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Scientists are confirming that COVID shots can damage the brain and devastate mental health. Studies reveal increases in ischemic strokes (up 44%), hemorrhagic strokes (up 50%), transient ischemic strokes (up 67%), myasthenia gravis (up 71%), Alzheimer's (up 22%), cognitive impairment (up 138%), depression (up 68%), anxiety disorders (up 44%), and sleep disorders (up 93%), all linked to toxic spike protein accumulation in the brain. To protect yourself, stop further exposure, support detoxification pathways, and ensure an anti-inflammatory diet that supports mitochondrial health.

COVID-19 injections are associated with neuropsychiatric disorders, according to an FDA and CDC study. The speaker claims that psychosis is 440 times more likely, dementia 140 times, schizophrenia 315 times, suicidal thoughts 150 times, and homicidal ideation 25 times. Brain clots are allegedly 3,000 times more likely, depression 530 times, and violent behavior 80 times. Cognitive decline is purportedly 115 times more likely and delusions 50 times. The speaker believes psychiatric harm is caused by the accumulation of toxic spike proteins, mRNA, lipid nanoparticles, and other unknown components.

I contracted SARS in South Korea during the outbreak. It caused neurological symptoms and was different from the flu or norovirus. I couldn't get a proper diagnosis, but I realized it was serious when I saw what was happening in Wuhan. There was an effort to suppress information beyond the official narrative. I believed it came from a lab and published a paper on it. I've been trying to inform people about the role of viruses in chronic neurodegenerative diseases. The spike protein in the virus can misfold and cause amyloidosis. There are safety concerns with gene transfection, and we're seeing excess deaths, especially in dementia cases. Synthetic peptides may be a contributing factor.

Speaker 0: The transcript cites multiple studies indicating severe behavioral changes in those who receive mRNA shots. A study by Oten colleagues found that the mRNA vaccine mRNA and spike protein were being produced in cerebral arteries of stroke patients. It is stated that the mRNA shot is based on the second largest COVID vaccine safety study ever conducted with eighty five million people in it, which purportedly found a two hundred percent increased risk of stroke after dose two of mRNA shots. The claim is that the vaccine goes to the brain, causes brain damage and neuronal destruction, and that this is reflected in neuropsychiatric conditions. This is linked to a study by Doctor James Thorpe and colleagues, which allegedly identified eighty-six neuropsychiatric safety signals for these COVID shots, including homicide, homicidal tendencies, psychosis, schizophrenia, Alzheimer's, cognitive impairment, and violent behavior, all claimed to be far in excess of what was reported with flu vaccinations, and described as corroborating multiple other studies. The transcript also references a study from Korea finding increased Alzheimer's risks and increased cognitive impairment risks, and another Korea study reporting a massive increased risk of depression, sleep disorders, and anxiety from these injections. The overall assertion is that, based on peer reviewed evidence, the injections damage the brain, cause brain damage resulting in neuropsychiatric conditions.

The speaker discusses how the spike protein in vaccines can lead to clotting issues, immune suppression, and reactivation of latent viruses like mono. This can also weaken the body's ability to fight off other viruses and cancers. An increase in cancer cases post-vaccination is noted anecdotally. The speaker attributes these effects to the spike protein in the vaccines.

Speaker 0 states that the study confirms suspicions from the past five years that common sense has deteriorated in the population. The study analyzed the VAERS system from the 1990s to 2024 and examined PRRs (proportional reporting ratios), which measure how many more adverse events occur with the COVID shots compared to the flu shot or other vaccines. It reports 8686 safety signals of neuropsychiatric adverse events, with some up to 3,000 times higher than the flu shot. The safety signal threshold defined by CDC/FDA for PRRs is greater than two, and all reported signals exceeded this threshold. The listed conditions include schizophrenia, dementia, Alzheimer's, cognitive impairment, strokes, brain clots, homicidal tendencies, homicidal behavior, and psychosis, described as people hallucinating and brain damage. The speaker notes that this large number of safety signals aligns with a recent study indicating that people who had strokes showed toxic spike protein production in their brains for up to seventeen months after vaccination, which the speaker suggests explains the observed deterioration in cognitive function.

