Did a Military Experimental Vaccine in 1918 Kill 50-100 Million People Blamed as "Spanish Flu"?

The “Spanish Flu” killed an estimated 50-100 million people during a pandemic 1918-19.

What if the story we have been told about this pandemic isn’t true? What if, instead, the killer infection was neither the flu nor Spanish in origin? Newly analyzed documents reveal that the “Spanish Flu” may have been a military vaccine experiment gone awry.

In looking back on the 100th anniversary of the end of World War I, we need to delve deeper to solve this mystery.

During the pandemic of 1918-19, the so-called “Spanish Flu” killed 50-100 million people, including many soldiers. Many people do not realize that disease killed far more soldiers on all sides than machine guns or mustard gas or anything else typically associated with WWI.

Public Petitions FDA to Investigate Gardasil Vaccine Fraud

The following open letter to FDA Commissioner, Dr. Scott Gottlieb, calling for immediate investigations into many facets of the clinical trials for Gardasil sponsored by Merck was emailed today.

Dear Dr. Gottlieb:

This open letter, written on behalf of medical consumers around the world, is an urgent request for you to investigate potential malfeasance perpetrated by Merck during their clinical trials of Gardasil, the human papillomavirus vaccine that the FDA approved in June 2006.

A new book, The HPV Vaccine on Trial: Seeking Justice for a Generation Betrayed, by Holland, Rosenberg, and Iorio, outlines at least four areas requiring the FDA’s urgent attention.

The Happy-go-Lucky Girl I had Pre-HPV Vaccine is Gone Forever

There is no doubt in my mind that HPV vaccines played a part in changing my daughter from a healthy young girl into one who was constantly sick with a long journey to recovery.

After all, the only change in her life prior to the appearance of all these new medical conditions was being vaccinated with Cervarix and Gardasil.

Fast forward three years to September 2018: Has my daughter recovered? Has Chelsea regained some sense of normality in her life? The answers to these questions are both “NO”!

Chelsea has had to battle mental health problems. I strongly believe these issues stem from the long term chronic illness she had to endure during her teenage years.

These years changed my daughter’s entire outlook on life. I rarely understand her reasoning with things. At times I despise her ways.

However, writing her story has made me stop and think. The happy go lucky girl I had pre-vaccine is probably gone forever.

World Health Organization Ensures More Children Die from Vaccines by Revising Vaccine Adverse Reaction Reporting

In April 2017, the World Health Organization (WHO) coordinated a joint project between teams of experts from the National AEFI (adverse events following immunization) committees of India and Zimbabwe with each country’s Ministry of Health.

However, doctors in private practice did not necessarily agree that the new guidelines helped protect the children of the world. In fact, they suspected just the opposite. Instead of accurately assessing potential vaccine-reactions, the new guidelines seemed to further hinder the discovery of real vaccine-reactions, particularly when a death occurred after vaccine administration.

In a letter published in the prestigious Indian Journal of Medical Ethics, two prestigious doctors from India, Dr. Jacob Puliyel and Dr. Anant Phadke, expressed their concerns over this new classification system.

“By simply denying deaths, the new AEFI classification is liable to miss the safety signals and therefore potential dangers with new vaccines.”

They note that Sri Lanka suspended the use of a pentavalent vaccine after five deaths within four months after its introduction in January 2008 and, in 2013 Viet Nam shelved the pentavalent vaccine because it had been associated with 12 deaths.

However, in both cases, the WHO teams which investigated the deaths declared they were ‘unlikely’ to be related to the vaccines used.

The authors point out that the consequences of using the new classification are illustrated starkly in the causality assessment of 134 serious AEFI cases uploaded on the website of the Ministry of Health and Family Welfare in India.

78 of these babies survived and 58 died.

Who is WHO protecting – children or vaccine manufacturers?

N.Y. Health Department Orders All Unvaccinated School Children to Miss 21 Days of School Over Measles "Outbreak"

The Rockland County Health Department in the State of New York has notified schools that students who are not vaccinated for measles cannot attend school for 21 days, due to a “measles outbreak” where 33 cases have allegedly been confirmed in the county.

This directive includes those who have legal vaccine exemptions for either medical or religious reasons.

Parents and members of the community are, of course, outraged at this tyrannical action being conducted by the Health Department, which is run by unelected medical professionals and administers “free” MMR vaccines purchased by the CDC (with U.S. taxpayer funds).

When these “outbreaks” of measles occur, and action is taken to target those who are not vaccinated, many facts are left out in educating the public regarding the truth about measles and the measles vaccine.

So here are the facts about measles and the measles vaccine, all of which are easily verified by anyone with an Internet connection.

1. There is NO measles vaccine. Only a 3-combo vaccine that includes measles (MMR).

2. Merck, the Manufacturer of the MMR Vaccine, is Being Sued in Court for FRAUD.

3. The MMR Vaccine is Linked to Autism.

4. More People Die from the Measles Vaccine than from Measles.

5. Measles Rates were Declining Long Before the Vaccine was Introduced.

The CDC’s Outlandish Lies About Mercury in Vaccines

The CDC says “the evidence is clear” that thimerosal is “merely a preservative” and not a neurotoxin.

However, no one who actually takes the time to examine the scientific literature can rationally conclude that mercury in any form—including the mercury in thimerosal—is safe for humans.

Robert F. Kennedy, Jr.’s book, Thimerosal: Let the Science Speak, describes hundreds of peer-reviewed scientific publications and the “broad consensus among research scientists that Thimerosal is a dangerous neurotoxin.”

The CDC falsely claims that “thimerosal was taken out of childhood vaccines in the United States in 2001.”

However, 25 micrograms of thimerosal remain in many of the influenza vaccines administered in the U.S., including to pregnant women and infants.

All eight studies included in the CDC fact sheet claiming that thimerosal is safe involve lead or co-authors accused of fraud or known to have been involved in behind-closed-doors data manipulation or weighed down by serious conflicts of interest.

'Unprecedented' Sales for Merck's Gardasil Vaccine as They Seek World Domination for HPV Vaccines

Merck’s Gardasil vaccine saw a 55% increase over last year’s third quarter, netting $1.05 billion in global sales for the third quarter of 2018.

Thanks to worldwide sales, the Gardasil vaccine has become the top money maker for Merck.

FiercePharma, the marketing trade publication for vaccine manufacturers, reports that Merck’s Gardasil has been propelling the pharma giant’s vaccine unit in recent quarters, and that doesn’t look like it’ll be changing.

The company sees more growth ahead thanks to an “unprecedented increase in worldwide demand” for HPV vaccines, an executive said.

Addressing the vaccine’s performance on a recent conference call, Merck’s president of global human health Adam Schechter said the company is “seeing unprecedented increase in worldwide demand for the HPV vaccines.”

He said global demand has “doubled in the last year alone.”

Meanwhile, the carnage left behind from mass Gardasil vaccination programs continues to get world-wide exposure, as doctors, scientists, and victims look for ways to oppose mass Gardasil vaccination programs.

A recent gathering in Ireland at an IFICA conference brought together many world leaders to discuss the Gardasil problem, and another meeting is scheduled in the U.S. in 2019 during the Autism One conference, at the 4th Annual International HPV Vaccine Education Symposium.

Vaccine Extremist and Industry Insider Dr. Paul Offit Losing Credibility with the Public

Dr. Paul Offit was at the National Press Club in Washington, DC last night peddling his new book, “BAD ADVICE: Or Why Celebrities, Politicians and Activists Aren’t Your Best Source of Health Information.”

It is clear that Dr. Offit desperately wants to be the authority on vaccines. He already is the industry shill, but is he the authority?

The opinion of the crowd in attendance at the event was a resounding NO.

Children’s Health Defense advocates, parents of vaccine-injured children, and scientists came from all over the United States to ask Dr. Offit questions.

They pointed out in their respectful, thoughtful questions that they do their own research.

Although Offit declined to take questions directly from the audience, it was a good day for parents everywhere to see Dr. Offit forced to have a moderator filter the written questions he did address down to the very basics so he could answer with one of his canned responses.

And the harder questions from the group were never presented to him.

Today’s intelligent parents don’t need a pharmaceutical tycoon physician from Philadelphia with a “gift of gab” telling them what the industry wants them to hear.

WARNING: Dangerous Flu Shots Being Given to Children Without Parental Consent

The annual influenza vaccine is, by far, the most dangerous vaccine in the United States.

This is evident from the quarterly reports the Department of Justice (DOJ) supplies every 3 months to the Advisory Commission on Childhood Vaccines (ACCV) as mandated by the National Vaccine Injury Compensation Program (NVICP).

Compensation paid through settlements in the federal Vaccine Court for injuries or deaths due to vaccines are highest for the annual flu shot, comprising more settlements than all other vaccines currently approved for the US market combined.

