@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…
@JesseMatchey - Jesse Matchey
Yeah, connect the fking dots Why don’t people care about this?
@JesseMatchey - Jesse Matchey
@swani741 I reached out years ago. No response.
@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.
@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 :)
@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.
@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.
@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.
@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.
@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.
@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.
@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
@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
@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
@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
@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:
@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.
@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%!
@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
@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
@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?
@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.
@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝
@BrokenTruthTV https://t.co/jKzHS52QIg
@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝
@BrokenTruthTV https://t.co/DNiBLgAkxQ
@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝
@BrokenTruthTV https://t.co/iaMSVSxCgI
@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝
@BrokenTruthTV https://t.co/ALQAS24QT7
@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝
@BrokenTruthTV https://t.co/rgfUu4FNWt
@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝
@BrokenTruthTV https://t.co/F5KMVFxL42
@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/
@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
@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.”
@JesslovesMJK - Jessica Rose 🤙
Please read this. It's almost as important as our paper. https://substacktools.com/sharex/5cOr45Tz@SecKennedy@SenRonJohnson@Kevin_McKernan@DJSpeicher@brownstoneinst@Honest_Medicine@DrJBhattacharya@HHSGov
@JesslovesMJK - Jessica Rose 🤙
link to paper: https://pubmed.ncbi.nlm.nih.gov/40913499/
@JesslovesMJK - Jessica Rose 🤙
link to Retraction Watch article: https://retractionwatch.com/2025/09/18/covid-vaccine-safety-acip-dna-contamination-study-autoimmunity/
@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/
@JesslovesMJK - Jessica Rose 🤙
link to original paper: https://www.tandfonline.com/doi/full/10.1080/08916934.2025.2551517#abstract
@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 🐺🐭🦝
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
@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
@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/
@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/
@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/
@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
@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
@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/
@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/
@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/
@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
@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
@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.
@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.
@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 🐭
@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
@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 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
@Jikkyleaks - Jikkyleaks 🐭
Just a reminder for those asking whether Mpox (monkeypox) was a manipulated virus. Absolutely.
@Jikkyleaks - Jikkyleaks 🐭
H/t @ClareCraigPath https://www.hartgroup.org/the-smallpox-vanishing-act/
@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 🐭
@drtaubraun @CharlesRixey @AGHuff Do you have a record of the report?
@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!
@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/
@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/
@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
@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
@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
@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
@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..
@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
@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
@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🐭
@Fynnderella1 - Dr. Lynn Fynn-derella🐭
@Fynnderella1 - Dr. Lynn Fynn-derella🐭
@IntuitAVC @NIHDirector_Jay Are you refuting this documented fact?
@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.
@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
@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
@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
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.
@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
@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
@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
@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
@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
@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
@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
@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
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
@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.
@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 💪🙏🔥
@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 🙏❤️
@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
@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 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
@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.
@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/
@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/
@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
@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
@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/
@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/
@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/
@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
@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
@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/
@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/
@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/
@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.
@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/
@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/
@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.
@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
@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
@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.
@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
@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 🏴👁&👁 🆓
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
@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
@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
@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
@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/
@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
@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
@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. 👇
@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?
@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.
@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 @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
@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 🐺🐭🦝
@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 🐺🐭🦝
@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 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 🐺🐭🦝
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
@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
@ChrisMasterjohn - Chris Masterjohn
SSRI Withdrawal Is Mitochondrial Dysfunction Installment seven in our series on understanding the truth about SSRIs. 🧵 https://t.co/IeABPwDvPK
@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.
@SabinehazanMD - sabine hazan md
Hello dear @grok can you answer @Kevin_McKernan ?
@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.
@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
@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. :-)
@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
@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
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]!🤬
@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
@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 🐭
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
@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
@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
@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
@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.
@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/
@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/
@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/
@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/
@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/
@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/
@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/
@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/
@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/
@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/
@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/
@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/
@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/
@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
@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/
@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/
@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/
@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
@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
@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/
@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/
@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
@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/
@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/
@Kevin_McKernan - Kevin McKernan
Strayer et al explains why SV40 plasmids integrate. https://pubmed.ncbi.nlm.nih.gov/12161189/
@Kevin_McKernan - Kevin McKernan
Nothing to see here https://aacrjournals.org/cancerres/article/64/11/3757/511331/Presence-of-Simian-Virus-40-DNA-Sequences-in-Human https://t.co/6tJw0dDTnX
@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.
@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.
@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
@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/
@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…
@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
@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
@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.
@joshg99 - Josh Guetzkow
@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
@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/
@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
@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
@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
@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
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
@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
@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 ——
@LewDrakePhD - Lewis Drake, PhD
From @MidwesternDoc https://www.midwesterndoctor.com/p/the-remarkable-history-and-safety?utm_medium=web&triedRedirect=true
@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.
@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/
@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!
@dbdugger - Daniel Brittain Dugger
Victoria, your country drew parallels to ME/CFS. You can give up! Better luck next time.
@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
@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/
@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/
@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/
@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/
@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/
@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
@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/
@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
@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
@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
@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/
@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/
@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
@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
@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.
@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
@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?
@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 :)
@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.
@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.
@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.
@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.
@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.
@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.
@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
@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.
