mRNA and Prion Diseases
dark days ahead
Greetings fellow Plebs & Peasants,
At the risk of coming across as one of the doom peddlers I have nothing but disdain for, I don’t think I can sit on this anymore. We are in dark times, an unprecedented situation of a highly coordinated biological and chemical war being waged by all governments of the world against the people, and if you still cannot come to terms with that, please catch up. This is not a failed medical product, and it doesn’t take a tin foil hat to see that. And if we want to win this war, we need to first acknowledge we are at war.
I first became aware of the potential for prion related diseases resulting from the covid injections early 2021 (here, here). Ok sounds bad, but as I wasn’t getting the jab, wasn’t my biggest concern. And it was still while a lot of the effects were still being figured out so it was a wait and see type situation for me. Well, a few months later, saw the first report (to my knowledge) of a woman dying from one of the prions diseases three months after her shot, which coincidentally times perfectly with the first reports of it being possible. Ok so that’s bad, but its only one person so not really something to lose sleep over yet. Well fast forward to late last year and fell head first into a whole new rabbit hole within the biowarfare rabbit hole, which lead me to the Dr. Kevin McCairn, the man discussed in the articles below. I see no reason to doubt there is prion risk in the injected. I’ve watched enough discussions on this over the past few months to feel pretty sure of that. The open question that Dr. McCairn is trying to figure out is was this actually the intent of the bioweapon (covid injection), or just an unfortunate side effect. So, I know there is a lot here with all the included videos and reference links, but please take the time and if you see merit to the arguments, please share. This needs more exposure. Very, very few are talking about it.
- jw
#donotcomply #nocompromise #nosurrender #gallowsandguillotines2024
also from 2021:
Source: Mercola
Doctors Predict Epidemic of Prion Brain Diseases
Analysis by Dr. Joseph Mercola
April 29, 2024
Story at-a-glance
Mounting research suggests a serious side effect of the COVID mRNA jabs could be dementia, and the prions that cause it may be contagious
Frameshifting, as we now know occurs in the COVID shots, can induce prion production and lead to neurodegenerative diseases such as Alzheimer’s and Creutzfeldt-Jakob disease (CJD)
Sid Belzberg's prions.rip website, which collected data on neurological side effects post-jab, found a notably high incidence of diagnosed CJD cases, suggesting an alarming trend
A series of articles highlight biases in clinical trials and observational studies, suggesting COVID-19 vaccines' safety and effectiveness have been massively overstated
The Global COVID Vaccine Safety Project study — funded by the U.S. Centers for Disease Control and Prevention — reveals significant side effects, including myocarditis, pericarditis, and blood clots, underscoring the need for reevaluation of COVID vaccine risks and benefits
According to mounting data, one of the more serious side effects of the COVID mRNA jabs appears to be dementia, and worse yet, this previously untransmissible disease may now be “contagious,” transmissible by way of prions.
In my 2021 interview with Stephanie Seneff, Ph.D., she explained why she suspected the COVID shots may eventually result in an avalanche of neurological prion-based diseases such as Alzheimer’s. She also published a paper detailing those mechanisms in the May 10, 2021, issue of the International Journal of Vaccine Theory. As she explained in that paper:1
“A paper published by J. Bart Classen (2021) proposed that the spike protein in the mRNA vaccines could cause prion-like diseases, in part through its ability to bind to many known proteins and induce their misfolding into potential prions.
Idrees and Kumar (2021) have proposed that the spike protein’s S1 component is prone to act as a functional amyloid and form toxic aggregates ... and can ultimately lead to neurodegeneration.”
In summary, the take-home from Seneff’s paper is that the COVID shots, offered to hundreds of millions of people, are instruction sets for your body to make a toxic protein that will eventually wind up concentrated in your spleen, from where prion-like protein instructions will be sent out, leading to neurodegenerative diseases.
What Are Prions?
The term "prion" derives from "proteinaceous infectious particle." Prions are known to cause a variety of neurodegenerative diseases in animals and humans, such as Creutzfeldt-Jakob disease (CJD) in humans, bovine spongiform encephalopathy (BSE or "mad cow disease") in cattle, and chronic wasting disease in deer and elk.