The last report from September of 2018, for example, listed 73 settlements from 198 cases, and of those 73 settlements for that 3-month period, 48 of the cases were for harm caused by the flu vaccine.

The actual number of people who are confirmed to have died with the influenza virus is only a few hundred each year, and most of those already have a compromised immune system that makes them more susceptible to the flu virus.

On the other hand, each year there are reports that healthy people are dying or being permanently injured after receiving a flu vaccine.

So there really is no good justification for anyone to give a child a flu vaccine and put that child at risk, without consulting with the child’s parents first.

And yet, news reports across the United States indicates that this is indeed happening.

In some of the reports we have heard, some parents have even signed statements that they did NOT want their child to receive a flu vaccine, but the child got one anyway.

So how can this be justified?

I asked Health Impact News foreign correspondent, Christina England, to look into this matter, as our initial reports indicated that the rationale for subverting parental consent to the flu vaccine might have come from a document published by the World Health Organization (WHO), defining something called “Implied Consent,” and is not unique to just the United States.

What do Doctors Learn in Medical School About Vaccines?

The idea that there are “medical experts” who, by virtue of the MD initials placed after their names, automatically know more than anyone else about vaccines is pervasive.

This commonly held belief persists, despite overwhelming evidence that doctors are taught almost nothing about vaccines in medical school.

Doctors are taught that vaccines have saved the world from infectious diseases and they are taught to follow the vaccine schedule promoted by the Centers for Disease Control and Prevention (CDC)—which tells them which vaccines to give and when.

They’re taught that they must always abide by the schedule and vaccinate every patient. That’s pretty much it.

Yes, it’s hard to believe, but don’t take my word for it.

In an article I wrote several years ago titled “Doctors Are No Experts On Vaccines,” I included quotes from several medical doctors to backup my allegation.

It is important to listen to them so that the magnitude of the myth that physicians are the experts on vaccines can fully sink in.

It is time to put this myth to rest because it is too often used as a way to disparage anyone who dares to disagree or even mildly question doctors about the safety and effectiveness of vaccination.

FDA Decision to Approve Gardasil Vaccine for Adults Will Likely Increase Cervical Cancer Rates

The HPV vaccine was just approved for adults, despite Merck’s concerning research data.

The FDA made its determination in the face of substantial evidence of the dangers of the HPV vaccine and the existence of safer alternatives.

For women who have already been exposed to certain strains of the HPV virus, vaccination can actually increase the risk of precancerous lesions by 44.6%.

That’s right: if you are already infected with HPV, getting vaccinated could increase your risk of getting cancer.

To put this in perspective, 79 million Americans are thought to be infected with HPV, and about 14 million are newly infected each year, making HPV the most common sexually transmitted infection.

Often there are no symptoms. The CDC says that “HPV is so common that almost every person who is sexually active will get HPV at some time in their life.”

A large, government-backed push to get more people vaccinated for HPV could actually increase many people’s risk of getting cancer.

Danish Doctor Issues Warning about HPV Vaccine: "The Vaccine Should be Stopped Immediately!"

The HPV vaccine controversy has been raging since the FDA approved Gardasil in 2006 in virtually every country utilizing this new medical intervention.

Dr. Stig Gerdes wrote this open letter to Danish Health authorities, the medical community, and local journalists hoping to shed some light on the very real consequences many Danish families were forced to deal with post-HPV vaccine use.

Dr. Gerdes wrote:

“The vaccine should be stopped immediately! There are so many unanswered questions that should be answered before we continue to vaccinate. With each injection, there is a risk of incapacitating a previously young strong human.”

Unfortunately, HPV vaccine stakeholders are still trying to deny the facts Dr. Gerdes was courageous enough to put in writing.

Is the Current Epidemic of "Mystery Illnesses," Similar to Polio, the Result of Vaccine Side Effects?

The CDC and other medical “authorities” refer to them as “mystery illnesses,” but they have been around and identified for the past 5 years now, and actually are not all that “mysterious.” Young children are affected the most.

They are the result of “enteroviruses,” the same as the polio virus, but they are not called “polio.”

There is currently another outbreak of enteroviruses being reported in the corporate media, usually referred to as acute flaccid myelitis (AFM). The symptoms are similar to polio, including paralysis.

Health Impact News first reported on these outbreaks back in 2014, providing information you are not likely to read in the corporate media. See our 2014 coverage:

As Enterovirus D68 Deaths Increase, Are Vaccine Contaminants to Blame?

Lyn Redwood, the president of Children’s Health Defense, addresses the current outbreaks and also provides information you are not likely to read in the corporate-sponsored “mainstream” media, which generally ignores all environmental factors, including vaccines, as a possible cause: The Non-Polio Illness That “Looks Just Like Polio.”

Parents, Scientists and Doctors from Around the World Gather to Discuss How to Handle Increasing HPV Vaccine Injuries

Earlier this year (2018) parents, scientists and doctors from all over the world gathered in Ireland at an IFICA conference to discuss the future of the HPV vaccine injured.

The theme was “Working Together.”

The Ireland Government HSE (Health Service Executive) was invited to send representatives to attend, but they refused the opportunity to speak or listen to the world-renowned experts who attended.

Instead, the HSE claims that the HPV vaccine is “100% safe” and labeled parents of HPV vaccine injured children as “Emotional Terrorists.”

As a result, victims suffering from Gardasil vaccine injuries in Ireland cannot get treatment, and must travel outside of the country to find medical help for their injuries.

FDA Approves Dangerous Gardasil Vaccine for Adults in the U.S.

Following a June, 2018 “Priority Review” by the FDA to approve Merck’s Gardasil 9 vaccine to be expanded to women and men, ages 27 to 45, after 10 years of the FDA denying Merck’s request to expand the Gardasil market to adults, the FDA approved Gardasil 9 to be expanded to adults, aged 27 to 45, on October 8, 2018.

Granting approval to a vaccine after a “Priority Review” by the FDA in only 3 months is a “fast nod” according to FiercePharma, the market trade publication of the pharmaceutical industry.

Merck did not even have to supply any new trials or data to get the vaccine approved for adults, in spite of the fact that the FDA denied their request for 10 years on the older Gardasil vaccine. According to FiercePharma:

“Because Gardasil 9 and sister shot Gardasil are manufactured similarly, the FDA based the Gardasil 9 decision on results from a study of its predecessor.”

The study the FDA relied upon to approve Gardasil 9 for adults, was considered insufficient for 10 years as the FDA denied Merck approval to market the vaccine to adults:

“Back in 2008, after agreeing to a faster review in the age group, the FDA decided against Merck’s case for an additional Gardasil approval in females 27 to 45. The agency in 2009 issued a second complete response letter for that application, demanding Merck to provide longer-term efficacy data in the age group.

That set of data apparently didn’t turn things around for Merck. In both Gardasil’s and Gardasil 9’s current labels, information about a study on 3,253 women, 27 through 45 years of age, states that there was “no statistically significant efficacy” demonstrated by the vaccine in preventing high-grade cervical lesions or cervical cancer.”

Yet somehow, that same study is now deemed to be sufficient to approve Gardasil 9 for adults.

Did 80,000 People Really Die from the Flu Last Year? Inflating Flu Death Estimates to Sell Flu Shots

The Centers for Disease Control and Prevention estimated that the 2017-2018 flu season killed 80,000 and hospitalized 900,000 Americans.

Of course, the mainstream media reported this as fact.

Deaths from flu are always estimates because if the Powers-That-Be reported the true numbers of deaths from actual influenza infections, the numbers would be much lower and people would not be so inclined to receive a flu shot.

How does the CDC overestimate the number of flu deaths? The CDC accomplishes this by reporting a combined pneumonia and influenza death rate.

For example, in 2001 the CDC reported that 62,034 died from influenza and pneumonia.

After a painful hour of searching the CDCs database, I found the true 2001 numbers: 257 died from influenza and 61,777 died from pneumonia.

80,000 deaths would lead one to conclude that 13,333 died per month (80,000/6 months) from the flu. Since the internet provides 24-hour news cycles, I think we all would have heard that about 9 people (267/30 days per month) in every state dying daily from the flu.

I have five practitioners in my office. We have over 100 years of experience in treating patients. None of us has can recall a single patient dying from the flu.

In fact, I can guarantee you that if 9 people were dying in my state daily from the flu, my partners and I would hear about it. In fact, there are always headlines on the internet when one person dies from the flu.

Studying the past CDC data shows that each year a few hundred to a few thousand die from the flu.

The War Against Vitamin D - A Threat to Big Pharma

Natural substances with tremendous healing capabilities that cannot be patented are a huge threat to the pharmaceutical industry and their FDA-approved drugs, and certainly vitamin D is at the top of this list.

