. So, the spike protein from these vaccines is not disappearing in 48 hours. It is going everywhere in the body and is maintaining expression. And that may have something to do with the fact that the DNA contamination during these shots, does not degrade as easily and may, in fact, integrate into the genome and give you prolonged expression of spike over time. Now this could be a risk for cancer. I don't think DNA alone is, is is gonna do it. But, it's not being delivered alone. It's being delivered with multiple other things that could aggravate this. Alright? So insertional mutagenesis is something that's in Moderna's patent. That is a risk. If there's DNA around, you can get insertional mutagenesis. That can increase the rates of cancer. Well, that alone may not do it. But if you have a weakened immune system that that can't clear those cells out, you more you're gonna be more prone to this, and we do know that from these vaccines. These vaccines, we know, reduce the innate immune system. There is an IGG four class which going on that makes your immune system somewhat blind, to many of these new insults. And we also have seen lymphocytopenia and neutropenia inside the Pfizer randomized controlled trial, this happened to patients for the 1st, like, few days after vaccination. They have lower white blood cell counts. On top of that, there's a few papers that have been published and controversially attacked, showing that the spike protein hits p 53 in in BRCA one. These are guardians of the genome. They're tumor suppressor genes. And if you inhibit those, on top of having a weakened immune system and more, DNA burden, cancer is certainly on the table. Perhaps other physicians will be speaking about that today. Now where do we stand from a regulatory standpoint? Well, all 3 regulators listed here have confirmed that they that the SV 40 sequence is in fact in the vaccines. Now they've also mentioned that Pfizer failed to disclose this to them. Most of them are still saying it's safe and effective, however, which is a bit unfortunate. But there is no longer a doubt that the s v forty sequence is present. That has been confirmed now by the regulators themselves. The question is, what does it mean? What is the clinical implications of this? We're gonna touch on some of the aspects of s p forty because it's not only a nuclear integration signal, but you're gonna see in a few slides forward, it it it binds to p 53, which is this tumor suppressor gene. This is just more, to to reiterate that this s v 40 sequence was given to the regulators, but the annotation of it was omitted. Now this is very bizarre. This is a real sign of of of intention

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

The presentation by Kevin McKernan is about the potential risks of DNA contamination in the mRNA COVID-19 vaccines. End https://t.co/mLzWzxpymm

Video Transcript AI Summary
In this video, the speaker discusses concerns about the Pfizer vaccine and the regulatory process. They mention that the plasmid used in the vaccine was intentionally modified, and regulators are aware of this but have not taken action. The speaker also highlights a Moderna patent that suggests quantitative PCR undercounts DNA in the vaccines. They discuss the potential risks of DNA contamination and its impact on tumor suppressor genes. The speaker raises concerns about the FDA's revolving door culture and the need to screen the blood supply and fertility clinics. They mention studies showing the presence of nucleic acids in breast milk and raise questions about transplant organ issues and cancer biopsies. The speaker offers PCR primers for testing and encourages others to try it themselves.
Full Transcript
Speaker 0: When you load a sequence like this into any commercial annotation tool to evaluate what the sequence is, it automatically decorates the plasmid with s v 40. So somebody at Pfizer had to go and intentionally delete that annotation and hand over a fabricated piece of information to the regulators, and the regulators have admitted that this has occurred, and they are still not retreating on this. Alright? That is a sign, of some capture that's going on that we'll we'll touch on momentarily. But I think this will also help like, to explain what you're seeing in documents like this and how discordant they are with what's actually occurring. These are guidelines from the FDA in the WHO and that all such open reading frames and promoters like the SB 40 promoter are in fact disclosed. And yet This is not, this is not giving them any pause after, after such a deception has been revealed. We can also see on this, Redacted paragraph on the right, this is taken from an EMA document from January, 2022 showing that they are still in discussions with Pfizer about the failure of this DNase reaction to properly remove all of the DNA. So they're very aware that this is a problem. They are demanding Pfizer fix it, yet they're not really holding their feet to the fire when the public finds it. Now just to, highlight that this is not something, that's too unexpected. This is a Moderna patent that predates the pandemic that, Stefan Bansal, the CEO of Moderna is actually inventor on. And it clearly spells out that quantitative PCR under counts the amount of DNA that's present in these vaccines. There's some other another Moderna patent. Stefan VanSylen, I believe is on this one, but other people inside his company have highlighted that mRNA technology is really the solution to the problem of using DNA scenes because the DNA prevents a alteration to the genome risk that you can get insertional mutagenesis with this. And this could get into the germ line and end up infecting daughter cells or cells in future generations. So their whole premise of wanting to use messenger RNA is to avoid the very risk that exists inside their products that we can now measure in the regulatory agencies admit is there. This is an important piece of the puzzle. This is Draymond all, they demonstrate that the very sequence that's in these vaccines is known as the SV 40, promoter, has these GC boxes that bind the tumor suppressor gene known as p 53. Alright? So we have a contaminant that not only is In a Trojan horse, like a lipid nanoparticle getting into the cell, it's going straight to the nucleus and it is binding a tumor suppressor gene. Now I don't know if that's enough to cause cancer, but I know it's enough to to pull the brakes. And that we should take a a real deep look at this, particularly given what we know is going on at the regulators. This was published in the BMJ very recently showing that 2 of the people who approved these vaccines at the FDA now work at Moderna. So we have a revolving door culture at the FDA that will see no evil and hear no evil because they are on the payroll. And, that's something that I hope your audience will take, serious consideration of. Now, what are we gonna do with these These PCR primers, none of the present. We are getting, constant requests from blood banks. People out there don't want this in their blood. The public is scared This, okay. So we we need to start screening the the the blood supply. We need to start looking at the fertility clinics. There's been a decrease in fertility since the vaccine program. Everyone's now worried. What does this do to sperm motility? What does this do to fertility rates? We've seen this in breast milk. There are The mother's nursing that don't wanna nurse now after vaccination or have if they need donor milk, they don't they wanna test it. So There's concern and there's already been multiple, papers published by Hannah et al that demonstrate that these nucleic acids are getting into the breast milk. And there's enough of it in there that with the amount that the baby has to consume and the weight of the baby, that is actually significant amount of RNA that's getting that's that's present. And it's in extracellular vessels in in the breast milk, which behaves just like an LNP. They're transfection vehicles for the nucleic acid that's in the breast milk. Right? There's transplant organ issues, and there's cancer biopsy questions. So we've kitted about 5,000 of these tests. The the sequences are public. They're online for anyone to download and use as open source. It takes about 60 minutes to run. It's about $100 per test. It can be done in under an hour. It's, it's open for anyone to try and test. If you need help making these primers, we've got some of them kitted. We have a limited supply of them, but, you can always make your own if you need to.
Saved - December 1, 2023 at 2:39 AM
reSee.it AI Summary
Title: SAVIMS: Unraveling Toxic Peptides, Amyloids, and Prions in Genetic Vaccines and SARS-CoV-2 In this comprehensive article, we delve into the intriguing world of toxic peptides, amyloids, and prions, exploring their relevance to genetic vaccines and the SARS-CoV-2 virus. Broken into concise sections, we examine the potential implications and emphasize the importance of informed consent. This thread is a valuable resource worth saving.

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

SAVIMS – Toxic Peptides, Amyloids & PRIONS: From Genetic Vaccines to SARS-CoV-2 Broken into 10 minute sections and upscaled the volume. I want to test something. @NestCommander Part 1 https://t.co/oCpGFU6X0I