@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝
@BrokenTruthTV https://t.co/jKzHS52QIg
@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝
@BrokenTruthTV https://t.co/DNiBLgAkxQ
@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝
@BrokenTruthTV https://t.co/iaMSVSxCgI
@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝
@BrokenTruthTV https://t.co/ALQAS24QT7
@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝
@BrokenTruthTV https://t.co/rgfUu4FNWt
@MeasslainteIRL - Thomas Anthony III 🐺🐭🦝
@BrokenTruthTV https://t.co/F5KMVFxL42
@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 🐺🐭🦝
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
@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
@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/
@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/
@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/
@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
@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
@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/
@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/
@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/
@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
@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
@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/
@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/
@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
@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
@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
@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
@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..
@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
@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!
@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.
@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
@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 🐺🐭🦝
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.
@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 💪🙏🔥
@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 🙏❤️
@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
@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 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
@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?
@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.
@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 @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
@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 🐺🐭🦝
@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 🐺🐭🦝
@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 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 🐺🐭🦝
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
@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.
@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 🐺🐭🦝
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
@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
@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
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
@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
@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/
@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/
@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/
@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!
@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
@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
@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/
@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/
@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/
@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!
@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
@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
@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
@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.”
@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!
@MeasslainteIRL - Thomas Anthony III
@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
@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
@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
@MeasslainteIRL - Thomas Anthony III
@Reseeit save thread
@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
@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.
@MeasslainteIRL - TAE III 1215 🍀
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.
@MeasslainteIRL - TAE III 1215 🍀
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.
@MeasslainteIRL - TAE III 1215 🍀
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.
@MeasslainteIRL - TAE III 1215 🍀
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.
@MeasslainteIRL - TAE III 1215 🍀
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.
@MeasslainteIRL - TAE III 1215 🍀
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.
@MeasslainteIRL - TAE III 1215 🍀
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.
@MeasslainteIRL - TAE III 1215 🍀
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/
@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
@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.
@MeasslainteIRL - TAE III 1215 🖖🏻 (Tomo)
@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
@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.
@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
@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
@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!
@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
@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
@MeasslainteIE - Thomas Anthony III
Very interesting what you can find on X. Sad that we are looking 4 years too late.
@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.
@MeasslainteIE - Thomas Anthony III
@AnneliseBocquet Post translated with thread reader! https://twitter-thread.com/t/en-US/1772902508886687757 The paper is in English.
@MeasslainteIE - Thomas Anthony III
Why yes we were !! https://www.facebook.com/share/p/nj9TESHJbYb57MBA/
@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/
@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/
@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).
@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.
@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
#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
@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!
@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
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
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.
@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. 😂
@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.
@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.
@MeasslainteIE - Thomas Anthony III
@MeasslainteIE - Thomas Anthony III
https://t.co/WHnlU96GCu 🦃 Tail #TurkeyTail #Cancer
@MeasslainteIE - Thomas Anthony III
https://t.co/P3oLUfCAEa #Vermox #AntiParasite
@MeasslainteIE - Thomas Anthony III
It's not just the jabs these chemicals are in the food and water. https://t.co/XCB583znR5
@MeasslainteIE - Thomas Anthony III
A great resource for all things glyphosate with many other avenues of research. https://t.co/hvvfAQLsjz
@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 🕊️
@MeasslainteIRL - Thomas Anthony III
@FineGael @LeoVaradkar @rodericogorman Vote No No resign now you frauds https://t.co/vqcRB65qrZ
@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
@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
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
@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
@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
@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/
@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
@MeasslainteIRL - Thomas Anthony III
@Reseeit save thread @threadreaderapp unroll
@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…
@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.
@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
@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.
@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
@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
@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
@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
@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
@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
@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
@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
@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋
SAVIMS – Toxic Peptides, Amyloids & PRIONS: From Genetic Vaccines to SARS-CoV-2 Part 3 https://t.co/vIBxwcuNId
@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
@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋
SAVIMS – Toxic Peptides, Amyloids & PRIONS: From Genetic Vaccines to SARS-CoV-2 Part 5 https://t.co/QIFH3McXgX
@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋
SAVIMS – Toxic Peptides, Amyloids & PRIONS: From Genetic Vaccines to SARS-CoV-2 Part 6 https://t.co/cyrFQHPmc2
@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋
SAVIMS – Toxic Peptides, Amyloids & PRIONS: From Genetic Vaccines to SARS-CoV-2 Part 7 https://t.co/WHS3imCVx9
@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋
SAVIMS – Toxic Peptides, Amyloids & PRIONS: From Genetic Vaccines to SARS-CoV-2 Part 8 https://t.co/k7HBB5MFYo
@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
@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋
@reSeeIt save this thread
@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
@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.
@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
@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.
@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋
#IrishBigots #FarRight #invasion https://youtu.be/tBtp6xeLjlo?feature=shared @KimIversenShow
@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/
@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/
@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
@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-/
@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋
@threadreaderapp unroll
@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/
@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/
@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
@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋
@jacksonhinklle @elonmusk https://www.turkiyenewspaper.com/politics/16892 Always follow the money. 🤷♂️
@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋
@MeasslainteIE - Thomas Anthony ≋T≋A≋E≋
@TheHorizonX @reSeeIt