An FDA panel just recently approved a so-called EUA, Emergency Use Authorization, for the Moderna and Pfizer-Biontech “COVID-19 Vaccine” for infants and children aged 6 months to 5 years. Why do I believe they are pushing this so hard? To reduce a very significant legal liability. In the recent FOIA request from the FDA and Pzifer reports of adverse events had huge implications.
The effects of the COVID-19 Vaccines can be transmitted through body fluids. This includes but is not limited to blood and breastmilk. A report out of Europe implied that the hepatitis outbreak among children is because of breastfeeding vaccinated mothers. Here are some pages from a Pfizer document released because of the FOIA request. The one that the FDA wanted 75 years to process!
I suspect there are millions of unvaccinated children of breastfeeding age that have been exposed to the adverse effects of experimental gene therapy injections because their mothers may have received self-amplifying mRNA from their COVID-19 inoculation. The breastmilk of the mothers may be contaminated with transcribed spike proteins. A significant portion of this age group were born before the EUA COVID-19 Vaccine was available. What does that mean?
A clear cut shot at an injury lawsuit because they have not been inoculated with the EUA COVID-19 Vaccine!! I believe the principal applies to the non-recipients of EUA COVID-19 Vaccines that have been injured from the COVID-19 Vaccine because blood/organ donations from an inoculated donor or inoculated sex partners. Doesn’t this make sense as to why hospitals deny “unvaccinated” organ recipients an organ donation? It’s likely the organ donation came from a deceased COVID-19 Vaccine recipient!
Here’s the link to the original article!
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