These diseases are collectively referred to as transmissible spongiform encephalopathies (TSEs). They’re characterized by long incubation periods, brain damage, the formation of holes in the brain giving it a sponge-like appearance, and failure to induce an inflammatory response.
Infectious prions propagate by transmitting their misfolded protein state to normal variants of the same protein.
In short, prions are infectious agents composed entirely of a protein material that can fold in multiple, structurally distinct ways, at least one of which is transmissible to other prion proteins, leading to a disease that is similar to viral infections but without nucleic acids.
Unlike bacteria, viruses, and fungi, which contain nucleic acids (DNA or RNA) that instruct their replication, prions propagate by transmitting their misfolded protein state to normal variants of the same protein.
According to the prion disease model, the infectious properties of prions are due to the ability of the abnormal protein to convert the normal version of the protein into the misfolded form, thereby setting off a chain reaction that progressively damages the nervous system.
Prions are remarkably resistant to conventional methods of sterilization and can survive extreme conditions that would normally destroy nucleic acids or other pathogens, which is part of why prion diseases are so difficult to treat.
More Evidence mRNA Shots Can Trigger Dementia
Today, there’s even more evidence to support Seneff’s theory. In August 2022, tech entrepreneur Sid Belzberg wrote2 about prions.rip, a website he’d set up to collect data on the neurological side effects of the jabs. (This site is no longer live.)
Within a few months, the site had received about 15,000 hits and gathered 60 reports from people who got the jab and suffered neurological deficits shortly thereafter, including six cases of diagnosed CJD.
“Normally this disease affects 1 in a 1,000,000 people,” Belzberg wrote.3 “To get 6 cases you would need 6,000,000 hits to the site assuming everyone reports. The chances of getting 1 case in 15,000 hits is 1 in 66. To see 6 cases in 1 group of 15,000 is 1/66^6 or 1 in 82,000,000,000, or 20 times more likely to win a Powerball lottery! ...
To reiterate, CJD is an exceptionally rare disease that is now a known and established severe adverse reaction (SAE) from the DEATHVAX™. Injecting this slow kill bioweapon can cause ailments that are about as likely to develop in the real word as getting struck by lightning twice. The proof is now irrefutable.”
Frameshifting Can Result in Prion Production
In mid-December 2023, researchers reported4,5,6 that the replacing of uracil with synthetic methylpseudouridine in the COVID shots — a process known as codon optimization — can cause frameshifting, a glitch in the decoding, thereby triggering the production of off-target aberrant proteins.
The antibodies that develop as a result may, in turn, trigger off-target immune reactions. According to the authors, off-target cellular immune responses occur in 25% to 30% of people who have received the COVID shot. But that’s not all.
According to British neuroscientist Dr. Kevin McCairn, this frameshifting phenomenon has also been linked to harmful prion production — and that frame shifted prions, specifically, are infectious and can be transmitted from one person to another. As reported in the Journal of Theoretical Biology in 2013:7
“A quantitatively consistent explanation for the titres of infectivity found in a variety of prion-containing preparations is provided on the basis that the etiological agents of transmissible spongiform encephalopathy comprise a very small population fraction of prion protein (PrP) variants, which contain frameshifted elements in their N-terminal octapeptide-repeat regions ...
Frameshifting accounts quantitatively for the etiology of prion disease. One per million frameshifted prions may be enough to cause disease. The HIV TAR-like element in the PRNP mRNA is likely an effector of frameshifting.”
McCairn explained this mechanism in a February 19, 2023, interview with Health Alliance Australia (video above). In it, he noted:
“Mis-folded proteins caused by prions can impact every level organ and tissue system in the body ... [They] bioaccumulate and are resistant to degradation, thereby building up ...”
Prions may in fact be the primary molecule that is being “shed” by COVID jab recipients, and if those prions are due to frameshifting, that could be very bad news indeed, considering their implication in dementia.
Another doctor who believes we’ll be facing an “epidemic of prion disease” is Dr. David Cartland. In late February 2024, he posted8 13 scientific papers linking the COVID jabs, prion diseases and CJD, noting that was just a “small selection” of what’s available in the medical literature.
