Dear President Donald J. Trump,

Upon your inauguration as the 47th President of the United States on January 20, 2025, you have the opportunity to make amends for the mistakes that were made during your first administration.

I call upon you to take the actions necessary to REVOKE the FDA licenses for the COVID-19 mRNA “vaccines” from Pfizer and Moderna, REMOVE the mRNA biological products from the marketplace and call for a halt to all clinical trials involving this technology.

Please hear this loud and clear:
Operation Warp Speed was NOT a success. From a health perspective, it was an absolute disaster, and as President you bear personal responsibility for the harm, devastation and death that has been inflicted upon millions of Americans and billions of people around the world.

Because of political pressure that you proudly claim to have exerted upon the FDA, the mRNA injectable biological products that were a result of Operation Warp Speed were not subjected to the required tests to ensure safety. As a result, they have caused unprecedented harm while providing absolutely no benefit. They do not fit the definition of a “vaccine,” but they do fit the definition of a biological weapon.

During your first term in office you proclaimed that there was an emergency and that immediate and decisive action needed to be taken.

By now, you must certainly know the following:
The Centers for Data Concealment (CDC) manipulated their data in order to create a fraudulent COVID-19 “casedemic” and they are ignoring VAERS, V-safe and DMED data while also manipulating the analyses of death certificates in order to hide the evidence that a massive number of deaths have been caused by the mRNA injections.

The pharmaceutical companies committed fraud by hiding very important data from the FDA and from the American people which clearly show that the mRNA injections are NOT safe and NOT effective.

Pfizer performed a “bait and switch” tactic in which they used one manufacturing method (“process 1”) to make the biological products that were used in the clinical trials in order to gain Emergency Use Authorization (EUA). Pfizer then switched to a different manufacturing method (“process 2”) to make the biological products that have been injected into billions of people worldwide. The biological products made via “process 2” have been shown to be adulterated with turbo-cancer-causing SV40 promoter sequences in amounts that are far beyond the regulatory limit. This is potentially an absolutely unmitigated disaster.

The hurried and pressured manner in which the mRNA products were brought to market did not stop or even slow down the so-called COVID-19 pandemic. Quite to the contrary, the more injections people have received the more likely they are to be diagnosed with COVID-19, as well as a whole host of vaccine-acquired immuno-deficiency diseases (VAIDS). By working at "warp speed," without concern for long- term safety and with blatant disregard for the fundamental rights of people and the principles of informed-dissent, our government colluded with the pharmaceutical hospital emergency industrial complex and the mainstream media to create an actual pandemic of long-term, chronic, horrifically disabling and enormously costly diseases.

Well over 1,000 VAERS reports have been filed on behalf of women who lost their unborn children on the very same day that they received the mRNA injections.

Over 38,000 VAERS reports have been filed documenting the deaths that are likely to have been caused by the mRNA injections.

The FDA has been captured by the pharmaceutical industry and has approved additional mRNA products without requiring the necessary long-term safety testing that has historically been required.

The FDA, the Environmental Protection Agency (EPA) and the Occupational Safety and Health Administration (OSHA) have absolutely failed to require the proper monitoring of the environment within research and manufacturing facilities. Everyone involved in such work is at risk of exposure to gene-altering and cancer-causing substances during the course of their research, clinical trials, manufacture and administration of the mRNA products. Due to the process known as “shedding,” it is believed that workers who may have been exposed to these experimental biological products may then spread contagion to their close family members as well as other members of their community. In essence, “lab leaks” may be occurring throughout America and the world on a daily basis due to the transmissibility of these experimental gene-based products.

video's and more here
https://jamesroguski.substack.com/p/an-open-letter-to-president-donald