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Wednesday, Apr 15, 2026

Lisa Marie Presley, singer and daughter of Elvis, dies aged 54

Lisa Marie Presley, singer and daughter of Elvis, dies aged 54

Lisa Marie Presley, singer and the only child of Elvis and Priscilla Presley, has died at the age of 54, after suddenly being hospitalised on Thursday.
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Brad 3 year ago
As we read through the DoD contract, it’s clear that Pfizer is in charge of communications with the FDA. Per the FDA documents, Pfizer exerted extreme influence over the FDA forcing the FDA to ignore safety flags during the clinical trials, thereby strong-arming the FDA to fraudulently authorize and then fraudulently approve a bioweapon as a safe and effective vaccine.

Pfizer is obviously the criminal in this case and can be criminally charged now. If I was an advisor in a criminal case, here’s a few examples on how I would eviscerate many of the fraudulent claims (extrinsic fraud) currently being made. Extrinsic fraud is when an attorney or expert witness misrepresents material facts or law so that victims are unable to take effective civil or criminal action

1. Pfizer’s DoD Contract was for a Prototype, NOT a Vaccine.

FALSE. Per the contract, the vaccine prototypes were part of a manufacturing demonstration, however the ‘vaccine prototypes’ would be categorized as emergency use authorized (EUA) or FDA-approved vaccines after receiving FDA authorization or FDA approval. If vaccine prototypes never received FDA authorization or approval, then they would have remained manufacturing prototypes and never distributed as vaccines to the US civilian population.

Pfizer’s Operation Warp Speed contract with the DoD was to produce 100 million doses of a vaccine (vaccine prototype) capable of providing protection against SARS-CoV-2 and related coronaviruses (variants) subject to FDA technical, clinical and regulatory success (laws and guidance).

Pfizer’s mRNA vaccines COULD NOT have been made available to the American public until after FDA regulatory approval per Sec 564 of the FD&C Act for an EUA authorized product or Sect 351 of PHS Act for a FDA-approval of a biological product based on successful clinical trial data.

The ‘vaccine prototypes’ would be categorized as emergency use authorized (EUA) vaccines after receiving FDA authorization and then FDA-approval.
Brad 3 year ago
JABRACADABRA (Abracadabra song parody from the makers of the 'Pure Blooded' song video) 15,400
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