NEW STUDY: COVID Vaccines Linked to Prion Brain Degeneration Similar to Mad Cow Disease
A new scientific report suggest that there may be potentially fatal risks involved with the experimental mRNA gene therapy vaccines being rushed into the public sphere without any real regulation or long-term safety testing.
The name of the report authored by Dr Greg Nigh is Worse Than the Disease? Reviewing Some Possible Unintended Consequences of the mRNA Vaccines Against COVID-19, which explicitly warns that “the exceptionally rapid movement of these vaccines through controlled trials and into mass deployment raises multiple safety concerns.”
This is what many critics, like former chair of the Council of Europe Health Committee, Dr Wolfgang Wodarg and former Pfizer executive Dr Micheal Yeadon have been warning for months, but instead of engaging with this potentially catastrophic situation, instead governments, corporate media and censorship engineers at YouTube, Facebook, Twitter have all sought to silence any criticism of the current range of experimental vaccines from well-connected pharmaceutical firms.
In the past, an “Emergency Use Authorization” (EUA) would only be for a limited period and only for use in section of the population who is most vulnerable to a disease. But the current EUA regime is being allowed to run indefinitely and for any “top-up vaccines” and is being used to try and vaccination the entire population – regardless of who is health or sick, or at risk or not.
Already, both in the US and also in the UK, vaccine injuries and deaths have far eclipsed anything seen before without a full government recall of the products in question.
Will government regulators admit they were wrong to wave the normal drug regulatory process, and instead capitulating to extreme political and corporate pressure?
The National File reports…
A new review of possible unintended consequences of COVID-19 vaccines suggests that the controversial mRNA vaccines – Moderna and Pfizer – may lead to unexpected neurological conditions similar to Mad Cow Disease.
The review by Stephanie Seneff, who works at the Computer Science and Artificial Intelligence Laboratory at MIT, and Dr. Nigh, who specializes in Naturopathic Oncologogy at Immerson Health in Portland, Oregon, was released this week in the International Journal of Vaccine Theory, Practice, and Research, and devotes a considerable space to discussing the research of Dr. J. Bart Classen, who first published a research paper on the possibility of prion-linked brain degeneration caused by the COVID-19 vaccine last month, and expands on his research.
The researchers explain that “researchers have identified a signature motif linked to susceptibility to misfolding into toxic oligomers, called the glycine zipper motif. It is characterized by a pattern of two glycine residues spaced by three intervening amino acids, represented as GxxxG. The bovine prion linked to MADCOW has a spectacular sequence of ten GxxxGs in a row,” and notes that “the SARS-CoV-2 spike protein is a transmembrane protein, and that it contains five GxxxG motifs in its sequence” and, thus, “it becomes extremely plausible that it could behave as a prion”.
“Recall that the mRNA vaccines are designed with an altered sequence that replaces two adjacent amino acids in the fusion domain with a pair of prolines,” the authors continue. “This is done intentionally in order to force the protein to remain in its open state and make it harder for it to fuse with the membrane. This seems to us like a dangerous step towards misfolding potentially leading to prion disease.”
Prions were first described as the method by which Mad Cow Disease causes brain degeneration due to misfolding proteins in the body. The CDC notes that “prion diseases are usually rapidly progressive and always fatal.” Mad Cow Disease “progressively attacks the brain but can remain dormant for decades,” per the BBC.
“Pfizer claims the RNA fragments ‘likely… will not result in expressed proteins’ due to their assumed rapid degradation in the cell,” the researchers note. They add, “While we are not asserting that non-spike proteins generated from fragmented RNA would be misfolded or otherwise pathological, we believe they would at least contribute to cellular stress that promotes prion-associated conformational changes in the spike protein that is present.”
Continue this story at the National File
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