🚨🚨🚨MUST WATCH🚨🚨🚨 I just unleashed the truth about COVID, its origins, and the tyrannical response of government. The government officials sitting in front of me had to listen to every one of the horrific things they did to our country. Source: https://x.com/repmtg/status/1857152546915471844

I agree! I told Dr. Fauci to his face that he should be in jail and prosecuted for crimes against humanity. Well, we might finally get the chance… Source: https://x.com/repmtg/status/1856364602386460761

pic.x.com/yUm7Zbsex3 Wow!!! You Can't Make This Up 🤯 "So Congress has paid over $17 million in hush money for s@xual misconduct...and what's more is that it was taxpayer money." Can you believe it? 🎥 @RepThomasMassie https://x.com/thrillarilla369/status/1854900778000875562?s=46

Dr. Robert Maloney: "We have the artifactual evidence of what was known in the form of the Pfizer common technical document that was first obtained by Byram Bridle from the Japanese it was prevented from being distributed by the US FDA and it revealed extensive understanding that we had this widespread biodistribution of these products that they caused the encoded protein to be manufactured in virtually every major tissue throughout the body." "It was known that there was a strong inflammatory and toxic reactions associated with these lipid nanoparticles. This is fundamental knowledge. It was in the field of these cationic-based lipid nanoparticle delivery systems. It was known that these particles will deliver both RNA and DNA into cells and tissues. It was known that the modification, the pseudo-uridine, altered the immune response to the RNA. That's the whole reason why the incorporation of pseudo-uridine was performed." "It was known that the pseudo-uridine would increase the longevity of these products, that this was not natural RNA. It was not known and not investigated as to whether or not these products would be quote shed. It was not known and not investigated whether or not these products would cause reproductive toxicity, whether they would be secreted in body fluids. A number of things that should have been investigated under normal FDA protocols and procedures not the least of which is characterization of the contamination or adulteration of the short DNA fragments, which are intrinsic to the manufacturing process, and which in prior FDA regulations have always been considered to be a risk for a form of genotoxicity called insertional mutagenesis." t.me/RevealedEye Source: https://x.com/toobaffled/status/1855603049273729429

Source: https://x.com/lisalu2024/status/1855788234392932353

Powerful testimony by dr. Kevin McKernan: "Thank you, Senator Johnson. I very much appreciate you giving us this audience. Many in this audience have been subjected to years of censorship on this topic. What I want to talk to you today is about the DNA contamination that our team at Medical Genomics discovered in the mRNA vaccines. We're specifically speaking about Pfizer and Moderna in this case. This work has been replicated by many labs around the world." "And now the FDA, the EMA, and even Health Canada have admitted to this. The regulatory agents have admitted that Pfizer also omitted the SV40 sequences that are in their vaccine. They've deemed this contamination to be of little consequence, claiming the DNA is of too little concentration to matter or to be containing DNA of no functional consequence. These statements are false and are not supported by any independent testing by these regulators." "After the regulators have admitted to being deceived, they ask the opinion of the party that deceived them, how bad was the deception? They shockingly believe the answer they were given, which is that these sequences have no relevance to plasma manufacturing. As someone millions of plasmids, I can assure you that this is an overt lie. DNA contamination can lead to insertional mutagenesis. This is actually declared in Moderna's own patents regarding mRNA vaccines." "This is US patent 10,898,574. This is also supported by LIM, et al., which speaks to the rate of spontaneous integration in the genome during transfection. We are using transfection, after all, with LNPs. The SV40 DNA is, in fact, functional. It is published as a potent gene therapy tool in a nuclear targeting sequence, as described by David Dean, et al. DNA is also known to bind to the tumor suppressor gene known as P53. This is described by Draymond et al. The DNA contains the promoter for the antibiotic resistance gene in this plasmid as well." "No plasmid manufacturing can occur without a promoter for the antibiotic resistance gene, so it is clearly functional and key to plasmid manufacturing despite the FDA's comments on this topic. The DNA quantity in many vials is over the 10 nanogram per dose limit, but it does vary substantially between lots. When we use both qPCR and fluorometry, these two tools give us different answers. This should be a concern that they're between these different tools. Moderna's own patents, US patent 10,000,077,439, teaches that qPCR underestimates the quantity of this contamination, and the DNA regulators are once again allowing them to cherry pick between these different measurement tools." "DNA guidelines used to be a thousandfold lower before the NCVIA Act was established, which provided liability protection for pharmaceutical companies. The limits were devised based on the 10 minute half-life of DNA in the blood, naked DNA in the blood. This DNA contamination is not naked. It's protected in lipid nanoparticles, which delivers this DNA to cells, which should arguably have limits set to the ones prior to the NCVIA." "We have since found Pfizer lots, 1F1042A, that are at least 10-fold over any lot we've measured before PCR, which is known to underestimate this quantity. For those not familiar with PCR, you may have received CT scores of 35 that called you positive for COVID. We're seeing CT scores of 13 on the DNA that you're injecting into children. We've applied these vaccines to some cancer cell lines and have evidence that it enters the cell and can survive several cell divisions." "We have preliminary evidence, although this requires replication in other labs, that this DNA can integrate into the genome. We found two spike sequence integration events in ovarian cancer cell lines of CAR3 into chromosome 12 and 19 very recently. Since these vaccines were expected to only contain mRNA, they were never assessed for genotoxicity studies. These studies were therefore. being conducted as guinea pigged U.S. citizens as we witnessed an unprecedented rise in cancer drug sales since the vaccines rolled out." "In summary, the vaccine manufacturers' own patents teach that the methods being used to monitor this DNA are not fit for purpose. Their patents teach the insertional mutagenesis risks present in L&P-based mRNA vaccines. The only people who are in denial of these facts are the regulators who are routinely hired to work for these very pharmaceutical companies." "Two of these regulators resigned over the wonton approval of these vaccines for young patients from them, it is time for our representatives to repeal or review the PDUFA Act of 1992. This act allows regulators to defray the costs of regulation by accepting payments directly from the companies they regulate. Over half of the FDA's budget is sourced through this act. They cannot be voted into office, they cannot be voted out, but they can approve dangerous library free mandated vaccines." "These policies have harmed the public torn our country part as immune nurses are forced to choose between their jobs and useless and even dangerous vaccines. DNA contamination was not part of any informed consent process. And many universities still mandate these shots based on the guidance and approval of our regulators who have become nothing less than a marketing division of the companies they regulate. Thank you for the time." Source: https://x.com/newstart_2024/status/1855703608890736709