Kevin, as I noted in the article I just posted https://wrestlingwithtruth.substack.com/p/flccc-conference-april-28 Ryan Cole commented on your work and said that he was seeking to replicate your findings. Of course "THEY" will dismiss his work as well, but each additional 'sequence drop' validates what you have done.
Any vials straight from Pfizer would be the least trusted of all. Pfizer is quite capable of "cherry picked" vials just for you. Vials from a vaccine station would be the ones that would reflect what is actually going into a recipients arm. The problem with that, is that no vaccination centre would agree, or certify chain of custody.
It has been tried before, and refusal is always the result. You would wonder why they would refuse, given the "faith" they have in them.
Regarding "mitotic" division, it was told to us, that once spike from the ribosome was presented on the cell wall, all cells which make spike would then be destroyed by the immune system. IF... that is true, mitosis would be moot.... and if that isn't true, then it's relevant. So that raises the question as to whether or not cells which make the spike are destroyed by killer T cells.
Interestingly the hcctv link refuses to work. Hopefully they put it up on several platforms.
Genotoxicity refers to the ability of harmful substances to damage genetic information in cells. Being exposed to chemical and biological agents can result in genomic instabilities and/or epigenetic alterations, which translate into a variety of diseases, cancer included.
Cytotoxicity is the degree to which a substance can cause damage to a cell. A substance or process that causes cell damage or death is referred to as cytotoxic, "cyto" meaning cell and "toxic" meaning poison.
Anadamide, I'm trying to get my head around this paper, but something feels very off with the assertion that NSl nuclear translocation of S protein spike mRNA only happens in infected airway epithelium. How does this paper sit with you?
I'm concerned about mRNA shot contaminants in donated blood. Re the dsDNA. Upon administration of a shot, is all the dsDNA, which I assume is primarily from the Ecoli, all covered by the LNP? Does it circulate in the blood? For how long? Is the only time the dsDNA exposed is when the LNP binds to a cell membrane? When the cell divides, does any part of the dsDNA then get into the blood stream? Whenever the dsDNA is in the blood stream, is that functional? Is it toxic? Can it break into pieces? What is the lifetime of the pieces? Are the pieces toxic?
Anandamide, you said on crpodcasts that there are lawsuits about this. Are you able to amplify on that? If that is too sensitive even though you said it, please delete.
dsDNA variance in Pfizer Docs
Kevin, as I noted in the article I just posted https://wrestlingwithtruth.substack.com/p/flccc-conference-april-28 Ryan Cole commented on your work and said that he was seeking to replicate your findings. Of course "THEY" will dismiss his work as well, but each additional 'sequence drop' validates what you have done.
Any vials straight from Pfizer would be the least trusted of all. Pfizer is quite capable of "cherry picked" vials just for you. Vials from a vaccine station would be the ones that would reflect what is actually going into a recipients arm. The problem with that, is that no vaccination centre would agree, or certify chain of custody.
It has been tried before, and refusal is always the result. You would wonder why they would refuse, given the "faith" they have in them.
Regarding "mitotic" division, it was told to us, that once spike from the ribosome was presented on the cell wall, all cells which make spike would then be destroyed by the immune system. IF... that is true, mitosis would be moot.... and if that isn't true, then it's relevant. So that raises the question as to whether or not cells which make the spike are destroyed by killer T cells.
Interestingly the hcctv link refuses to work. Hopefully they put it up on several platforms.
Genotoxicity refers to the ability of harmful substances to damage genetic information in cells. Being exposed to chemical and biological agents can result in genomic instabilities and/or epigenetic alterations, which translate into a variety of diseases, cancer included.
Cytotoxicity is the degree to which a substance can cause damage to a cell. A substance or process that causes cell damage or death is referred to as cytotoxic, "cyto" meaning cell and "toxic" meaning poison.
Thank you for your amazing work ♥️
Anadamide, I'm trying to get my head around this paper, but something feels very off with the assertion that NSl nuclear translocation of S protein spike mRNA only happens in infected airway epithelium. How does this paper sit with you?
https://pubmed.ncbi.nlm.nih.gov/36778849/
Anadamide, have you read this?
https://pubmed.ncbi.nlm.nih.gov/35627104/
I'm concerned about mRNA shot contaminants in donated blood. Re the dsDNA. Upon administration of a shot, is all the dsDNA, which I assume is primarily from the Ecoli, all covered by the LNP? Does it circulate in the blood? For how long? Is the only time the dsDNA exposed is when the LNP binds to a cell membrane? When the cell divides, does any part of the dsDNA then get into the blood stream? Whenever the dsDNA is in the blood stream, is that functional? Is it toxic? Can it break into pieces? What is the lifetime of the pieces? Are the pieces toxic?
I like your use of the Ferguson as the gold standard unit for measuring large errors in prediction. I hope it catches on. 😀
Anandamide, you said on crpodcasts that there are lawsuits about this. Are you able to amplify on that? If that is too sensitive even though you said it, please delete.
Good Day, Kevin,
First, thanks for your work.
2 questions:
1. About the 1ng/mg to 815ng/mg of DNA/RNA: is that per dose or per vial?
2. I've heard about plasmid DNA. How does that relate to dsDNA?
Thanks.