It's madness

This post is not intended to create fear or anxiety. Rather, I am driven to disseminate this information in the hope that it contributes to the immediate and comprehensive cessation of the genetic-immune modifying jabs and the termination of all existing vax mandates. Since I am a neuroscience-based specialist, the neurological findings that I share have a direct relevance to the principles and practice of my speciality.
Proteins consist of chains of amino acids termed polypeptides which are folded in a very specific way. The folding of a protein directly influences its functions. The folding reflects primarily the arrangement and type of amino acids in the polypeptide chains. If the type of amino acids or their order in the chains is changed, the resulting protein folds in a different way. This abnormally folded protein functions differently or has no function at all. Equally important – the abnormally folded protein can interfere with normally folded protein rendering that protein pathological by interfering with its folding. The abnormally folded protein is referred to as prion protein. Prion protein occurs most frequently in the brain where its slow build up gives rise to the neurodegenerative conditions such as Alzheimer’s and Parkinson’s disease. Most importantly prion protein may spread between different organisms – either of the same species or between species. An example of this is Mad Cow Disease or Bovine Spongiform Encephalopathy – a prion protein-based disease of cows. This condition may spread between the animals but if the animals are eaten by man, particularly their brains, this may result in the condition called Creutzfeldt-Jakob Disease (CJD) in man.
The prion protein results in a loss of all neurological function over time, progressing to dementia and death in all cases. CJD has been the condition feared by generations of neurosurgeons because in the course of our practices we have been called upon to biopsy the brains of those suspected of having CJD. Since the prions of this condition are transmissible, the surgeon may contract CJD as a result of doing the biopsy. Additionally prion proteins are particularly resistant to heat neutralization and so sterilized instruments may remain contaminated with prions and possibly be transferred to a subsequent patient.
Enter Covid center stage. In the early days of the plandemic, two articles appeared (1, 2) which warned of the specific danger of the vax giving rise to prion proteins. The warning was based on the fact that the mRNA code had been changed to make it more resistant to the immune attack on its way to the cell. But as indicated previously if you change the code you change the amino acids and thus the folding of the protein. Consequently several of us have been greatly concerned by the possibility of prion formation particularly in the brain resulting from the vax. Sure enough this has occurred, true to prediction.
In a recent article, both published and presented at a recent neurology congress in the UK, 26 cases of CJD have been diagnosed following mRNA jabs of whom 20 have died. What makes this even more ominous is that the authors describe an acute form of CJD where progression to debilitating neurological pathology and death occurred over a relatively short period of time.
In the face of the failure of the vax to prevent illness, spread and death as well as the mounting adverse reactions, this new and ominous finding must surely put an immediate end to all further jabs. The Nuremberg Code is being violated with impunity to the point that one begins to ask whether the vax is indeed an instrument of extermination. With the burgeoning exposure of documented adverse reactions, mandating further vaxes must surely represent the worst of crimes against humanity.
References
Articles from Ian Weinberg
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