Video Transcript AI Summary
The speaker discusses their background and conflict of interest before delving into their opinions on the origin of SARS-CoV-2 and the vaccines. They mention the OpenVAERS website and the underreporting of adverse events. They analyze all-cause mortality data from the CDC and ONS, noting sustained mortality rates in the UK and the presence of cardiovascular and neurodegenerative disorders. They also mention the lack of a respiratory disease signal in excess death data, with Alzheimer's disease, dementia, cardiovascular diseases, and cancer being the leading causes. The speaker suggests that something other than respiratory diseases is affecting the population.
Full Transcript
Speaker 0: And where I specialized in all SARS emerged, you can go to ResearchGate. There you'll find a bunch of metrics. Myself, all my publications, academic publications there for reading, should you so wish. And we have or I have a conflict of interest statement to make, which is that I'm the founder, CEO CSO of Synaptek Deep Learning Systems based in Japan, and it has very little, actually, to do with The work that's being presented here, this company was started way back, when I was, I would have Made the devices that would have formed part of the the digital Panopticon that they're making for you. You should be You should be glad that that deck in it well. I'm sure it is emerging, but, I I don't have the atomic debt from it. So Let us, Speaker 1: let's move on. And, I'm gonna make Speaker 0: a bunch of a priori assumptions, about SARS CoV two and the vaccines themselves. So to give some background, as the pandemic started, I was one of a number of researchers which were They formed an organization called DRASTIC. Again, it's a loose aggregation of public and anonymous researchers who have tried to address questions around the, the pandemic. I was not officially part of Fantastic. I just I was just vocal enough at the beginning that they asked me to contribute to the to a manuscript which, was one of the first in anything approximating a orthodox scientific journal who take the arguments about the laboratory origin of SARS CoV-two. There's the title of it on the screen. Of course, I wanna give credit to Rosanna Segretto, Yuri Dugan, maybe the ones that were the driving force behind, that particular piece of work. I will state for the record that SARS CoV 2, in my professional opinion, is a consequence of bioballfare medical countermeasures, research, the use of those medical countermeasures, particularly, Scenes violated informed consent laws. The construction of synthetic SARS chimeras constitutes a crime against humanity, and people Speaker 1: Could be, hold to account, the base well, I it was getting hot in here. Speaker 0: I wondered if the PC shut down because it it got overheated or something, so Speaker 1: I put the AC on. Speaker 0: Oh, it's cold now. Speaker 1: So I got my hat and, alright. Speaker 0: So let's need to progress. Speaker 1: I'll try Speaker 0: and get through these quickly. So the The position that we find ourselves in as the general public that have been on the receiving end of these biowarfare medical countermeasures industries, is that we are very much reliant on open source data and trying to interpret what that means for Speaker 1: disease itself and also the consequences to the countermeasures. In this case, Speaker 0: I'm gonna focus on the vaccines. Speaker 1: If you look at the OpenVAERS website, Speaker 0: you can there's approximately 2 a half 1000000 reports in there. There's considered to be massive underreporting with that system, so perhaps you could times that amount by 10. Again, I'm not here to sort of argue the veracity of these numbers. I We'll stay for the record that I do think I've seen severe adverse events on vaccines. I've also seen severe cases of COVID and the consequences of that. So, you can take the data from OpenVAIRs. It plots, nicely relative to other years. We have a peak in 2021 and it's thankfully dropping off. And in 2023, Uptake of vaccines is much lower. And, importantly, the the reports to VAERS have dropped off. Let's hope they go back to normal. Speaker 1: What I wanna do is to look at, at Speaker 0: All cause mortality and the data that makes Speaker 1: up all cause mortality. What what are the types of deaths that we can Speaker 0: extract from that type of data. So we're gonna look at a number of a couple of countries' data with respect that all cause mortality because there's still some ambiguities there, which I think need going over. So this This is from the CDC's website. It shows Speaker 1: the sinusoidal, deaths as they occur across seasons. So you'll get a Speaker 0: dip in the summer, increase winter and then the pandemic started, we had a sustained increase in all cause mortality that continued several years. In the US, it appears to be returning to normal. But if we look at the latest ONS data, again, when I'm using open source data and people that have put their work in and put it out there for people to use. I wanna give credits. This is, Twitter user called Outside Alan has put it this data, ONS data, into a nice visualization table. And what we what can we extract from this? Well, if we look in the year 2020, Speaker 1: laser pen, We can see the Speaker 0: so we can see the initial spikes in all cause mortality. Now there's much debate about what made those up, were they consequence of hospital protocols, etcetera. Speaker 1: Again, I'm not here to sort of argue causes in this instance because we'll take Speaker 0: a look what the actual causes of death are in a minute. But what's interesting and what I would like to draw people's attention to in this data is, as we go down in years, so as we go down in rows, We get to 2022, and we're seeing sustained all cause mortality. This is in the case of the UK and particularly in the young. And there's only so many ways that you can take out young people, And, primarily, that would have Speaker 1: to be some cardiovascular, Speaker 0: major event or something like and so the neurodegenerative side of the equation will end towards the older end of the spectrum still, but, something is still going on. Now I'm gonna jump back to US data and try to make meaning of what we see with respect to excess deaths. Speaker 1: Now SARS was touted as an acute respiratory distress disease. And, you would expect or the prediction would be But in Speaker 0: terms of excess deaths, you should see respiratory pneumonia type disorders leading the pack. So if we go to, Hang on a minute. I've got a different presentation, so I might be missing some slides. Doesn't matter. I will just push on. So, in terms of all cause mortality, the, What we saw over the course of the pandemic was you expect a, stable baseline with respect to the ways that people die. And in this, plot, what we can see at the top is respiratory diseases. And this is above the expected baseline that you would expect for those types of conditions. So the yellow bars are an indication of the proportion of total excess deaths, and in this case, influenza, pneumonia, chronic lower respiratory disease and other diseases of the respiratory system, out for this very small fraction of, the all cause deaths. The majority of them land in the Alzheimer disease and dementia category. Here you can see one of the leading, causes of death It was a year over a year ago now, April 2022. Last time I checked this data was 26th August 2023. The patent is holding, and the other areas where we see excess death are cardiovascular, Speaker 1: vents and, also, malignant neoplasms. What that means is cancer in this case. And so, we don't seem Speaker 0: to have a signal in the all cause data that would point at a, respiratory disease, taking its toll on the population. So something else is going on. So the next slide, I tried to introduce this slowly, and

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

SAVIMS – Toxic Peptides, Amyloids & PRIONS: From Genetic Vaccines to SARS-CoV-2 Part 3 https://t.co/vIBxwcuNId

Video Transcript AI Summary
In this video, the speaker discusses some findings from their investigations into COVID-19 vaccines. They mention a sample that showed no phosphorus, which could be experimental error. They also found small specks of copper in some vaccines, but the reason for this is unknown. The speaker then talks about their own experiment where they added the Pfizer vaccine to blood and observed discoloration and clumping of red blood cells. They suggest that this could be due to the cationic lipid in the vaccine coming into contact with cell membranes. They emphasize the importance of informed consent and the need for more research on these vaccine effects.
Full Transcript
Speaker 0: Findings that we did see in, in our investigations. And so this is just the, the SEM edX, and this is what leapt out with respect to, oddities and what we would would predict. And in the left hand corner, one of the samples that we had, it failed to show any phosphorus in its, EDX mapping. And this was a one off. I was unable to repeat it. There's been one other person who's reported a lack of phosphorus, that's doctor Daniel Nagase in Canada. I again, I'm showing this just because we saw a similar effect. Again, could be experimental error. An n of 1 doesn't mean much, but you look at another batch, Pfizer and we see the expected, phosphorus, peaks. And another finding that we came across was the this was in Janssen, so the adenoviral vector based vaccines. And what you can see, these little light gray inclusions. They're colored, green on, the elemental map. And these were, small specks of copper. Now, why is copper in there? I don't know. It could be contamination on the industrial process, has it been added, deliberately? Again, I don't know, but this is, this was about the most that we found with respect to just Hemicort analysis of the vaccine vials, and I'm pretty confident that we can remove any any of the claims. We can rebut any of the claims that those crystals that people are looking at are graphene self assembling under five gs. That's, nonsense distraction environment designed to pull you in down rabbit holes, like, essentially, no virus type claims. So one of the other things that we did once we got hold of vaccines was actually do challenged with blood. We actually did get it into a manuscript, but, simply, nondescript. No one wanted to touch this data. And but what did we see? It's an observation. I think it's important that it's put out there, particularly as we're seeing the example that we looked at earlier, which was the, the clot being extracted from an individual's arm and the loss of the arm and also, the cardiovascular events are leading the all cause mortality, aggregation of, data, the pool of where, excuse me, where people are dying. And so, in November of 2021, I added, I did a blood draw of myself. This was I wouldn't have done it except for people asking me to do it in the live stream chat. So live on camera, I had the equipment available, took a IV blood draw and dropped a drop of my blood onto a microscope slide and then a drop of Pfizer vaccine. And this will, resolve into focus. And what became apparent quickly was that there seemed to be a pumping around the edges of where the vaccine was contacting but also the erythrocytes themselves began to discolor. This was a phenomenon that we saw primarily with Pfizer. We're gonna look, a little bit, work that was done by doctor Richard Fleming. So I was the 1st to, sort of, show this effect in real time. He managed to get more subjects, more vaccine samples and, again, in real time, show what happens when you add vaccine directly to blood. And I wanna just give a little caveat here, which is that the the effect that we observed, I think it was possible because we didn't or I didn't smear out the blood as is usually done when you do, wet mount slide. A drop on there and the blood was relatively thick, so the discoloration was visible under light microscopy conditions. And this is, Richard attempting to do this. Again, it was in real time. Thank you to Mike Adams for the use of, his laboratory equipment to test this. And here you can see blood being exposed to Pfizer, and I'll let Richard do the talking. Minutes. Speaker 1: Try the side light. No more asphalt light getting pumped into it. Okay. That's perfect. We might get better with contract. Speaker 2: See, and you can actually see now. You can see a strip of red blood cell cells still holding some of their Speaker 1: oxygen and then other strips of red blood cells that are just they've lost Speaker 2: And that's a good picture of what the Pfizer vaccine is just being placed into contact with red blood cells. So you actually see a demarcation there between where the where the vaccine is even though, a bubble from the vaccine going in and then the blood to the edge of that. Mhmm. And then 150, that last north of 100, this is 150. Speaker 0: Hey. Can you Speaker 2: span 200, and then we will go to a higher magnification. This is now 200 again. Yeah. Sadly, it loses it just keeps losing its saturation back to the original, Which is interesting. Okay. Even with the little that we got, You the 3rd? Uh-huh. Speaker 1: Let me get a quote on this. Speaker 2: Okay. We're good at 50. The little area that we were able to get. Is that what we're looking at, doctor? Those are all clots that form. Well, I mean, they're certainly clumping together and they shouldn't be clumping together quite that nicely. What is Obvious is there's more paleness to what I'm seeing. Again, this was not even quite a drop of Pfizer because I thought it was left in that particular vial. Speaker 0: So I'm gonna stop it there. The all videos available on Doctor Fleming's Rumble channel. You can go watch it there. And it I'll try to address some of the questions that were asked me in the presentation that I gave earlier to the South African group. And the gist of those questions, where what's what are we looking at there, what's happening, and is this the same as blood being exposed to spike protein? And I would put forward the argument that what we're seeing here, because it was so rapid that it's a it it can't be down to protein expression and, like product being produced. Erythrocytes don't contain, the apparatus necessary to translate, RNA into protein structures. And so what I think we were looking at is a result of the cationic lipid and it coming into contact the cell membrane. The next question was, well, is this a sort of self amplifying phenomenon? And my response was, well, we didn't see that under the microscope. Though, yes, it caused problems with blood it came into contact to, but it didn't spread across the slide where there Quasiant vaccine. And so, you know, is there there would be a dilution effect once you inject it into the body. But, potentially potentially, the someone who may be prone to clotting when that type of reaction happens with their blood maybe an adverse event that happened in this instance. Again, this was just a phenomenon we were able to observe right at the beginning of the rollout of these vaccines indicating that there was chemistry at play that they hadn't they hadn't informed the public about, and this is about informed consent. And no one

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

SAVIMS – Toxic Peptides, Amyloids & PRIONS: From Genetic Vaccines to SARS-CoV-2 Part 4 #Informedconsent https://t.co/d0QbTY2iaU