Prions Implicated in Long COVID as Well
According to genomics expert Kevin McKernan, Ph.D., prions are also involved in long COVID (or as McKernan calls it, “long vax”).9 In one 2024 study,10 96.7% of long COVID sufferers had received the jab. In an interview with the Front Line COVID-19 Critical Care Alliance (FLCCC), McKernan stated:11
“If you frameshift over the stop codons, you’re going to be making proteins that are spike-mito proteins. When I talk to a lot of the long vax patients I hear of all these things that remind me of my time in the mitochondrial disease sequencing space ...”
McKernan claims he tried to publish a paper on this in 2021 with Dr. Peter McCullough, but the editor of the journal “stepped in and torpedoed the paper.”12
World’s Largest Side Effect Analysis Has Been Published
In related news, the largest study13 to date on the side effects of the COVID jabs was published in the journal Vaccine in February 12, 2024, and it confirms what I and many other alternative news sources have been saying all along, namely that the mRNA jabs are the most dangerous medical products to ever hit the market.
The study — performed by the Global COVID Vaccine Safety (GCoVS) Project and funded by the U.S. Centers for Disease Control and Prevention, Public Health Ontario and the Canadian Health Research Institute — evaluated the risk of "adverse events of special interest" (AESI) following COVID-19 “vaccination.”
Data from 10 sites in eight countries (Argentina, Australia, Canada, Denmark, Finland, France, New Zealand and Scotland) were included, encompassing more than 99 million jabbed individuals.
Of the thousands of side effects Pfizer listed in its confidential report of post-authorization adverse events submitted to the U.S. Food and Drug Administration,14 the GCoVS focused on 13 AESIs that fall into three primary categories: Neurological, hematologic (blood-related) and cardiovascular conditions.
They calculated the AESI risk for each of the 13 AESIs based on the number of observed versus expected (OE) incidents occurring up to 42 days after injection. The “expected” number of side effects were based on vaccine adverse event data from 2015 to 2019. These rates were then compared to the adverse event rates observed in those who got one or more of the COVID jabs, either Pfizer's BNT162b2, Moderna's mRNA-1273, or AstraZeneca's ChAdOx1.
Largest Study to Date Confirms COVID Jab Dangers
The analysis15 revealed several concerning side effects, including increased risks of myocarditis, pericarditis, blood clots in the brain, and various neurological conditions. Here’s a quick summary of the findings:
• Myocarditis and pericarditis:
◦ Pfizer vaccine — OE ratios for myocarditis were 2.78 and 2.86 after the first and second shots, with the risk remaining doubled after the third and fourth shots.
◦ Moderna vaccine — OE ratios for myocarditis were 3.48 and 6.10 after the first and second shots. Doses 1 and 4 also showed OE ratios of 1.74 and 2.64 for pericarditis.
◦ AstraZeneca vaccine — OE ratio for pericarditis was 6.91 after the third shot.
• Blood clots in the brain (cerebral venous sinus thrombosis, CVST):
◦ An OE of 3.23 for CVST was observed after the first AstraZeneca shot.
◦ A significant increase in CVST risk was also noted after the second Pfizer dose.
• Neurological conditions:
◦ Guillain-Barré syndrome — An OE ratio of 2.49 was observed following the AstraZeneca jab.
◦ Transverse myelitis — Risk nearly doubled with the AstraZeneca shot.
◦ Acute disseminated encephalomyelitis — OE ratios of 3.78 (Moderna) and 2.23 (AstraZeneca) were noted.
These findings really underscore the potential for serious side effects from the COVID shots, including conditions that may lead to other consequences in the longer term, such as stroke, heart attack, paralysis and death.
Effectiveness and Safety Was Wildly Exaggerated in Trials
Considering those findings, it’s no surprise to find that effectiveness and safety were exaggerated in clinical trials and observational studies. In a guest post on Dr. Robert Malone’s Substack, Raphael Lataster, Ph.D., writes:16
“An unofficial series of four crucially important medical journal articles, two by me, appearing in major academic publisher Wiley’s Journal of Evaluation in Clinical Practice reveals that claims made about COVID-19 vaccines’ effectiveness and safety were exaggerated in the clinical trials and observational studies, which significantly impacts risk-benefit analyses.
