There is now enough information on this website to piece together the links in a puzzle that has taken independent researchers three years to unravel. Each one provided a link or a brick in a massive crossword puzzle, as it were. These researchers and investigators are doing a process of reverse engineering. They are beginning with a finished product (either the virus made in a laboratory or the mRNA vaccine) and trying to understand what it is and how it works. They are reconstructing at least ten years of bio-engineering financed by DARPA (a branch of the US Military) and they are doing this research on limited funds.The actual work financed by DARPA has been done in Universities and in U.S. Biological Warfare Labs.
“Emergency Use Authorization” does not mean Approved. It means Authorized. Perhaps a legal technicality but that is what it is. Manufacturers of EUA Vaccines are not required to report the contents of these vaccines to the CDC. Hence there are wild variations in lot numbers and batches. Some batches , called “Hot Lots” are 50X more toxic than other lots that are more benign. Further, it may be that many vaccine doses are no more than saline solutions.
It could be that in Israel most vaccine doses were benign because Pfizer was using Israel as a showcase to the world in order to promote distribution world-wide. Nevertheless, the Israeli Authority did not see fit to institute a public VAERS System to report adverse effects when they did occur. Hence it required independent researchers to gather interviews to document serious Adverse Events.
There have been two groups of independent researchers. Some uncovered the residues of synthetic snake venom in the vaccines. On a separate track, as many as 26 independent laboratories uncovered via High Powered Dark Field Microscopy strange metallic particles in the Vaccines and Blood Samples of those who have been vaccinated. The list of metallic substances in the vaccines, including Graphene Oxide have been well documented.
We posit that because of the no-reporting requirement concerning the contents of the EUA vaccines, the Drug companies were experimenting worldwide with different doses and different compositions of the vaccines, which would explain the randomness of adverse events.
Gerald Parkoff, Efrat, Israel gparkof1@gmail.com
