Dr. Rima Laibow joins Maria Zeee for the second time, dropping truth bomb after truth bomb about what future awaits dissidents if we don’t stand up, including re-education camps, the liquifying of human corpses, and the WHO’s special diagnoses for the “undervaccinated”.
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To prepare you and your family, head to Heaven’s Harvest on the link below (available only in the United States):
verb [ with obj. ]
compose the sequence of steps and moves for (a performance of dance or ice skating): he is now choreographing a ballet.
• plan and control (an event or operation): the committee choreographs the movement of troops.
“United Nations” is here, folks. The puppets / robots / clones who stand before the cameras are reading from a common script provided by – WHOM? Anyone want to venture a guess? And to what end?
I will guess: the ages-old Luciferian wet-dream of a small population under a tiny world government, absolute control, a cruel dictatorship (see the book “1984”), totalitarianism?
The fall and destruction of the Georgia Guidestones eloquently express the informed well-American citizens’ view of the NWO plan.
Alex Jones breaks down the open admissions of globalist elites to working towards collapsing society to eradicate humanity ahead of the Great Reset.
According to an ex-pharmaceutical industry and biotech executive, documents obtained from the U.S. Department of Health and Human Services (HHS) on Moderna’s COVID-19 vaccine suggest the U.S. Food and Drug Administration (FDA) and Moderna colluded to bypass regulatory and scientific standards used to ensure products are safe.
Alexandra Latypova has spent 25 years in pharmaceutical research and development working with more than 60 companies worldwide to submit data to the FDA on hundreds of clinical trials.
After analyzing 699 pages of studies and test results “supposedly used by the FDA to clear Moderna’s mRNA platform-based mRNA-1273, or Spikevax,” Latypova told The Defender she believes U.S. health agencies are lying to the public on behalf of vaccine manufacturers.
“It is evident that the FDA and NIH [National Institutes of Health] colluded with Moderna to subvert the regulatory and scientific standards of drug safety testing,” Latypova said.
“They accepted fraudulent test designs, substitutions of test articles, glaring omissions and whitewashing of serious signs of health damage by the product, then lied to the public on behalf of the manufacturers.”
In an op-ed on Trial Site News, Latypova disclosed the following findings:
- Moderna’s nonclinical summary contains mostly irrelevant materials.
- Moderna claims the active substance — mRNA in Spikevax — does not need to be studied for toxicity and can be replaced with any other mRNA without further testing.
- Moderna’s nonclinical program consisted of irrelevant studies of unapproved mRNAs and only one non-GLP [Good Laboratory Practice] toxicology study of mRNA-1273 — the active substance in Spikevax.
- There are two separate investigational new drug numbers for mRNA-1273. One is held by Moderna, the other by the Division of Microbiology and Infectious Diseases within the NIH, representing a “serious conflict of interest.”
- The FDA failed to question Moderna’s “scientifically dishonest studies” dismissing an “extremely significant risk” of vaccine-induced antibody-enhanced disease.
- The FDA and Moderna lied about reproductive toxicology studies in public disclosures and product labeling.
“Moderna’s documents are poorly and often incompetently written — with numerous hypothetical statements unsupported by any data, proposed theories, and admission of using unvalidated assays and repetitive paragraphs throughout,” Latypova wrote.
“Quite shockingly, this represents the entire safety toxicology assessment for an extremely novel product that has gotten injected into millions of arms worldwide.”….