For example, published scientific literature shows that vitamin D is more effective in preventing annual influenza than the dangerous flu shot.

Since the best and primary source of vitamin D is from the sun, most people in North America are vitamin D deficient, even during the summer months when we are told to block the sun’s rays due to the fear of skin cancer.

When a natural substance like vitamin D can cure and prevent so many diseases, usually in ways far superior to FDA-approved drugs and vaccines, it should come as no surprise that Big Pharma will pull out all the stops to discredit the science behind these natural substances, as they affect their profits from pharmaceutical products.

This is routinely done by funding their own biased studies, and then attacking medical doctors and scientists who promote natural cures.

One of the areas of vitamin D deficiency that affects many of the families we work with here at Health Impact News, is in the area of Medical Kidnapping and the widely debunked theory of Shaken Baby Syndrome (SBS) that is used to medically kidnap children.

Vitamin D deficiency can lead to brittle bones in infants and children, where multiple hairline fractures occur giving the appearance of “abuse” according to proponents of the Shaken Baby Syndrome medical theory.

One doctor who is a world-renown authority on vitamin D and has testified in court on behalf of parents falsely accused of SBS, is Dr. Michael Holick. He has recently come under fire and was attacked in the corporate-sponsored “mainstream” media that derives much of its advertising revenue from Big Pharma.

William B. Grant, PhD, the director for the Sunlight, Nutrition, and Health Research Center, and former senior research scientist at SRI International, the Jet Propulsion Laboratory, and the NASA Langley Research Center, has recently published a commentary with the Orthomolecular Medicine News Service exposing Big Pharma’s “disinformation playbook” and how they attack natural cures, and vitamin D health benefits specifically.

Dr. Grant has authored or coauthored over 60 articles in peer-reviewed journals.

Fraud Uncovered in U.S. Government's Claim that Vaccines do not Cause Autism - Will Congress and DOJ Act?

Robert F. Kennedy Jr., Chairman of Children’s Health Defense (CHD) and Rolf Hazlehurst, the father of a vaccine-injured child have petitioned Michael Horowitz, the Inspector General of the Department of Justice (DOJ) to investigate the conduct of two DOJ attorneys, Vincent Matanoski and Lynn Ricciardella.

The two attorneys represented the Secretary of Health and Human Services in the National Vaccine Injury Compensation Program (NVICP), otherwise known as the “Vaccine Court”, in the Omnibus Autism Proceedings (OAP), which ruled that vaccines do not cause autism.

The alleged actions of the two attorneys in the OAP were fraudulent and obstructed justice.

Kennedy and Hazlehurst allege that Matanoski and Ricciardella acted together to intentionally misrepresent the opinion of one of their own witnesses, Dr. Andrew Zimmerman, to conceal evidence of his true opinion from the Special Masters who presided in the “Vaccine Court” and the petitioners who were seeking justice and compensation.

The evidence that Matanoski and Ricciardella concealed was a report authored by Dr. Zimmerman showing how vaccines may cause autism in a subset of children with underlying mitochondrial issues.

After Dr. Zimmerman submitted his report, the DOJ attorney informed Dr. Zimmerman that he would no longer be needed as a witness.

Zimmerman’s full opinion was devastating to the government’s case. Simply stated, it was now entirely possible that the government would lose thousands of the OAP cases.

The cost could be into the billions and the fund that compensated the vaccine injured would be bankrupted.

Even worse, the government’s claim that vaccines are “safe and effective” would evaporate and the claim that “vaccines don’t cause autism” would be debunked.

Why was the Dangerous and Contagious FluMist Vaccine Approved by the CDC?

In February 2018, the U.S. Centers for Disease Control and Prevention’s (CDC) Advisory Committee on Immunization Practices (ACIP) voted to re-recommend the live virus nasal spray influenza vaccine, FluMist, for the 2018-19 “flu season” after a two-year hiatus.

The live attenuated influenza vaccine (LAIV) is popular, particularly with children, since it is sprayed up the nose and does not require a needle for administration.

The ACIP voted against recommending the quadrivalent FluMist for the 2016-17 and 2017-18 influenza seasons due to the vaccine’s ineffectiveness in protecting against the H1N1 strain (Influenza A).

It is important to note that there are cases reported in the medical literature that FluMist has resulted in shedding and transmission of vaccine strain influenza virus.

Despite the fact that the efficacy and effectiveness of this vaccine is unknown, Cynthia Pellegrini, senior vice president of public policy and government affairs for March of Dimes stated,

“This vaccine is better than not being vaccinated and there are kids who will not be vaccinated without this option…”

The assumption that using FluMist is better than not being vaccinated given the lack of data on the efficacy is not rational because it is not based on scientific evidence.

Financial Incentives for Doctors to Vaccinate as Many Children as Possible - Keep Patients on Statins

There are monetary awards for doctors and other mainstream medical practitioners who maintain high levels of compliance for prescription drugs (including vaccines), and doctors’ visits.

These incentives to get more patients into their offices and to receive as many vaccines and prescription drugs as possible come from the insurance industry.

The busier a doctor, pediatrician, or clinic is to maintain quotas for vaccinations and drugs, the more insurance awards them with kickbacks. Despite the ostensible stated reason of ensuring a high level of healthcare, this practice can lead to more health problems due to known side effects of these pharmaceutical products.

Educating patients on prevention, such as learning how to eat healthy and avoiding environmental toxins, provides no financial benefits to medical professionals.

Legislative Update on Battle to Oppose Mandatory Vaccines in Each State

The corporate-sponsored “mainstream” media, along with Big Pharma and the U.S. Government, would like the public to believe that the “science is settled” when it comes to vaccines, and that all vaccines are safe and effective. They spend a great deal of effort to try to convince the public that this is the only view held by medical doctors and scientists.

This message to the public, however, is not true, and can be properly called “propaganda.”

As we have previously written, there are a variety of opinions and viewpoints regarding the science of vaccines among medical doctors and researchers.

The extremist view regarding vaccines, and not the one necessarily held by most doctors and scientists, is the view that ALL vaccines are safe and effective for ALL people, ALL the time, by force if necessary.

Propaganda is used to try and achieve their agenda, which is a form of medical tyranny by taking away people’s choice to refuse vaccines for themselves or their children.

Fortunately, the National Vaccine Information Center has volunteers in all 50 states opposing legislative efforts to impose mandatory vaccines and take away informed consent and the freedom to refuse medical treatments like vaccines.

They have successfully mobilized the American public through grassroots efforts to oppose most of these bills that have been proposed in recent years.

The following is their 2018 annual report. To keep up to date on what is going on in your state regarding vaccine laws, be sure to sign up for their portal on their website.

The Pertussis Vaccine and Children Brain Damage: America's Dark Vaccine History

It is a primitive bacterial vaccine licensed in 1914. It has not been given to babies in America for 20 years.

It is the vaccine that had brain damaged so many children and caused so many vaccine injury lawsuits that Big Pharma used it to blackmail Congress into giving vaccine manufacturers a partial product liability shield in 1986, which the U.S. Supreme Court made even bigger in 2011.

I’m talking about whole cell pertussis vaccine in DPT, a crude brew of whole B. pertussis bacteria heated and washed with formaldehyde but still full of neurotoxic aluminum and mercury along with shock-inducing endotoxin, as well as brain damaging bioactive pertussis toxin, a toxin so lethal that researchers use it to deliberately induce acute experimental autoimmune encephalomyelitis (EAE) in lab animals.

Whole cell pertussis vaccine: the most reactive vaccine still given to infants and children in developing countries because it costs drug companies just pennies to make a dose of it.

U.S. Zika Vaccine Trial: A Vaccine Looking for a Disease to Cure - Natural Immunity has Already Eliminated the Zika Virus

The experimental Zika vaccine is a controversial DNA vaccine, never before used in humans. An earlier NIH attempt to develop a West Nile DNA vaccine was aborted.

But the unexpected happened; the virus has disappeared.

The adults who had been infected recovered without treatment—and they have gained the advantage of lifetime immunity.

Zika no longer poses a health problem for humans.

In 2017, when “new cases have dropped to a trickle throughout the Americas” Sanofi pulled the plug on its Zika vaccine.

Dr. Fauci acknowledges that:

“Right now, there are no infections, and certainly not enough to even think about an efficacy signal at this point”.

Science Magazine, notes:

“Further complicating the trial, many people throughout Latin America and the Caribbean have already been infected with Zika and recovered, which has left them immune to the virus and hence ineligible for vaccine trials.”

To overcome “the problem” that Mother Nature resolved – NIAID officials and the researchers are intent on facilitating the continuation of the vaccine trial.

They propose to intentionally infect people who may then spread the virus and create an epidemic that has receded.

