Vaccine News – Vaccine-Autism Link Study is Allegedly Part of Trump Administration’s $54 Billion Budget Cut

Vaccine-Autism Link Study is Allegedly Part of Trump Administration’s $54 Billion Budget Cut
Regin OlimberioMar 13, 2017 12:50 AM EDT
President Donald Trump’s stance to study the alleged link between vaccine and autism stirs fear of hampered study and minimal funding among health sector. A previous study has already debunked the myth that vaccines can cause autism but Trump opened the doors to further research. Advocates of mass vaccination fear that they have to turn their energy defending vaccines instead of moving forward with a medical breakthrough.
To recall, the renewed vigor started in 2008 when the National Vaccine Advisory Committee pushed for a safety agenda about the issue. Parents were assured of transparent access to results of research about vaccine’s link to autism. The agenda resurged at the start of Trump administration.
Health experts argued that Trump’s policy might delay or hamper the administration of vaccines. By doing so, children will be more susceptible to natural infections. This heightened risk can occur even at small delay between vaccine shots.
Another implication could be the difficulty in availing health insurance being stipulated under Affordable Care Act or Obamacare. The said law assures health coverage for pre-existing condition. Health insurance companies can simply imply that autism is not part of coverage since it is debatably not pre-existing but aggravated by vaccines. Another law that will suffer a setback is Disabilities Education Act that ensures education for autistic children, Live Science reported.

Vaccines and Autism Revisited — The Hannah Poling Case
Paul A. Offit, M.D. N Engl J Med 2008
On April 11, 2008, the National Vaccine Advisory Committee took an unusual step: in the name of transparency, trust, and collaboration, it asked members of the public to help set its vaccine-safety research agenda for the next 5 years. Several parents, given this opportunity, expressed concern that vaccines might cause autism — a fear that had recently been fueled by extensive media coverage of a press conference involving a 9-year-old girl named Hannah Poling.
When she was 19 months old, Hannah, the daughter of Jon and Terry Poling, received five vaccines — diphtheria–tetanus–acellular pertussis, Haemophilus influenzae type b (Hib), measles–mumps–rubella (MMR), varicella, and inactivated polio. At the time, Hannah was interactive, playful, and communicative. Two days later, she was lethargic, irritable, and febrile. Ten days after vaccination, she developed a rash consistent with vaccine-induced varicella.
Months later, with delays in neurologic and psychological development, Hannah was diagnosed with encephalopathy caused by a mitochondrial enzyme deficit. Hannah’s signs included problems with language, communication, and behavior — all features of autism spectrum disorder. Although it is not unusual for children with mitochondrial enzyme deficiencies to develop neurologic signs between their first and second years of life, Hannah’s parents believed that vaccines had triggered her encephalopathy. They sued the Department of Health and Human Services (DHHS) for compensation under the Vaccine Injury Compensation Program (VICP) and won.
On March 6, 2008, the Polings took their case to the public. Standing before a bank of microphones from several major news organizations, Jon Poling said that “the results in this case may well signify a landmark decision with children developing autism following vaccinations.”1 For years, federal health agencies and professional organizations had reassured the public that vaccines didn’t cause autism. Now, with DHHS making this concession in a federal claims court, the government appeared to be saying exactly the opposite. Caught in the middle, clinicians were at a loss to explain the reasoning behind the VICP’s decision.
The Poling case is best understood in the context of the decision-making process of this unusual vaccine court. In the late 1970s and early 1980s, American lawyers successfully sued pharmaceutical companies claiming that vaccines caused a variety of illnesses, including unexplained coma, sudden infant death syndrome, Reye’s syndrome, transverse myelitis, mental retardation, and epilepsy. By 1986, all but one manufacturer of the diphtheria–tetanus–pertussis vaccine had left the market. The federal government stepped in, passing the National Childhood Vaccine Injury Act, which included the creation of the VICP. Funded by a federal excise tax on each dose of vaccine, the VICP compiled a list of compensable injuries. If scientific studies supported the notion that vaccines caused an adverse event — such as thrombocytopenia after receipt of measles-containing vaccine or paralysis after receipt of oral polio vaccine — children and their families were compensated quickly, generously, and fairly. The number of lawsuits against vaccine makers decreased dramatically.

Whooping cough increase related to current vaccine
Friday, 24 April 2015 Dani Cooper ABC
The move to an artificially created vaccine for whooping cough is behind an increase in cases of the deadly disease in the US, a new study suggests.
The findings highlight the need to do similar research in Australia where whooping cough cases have spiralled upward in the past decade, co-author Associate Professor Manoj Gambhir, from the University of Monash, says.
In 2012 the US saw the highest number of pertussis (whooping cough) cases since 1955.
At the same time there has been a shift in the age group reporting the largest number of cases from adolescents to 7 to 11 year olds.
In the paper, published today in PLOS Computational Biology, Gambhir and colleagues use mathematical modelling of 60 years of pertussis disease data to determine what best explains this increase.
Their research finds the level of protection of the currently used acellular vaccine is lower than that of the previously used whole-cell vaccine.
Gambhir says the original whole-cell vaccine developed in 1942 was very effective.
Following introduction of vaccination, the reported disease incidence in the US dropped from 150 cases per 100,000 each year before 1940, to the point of near elimination in the mid-1970s when there were just 0.5 reported cases per 100,000 population.
“Now in the past decade we have seen a rise from that low to about 10-20 cases per 100,000,” says Gambhir.
Gambhir, who led the study with Dr Thomas Clark at the Centers for Disease Control and Prevention, in Atlanta, Georgia, and Professor Neil Ferguson, of the Imperial College London in the UK, says while the number of cases remains low the trend is upward.
“It’s the sort of five-year by five-year rise that is the concern because the worry is it could go back to those levels at which we would start seeing infant deaths,” he says.
New vaccine to blame
Gambhir says in 1991 researchers developed a new vaccine to address public concerns that the whooping cough vaccine caused a reaction in some children.