Video Transcript AI Summary
This video discusses concerns about informed consent and the presence of SV40 promoters in Pfizer vaccines. The speaker mentions Kevin McKernan's findings of plasmid DNA in the vials. Legal proceedings in Australia are mentioned, questioning the classification of these vaccine products. The speaker also talks about amyloidogenic sequences associated with viruses and their presence in SARS-CoV-2. They discuss a study on amyloidogenesis of the spike protein and how it could trigger amyloidogenic aggregation. The speaker highlights the increased attractiveness of the spike protein to neutrophil elastase due to added amino acids. They mention an analysis that shows similarities in amyloidogenic properties between the natural virus spike protein and the one translated in vaccine recipients. The video concludes with a mention of the cleavage of the spike protein and its potential implications.
Full Transcript
Speaker 0: This is about informed consent, and no one no one has refuted, this observation. I would be happy if they did. And these are just stills on that manuscript, if you wanna go look at it, showing discoloration, responses to different vaccines under different magnifications. And Next, we're gonna come to well, so what I was saying in the seminar earlier was, as bad as this looks With respect to immediate reactivity of the, constituents of those vials, Recently, there have been other findings which make the contents of those files even more suspect, and, of course, we should give a shout out to Kevin McKernan, Plasmidgate, and his finding of, plasmid DNA in the vials, I'm gonna focus on Pfizer as, it constrains the discussion. And What he was able to show was that there was a SV 40, 72 base pair, SV 40 promoter In the, in the genetic material, if it was sampled using next generation sequencing, as Kevin did in his laboratory. Speaker 1: So one of the or a Speaker 0: bunch of Criticism was thrown Kevin's way, which was you used vials that had been opened, there wasn't any cold chain of custody, they were out of date, etcetera, etcetera. So recently, Speaker 1: in this Speaker 0: issue of his newsletter. I was able to get Kevin cold chained in day And sealed samples of Pfizer, and he was again able to show that these SV 40 promoters were in there. Speaker 1: And there's I mean, I don't wanna spend too Speaker 0: much time about What this means for people who have been exposed, etcetera, just to say that this wasn't declared to health authorities, etcetera, Right now, there's legal proceedings going on down, in Australia, Julian Gillespie, and, basically, Speaker 1: The arguments there are such that these vaccine, Speaker 0: quote, unquote, vaccine products It should Speaker 1: have been considered, interventions that should have been classed under PMO type Speaker 0: PMO and gene engineering technologies that require a whole different regulatory apparatus than is required with normal, small molecule type drugs which, make up the bulk of pharmaceuticals. Speaker 1: Now One of the issues that I talk about Speaker 0: a lot, have been doing for many years now, around SARS, is that there are amyloidogenic sequences associated with viruses And there are amyloidogenic sequences in SARS CoV-two. I asked Kevin, On the open reading frame Speaker 1: for the vaccines oh, there Speaker 0: is another slide. So this just shows the, quantitative PCR for the Japanese samples versus a sample that he Speaker 1: had or, Speaker 0: A batch that's been associated with a large number of adverse events, and there's a difference of, a couple of cycle counts with respect to the identification of that, SV40 sequence. Now, getting back to the Amyloid sequences. So I asked Kevin there's, a number of amyloidogenic sequences, by this time, we know particularly suspect. I'm gonna get into that. And I asked him if that sequence was present in the plasmid, So would it be in the RNA products, etcetera? He was able to identify that, that's down here In the bottom left hand quadrant of the, of the plasmid. Speaker 1: That's, that's it blown up a little. And so, Speaker 0: we're gonna change the pack somewhat and start talking about amyloidogenesis prions, what they are, etcetera. And so, relatively early in the Scientific literature. The orthodox scientific literature, Nystrom and Hammerstrom published a paper, I'm alloidogenesis of SARS CoV-two spike protein. And what they what, essentially, what this study shows is that there are a whole bunch of, short epitopes that can trigger or were predicted to trigger amyloidogenic, Speaker 1: aggregation. And The well, what I discussed earlier was that they Speaker 0: put a preprint Up on to, bioRxiv, and in that preprint, they go to great lengths to say that the expression products of the vaccines would match those of the viruses and thus you would be exposing people to these amyloidogenic peptides were you to go and gene transfect them en masse in, in large populations. And so the next slide is just, Speaker 1: one of the mechanisms that they looked at is, How Speaker 0: would these epitopes become exposed and increase the chances of seeding and causing amyloidogenic cascades? And, they, again, they focused on neutrophil elastase, looking at the, Representations of the amino acid sequence and the confirmation shape that it changes, they identified Where these, where these sequences were, I encourage everyone to get very familiar with this paper. Speaker 1: And, Also, I mentioned Speaker 0: at the beginning that I'm very much of the opinion that because ours is a consequence of fire warfare, medical countermeasures, research. So we should be very, very sensitive to What appears to be changes that wouldn't make sense were it to have just sprung out from a bat cave naturally. And what Nystrom and Hammerstrom showed in that paper was Speaker 1: where the, The Speaker 0: cleavage sites are on the on the spike protein with respect to neutrophil elastase. The length of it is actually increased, so it's more attractive to neutrophil elastase so it gets chewed up. And in this instance, I would, again, under the current circumstances in which we're operating, that would be considered particularly if amyloidogenic peptides have been weaponized as a something that's highly suspicious and Could be Speaker 1: looked at in more detail to see this, what is essentially, Speaker 0: about Eleven extra amino acids that have been added Speaker 1: to SARS CoV-two peptide that makes the attraction to neutrophil elastase more, more attractive in terms of proteolysis. So, by for streaming. I'm, a bit paranoid about, Speaker 0: tech glitches at the moment. Speaker 1: So We had Speaker 0: the we had the vaccines released, and one of the Speaker 1: earliest Analyses that were done, came out of Harvard, Speaker 0: Yong et al, And they did next generation sequencing and published the sequences of the RNA Speaker 1: products that were meant to be translated in individuals. And Speaker 0: you Can take this data, and you can run the same analysis like Nystrom and Hammersdram did. They used the WALTZ algorithm. And you can see that there is a, close match in terms of amyloidogenic Properties, whether it's the natural virus spike protein Speaker 1: or the one that would be translated Speaker 0: and expressed And people who were recipients of the vaccines, I want to highlight the bounding box here. We're gonna take a look at that in a minute. Also, I made mention I probably should have made this slide larger with respect to, there was some Well, I don't wanna say misunderstanding, but that there was questions about, well, the spike protein is Stabilized by proline locks. Well, okay, that's all well and good, but The spike protein does get cleaved up and chopped up in intracellular

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

SAVIMS – Toxic Peptides, Amyloids & PRIONS: From Genetic Vaccines to SARS-CoV-2 Part 5 https://t.co/QIFH3McXgX

Video Transcript AI Summary
The video discusses the potential adverse effects of the spike protein in SARS-CoV-2 on human prion protein and amyloid fibril formation. The speaker highlights a study showing that spike amyloid fibrils can accelerate the formation of amyloid fibrils associated with prion diseases and Alzheimer's. They also mention recent research suggesting that other viruses, like H5N1 influenza, may impact and misfold prion protein. The speaker emphasizes the importance of understanding these interactions and their potential implications. They briefly mention the symptoms and diagnostic challenges of prion diseases like Creutzfeldt-Jakob disease. Overall, the video explores the role of the spike protein in amyloidosis and its potential impact on neurological tissues.
Full Transcript
Speaker 0: And on membrane surfaces. And the spike epitope that we're interested in, in Speaker 1: this instance, sits on the s one segment, which isn't locked by that proline and essentially is released. This study in trends in molecular medicine, bike bike protein hypotheses for adverse events, something along those lines, was the title of the paper, St.el 2022. And they come up with this nice diagram of Speaker 0: how, Reactive peptides could be being released, in, in within the body, such that they could be causing problems, a whole suite Speaker 1: of problems that we've come to know, things like myocarditis and also, the impact on neural tissue, which I'm interested in. And Speaker 0: What I want to do is highlight this work, again from Hamnerstrom and Nystrom, Speaker 1: SARS CoV-two spike amyloid fibrils specifically and selectively accelerate amyloid fibril formation of human prion protein and the amyloid beta peptide. Now amyloidosis is a phenomenon that's Speaker 0: been understood for quite some time, but there are degrees of, toxicity with respect to the type of amyloid and prion Speaker 1: that you're dealing with. And I'm just going to read a little bit from their abstract. We here provide evidence of significant spike amyloid fibril aided acceleration of amyloid formation of CJD associated human prion protein using an in vitro conversion assay. By seeding the human prion protein conversion assay with other in vitro generated disease associated amyloid fibrils, we demonstrate that this is not a general effect, but a specific feature of spike amyloid fibrils. We also showed that the amyloid fibril formation of Alzheimer dementia associated amyloid beta 142, was expecelerated by spike amyloid fibril seeds. 7 different 20 amino acid long peptides, Spike 532 to 551, was most efficient in seeding human PRP protein. Like 601 to 620, was most efficient at seeding amyloid beta Speaker 0: 1 to 42. And I reiterated in the presentation that I did yesterday and why it's able to jump. Something's going on. Speaker 1: I've got new keyboard setup and new mixer, so, Speaker 0: I don't Speaker 1: know why they just Speaker 0: but what I what I was saying was in my domain, in neuroscience. It's been established that there is no safe dose of grapey form of the prion protein, Speaker 1: which is what they're talking about here in the conversion of the prion protein into its amyloidogenic form. And so in this instance, Speaker 0: we're in a new new world. Now are there other viruses which would Speaker 1: could influence the expression Creon protein. And this is very, very recent work. There's not much on PubMed with respect to it, but it appears that, H5N1 influenza, another neurotropic virus, in cell culture is able to impact and misfold prion protein. And, which epitope is doing that? How much does it differ from what we see in SARS CoV-two, etcetera? We don't know. The work hasn't been published. And so In the public domain, we're still very much feeling our way through this data, but it should be a The alarm bells should start sounding Speaker 0: for you when mention of interaction with human prion protein being converted into the scrapy form, not by other prion proteins itself, but in this case, more epitope segments acting as catalytic seeds, within the cellular environment. So Speaker 1: just to look at that data from Amherstom and Nystrom, here you can see what they're looking at is the Time to form these misfolded prion like peptides. And you can see that the lag is the least, so it happens fastest with that human prion protein selective segment. That segment I've shown, on multiple occasions. You can take it. You can search for it in BLAST. There's no other overlap with any other viral sequences except SARS CoV-two unique to SARS. I would say that would make SARS CoV-two a unique virus, particularly when dealing with phenomenon like prion protein and, scrapey, transmissible spongiform encephalopathies. Move on. I've played this movie, in numerous times. You can go find it on the Internet. Just look for, Speaker 0: transmissible spongy encephalopathies, Speaker 1: Peru. And you can find, archive footage of someone who shows all the symptoms of well, actually, I Speaker 0: better play it we're gonna look at a monkey, version. But there are a Speaker 1: few things to look at. So one of the things that you see is, postural abnormalities, hystonic posturing, twitching, kicks. And, in this instance, Kuru has the, well, the They call it laughing disease because the people who develop it develop uncontrollable laughter, but the person you're looking at on the screen here doesn't have long to live as the prion cascades are taking over and destroying central nervous system. So Speaker 0: Again, I'm not gonna, all the way through. I'm conscious of mine, but you Speaker 1: can see the tics, the abnormal movements, etc. And this is indicative of Freon CJD guru like disorders. Speaker 0: So let's move to the next slide. So what Speaker 1: are prion proteins? So canonically, preon protein has been the, the protein that has received the most tension because of the dramatic effects that it can have on individuals Speaker 0: who are exposed. So what's happening to the prion protein? Well, basically, it's what's called confirmation change. The normal prion protein, which is involved in cell trafficking, signal propagation, synapse stability, but it's also Speaker 1: a peptide that's found throughout the body and essentially has a number of alpha helices that form up the core of the peptide. And when it's catalyzed into the scrapy form, it develops a, basically, a A series of beta pleated sheets. And you can think of these as, planar forms of amino acids, which in this instance are hydrophobic, meaning they don't like aqueous environments. So what happens is is those de depleted sheets begin to oligomerize and extend out like you are adding Lego bricks together. And this is what they think is the, Speaker 0: toxic substrate to these transmissible spongiform encephalopathies. So This process Speaker 1: can be, I'll explain that in a minute, but just to show, you can go I just grabbed this off Wikipedia just to show you that there are a number of, monoclonal signatures that we would look with with MRI, just to help orientate people. Primarily, they show up, in these instances. You can see the, when I say hyperintensity, bright areas here, These are the basal ganglia, and this could account for why you're seeing a lot of the movement disorders that we were seeing in the individual who was suffering from kuru, Speaker 0: an interesting feature with Brion disease, Creutzfeldt Jakob disease. So it's a diagnosis that can only be made postmortem. Right? So you can present with a Speaker 1: bunch of symptoms of rapid onset of dementia, the movement disorders, And they can do some diagnostic tests, which would say, oh, we think this person might have CJD, but they cannot make the definitive diagnosis until after death. Brain is taken out, and then they look for the microscopic, or in this case, can be macroscopic changes to the brain tissue. And, what does it mean when they're talking about spongiform encephalopathies, where you get a spongy appearance to the brain? There's lots of little holes where the tissue has died back, but you also get these amyloid black build ups as well. And these are these, filamentary like structures you can see on the screen as well. So there's multiple