The speaker discusses the harmful effects of the spike protein found in COVID-19 vaccines. They mention a study showing that almost a third of patients experienced neurological issues from the spike protein. They express concern about the lack of an off switch for this gene and the potential for autoimmune and neurological harm. The speaker also addresses criticism of fearmongering and highlights the connection between the spike protein and HIV. They mention studies linking COVID-19 vaccines to autism in rats and discuss the use of edible vaccines in plants. The speaker emphasizes the importance of sharing information and concludes by promoting their video game.

In a deceased patient, spike protein was found in the heart but not nucleocapsid protein. The autopsy revealed bronchopneumonia, Parkinson's disease, necrotic encephalitis, and myocarditis. The author suggests that the spike protein in affected tissues was likely from gene-based COVID-19 vaccines, not a SARS CoV-2 infection, as nucleocapsid protein was absent. Spike protein was found in areas with brain and heart inflammation, possibly contributing to the disease.

Speaker 1 asks for information on how the vaccine links to dementia, citing a grandmother who suffered from dementia after the COVID vaccine. Speaker 0 responds: "I'm so sorry, and thank you for bringing that up." He notes: "lipid nanoparticles traverse the blood brain barrier" and "lipid nanoparticles were developed and understood to traverse the blood brain barrier." He cites "the indoctrinated brain" by doctor Michael Nels and says "the combination of propaganda, repetition of messages while people are in a state of fear actually damages and rewires the brain" and that there is "this actual brain damage from the injection specifically destroying or damaging the prefrontal cortex." He mentions "lost their memories of themselves" and "there's so much dementia and Alzheimer's type damage in the Pfizer documents." He adds "these lipid nanoparticles damage the brain as they circulate through the system, you know, crossing the blood brain barrier." He suggests "traumas based interventions" and "you can possibly rebuild the myelin sheath of the nervous system." "So that's the best I can do, and I'm really sorry that that happened to your grandma."

A study from the Oxford Academic QJM Medical Journal suggests a potential association between COVID-19 vaccination and the development of Alzheimer's disease. The study, conducted in Seoul, South Korea, analyzed data from a random 50% sample of city residents aged 65 and above. Findings showed an increased incidence of mild cognitive impairment (MCI) and Alzheimer's disease (AD) in vaccinated individuals, particularly those receiving mRNA vaccines within 3 months post-vaccination. No significant relationship was found with vascular dementia or Parkinson's disease. Preliminary evidence suggests a potential link between COVID-19 vaccination, particularly mRNA vaccines, and increased incidences of AD and MCI. The study underscores the need for further research to elucidate the relationship between vaccine-induced immune responses and neurodegenerative processes, advocating for continuous monitoring and investigation into vaccines' long-term neurological effects. The CDC and FDA still recommend COVID-19 vaccines.

The speaker discusses issues with RNA vaccines, such as frame shifting and template switching, potentially leading to the production of abnormal proteins. They highlight concerns about mitochondrial sequences in vaccines causing adverse effects in patients. The conversation delves into the risks of amyloidogenic proteins and their ability to trigger a chain reaction of misfolding, leading to serious health implications. The speaker emphasizes the need for further research and vigilance in monitoring potential risks associated with RNA vaccines.

The speaker observed vasculitis, or inflammation of the blood vessels, in the brain tissue of almost all cases examined post-vaccination. Lymphocytes aggregate around small vessels, indicating inflammation possibly triggered by an antigenic structure like spike protein. This was described as one of the most alarming findings. Individuals with this complication may experience transient defects like loss of speech, unconsciousness, or blindness, but the brain can compensate if there is no major inflammation or hemorrhage. The speaker clarified that the individuals did not die from the vasculitis itself. It's possible for vaccinated individuals to experience these symptoms without knowing the underlying cause. Changes in character have been reported in some vaccinated individuals, which may be related to this inflammation.