Study – A Change in Vaccine Efficacy and Duration of Protection Explains Recent Rises in Pertussis Incidence in the United States
Published: April 23, 2015
PDF version
Abstract
Over the past ten years the incidence of pertussis in the United States (U.S.) has risen steadily, with 2012 seeing the highest case number since 1955. There has also been a shift over the same time period in the age group reporting the largest number of cases (aside from infants), from adolescents to 7–11 year olds. We use epidemiological modelling and a large case incidence dataset to explain the upsurge. We investigate several hypotheses for the upsurge in pertussis cases by fitting a suite of dynamic epidemiological models to incidence data from the National Notifiable Disease Surveillance System (NNDSS) between 1990–2009, as well as incidence data from a variety of sources from 1950–1989. We find that: the best-fitting model is one in which vaccine efficacy and duration of protection of the acellular pertussis (aP) vaccine is lower than that of the whole-cell (wP) vaccine, (efficacy of the first three doses 80% [95% CI: 78%, 82%] versus 90% [95% CI: 87%, 94%]), increasing the rate at which disease is reported to NNDSS is not sufficient to explain the upsurge and 3) 2010–2012 disease incidence is predicted well. In this study, we use all available U.S. surveillance data to: 1) fit a set of mathematical models and determine which best explains these data and 2) determine the epidemiological and vaccine-related parameter values of this model. We find evidence of a difference in efficacy and duration of protection between the two vaccine types, wP and aP (aP efficacy and duration lower than wP). Future refinement of the model presented here will allow for an exploration of alternative vaccination strategies such as different age-spacings, further booster doses, and cocooning.

Vaccine Detox: Do This IMMEDIATELY if Baby Regresses after Shots
by Sarah Updated: December 23, 2016
When it comes to childhood immunizations, the approach with the least long term risk to your child’s health is refusing the shots in the first place. It’s a better strategy to avoid the myriad of vaccine related health problems from the start rather than scrambling for an effective vaccine detox to unwind the immune system damage later.
You can always get vaccinated, but undoing vaccine damage is a challenging process. Procrastination is a virtue when it comes to shots!
Science is not on your side if you choose to vaccinate, contrary to the drone of government officials, the media, misinformed school officials, and even pediatricians, some of whom are fearful of reprisal if they speak out with a differing opinion on the subject.
Emergency Vaccine Detox if a Child Regresses after Vaccination
Loss of eye contact, unresponsiveness to sounds or other stimuli, and the sudden inability to walk are common observations by parents of young children after a round of vaccinations. They are so common, in fact, that more than 1 in 50 children is currently on the autistic spectrum. This is up from one in every 300 children when my first child was born in 1998. In the 1980s, about 1 in every 10,000 children was autistic. Scientific projections are that 1 in every 2 boys will be on the spectrum by 2030 at the current rate of growth.
What should you do if you decide to vaccinate and your child suddenly starts to regress?
Developmental pediatrician Dr. Mary Megson of the University of Virginia has answers for you based on her extensive clinical experience treating autistic children for over 25 years.
Dr. Megson has developed a framework for treating autism based on the piece of the puzzle she has discovered clinically – blocked Vitamin A pathways in the brain.

Six Reasons To Say NO to Vaccination
by Sarah Updated: February 25, 2017
Vaccination is an extremely controversial topic these days. Whatever side of the aisle you may fall with regard to your opinion about vaccination, one thing is for certain. The choice to vaccinate or not vaccinate is a decision that has the potential to greatly impact the health of you and most importantly, your children for the rest of their lives.
As a result, this decision should not be taken lightly and it should not be made in a vacuum.   In other words, don’t just take your pediatrician’s word that shots are safe.    It is possible for doctors to be wrong.    They are human, after all.   In reality, your doctor is simply parroting the standard line about vaccination from the American Medical Association (AMA) playbook.    If you think you are getting their honest assessment, think again.
You should neither assume shots are dangerous just because your friend down the street doesn’t vaccinate her kids.