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

SAVIMS – Toxic Peptides, Amyloids & PRIONS: From Genetic Vaccines to SARS-CoV-2 Part 6 https://t.co/cyrFQHPmc2

Video Transcript AI Summary
Protein misfolding is a recent phenomenon in the study of neurodegenerative disorders like Parkinson's and Alzheimer's. Other peptides besides the prion protein can also misfold and form toxic fibrils. Prions have been studied as potential biological warfare agents due to their robustness and toxicity. The transmission of prions is difficult, but recent research suggests that small epitopes on viruses and bacteria may also have amyloidogenic properties. Neuroinvasion and anosmia are independent phenomena caused by SARS-CoV-2 infection, indicating ongoing pathology at a fundamental level. The spike protein of SARS-CoV-2 has been found to cause amyloidogenic clots in the blood, potentially contributing to long-haul symptoms. There are also concerns about the homology between SARS-CoV-2 and HIV, as HIV epitopes have amyloidogenic properties and have been the focus of bioweapon research.
Full Transcript
Speaker 0: Protein misfolding, phenomena occurring in this particular condition. So a fairly recent phenomenon in my domain was that In order to try to understand nonical neurodegenerative disorders, age related: Parkinson's, dementia, Alzheimer's, Lewy body dementia, amyotrophic lateral sclerosis, etcetera, multisystem atrophy. The list goes on and on. It was, the the data converged on the fact that there were other peptides other than the prion protein which were essentially doing the same phenomenon. They were misfolding and then beginning to aligmarize and form out these, toxic fibrils, amyloidogenic fibrils. And, I'll I'll skip through this just dramatic of how you get but Technically, we talk about a propagon. A propagon could be the misfolded protein itself, or it could be the catalyzing epitope and peptide. Here we have just a list, if you want to screenshot this, of, some of the different types of peptides that are under investigation with respect to amyloidogenic and prion like disorders. We're gonna take a look alpha synuclein, as that is a, candidate misfolding peptide in exposure to SARS CoV-two spike protein. Speaker 1: Let's move on. And one of the Speaker 0: things that I would like to highlight is Speaker 1: the prions, and their because of their Robustness Speaker 0: in the environment Speaker 1: and their toxicity have been a Various area of research in the bi warfare domain. It's not very public. Speaker 0: Here's a little inkling that, they have been studying it. This is, a little article in Defense IQ and Military Journal by 1 James Giordano, and again alluding to Speaker 1: the fact that prions could be a very interesting biological warfare agent. Now the issue that they had is that the peptide itself is you can only, Speaker 0: you can aerosolize it and you can infect people that way. But in order to transmit it, Generally, the route of exposure is important. So like the, Kura example, you'd have to be eating issue, etcetera. If you're handling, tissue with a high infective load of prions, it can transfer through skin, etcetera. But it's hard It's not a self amplifying and Speaker 1: spreading, disease as we as we would understand it. Speaker 0: But this is this is changing now as we come to understand that these small epitopes on contagions, on viruses, And I would the simple fact is is that we don't we don't we haven't catalogued everything, and toxic epitopes probably live across the bacterial and viral Speaker 1: and, excuse me, and yeast domains, And anyone whose physiological condition is not in the best of states, you allow those, pathogens to take a Speaker 0: hold, is gonna increase their chance of being exposed to these amyloidogenic preenergic type peptides. Speaker 1: So One of the things I Speaker 0: tried to reiterate yesterday because that's a group that is highly focused on the impact from vaccines. I would say all the time that we have a risk from Freon catalyzing epitopes in this transmissible agent, we should be paying attention to the data and the all cause mortality data, where we're seeing big spikes Speaker 1: in neurodegenerative processes. And Speaker 0: This paper came out recently. Neuroinvasion and anosmia are independent phenomena on infection with SARS CoV-two, importantly, and its variants. I'm just gonna read 1 sentence from this. Conversely, all SARS CoV two variants are neuroinvasive regardless of the clinical presentation they induce. This is the phenomenon where people become infected And they then develop what's called the long hauler state. And so that tells you that there's some ongoing pathology that's separate to exposure to the initial pathogen itself. And I would argue that it's happening at this deeper, more fundamental level where the protein peptide interactions are occurring rather Speaker 1: than the response to an infectious particle, called bacterium. Speaker 0: Some of the earliest work which identified that there was Speaker 1: a amyloidogenic response Speaker 0: occurring to the spike protein came from South Africa, Risia Pretorius. Speaker 1: They showed that Speaker 0: Plasma exposed to BiC protein, the S1 subunit, in this instance, caused fibrinogen resistant amyloidogenic clots to build up, in the blood, and they have proposed that this might be one of the causal mechanisms for the long haul, post viral me CFS like state. And again, this was great work and, again, came out early on, say, Anyone? Yes. And, reported the contention that I was making that, these agents have this propensity, and when if we're dealing with something that comes out of a laboratory, we probably should be paying attention to how it shakes out epidemiologically. Speaker 1: So as well as the Brion Speaker 0: catalyzing epitopes that I've spoken about here. There are other epitopes that are of concern. This came up much earlier in the research around SARS CoV two, and that's the homology with, HIV. And, here you can just see Three d representation of the spike protein, the yellow balls or bubbles on this, injection, are areas that have overlap with HIV, and they come from different clades of HIV, which would indicate that they would appear to be synthetic. They also cover the what Speaker 1: Everyone knows now, excuse me, as the, I should probably just turn off this code. Speaker 0: The furin cleavage site, the furin chemistry around the furin cleavage site is even worse though than what was initially described with respect to properties of furin, its, cleaving of the peptide, and that sequence, essentially what's called a nuclear localization signal, It means it Speaker 1: can Speaker 0: What the technical term is of getting into the nucleus in this instance, but migrate across the nuclear membrane into where the chromosomes, and your genetic information is stored. And I don't want to get into that particular, pathology or mechanism Speaker 1: in this instance. But one of Speaker 0: the things I wanna Draw your attention to is, again, the early identification of HIV like epitopes came from Pradman et al. It went up on preprint servers in February, I think, January Speaker 1: 2020, 130, nearly. And the Speaker 0: This paper was shut down rapidly by scientific authorities. They did not want people knowing about these homologies with HIV. And Why? Because these HIV epitopes have been the focus again of bioweaponics research, and they have amyloidogenic properties as well, which we'll briefly go over. So, this was also confirmed by Luc Montagnier.

