We’ll cover the truth regarding the dangers of prescription medicines and vaccines.
Whistleblower Doctor Claims Tamiflu Drug Fraud Bilked $1.5 Billion from Government to Stockpile Drug that is Ineffective in Stopping the Flu
Drug company Hoffmann-La Roche (OTCMKTS – RHHBY) bilked U.S. federal and state governments out of $1.5 billion by misrepresenting clinical studies and falsely claiming that its well-known influenza medicine Tamiflu was effective at containing potential pandemics, according to a recently unsealed whistleblower lawsuit. The lawsuit claims the drugmaker’s scheme involved publishing misleading articles falsely stating that Tamiflu reduces complications, severity, hospitalizations, mortality and transmission of influenza. The company then used those articles to aggressively market the drug to the government for pandemic use. Relying on the supposed truthfulness of Roche’s claims, federal and state governments spent about $1.5 billion to stockpile Tamiflu to combat influenza pandemics, according to the complaint.
Less Than 1% of Vaccine Injuries Reported in the Government National Vaccine Adverse Event Reporting System
The Vaccine Adverse Event Reporting System (VAERS) was created by Congress under the National Childhood Vaccine Injury Act of 1986 and became operational in 1990 in response to growing public concern about the safety of vaccines, particularly the DPT (diphtheria-pertussis-tetanus) vaccine. VAERS is jointly operated by the U.S. Food and Drug Administration (FDA) and U.S. Centers for Disease Control and Prevention (CDC). Since VAERS began collecting reports in 1990, as of Nov. 14, 2019 there have been 8,087 vaccine-related deaths reported and about 47 percent of those death reports were for children under the age of three. There have been 17,394 reports of permanent disability following vaccinations, with about 30 percent occurring in children under age 17, while about 40 percent are in adults between 17 and 65 years old. A 2011 report by Harvard Pilgrim Health Care, Inc. for the U.S. Department of Health and Human Services (HHS) stated that fewer than one percent of all vaccine adverse events are reported to the government.
As year 2020 gets underway, we are seeing more and more mainstream media sources covering medical kidnapping stories, especially when Child Abuse Pediatricians are involved. One of the latest investigative reports comes from the Tampa ABC News I-Team Investigations. Katie LaGrone, reporting with ABC Action News, writes: "A Florida lawmaker believes the state’s medical experts on child abuse need more checks and balances after an I-team investigation revealed several pediatricians have made questionable calls against parents who appeared to have done everything right. 'Any position of authority that isn’t checked by something is concerning,' said Florida Democratic Representative Anna Eskamani of Orlando. Eskamani was responding to our investigation that found several cases where child abuse pediatricians, who were hired to be the state’s experts on abuse, wrongly accused Florida parents of child abuse."
Pro-Vaccine NJ Senator Caught Denying Aborted Fetal Tissue is Used in Today’s Vaccines to try to Stop Religious Exemptions
New Jersey is one of the most recent states where lawmakers want to remove vaccine exemptions, specifically religious exemptions. Del Bigtree's HighWire program has captured Senator Sweeney's denial that today's vaccines contain human DNA from aborted babies, and then presents the truth that contradicts Senator Sweeney's denial. In fact, today's vaccines use more aborted DNA than ever before.
Zantac, once called the "best-selling drug in the world," has been linked to cancer. Michele Cohen Marill, writing for Wired, states: "That burning feeling in your chest after you eat a heavy meal could be heartburn. Or it could be worry over the drugs you’ve taken to treat that heartburn. Among the top medical stories of 2019 was the discovery of contaminants in common medicines, and ranitidine—best known as Zantac—took up a large share of those headlines. A cancer-causing substance known as NDMA has been repeatedly found in one of the most popular antacid drugs in the United States. The scary news continues in 2020. On Wednesday, the Food and Drug Administration announced voluntary recalls of prescription forms of ranitidine by two generic drug companies, Appco Pharma and Northwind Pharmaceuticals, bringing the total number of ranitidine recalls to 14 in the past five months. The agency also reported that Mylan Pharmaceuticals recalled three lots of Nizatidine (Axid), a similar drug, again because of NDMA. This week’s recalls are a new cause for alarm for the 15 million Americans who take ranitidine at prescription levels, and the millions more who regularly take lower-dose, over-the-counter versions. More than 60 million Americans experience heartburn at least once a month. Zantac was once the best-selling drug in the world."
California Medical Doctor Explains How Doctors Receive No Medical Training on Vaccines – Indoctrination on Belief in Vaccines
Dr. Gary Foresman was recently interviewed by Polly Tommey on the VAXXED II tour bus. Dr. Foresman compared today's medical training, which forces most doctors into huge debts, as "the indoctrination, almost the indentured servitude of the average physician" coming out of medical school. He goes on to explain that doctors come out of their training wanting to think they have all the knowledge after spending so much money, and that it is hard for them to admit there are gaps in their knowledge. "Today's doctor, they're spending hundreds of thousands of dollars, and then when you go through medical school and residency, and you put your life on the line, you've been on call every four nights - you've had some of the worst nights of your life overnight in the ICUs, and I have, you do not like to come out of that training, and think you don't have all the knowledge. So you start to act like you do. Even when you haven't had training in that area."
