February 23, 2021 (Children’s Health Defense) — In December, the U.S. Food and Drug Administration (FDA) granted Emergency Use Authorization to two messenger RNA (mRNA) vaccines against COVID-19. Because the unapproved vaccines’ status is investigational, anyone who gets an injection (whether they realize it or not) is agreeing to participate in an ongoing experiment.
Recognizing that there are many unknowns, many Americans have refused the experimental jab, including members of the armed forces and healthcare workers, but with one notable exception: healthcare providers who are pregnant.
Even without data from Pfizer or Moderna sufficient “to inform vaccine-associated risks in pregnancy,” expectant doctors, nurses and others appear eager for the shots, perhaps influenced by the American College of Obstetricians and Gynecologists, which states that neither a conversation with a clinician nor even a pregnancy test are necessary prerequisites.
Do these individuals know that as of Feb. 12, the Vaccine Adverse Event Reporting System (VAERS) had already received 111 reports of adverse events experienced by women who were pregnant at the time of their Pfizer or Moderna injection?
The first such report was submitted Dec. 22, just 10 days after authorization of the Pfizer vaccine. Nearly a third (31%) of the women had miscarriages or preterm births, which occurred within as little as one day of injection — the majority after a single dose of vaccine.
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