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

SAVIMS – Toxic Peptides, Amyloids & PRIONS: From Genetic Vaccines to SARS-CoV-2 Part 7 https://t.co/WHS3imCVx9

Video Transcript AI Summary
The speaker discusses the inflammatory and amyloidogenic effects of small sequences called epitopes, which can cause memory dysfunction in mice. They also mention a study that found the introduction of gene transfection technologies containing the spike protein can induce amyloidogenic cascades. The speaker highlights a 200% increase in the diagnosis of CJD in France after the rollout of vaccination programs, suggesting a potential link. They discuss the loss of cognitive function associated with exposure to the spike protein and propose that amyloidogenic disease processes may underlie long-haul COVID-19 symptoms. The speaker mentions the role of viral infections in facilitating intercellular aggregate dissemination and shares examples of misfolding prion amyloidogenic diseases.
Full Transcript
Speaker 0: Luke Montagnier is not with us anymore, but we miss his input into this discussion. Here, I'm just showing, literature that shows that these epitopes, again, small, short sequences, are inflammatory an amyloidogenic, in this instance, causing memory dysfunction in mice. So does this really matter with respect to the vaccines and the gene transfection technologies? Well, what we have here. Are they causing amyloidogenic cascades when you inject them into individuals? And so, again, very early on, after the vaccine rollout, we got this case reported. Now this study wasn't intending to look at the response to vaccination in this instance. What they were doing. This person was scheduled to go into hospital for a PET image, look for amyloidogenic load in the brain and heart because of a suspected, case of Alzheimer's. What they found was that when they did the scan, they could see where the injection site was with the ligand that they used to bind to amyloidogenic peptides in the body to say whether the load is higher than would be expected, in a in a healthy individual. This shows that the introduction of gene transfection technologies that contain the spike protein induced amyloidogenic cascade. It was, Luke finding in this instance, but it's there as a demonstration that these reactions are occurring, and we should probably should be paying more attention to this, particularly in terms of the, the all cause mortality data. So what do we have coming up next. Again work from Luc Montagnier. And what they were able to show was in the year of rollout, there was a 200% increase in the diagnosis of CJD in France, and, disturbingly, there was about, on average, 12 days, 11 11 days between the person receiving the transfection shots and the emergence of symptoms. Now France is because of its proximity to the UK, UK had the BSE mad cow outbreak in the eighties nineties. They have very sophisticated and, highly attuned laboratory setups and surveillance look for CJD like disorders, and it had been ticking along approximately 1 per year for 20 years. And then SARS comes along and then the vaccination programs come along and we get this, peak in diagnosis of CJD. Is it still ongoing? I haven't seen data to confirm that. But, again, it's a signal that we should be paying attention to, because we don't know what the consequences are of seeding the environment with these types of toxic peptides like they have done. And from if I was to make an assessment, what you would see would be neurodegenerative processes. And, and this is a study that I looked at the other day which was, loss of cognitive, processing. And it the numbers thrown out by that study was that, essentially, those who have come into contact with the spike protein in terms of, in this case, it was infection, lose approximately 10 plus years of cognitive function after exposure. So one of the things that I've been concerned about is that these types of disease processes, these amyloidogenic disease processes, what underlies the emergence of these long haul estates. I'm not the only person thinking this. These are just some examples of, publications that have been put out there. We're proposing the same thing, and, it's it's a theory that was sort of floating around the edges of neuroscience and the MECFS community prior to SARS, but it didn't get much attention, one because it's difficult to study in laboratory animals. So, you don't, you don't have a good model. It's difficult to test the premises, and you just have the clinical picture, and the problem we have is that, for many years, doctors and clinicians and scientists would ignore this postviral state. And, again, I would, I've always been of the opinion that they could be, a consequence of this these misfolding cascades occurring in the organism. What's the nature of those cascades? Another question I've done many lectures about how they may be, part of the innate immune system that are there to wrap, things like epitopes, short sequences of toxic peptides and make sure that they're not, traveling around and causing problems in the intracellular and extracellular environment. So, I want to just read a little bit from this abstract. A note from this paper. It's an important paper, which is highly efficient intercellular spreading of protein misfolding mediated by viral ligand receptor interactions. And this in in this study, they're basically using in vitro testing, which is cell cultures. And they show that propagating prions or pathogenic tau aggregates demonstrate that, in this instance, they're using a couple of viruses, a vesticular thymatitis virus, glycoprotein and SARS CoV-two, Bi protein, increase aggregate induction by cell contact or ligand decorated extracellular vesicles or exosomes, as receptor ligand interactions are important determinants of intercellular aggregate dissemination. Our data raised the possibility that viral infections contribute to proteopathic seed spreading by facilitating intercellular cargo transfer. What does that mean. When the cell begins the misfolding cascade, as the cell tries to restore homeostasis in this instance, it will try to what will happen is is that those misfolded proteins will be packaged up into these exosomes. They will be secreted. They will then travel 2 neighboring and distant cells and tissues. And once they're taken into those cells, they will then initiate the misfolding cascade again. So it's, you can think of it as a sort of infective process but, again, at a lower lower functional level than what normal people or what we would normally associate with viral particles, bacteria. So I want to take a look at an example from, the real lab, example of these misfolding prion amyloidogenic diseases. This, this happened in my laboratory, and we had, as far as we know, the world's only recorded early onset Parkinsonian like condition, and I mentioned alpha synuclein as being one of those peptides which is, under suspicion right now, particularly with SARS, but also, other viral epitopes and assaults that come from the environment. So, this here is Human Proteome Atlas, and it just shows the distribution of alpha synuclein, and it's particularly present in brain, but also bone marrow and lymphoid tissue. This was a study recently which shows that the SARS CoV-two spike protein fragment eases amyloidogenesis of alpha synuclein. Again, I'm not going to go into the details. It's just to let you know that, it is on the radar in the scientific literature. And one of the earlier studies which came out in 2020 was this one which showed that McCaques, who had been exposed to SARS CoV, who developed alpha synuclein aggregates after they'd been infected. Again, what what are we looking at here. Perhaps this middle row is most important, but they see activated microglia. This is the immune cells, basically, of the central nervous system but also, the appearance of Lewy bodies. Lewy bodies are a form of protein aggregate that we can think of, you can transpose cross amyloid

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

SAVIMS – Toxic Peptides, Amyloids & PRIONS: From Genetic Vaccines to SARS-CoV-2 Part 8 https://t.co/k7HBB5MFYo

Video Transcript AI Summary
In this video, the speaker discusses a monkey with Kuru, a condition that causes tremors and stoop posture. The monkey also exhibits trichotillomania, a behavior similar to OCD. The speaker compares the monkey's Parkinsonian symptoms to those induced by neurotoxins in model systems. They mention the Universal Parkinson's Disease Rating Scale and PET imaging with a ligand for alpha-synuclein. The speaker explains how Parkinsonian disorders are diagnosed and mentions multisystem atrophy. They discuss the dopaminergic system in the monkey's brain and the presence of iron deposits in the basal ganglia. The speaker briefly mentions a treatment for amyloidogenic buildups in the blood and concludes the presentation.
Full Transcript
Speaker 0: Arms, etcetera. They're, they're toxic byproducts. So moving on, here's a video of that monkey. I'd like you to think about what you saw with the individual who had Kuru. You can see she's got stoop posture, she's tremulous. You can see that her fur isn't good isn't in good condition because basically she's plucked it out. That's a condition called tricotillomania and it's a surrogate marker in animals, for potentially OCD like, behaviors. And she was, a unique animal. Again, because she had Parkinsonian like symptoms, we were looking at it through the Parkinsonian lens. We gave her a rating, there's something called the Universal Parkinson's Disease Rating Scale. There's a primate equivalent and basically she classed as slight to moderate, Parkinsonian conditions, compared to the model systems we would use where we would use neurotoxins that would knock out dopamine to induced Parkinsonism. Speaker 1: So by that, this is just, Speaker 0: the measure of the EMG activity, there's a lot of data here that I skipped through in the presentation as well just to show that we did we did it and we have it. Here we can see, PET imaging again, this time with a ligand 4 alpha synuclein. What you can see is in the brainstem there's a far stronger signal from what we see in a age matched control. And, the way that, clinically, you make a classification of these disorders when you turn up your doctor, and you've got these Parkinsonian like symptoms, is you will get challenged with something called L Dopa. You'll go away for a couple of weeks, and then you'll come back and tell the doctor if the L DOPA made a difference. If you're lucky, the L DOPA did, and you'll get a diagnosis of Parkinson's. If it was not, and you were L DOPA unresponsive with Parkinsonian symptoms, it's more than likely that you have an aggressive form of, multisystem Parkinsonism called multisystem, atrophy. And, should you be diagnosed with such condition? Basically, you have about 5 years Speaker 1: left to live. Does Speaker 0: she seem to fit the profile of having multi system atrophy, the dopaminergic system seemed relatively intact. On the top row, A and B, you can see a normal monkey undergoing, measurement of dopamine levels in the, in the basal ganglia. And you can see the bright colors indicate that there's generally normal dopamine there. After, lesioning with MPTP, we can see a large reduction, and you can see in our target animal, she generally had, what would seem to be an intact dopaminergic system relative to the Parkinsonian models we would use, we had a poly single nucleotide polymorphism, one base pair insertion in a specific gene that I'm not going to get into right now, which those overlap with individuals that have multisystem atrophies. K. This is just to show that we've done those studies. And, but what I want to get to is how does the pathology manifest in the brain, compared to the, at the model systems where we've used chemical lesioning, and what I would like to do so I can use this slide. And so again, looking at these deep brain structures, in MRI, you can see that they look very dark. And you can compare that to, sections equivalent anatomical sections on the right from a monkey that we've made Parkinsonian using neurotoxin, you can see that the colors of the brain are essentially homogeneous through the MRI imaging. So what is this dark, aggregation in the in this animal's brain, well, what it was was, iron, basically. These cells had been undergoing ferroptosis and we're just depositing large amounts of iron in the basal ganglia. And so I Speaker 1: think, I Speaker 0: was done with a bunch of electrophies. I'm just gonna Hit Buy, there is some good news, Speaker 1: and I wanna, I'll shout Speaker 0: out to Beata Jaeger, who's been doing a heparin form of extracorporeal, apheresis, where they're essentially cleaning the blood of these amyloidogenic buildups. And, I'm not gonna show too much from the paper. It's, it's still up for review, etc. But you can see, in this instance, long COVID, so someone who's been exposed to the virus develops this amyloidogenic, buildup in the blood. They're able to do the treatment, and then they find a significant reduction and also a, a recovery of symptoms. And so with that, that brings me to the end of the presentation that I did for the discussion, for the South African doctors, again, sorry for the technical problems, during this talk. Here's what it is. So, I'll look through that just to see if there's any questions, etcetera, then I can So, COX runs without central fiber. I don't know what Speaker 1: that means. Problems, old stuff. Speaker 0: Kevin's going to redo the science slide. Yes. Black and rumble. Yes. A, La Quinta column, La Quinta equals 5th column, yes. How much if determinism much. That means, piss crystals. Yes. We did find them in, urine samples. So I wonder if doc is gonna go into what that doc from Texas was upset about with IC, intelligence community and lies. I'm not sure what that means. The says, this really is a top grade presentation. Thank you, Kev. This I'll share wherever I can. Speaker 1: More than welcome. Mike says, I'm Speaker 0: always confused how virus diseases always seem to evolve more dangerous, if not a living thing. How is that possible? Well, generally, that's not the case. In most instances, generally, a new virus tends towards less lethality as it, emerges in the environment. At MIND. All literature prior to the COOPH shows evolution towards greater infectivity, lower path Misty, and generally, that's what you've seen with SARS. It's become less, the initial infection is less overwhelming for the body. Again, go back to the data point, which shows that all all versions of SARS are neurotropic, meaning brain invasive, and the No amino acid sequence that is, Freon catalyzing. It's only changed slightly the last 5 amino acids, but we still don't know if it's causing the, the prion catalysis that, we're potentially looking at to problematic. So I think there's still a lot to find out and learn. My argument is pathogenic viruses are elements of protist symbiont mimicking mitochondrial virus like particles. Maybe. Keep working on it. With the crisis of SARS CoV-two still walking the air, we can't safely assume that variants are the product of natural pollution. No. And as the Japanese scientist who came out, published a paper, it basically showed you're getting a systemic or systemic release of mutations that is not natural, which would indicate that there's still some lab, jiggery hokery going on, Virus like particles, definitely part of the show. Well, if you're talking about exosomes and them carrying, toxic cargoes, yes, this has been known about for a long time in my field. Again, we're just gonna there's nothing you can do right now about the release and if you've been exposed either via infection or, via gene transfection, you've been exposed now. How that shakes out? Well, you hope that the luck of the draw favors you and the complexity of biology is far more sophisticated than bioweapon is with credit