Also discussed are the concerning topics of myocarditis, with evidence indicating that this one adverse effect alone means that the risks outweigh the benefits in the young and healthy; and perceived negative effectiveness, which indicates that the vaccines increase the chance of COVID-19 infection/hospitalization/death, to say nothing about other adverse effects.”
Summary of Papers
The four papers in question include:
1. “Sources of Bias in Observational Studies of COVID-19 Vaccine Effectiveness” published in the Journal of Evaluation in Clinical Practice in March 2023, co-authored by BMJ editor Peter Doshi, Ph.D., statistician Kaiser Fung and biostatistician Mark Jones, which concluded that “case-counting window bias” had a significant effect on effectiveness estimates.17
As explained by Lataster, this “concerns the 7 days, 14 days, or even 21 days after the jab where we are meant to overlook jab-related issues, such as COVID infections, for some odd reason as ‘the vaccine has not had sufficient time to stimulate the immune system.’
This may strike you as quite bizarre since all of the ‘fully vaccinated’ must go through the process of being ‘partially vaccinated,’ sometimes even more than once. To make matters worse, the unvaccinated do not get such a ‘grace period,’ meaning that there is also a clear bias at play.
In an example using data from Pfizer’s clinical trial, the authors show that thanks to this bias, a vaccine with effectiveness of 0%, which is confirmed in the hypothetical clinical trial, could be seen in observational studies as having effectiveness of 48%.”
2. “Reply to Fung et. al. on COVID-19 Vaccine Case-Counting Window Biases Overstating Vaccine Effectiveness,” authored by Lataster, which discussed how the counting window bias not only affected effectiveness estimates in observational studies but also safety estimates, suggesting a need for reassessment of vaccine safety.18 The article also addresses “the mysterious rise in non-COVID excess deaths post-pandemic.”19
3. “How the Case Counting Window Affected Vaccine Efficacy Calculations in Randomized Trials of COVID-19 Vaccines,” again co-authored by Doshi and Fung, which detailed how case-counting window issues also overestimated effectiveness in Pfizer and Moderna clinical trials.20
4. A second article by Lataster, in which he highlighted and summarized the evidence showing that clinical trials were affected by adverse effect counting window issues that led to exaggerated safety estimates.21
“Together, these four articles make clear that claims made about COVID-19 vaccines; effectiveness and safety were exaggerated in the clinical trials and observational studies, whilst also finding time to discuss myocarditis and perceived negative effectiveness, meaning that new analyses are very much needed,” Lataster writes.22
Resources for Those Injured by the COVID Jab
Based on data from across the world, it’s beyond clear that the COVID shots are the most dangerous drugs ever deployed. If you already got one or more COVID jabs and are now reconsidering, you’d be wise to avoid all vaccines from here on, as you need to end the assault on your body. Even if you haven’t experienced any obvious side effects, your health may still be impacted long-term, so don’t take any more shots.
If you’re suffering from side effects, your first order of business is to eliminate the spike protein — and/or any aberrant off-target protein — that your body is producing. Two remedies shown to bind to and facilitate the removal of SARS-CoV-2 spike protein are hydroxychloroquine and ivermectin. I don’t know if these drugs will work on off-target proteins and nanolipid accumulation as well, but it probably wouldn’t hurt to try.
The Front Line COVID-19 Critical Care Alliance (FLCCC) has developed a post-vaccine treatment protocol called I-RECOVER. Since the protocol is continuously updated as more data become available, your best bet is to download the latest version straight from the FLCCC website at covid19criticalcare.com.23
For additional suggestions, check out the World Council for Health’s spike protein detox guide,24 which focuses on natural substances like herbs, supplements and teas. Sauna therapy can also help eliminate toxic and misfolded proteins by stimulating autophagy.
