Scientific research now shows that the Covid-19 vaccines will bring about an avalanche of neurological diseases.
The COVID-19 vaccinations were discussed in an interview by Dr. Joseph Mercola, the founder of Mercola.com and an osteopathic physician, best-selling author, and recipient of multiple awards in the field of natural health, with Stephanie Seneff, Ph.D., a distinguished research scientist at MIT for more than 50 years. Since 2008, glyphosate and sulphur have been her main areas of interest. However, in the past year, she has delved deeply into the science behind these innovative injections and has just released an excellent paper on the subject.
She says: “To have developed this incredibly new technology so quickly, and to skip so many steps in the process of evaluating [its safety], it’s an insanely reckless thing that they’ve done. My instinct was that this is bad, and I needed to know [the truth]. So, I really dug into the research literature by the people who’ve developed these vaccines, and then more extensive research literature around those topics. And I don’t see how these vaccines can possibly be doing anything good. When you weigh the good against the bad, I can’t see how they could possibly be winning, from what I’ve seen.”
According to Seneff, significant death toll will rise in months and years to come. Seneff cites research and statistics from months into the vaccine program that shows deaths are 14.6 times more common in persons over 60 over the first 14 days following the initial COVID injection as compared to those who aren’t vaccinated.
Currently, hundreds of millions of people have received vaccinations all around the world. She said that it is alarming to note that while sudden death is one obvious side effect, most adverse effects won’t be understood for at least ten years. She thus predicted that in the next 10 to 15 years, we are likely to see spikes in prion diseases, autoimmune diseases, neurodegenerative diseases at younger ages, and blood disorders such as blood clots, haemorrhaging, stroke, and heart failure.
In her paper, Seneff describes key characteristics of the SARS-CoV-2 spike protein that suggests it’s a prion and why are we to expect long-term neurological damage to the vaccinated:
“Neurological symptoms associated with COVID-19, such as headache, nausea and dizziness, encephalitis and fatal brain blood clots are all indicators of damaging viral effects on the brain. Buzhdygan et al. (2020) proposed that primary human brain microvascular endothelial cells could cause these symptoms …
In an in vitro study of the blood-brain barrier, the S1 component of the spike protein promoted loss of barrier integrity, suggesting that the spike protein acting alone triggers a pro-inflammatory response in brain endothelial cells, which could explain the neurological consequences of the disease.
The implications of this observation are disturbing because the mRNA vaccines induce synthesis of the spike protein, which could theoretically act in a similar way to harm the brain. The spike protein generated endogenously by the vaccine could also negatively impact the male testes, as the ACE2 receptor is highly expressed in Leydig cells in the testes …
Prion diseases are a collection of neurodegenerative diseases that are induced through the misfolding of important bodily proteins, which form toxic oligomers that eventually precipitate out as fibrils causing widespread damage to neurons …
Furthermore, researchers have identified a signature motif linked to susceptibility to misfolding into toxic oligomers, called the glycine zipper motif… Prion proteins become toxic when the α-helices misfold as β-sheets, and the protein is then impaired in its ability to enter the membrane.”
In conclusion, the lesson to be learned from this is that COVID-19 vaccines, which are given to hundreds of millions of people, are blueprints for your body to create a toxic protein that will eventually concentrate in your spleen, from which prion-like protein instructions will be sent out, resulting in neurodegenerative diseases.
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The synthetic mRNA contains a substitution of the nucleotide uracil with the synthetic version called methylpseudouracil. The synthetec substitution is more resistant to enzyme degredation and can result in misfolded proteins, resulting in lethal prion disease that can result in sudden adult death syndrome.
The synthetic mRNA produces a spike protein that contains 2 extra proline molecules that do not exist in the viral spike protein. The proline molecules attach to H2 receptors, where the misfolded proteins fail to enter the cell membrane and instead block the H2 receptors.
The synthetic spike protein peptides that escape the cellular membrane attachment are subsequently attacked by the body. Neutrophilic elastase, an enzyme used to degrade bacteria and necrotic host tissue, is deployed to fight the invading peptide army.
Once the spike 1 protein peptides are cleaved into smaller molecules, those toxic protein particles then concentrate in the arteries and veins, resulting in these strange, white, amyloid-like plaques that are being pulled out of sudden adult death cadavers.
This is my literature review research and if the calculations play out, there will be an average of 27,000 American deaths, everyday, for the next five years before this tragedy is fully understood.