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

SAVIMS – Toxic Peptides, Amyloids & PRIONS: From Genetic Vaccines to SARS-CoV-2 Part 9 end https://t.co/UTsa5dkxaQ

Video Transcript AI Summary
The speaker discusses various topics including the need for research in gain of function for Freon Science, the possibility of iron dysregulation causing neurodegenerative states, and the difficulty in treating amyloidogenic peptides. They also mention a research accident in Guangzhou, China that may have released a cancer-causing virus. The speaker expresses suspicion towards research programs in certain countries and urges caution in believing their claims of innocence. They thank some individuals for their support and apologize for technical difficulties. The speaker concludes by emphasizing the challenges of breaking down amyloids and prions through autophagy and encourages sharing the lecture to spread awareness.
Full Transcript
Speaker 0: It's far more sophisticated than bioweapon is give it credit for. Research is needed in to gain a function for Freon Science. Yeah. I don't know. I think we know enough. All of it's artificial nowadays. My suspension is to locate the source of replicons, knock it out, allow the body to learn from the let's see. Pathogen is where some people are immune to malaria. That might Speaker 1: be because they've got sickle cell. Speaker 0: We are being bombarded with government fleet programs. Speaker 1: Maybe. People should be translating Kevin's presentations into other languages. I agree. Speaker 0: We do have AI that can do that. Speaker 1: Doc, did you see this come Speaker 0: up recently? Don't see anyone talking about it, really. Speaker 1: Did I see this come up? Well, I'm not sure what you mean. The Speaker 0: iron deposition has led some people to conclude that iron is the cause and not the effect of Parkinson. Speaker 1: Well, again, it's very difficult to, in complex systems, point out one causal agent. Speaker 0: Can iron dysregulation lead to neurodegenerative states? Speaker 1: Yes. Is it the only thing? No. Speaker 0: How do they clean out amyloids? Speaker 1: So basically, it's kind of like a dialysis. And, like a sort of Ligand capture and filtering of blood. And the it It seems Speaker 0: but with respect to how difficult it is to treat amyloidogenic peptides because they're generally proteolytic resistant. And they just keep building up and building up. And it's the speed of aggregation which defines the disease state. And so, Speaker 1: cleaning the blood may be one of the more cogent ways of going about treating these issues. Speaker 0: I don't think you're gonna break them down chemically. Prions are notoriously tough. They they can survive all manner of caustic substances and high temperatures and still be infected. So the last 25 minutes Yeah. Again, that stream wasn't supposed to happen, and some things are happening with respect to this new setup where things are triggering, etcetera, and, I'm not sure what's causing it. Too long didn't read. A research accident in Guangzhou, China I've released Speaker 1: cancer causing virus in the world. I'm not biting down on the It was the Chinese at Speaker 0: the moment. There's too much overlap with, research in countries that we know I have these programs. All of them should be held, Speaker 1: or you should be suspicious of them all. Speaker 0: And anything that they say to protest their innocence. Don't buy it. Speaker 1: Afraid. Alright. Speaker 0: I think I'm done. I would remind everyone again, it is Saint Arafat Day. Please please please help me feed, Simon on the plantation. Speaker 1: They, and I want to say thank you Speaker 0: to, Jonathan and Carl. Much, much appreciated. And, There was, yes, someone on literally someone on Buy Me A Coffee, Brought me coffee earlier. Thank you very much. I'll come back with, more of the normal fare, hopefully, More entertaining, stream. Hopefully, this sort of brings you up to date with where we are with the literature. Amyloids and prions are playing a big Part of what we're dealing with as predicted and, autophagy. Sorry, but autophagy doesn't work With amyloids and prions, I'm afraid. We're just releasing them. They don't go away. How are you gonna break them down through, Autophagotic processes doesn't happen. This is the problem, and people have a job Wrap their mind around what this means. So, like, literal cleaning out the blood, like, physically removing the amyloidogenic Build up. Yes. Autophagy, generally, is just gonna release more amyloidogenic peptide into the environment. Where does it go? Alright. So I'm out of here. I'm just gonna end the stream there. So you've got a relatively Straightforward lecture if you wanna spread it around and give it to people, get them up to date. So thank you for listening. Again, apologies for the, technical problems. It is what it is. I'll be back later. Take care.

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

@reSeeIt save this thread

Saved - November 30, 2023 at 1:12 AM
reSee.it AI Summary
The COVID jabs and lockdowns have resulted in more deaths than those caused by migrants and organized crime in the past three decades. A crucial regulator of the cell cycle, p53, is inactivated by SV40, a virus with oncogenic and mutagenic capabilities. This raises concerns about bioweapons and calls for a Covid inquiry.

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

LMAO, more murders have occurred with COVID jabs and lockdowns than the combined deaths caused by migrants and organized crime over the last three decades.@LeoVaradkar#ResignLeotheleak https://youtu.be/Klja0qOJQxo?feature=shared…

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

#Bioweapons #CovidInquiry #Genomics #P53 dubbed #TheGuardianoftheGenome https://www.mskcc.org/news/new-findings-clarify-how-guardian-genome-works

New Findings Clarify How the “Guardian of the Genome” Works Surprise! It has to do with metabolism. mskcc.org

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

#SV40 #plasmids with oncogenic & mutagenic capabilities. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC452549/ SV40 has the ability to bind to and inactivate p53, which is a crucial regulator of the cell cycle and plays a role in preventing the formation of tumors.

Emergent Human Pathogen Simian Virus 40 and Its Role in Cancer The polyomavirus simian virus 40 (SV40) is a known oncogenic DNA virus which induces primary brain and bone cancers, malignant mesothelioma, and lymphomas in laboratory animals. Persuasive evidence now indicates that SV40 is causing infections in humans ... ncbi.nlm.nih.gov
Saved - November 30, 2023 at 12:51 AM
reSee.it AI Summary
Leo Varadkar's decision to allow a knife-wielding individual to stay in Ireland has sparked controversy. Concerns have been raised about the potential consequences, including the harm caused to innocent individuals. Additionally, a cautionary note highlights the support for Sharia Law among a percentage of British Muslims and the advocacy for it by a senior Muslim cleric in Ireland. These incidents have fueled debates around immigration and religious extremism. #Controversy #ImmigrationDebate

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

Yes this is factual. @LeoVaradkar weren't you responsible for filing the papers to allow this knife wielding fiend to stay in Ireland? and it has cost the innocence of babies. @griptmedia @rtenews @IrishInquiry @Mickbraz1 @VirginMediaNews @IrexitFreedom

@keira_con - Keira Connnolly

I wonder who from Dublin 15 Did @LeoVaradkar & @FineGael petition the minister for justice to allow to remain in Ireland "Dublin 15 lies to the west of Fingal, encompassing the areas of Blanchardstown, Mulhuddart, Clonsilla, Castleknock and Tyrrellstown" https://t.co/GdA9AHvXjq

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

They should have thrown the invader out. #deport #IrelandExit #ResignLeo

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

https://t.co/NSM660tHgL I really hope this is nonsense.