#1:   Pharmaceutical Companies Can’t Be Trusted (Ever)
#2:   ALL Vaccines are Loaded with Chemicals and Heavy Metals
#3:   Vaccinated Children are the Unhealthiest, Most Chronically Sick Children
#4:   Other Countries Are Waking Up to the Dangers of Vaccination
#5:   Numerous Vaccines Have Already Had Problems/Been Removed from the Market
#6   You Can Always Get Vaccinated, But You Can Never Undo a Vaccination

Govt. Still Pushing HPV Vaccine on Kids a Decade after JW Exposed Deadly Side Effects
MARCH 09, 2017
A decade after Judicial Watch exposed the dangers of a government-backed cervical cancer vaccine, a federal lawsuit highlights its perilous side effects including paralysis, seizures, nausea and death. Litigation was initiated by disgruntled parents because the government is still pushing the hazardous vaccine, manufactured by pharmaceutical giant Merck, on children as young as nine years old to treat a sexually transmitted disease.
The vaccine is called Gardasil and in the last ten years Judicial Watch has uncovered troves of government records documenting its harmful side effects. The vaccine was scandalously fast-tracked by the Food and Drug Administration (FDA) and was ardently promoted by the Obama administration as a miracle shot that can prevent certain strains of cervical cancer caused by Human Papillomavirus (HPV). Instead it’s been linked to thousands of debilitating side effects, according to the government’s own daunting statistics. This includes thousands of cases of paralysis, convulsions, blindness and dozens of deaths. Back in 2008, after receiving the first disturbing batch of records from the Centers for Disease Control and Prevention (CDC), Judicial Watch published a special report detailing Gardasil’s approval process, side effects, safety concerns and marketing practices. Undoubtedly, it illustrates a large-scale public health experiment.
Regardless, the government has continued promoting the vaccine while covering up its debilitating side effects, recommending it for girls—and more recently boys—starting at age 9. The Obama administration gave dozens of state and municipal health agencies tens of millions of dollars to boost the number of adolescents that get Gardasil. This includes targeting low-income and ethnic minority populations that receive “culturally sensitive” intervention in a variety of languages, including Spanish, Mandarin, Armenian and Korean. U.S. law forbids lawsuits against vaccine manufacturers, but Judicial Watch has obtained records from the Department of Health and Human Services (HHS) revealing that its National Vaccine Injury Compensation Program (VICP) has awarded nearly $6 million to dozens of victims in claims made against the very HPV vaccine it is pushing on children.
In 2014 a physician who worked at Merck denounced Gardasil as an ineffective vaccine with deadly side effects that serves no other purpose than to generate profit for its manufacturer. The former pharmaceutical industry doctor, Bernard Dalbergue, said Gardasil is useless, costs a fortune and that decision-makers at all levels are aware of it. “I predict that Gardasil will become the greatest medical scandal of all times because at some point in time, the evidence will add up to prove that this vaccine, technical and scientific feat that it may be, has absolutely no effect on cervical cancer and that all the very many adverse effects which destroy lives and even kill, serve no other purpose than to generate profit for the manufacturers,” Dr. Dalbergue said. He added that there is far too much financial interest for the vaccine to be withdrawn. Dr. Dalbergue’s statements were used by a member of the French Parliament as part of a broader campaign blasting Gardasil’s horrible safety record in Europe.

New FDA Records Obtained by Judicial Watch Indicate 28 Deaths Related to Gardasil in 2008
JUNE 22, 2009
Judicial Watch, the public interest group that investigates and prosecutes government corruption, announced today that it has obtained records from the Food and Drug Administration (FDA) documenting 28 deaths in 2008 associated with Gardasil, the vaccination for human papillomavirus (HPV), up from 19 deaths in 2007. The total number of Gardasil-related deaths is 47 since the vaccine was approved in 2006. Overall, the FDA documented 6,723 “adverse events” related to Gardasil in 2008, of which 1,061 were considered “serious,” and 142 considered “life threatening.”
The following are several “adverse events” documented by the FDA’s Vaccine Adverse Event Reporting System (VAERS):
“15 months from the completion of the GARDASIL HPV vaccination, I had full blown cervical cancer. My oncologist would like to do a hysterectomy at this time, but [as I have] always wanted children, I have chosen to wait . . . I have two of the [strains] that the shot is suppose to prevent . . . I now have cervical cancer and I am left wondering what role the GARDASIL HPV vaccination played in the hasty onset.” (ID: 319836)
“After receiving her second dose of GARDASIL … she could crawl but … needed to use crutches or a wheel chair … She was experienced problems breathing and had ‘super migraines’ that never went away … She had swelling in her face, jaw and wrists. The patient was diagnosed with GUILLAIN-BARRE syndrome, myelin sheath degeneration and peripheral neuropathy. Patient was hospitalized twice … patient has not recovered from symptoms.” (ID: 318052)
A 19-year-old girl with no medical history immediately experienced side effects after receiving the Gardasil vaccine. Within eleven days her symptoms included “Aggression, Arthralgia, Complex partial seizures, Confusional state, Convulsion, Crying, Dizziness, Epilepsy, Fatigue, Feeling abnormal, Grand mal convulsion, Immediate post-injection reaction, Irritability, Myalgia, Nausea, Pain, Postictal state, Somnolence, Syncope, Tremor, and Unresponsive to stimuli.” (ID: 320598)
“Two weeks after the third dose, the patient developed a complication. She was taken to the hospital by ambulance but passed away during the transport from an unknown cause…Upon arrival in ER unresponsive, pupils fixed and dilated, no cardiac activity. Resuscitation unsuccessful and patient expired.” (ID: 314769)
The FDA VAERS reports show that since last June, 235 cases detailed permanent disability. There were also 29 new cases of Guillain-Barre Syndrome, and 147 cases of “spontaneous abortions,” or miscarriages, when the vaccine was given to pregnant women.

