Posted on 04/19/2024 6:44:22 AM PDT by Paul46360
[Yeah, I’m not into squirrel brains- but have eaten the tree rats before- they are tough, and not very palatable- although they get pretty tender is pressure cooker. Not real crazy about the flavor though, but might be good pressure cooked then made into a stew.]
Possible, but hard to believe certain as the headline suggests. There are about 350 cases a year of Creutzfeldt Jakob Disease. It can be diagnosed and confirmed after death. Chronic Wasting Disease can also be diagnosed after death. That's how various DNRs monitor it's spread. It's hard to believe they couldn't test the deceased's brains.
Another cover story for the death jab.
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Prion diseases are no joke
The people ‘in charge’ don’t know what a prion is...
https://jessicar.substack.com/p/prion-diseases-are-no-joke
UPDATE JUNE 7, 2022: there are 42 reports of Creutzfeldt-Jakob disease in VAERS now.
UPDATE JAN 1, 2022: there are 24 reports of Creutzfeldt-Jakob disease in VAERS now.
Luc Montagnier claims to have detected five cases of prion disease in young and healthy people in temporal proximity to COVID-19 injectable product administration. I stand behind his claim.
There are, in fact, 6 cases of Creutzfeldt-Jakob disease reports in VAERS as we speak (write).
The first report was filed in February and the onset occurred within 2 days of the injection. The latest report was filed on June 1st, 2021 and the individual was dead within 6 months of the injection on January 27th, 2021.
Prion diseases manifest in the presence of prions that cause normal proteins to fold abnormally and thus destroys their normal function. Creutzfeldt-Jakob disease (CJD) is a type of prion disease. In the case of CJD, otherwise known as subacute spongiform encephalopathy or neurocognitive disorder, this happens in the brain. Death from a prion disease usually occurs within a year.
Prion diseases are rare with 300 cases reported in the U.S. per year,2 so the fact that there are 6 reports in VAERS in the context of the COVID-19 products may, or may not, be very telling. Time will tell. The average age of the individuals who filed VAERS reports is 67. Sporadic CJD tends to develop later in life, usually around age 603 so this might actually represent 6/300 individuals who might have succumbed to CJD anyway. But… might? Who wants to make a decision so big on a ‘might’ in the context of an exceedingly curable disease like COVID-19?
Human-created prion disease outbreak has happened before. A CJD health scandal occurred in France in the early 1980s where 120 children died from CJD following receipt of an injection of pituitaries harvested from elderly people in a retirement home.”4 So it’s not unfathomable that these products are the reason for the CJD occurrences due to lack of true safety monitoring along the development pathway.
My personal opinion with regards to prion diseases is that they are scarier than anything. Scarier than Ebola. Way scarier. Impairment of normal functioning of necessary proteins is equivalent to dissolving from the inside, which, speaking of Ebola, is what happens. But Ebola is not fatal in every single case. Prion diseases are. There’s no getting out of it once you are in. Brain = over.
Once again, this information needs to be addressed and assessed by doctors, parents, nurses, policy makers - everyone.
Go Luc.
In Michigan, you can get test kits or take your deer to a MDNR check station.
Pretty much nothing can destroy the prions. Maybe burning.
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