Dear John, The U.S. Food and Drug Administration (FDA) is likely to grant Emergency Use Authorization (EUA) for Pfizer’s BioNTech SARS-CoV-2 vaccine for children ages 6 months through 4 years and Moderna’s COVID-19 mRNA vaccine for infants and children ages 6 months through 5 years and 6 years through 17 years in their upcoming meetings today and tomorrow (June 14-15). CHD is poised to take legal action against the FDA should they grant these emergency use authorizations. We seek to hold FDA accountable for recklessly endangering our children with products that have little, no or even negative net efficacy. These products may put them, without warning, at risk of many adverse health consequences, including heart damage, stroke, other thrombotic events and future reproductive harm. Please join Children’s Health Defense in telling the FDA to get their #HandsOffOurChildren and let regulatory authorities know that we will not stand idly by while they subject the youngest, most vulnerable population to these experimental shots. We need Defenders like YOU to hold the line as we try to stop the approval of EUA amendments that profoundly impact the health and safety of our kids. Urgent: Take Action & Advocate Today on Behalf of Children! We have two action alerts. First, demand the FDA, CDC and VRBPAC members vote NO on the EUAs, and second, share Robert F. Kennedy, Jr.’s letter directly with your federal legislators. Please complete and share these action alerts today!   | 
