Keeping You Informed

Quote: "Merck's Gardasil Vaccine Continues to Kill and Maim Young Girls as Two New Lawsuits are Filed. Prior to 2020 and the COVID Scam, the #1 most-read topic on the Health Impact News network, by far, was the Gardasil HPV vaccine, and the carnage this vaccine has caused in the U.S., and around the world. If you type in "Gardasil" into the search feature of Health Impact News, you will get a result of 475 articles we have published on this topic. Just one article, the story of Katie Robinson, as told by her mother and originally published on Sanevax.org, is the most-read article ever published on Health Impact News, having been read by many millions of people and shared over a million times on Facebook. Gardasil is back in the news this week, as Judicial Watch has reported on two new lawsuits filed against Merck by plaintiffs who were young teenage girls when they received the vaccines. Under U.S. law, vaccines approved by the FDA and part of the CDC recommended vaccine schedule for children are covered by the National Vaccine Injury Compensation Program, where the manufacturer of the vaccine cannot be sued. You have to sue the U.S. Government in their special "Vaccine Court." So the lawsuits against Merck, as the manufacturer of the vaccine, are limited to the fraud that was committed in bringing the product to market for FDA approval. And the evidence that Merck committed fraud in bringing Gardasil to market, along with the FDA and CDC committing fraud in approving it, is overwhelming."    Merck’s Gardasil Vaccine Continues to Kill and Maim Young Girls as Two New Lawsuits are Filed (healthimpactnews.com)  

Quote: "17-Year-Old Died ‘Suddenly in Sleep’ 6 Months After 2nd Pfizer Shot. VAERS data released Friday by the Centers for Disease Control and Prevention included a total of 1,205,755 reports of adverse events from all age groups following COVID vaccines, including 26,396 deaths and 214,521 serious injuries between Dec. 14, 2020, and March 25, 2022. The Centers for Disease Control and Prevention (CDC) today released new data showing a total of 1,205,755 reports of adverse events following COVID vaccines were submitted between Dec. 14, 2020, and March 25, 2022, to the Vaccine Adverse Event Reporting System (VAERS). VAERS is the primary government-funded system for reporting adverse vaccine reactions in the U.S. The data included a total of 26,396 reports of deaths — an increase of 337 over the previous week — and 214,521 of serious injuries, including deaths, during the same time period — up 2,937 compared with the previous week.        Excluding “foreign reports” to VAERS, 799,732 adverse events, including 12,103 deaths and 78,227 serious injuries, were reported in the U.S. between Dec. 14, 2020, and March 25, 2022. Foreign reports are reports foreign subsidiaries send to U.S. vaccine manufacturers. Under U.S. Food and Drug Administration (FDA) regulations, if a manufacturer is notified of a foreign case report that describes an event that is both serious and does not appear on the product’s labeling, the manufacturer is required to submit the report to VAERS. 

       Of the 12,103 U.S. deaths reported as of March 25, 17% occurred within 24 hours of vaccination, 21% occurred within 48 hours of vaccination and 59% occurred in people who experienced an onset of symptoms within 48 hours of being vaccinated. In the U.S., 559 million COVID vaccine doses had been administered as of March 18, including 330 million doses of Pfizer, 210 million doses of Moderna and 19 million doses of Johnson & Johnson (J&J).

Quote: "Heart Damage Found in Teens Months After Second Pfizer Shot, Study Shows. A new peer-reviewed study shows more than two-thirds of adolescents with COVID-19 vaccine-related myopericarditis had persistent heart abnormalities months after their initial diagnosis, raising concerns for potential long-term effects and contradicting claims by health officials that the condition is “mild.” A new peer-reviewed study shows more than two-thirds of adolescents with COVID-19 vaccine-related myopericarditis had persistent heart abnormalities months after their initial diagnosis, raising concerns for potential long-term effects. The findings, published March 25 in the Journal of Pediatrics, challenge the position of U.S. health agencies, including the Centers for Disease Control and Prevention (CDC), which claim heart inflammation associated with the Pfizer and Moderna mRNA vaccines is “mild.” Researchers at Seattle Children’s Hospital reviewed cases of patients younger than 18 years old who presented to the hospital with chest pain and an elevated serum troponin level between April 1, 2021, and Jan. 7, 2022, within one week of receiving a second dose of Pfizer’s vaccine.

        While 35 patients fit the criteria, 19 were excluded for various reasons. Cardiac magnetic resonance imaging (MRI) of the remaining 16 patients was performed three to eight months after they were first examined. The MRIs showed 11 had persistent late gadolinium enhancement (LGE), although levels were lower than in previous months. According to the study, “The presence of LGE is an indicator of cardiac injury and fibrosis and has been strongly associated with worse prognosis in patients with classical acute myocarditis.” In a meta-analysis of eight studies, LGE was found to be a predictor of all-cause death, cardiovascular death, cardiac transplant, rehospitalization, recurrent acute myocarditis and requirement for mechanical circulatory support.

Quote: 425 Different Tests for COVID Still Have Emergency Use Authorizations from the FDA in Third Year of "Pandemic". Almost 2 years ago, on May 5, 2020, we published an article reporting that not a single test being used to allegedly detect the COVID-19 virus was approved by the FDA, and that the ones that were granted emergency use authorizations (EUAs) were admitted to be unreliable by the FDA and the pharmaceutical manufacturers. I included testimony from a reader of Health Impact News who had 43 years of experience in Clinical Diagnostics and was appalled that our nation was being locked down over an alleged virus for which there was no accurate test. Fast forward now 2 years to today, and the only thing that has changed over these faulty tests is that now there are a lot more of them that have been given EUAs, and still none of them have been granted FDA approval. We have previously reported on how the CDC withdrew their EUA request on certain PCR tests at the end of 2021 because they claimed that some of these COVID tests could not distinguish between an influenza virus, or a COVID-19 virus. We have also previously reported how the CDC changed how they reported deaths at the end of 2020, because the statistics at the end of the year were not showing excess deaths in the year the COVID "pandemic" started, and they added about 400,000 deaths to make COVID appear to be a serious killer virus, which then hid the real increase in deaths that occurred in 2021 after the COVID-19 vaccines were rolled out. This is the biggest scam in the history of the world, as the flu disappeared in 2020 and still remains absent here in 2021, because there just are not enough sick people dying to inflate both flu and COVID numbers. And the real tragedy that this corruption has caused, besides the fact that the COVID-19 vaccines are destroying people's lives, is that this group of upper respiratory symptoms that used to be called "influenza" but is now called "COVID-19" is very easily treatable, by either using older drugs that are generally safe such as Ivermectin, or even natural products such as high-dose Vitamin C IV treatment. But to make sure these existing treatments do not interfere with the new vaccines and drugs that have been given EUAs by the FDA, the FDA has issued 215 warning letters for "Fraudulent Coronavirus Disease 2019 (COVID-19) Products" to protect the pharmaceutical industry and their EUA products "by pursuing warning letters, seizures, injunctions or criminal prosecutions against products and firms or individuals" that dare to defy the FDA by using unauthorized products to actually heal people."     425 Different Tests for COVID Still Have Emergency Use Authorizations from the FDA in Third Year of “Pandemic” (healthimpactnews.com)