@IrishInquiry - TheIrishInquiry

A NOTE OF CAUTION: This year a poll published in the Sunday Telegraph demonstrated that 40% of British Muslims want Sharia Law. The findings were that this percentage of British Muslims supported "there being areas in Britain which are predominately Muslim and in which sharia law is introduced". Sharia law condones public stoning of adulterers (female), executing apostates and amputating the limbs of thieves. Regarding reactions to the cartoons of the Prophet Mohammed, 14% of British Muslims thought it was right for protesters in Muslim countries to attack Danish embassies and 12% thought it was right for "demonstrators to carry placards calling for the killing of those who insult Islam". 13% said it was right "to exercise violence against those who are deemed by religious leaders to have insulted them". In Ireland, senior Muslim cleric and spokesperson for the #ClonskeaghMosque, #DrAliSelim, advocates for Sharia Law (if Muslims were a majority in Ireland). Selim lost his role as a lecturer in Trinity College Dublin for stating on Irish Television that Female Genital Mutilation was acceptable in certain circumstances. He came under pressure to apologise, which he did so. He later won a case against TCD for unfair dismissal.

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

#IrishBigots #FarRight #invasion https://youtu.be/tBtp6xeLjlo?feature=shared @KimIversenShow

Saved - November 28, 2023 at 1:33 AM
reSee.it AI Summary
Spike Detox by Measslainte is a meticulously crafted blend of nature's finest ingredients, including ancient pine needle tea, foxglove buds, loinsmane mushrooms, and more. Fasting and fruit fasting are beneficial practices to explore for improved well-being. Grounding, just 15 minutes a day, can have a profound impact on overall health. Cucumbers offer versatile health benefits, while nanoporous silica shows potential in detoxification therapies. Parsley tea aids kidney detoxification, but moderation is key. Glutathione provides antioxidant, detoxification, immune, and anti-aging benefits.

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

Spike Detox by Measslainte is a meticulously crafted blend of nature's finest ingredients. Our ancient old-growth pine needle tea, delicately infused with the flowering buds of foxglove, is expertly combined with a harmonious medley of premium components. This exclusive formula includes loinsmane mushrooms, seamoss, bladderwrack, invigorating natural peppermint, quercetin for added antioxidants, bromelain for digestive support, the cholesterol-balancing power of red yeast rice, CoQ-10 for heart health, NAC for detoxification, the exotic graviola soursop, the liver-loving milk thistle, and chelated zinc for overall wellness. Experience the revitalizing effects of Spike Detox and embark on a journey to enhanced well-being

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

Fasting is a practice that has gained significant attention in recent years due to it's health benefits. When you are feeling unwell, understanding the significance of fasting can be crucial. You can read more about it in this article: https://measslainte.ie/post/water-fasting/ , fruit fasting is another viable option to explore. It's a method of fasting that involves consuming only fruits for a specified period. This approach can have its unique advantages, and it's worth considering as part of your wellness routine."Grounding: How Just 15 Minutes a Day Can Change Your Life"Grounding, also known as earthing, is a simple yet powerful practice. Devoting just 15 minutes a day to grounding can have a profound impact on your overall well-being. The best part is that it costs nothing. To learn more about the benefits and how to get started with grounding, check out this informative article: https://measslainte.ie/post/grounding-natures-antioxidant/

Unveiling the Marvels of Autophagy through Water Fasting Embracing Autophagy: A Cellular Symphony of Renewal Welcome to the captivating world of autophagy – a mesmerizing cellular symphony where renewal takes center stage. Derived from the Greek words “auto” (self) and “phagy” (eating), autophagy invites you to witness a remarkable process of cellular self-cleansing and rejuvenation that holds the key to enhanced well-being and longevity. The Dance of Cellular Renewal Autophagy orchestrates an intricate dance within your cells, where components are meticulously broken down and recycled. measslainte.ie

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

#Cucumber #Silca #Detox #Nutrition https://measslainte.ie/post/cucumber-nutrition/ cucumbers stand tall as a versatile, nutrient-packed superfood. With their myriad benefits, from connective tissue support to silica-rich skin enhancement and detoxifying properties, cucumbers are your allies in the quest for vibrant health The results indicate that nanoporous silica, which has been functionalized with organic ligands, possesses substantial potential as a versatile material in the realm of detoxification therapies. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3429124/

Functionalized Nanoporous Silica for the Removal of Heavy Metals from Biological Systems: Adsorption and Application Surface-functionalized nanoporous silica, often referred to as self-assembled monolayers on mesoporous supports (SAMMS), has previously demonstrated the ability to serve as very effective heavy metal sorbents in a range of aquatic and environmental systems, ... ncbi.nlm.nih.gov

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

Parsley tea has been traditionally used as a natural remedy for various health issues, including detoxifying the kidneys. The kidneys play a crucial role in filtering waste products and toxins from the body, and they can be affected by various factors such as diet, medication, and environmental pollutants. Parsley contains various compounds such as flavonoids and volatile oils, which have been shown to have diuretic and anti-inflammatory properties. These properties can help increase urine output and promote the elimination of toxins from the body, thus reducing the workload on the kidneys. To make parsley tea, you can follow these simple steps: Wash a bunch of fresh parsley leaves thoroughly and chop them into small pieces. Add the chopped parsley to a teapot or a cup. Pour boiling water over the parsley leaves. Cover the teapot or cup and let it steep for 5-10 minutes. Strain the tea and drink it warm or cold. It is important to note that parsley tea should not be used as a replacement for medical treatment, and people with kidney problems should consult their healthcare provider before using it. Additionally, excessive intake of parsley tea may cause side effects such as stomach upset, diarrhea, and allergic reactions. Therefore, it is recommended to consume it in moderation. https://www.healthline.com/nutrition/parsley-benefits

8 Impressive Health Benefits and Uses of Parsley Widely used as a fresh culinary herb or dried spice, parsley has been labeled as one of the most powerful disease-fighting plants. Here are 8 impressive health benefits and uses of parsley. healthline.com

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

Benefits of Glutathione# Glutathione has numerous health benefits, including: Antioxidant Protection Glutathione is a powerful antioxidant that protects the body against oxidative stress and free radical damage. Detoxification Glutathione plays an important role in the detoxification of harmful toxins and chemicals in the body. Immune Function Glutathione is essential for the proper functioning of the immune system. It helps to boost the immune response and protect against infections. Anti-Aging Glutathione is believed to have anti-aging properties due to its ability to protect the body against oxidative stress and free radical damage. https://measslainte.ie/post/selenium-/

Selenium Selenium Supplementation and its Conversion to Glutathione measslainte.ie

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

@threadreaderapp unroll

Saved - November 22, 2023 at 10:56 PM
reSee.it AI Summary
Mental health is a preventable concern. Gluten, which often contains glyphosate herbicide, blocks serotonin production in the gut. Shockingly, 11% of Americans over 12 rely on antidepressants. Did you know that Bayer's Monsanto Roundup with glyphosate is an antibiotic? #MentalHealthAwareness #PreventionIsKey

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

Mental health is a huge concern and the sad truth is, it's preventable. Most serotonin is produced in the gut, but #gluten blocks it, and most gluten contains #glyphosate herbicide, making it even worse #MentalHealthAwareness #PreventionIsKey https://measslainte.ie/post/glyphosate/

@TheRabbitHole84 - The Rabbit Hole

11% of Americans over the age of 12 take an antidepressant.

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

@Bayer #Monsanto #Roundup #Glyphosate did you know it was an anti biotic ?

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

https://supergreentonik.com/glyphosate-and-the-possible-connection-to-gluten-intolerance/

Glyphosate And The Possible Connection To Gluten Intolerance We explore Glyphosate and the possible connection to gluten intolerance. What causes celiac disease and the rapid rise of gluten intolerance? supergreentonik.com
Saved - November 7, 2023 at 10:40 AM
reSee.it AI Summary
Investing time in health matters has been rewarding. I'm proud to have saved a life without seeking profit. Sharing a foolproof detox method and expertise in neurological disorders. Check out the link for more detox techniques. Acknowledging mistakes is crucial for fixing them. Have a great day!

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

I've invested a significant amount of time in health matters, Not a doctor but I'm genuinely glad I did. I can proudly say that I've saved at least one life, and I don't do it for profit. I wouldn't let anyone label me a grifter. The detox method I've shared below is foolproof, and I have a knack for dealing with neurological disorders. Don't forget the selenium #Gluthathion I can also provide information on other detox techniques. https://measslainte.ie/categories/detox/ Have a great day now. I don't want to alarm you but it is what it is. The first thing people need to do is acknowledge they messed up or they will never fix it. End

Detox Discover Nutritional Supplements for Multiple Sclerosis and other Demyelination Illnesses measslainte.ie

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

#SpikeDetox #nutrition #detox #vaccines #Myocarditis #antiinflammatories https://threadreaderapp.com/thread/1710277894251909141.html I think it missed the bottom link on glutathione. https://measslainte.ie/post/selenium-/ #Health #advice #Healthtips

Thread by @MeasslainteIE on Thread Reader App @MeasslainteIE: Spike Detox by Measslainte is a meticulously crafted blend of nature's finest ingredients. Our ancient old-growth pine needle tea, delicately infused with the flowering buds of foxglove, is expertly ...… threadreaderapp.com
Selenium Selenium Supplementation and its Conversion to Glutathione measslainte.ie
Saved - November 1, 2023 at 3:04 PM

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

@jacksonhinklle @elonmusk https://www.turkiyenewspaper.com/politics/16892 Always follow the money. 🤷‍♂️