The motivating factors for completing the trial by resorting to unethical exposure of human subjects to potentially serious harm, is that a Zika vaccine will be brought to market – whether or not Zika poses a threat.

The trial is about protecting the financial investment, career advancement for the researchers, and launching yet another profit generating vaccine.

Vaccine Awareness Week: National Vaccine Information Center Calls on Health Officials to Protect Babies in U.S. from Toxic DPT Vaccine

During the Ninth Annual Vaccine Awareness Week co-sponsored by the non-profit charity National Vaccine Information Center (NVIC) and Dr. Joseph Mercola, NVIC is calling on the U.S. Department of Health and Human Services (DHHS) to protect newborns from being subjected to the risks of an old and crude whole cell pertussis vaccine in DPT that has not been given to babies in America for 20 years.

During this year’s Vaccine Awareness Week, NVIC is also releasing a 2018 Annual Report on U.S. State Vaccine Legislation: Breakdown, Trends and Predictions.

The report is an analysis of which state legislatures passed bills that affected vaccine exemptions or added new vaccine mandates, enrolled citizens in electronic vaccine tracking registries, approved vaccine promotion programs in daycares and schools or enacted other vaccine-related legislation. NVIC reports that for the third year in a row, exemptions in vaccine laws remained stable with no losses in any state.

Vaccine Awareness Week Sept. 23-30, 2018 was launched with an article and video reviewing the risks and failures of influenza vaccines and will include an article on fast tracking and marketing of vaccines, such as Gardasil (HPV) vaccine, by federal health agencies. Saturday will feature online viewing of excerpts from the international award winning HPV vaccine documentary, Sacrificial Virgins.

After 20 Month Old Son Dies from Vaccines Professional Fighter with Nurse Wife Put Up Billboards as Warning

Nick Catone is a professional MMA martial arts fighter, and his wife, Marjorie Catone, is a registered nurse who works in an intensive care unit at a local hospital where they live.

17 days after their 20 month old healthy and active son, Nicholas, was vaccinated with the DTaP (Diphtheria, Tetanus, Pertussis) vaccine, his parents found him dead in his bed one morning.

In an interview with Del Bigtree, Marjorie comments about how her nursing education never trained her in the possible adverse reactions to vaccines, and she never bothered to check the ingredients of the vaccine, even though as a wife of a professional MMA fighter and mother she was meticulous to check ingredient lists of foods to make sure her family was eating healthy.

The autopsy report of their son listed the cause of death as “sudden unexplained” (SIDS) and “natural,” as medical authorities apparently refused to consider their son’s vaccines as a contributing factor to his death, and they allegedly did not conduct a thorough exam during the autopsy.

Nick and Marjorie now want to warn others about the dangers of vaccines, so that parents can be informed before making a decision to vaccinate their children, before it is too late and they find themselves in the same situation as they are, grieving over the death of their formerly healthy child. They are putting up billboards in several states in an effort to educate the public on the risks of vaccines.

Vaccine Safety Untested on Pregnant Women, But Big Pharma Not Liable for Vaccine Injuries to Unborn Children and Pregnant Mothers

We are here today because in 2016, Congress amended the 1986 National Childhood Vaccine Injury Act to add vaccines recommended by the CDC for routine administration to pregnant women to the Vaccine Injury Table.

Congressional action was required to do it because the 1986 Act was not about vaccines recommended for adults or unborn babies developing in the womb.

As stated in multiple congressional hearings between 1982 and 1986, the National Childhood Vaccine Injury Act was created by Congress for one purpose: to protect the availability and lower the costs of federally recommended vaccines for children that are state mandated for school attendance.

Although this NPRM requests public comment on how the addition of this new maternal vaccination category should be formatted on the Vaccine Injury Table, the public is hampered from making informed comments because of knowledge gaps about the safety and effectiveness of administering vaccines to pregnant women and potential negative health outcomes for the unborn child developing in the womb.

Various package inserts for these vaccines contain warnings such as “it is not known whether the vaccine can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity;” and “there are no adequate and well controlled studies in pregnant women;” and “available data on the vaccine administered to pregnant women are insufficient to inform vaccine associated risks in pregnant women;” and “the vaccine should be given to pregnant women only if clearly needed.”

There is no single vaccine-related issue of more concern to Americans than protection of this internationally recognized human right for pregnant women, parents of minor children and adults of all ages, who are too often being threatened and sanctioned if they do not agree to receive all government recommended and mandated vaccines for which the pharmaceutical industry has had no product liability since 2011.

Robert F. Kennedy, Jr. Demands the Office of the Inspector General and Congress Investigate Fraud in Vaccine Court by Denying Autism Vaccine Injuries

Robert F. Kennedy Jr., Chairman of Children’s Health Defense (CHD), and Rolf Hazlehurst, parent of a vaccine-injured child, petitioned the Department of Justice (DOJ) Office of Inspector General (OIG), and the Senate and House Judiciary Committees today to investigate actions taken by federal personnel during the “Vaccine Court” Omnibus Autism Proceedings (OAP).

Recently discovered evidence provided by Kennedy and Hazlehurst details obstruction of justice and appallingly consequential fraud by two DOJ lawyers who represented the Department of Health and Human Services (HHS) in 2007. These actions led to a denial of justice and compensation for over 5,000 families who filed claims of vaccine injury leading to autism in their children.

The fraud by the two DOJ attorneys directly influenced the 2011 Bruesewitz v. Wyeth Supreme Court decision which all but shut the door forever for families seeking redress for vaccine injury in the civil court system.

Since this miscarriage of justice, roughly one million children have been diagnosed with autism. An unknown percentage of these cases are the result of vaccine injury.

Are Vaccine Manufacturers Concealing Deaths Caused by Vaccines by Manipulating Post-marketing Data?

National and international health agencies such as the Centers for Disease Control and Prevention (CDC), the European Medicines Agency (EMA) and the World Health Organization (WHO) routinely and emphatically claim that serious adverse events following vaccination are rare.

Nowhere is officialdom’s minimization of vaccine risks more apparent than in these agencies’ position on vaccine-related deaths. The WHO, for example, states that “so few deaths can plausibly be attributed to vaccines that it is hard to assess the risk statistically.”

Nevertheless, once regulators have deemed that a given vaccine is safe enough to be licensed and widely marketed, vaccine manufacturers are supposed to do just that—that is, continue to statistically assess a vaccine’s risks, including the risk of death—and regulators are supposed to carefully review the postlicensure data that pharmaceutical companies submit.

A 2017 commentary by India-based physicians Jacob Puliyel and C. Sathyamala in the Indian Journal of Medical Ethics describes a shocking dereliction of duty on the part of regulators who were presented with vaccine data carefully tailored to obscure serious risks.

Tackling concerns about infant deaths that have occurred following hexavalent vaccination in several European countries, the authors of the commentary show that GlaxoSmithKline (GSK) neglected to report to regulatory authorities that there was a statistically significant increased risk of sudden infant death in the four days after administration of its hexavalent vaccine—and the regulatory agency in question (the EMA) ignored the omission and accepted GSK’s apparently whitewashed data at face value.

The End of Scientific Integrity? Cochrane Collaboration Expels Critic of Big Pharma - 4 Other Board Members Resign

Dr. Peter Gøtzsche recently sent out an email to the public explaining that he is the first person in 25 years to be expelled from the Cochrane Collaboration. He writes:

“No clear reasoned justification has been given for my expulsion aside from accusing me of causing ‘disrepute’ for the organization. This is the first time in 25 years that a member has been excluded from membership of Cochrane.”

Four other board members have resigned from the Cochrane Collaboration as a result of this action.

Health Impact News has covered the work of Dr. Gøtzsche frequently over the years, as he is an outspoken critic of Big Pharma, referring to them as “organized crime.”

He is author of the book, “Deadly Medicines and Organized Crime: How big pharma has corrupted healthcare.”

The Cochrane Collaboration is considered to be the “gold standard” in scientific integrity, but they have come under fire recently for what appears to be biased reviews influenced by the pharmaceutical industry.

They received a $1.15 million “gift” from the Bill & Melinda Gates Foundation to fund “project work” from 2016 to 2017.

Earlier this year (2018), researchers from the Nordic Cochrane Centre published a critique in the British Medical Journal stating that the Cochrane’s review of the HPV vaccine “does not meet the standards for Cochrane reviews or the needs of the citizens or healthcare providers that consult Cochrane reviews to make informed decisions.”

Illinois Teen Dies Three Weeks After Being Injected with HPV Gardasil Vaccine

Christopher Bunch, 14 years old, died on Aug. 14, 2018 of complications from a rare neurological disease called Acute Disseminated Encephalomyelitis (ADEM). The teenager began experiencing symptoms, including headaches, nausea and vomiting, on Aug. 6. He spent much of the next two days sleeping.

