Specific regulatory guidance for mRNA-based vaccines has yet to be developed. Pfizer is using a different method to produce RNA for mass production than they did for the initial trials. The mass production RNA is not as clean. BioNtech has admitted there are DNA contaminants. Many different outcomes after vaccination are possible depending on where the DNA lands. But it must hit a dividing cell to contaminate it. Therefore it is not recommended for pregnant women.
They have not done a transport verification study. The integrity and quality of the RNA varies from batch to batch. The lipid nanoparticles get into all cells, not just the muscle cells. Lipids in some batches are contaminated too. The EMA committee issued complaints about 20 points in total regarding Good Manufacturing Practice. Pfizer has until July to address these issues. Of the three levels of doses tested, the benefit was the same for all, but the higher doses had more adverse events. They skipped a correlation test which would have documented that. Nevertheless, the highest dose is being used for the public. The Pfizer vaccine arrives dehydrated and has to be mixed with saline. They didn't test properly whether a second dose actually raised antibody titers relative to the first dose. Because the different vaccines are being mixed (i.e. the two shots are not from the same company), we can't tell what the effects of one vaccine over another are. She has not investigated Moderna and Astrazenica yet.
LNP's (lipid nanoparticles) are a problem because of their size. They interact with cell components. For awhile, the affected cells are full of spike proteins. That is a temporary genetic modification. T-cells are formed in response and signal the cell to commit apoptosis. The cationic lipid component has a positive charge, and that is very very toxic. They can react with the negatively-charged DNA and amino acids. Cationic lipids can destroy mitochondrial membranes, leading to oxygen radicals not being disabled, which they otherwise would be. The resulting oxidative stress either kills the cell or turns it into a cancer cell. This technology is used in cancer treatments because it can target cancer cells locally, but in a vaccine the effect is not localized. LNP's were found in many organs after just 15 minutes. Cationic lipids were still in the plasma 12 days later. Half life in the liver is 3 weeks. 2 micrograms of RNA were used in that test, but the vaccine dosage given to the public is 30 micrograms. There is no information on the effect of LPN in excreted matter on the environment (i.e. will they be filtered out by sewage plants, and end up in the drinking water? Would stomach enzymes break them down? Could they cause anaphylactic shock in those who drink?)
Myofascial degeneration was seen in mice given three shots. They lost weight and showed signs of subcutaneous inflammation and hepatocellular periportal vacuolisation. The vacuoles commit apoptosis. The presence of cationic lipids in the vacuoles can be confirmed by autopsy. Pfizer found a moderate to strong reduction in red blood cells and reticulocytes, particularly sensitive to oxidative stress - leads to hypoxia. They also saw inflammation of the perineural tissue of the iscias nerve. In a healthy organism, the liver will completely regenerate. Dr. VSK is extremely critical of the EMA for not investigating any of these things that they found were not investigated in human beings in the clinical study. It would have been easy enough to measure all the blood parameters, but it wasn't done, or results were hidden. So we don't know if the same effects are in humans. Subjects suffer from lymphopenia in 1 -3 days, but we don't know why.
A pharmacist died after vaccination and her organs were harvested for transplantation. We don't know the implications of that. Cremation should not be allowed when the deceased had been recently vaccinated. That destroys evidence. They did not investigate the Syncytin issue in pregnant women. Long-term studies and studies on possible autoimmune conditions were not conducted. They didn't investigate whether the vaccine can be transferred to the foetus. This mechanism crossed the blood-brain barrier, so LNP's can damage the brain. Damage can occur as long as lipids are there, which is 4 to 5 months. We can't say whether the RNA in one vaccine can cross-react with another vaccine. Further discussion that there are other viruses present. The wider picture hasn't been taken into account.
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