By Faye Gaston
On May 19, 2021, "America's Frontline Doctors" filed a lawsuit against the Federal Government in the U.S. District Court for the Northern District of Alabama seeking a temporary restraining order against using the experimental emergency COVID-19 vaccines on children under age 16.
The lawsuit seeks to prevent forcing experimental DNA altering COVID-19 vaccines on United States children. The founder of "America's Frontline Doctors" on July 16, 2020, is Simone Melissa Gold, an anti-vaccine activist, physician, attorney, and author. The group consists of doctors that report information on COVID-19 from a conservative perspective.
The lawsuit brings up the point that there isn't enough reliable data to see what is happening with the vaccines. Reported side effects are bad, but how many more side effects will there be. The attorney says that "informed consent" is not being given. Dr. Angelina Farella, pediatric medical director for "America's Frontline Doctors," stated, "We've never seen this level of side effects for any vaccine without the FDA taking action.
The Rotavirus vaccine was pulled for 15 cases of non-lethal side effects, and the Swine Flu vaccine was pulled for 25 deaths. But now, by the CDC's data, we see a 12,000 percent increase in deaths with these vaccines, and they're still talking about giving this to our kids." She said children are statistically at zero risks for COVID-19.
The data shows that the recovery rate for COVID-19 patients under the age of 20 is 99.997 percent. Dr. Teryn Clarke, Executive Communications Director for "America's Frontline Doctors," said, "People are being misled here, and we need to ensure that we don't rob our children of their future because of a rush to administer a vaccine that has not been fully tested and approved."
A statement by "America's Frontline Doctors" said that researchers are concerned that spike proteins from the vaccines could cause disease even without the virus and could increase auto-immune disorders.
The plaintiffs' leading attorney, Lowell H. Becraft, said, "There is no public interest in subjecting children to an inoculation program to protect them from a disease that simply does not threaten them. Children are inherently incapable of providing informed consent.
Neither the children nor their parents can possibly give informed consent to these vaccines since the DHHS Secretary has failed to make even the minimum statutory disclosures regarding risks and alternative treatments." According to CDC's own medical and scientific data, in the last four months, more than 4,000 deaths from the COVID-19 vaccines were reported as opposed to 1,400 deaths in the previous ten years from all other vaccines combined. The CDC said it investigates reports of heart inflammation in teenagers and youngsters who received a vaccine against the virus.
The CDC reports that over 77,000 children under the age of 12 have received at least one shot as of May 24, and another 2.1 million between the ages of 12 and 15 have gotten at least one shot. At least 18 teens and young adults in Connecticut were hospitalized for myocarditis (heart condition) after receiving COVID-19 vaccines.
The FDA expanded the use of Pfizer's COVID-19 vaccine to children as young as 12 on May 10, saying the vaccine is safe and offers strong protection for younger teens. The Advisory Committee on Immunization Practices voted unanimously to approve the use of this vaccine to children aged 12 to 15.
The lawsuit is against the U.S. Department of Health and Human Services (HHS) and its relevant sub-agencies and personnel, including but not limited to the Food and Drug Administrator (FDA), Centers for Disease Control and Prevention (CDC), National Institutes of Health (NIH), Becerra, the HHS Assistant Secretary for Preparedness and Response, and the HHS Vaccines and Related Biological Products Advisory Committee. The analysis by "America's Frontline Doctors" suggests that the vaccines are a likely cause of reported deaths, spontaneous abortions, anaphylactic reactions, cardiovascular, neurological, and immunological adverse effects.