“We the People 50, Recall the Shots” Initiative

Demand letter filed with AG of Mississippi, more letters to state AGs to follow

I have submitted an affidavit on cGMP noncompliance to this initiative. They plan on submitting these complaint letters and affidavits to all AGs.

Press release here.

An Emergency Referral Letter has been sent to Attorney General Lynn Fitch of Jackson, Mississippi to bring to her attention the ongoing fraud and misrepresentation of the safety, efficacy and FDA-approval status, of the COVID gene therapy shots available and administered to the public. These shots have been mislabeled and misrepresented as “safe and effective” and “fully approved products” under cGMP compliance, which they are not. This action is brought in order to protect Mississippians from unfair and deceptive business practices that are harming and taking lives. Besides the inherent lack of safety of the experimental genetic vaccine technology platform, there is recent scientific evidence of contamination of the COVID mRNA shots with the DNA plasmids used to create them, as well as evidence, with failure to ameliorate, of significant degradation of the mRNA within these shots. Batch to batch variation in deaths and injuries, with some batches highly associated with harm, over others, supports lack of cGMP compliance and regulatory oversight. These are clear violations of Good Manufacturing Practice by the manufactures, as stipulated is required by the US Code of Federal Regulations, Title 21 parts 210, 600, 611. There is documented evidence of excessive deaths and disability in the CDC VAERS system attributed to these experimental products, in numbers far above those, that in the past, led to the recall of other shots. For example, in the past, 26 deaths from Guillain- Barre prompted the recall of the swine flu vaccines, while the VAERS system currently lists 34,965 deaths attributed to the COVID genetic vaccines overall and 17,315 deaths in the US alone. Additionally there are 64,573 permanently disabled, 3,884 cases of myocarditis and pericarditis in 6 months to 25 year-olds, and 44 deaths in children aged 6 months to 12 years old. These figures in VAERS are known to be under-reported. The risk of harm from these genetic vaccines far outweighs any benefit they were thought to possess, especially for once-healthy children and adolescents who are at essentially zero risk of mortality from COVID, but who are now suffering heart attacks and strokes and dying in their sleep in unprecedented numbers, with no investigations by the CDC and no outrage by the medical community. These deaths and injuries as well as the allegations of contamination, requires that previous precedent be met and prompt, swift action be taken in this matter, to seize and recall these products. This Demand requires that the Attorney General litigate against the manufacturers and the agencies that did not enforce or comply with these cGMP statutes and seek damages for those harmed. In this letter, we are asking AG Fitch to open immediate investigations into the contamination findings and the misrepresentations of these shots as being “safe and effective”. Because the FDA and CDC no longer seem to be functioning properly in their regulatory oversight of these products, as compared to past practices, we’ve gone to the State level to get these gene therapy shots recalled, as it the right of each state to do, to protect its citizens from unreasonable harm.

Art for today: Plein air sketch of CA hills, 8x10 in