Posted originally on Jan 4, 2024 By Martin Armstrong 

The truth is coming out about the vaccines in 2024. Those living in Florida may have received a notification this week from Florida Surgeon General Joseph Ladapo’s office warning the public that the vaccination is not safe. The FDA warned Lapado last month that questioning the vaccine would be considered “misinformation,” but he ignored their threats and reported what they found.

Lapado has been attempting to warn the public about the dangers of the vaccine to no avail. Florida was the first state to recommend against vaccinations for healthy children. Lapado later came out and said that healthy people under the age of 65 should not take the booster shots. DeSantis has supported Lapado and has even brought him on the campaign trail. However, this bold move is sure to anger the establishment.

I will post the full letter distributed to residents of the state at the end of this blog post. The FDA sent a letter to Dr. Lapado on December 14, 2023, but he felt that they failed to adequately address his concerns. This is the FDA’s response (read the full letter here):

1. In response to the question regarding potential genotoxicity of the mRNA COVID-19 vaccines: No SV40 proteins are encoded for or are present in the vaccines. On first principle, it is quite implausible that the residual small DNA fragments located in the cytosol could find their way into the nucleus through the nuclear membrane present in intact cells and then be incorporated into chromosomal DNA.2 Additionally, studies have been conducted in animals using the modified mRNA and lipid nanoparticle together that constitute the vaccine, including the minute quantities of residual DNA fragments left over after DNAse treatment during manufacturing, and demonstrate no evidence for genotoxicity from the vaccine.3 Pharmacovigilance data in hundreds of millions of individuals also indicate no evidence indicative of genotoxicity.
2. Regarding whether FDA considers the lipid nanoparticle delivery system in setting the safe levels of DNA in the mRNA vaccine: The agency has taken into account the totality of the mRNA COVID-19 vaccine product, including the lipid nanoparticles, as it reviewed the manufacturers’ specifications for residual DNA fragments present. Any contamination with residual DNA fragments is monitored routinely as a product specification.
3. Regarding concern for possible integration of the residual DNA fragments into reproductive cells: Please see the response to the first question above regarding the implausibility that the minute amounts of small DNA fragments present could find their way into the nucleus of these cells. Additionally, reproductive toxicology studies have been conducted to evaluate the mRNA COVID-19 vaccines and have found no concerns.

The FDA admits that the mRNA vaccine has the potential to alter DNA, but says it is “quite implausible.” Dr. Lapado responded by sending the FDA their own guidelines for DNA vaccines issued in 2007: Guidance for Industry: Considerations for Plasmid DNA Vaccines for Infectious Disease Indications (Guidance for Industry). He then points out that the FDA’s own guidelines before COVID said that DNA integration had the potential to transform healthy cells into cancerous cells and cause chromosomal instability. The guidelines from 2007 note that such vaccines could impact every bodily organ, muscle, and blood.

Furthermore, Lapado said that the reply on December 14 provided no evidence that DNA assessments were conducted on the COVID vaccines, and instead, the letter only validated that DNA fragments were present in these vaccinations. Plain and simple – “THESE VACCINES ARE NOT APPROPRIATE FOR USE IN HUMAN BEINGS.”

Below is the full message from the Surgeon General that will cause an uproar amongst the establishment in the coming weeks:

Florida State Surgeon General Calls for Halt in the Use of COVID-19 mRNA Vaccines

Tallahassee, Fla. – On December 6, 2023, State Surgeon General Dr. Joseph A. Ladapo sent a letter to the United States Food and Drug Administration (FDA) Commissioner Dr. Robert M. Califf and Center for Disease Control and Prevention (CDC) Director Dr. Mandy Cohen regarding questions pertaining to the safety assessments and the discovery of billions of DNA fragments per dose of the Pfizer and Moderna COVID-19 mRNA vaccines.

The Surgeon General outlined concerns regarding nucleic acid contaminants in the approved Pfizer and Moderna COVID-19 mRNA vaccines, particularly in the presence of lipid nanoparticle complexes, and Simian Virus 40 (SV40) promoter/enhancer DNA. Lipid nanoparticles are an efficient vehicle for delivery of the mRNA in the COVID-19 vaccines into human cells and may therefore be an equally efficient vehicle for delivering contaminant DNA into human cells. The presence of SV40 promoter/enhancer DNA may also pose a unique and heightened risk of DNA integration into human cells.

In 2007, the FDA published guidance on regulatory limits for DNA vaccines in the Guidance for Industry: Considerations for Plasmid DNA Vaccines for Infectious Disease Indications (Guidance for Industry). In this Guidance for Industry, the FDA outlines important considerations for vaccines that use novel methods of delivery regarding DNA integration, specifically:

• DNA integration could theoretically impact a human’s oncogenes – the genes which can transform a healthy cell into a cancerous cell.
• DNA integration may result in chromosomal instability.
• The Guidance for Industry discusses biodistribution of DNA vaccines and how such integration could affect unintended parts of the body including blood, heart, brain, liver, kidney, bone marrow, ovaries/testes, lung, draining lymph nodes, spleen, the site of administration and subcutis at injection site.

On December 14, 2023, the FDA provided a written response providing no evidence that DNA integration assessments have been conducted to address risks outlined by the FDA themselves in 2007. Based on the FDA’s recognition of unique risks posed by DNA integration, the efficacy of the COVID-19 mRNA vaccine’s lipid nanoparticle delivery system, and the presence of DNA fragments in these vaccines, it is essential to human health to assess the risks of contaminant DNA integration into human DNA. The FDA has provided no evidence that these risks have been assessed to ensure safety. As such, Florida State Surgeon General Dr. Joseph A. Ladapo has released the following statement:

“The FDA’s response does not provide data or evidence that the DNA integration assessments they recommended themselves have been performed. Instead, they pointed to genotoxicity studies – which are inadequate assessments for DNA integration risk. In addition, they obfuscated the difference between the SV40 promoter/enhancer and SV40 proteins, two elements that are distinct.

DNA integration poses a unique and elevated risk to human health and to the integrity of the human genome, including the risk that DNA integrated into sperm or egg gametes could be passed onto offspring of mRNA COVID-19 vaccine recipients. If the risks of DNA integration have not been assessed for mRNA COVID-19 vaccines, these vaccines are not appropriate for use in human beings.

Providers concerned about patient health risks associated with COVID-19 should prioritize patient access to non-mRNA COVID-19 vaccines and treatment. It is my hope that, in regard to COVID-19, the FDA will one day seriously consider its regulatory responsibility to protect human health, including the integrity of the human genome.”

In the spirit of transparency and scientific integrity, State Surgeon General Dr. Joseph A. Ladapo will continue to assess research surrounding these risks and provide updates to Floridians.