FDA’s Vaccine & Related Biological Products Advisory Committee (VRBPAC) To Meet To Formulate Recommendations For Updated CONvid Bioweapons Shots

Article posted with permission from the author, Suzanne Hamner

Controversy still surrounds the CONvid-1984 modified mRNA gene therapy bioweapon shot four years on after numerous databases, including the Vaccine Adverse Event Reporting System (VAERS), indicate these bioweapons are extremely harmful and in many cases deadly. The question is why is it controversial? Those supporting the “Make America Healthy Again” agenda are confident with their “Healthketeers” in prominent positions at the Food and Drug Administration (FDA), the Department of Health and Human Services (HHS), the National Institute of Health (NIH), and the Centers for Medicare and Medicaid Services (CMS) to stop the continued used of these bioweapons and thwart the development of others. However, the only offer to the public has been to “consider” removing these bioweapon shots from the Center for Disease Control (CDC) recommended childhood immunization schedule. In a not so surprising move, the FDA’s Vaccine and Related Biological Products Advisory Committee (VRBPAC) is convening in May 22, 2025, to discuss recommendations for updated CONvid-1984 modified mRNA gene therapy bioweapon shots, including which “variants” to target and if “boosters” should be promoted.

The Food and Drug Administration (FDA) will convene a panel of experts in a critical meeting on May 22 to discuss recommendations for the next round of Wuhan coronavirus (COVID-19) vaccines.

The virtual meeting of the FDA’s Vaccines and Related Biological Products Advisory Committee (VRBPAC) will weigh in on which COVID-19 variant should be targeted in updated booster shots, or whether boosters would be promoted at all. While the VRBPAC’s advice isn’t binding, it could shape immunization efforts for the fall and winter seasons.

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The May 22 meeting also comes amid significant leadership changes in the FDA. Dr. Marty Makary was named as the new head of the agency, while Dr. Vinay Prasad was named as the new director of the FDA’s Center for Biologics Evaluation and Research (CBER). Incidentally, both Makary and Prasad have publicly questioned aspects of the government’s COVID-19 vaccine approach.

Makary and Prasad question “aspects” of the government’s CONvid-1984 modified mRNA gene therapy bioweapon shot approach; but, are these two questioning the shot itself? Apparently not, since they are continuing to develop recommendations for the next round of bioweapon shots, including target “variants” in the boosters and whether boosters are “promoted”. The only concession being offered the public is “possible” removal of the CONvid-1984 bioweapon shots from the childhood immunization schedule. These bioweapon shots harm adults as well as children. Why are the “Healthketeers” refusing to look at removing these bioweapons from the market? Makary, Prasad, Kennedy, Bhattacharya, and Oz should be asked that question so the public can hear their excuses. How long does it take to determine these bioweapon shots should be ceased for children? The Healthketeers should answer that question as well.

Do we really need a group of supposed “experts” to provide any recommendations on taking a bioweapon shot? The only sane recommendation is to refrain from injecting yourself with a bioweapon. Anything else is utter insanity. Whatever recommendation this group makes, Americans would be wise to ignore it – so would States.

The FDA has delayed the approval of Novavax’s protein-based “vaccine”, requesting additional clinical trials. “Moderna has similarly faced hurdles, with the agency requesting more data on its experimental flu-COVID combination vaccine.”

So, the development of these products continues, with Moderna developing a combo flu/CONvid-1984 modified mRNA gene therapy bioweapon shot, with the FDA only requesting more data. Remember, the CONvid-1984 emergency declaration triggering the PREP Act issued by Xavier Becerra is effective until December 31, 2029. Aren’t the “Healthketeers”, particularly Robert F. Kennedy, Jr. going to address that declaration? After all, the only time the Secretary of HHS can declare an emergency is due to chemical, biological, radiological, or nuclear (CBRN) agents or illnesses that can be attributed to those type of agents. Where are they on the “MAHA” agenda they have touted?

The FDA has historically followed an influenza-like model for COVID-19 vaccines, updating formulations annually without requiring new clinical trials. But recent demands for placebo-controlled studies suggest a pivot toward more rigorous standards. Critics argue this could slow vaccine availability, while supporters contend it ensures greater safety scrutiny.

Meanwhile, the CDC is considering narrowing its universal COVID-19 vaccine recommendation – potentially shifting to a risk-based approach. Such a move would mark a significant departure from earlier policies, reflecting evolving scientific understanding and public skepticism.