Merck Dr. Exposes Gardasil Scandal: Ineffective, Deadly, Very Profitable
APRIL 21, 2014
A controversial government-backed cervical cancer vaccine is ineffective, has deadly side effects and serves no other purpose than to generate profit for its manufacturer, according to a physician who worked at the major pharmaceutical company that’s made huge profits selling it to girls and young women.
It marks the most disturbing inside information exposed about the vaccine, Gardasil, which is manufactured by pharmaceutical giant Merck. The vaccine was scandalously fast-tracked by the Food and Drug Administration (FDA) and has been ardently promoted by the Obama administration as a miracle shot that can prevent certain strains of cervical cancer caused by Human Papillomavirus (HPV).
Instead it’s been linked to thousands of debilitating side effects, according to the government’s own daunting statistics. Since 2007 Judicial Watch has been investigating the Gardasil scandal and exposed droves of government records documenting thousands of adverse reactions associated with the vaccine, including paralysis, convulsions, blindness and dozens of deaths. Based on the records JW published a special report in 2008 detailing Gardasil’s approval process, side effects, safety concerns and marketing practices. Undoubtedly, it illustrates a large-scale public health experiment.
Now a one-time pharmaceutical industry physician, Dr. Bernard Dalbergue, who worked with Merck has come forth with shocking inside information that confirms what JW has exposed about Gardasil in its ongoing investigation. Dr. Dalbergue delivered the details in a French health magazine and a U.S. counterpart called Health Impact News Daily translated excerpts of the interview.
The physician confirms that Gardasil is useless, costs a fortune and that decision-makers at all levels are aware of it. “I predict that Gardasil will become the greatest medical scandal of all times because at some point in time, the evidence will add up to prove that this vaccine, technical and scientific feat that it may be, has absolutely no effect on cervical cancer and that all the very many adverse effects which destroy lives and even kill, serve no other purpose than to generate profit for the manufacturers,” Dr. Dalbergue says. He adds that there is far too much financial interest or the vaccine to be withdrawn.

Examining the FDA’s HPV Vaccine Records: PDF source
Detailing the Approval Process, Side-Effects, Safety Concerns and Marketing Practices of a Large-Scale Public Health Experiment June 30, 2008

Push for nation-wide ‘no jab, no play’ at childcare centres
11:40pm March 12, 2017
Unvaccinated children could be banned from attending childcare centres and preschools across Australia as part of a renewed push by the federal government.
Prime Minister Malcolm Turnbull has written to state and territory leaders in a move towards introducing consistent laws to protect children across the country.
“If you don’t vaccinate your child you are not just putting their own life at risk, but you are putting everyone else’s children at risk,” Mr Turnbull wrote.

Settlement for Saba Button, severely disabled after flu vaccine
Updated 8 Jun 2014, 2:26am
The family of a West Australian child left severely disabled after receiving a flu jab has reached a settlement with the vaccine’s manufacturer and the State Government.
Saba Button suffered brain and organ damage after getting the Fluvax shot when she was 11 months old in 2010.
Her parents launched legal action in the Federal Court against the vaccine’s manufacturer, CSL Limited.
CSL cross-claimed against the State of WA and the Health Minister.
All parties have reached a confidential settlement which has today been accepted by Federal Court Justice Michael Barker.
Saba’s father, Mick Button, said it had been a long battle for compensation.
“Today is a bittersweet feeling for us,” he said.
“It’s a relief to have the legal case behind us.
“We now have the ability to be able to supply Saba with the care, the therapy, the equipment, all the things that she needs to give her the best quality of life.”
Her mother Kirsten Button said she was relieved the legal action had been finalised.
“It doesn’t matter how much you have because you can’t buy your health but it is a good outcome, and the fact that it’s settled, we’re quite a strong family and we have moved forward but I think having that hanging over your head as such can be stressful so now we can move forward knowing that it’s all over.”
Mr Button said the funds would help Saba continue ongoing therapy and explore new options both in Australia and overseas.
“This doesn’t just stop now, once all the cameras are gone, it’s back to business and we’ve got a lot to do with Saba,” he said.

VACCINE STUDY: Peer-reviewed study shows vaccinated children have a 700% higher chance of neurodevelopmental disorder
Tuesday, March 07, 2017 by: Vicki Batts
(Natural News) On Valentine’s Day, a 34-page study that illustrated some of the harmful effects of vaccination was made available for viewing online. Six hours later, the URL had vanished, and the study was seemingly erased from the depths of the internet — likely in the hopes that the “controversial” information it contained would be forgotten.
Vaccination and Health Outcomes: A Survey of 6- to 12-year-old Vaccinated and Unvaccinated Children based on Mothers’ Reports, by Anthony R. Mawson, et al. seemed like any other standard report on vaccination at first glance, according to author James Grundvig. The paper had been linked to Grundvig, and he recently published an article about the study, how he authenticated it with the study’s author, and he even described how the publishing journal went about censoring the information.
Grundvig writes that after reading Mawson’s conclusions in the study, it appears that perhaps the CDC has purposefully avoided conducting such research themselves because “it would have run counter to CDC’s messaging that all ‘vaccines are safe.’”
Research: vaccines and neurodevelopmental disorders
To conduct their research, Mawson and his team engaged in a cross-sectional survey of mothers of children who were educated at home. Homeschooling organizations from Florida, Louisiana, Mississippi, and Oregon were asked to forward an email to their members, requesting mothers to fill out an anonymous online survey. The questionnaire gathered information on vaccination status and health outcomes of their biological children who were between the ages of 6 and 12. In total, 415 mothers provided information about 666 children. Of those, just 261 (or 39 percent) had not been vaccinated. Information on pregnancy experiences, birth histories, acute and chronic conditions, and the usage of medication and health care services was also included in the data collection.
Overall, the results of the study showed that while vaccinated children were less likely to have had chicken pox or pertussis, they were significantly more likely to develop other types of infections, allergies, and were more likely to be diagnosed with a neurodevelopmental disorder (referred to in the study as an NDD). NDDs were defined as autism spectrum disorders, attention deficit hyperactivity disorder (ADHD), a learning disability, or any combination of the three. Could it be that unvaccinated children are in many ways healthier? It certainly seems that way.
Data reveals shocking disparities

