by Chris Black
You should read this friends. Through and through.
https://twitter.com/718Tv/status/1480082895075266561
mRNA technology has been around for a while. What kept it from being used in widespread vaccination was lacking a way to protect the mRNA long enough to get inside of cells and ribosomes, where it can be "read" to construct a protein. Instead of admitting this they (Moderna,
— stained hanes (@718Tv) January 9, 2022
normal lymph flow and end up in lymph-nodes local to site of injection where foreign, antigenic molecules are processed by dendritic cells and stay in the extracellular space otherwise (outside and in-between cells, the interstitium), the mRNA injected in these vaccines ends up
— stained hanes (@718Tv) January 9, 2022
is a molecule called ACE2.) In "normal" vaccination only dendritic and a few other immune cells (which are designed to ingest and deal with antigenic molecules) end up with viral proteins in them. These specific cells are part of the immune reaction that ends up with long term
— stained hanes (@718Tv) January 9, 2022
…
https://twitter.com/718Tv/status/1480082895075266561
The thing about most vaccine related injuries is that you don’t know that they happened.
Myocarditis doesn’t have many symptoms if it is mild, and you might just brush it off as heartburn.
The destruction of T-cells is something you won’t notice right away, nor the emergence of soft tissue cancers.
Reproductive harm and DNA damage also doesn’t just appear in a few days or months.
It is why they normally test vaccines for five to ten years.