FDA Moves to Apply Vaccine to 6-Month Old Infants – Here’s How to Fight Back
On June 14, 2022, VRBPAC (FDA advisors) will meet to discuss amending the EUA of the Moderna COVID-19 mRNA vaccine to include the administration of the primary series to children and adolescents 6 years through 17 years of age. On June 15, 2022, they will discuss amending the EUA of the Moderna COVID-19 mRNA vaccine to include the administration of the primary series to infants and children 6 months through 5 years of age, and also to discuss amending the EUA of the Pfizer-BioNTech COVID-19 mRNA vaccine to include the administration of the primary series to infants and children 6 months through 4 years of age.
The FDA is establishing a docket for public comment on this meeting. The docket number is FDA-2022-N-0904. Submit either electronic or written comments on this public meeting by June 13, 2022.
Comments received on or before June 7, 2022, will be provided to the committee.
Comments received after June 7, 2022, and by June 13, 2022, will be taken into consideration by FDA.
Interested parties can also do a formal oral presentation–several minutes depending on how many public speakers there are. If there are too many people requesting this, there’s a lottery to see who can speak. Deadline to request this is 6 pm ET on June 8.
Here’s the link to search for the docket FDA-2022-N-0904:
- Go to https://www.regulations.gov/
- Type in Search: FDA-2022-N-0904-0001
- Click on Comment button
Here is the link to the meeting page for reference and more details:
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“Authorized for use” isn’t the same as “medically indicated.” Why are politicians behaving as if the two are the same? They are not. If a vaccine is “authorized for use” in children, that means it’s OK to give the vaccine to children for whom vaccination is medically indicated (due to health conditions that make them vulnerable to COVID). It does not mean that all children should be vaccinated, or that that is a good idea.
They have removed the comments on this reg.
You can still comment.
https://www.regulations.gov/commenton/FDA-2022-N-0904-0001
The human immune system is not fully developed until at least three years of age. At six months the thymus gland is still busy distinguishing self from non-self. vaccines administered at six months might well be identified as “self” thereby precluding any immune response to contact with the pathogen. This is why humans, in fact all mammals, secrete antibodies (immunoglobulins) in colostrum and later in breast milk. Too many antigens introduced at or near the same time are likely to trigger autoimmune diseases,.especially in young children.
The reason our children are being aggressively targeted by COVID mandates is because vaccine makers want to get the shots onto the childhood vaccination schedule (even though they are not at serious risk from COVID) Once a vaccine is added to the childhood schedule, the vaccine maker is shielded from financial liability for injuries, unless the manufacturer knows about safety issues and withholds information! I believe the manufacturers have definitely withheld safety information along with lack of testing of the vaccines. Our children do not need these Ill prepared vaccines that have more of a chance of harming them than protecting them from COVID which is what a vaccine is supposed to do. This is the first vaccine I’ve ever heard of that doesn’t keep the recipient from getting the virus it’s supposed to protect you from. This is all about control and keeping the pharmaceutical companies from being liable for the deaths and injuries. To the FDA, don’t you dare allow the vaccine to be given to our most vulnerable citizens, the CHILDREN!!!