The “Healthketeers” have touted injectable products should go through “placebo-controlled” trials for safety. However, what they have failed to indicate is the products do go through “placebo-controlled” trials – the placebo is just not an inert placebo, such as normal saline. The FDA’s own “regulations” indicate that another product, other than an inert placebo, can be used when that product’s safety is well-known. Why are they not telling this to the public? Why is it the public has to demand “inert placebo” controlled trials? Inert placebo-controlled trials are the gold standard to determine safety.

While the CONvid-1984 modified mRNA gene therapy bioweapon shots did undergo a placebo-controlled trial using normal saline as the placebo, Pfizer, knowingly, undermined that trial by injecting the placebo group with the bioweapon shot. This was accepted by the FDA to approve the first CONvid-9184 bioweapon shots. However, Kennedy and Makary have not indicated any intention of suspending or ending these bioweapon injections for adults.

As the FDA prepares for its May 22 meeting, the outcome could redefine the future of COVID-19 vaccination in the U.S. With new leadership in place and growing debate over vaccine mandates, the agency’s decisions will be closely watched.

Let’s be clear – the States mandate the shot on the CDC recommended childhood immunization schedule, not the federal government. So, even if the Healthketeers do not get those removed from the childhood schedule, State residents can approach and lobby State legislation in their state to do just that. And, there is always refusal to inject you or your child with a bioweapon shot.

Has everyone forgotten about the hundreds of millions of dollars the federal government paid Moderna to make “new” modified mRNA gene therapy bioweapon shots for the “bird flu” (H5N1) and other so-called variants of “bird flu”? Where are these MAHA Healthketeers occupying offices in these unconstitutional health agencies on those? Because of the addition of the H5N1 “bird flu” to an existing emergency declaration for H7N9 due to CBRN agents, all of this falls under the PREP Act.

The four “Healthketeers” were nominated and confirmed just to appease the public. It was a public relations maneuver plain and simple. Neither Kennedy nor Makary have any intention of slowing down the production of current and future modified mRNA gene therapy bioweapon shots nor do either have any intention of stopping those products. They are there to lull those gullible “medical freedom” fighters into supporting their MAHA agenda, which will not do anything regarding “medical freedom”. Government is not authorized to conduct any intrusion into medical care or health care. Individuals are responsible for their own health.

As far as medical freedom goes, your right to choose based upon proper informed consent and your right to refuse based on the same is recognized, guaranteed and protected by the Ninth Amendment to the Constitution for the united States of America.

Department and agency appointees change with every president. There is absolutely no way these Healthketeers can make any lasting change. The “policies” implemented during their tenure can and will be done away with upon the next presidential change. Moreover, Kennedy and Makary are not going to try and stuff the modified mRNA gene therapy bioweapon shot genie back into the bottle – that is going forward because that is what Big Pharma wants and so does the Department of Defense (DOD). These modified mRNA gene therapy bioweapon shots are being developed under the DOD through the PREP Act. DOD never relinquishes their “weapons”. In fact, CBRN agents, which are also weapons of mass destruction, are being used on the people by the government. And, because of the dis-ease caused by these government released agents, the government then helps develop and promote the “cure” – a bioweapon shot. It happened under Trump the first time and it’s happening now.

The American public needs to wise up and quit running for the pitiful bones the MAHA Healthketeers are throwing in appeasement. Kennedy, Makary, Bhattacharya, Oz, and Prasad were “confirmed” because they will “play ball” with government and Big Pharma. After all, Big Pharma and other corporations own the federal government. If Americans want change, Americans will have to do the fighting for it themselves at the local and State level.

In fact, Dr. Joseph Sansone has compiled potential legislation for all 50 states to recognize the mRNA bioweapon shots as illegal under all current State laws. The legislation has been introduced in Minnesota by Rep. Shane Mekeland. Dr. Francis Boyle prepared a sworn affidavit for Dr. Sansone to attach to each State’s proposed bill declaring the CONvid-1984 modified mRNA gene therapy injections meet the criteria of biological weapons and weapons of mass destruction and are illegal in all US States according to existing State laws. Deadlines may have passed in many States to submit new legislation; however, residents can begin to contact state district representatives in preparation for next year. When you access the proposed bill for your state, be sure and search for the appropriate law referenced in the bill, print it (if possible) and have it in the package for your representative.

In order to get these modified mRNA gene therapy bioweapons stopped, the people are going to have to mobilize and get legislation in each State to prohibit the bioweapons in their State. You can’t rely on “windsock Healthketeer” Kennedy nor his other three Healthketeers to do it. Besides, why rely on an unconstitutional agency head to do for you what you should be doing for yourself?

Article posted with permission from Sons of Liberty Media