While American Big Media in 2023 was focused on the history and events of September 11 in American history, the FDA obediently approved a new round of Big Pharma jabs that day.

Not surprisingly, these shots from Pfizer and Moderna are technically called updates (rather than boosters), because they are made against the newer XBB1.5 variant. 

The XBB1.5 variant that the shots were designed to neutralize is almost gone, comprising only 3.1% of new infections. 

“It is now abundantly clear that the shots were never designed to prevent transmission,” says America’s Frontline Doctors (AFLD) in an October 2023 report. “They are ineffective at even preventing severe injury and death as their protection starts waning almost immediately.”

“Scientifically, the production of new boosters or updates for a quickly mutating RNA virus makes no sense,” the report emphasizes. “By the time the new shots come to market, they are no longer a match to the variants currently in circulation.”

AFLD stresses that a “mountain of data now shows that the shots are inherently unsafe. Yet, they continue to be pushed on our children. This most recent round was authorized for children under an Emergency Use Authorization. What’s the emergency?? Most children have natural immunity already.”

“The push for these new ‘vaccine’ updates appears to have come out of nowhere,” their report states. “The Advisory Committee on Immunization Practices (ACIP) never announced that it would be reviewing these new shots and voting on their approval. At the September meeting, during which the inoculations were approved, the public comments were limited to ONE person.”

“This total lack of transparency by the ACIP and the CDC is to the point of criminality,” they emphasized. “It is ALMOST as criminal as approving them without any clinical trial data, which is exactly what occurred.”

“The public has been consistently told that double-blind, placebo-controlled clinical trials are the only standard that can be used to determine the safety and efficacy of a new product,” they revealed. “However, a surrogate of antibody production was used to evaluate these new monovalent shots with no data presented on safety or real-world effectiveness.”

The FDA approval came even as the most recent study by the Cleveland Clinic found that a person’s risk of getting COVID increased with every dose of the “vaccine” they received. 

“Since natural immunity has been shown to be more than 95% effective at preventing severe illness and death from COVID, these data beg the question of why this program of shots is still being pushed on the population.”

Even the government run VAERS (which is known to understate reality) reports:

• Over 36,000 people have died concomitant with vaccination.

• 27,000 have been diagnosed with myocarditis or pericarditis.

• Almost 68,000 people are now disabled because of unsafe, ineffective COVID shots.

• Excess mortality has increased 25% in some localities with the incidence of stillbirths paralleling those numbers.

Alarmingly, the approval of Pfizer and Moderna’s new monovalent shots applies to those 12 and older.

New shots for children under 12 years old were authorized under an Emergency Use Authorization. Manufacturers of all COVID shots continue to be free from liability until December 31, 2024, under the PREP Act (Public Readiness and Emergency Preparedness Act).

The recent FDA authorization was quickly followed by a meeting of the CDC-run Advisory Committee on Immunization Practices (ACIP) on September 12, 2023, in which the shots were approved for recommendation.

Meanwhile, the authorization for the older bivalent shots has been withdrawn, so the only shots available will be the new monovalent ones made against the XBB1.5 variant.

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IN GOD WE TRUST

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