Christopher had apparently received the HPV (human papillomavirus) vaccine Gardasil three weeks prior to his death. ADEM is a reported side effect of Gardasil. It is listed in the Gardasil package insert.

Michigan Department of Health Tracking Student Vaccination Status in Violation of Federal Law

The group Michigan for Vaccine Choice has sent a letter to parents in Michigan informing them that the Michigan Department of Health and Human Services (MDHHS) and the Michigan Department of Education (MDE) are violating federal law (FERPA) by transferring private medical records about minor children, without the consent of their parents, regarding each student’s vaccination status into a vaccine tracking database.

American Academy of Pediatrics Concerned About Unregulated Food Additives, but Not Vaccine Additives

In July, 2018, The American Academy of Pediatrics (AAP) released a policy statement titled, Food Additives and Child Health. The report begins by stating, “Our purposes with this policy statement and its accompanying technical report are to review and highlight emerging child health concerns related to the use of colorings, flavorings, and chemicals deliberately added to food during processing (direct food additives) as well as substances in food contact materials, including adhesives, dyes, coatings, paper, paperboard, plastic, and other polymers, which may contaminate food as part of packaging or manufacturing equipment (indirect food additives); to make reasonable recommendations that the pediatrician might be able to adopt into the guidance provided during pediatric visits; and to propose urgently needed reforms to the current regulatory process at the US Food and Drug Administration (FDA) for food additives.”

However, one important subject that the AAP doesn’t address is the toxins in pediatric vaccines. Mercury, the second most dangerous substance known to mankind is still in childhood vaccinations–influenza, meningitis, HIB, Tdap, and Td; aluminum, a neurotoxin, is in a plethora of vaccines including hepatitis A and B, DTaP, Td, HIB, HPV; formaldehyde a known carcinogen is found in DTaP, Td, Hepatis A, Hib, influenza, and Tdap. There are other toxic substances in many different vaccines.

Our children are the most vaccinated young people on the planet. Unfortunately, our children are the sickest when compared to any major Western country.

It is long overdue for the AAP to address the elephant in the room; toxic additives in childhood vaccines.

Should the CDC Oversee Vaccine Safety When They Purchase Over $5 Billion of Vaccines from Big Pharma?

The U.S. Centers for Disease Control and Prevention (CDC) is tasked by the U.S. Government with overseeing vaccine safety.

They claim on their website:

“The United States’ long-standing vaccine safety program closely and constantly monitors the safety of vaccines.

A critical part of the program, CDC’s Immunization Safety Office identifies possible vaccine side effects and conducts studies to determine whether health problems are caused by vaccines.

Data show that the current U.S. vaccine supply is the safest in history.”

However, the CDC is the largest purchaser of vaccines in the world, and their budget to purchase vaccines from pharmaceutical companies was over $5.1 BILLION in 2018, and is set to increase to over $5.4 BILLION in 2019.

Can we trust the CDC to oversee vaccine safety with such a blatant conflict of interest?

Get Your Flu Shot? DOJ Report From Vaccine Court Reveals Flu Shot is Most Dangerous Vaccine in U.S.

The 2018 push for the flu shot is now in full swing. Pharmacies are advertising enticing offers, including free flu shots with discounts on other products (CVS), and the opportunity to give a free flu shot to children in Africa (Walgreens).

These retail outlets offer no-wait shots, making it appear to be as easy as purchasing candy or tissue paper in your visit to your local drug store.

What these retail outlets will most likely fail to mention, however, is that according to the Department of Justice’s quarterly reports listing compensations for injuries and deaths due to vaccines from the Vaccine Court, the flu shot is the most dangerous vaccine in the U.S. with crippling and fatal side effects.

How many people taking advantage of “free” flu shots will know that there is a long list of debilitating side effects from the flu shot, as compensated by the U.S. Government in the federal Vaccine Court?

These side effects include (among others):

GBS – Guillain–Barré syndrome is a rapid-onset muscle weakness caused by the immune system damaging the peripheral nervous system.

TM – Transverse myelitis is an inflammation of both sides of one section of the spinal cord. This neurological disorder often damages the insulating material covering nerve cell fibers (myelin).

ADEM – Acute disseminated encephalomyelitis, or acute demyelinating encephalomyelitis, is a rare autoimmune disease marked by a sudden, widespread attack of inflammation in the brain and spinal cord.

CIDP – Chronic inflammatory demyelinating polyneuropathy is a neurological disorder — a condition that targets your body’s nerves.

MS – Multiple sclerosis is a demyelinating disease in which the insulating covers of nerve cells in the brain and spinal cord are damaged.

SIRVA – SIRVA stands for “Shoulder Injury Related to Vaccine Administration.” SIRVA can lead to intense, prolonged pain, limited range of motion, and shoulder-related injuries such as Adhesive Capsulitis or Frozen Shoulder Syndrome.

Myasthenia gravis is a long-term neuromuscular disease that leads to varying degrees of skeletal muscle weakness.

Peripheral Neuropathy is damage to or disease affecting nerves, which may impair sensation, movement, gland or organ function, or other aspects of health, depending on the type of nerve affected.

DEATH by the flu vaccine.

All of these debilitating side effects were reported as being compensated in recent DOJ reports.

Was Texas Mom's Baby who was Accidentally Vaccinated with Gardasil Medically Kidnapped for Medical Research?

When Anita Vasquez sought medical care for the reactions her baby girl was having after mistakenly being given the Gardasil vaccine at only 4 months old, she had no way of knowing that she was walking into a hospital that was working on vaccine development in collaboration with one of the largest pharmaceutical companies in the world.

She found herself tangled in what appeared to her to be a deep web of interests that were in direct conflict with her only goal, which was simply trying to get help for her baby.

Instead of finding help, she was met with accusations that she had somehow caused harm. Doctors and social workers testified that Anita had Munchausen Syndrome by Proxy (also known as “factitious disorder”), which means she was accused of making up her daughter’s medical conditions when there were none. Anita is a licensed nurse by profession.

The state of Texas recently terminated her parental rights to her daughter Aniya Blu.

It was apparent to Anita from the very beginning that there was more going on than meets the eye.

Evidence was hidden. Medical records were kept from her and her attorneys. Medical diagnoses of real problems were covered up.

The deception continued throughout the ordeal with Child Protective Services, and it followed Anita into the courtroom. There were many facts of the case that Anita didn’t learn about until just before the termination hearing. Even then, the evidence was ignored.

Anita Vasquez has appealed the termination of her parental rights for her daughter, who was mistakenly injected at 4 months old with the Gardasil 9 vaccine intended for her older brother. Anita received a letter on August 31, 2018, from the Thirteenth District of Texas Court of Appeals noting that her appeal was accepted.

Japan has the Lowest Infant Mortality Rate Following Ban on Mandatory Vaccinations

Fact: Japan has the lowest infant mortality rate following ban on mandatory vaccinations, and they urge other countries to follow this firm stance.

The citizens of Japan are statistically proven to be the healthiest and longest-living people in the world. The country also has the lowest infant mortality rate on the planet.

It may come as no surprise to many that the Japanese Government banned a number of vaccines that are currently mandatory in the United States and has strict regulations in place for other Big Pharma drugs and vaccines in general.

Japan’s anti-vax policies have long been criticised by vaccine pushers in the US who claim that vaccinating the public “promotes health.”

However, Japanese people live longer, healthier lives than Americans, with babies born in the US twice as likely to die in infancy than those born in Japan.

It’s clear to see that Western nations have a lot to learn from the Japanese when it comes to their approach to vaccinations and issues facing public health.

The Japanese are vaccine sceptics, to put it simply, and due to adverse reactions suffered by Japanese children, have banned many vaccines.

The Japanese are well educated on the dangers of over-vaccinating their children and oppose the use of multi-shot vaccinations such as the MMR vaccine.

Following a record number of children developing adverse reactions, including meningitis, loss of limbs, and even sudden death, the Japanese government banned the measles, mumps, and rubella (MMR) vaccine from its vaccination program, despite facing serious opposition from Big Pharma.

Do You Know How to Recognize a Vaccine Reaction?

Do you know how to recognize a vaccine reaction?

Like with prescription drugs and other pharmaceutical products, reactions to vaccines can be mild or severe. There can be complete recovery or long lasting health problems after vaccine reactions. Rarely, vaccine reactions can be fatal.

If you are making a decision about vaccination for yourself or your child, it is important to first become fully informed about each vaccine’s reported side effects, precautions and contraindications, which means reasons for why a person may be at risk for having a serious reaction.

It is especially important for parents to become informed about vaccine complications and how to recognize the symptoms of a vaccine reaction.