Protein misfolding is a recent phenomenon in the study of neurodegenerative disorders like Parkinson's and Alzheimer's. Other peptides besides the prion protein can also misfold and form toxic fibrils. Prions have been studied as potential biological warfare agents due to their robustness and toxicity. The transmission of prions is difficult, but recent research suggests that small epitopes on viruses and bacteria may also have amyloidogenic properties. Neuroinvasion and anosmia are independent phenomena caused by SARS-CoV-2 infection, indicating ongoing pathology at a fundamental level. The spike protein of SARS-CoV-2 has been found to cause amyloidogenic clots in the blood, potentially contributing to long-haul symptoms. There are also concerns about the homology between SARS-CoV-2 and HIV, as HIV epitopes have amyloidogenic properties and have been the focus of bioweapon research.

Spike is a toxin that can cross the blood-brain barrier, causing disruption to the brain's blood vessels and leading to inflammation. This inflammation is responsible for the brain fog experienced by both COVID patients and those who have been vaccinated. Despite claims that there have been no deaths or injuries from the vaccine, this is not true. The image shown reveals the presence of inflammation in the brain, indicated by the blue color. This inflammation is a result of the spike toxin.

Truth is out. Scientists are now confirming what many have long suspected. The COVID shots don't just impact your immune system. They can damage your brain and devastate mental health, and the evidence is overwhelming. A recent wave of studies have revealed shocking increases in ischemic strokes up forty four percent, hemorrhagic strokes up fifty percent, transient ischemic strokes or mini strokes up sixty seven percent, myasthenia gravis, a debilitating autoimmune condition up over seventy one percent, Alzheimer's up twenty two percent, cognitive impairment up nearly a hundred and thirty eight percent, depression up over sixty eight percent, anxiety disorders up nearly forty four percent, and sleep disorders up over ninety three percent, all linked to one thing, toxic spike protein accumulation and persistence in the brain. This isn't a conspiracy theory. There's a documented peer reviewed research published studies by documented experts, including by epidemiologist Nicholas Holcher, who says using mRNA to hijack cells in various organ systems to produce a highly toxic spike protein that persists in the body for months or even years was one of the worst ideas in medical history. So what can you do?

Some individuals are experiencing health issues that resemble long COVID, but are actually due to mRNA vaccines. These can include cognitive dysfunction, such as severe word recall problems, and a condition where patients feel suffocated despite normal heart and lung function. This is linked to issues with blood returning to the heart. Autonomic dysfunction is also noted, with some patients unable to sit up without severe symptoms. While these conditions can be serious, they are often reversible over time, potentially driven by residual spike protein from the vaccines. The mRNA vaccines turn the body into a spike protein factory, which raises concerns about their safety. An alternative, the Novavax protein vaccine, provides a controlled amount of spike protein without these risks and should be considered more critically.

Inflammation in the brain from COVID can lead to long-term cognitive issues. The high levels of inflammation seen in even mild cases of COVID worried me about a potential neurological crisis. The rates of lasting cognitive symptoms in COVID survivors are concerning. Effective therapy is crucial to help the millions who may suffer from these symptoms.

White fibrous clots found in the living and dead recipients of mRNA vaccines are being ignored, but research reveals their composition and cause. The spike protein mutates fibrin into jagged, misfolded, insoluble amyloid, similar to prionic infections. Microclots form and align into large white clots, initiated by spike protein fragments like spike 601. Prolene, a "kinker protein" added to the spike protein, causes misfolding, with proline being prevalent in the clots. A 2021 paper showed the SARS CoV-2 spike induces abnormal blood clots due to the fibrinogen beta chain. Plasma exposed to the spike protein is imbalanced, with the fibrinogen beta chain being dominant. These clots contain four times the normal amount of phosphorus, released from lipid nanoparticles. Similar clots in 1988 were caused by sulfur-based heparin, which was resolved by reducing sulfur content. A 2017 paper showed altered phosphorus levels cause cancer. Thomas Havilland, who shares this information, is being ignored by mainstream and alternative media. Undertakers are seeing massive white fibrous clots at record levels.