First Peer-Reviewed Study of Vaccinated versus Unvaccinated Children (Censored by an International Scientific Journal) Now Public
Results: Vaccinated children were significantly less likely than the unvaccinated to have been diagnosed with chickenpox and pertussis, but significantly more likely to have been diagnosed with other infections, allergies and NDDs (defined as Autism Spectrum Disorder, Attention Deficit Hyperactivity Disorder, and/or a learning disability).
Chronic Illness Detail:
Vaccinated children were significantly more likely than the unvaccinated to have been diagnosed with the following chronic illnesses:
7-fold higher odds of any neurodevelopmental disorder (i.e., learning disability, ADHD, or ASD)

        2-fold increase in Autism Spectrum Disorder (“ASD”)
2-fold increase in ADHD
2-fold increase in learning disabilities
1-fold increase in allergic rhinitis
9-fold increase in other allergies
9-fold increase in eczema/atopic dermatitis
4-fold increase in any chronic 
illness

No significant differences were observed with regard to cancer, chronic fatigue, conduct disorder, Crohn’s disease, depression, Types 1 or 2 diabetes, encephalopathy, epilepsy, hearing loss, high blood pressure, inflammatory bowel disease, juvenile rheumatoid arthritis, obesity, seizures, and Tourette’s syndrome. However, larger samples would be needed to detect group differences in these less common conditions.
Acute Illness Detail:
Vaccinated children were significantly less likely than unvaccinated children to have had chickenpox or whooping cough (p<0.001).
Vaccinated children had a 3.8-fold increased odds of middle ear infections and a 5.9-fold increased odds of being diagnosed with pneumonia compared to unvaccinated children.
No significant differences were seen between the two groups with regard to Hepatitis A or B, high fever in the past 6 months, measles, mumps, meningitis (viral or bacterial), influenza, or rotavirus.

US Immunization Schedule Recommends 26 Vaccinations For Children Under 1, Highest In World And Ranks 34th In Infant Mortality
Print Friendly MARCH 12, 2017
A new study published today in the Journal of Human and Experimental Toxology found that countries that administer a higher number of vaccines during the first year of life experience higher infant mortality rates.
The infant mortality rate (IMR) of a country is one of the most accepted and critical indicators of the socioeconomic well being of its citizens. It also reflects public health conditions and whether those conditions are improving or worsening over time.
The United States ranks 34th in infant mortality rate which means that 33 countries outrank the USA in this critical measure of public health. In addition, the United States’ immunization schedule for infants under 1 year of age recommends 26 vaccinations – the highest in the entire world.

Vaccine pioneer admits adding cancer-causing virus to Vaccine

Vaccine pioneer admits adding cancer-causing virus to Vaccine
In this interview Dr. Maurice Hilleman reveals some astounding revelations. He admits that Merck drug company vaccines (Polio) had been deliberately contaminated with SV40, a cancer-causing monkey virus from 1953 – 63.
For years, researchers suggested that millions of vials of polio vaccine, contaminated with SV40, infected individuals which caused human tumors, and by 1999, molecular evidence of SV40 infections were showing up in children born after 1982. Some experts now suggest the virus may have remained in the polio vaccine until as late as 1999.
In 2002, the journal Lancet published compelling evidence that contaminated polio vaccine was responsible for up to half of the 55,000 non-Hodgkin’s lymphoma cases that were occurring each year. And there is the likelihood that there was an importing and spreading of the AIDS virus in the same manner, as revealed in the video.
At first no one could fathom how the virus had been transmitted into the human population, but this shocking video proves that it was deliberately added to the vaccine by Dr. Maurice Hilleman, which was “good science” at that time.
Just Who is Dr. Maurice Hilleman?
Now, for those of you who may think Dr. Hilleman was just another crackpot (he passed away in 2005), think again. He was, and still is, the leading vaccine pioneer in the history of vaccines. He developed more than three dozen vaccines—more than any other scientist in history—and was the developer of Merck’s vaccine program.
He was a member of the U.S. National Academy of Science, the Institute of Medicine, the American Academy of Arts and Sciences, and the American Philosophical Society, and received a special lifetime achievement award from the World Health Organization.
When he was chief of the Department of Respiratory Diseases with what’s now the Walter Reed Army Institute of Research, he discovered the genetic changes that occur when the influenza virus mutates, known as shift and drift. He was also one of the early vaccine pioneers to warn about the possibility that simian viruses might contaminate vaccines.So Dr. Hilleman knew what he was talking about. And in his own words, “vaccines have to be considered the bargain basement technology for the 20th Century.”