Lawsuits Mount Against Shingles Vaccine

Drugwatch.com is reporting that Merck’s shingles vaccine, Zostavax, is facing several lawsuits for causing shingles, the very thing the vaccine is supposed to protect against.

Eighteen people from across the country filed one of the first Zostavax lawsuits in New Jersey.

The lawsuit alleges the vaccine caused people to develop shingles. The outbreak led to hospitalization and chronic nerve pain called post-herpetic neuralgia.

“Merck knew or should have known that its product caused viral infection and was therefore not safe,” the suit said.

Jane Boda filed one of the early lawsuits in Wisconsin in May 2018. The lawsuit claims Zostavax gave Boda shingles. She says she suffered chronic nerve damage as a result.

Whistleblower Accuses CDC of Manipulating Shingles Data with Chickenpox Vaccine

The controversy over varicella vaccine safety and mandates has raged since its introduction in the U.S. nearly 25 years ago. When it was licensed in 1995, the National Vaccine Information Center (NVIC) questioned the strength of the scientific evidence for safety and effectiveness used by CDC and the American Academy of Pediatrics (AAP) to make a universal use recommendation and argued the vaccine should not be mandated because, in part, universal use of the vaccine could drive chickenpox into older children and adults and raise the risks for shingles later in life.

Gary S. Goldman, PhD served for eight years as Research Analyst for the Varicella Active Surveillance Project (VASP) in a cooperative project with the CDC.

In March 2018, Dr. Gary S. Goldman published an article in Annals of Clinical Pathology, “The US Universal Varicella Vaccination Program: CDC Censorship of Adverse Public Health Consequences.”

In that article he provided evidence to support his allegation that CDC officials manipulated varicella data to affirm the CDC’s support for chickenpox vaccine mandates that that will require a lifetime of expensive vaccine boosters.

In what Goldman described as a deliberate “attempt to quash the unwanted outcomes in the years following 2000,” he said it became apparent that the methods for interpretation of data were flawed, skewing CDC and VASP conclusions in favor of the varicella mass vaccination program.

Pro-Vaccine Maryland Parent Outraged over Corruption in Mass Gardasil Vaccination Policies

Maryland parent Josh Mazer is a pro-vaccine parent. He has stated: “A properly administered, robust vaccine policy is instrumental in promoting the public welfare.” (We disagree on this point.)

However, there is one vaccine he does not promote, and after the local health department started promoting this vaccine to 12 and 13-year-old children without parental consent or knowledge, he decided to do some investigating behind this large public campaign of mass vaccination.

The vaccine in question is Merck’s HPV vaccine Gardasil, which is well-known to the readers of Health Impact News, but less so among the general public.

Mazer was notified of the policy earlier this year (2018) by a “a career public school nurse” who told him that she was “being forced” to market Gardasil to 11 and 12-year-old kids at her school.

Mazer decided to investigate why this was being presented as a “public health crisis,” but none of the local health department officials gave him any useful facts or information to justify the mass HPV vaccine campaign.

So he filed a Public Information Act request with the local government Prevention and Health Promotion Administration.

He learned the state health department received $91.6 million just since 2012 from pharma funded non-profits to promote the HPV vaccine in Maryland.

Bingo. Welcome to our world, Mr. Mazer.

4 Years After CDC Whistleblower Reveals Vaccine Fraud Still Nothing Happens

It was four years ago, August 2014, that a senior CDC scientist—Dr. William Thompson–claimed whistleblower protection by claiming that the CDC had committed fraud by hiding and manipulating data that showed the MMR vaccine was associated with a higher risk of autism.

According to the CDC, we are currently suffering through an exponential increase in autism since the 1970s. In 1970, the autism rate was 1 in 10,000. In 2018, the rate of autism epidemically increased to 1 in 59 children. That is a 169-fold increase in autism in U.S. children over nearly 50 years!

You would think a senior CDC scientist who claims malfeasance at the CDC is responsible for the rapid rise in autism would immediately trigger Congressional investigations to find out the truth.

However, our dysfunctional Congress would prove you wrong.

U.S. Children Have Highest Rates of Diabetes and the Most Vaccines in the World

Type 1 diabetes—also called insulin-dependent diabetes mellitus (IDDM) or juvenile diabetes— is one of the most common and rapidly increasing autoimmune diseases in children. The U.S. has more children with type 1 diabetes than any other country in the world, with a prevalence in children and adolescents that grew by 21% from 2001 to 2009. The U.S. also has the highest number of new cases annually, well ahead of India (with a population four times bigger).

Puzzling over the dramatic rise of type 1 diabetes in young children over the past several decades, scientists are reaching consensus that environmental factors play a significant role.

Two of the most widely discussed environmental candidates are dietary factors and viral infections. In light of the hypothesis that viruses can be precipitating factors, it has appeared logical to at least some researchers to consider whether live virus vaccines also could be contributors, particularly given the temporal association between expansion of the childhood vaccine schedule and the escalating type 1 diabetes rates.

Are Front-line Emergency Room Doctors the Key to Identifying Vaccine Injuries and Reporting Them?

Are front-line emergency room doctors the key to identifying vaccine injuries and reporting them?

At least one ER doctor thinks so.

David Denton Davis MD, a former Emergency Physician, claims neither our Centers for Disease Control (CDC) nor our Department of Health and Human Services (HHS) has requested help from the American College of Emergency Physicians (ACEP) in identifying illnesses and deaths occurring hours, days and weeks following childhood vaccinations.

In his soon-to-be-published book “Who Can Parents Trust? Vaccines: Avoidable and Unsafe,” he claims the vast majority of serious vaccine related illnesses coming into Emergency rooms will continue to go unrecognized, unless nurses and physicians ask the last vaccination date (LVD).

He believes during the past thirty years several million serious Adverse Events (AE’s), including deaths presenting nationwide to more than 5,000 Emergency rooms have never been recognized, documented or submitted for investigation, in accordance with our National Childhood Vaccine Injury Act (NCVIA). All suspicions of a vaccine related adverse event are required by law to be submitted using our Vaccine Adverse Event Reporting System (VAERS).

Sadly, he goes on, very few Emergency Physicians or Nurses have received any NCVIA or VAERS education.

As a charter member of ACEP, Dr. Davis served on the Board of Directors during the creation of Emergency Medicine (EM) as a specialty. He admits his own reporting failures were due to a lack of vaccine education.

Dr. Davis states he is concerned many pediatricians know, but are not reporting illnesses following vaccinations, for financial reasons. Although neither makers nor physicians are liable for vaccine damage, the ultimate truth for safety was made contingent on investigating physician, parent or third party VAERS submissions.

With only a very small percentage being reported, no one can honestly say vaccines are safe.

French Oncologist Analysis of Gardasil Vaccine Finds Higher Rates of Cervical Cancer Associated with High Vaccination Rates

A medical doctor in France, Dr. Gérard Delépine, an oncologist, has published an analysis of the HPV vaccine Gardasil on the independent news site, Agora Vox, showing how increased rates of Gardasil vaccinations are actually correlated with a higher rate of cervical cancer.

The analysis was published as an Open letter to parliamentarians, and to all citizens, in response to a recent meeting between French President Emmanuel Macron and “thirty leaders of the world’s largest pharmaceutical groups,” and to the call among some politicians to make the HPV vaccine Gardasil mandatory in France.

Using statistics from several countries, Dr. Delépine shows that cervical cancer was decreasing in all these countries due to the implementation of regular pap smears.

However, in some countries where mass Gardasil vaccination took place, the incidence of cervical cancer actually increased.

15 Year Old French Girl's "Descent into Hell" After Gardasil Vaccine - Wheelchair Bound and Paralyzed

Jean-Jacques and Yveline say that their daughter Océane was a girl full of joy, health, and laughter before her 15th birthday. They affectionately called her their ‘little pearl.’ She never had to visit the doctor for an illness. That is until her life was turned upside-down because of trust.

Océane was 15 years old when she went to her family doctor to get a medical certificate for dancing with a friend. The doctor suggested Gardasil for cervical cancer prevention. Her parents trusted their family doctor and consented to the vaccination. They did not realize this decision would set off a chain of events that would make Dante’s Inferno look like a picnic.

The year 2011 was a descent into hell for Océane’s parents. One stroke had left their daughter in a wheelchair without vision or hearing due to the acute encephalomyelitis.

For two years, Océane could not attend school. Wheelchairs, facial paralysis, dizziness and great fatigue kept her home.

Today, they seek justice in court, not only for their daughter, but for the more than 700 other French families who have suffered injuries due to the Gardasil vaccine.

