On Sept. 11, 2023, the FDA approved a new round of shots from Pfizer and Moderna that are technically called updates (rather than boosters), because they are made against the newer XBB1.5 variant. A new monovalent version of the more traditional Novavax vaccine is still under review by the FDA. The FDA approval of Pfizer and Moderna’s new monovalent shots applies to those 12 and older. New shots for children under 12 years old were authorized under an Emergency Use Authorization. Manufacturers of all COVID shots continue to be free from liability until December 31st, 2024, under the PREP Act (Public Readiness and Emergency Preparedness Act). The recent FDA authorization was quickly followed by a meeting of the CDC-run Advisory Committee on Immunization Practices (ACIP) on September 12, 2023, in which the shots were approved for recommendation. Meanwhile, the authorization for the older bivalent shots has been withdrawn, so the only shots available will be the new monovalent ones made against the XBB1.5 variant.
The push for these new “vaccine” updates appears to have come out of nowhere. The Advisory Committee on Immunization Practices (ACIP) never announced that it would be reviewing these new shots and voting on their approval. At the September meeting, during which the inoculations were approved, the public comments were limited to ONE person. This total lack of transparency by the ACIP and the CDC is to the point of criminality. It is ALMOST as criminal as approving them without any clinical trial data, which is exactly what occurred. The public has been consistently told that double-blind, placebo-controlled clinical trials are the only standard that can be used to determine the safety and efficacy of a new product. However, a surrogate of antibody production was used to evaluate these new monovalent shots with no data presented on safety or real-world effectiveness.
It is now abundantly clear that the shots were never designed to prevent transmission. They are ineffective at even preventing severe injury and death as their protection starts waning almost immediately. Scientifically, the production of new boosters or updates for a quickly mutating RNA virus makes no sense. By the time the new shots come to market, they are no longer a match to the variants currently in circulation. The XBB1.5 variant that the shots were designed to neutralize is almost gone, comprising only 3.1% of new infections. This raises the question of whether this newest rollout of injections will have any protective effect at all against the variants that ARE currently circulating. The Eris variant EG.5 currently comprises 21.5% of new infections with variant FL.1.5.1 following closely with 14.5% of new infections. Vaccine manufacturers are now playing a game of variant “whack-a-mole,” where they struggle to keep pace with the mutational capacity of the virus. Manufacturers are producing products that not only are less and less able to neutralize new strains but appear to mistrain the immune system in important ways that make recipients MORE likely to catch COVID.
A recent study by the Cleveland Clinic found that a person’s risk of getting COVID increased with every dose of the “vaccine” they received. Since natural immunity has been shown to be more than 95% effective at preventing severe illness and death from COVID, these data beg the question of why this program of shots is still being pushed on the population.
This brings us to the most egregiously unethical aspect of this campaign, which is that a mountain of data now shows that the shots are inherently unsafe. Yet, they continue to be pushed on our children. This most recent round was authorized for children under an Emergency Use Authorization. What’s the emergency?? Most children have natural immunity already.
THE REAL MISINFORMATION
Alarmingly, the media has been complicit by pushing this newest rollout of shots without even mentioning that several groups of scientists recently demonstrated that the Pfizer vaccine is adulterated/contaminated with DNA that is likely to become a part of the recipient’s DNA. Until recently, the media labeled this possibility misinformation. However, molecular biologists have known from the start that the possibility of genomic integration is a serious risk of these gene-transfer platforms.
Dr. Phillip Buckhaults, head of a lab that studies genomic integration, recently testified before the South Carolina Senate that the DNA contamination in the Pfizer vaccine would create genomic integration, causing cells to produce the toxic, foreign spike protein indefinitely. Dr. Buckhaults further testified that his own work demonstrated that each dose of Pfizer vaccine contains around 200 billion fragments of DNA with the ability to become part of the DNA of the recipient. He shared that genomic integration would increase cellular dysfunction and the incidence of cancer. He expressed dismay that our regulatory agencies have repeatedly failed to address this issue and were unlikely to do so, because there is an overwhelming financial incentive to ignore all problems with the shots.
VAERS reports that over 36,000 people have died concomitant with vaccination, 27,000 have been diagnosed with myocarditis or pericarditis, and almost 68,000 people are now disabled because of unsafe, ineffective COVID shots. Excess mortality has increased 25% in some localities with the incidence of stillbirths paralleling those numbers. It’s time to stop the madness and concede that natural immunity is superior!!
Shrestha, Nabin K et al. “Effectiveness of the Coronavirus Disease 2019 Bivalent Vaccine.” Open forum infectious diseases vol. 10,6 ofad209. 19 Apr. 2023, doi:10.1093/ofid/ofad209 https://pubmed.ncbi.nlm.nih.gov/37274183/
Chemaitelly, Hiam et al. “Duration of immune protection of SARS-CoV-2 natural infection against reinfection.” Journal of travel medicine vol. 29,8 (2022): taac109. doi:10.1093/jtm/taac109
Chase safety not variants: Advisory Committee on Immunization Practice September 12, 2023. XBB1.5 variant: likely rapid waning and escape by emerging variants will quickly render this vaccine obsolete with more risk than benefit. v2 September 2023 DOI:10.13140/RG.2.2.26411.62248
South Carolina Senate Hearing September 15th, 2023. https://www.youtube.com/watch?v=IEWHhrHiiTY
UKCauseof DeathProject Death&DisabilityTrends,Ages 15-44:Cardiovascular Diseases Data Sources: UK Office of National Statistics (ONS)
Perinatal mortality rates by trust/health board. United Kingdom and Crown dependencies, for births in 2021 https://timms.le.ac.uk/mbrrace-uk-perinatal-mortality/data-viewer/