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Naïve, learning, adapting, innate immune systems of the young are not to be tinkered with because then there is no hope for sterilising natural immunity. C-19 doesn’t or rarely affects children. Autoimmune, vaccine induced CD8 T-cell dependent acute hepatitis does which is at least a red flag. Vaccine shedding is real. Also, the liver is…
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Naïve, learning, adapting, innate immune systems of the young are not to be tinkered with because then there is no hope for sterilising natural immunity. C-19 doesn’t or rarely affects children. Autoimmune, vaccine induced CD8 T-cell dependent acute hepatitis does which is at least a red flag. Vaccine shedding is real. Also, the liver is where the vaccine spike protein converts into DNA, causing inflammation, one may join the dots. This is an experimental, LNP mRNA, non sterilising, gene therapy, (very recently included on the NIH website as the definition of a vaccine), “vaccine”. And for corona viruses! With a non sterilising vaccine for a start! WHO are they trying to bullshit! They have been unsuccessfully mucking around with corona virus vaccines for decades only to end up with disease enhancement or antibody dependent enhancement. Marek’s disease and dengue fever are other failed vaccine examples of this. This abomination of a so called vaccine is now common knowledge and I hear people talking about it. Keep spreading the word. First there was vaccine resistance, viral immune escape variants, negative efficacy and now antibody dependent enhancement appears and dormant viruses evolving. (Monkey pox is on the public record as gain of function , complete with another so called vaccine. The genome sequence of this is out a week or so ago). My guess is that this is an unfortunate combination.
The C-19 lipid nanoparticle vaccine spike protein enters the nucleus of the cells and down regulates DNA repair and the immune system. (Swedish study Nov 2021, major game changer in molecular biology. Merogenomics 18 YouTube). I couldn’t think of anything worse for a vaccine design.