FDA Approves Experimental Hepatitis B Vaccine for Adults Despite Higher Incidence of Heart Attacks

In February 2018, the FDA and CDC approved the recommendation for a new hepatitis B vaccine, Heplisav-B targeting adults over the age of 18.

The U.S. Food and Drug Administration (FDA) had twice rejected the application for licensure for Heplisav-B in the past four years because of safety signals.

Heplisav-B differs from other licensed hepatitis B vaccines in that it contains a new synthetic adjuvant known as cytosine phosphoguanine 1018 (CpG 1018) composed of short synthetic DNA molecules.

In 2016, the FDA rejected an application for licensure for the Heplisav-B vaccine, because the agency was concerned about an increased rate of heart attacks and deaths in people who had been given the vaccine. During the trial, approximately 14 subjects had heart attacks.

In July 2017, the FDA committee convened to re-evaluate the scientific evidence and make a decision on whether Heplisav B should or should not be approved for use in the U.S.

This committee had only one cardiologist on the team, Milton Packer, MD, who is a distinguished scholar in cardiovascular science at the Baylor University Medical Center in Dallas, Texas.

According to Dr. Packer, it was possible that the Heplisav B vaccine’s novel adjuvant was related to the higher number of heart attacks in study participants who received the experimental vaccine. He stated: “To know if the 7 -1 heart attack imbalance represented a real risk, we’d need comparative data in 50,000 people.”

However, the only way to conduct such a large trial would be to approve the vaccine and see what happens in the public.

With Dr. Packer abstaining in his vote to recommend the vaccine, the FDA committee approved it anyway. Dr. Packer stated: “Why did I abstain? Based on the available data, it was impossible for anyone to know if the increase in heart attack risk was real. There is a simple rule in life: if you don’t know, you should say you don’t know.”

The vaccine is now available to the public, and all those who receive it are basically guinea pigs to find out if heart attacks will result from the experimental vaccine, and if it will continue to have FDA approval.

HPV Vaccine Scandal Affects Cochrane Biased Review as Critics Speak Out in BMJ

In May 2018, Cochrane, the research organization that bills itself as the “international gold standard for high quality, trusted information,” released a flattering review of human papillomavirus (HPV) vaccines. The Cochrane review methodology involves pulling together data from clinical trials and reviewing the assembled evidence in what is supposed to be a standardized, systematic and neutral manner.

In June, we reported that Cochrane’s sources of funding—agencies and foundations that are unwilling to brook any questions about vaccine safety—raise reasonable doubts about Cochrane’s conflicts of interest and ability to remain independent from its funders’ agendas. Now, researchers affiliated with one of Cochrane’s regional member centers (the Nordic Cochrane Centre) and with the Oxford-based Centre for Evidence Based Medicine (OCEBM) have come out with an exhaustive critique of Cochrane’s HPV review, published in BMJ Evidence-Based Medicine. Not mincing their words, the authors state:

“We believe that the Cochrane [HPV vaccine] review does not meet the standards for Cochrane reviews or the needs of the citizens or healthcare providers that consult Cochrane reviews to make ‘Informed decisions,’ which…is part of Cochrane’s motto.”

The Nordic and OCEBM authors make many solid arguments about the Cochrane reviewers’ omissions and errors, including the reviewers’ inexplicable characterization of the higher death rate in the HPV group as “a chance occurrence.”

UK Government to Begin Giving HPV Vaccine to Boys Amid Public Outcry

The UK government has recently announced that, by September 2019, boys aged 12 to 13 years will be given the human papillomavirus (HPV) vaccine, a vaccine that has been available to girls in the UK for the past ten years.

There has been documented evidence that the HPV vaccine has caused more injuries than any other vaccination in history. Despite this evidence, however, the HPV vaccination has continued to be hailed a success by the pharmaceutical industry and governments alike.

According to the MHRA, the adverse event reporting system in the UK, there have been a total of 9,119 reports of adverse reactions reported in the UK since the vaccine was launched in 2008. These reports equate to 23,882 different ailments and include a total of 8 deaths.

The UK’s decision to include boys into the equation has alarmed many parents whose daughters have already been injured by the vaccine.

Lawfirm Announces $101 Million Measles Vaccine Settlement for Infant that Suffered Brain Injury

The lawfirm of Maglio Christopher & Toale, P.A. announced earlier this month (July, 2018) that they had negotiated a $101 million dollar settlement for an infant who suffered a severe reaction to the Measles Mumps Rubella (MMR) vaccine.

A one-year-old healthy baby girl, who was already walking and climbing, received vaccinations for Measles Mumps Rubella (MMR), Hepatitis A, Haemophilus Influenzae type B (Hib), Prevnar (pneumonia), and Varicella (chickenpox) on February 13, 2013.

That evening, the mother noticed the baby was irritable and feverish.

After a call to the pediatrician, the doctor advised Mom to give her Tylenol and Benadryl. The fever continued for several days, and on the evening before the baby’s scheduled pediatrician visit, the baby began having severe seizures.

She was rushed to the emergency room. She went into cardiac and respiratory arrest, and doctors placed her on a ventilator.

The seizures and cardiac arrest left the baby with a severe brain injury, encephalopathy, cortical vision impairment, truncal hypotonia (low muscle tone), and kidney failure.

After months of treatment at the hospital, the baby finally went home, but her disabilities required specialized medical care and supervision around the clock for the rest of her life.

The $101 million dollar settlement will pay for the child’s constant high-level medical care for the rest of her life. The family received a lump sum of $1 million dollars to cover the immediate costs of medical bills and expenses. The rest will be paid out through an annuity over the child’s lifetime.

Don’t expect to read this story in the Big Pharma-sponsored corporate “mainstream” media, where the official doctrine is that vaccines are “safe and effective.”

Are Vaccines Linked to Increase in Mast Cell Disease and Allergies?

Do you or does someone you know have severe symptoms of itching, rashes, flushing, stomach or other body pain, frequent diarrhea, nausea, fatigue, brain fog, headache and severe allergies to certain foods, medications or insect stings that may include fainting episodes or anaphylaxis?

Although it has been classified as a rare immune system disorder, there are indications that Mast Cell Activation Syndrome (MCAS) may be more prevalent than previously thought and people can suffer for years without being correctly diagnosed.

With severe allergies and chronic inflammatory diseases increasing in populations around the world, scientists are investigating the association between mast cell dysregulation and various brain and immune system disorders ranging from asthma, inflammatory bowel disease and chronic fatigue syndrome to ADHD, depression, autism and cancer.

Mast cells play an important part in keeping the body healthy, but when they malfunction, can cause system wide chronic inflammation in the body that interferes with quality of life or can even cause death.

Although for the past several decades, most pediatricians and public health officials have rejected the possibility of a relationship between vaccination and the development of allergic and autoimmune disorders, the apparent increase in mast cell dysregulation in highly vaccinated populations deserves more in-depth investigation.

Soaring Infertility Rates Linked to Vaccines

A plague is spreading silently across the globe. The young generation in America, the United Kingdom, France, Italy, Japan, Australia – in virtually every western country — is afflicted by rapidly increasing rates of infertility.

This spring, the United States reported its lowest birth rate in 30 years, despite an economic boom. Finland’s birth rate plummeted to a low not seen in 150 years. Russian President Vladimir Putin recently introduced a string of reforms aimed at stemming the country’s “deep demographic declines.” The government of Denmark introduced an ad campaign to encourage couples to “Do it for Denmark” and conceive on vacations, and Poland produced a campaign urging its citizens to “breed like rabbits.”

The “population bomb” we were all endlessly warned about by environmentalists failed to blow, and instead, demographers have been trying to raise the alarm about the population implosion crisis unfolding across the West — the graying of societies facing an unprecedented aging demographic in which there will be too few young to support the old. Most often, they blame social factors: young women embracing careers instead of motherhood, men shunning marriage and fatherhood, rising consumerism or couples choosing to delay raising a family until the economy settles.

But there is another phenomenon that is rarely mentioned – the growing numbers of young people who are not childless by choice but who are incapable of bearing children.

So, earlier this month, when an unprecedented study was released that looked at a database of more than eight million American women and singled out a whopping 25 percent increase in childlessness associated with one particular vaccine that young women have been taking for only a decade — in tandem with a marked decline in fecundity — you would have thought there would be significant interest from public health, the medical profession and the media, wouldn’t you?

Unable to Sue Big Pharma, Vaccine Injury Victims Now Being Denied Legal Counsel in Vaccine Court

How does the National Vaccine Injury Compensation Program (NVICP) and the Federal Court of Claims deprive petitioners, who are seeking compensation for their injuries, the opportunity to seek and retain legal counsel?

Very cleverly.

But it takes some understanding of how legal representation in the program has evolved and more importantly, how fees are paid.

Today, our government is shutting the door on those who have been injured or have died as a result of a vaccine.

