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Anne Reed of Operation Rescue reported last week that recently released documents from Pfizer that were submitted to the FDA prior to approving their COVID-19 vaccine in early 2021 showed that 82% – 97% of the documented pregnancy outcomes resulted in death in their post-marketing analysis.
This is more evidence that Pfizer and the FDA colluded together to conceal damaging data related to the roll out of the Pfizer COVID-19 vaccines.
Back in May of 2021, Operation Rescue published a report from a whistleblower who had examined the Pfizer documents submitted to the European Medicines Agency (EMA) which authorized the Pfizer COVID-19 vaccines for emergency use in the UK back in December of 2020, and among those documents (which we assume were also submitted to the FDA but not yet made public) were the results of animal trials showing serious birth defects occurred in rat specimens injected with the vaccines. See:
Health Impact News | By Brian Shilhavy – May 6, 2022 Editor, Health Impact News
The U.S. Government Vaccine Adverse Events Reporting System (VAERS) was updated today, and there have now been 1,255,355 cases of adverse reactions filed following COVID-19 vaccines since December of 2020, a 17-month time frame.
This includes 27,758 deaths and 51,600 permanent disabilities. (Source.)
(NaturalHealth365) Sections 8.1 and 13.1 of the drug insert for Pfizer’s FDA-approved COVID shot, COMIRNATY, feature several concerning statements: “Available data on COMIRNATY administered to pregnant women are insufficient to inform vaccine-associated risks in pregnancy.”“COMIRNATY has not been evaluated for the potential to cause carcinogenicity, genotoxicity, or impairment of male fertility.”
(NaturalHealth365) The U.S. government’s vax surveillance program – or Vaccine Adverse Event Reporting System (VAERS) – is an essential and historically underutilized tool intended to help keep the public as safe as possible from the adverse effects of vaxxes, including the flu shot, the COVID-19 shot, and the dozens of other shots contained within the childhood jab schedule. The U.S. Centers for Disease Control and Prevention (CDC) and the U.S. Food and Drug Administration (FDA) rely on VAERS data to identify potential safety concerns or patterns that require further investigation.
Dr. Ryan Cole was recently interviewed by Maria Zeee where he stated that he is getting reports all across the world from doctors observing that cancer rates are “taking off like wild fire” following COVID-19 vaccinations.
Pfizer announced this week that they were asking the FDA to issue an emergency use authorization (EUA) for a “booster” COVID-19 vaccine for children between the ages of 5 and 11. (Source.)
The FDA issued an EUA for the first Pfizer COVID-19 shots for this age group of children in October of 2021. (Source.)
At the time, a doctor on the FDA Advisory Committee deliberating on whether or not an EUA should be given for this age group, stated that the only way to find out if the Pfizer COVID-19 vaccines were safe for this age group was to start injecting them with it.
(NaturalHealth365) Despite not being tested on pregnant women for ethical reasons, the COVID shot was immediately pushed onto expecting, breastfeeding, and trying-to-conceive moms. This is obviated in Section 13.1 of Pfizer’s package insert for its version of the COVID shot, COMIRNATY, which has received approval by the U.S. Food and Drug Administration. Section 13.1 states that this drug “has not been evaluated for the potential to cause carcinogenicity, genotoxicity, or impairment of male fertility,” adding that only a single developmental toxicity study in rats indicates no vax-related effects on female fertility.