The speaker asserts that COVID-19 shots do more than affect the immune system; they can damage the brain and worsen mental health. They claim a wave of studies shows sharp increases in various strokes: ischemic strokes up to 44%, hemorrhagic strokes up to 50%, and transient ischemic attacks (mini strokes) up to 67%. They also report increases in neurological and autoimmune conditions, including myasthenia gravis up 71% and Alzheimer’s disease up 22%. Cognitive impairment is claimed to have risen by nearly 138%, while depression is up 68%, anxiety disorders up 44%, and sleep disorders up 93%. The speaker links all of these increases to “toxic spike protein accumulation and persistence in the brain.” The speaker states this is not a conspiracy theory and cites what they describe as documented peer‑reviewed research and studies by experts. They name epidemiologist Nicholas Holcher, who allegedly says that using mRNA to hijack cells in various organ systems to produce a highly toxic spike protein that persists in the body for months or years was “one of the worst ideas in medical history.” The speaker then asks, “So what can you do?” as a transition to presumably recommendations or actions, though no specific actions are listed in the provided segment.

The video discusses the potential adverse effects of the spike protein in SARS-CoV-2 on human prion protein and amyloid fibril formation. The speaker highlights a study showing that spike amyloid fibrils can accelerate the formation of amyloid fibrils associated with prion diseases and Alzheimer's. They also mention recent research suggesting that other viruses, like H5N1 influenza, may impact and misfold prion protein. The speaker emphasizes the importance of understanding these interactions and their potential implications. They briefly mention the symptoms and diagnostic challenges of prion diseases like Creutzfeldt-Jakob disease. Overall, the video explores the role of the spike protein in amyloidosis and its potential impact on neurological tissues.

The spike protein from the COVID-19 virus circulates in the body and can land in multiple organs, causing various diseases. Lab studies have shown that even without the virus, just injecting the spike protein can induce the same lung, vascular, heart, and brain diseases as COVID-19. The spike protein is considered the toxin responsible for causing the disease. This raises questions about why we are injecting something that is essentially a toxin into the human body, as it is not a traditional vaccine.

Speaker 0 asserts that truth is out and that scientists are now confirming long-suspected effects of the COVID-19 shots beyond the immune system, specifically that they can damage the brain and devastate mental health. The claim is that the evidence is overwhelming and that a new wave of studies has revealed significant increases in various neurological and psychiatric conditions, all linked to the presence of toxic spike protein accumulation and persistence in the brain. The summary of claimed study findings includes: - Ischemic strokes: up forty-four percent. - Hemorrhagic strokes: up fifty percent. - Transient ischemic strokes (mini strokes): up sixty-seven percent. - Myasthenia gravis, described as a debilitating autoimmune condition: up over seventy-one percent. - Alzheimer’s disease: up twenty-two percent. - Cognitive impairment: up nearly one hundred and thirty-eight percent. - Depression: up over sixty-eight percent. - Anxiety disorders: up nearly forty-four percent. - Sleep disorders: up over ninety-three percent. Speaker 0 links all of these increases to one cause: toxic spike protein accumulation and persistence in the brain. The statement "This isn't a conspiracy theory" is used to bolster the claim that there is documented peer-reviewed research and published studies supporting these observations. The speaker cites epidemiologist Nicholas Holcher as an example of an expert who has commented on the issue. The quote attributed to Holcher describes using mRNA to hijack cells in various organ systems to produce a highly toxic spike protein that persists in the body for months or even years, and characterizes this approach as one of the worst ideas in medical history. In closing, Speaker 0 poses a question, "So what can you do?" signaling a transition from presenting the alleged findings to offering potential actions or recommendations. The overall message is that COVID-19 vaccines are claimed to cause widespread brain toxicity and mental health problems through persistent spike protein, with purported evidence from peer-reviewed studies and expert commentary cited to support the assertions.

