Important

Rarely used.  Reserved for things that are from leading scientists, scientific evidence, governments, and has a massive effect on medical freedom.  Important things will be relevant 10 years from now and not just a sensational headline like “Paris Hilton died of COVID” or “Mom protests school board”.  These are things that the 5 minute sound-bite reader must see first.

Planet Lockdown – Dr. Michael Yeadon (former Pfizer VP & Chief Scientist)

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https://www.bitchute.com/video/8YLXDB9aHRFj/

Dr. Malone (inventor of mRNA vaccine) – Stop Vaccinations Now Because of Antibody Dependent Enhancement (ADE)

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https://www.bitchute.com/video/eih5uxE5ZhQg/

CDC Quietly Revokes RT-PCR Emergency Use Authorization Because They Counted Covid-19 and Influenza Together

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Original article:    https://thelibertydaily.com/cdc-quietly-revokes-rt-pcr-emergency-use-authorization-because-they-counted-covid-19-and-influenza-together/ Here’s a punch in the gut for a nation that’s already hurting. As it turns out, the so-called “gold standard” testing referenced by so many “doctors” like Anthony Fauci, as well as government officials across the board, has had its Emergency Use Authorization revoked. The CDC announced, albeit quietly, on Wednesday … Read more

Informed Consent? AFLD Lawsuit Seeks Halt to EUA and FDA Approval

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source:  https://uncoverdc.com/2021/07/26/informed-consent-afld-lawsuit-seeks-halt-to-eua-and-fda-approval/   America’s Frontline Doctors filed a motion on July 19 to stop Emergency Use Authorization (EUA) of the experimental COVID-19 gene therapy injections. The lawsuit, filed in Alabama Federal Court against Xavier Becerra, Secretary of the Department of Health and Human Services (DHHS), and others, argues for immediate injunctive relief against the COVID-19 “Vaccines” … Read more

FDA Issues Recall for Defective COVID Tests Made by ‘World’s Largest Manufacturer’ of Rapid Tests

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FDA Issues Recall for Defective COVID Tests Made by ‘World’s Largest Manufacturer’ of Rapid Tests     July 28, 2021 by Kyle Becker The Food & Drug Administration issued a class I recall for a defective COVID rapid test that had been the “benchmark” for testing in the United States. It continues an alarming trend of problems with … Read more