Sources and References
1 International Journal of Vaccine Theory, Practice and Research May 10, 2021; 2(1): 402-444
9, 11, 12 LifeSite News March 4, 2024
16, 19, 22 RW Malone MD Substack March 6, 2024
17 Journal of Evaluation in Clinical Practice March 26, 2023; 30(1): 30-36
18 Journal of Evaluation in Clinical Practice July 4, 2023; 30(1): 82-85
20 Journal of Evaluation in Clinical Practice July 15, 2023; 30(1): 105-106
21 Journal of Evaluation in Clinical Practice January 18, 2024
24 World Council for Health Spike Protein Detox Guide November 30, 2021
Source: Health Alliance Australia
The silent disaster of bio-warfare prions infecting humanity
If the spike protein of both the infection and the jab is an engineered prion, a result of bio-warfare research and development then this has grave implications for humanity because these weaponized prions are far more dangerous than viruses. The most commonly known prion disease is CJD or Creutzfeldt-Jakob disease, which is a spongiform encephalopathy where the brain becomes spongy, wastes away and ultimately leads to a horrible death. Alzheimer’s and Parkinson’s are other neurodegenerative diseases associated with prions.
Prions means proteinaceous, infectious particles; substances that lack nucleic acids and that stick together and form cascades. Prions are said to be in the border zone between nonliving and living things because they have no need to metabolize or the capacity to reproduce but they are capable of replication within the body of a human or of some mammals. Prions according to medical science survive heat, can travel through the stomach to the brain and once someone is infected, leads to protein mis-folding and accumulate in the body. Treatment of prion diseases remains supportive; no specific therapy has been shown to stop the progression of these diseases.
History of spike protein prion
The SARS-cov-2 spike protein is an engineered prion like incapacitating agent that causes proteins to mis-fold, otherwise known as amyloidosis. In early 2020, Dr Kevin McCairn, a systems neuroscientist of the Principal Investigator at Korea Brain Research Institute – Systems Neuroscience and Movement Disorders Laboratory raised the alarm on prion disease associated with SARS-cov-2 infection, that was the result of biological warfare research.
In this episode he discusses how there was a co-ordinated effort from the very beginning of the Wuhan outbreak, at the highest levels of NIH to suppress the priogenic nature of SARS-cov-2. He reveals that mRNA technology used in the COVID jabs causes frame shifting that leads to prions being produced, and transfected and as a result of prions being released into the environment, we now have a situation where these lab engineered toxins are being absorbed by living things, potentially leading to a host of disease from neurological to heart disease and cancer in anyone infected. He discusses mRNA technology and how recent published research has revealed that mRNA jabs can lead to frame shifting of the DNA but also the formation of harmful pathogenic proteins. This finding is significant and concerning.
Prion disease explains the mechanism for phenomena of “silent hypoxia”, the formation of fibrous, white clots, the sudden deaths of athletes, turbo CJD, turbo cancer, amyloidosis, neurological diseases, long covid being brain inflammation.
A paper released and withdrawn on SARS-cov-2 in early 2020 called, “Uncanny similarity of unique inserts in the 2019-nCoV spike protein to HIV-1 gp120 and Gag describes prions” can be found https://www.biorxiv.org/content/10.1101/2020.01.30.927871V1.full
“Our results highlight an astonishing relation between the gp120 and Gag protein of HIV, with 2019-nCoV spike glycoprotein. These proteins are critical for the viruses to identify and latch on to their host cells and for viral assembly (Beniac et al., 2006). Since surface proteins are responsible for host tropism, changes in these proteins imply a change in host specificity of the virus. According to reports from China, there has been a gain of host specificity in case 2019-nCoV as the virus was originally known to infect animals and not humans but after the mutations, it has gained tropism to humans as well.
This paper published on 30th January 2020 is incredibly indicative of the cover-up that is only recently making it’s way into the political sphere.
and it’s taken several years for the coverup to be exposed. Listen to the recent talk by Senator Rand Paul on the COVID Cover-up, he reveals many details of the coverup in early 2020. We also know they were desperate to conceal the lab origins because it would link back bioweapons research, which in America is punishable by lifetime imprisonment under the S.993 – Biological Weapons Anti-Terrorism Act of 1989. See our interview with Professor Francis Boyle.
Recent research
In December 2023, researchers from Oxford showed that 8 percent of the time, the body does not make spike protein from Pfizer mRNA vaccines but may form aberrant proteins instead. This has led researchers to investigate the potential risks of such unintentional formations. Subsequently, on Jan. 12, retired French bio-mathematician Jean-Claude Perez published a preprint study discussing whether such mistakes could lead to the formation of prion-like proteins. He concluded that prion-like protein formation is possible.
