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Have you heard of Prion disease?
Over the last two decades there has been a concern among certain scientists that prions could be used as bioweapons. Even though prion diseases do come in slightly different forms, they have a whole lot in common. In each disease, the prion protein (PrP) folds up the wrong way, becoming a prion, and then causes other PrP molecules to do the same. Prions can then spread “silently” across a person’s brain for years without causing any symptoms. Eventually prions start to kill neurons, and once symptoms strike, the person has a very rapid cognitive decline. All known prion diseases are untreatable and fatal.
Analysis of the Pfizer vaccine against COVID-19 identified two potential risk factors for inducing prion disease in humans.
Creutzfeldt-Jakob (KROITS-felt YAH-kobe) disease (CJD) is a degenerative brain disorder that leads to dementia and, ultimately, death. Individuals experience problems with muscle coordination. Personality changes (including impaired memory, judgment, and thinking), and impaired vision. insomnia, Depression, and Unusual sensations.
As the illness progresses, peoples’ mental impairment becomes severe. They often develop involuntary muscle jerks called myoclonus, and they may go blind. They eventually lose the ability to move and speak, and enter a coma. Pneumonia and other infections often occur in these individuals and can lead to death.
Variant CJD begins primarily with psychiatric symptoms, affects younger individuals than other types of CJD, and has a longer than usual duration from onset of symptoms to death. Some symptoms of CJD can be similar to symptoms of other progressive neurological disorders, such as Alzheimer’s and Huntington’s disease. CJD causes unique changes in brain tissue and Causes more rapid deterioration of a person’s abilities than Alzheimer’s disease or most other types of dementia.
More recently there has been a concern that ubiquitous intracellular molecules
could be activated to cause prion disease. This concern originates due to potential for misuse of research data on the mechanisms by which certain RNA binding proteins like TDP-43, FUS and others can be activated to form disease causing prions.
RNA is software. It can be programmed to do ANYTHING. If it is causing prion disease we are in a world of trouble as prion disease is fatal.
Oh... and prion research is funded by several questionable private organizations including the military industrial complex, Bill and Melinda Gates Foundation, and Ellison Medical Foundation
Maybe this is the reason the CDC just put up “Tips on Surviving a Zombie Apocalypse”.
-Chanda Morse
