The so-called “side-effects” of the COVID jab are well known: myocarditis and pericarditis, heart inflammation problems that have plagued children and young people given the experimental injection. This is the condition that killed Ernest Ramirez’s son and it’s the reason healthy young athletes are dropping dead on sports fields by the dozens around the world.

The problem has been so severe that the FDA added warnings to the Pfizer-BioNTech and Moderna shots stating that “reports of adverse events suggest increased risks of myocarditis and pericarditis, particularly following the second dose and with onset of symptoms within a few days after vaccination” and “vaccine recipients should seek medical attention right away if they have chest pain, shortness of breath, or feelings of having a fast-beating, fluttering, or pounding heart after vaccination.” 

That was before the shot was authorized for kids as young as 5. So, how did the FDA justify giving a shot known to cause heart problems to kids?

Pfizer-BioNTech changed their jab’s ingredients, adding a heart medication (tromethamine, also known as Tris) to the shot for kids ages 5 to 11.

And, these experimental COVID injections don’t even work! They are ineffective at preventing infection and death. It doesn’t make sense to apply a risk-benefit analysis to a useless and dangerous vaccine, but it’s worth pointing out that babies and preschoolers are at virtually no risk of COVID.

According to CDC data, only 442 kids under 5 have died with COVID since the pandemic began. COVID is linked to just 1 percent of deaths in this age group!

Babies as young as 6 months don’t need the vaccine and they shouldn’t be subjected to its risks.

A letter to the FDA from 18 members of Congress asked questions about the safety of COVID-19 vaccines for young children.

“The data show that the risks of serious adverse outcomes for COVID for children five and under is very low and as such the standard for evaluating EUA interventions must be very high,” the letter states.

“We believe it is prudent and necessary that the FDA provide answers to a number of questions before approving EUA vaccines for children under age 5, including more than 70% of whom are already seropositive for COVID-19.”

They ask the FDA to explain, among many other things:

• What the cardiac risk factor is for children who receive EUA COVID-19 vaccines.

• Why the FDA recently lowered the efficacy bar for COVID-19 vaccines for the youngest children.

• When the FDA and the Centers for Disease Control and Prevention (CDC) will provide the public with more details on children’s serious adverse outcomes from COVID-19 infections.

• If it is possible that administering the vaccines in young children could predispose them to increased risk from future novel COVID-19 variants.

• How many children ages 5 and under with and without pre-existing medical conditions have died from COVID-19 or its variants.

Finally, the letter asks Commissioner Califf to “please list the medical emergencies [among] children 0 to 4 years old that enable the FDA to approve the COVID vaccine for children using its EUA.”

For the pharmaceutical companies that run the FDA, this isn’t about science or health, it’s about money and control. 

Because of vaccination requirements for school attendance, the pharmaceutical companies have the greatest control over our kids and they can make the most money by exploiting them. 

As Toby Rogers, Ph.D. points out, the real reason the pharmaceutical companies are going after our kids is so they “can have liability protection forever.” Eventually, they’ll lose the protections they have under Emergency Use Authorizations for COVID, so they’re planning to make use of the protections they can get if the COVID vaccines are added to the childhood vaccination schedule. 

We can’t let them carry out this deadly assault on our children.

TAKE ACTION! Tell the FDA: Don’t Break Babies’ Hearts! No COVID Jabs for Babies!