Previously, TFTP reported how a disturbing push was made to attempt to normalize pedophilia as a mainstream “sexual orientation.” The move involved pedophiles rebranding themselves as “Minor Attracted Persons” (MAP) with the hope that they will be accepted like the LGBTQ community. Disgustingly enough, it was somewhat effective as multiple outlets reported it like it was totally acceptable to be sexually attracted to children. While this incident was extremely disturbing, even more worrisome is that this normalization appears to be spreading and as some recent activity on Twitter illustrates, it’s condoned by social media giants. Since we reported on Minor Attracted Persons several years ago, the terminology became so popular that it morphed into multiple categories and abbreviations. There are now NOMAPS, which apparently are the “best kind” of MAP because the “NO” means they don’t want to have sex with children. That’s where the pro-c MAPs come in. The “pro-c” denotes pro-contact as in the belief that children can consent into having physical contact and sex with an adult. Children cannot consent to sex with an adult.
In her meticulously referenced testimony submitted to the Massachusetts legislature which is considering whether to eliminate religious exemptions from the childhood vaccination schedule, Meryl Nass, MD, board member of the Alliance for Human Research Protection, laid out the facts to refute the Pharma-orchestrated propaganda about vaccines. First: “there is no crisis (no epidemic of deaths or disabilities) from infectious diseases caused by unvaccinated children, either in Massachusetts or the United States.” She pointed out that “the elephant in the auditorium today is Pharma profits.” Merck lists on its website over 1,000 candidates for state and federal offices to whom it “contributed” money in 2018. Pharma money purchases the allegiance of our major media corporations: in addition to its expenditure for advertising to consumers — $6.4 billion — Pharma spent in 2016, Pharma spent $29.9 billion on medical marketing. “Pharma’s latest risky strategy is trying to rid the world of vaccine exemptions, to prevent vaccine opt-outs–before a new crop of vaccines, with inadequate safety and efficacy testing. Vaccines for which Pharma will have no liability once they are placed on the childhood schedule.” Dr. Nass points out the added danger that government waivers of vaccine liability posed for children. “Waivers discourage manufacturers from ensuring that the vaccines they sell are as safe and effective as possible. The removal of vaccine exemptions, combined with liability waivers for vaccine side effects and recently loosened standards for licensing vaccines, create a highly toxic mix. Dare I say out loud that our children’s arms and bodies are the delivery system for transferring money from the citizens of the Commonwealth to the pharmaceutical industry?”
Ashley from San Jose, California was recently interviewed by Polly Tommey on the VAXXED II tour bus. Ashley was quite emotional when she saw all of the signatures on the bus, and Polly tells her that seeing the VAXXED bus and sitting in it is an emotional experience for most people. Ashley received the Gardasil vaccine when she was 20 years old, and immediately suffered pain. Soon afterwards, her monthly periods stopped. She also experienced some paralysis on the right side of her body. She tried to get help from medical doctors, but she was only recommended to get psychiatric help, as they did not believe her symptoms could be related to the vaccine. Even her family doubted her, and accused her of buying into "conspiracy theories." #getversed
It is far from uncommon for vaccines—including the measles-mumps-rubella (MMR) and MMR-plus-varicella (MMRV) vaccines used in the United States—to fail to live up to their textbook promises. As of 2019, in fact, leading vaccine scientists admitted that “the ability of the current measles vaccine to sustain long-term protective immunity and adequate herd immunity in settings with no wild type virus exposure” is “still a subject of debate.” Right at the starting gate, anywhere from 2% to 12% of children who receive their first measles-containing vaccine exhibit “primary vaccine failure”—defined as vaccine non-responsiveness. For largely unknown reasons, this subset of children (and also adults) fails to mount the expected antibody response after either an initial vaccine or a booster shot. Even in those for whom the vaccine appears to “take,” vaccinated individuals “have lower levels of measles-specific antibody than do those with immunity derived from exposure to wild-type” measles virus. Secondary vaccine failure (waning immunity) is also a built-in feature of measles (and other) vaccines, with vaccine efficacy acknowledged to be “lower and not life-long compared to the wild type virus infection.” Studies show that levels of measles antibody progressively decreasewith increased time since vaccination. Moreover, additional boosters do not solve the problem. In a CDC study of 18-28 year-olds who were given a third dose of MMR vaccine, protection petered out in less than a year—a fact that forced the study’s authors to argue against a routine third dose.