A previous peer-reviewed paper by Mr. Perez and his co-authors in January 2023 recorded 26 cases of CJD. Those afflicted reported that their first symptoms manifested within one to 31 days of their last COVID-19 vaccination or infection. All patients experienced a rapid worsening of their condition over the ensuing months and died. (Source https://www.theepochtimes.com/health/mrna-vaccines-contain-prion-region-may-be-linked-to-prion-like-diseases-5573131 )
From the recent paper published by Jean Claude Perez, January 2024
“In COVID-19 mRNA vaccines, natural uracil bases are replaced with modified pseudouracil. This study investigates the potential consequences of this modification on protein synthesis. Occasionally, ribosomes may overlook these modified bases, leading to a shift in the reading frame of the genetic code. We examine the spike protein in the context of these shifted reading frames and identify the resulting proteins. Our analysis focuses on the potential formation of prion-like or amyloidogenic proteins due to this frame-shifting process”
He goes on to say, that the emergence of these proteins, suggest a possible link between the vaccines mRNA technology and it’s unintended consequences. The output according to the author, pinpointed both the “unknown proteins but also the presence of the potential prion region.” It is a problematic, troubling observation should it be accurate, given the inherent risks linked to prion diseases, and the implication for neurological health.” Also does the use of pseudouridine in the mRNA vaccines, which were delivered at a massive scale raise the prospect of a “broad impact of any unintended protein creation across different vaccine batches and formations?”
This is a huge finding that the “jabs” are releasing prions that lead to disease not just in the recipient but also contaminate the environment and ability to transfect other people.
In our interview with Dr Kevin McCairn he says, “Misfolded proteins caused by prions can impact every level organ and tissue system in the body, bioaccumulate and are resistant to degradation, thereby building up in the environment, is that we do not need the like for like peptide to cause the misfolding in the next one, for the cascade to occur, in this instance we have cross seeding epitomes, that no longer need the whole protein, only certain segments to be digested and released to then come into susceptible proteins in the body, to misfold and then the process starts a chain reaction.” We also discuss the staged assault on humanity, potential treatments, evolutionary pressure, and where the road may lead.
Dr McCairn cautions that we are in a “highly controlled, information eco-system”, where there is censorship, narrative and counter narrative control, behavioral control and advanced neuro-psychological techniques. He has been highly censored and had to restart his social media accounts.
Links to Dr Kevin McCairn’s work and profile
https://www.researchgate.net/profile/Kevin-Mccairn
https://neurotree.org/beta/publications.php?pid=22671
https://loop.frontiersin.org/people/78255/overview
https://www.linkedin.com/in/dr-kevin-mccairn-phd-619b411a/?originalSubdomain=uk
https://twitter.com/NestCommander
COVID-19 RNA Based Vaccines and the Risk of Prion Disease
J. Bart Classen, MD
ABSTRACT
Development of new vaccine technology has been plagued with problems in the past. The current RNA based SARS-CoV-2 vaccines were approved in the US using an emergency order without extensive long term safety testing. In this paper the Pfizer COVID-19 vaccine was evaluated for the potential to induce prion-based disease in vaccine recipients. The RNA sequence of the vaccine as well as the spike protein target interaction were analyzed for the potential to convert intracellular RNA binding proteins TAR DNA binding protein (TDP-43) and Fused in Sarcoma (FUS) into their pathologic prion conformations. The results indicate that the vaccine RNA has specific sequences that may induce TDP-43 and FUS to fold into their pathologic prion confirmations. In the current analysis a total of sixteen UG tandem repeats (ΨGΨG) were identified and additional UG (ΨG) rich sequences were identified. Two GGΨA sequences were found. Potential G Quadruplex sequences are possibly present but a more sophisticated computer program is needed to verify these. Furthermore, the spike protein, created by the translation of the vaccine RNA, binds angiotensin converting enzyme 2 (ACE2), a zinc containing enzyme. This interaction has the potential to increase intracellular zinc. Zinc ions have been shown to cause the transformation of TDP-43 to its pathologic prion configuration. The folding of TDP-43 and FUS into their pathologic prion confirmations is known to cause ALS, front temporal lobar degeneration, Alzheimer’s disease and other neurological degenerative diseases. The enclosed finding as well as additional potential risks leads the author to believe that regulatory approval of the RNA based vaccines for SARS-CoV-2 was premature and that the vaccine may cause much more harm than benefit.