CDC admits 98 million Americans were given cancer virus via the polio shot
The CDC has admitted that between 1955–1963 over 98 million Americans received one or more doses of a polio shot which was contaminated with a cancer-causing virus called Simian vacuolating virus 40 (SV40).  The CDC quickly took down the page, along with Google, but the site was luckily cached and saved to symbolize this grand admission.

Historical Vaccine Safety Concerns
Simian Virus 40(SV40) – 1955-1963
Some of the polio vaccine administered from 1955 to 1963 was contaminated with a virus called simian virus 40 (SV40). The virus came from the monkey kidney cells used to produce the vaccines.  Once the contamination was discovered in the Salk inactivated polio vaccine in use at that time, the U.S. government established requirements for vaccine testing to verify that all new batches of the polio vaccine were free of SV40. Because of research done with SV40 in animal models, there was some concern that the virus could cause cancer. However, evidence suggests that SV40 has not caused cancer in humans.

Volume 3, Number 2—June 1997
Simian Virus 40 (SV40), a Possible Human Polyomavirus (Workshop Held at NIH)
During the past 4 years, polymerase chain reaction (PCR) assays have detected DNA sequences related to SV40 (an oncogenic simian polyomavirus) in a variety of human tissues, especially choroid plexus tumors, ependymomas, mesotheliomas, and osteosarcomas (1-7). These findings were supported by the isolation of infectious SV40 from a choroid plexus tumor (8).
Although another paper reported the failure to detect SV40 DNA in mesotheliomas (9), these studies have reawakened interest in inadvertent human exposure to SV40 in the late 1950s and early 1960s when polio and adenovirus vaccines prepared in rhesus monkey cells containing SV40 were used (10,11). In response to the implications of detecting SV40 DNA in human tumors, the Food and Drug Administration, National Institutes of Health, National Vaccine Program Office, and Centers for Disease Control and Prevention sponsored a workshop on SV40 on January 27-28, 1997 at the National Institutes of Health to examine the possibility that SV40 is an infectious agent in humans.

The following statement is an introduction for a more detailed packet on SV-40 and animal viruses in the production of vaccines.

Statement by Barbara Loe Fisher, Co-Founder & President
National Vaccine Information Center
Workshop on Simian Virus-40 (SV-40): A Possible Human Polyomavirus
January 27-28, 1997
Bethesda, Maryland
The National Vaccine Information Center (NVIC), which was founded in 1982 and represents health care consumers and health care professionals concerned about vaccine safety, became actively involved in 1994 in researching reports of contamination of childhood vaccines with animal viruses and the possibility that inter-species transfer of animal viruses into humans via vaccines has had a negative impact on public health. Our concern was that government health agencies and industry had not adequately addressed many of the most important questions that remained unanswered about the contamination of polio vaccines with simian (monkey) viruses.

Should I Get the Flu Shot? CDC Data Raise Concerns

Should I Get the Flu Shot? CDC Data Raise Concerns
In February the CDC revealed that the 2014-2015 influenza vaccine had an efficacy rate of only 19 percent. If that was not bad enough, in June the CDC’s committee that advises on immunization practices announced that nasal spray flu vaccines should not be used in the 2016-2017 flu season because, in the CDC’s own words, “no protective benefit could be measured” from taking them.
Indeed, numerous peer-reviewed scientific studies have shown that the flu vaccine is not effective either at reducing the flu or reducing flu-related deaths.
When a team of researchers at the National Institutes of Health compared flu vaccine rates with influenza-related illness over a 19-year period, from 1980 to 1999, they found that deaths from the flu increased as vaccination rates increased. “In conclusion, the increase in elderly influenza vaccination coverage in the U.S. after 1980 was not accompanied by a decline in influenza-related mortality,” the researchers concluded.
A study, led by a researcher at the National Institute of Allergy and Infectious Diseases and published in the journal Archives of Internal Medicine, found that increasing vaccination coverage did not correlate with declining mortality and the decline in influenza-related mortality could not be attributed to the flu vaccine but was rather the result of naturally acquired immunity. Observational studies crediting the flu vaccine with contributing to decreased deaths from the flu, “substantially overestimate vaccination benefit,” these researchers concluded.
A study published in the American Journal of Perinatology of vaccine effectiveness in pregnant women in Northern California across five flu seasons found that women who received flu vaccines during pregnancy had the same risk for influenza-like illness as unvaccinated women, and infants born to women who received flu vaccines also had the same risks for influenza or pneumonia as infants born to unvaccinated women. In other words, vaccine status made no difference to whether or not pregnant women or their offspring got the flu.
A study published in Pediatrics International of Japanese children ages 6 months to 2 years who were vaccinated against the flu found that the influenza vaccine did not reduce the rate of influenza A infections in children under two.

