We Have a Long Way to Go, MAHA
Moderna's mRNA "SpikeVax" Covid shot was just fully approved by the FDA yesterday for "at risk" pediatrics aged 6 months to 11 years. WHAT?
MAHA is off to a bumpy start in the “vaccine” realm. Yesterday, July 10, 2025, the FDA fully approved Moderna’s Spikevax, the company’s COVID-19 vaccine, in children 6 month to 11 years of age who are at increased risk for Covid-19.
Photo by Airman 1st Class Anna Nolte
With American kids facing a staggering risk of chronic disease, the “at risk” pediatric population can include factors such as prematurity, obesity, asthma, and diabetes. Who will define “at risk?” Will it include kids with ADD? Allergies? Autism?
Both parents and doctors may face unrelenting pressure to comply with this recommendation … all IN SPITE OF hundreds of studies over the past 5 years linking these shots to myocarditis, pericarditis, strokes, dangerous clots, brain injury, cancer risks, and the list goes on.
This risk of the shot was taken right off the Moderna website:
“Myocarditis (inflammation of the heart muscle) and pericarditis (inflammation of the lining outside the heart) have occurred in some people who have received mRNA COVID-19 vaccines. Myocarditis and pericarditis following mRNA COVID-19 vaccines have occurred most commonly in males 12 years through 24 years of age. You should seek medical attention right away if you or your child has any of the following symptoms after receiving Spikevax, particularly during the 2 weeks after receiving a dose of the vaccine: chest pain, shortness of breath, feelings of having a fast-beating, fluttering, or pounding heart. Additional symptoms in children may include fainting, irritability, poor feeding, lack of energy, vomiting, pain in the abdomen, or cool, pale skin.”
How will a 6 month old infant report symptoms of chest pain?
If your one year old has a seizure, will the pediatrician suspect the covid shot? Will it be reported to VAERS, which has been significantly underreported for years?
Will this recommendation open the door to more vaccine mandates?
We now know how successful early treatment is for the Covid-9 virus. It is inexcusable that this approval has been given with the lack of long-term safety data.
What happened to Health and Human Services Secretary Robert F. Kennedy’s promise that all new vaccines will undergo placebo-controlled trials before approval? What happened to transparency, a return to gold standard science, and a return to vigorous scientific debate over serious safety concerns?
Many of us in the medical freedom arena feel deeply let down and betrayed by this latest move. Our voices need to be heard on this issue.
Time to Act:
Flood the phone lines of the Department of Health & Human Services-
1-202-690-7000
Share your concern and disappointment with Secretary Kennedy and Dr Marty Makary, FDA Commissioner, that this dangerous product has been fully approved for kids without adequate long-term testing.
I just left my message. Let there be hundreds of messages waiting as they open for business on Monday.
Our duty is to protect our children— especially when our government won’t.
