Docket No. CDC-2026-0199 Public Comments to Meeting of the Advisory Committee on Immunization Practices

Docket No. CDC-2026-0199

Public Comments to Meeting of the Advisory Committee on Immunization Practices

The mRNA vaccine platform is deeply flawed. The mRNA vaccine is in fact a scientific fraud by violating the scientific mechanism of vaccines to minimize viral toxicity but provide immunity. First, those mRNA vaccines, including Covid and Flu vaccines, don’t provide the long-term immunity (e.g., adding immunological memory to body’s immune system by generating memory immune cells for rapid response to fight off future infections) --- the only benefit outweighs risk. Second, Pfizer and Moderna didn’t minimize viral toxicity by using highly toxic viral spike protein as the antigen. Third, Pfizer and Moderna bioengineered the mRNA vaccines to dangerous GOF to make the vaccines even more dangerous, toxic, and deadly than the viruses, such as using lipid-nanoparticles traverse biological membranes for wide biodistribution to whole body to deliver wide-spread damages to many vital organs, viral mRNA stabilization for long-term production of viral toxicity and even permanent viral genome integration. It is absolutely unsafe to use such an invasive experimental technology for lab rats (e.g., lipid-nanoparticles) to deliver bioengineered viral mRNA across biological membranes to brains and hearts, causing strokes and heart attacks in children and youth we had never seen before the mass Covid mRNA vaccination and booster shots. Fourth, the mechanism of mRNA vaccines to hijack human cells as viral manufacturers and make human cells the target of its own immune system --- downright causing autoimmune diseases --- should have completely disqualified viral mRNA as vaccines in the first place, and mRNA vaccines or viral mRNA should have never been allowed to be injected into any healthy individuals to cause the massive epidemic of vaccine injury (MEVI) we have to face today.

Covid vaccine injuries were widely felt among the American people during Covid mass vaccination, and caused wide-spread vaccine hesitancy in the American public. Even according to CDC VAERS data, which is highly underreported by a factor of at least 10 folds, there are close to 40,000 deaths and over 1.6 million SAEs associated with Covid vaccines, higher than all the previous vaccines combined.

It is widely acknowledged that Moderna and Pfizer mRNA Covid vaccines caused myocarditis and pericarditis, blood clots, stroke, accelerated neurodegeneration like Alzheimer’s disease, and turbo cancers (e.g., hundreds of peer-reviewed scientific publications). The mRNA shots significantly increased risk of all cancers, including breast cancer, bladder cancer, colon cancer, blood cancer, uterine cancer, ovarian cancer, thyroid cancer, lung cancer, prostate cancer. The genetic “fingerprint” of Covid mRNA vaccines was found embedded in the DNA of cancer patients, and 98% of new cancer diagnosis are among mRNA vaccinated people. The mRNA vaccine shots have led to unprecedented explosions of aggressive, fast-growing cancers in young people (20s-30s) and children, and strokes and heart attacks in children and youth we had never seen before the mass Covid mRNA vaccination and booster shots.

Moderna and Pfizer mRNA Covid vaccines had never even passed animal safety testing before mass rollout to vaccinate the entire US population, including vulnerable children and babies who were not even at risk, and Pfizer even admitted themselves (Moderna should too) they never even did any test to show the mRNA vaccine preventing transmission before they had the government to implement vaccine mandates and enforce censorship, and they still have not done any test for any of those booster shots.

Moderna and Pfizer mRNA Covid vaccines violate Biological Weapons Convention (BWC), engineered with dangerous gain of function traits, such as using pseudouridine to stabilize mRNA, spike protein encoded with furin cleavage site, HIV like & SEB superantigen motifs, mRNA recoded with synthetic base, aberrant protein, the antigen spike protein is a viral toxin, lipid-nanoparticles traverse biological membranes and barriers (e.g., blood-brain barrier, blood-placental barrier, blood-testis barrier) to deliver wide-spread harms to many vital organs. Moderna and Pfizer mRNA Covid vaccines violate BWC, which makes them UNLAWFUL. Moderna and Pfizer mRNA Covid vaccines also violate Nuremberg code, Helsinki declaration, and the US constitutional protections (e.g., 1st, 10th, 14th amendments).

The scientific mechanism of vaccine is that a vaccine is supposed to provide immunological memory, the long-term immunity, with a single shot, not just elevating the antibody level. Booster shots are evidence of ineffectiveness of vaccines, like assisted suicide. The method of delivery --- the revolutionary novel mRNA vaccines via lipid-nanoparticles that traverse biological membranes, such as blood-brain barrier and blood-placenta barrier --- is a core problem and a key reason why such an invasive experimental technology for lab rats had never been commercially marketed, until the Covid-19 pandemic through fast track under emergency use authorization (EUA). Needless to say, mRNAs are potent mutagens or cancerogenic to cause cancers, which is why mRNAs are very unstable and quickly degraded inside cells. However, mRNA vaccines are genetically stabilized to produce toxic spike protein for at least 60 days post vaccination, which significantly increases the risk of cancer. It is absolutely unsafe to use such an invasive experimental technology for lab rats (e.g., lipid-nanoparticles) to deliver bioengineered viral mRNA across biological membranes to brains and hearts, causing strokes and heart attacks in children and youth we had never seen before the mass Covid mRNA vaccination and booster shots.

The next-generation gene-therapy vaccines, such as mRNA (Pfizer and Moderna) and adenovectorDNA (AstraZeneca and Janssen) COVID-19 vaccines, employ viral-like invasive experimental technology platforms that use viral genetic-codes to hijack human cellular machinery to make toxic viral proteins protruded from the human cell surface as the antigens, which makes our body’s own cells, including immune cells, brain cells, heart cells, become the target of its own immune system, causing auto-immune diseases and wide-spread human cell and tissue damages across many vital organs. Such invasive experimental technologies for vaccine delivery, such as AAV virus vector and lipid-nanoparticles, are designed to study genes in lab animals, which could cause severe tissue damages to liver, heart, and other vital organs, should never be used in humans. To make matter worse, the FDA even granted many of those gene therapy and gene therapy vaccine companies fast track status to bypass FDA standard regulations. The FDA has even abused the Regenerative Medicine Advanced Therapy (RMAT) designation and granted approximately 151 RMAT designations, a significant portion of these designations are for gene therapies with some companies operating in stealth mode, even though gene therapies could not regenerate damaged or lost tissues and have nothing to do with RMAT.

The FDA prioritizing rapid access and speed approval to new treatments over safety is one of the root causes of the rising rates of many chronic diseases. Gene therapy only targets a small group of patients, so we only heard a few deaths, though way too common, from those gene therapy companies. Gene therapy vaccines, such as mRNA (Pfizer and Moderna) and adenovectorDNA (AstraZeneca and Janssen) COVID-19 vaccines, target mass populations that most people are actually healthy, so it is unethical for those FDA and CDC experts not to warn the public about the health risks of gene therapy vaccines, and continue to hide safety data and the staggering numbers of SAEs and deaths associated with Covid mass vaccination, raising enormous public sentiment and vaccine hesitancy. The FDA should re-evaluate the safety of invasive experimental genetic-engineering technologies used in next-generation bioengineered vaccine and drug development and the guidelines of regulatory approval and recommendation for gene-based or genetically-engineered GOF novel vaccines and products, and should never use fast track, RMAT designation, or EUA, to bypass FDA standard regulations at the cost of public safety.