A Potential Role of the Spike Protein in Neurodegenerative Diseases: A Narrative Review
Stephanie Seneff, Anthony M Kyriakopoulos, Greg Nigh, and Peter A McCullough
Abstract
Human prion protein and prion-like protein misfolding are widely recognized as playing a causal role in many neurodegenerative diseases. Based on in vitro and in vivo experimental evidence relating to prion and prion-like disease, we extrapolate from the compelling evidence that the spike glycoprotein of SARS-CoV-2 contains extended amino acid sequences characteristic of a prion-like protein to infer its potential to cause neurodegenerative disease. We propose that vaccine-induced spike protein synthesis can facilitate the accumulation of toxic prion-like fibrils in neurons. We outline various pathways through which these proteins could be expected to distribute throughout the body. We review both cellular pathologies and the expression of disease that could become more frequent in those who have undergone mRNA vaccination. Specifically, we describe the spike protein’s contributions, via its prion-like properties, to neuroinflammation and neurodegenerative diseases; to clotting disorders within the vasculature; to further disease risk due to suppressed prion protein regulation in the context of widely prevalent insulin resistance; and to other health complications. We explain why these prion-like characteristics are more relevant to vaccine-related mRNA-induced spike proteins than natural infection with SARS-CoV-2. We note with an optimism an apparent loss of prion-like properties among the current Omicron variants. We acknowledge that the chain of pathological events described throughout this paper is only hypothetical and not yet verified. We also acknowledge that the evidence we usher in, while grounded in the research literature, is currently largely circumstantial, not direct. Finally, we describe the implications of our findings for the general public, and we briefly discuss public health recommendations we feel need urgent consideration.
Worse Than the Disease? Reviewing Some Possible Unintended Consequences of the mRNA Vaccines Against COVID-19
Stephanie Seneff and Greg Nigh
ABSTRACT
Operation Warp Speed brought to market in the United States two mRNA vaccines, produced by Pfizer and Moderna. Interim data suggested high efficacy for both of these vaccines, which helped legitimize Emergency Use Authorization (EUA) by the FDA. However, the exceptionally rapid movement of these vaccines through controlled trials and into mass deployment raises multiple safety concerns. In this review we first describe the technology underlying these vaccines in detail. We then review both components of and the intended biological response to these vaccines, including production of the spike protein itself, and their potential relationship to a wide range of both acute and long-term induced pathologies, such as blood disorders, neurodegenerative diseases and autoimmune diseases. Among these potential induced pathologies, we discuss the relevance of prion-protein-related amino acid sequences within the spike protein. We also present a brief review of studies supporting the potential for spike protein “shedding”, transmission of the protein from a vaccinated to an unvaccinated person, resulting in symptoms induced in the latter. We finish by addressing a common point of debate, namely, whether or not these vaccines could modify the DNA of those receiving the vaccination. While there are no studies demonstrating definitively that this is happening, we provide a plausible scenario, supported by previously established pathways for transformation and transport of genetic material, whereby injected mRNA could ultimately be incorporated into germ cell DNA for transgenerational transmission. We conclude with our recommendations regarding surveillance that will help to clarify the long-term effects of these experimental drugs and allow us to better assess the true risk/benefit ratio of these novel technologies.
related:
Coronavirus Contains "HIV Insertions", Stoking Fears Over Artificially Created Bioweapon
Could certain COVID-19 vaccines leave people more vulnerable to the AIDS virus?
Daily briefing: Australian COVID vaccine trial abandoned after HIV ‘false positives’
Researchers Warn COVID-19 Vaccines May Cause HIV Infection
Possible false-positive HIV test results in persons vaccinated against Sars-CoV-2 virus?
Increase in False-Positive Fourth-Generation Human Immunodeficiency Virus Tests in Patients With Coronavirus Disease 2019
Quercetin Disaggregates Prion Fibrils and Decreases Fibril-Induced Cytotoxicity and Oxidative Stress
Neurodegenerative Disease Linked to FUS Protein Aggregates’ Prion-like Mechanism
Canada releases 70-year-old document that accuses U.S. of genocide, biological warfare during Korean War
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