CDC Presents Updated Estimates of Flu Vaccine Effectiveness for the 2014-2015 Season
Flu vaccine did not protect against drifted H3N2 viruses, but protected against vaccine-like H3N2 and B viruses
On February 26, 2015, updated interim influenza (flu) vaccine effectiveness (VE) estimates for the current 2014-2015 season were presented to the Advisory Committee on Immunization Practices (ACIP). The updated VE estimate against influenza A H3N2 viruses was 18% (95% confidence interval (CI): 6%-29%).This result is similar to the VE point estimate of 23%, which was reported in a January 16 Morbidity and Mortality Weekly Report (MMWR) and confirms reduced protection against H3N2 viruses this season. The VE estimate against influenza B viruses this season was 45% (95% CI: 14% – 65%).
How well the flu vaccine works can vary depending on a number of factors, including the similarity between circulating influenza viruses and vaccine viruses, and the age, health or immune status of the person vaccinated. The findings for VE against H3N2 viruses this season are about one-third of the VE expected when the flu vaccine is well matched to circulating influenza viruses. The VE against influenza B viruses this season is similar to the effectiveness observed when vaccine viruses and most circulating viruses are well matched.

ACIP votes down use of LAIV for 2016-2017 flu season
Media Statement
For Immediate Release: Wednesday, June 22, 2016
CDC’s Advisory Committee on Immunization Practices (ACIP) today voted that live attenuated influenza vaccine (LAIV), also known as the “nasal spray” flu vaccine, should not be used during the 2016-2017 flu season. ACIP continues to recommend annual flu vaccination, with either the inactivated influenza vaccine (IIV) or recombinant influenza vaccine (RIV), for everyone 6 months and older.
ACIP is a panel of immunization experts that advises the Centers for Disease Control and Prevention (CDC). This ACIP vote is based on data showing poor or relatively lower effectiveness of LAIV from 2013 through 2016.

Vaccine injury testimony – Gardasil – Hannah M. Robinson

Vaccine injury testimony – Gardasil – Hannah M. Robinson
My vaccine injury, I have several photos and videos I feel ready to upload… Just a very small part of it… Thanks Gardasil! If you have a popular public profile and wish to share this or are close to one of the “higher ups” in our groups please private message me so I can send it to you.

New Concerns about the Human Papillomavirus Vaccine
It has recently come to the attention of the College that one of the recommended vaccines could possibly be associated with the very rare but serious condition of premature ovarian failure (POF), also known as premature menopause.
American College of Pediatricians – January 2016
The American College of Pediatricians (The College) is committed to the health and well-being of children, including prevention of disease by vaccines. It has recently come to the attention of the College that one of the recommended vaccines could possibly be associated with the very rare but serious condition of premature ovarian failure (POF), also known as premature menopause. There have been two case report series (3 cases each) published since 2013 in which post-menarcheal adolescent girls developed laboratory documented POF within weeks to several years of receiving Gardasil, a four-strain human papillomavirus vaccine (HPV4).1,2 Adverse events that occur after vaccines are frequently not caused by the vaccine and there has not been a noticeable rise in POF cases in the last 9 years since HPV4 vaccine has been widely used.
Nevertheless there are legitimate concerns that should be addressed: (1) long-term ovarian function was not assessed in either the original rat safety studies3,4 or in the human vaccine trials, (2) most primary care physicians are probably unaware of a possible association between HPV4 and POF and may not consider reporting POF cases or prolonged amenorrhea (missing menstrual periods) to the Vaccine Adverse Event Reporting System (VAERS), (3) potential mechanisms of action have been postulated based on autoimmune associations with the aluminum adjuvant used1 and previously documented ovarian toxicity in rats from another component, polysorbate 80,2 and (4) since licensure of Gardasil® in 2006, there have been about 213 VAERS reports (per the publicly available CDC WONDER VAERS database) involving amenorrhea, POF or premature menopause, 88% of which have been associated with Gardasil®.5 The two-strain HPV2, CervarixTM, was licensed late in 2009 and accounts for 4.7 % of VAERS amenorrhea reports since 2006, and 8.5% of those reports from February 2010 through May 2015. This compares to the pre-HPV vaccine period from 1990 to 2006 during which no cases of POF or premature menopause and 32 cases of amenorrhea were reported to VAERS.
Many adolescent females are vaccinated with influenza, meningococcal, and tetanus vaccines without getting Gardasil®, and yet only 5.6% of reports related to ovarian dysfunction since 2006 are associated with such vaccines in the absence of simultaneous Gardasil® administration. The overwhelming majority (76%) of VAERS reports since 2006 with ovarian failure, premature menopause, and/or amenorrhea are associated solely with Gardasil®. When VAERS reports since 2006 are restricted to cases in which amenorrhea occurred for at least 4 months and is not associated with other known causes like polycystic ovary syndrome or pregnancy, 86/89 cases are associated with Gardasil®, 3/89 with CervarixTM, and 0/89 with other vaccines administered independently of an HPV vaccine.5 Using the same criteria, there are only 7 reports of amenorrhea from 1990 through 2005 and no more than 2 of those associated with any one vaccine type.
Few other vaccines besides Gardasil® that are administered in adolescence contain polysorbate 80.6 Pre-licensure safety trials for Gardasil® used placebo that contained polysorbate 80 as well as aluminum adjuvant.2,7 Therefore, if such ingredients could cause ovarian dysfunction, an increase in amenorrhea probably would not have been detected in the placebo controlled trials. Furthermore, a large number of girls in the original trials were taking hormonal contraceptives which can mask ovarian dysfunction including amenorrhea and ovarian failure.2 Thus a causal relationship between human papillomavirus vaccines (if not Gardasil® specifically) and ovarian dysfunction cannot be ruled out at this time.