Bonjour à tous, Anaïs Bloqué, docteur en biologie santé, explique les impacts de la protéine Spike du SARS-CoV-2 sur le système immunitaire inné, basés sur son article récent. La Spike seule n'active pas complètement le TLR 4, un récepteur immunitaire, et ne produit pas d'interférons de type 1, essentiels pour la réponse antivirale. Pour une activation complète, la Spike doit s'associer au LPS (des bactéries Gram négatif). L'activation des interférons 1 augmente l'expression d'ACE2, le récepteur du virus, via les ISG, sensibilisant l'organisme à l'infection. Les ARN messagers des vaccins peuvent aussi lancer la production d'interférons 1 via MDA5. La Spike, protéine amyloïde, peut aussi déclencher le TLR 4 avec des fibres amyloïdes, entraînant un "double effet amyloïde". L'augmentation de NF-κB par les ISG peut bloquer la p53, potentiellement cancérigène. De plus, NF-κB induit le MIR-200c, qui bloque l'ACE2. Chez les individus avec comorbidités, une boucle d'amplification inflammatoire se crée : Spike-LPS-TLR4 induit interférons 1, ISG, surexpression d'ACE2, augmentation de NF-κB, MIR-200c, diminution d'ACE2 et augmentation d'angiotensine 2. La Spike persiste longtemps, et ses propriétés amyloïdes font craindre des pathologies dégénératives à long terme. --- Hello everyone, Anaïs Bloqué, PhD in health biology, explains the impacts of the SARS-CoV-2 Spike protein on the innate immune system, based on her recent article. Spike alone does not fully activate TLR 4, an immune receptor, and does not produce type 1 interferons, which are essential for the antiviral response. For complete activation, Spike must associate with LPS (from Gram-negative bacteria). Activation of interferon 1 increases the expression of ACE2, the virus's receptor, via ISGs, sensitizing the body to infection. Vaccine mRNAs can also trigger the production of interferon 1 via MDA5. Spike, an amyloid protein, can also trigger TLR 4 with amyloid fibers, leading to a "double amyloid effect." The increase in NF-κB by ISGs can block p53, which is potentially carcinogenic. In addition, NF-κB induces MIR-200c, which blocks ACE2. In individuals with comorbidities, an inflammatory amplification loop is created: Spike-LPS-TLR4 induces interferon 1, ISG, ACE2 overexpression, increased NF-κB, MIR-200c, decreased ACE2 and increased angiotensin 2. Spike persists for a long time, and its amyloid properties raise concerns about long-term degenerative pathologies.

COVID-19 vaccines have been linked to serious neurological and psychiatric issues, including ischemic and hemorrhagic strokes, transient ischemic attacks, myelitis, myasthenia gravis, Alzheimer's disease, cognitive impairment, depression, anxiety, and sleep disorders. A study of 8 million Italians indicated that vaccinated individuals had a higher incidence of these disorders. Further research in South Korea found increased risks of Alzheimer's and various psychiatric conditions among older adults post-vaccination. The potential cause is the accumulation of toxic spike proteins in the brain. Concerns about vaccine side effects and government accountability persist, especially with ongoing global tensions. Preparedness is emphasized, suggesting the importance of having emergency food supplies for safety and community support.

The speaker believes mRNA vaccines are producing an abnormal spike protein that doesn't enter the membrane, potentially leading to prion problems. Prion proteins misfold into beta sheets in the cytoplasm, forming crystals that attract other proteins and create fibrils like Alzheimer's plaque. The speaker claims the vaccines produce many spike proteins that cannot enter the membrane, increasing the likelihood of becoming problematic prion proteins. This is described as a setup for Parkinson's disease, potentially causing earlier onset or new cases in vaccinated individuals. The speaker suggests annual boosters may accelerate the development of Parkinson's.