Texas Mom Who is a Nurse Fights to Regain Custody of Daughter Taken Away After Gardasil Vaccine Injury

Social workers told a Texas mother that Monday was her last visit with her daughter. Aniya Blu Vasquez was medically kidnapped from her family after she became ill following a medical error in which her pediatrician injected her with the Gardasil 9 vaccine intended for her older brother. Aniya was just 4 months old at the time.

A Texas court decided last month that the parental rights of her mother, Anita Vasquez, should be terminated, devastating the family and supporters alike.

However, their story is not over.

In a quirk of legalities, Anita Vasquez filed a Declaration of Recision of Signature/Contracts before the court was able to file the entry of judgement on the termination of parental rights.

As a result, there will be another hearing on Monday, July 23, 2018, at the Victoria County Courthouse at 9 a.m.

She says that there is substantial new evidence in her case that was not considered by the court. Anita asserts that the very basis upon which CPS seized custody of Aniya was fraudulent, and CPS knew it all along.

Concerned citizens are rallying around the family that they believe is suffering a grave injustice.

Gardasil Vaccine Legal Victory: Canada Federal Court Rules to Release Clinical Trial Data to American Researcher

CBC News and the British Medical Journal (BMJ) are reporting that Professor Peter Doshi has won a major legal victory against pharmaceutical companies trying to hide clinical trial data from the public due to “confidential agreements” for 5 pharmaceutical products.

Doshi sued Health Canada to release clinical trial data submitted to Health Canada by the manufacturers of the HPV vaccines Gardasil, Gardasil 9 and Cervarix, and the anti-viral flu medications, Tamiflu and Relenza.

A Canadian Federal Court judge ordered Health Canada to release the pharmaceutical clinical trial data, undercutting the Canadian government’s attempts to keep the information confidential.

As far as I can determine, this landmark court ruling out of Canada has been completely censored in the U.S. corporate-sponsored “mainstream” media.

This appears to be a brilliant legal strategy by Doshi and his attorneys, since they had little to no chance of obtaining this clinical trial data from any court in the U.S., where pharmaceutical companies enjoy legal immunity from most lawsuits.

The importance of receiving this data, particularly on Merck’s Gardasil vaccine, cannot be overstated.

As we have reported many times here at Health Impact News, the entire medical approval process to bring the HPV vaccine into the U.S. market is full of scandals and cover-ups, which has resulted in the injuries and deaths of many young people, particularly young women aged 12 to 26, many of whom can no longer bear children due to the vaccine making them infertile.

“I hope my case sets a precedent and allows researchers, clinicians, and the public easy access to clinical trial data,” Doshi reportedly stated in an email to CBC News.

“Regulators shouldn’t have a monopoly on judging the risks and benefits of medicines or hinder others from doing the same via confidentiality agreements.”

HHS Sued for Not Upholding Vaccine Safety Testing Mandated by Law

In 2017, Health Impact News reported that the Informed Consent Action Network (ICAN), supported by 55 organizations, representing over 5 million people, had taken the unprecedented step of serving a notice to Mr. Don Wright, M.D., M.P.H., who was the acting secretary of the Health and Human Services (HHS) department at the time, stating that HHS had failed in their duty to conduct the proper scientific research required to demonstrate vaccine safety as was required by law, and that they should take immediate action to remedy this negligence.

Last week (July, 2018), Del Bigtree interviewed Robert F. Kennedy Jr. on his program HighWire, announcing that they had filed a lawsuit against HHS for violating U.S. law on vaccine safety, and won.

Hundreds of HPV Vaccine Victims Take to the Streets in Dublin to Protest - 2 Girls Suffer Seizures During Protest

Hundreds of HPV vaccine-injured people took to the streets to protest at Leinster House, Dublin, on July 9th, 2018, while Professor Ian Frazier, one of the co-inventors of the vaccine, gave a speech next door at the Royal College of Physicians.

During the protest, 3 Gardasil vaccine victims took ill, with 2 of them having seizures. Both of the girls suffering seizures had to be taken to the hospital.

The following video was taken of the protest, and towards the end of the video you can see one of the girls having a seizure.

This protest has been mostly censored in the “mainstream” corporate-sponsored media.

Samoa Seizes All MMR Vaccines After Two Infants Die Minutes After Receiving the Vaccine

TV1 in Samoa is reporting that two infants have died within minutes of receiving the measles, mumps, and rubella (MMR) vaccine.

“Tala Fou brings you breaking news on the death of two young children both aged 1-year-old from the villages of Safotu and Sasina in Savaii. Both children died within minutes of being vaccinated with the MMR vacine at Safotu Hospital on Friday morning the 6th of July.

Our News Reporter Alisa Faamaoni met with both families in Savaii today. The parents of the first child Marietta and Samuelu Tuisuesue of Sasina explained in detail to Tala Fou that within three minutes of their 1-year-old daughter Lannacallystah Samuelu being injected with the MMR vacine by a nurse she was dead.”

What is so tragic, and has this island nation in such an uproar, is that the parents of the second child who died had reportedly already learned about the first infant’s death a couple hours earlier and declined to have their child receive the same MMR vaccine. The mother reports that the nurse administered the vaccine against her consent, leading to the child’s immediate death upon receiving the vaccine.

Should Women be Given the Tdap Vaccine During Pregnancy?

A great debate is raging about whether we should have mandatory vaccination to prevent childhood illnesses. Mandatory vaccination would do away with a religious, ethical, or scientific disapproval of a vaccine.

A study from the University of North Carolina School of Medicine reported that the Tdap vaccination during pregnancy reduced the occurrence of infantile pertussis. This study is a perfect example of why we need informed consent on the safety and efficacy of vaccines and why we should not have government mandates about vaccines.

The researchers looked at infants admitted to the hospital with pertussis and compared two groups of pregnant women: one group who received the Tdap and the other group that did not.

This study showed that the Tdap vaccine is 0.02% effective at preventing hospitalization from pertussis. In other words, the vaccine will not benefit 99.98% who take it.

The Tdap vaccine contains a known neurotoxin (aluminum) and carcinogen (formadehyde). There are ZERO safety studies shown that it is safe to inject either substance into a human much less a pregnant human.

When I was trained, I was taught to be very careful when prescribing any therapy for a pregnant woman. I was always taught to err on the side of caution.

I think that was sage advice.

Tdap for pregnant women? Give women the appropriate information and let them decide.

World Health Organization's New Lax Vaccine Safety Policy Leads to More Child Deaths by Vaccines

Two leading pediatricians in India have published a critique of the World Health Organization’s (WHO) newly revised manual on the classification of Adverse Events Following Immunization (AEFI).

The doctors claim that the new guidelines are too lax, resulting in more children dying from adverse reactions to vaccines, with no accountability for the vaccine manufacturers to produce safer vaccines.

In the U.S., pharmaceutical companies manufacturing vaccines cannot be sued due to faulty vaccines, which allows them to put as many vaccines into the market as they want, with no repercussions if the vaccine proves to be faulty or have a high injury and death rate. Victims must sue the U.S. government and top DOJ attorneys who protect the drug companies.

This move by the WHO may very well be an attempt to protect drug companies manufacturing vaccines by preventing lawsuits in the rest of the world for faulty vaccines.

According to the report of these two doctors, the consequence of India adopting WHO’s new classification can be seen from the causality assessment of 132 serious AEFI cases uploaded on the website of the Ministry of Health and Family Welfare. Of the total AEFI cases, 54 babies died and 78 survived, “but not even one death was classified as vaccine-related. Nearly all the deaths were simply classified as unclassifiable or coincidental.”

Japanese Attorneys Representing HPV Vaccine Victims Urge Government to Ban HPV Vaccines

In a recent press release commemorating the 5-year anniversary of the Japanese Government suspending its recommendation of the HPV vaccine, the National Attorneys Association for the HPV Vaccines Lawsuits called upon the Japanese Government to ban the HPV vaccine completely.

This is the type of news that is routinely censored in the corporate-sponsored “mainstream” media in the United States. The fact that there is a national organization of attorneys litigating against one specific vaccine and the injuries it is causing, is itself newsworthy.

The vaccine manufacturers who are being sued in Japan, GlaxoSmithKline PLC and Merck Sharp & Dohme Corp., enjoy 100% legal immunity in the United States, due to the 1986 National Childhood Vaccine Injury Compensation Act.

We must look outside of the U.S., therefore, to learn about just how devastating Gardasil and the HPV vaccine is, as the National Association for the HPV Vaccines Lawsuits reports:

“Compared to other routine vaccinations, an average of over seven times the number of serious adverse effects per one million HPV vaccinations have been reported, and the number of disability certifications by the Adverse Drug Reaction Relief System is almost ten times higher.”