Are prions, a biotechnological weapon, the secret genocidal component of the Covid-19 vaccines?
Prions are unprecedented infectious pathogens that cause a group of deadly neurodegenerative diseases by a novel mechanism. They are transmissible particles that lack nucleic acid. Due to their unique characteristics, prions emerge as a potential danger as they can be used in the development of such weapons. They cause deadly infectious diseases, and to date there is no therapeutic or prophylactic approach against these diseases. In addition, they are resistant to food preparation treatments, such as intense heat, and can pass from the digestive system to the nervous system; recombinant prions are infectious, either bound to soil particles or in aerosols. Therefore, lethal Prions can be developed by malicious researchers who could use them to attack political enemies since such weapons cause disease beyond suspicion.
“Development of new vaccine technology has been plagued with problems in the past. The current RNA based SARSCoV-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.”
Also, Dr. Tenpenny Explains In Simple Terms Some Of The Dangers of The Covid-19 “Vaccine”
“It takes at least 6 weeks from the time you get your injection for the spike antibody to start to develop. So, somewhere between 3 months and quite frankly 20 years. The immunologist I spoke to said that over the next 10 years we are going to see this go on in perpetuity, because it can take anywhere from 2 years to 19 years to get full blown auto-immune disease. I think we will see massive injuries and a lot more deaths starting somewhere between 4 and 18 months from now. This Vaccine will permanently alter your immune system.”