Video Transcript AI Summary
The US, UK, and France support Israel because of the potential financial benefits of the proposed Ben Gurion Canal. The Suez Canal, owned by the French and British, is currently used for trade and oil distribution. However, it has limitations and caused significant losses when a ship got stuck in 2021. The Ben Gurion Canal, deeper and wider than the Suez Canal, would generate billions of dollars in revenue for Israel. It would also bypass the inconvenient placement of the Gaza Strip, potentially leading to the annexation of Gaza by Israel. This move would increase Israel's geopolitical standing and weaken Arab states' leverage against the US, UK, France, and Israel.
Full Transcript
Speaker 0: I think I just figured out why the US, UK, and France are so adamantly pro Israel right now. If we all knew what had to do with money, but I'm gonna tell you exactly how. There's is a shout out to my uncle who told me to do some research on the Ben Gurion Canal. And I did, and I took notes. Now who is Ben Gurion, he is known as the founding father of Israel. He was the 1st prime minister. Yes, you guessed it in 1948. And this canal is a proposal to connect The Red Sea to the Mediterranean Sea through here. Right? But we already have a connection, and it's called the Suez Canal. And if you don't know the history, let's get into The Suez Canal was opened in 18/69, and the Suez Canal Company was given a 99 year lease to own the Suez Canal. And guess who owned the Suez Canal company. The French and the British. I think it's also important to note that the British Empire originally was The post surveilling the canal because they thought it would directly threaten their economy, but instead they just decided let's benefit from it. Bought 44% of the shares in 18/75, So they were all good. Now in 18/88, the maritime powers, Great Britain, Germany, Austria Hungary, Spain, France, Italy, Netherlands, Russia, and Turkey signed this thing called the convention of Constantinople. What's important about this is it said that every single nation should be able to use the canal, Whether at war, at peace, it cannot be denied access to anyone. In 1949, Egypt denied Israel access After the Nakba, after they did what they did. That was a huge deal. It was a big statement because of this. Now in 1956, when the US was basically having a proxy war with the The Soviet Union in that region. The Egyptian president at the time, Gamal Abdel Nasser, decided to nationalize the Suez Canal, so taken away from the British and French owned company. Essentially because the US, reneged on a previous agreement to finance the Aswod Dam project that was for the Nile, getting water and electricity to Egyptian population, etcetera, etcetera. This was a massive shift, a huge move in the region and globally. Probably why it was also used as a battleground In the 1967 Arab Israeli war. Now after the Arab Israeli war and the Geneva conference, etcetera, etcetera, what you need to know is Israel and Egypt It signed a peace treaty at Camp David signed by Jimmy Carter. This is from a US government website, By the way, my sources are checked, tried, and trusted. And the US was given credit for orchestrating a peace treaty between these These 2 countries, again, why were they involved from the beginning? Who knows? The US has always been here. We're in 1979 now. Should all be cool. A peace treaty was signed. Like, everything is perfect. Suez Canal is open to everyone. Cool, cool, great. Right? Wrong. 16 years before this, and even before the Arab Israeli war, the US Department of Energy and the Lawrence Livermore National Laboratory Tory had been making a plan for something else. In 1963, they made a classified plan to help excavate The Negev Desert Hills with 520 nuclear bombs to help create a canal. This was only made public in 1993, 1994, depending on the sources you check. So at the time of the peace treaty, nobody knew this was going on, except of course, Jimmy Carter. Now we could also talk about how the war was a product of collusion between Britain, France, and Israel, and they decided to initiate the war, but we'll save that for another time. You might be asking yourself, why do they wanna build another canal? Like, we have the Suez Canal right here. Why do we need a canal through here? This is where the money comes in, baby. Without the Suez Canal right here, ships from Asia would have to go all the way down and around Africa in order to reach Europe. This canal right here currently sees the passage of 12 to 15%, depending on the source you check, Of the world's trade and 10% of the global oil distribution. Just this little canal right here. And who benefits from this? Egypt, of course, it's their canal, right? In 2023, they broke records and made a revenue of 9,400,000,000 US dollars. Yay for Egypt, right? Well, how do you think the US, the UK, France, and Israel feel about that? Not good. So it's canal is not ideal. Up until 2014, you could only go one way, which meant for 6 hours, it went in one direction and 6 hours it went in the other, which was super not efficient. It was also not wide enough to accommodate some of the largest ships in the world. So what happened in 2021? You might remember this. One of the world's biggest ships jammed the Suez Canal leading to approximately $900,000,000 of losses. The US was really not happy about this, and the Pentagon released a statement that this made it difficult for the movement of their military vessels, specifically to Israel, but not to worry they had other ways. Now when they're planning the Ben Gurion Canal, they're planning to have it 50 meters deep, which is 10 meters deeper than the Suez Canal, and 200 meters wide, which will facilitate the biggest ships in the world going in both directions. Not only that, but directly competing with the Suez Canal, Israel projects that it would make them an annual revenue of about $6,000,000,000 a year Plus. And now for the interesting part, there's one feature about the Suez Canal that's also really inconvenient And that's the fact that it's built on pretty sandy shores. Now, I'm not an engineer. Now from what I read, sandy shores are Pretty inconvenient for a canal. They constantly need maintenance. But where Israel wants to dish it out to the Mediterranean Sea, it's It's a rocky land texture which is ideal for these conditions. Let's zoom into this. That's the Gaza Strip. How annoying is the placement of the Gaza Strip for them? They have to actually turn the canal around so that it avoids this piece of land. Do you see where I'm getting at? They don't want ships to have to do this Tie around and add a little time and inconvenience to their journey and have such close proximity to Gaza, What if they just built it through Gaza? Oh no, wait. They don't want to do that. They don't want to help the Palestinian economy. What do you mean? That would defeat the entire purpose, wouldn't it? Unless they took that land. Yeah. That's what's going on. Israel wants to seize Gaza, annex the land, take it over so they can build their canal through it. And the US, the UK, and France are all for that Because it's gonna make them a lot of money at the cost of millions of lives destroyed. Unfucking believable. Building this canal will not only redirect trade, but historically, Arab states use the Suez Canal to put pressure on Israel. So it will not only increase Israel's geopolitical standing, but it'll also become a strategic asset for diplomatic negotiations for Israel And take away the most powerful thing the Arab states had against the US, UK, France, and Israel to keep them in line. And there you have it. That's the reason.
Israel's goal to open Ben Gurion Canal: Sources - Turkiye Newspaper Israel, which has been bombarding Gaza for days, aims to realize the Ben Gurion Canal, which will create a new route for global energy and trade. turkiyenewspaper.com
Saved - October 25, 2023 at 11:51 PM

@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋

https://t.co/2rBFDOm6FE

Video Transcript AI Summary
Kevin McKernan, an experienced genomic expert, discusses his findings regarding mRNA vaccines. He discovered that the expression vectors for the vaccines are still present in the vials, exceeding the guidelines set by the EMA and FDA. These vectors, derived from E. Coli, can be challenging to remove and may lead to residual plasmids in the vaccines. McKernan's team designed quantitative PCR assays that confirmed the presence of the vectors in the vaccines. The CT values obtained were consistently above the recommended limits. This poses a significant concern as the contamination levels are much higher than those found in COVID diagnostic tests. McKernan urges others to replicate his work using the publicly available primer sequences to gain a better understanding of the situation.
Full Transcript
Speaker 0: Next is mister Kevin McKernan. Thank you. I have no conflicts to disclose. I have 25 years of experience in the genomic space. I've worked as a team leader of R&D at the Human Genome Project at Whitehead, MIT. And I have over 57,000 citations to publications, in my space in multiple patents on on PCR and sequencing. Next slide, please. No conflicts. Next slide. In February, I used mRNA vaccines as the spike in control for some RNA sequencing libraries, and, to my shot, discovered that the expression vectors for the Vaccines are still in the vials. I looked at this in over a dozen vials, and it appears that this expression vector is above the EMA guidelines and the FDA guidelines. You can see this in this preprint that's described here. Next slide. As a refresher, there's 2 different processes that have been discussed in this BMJ article. The clinical trials running process 1, which uses in vitro transcription off of synthetic DNA, but they switched to process 2 for a scale up, which used E. Coli to amplify plasmids. And those plasmids are what still remain in the vials, and we're not within the clinical trial. Next slide. This is another depiction of this process. You can see getting plasmids out of these E. Coli is a challenge and can sometimes lead to residual plasmids inside the vaccines. Next slide. These are the expression vectors that we discovered on the left in Pfizer vaccines. They also exist in the Moderna vaccines, but they're a little bit different. The Pfizer vaccines specifically have this SV 40 promoter, which was not disclosed in the expression vector map that was given to the FDA, or I'm sorry, the EMA, but the expression factor has a 3 44 base pair promoter with a nuclear localization signal known as this SV40 promoter. Next slide. So we want to verify this by designing quantitative PCR assays that target the spike sequence and the vector sequence. Next slide. And this work demonstrated that, with even 1 to 100 dilutions, you could get CTs of 22 for the DNA that's in these vials for the vector, which is not part of, what should be in these vials. We did this in triplicate across 8 vials. It's very consistent, and they are over the EMA and the FDA's, limits. Next slide. The EMA has a ratiometric limit that looks at RNA to DNA ratios, and you can measure you should expect an 11.5 CT offset between the spike in between the vector. What we see is only 5 to to 7 CT difference, which means there's an 18 to 70 fold over the limit of the 3 30 nanogram per milligram recommended by the EMA. Next slide. You can readily, assay this in any other lab around the world now. If you put these vaccines directly into quantitative PCR, you can get CTs as low as 17. This is very important to know because COVID was diagnosed with CTs less than 40, which is over a 1000000 fold higher contamination being injected than what you might get from a nasal swab. Next slide. We know these vials, were these vials were sent to us anonymously in the mail, so we do not have the cold chain. However, we can measure the RNA integrity by putting them on electrophoresis systems, and we do not see a substantial difference in the RNA integrity from the files that we received versus what's been published about these in the past. Next slide. Various people on Twitter have now begun to to reproduce this. In addition, I'd point to the EMA's documentation, where they have an 8 15 fold variance across ten lots of double stranded DNA contamination documented in the EMA process. Next slide. There are some risks to this. There is double stranded DNA can create interferon responses, and Keith Petten at the FDA has done great work demonstrating the risks of DNA integration into the genome if these things are in vaccines. Next slide. The call to action here is all of these primer sequences are now public, and people are downloading them and trying to reproduce this work. You can reproduce this work in 60 minutes with a microliter of the vaccine, which is 1 3 100th of a dose for less than $10. I encourage everyone to try and do this to understand what we have at foot. I will note we did not measure any of the bad lots that are in the Schmeling et al paper that demonstrated high adverse events in certain lots. To be measuring what seemed to be normal lots. Next slide. And thank you for your time and consideration. Great. Thank you so much, mister McKernan, for your presentation.
Saved - October 23, 2023 at 11:36 AM

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