+ + + + + +

 

A little while back – and it was actually covered by some of our Canadian media – Health Canada CONFIRMED what independent scientists had discovered and were making public, ie., that there was foreign DNA in the mRNA needles.

 

Health Canada further disclosed that the company had not disclosed that information in their documentation submitted for emergency use authorization.

 

The Canadian regulatory approval system is entirely based on a self-regulatory framework model, where all of the studies and trial data is undertaken by the company, not Canadian government or independent third-party scientists.

 

The “safe and effective” claims we’ve therefore been hearing from the very “get-go” have all been based on the word of people making those claims [Premier King and Dr. Morrison here in Prince Edward Island] BLINDLY TRUSTING that Moderna and Pfizer were trustworthy and telling the truth. We know now that was beyond foolish and irresponsible.

 

We can now properly characterize those pushing the needles and assuring us of their safety as the official “spokespersons for global liars,” pursuing genocide.

 

These lackeys were bribed with tons of money to be enlisted as foot soldiers in the malicious plans, so the globalists who we don’t know could access the “trust factor” for successful delivery of their lies and the implementation of their steps in their plans with the local population.

 

There was a lot of noise made about Health Canada’s admission of foreign DNA contaminating the needles made by a lot of people across the country – ie., there were a number of social media posts from me and Dr. Laura Braden here in PEI on this news – but NOTHING was done about it anywhere in the country.

 

Despite the absolutely top-shelf priority of this serious matter, [something that could potentially alter forever what it means to be human] NOT A PEEP from a single leader in Prince Edward Island. Neither in the government nor the churches!

 

Recommendations to continue taking those poisonous needles continue, with all the same propaganda and false advertising same as usual.

 

Not only is this DNA in the jabs a clearly-deliberate, planned facet of the contents employed to cause turbo cancers” from the corruption of our human DNA with foreign DNA injected into people, but that foreign DNA then may ALTERS the “human” DNA, making us no longer human, but “transhuman”.

 

The Surgeon General of Florida concludes his somewhat technical but quite understandable statement that explains his decision with the following shocking comment, one that highlights how the FDA is obviously willing to turn a blind eye to this critically-important, historically-significant issue and challenge now facing the entire human race as a result of the immoral misuse of biotechnology.

 

And keep in mind that what the FDA approves Canada approves in lockstep the day after after, so an equal partner in the same corruption until action is taken to stop this genocide from proceeding any further:

 

 

The mainstream media will quickly attempt to portray the public announcement from the Surgeon General for Florida that the MRNA injections are dangerous and unfit for human use, so I am posting here the words from the Surgeon General himself, as found on Florida’s Health Website.

 

 

 

 

In 2007, the FDA published guidance on regulatory limits for DNA vaccines in the exit disclaimer iconGuidance 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 bio-distribution 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 exit disclaimer icon 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:

 

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.”