The mother of 10-year-old Isabella shares her story. She trusted the doctors and was told that the HPV Vaccine was needed to prevent cervical cancer, which she was told could kill her daughter if contracted.
Within a few days after receiving the HPV vaccine, Isabella started having uncharacteristic headaches that wouldn’t go away. She was admitted to the Children’s Hospital, evaluated for migraines, medicated, and sent home. She continued getting worse with excruciating pain until there was nothing left to do for her.
Please share this 11-minute story of a real family’s experience. They want to spread awareness of the risks of Gardasil, and prevent this from happening to someone else’s child.
“The European (EEA and non-EEA countries) database of suspected drug reaction reports is 
“In 2012, when she was 20 years old, Rochelle was so injured by Merck’s Gardasil vaccine that she had to give up her pre-med studies. Ten years later, her mother was injured by Moderna’s COVID-19 vaccine, and shortly after, her grandmother died just a few weeks after getting Pfizer’s vaccine.”
“Since the emergency use authorization of the COVID-19 vaccines in December of 2020, through the latest update of the VAERS database on October 14, 2022, 84% of all deaths reported after vaccination for the past 31+ years have been reported following COVID-19 vaccines. ”
The U.S. Food and Drug Administration (FDA) has refused a Freedom of Information Act (FOIA) request to release the autopsy results of people whose deaths were reported to the Vaccine Adverse Event Reporting System (VAERS) after receiving a COVID-19 shot.
“Baum Hedlund Aristei & Goldman and Robert F. Kennedy, Jr., chairman of Children’s Health Defense, this week filed a wrongful death suit against Merck alleging the drugmaker’s Gardasil HPV vaccine caused the death of 13-year-old Noah Tate Foley.”
“The Journal of Insulin Resistance published a two-part research paper, “Curing the pandemic of misinformation on COVID-19 mRNA vaccines through real evidence-based medicine.”
“The problem in issuing the existing smallpox/monkeypox vaccine an EUA, is that it was already approved by the FDA, even though it has not been tested in the public much beyond the initial trials conducted by the drug company.