HPV Vaccine Being Tested To Give To Infants

HPV Vaccine Being Tested To Give To Infants
You’d be naive if you hadn’t considered the disturbing possibility of infants having to take the Gardasil vaccine. Of course, you’ve considered that the powers that be could move to add it to the regular vaccine schedule. When it comes to pharmaceutical companies and their mission statements, expanding medications based on profits doesn’t have to be clearly stated; it is assumed a truth and for good reason.
A new clinical trial is in the works, sponsored by Merck, to look at the effects of the HPV vaccine in infants. Sadly, this is a cold reality.

Side effects in young girls take Gardasil out from Japanese market
Around 2,000 reported side effects after using Gardasil cervical cancer vaccine have determined Japanese government officials to withdraw Gardasil from the market in 2013, despite the vaccine being highly promoted in the United States and now approved by the European Union.
“Japanese health officials have recorded nearly 2,000 adverse reactions – hundreds of them serious,” reported Judicial Watch, the Washington-based corruption watchdog that has been monitoring the effects – and health costs – of the drug’s use in the United States for years.
“The alarming reports have led Japan’s government to take action, suspending recommendation for the controversial vaccine which is billed as a miracle shot that can prevent certain strains of cervical cancer caused by Human Papillomavirus (HPV).”

HPV Vaccine: American College of Pediatricians Issues Rare Warning Against Vaccine Due to Premature Ovarian Failure
In an unprecedented move, the American College of Pediatricians has issued a warning against a vaccine that has been approved by the FDA and CDC. The College says that they are committed to the health and well-being of children, and due to their commitment to children’s health, they feel that safety concerns regarding the Human Papillomavirus Vaccine Gardasil should be made public.
The College says that in addition to concerning correlations between Gardasil and Premature Ovarian Failure, they are also concerned with the pre-release vaccine testing methods utilized by Gardasil maker Merck. Pre-licensure safety trials for Gardasil used a placebo that contained polysorbate 80 as well as an aluminum adjuvant, which are both contained within the vaccine. Therefore, if either of these ingredients could cause ovarian dysfunction, an increase in amenorrhea probably would not have been detected. The College notes that the placebo-controlled trials were highly questionable due to the fact that the placebos were actually not placebos at all.
The American College of Pediatricians just released their statement concerning the HPV vaccine, noting that they feel parents should be made aware of possible safety concerns regarding the use of the popular vaccine. The ACPEDS notes that they released the warning following new information presented to them about the potentially harmful vaccine.
“It has recently come to the attention of the College that one of the recommended vaccines could possibly be associated with the very rare but serious condition of premature ovarian failure (POF), also known as premature menopause.”

New Concerns about the Human Papillomavirus Vaccine
American College of Pediatricians – January 2016
The American College of Pediatricians (The College) is committed to the health and well-being of children, including prevention of disease by vaccines. It has recently come to the attention of the College that one of the recommended vaccines could possibly be associated with the very rare but serious condition of premature ovarian failure (POF), also known as premature menopause. There have been two case report series (3 cases each) published since 2013 in which post-menarcheal adolescent girls developed laboratory documented POF within weeks to several years of receiving Gardasil, a four-strain human papillomavirus vaccine (HPV4).1,2 Adverse events that occur after vaccines are frequently not caused by the vaccine and there has not been a noticeable rise in POF cases in the last 9 years since HPV4 vaccine has been widely used.
Nevertheless there are legitimate concerns that should be addressed: (1) long-term ovarian function was not assessed in either the original rat safety studies3,4 or in the human vaccine trials, (2) most primary care physicians are probably unaware of a possible association between HPV4 and POF and may not consider reporting POF cases or prolonged amenorrhea (missing menstrual periods) to the Vaccine Adverse Event Reporting System (VAERS), (3) potential mechanisms of action have been postulated based on autoimmune associations with the aluminum adjuvant used1 and previously documented ovarian toxicity in rats from another component, polysorbate 80,2 and (4) since licensure of Gardasil® in 2006, there have been about 213 VAERS reports (per the publicly available CDC WONDER VAERS database) involving amenorrhea, POF or premature menopause, 88% of which have been associated with Gardasil®.5 The two-strain HPV2, CervarixTM, was licensed late in 2009 and accounts for 4.7 % of VAERS amenorrhea reports since 2006, and 8.5% of those reports from February 2010 through May 2015. This compares to the pre-HPV vaccine period from 1990 to 2006 during which no cases of POF or premature menopause and 32 cases of amenorrhea were reported to VAERS.

How Big Pharma Plans to Fool You Into Giving Gardasil to Your Child

How Big Pharma Plans to Fool You Into Giving Gardasil to Your Child
Trust in the HPV vaccines is extremely low due to pressing concerns about safety and effectiveness. Many medical doctors concur. A prominent MD in women’s health writes about how Gardasil is gutting rather than “guarding” our youth. The American College of Pediatricians has officially sounded the alarm about Gardasil and how it is triggering premature ovarian failure (infertility) in young girls at an alarming rate.
In Japan, a class action lawsuit is in process with dozens of families suing the vaccine manufacturers for the debilitating health effects suffered by their daughters (1).  In addition, the Japanese government suspended the HPV vaccine in 2013 in response to numerous cases of serious adverse events.
In the United States, citizens are barred from suing vaccine manufacturers per the National Childhood Vaccine Injury Act of 1986. The only way to get compensation for vaccine injuries in the USA is from the National Vaccine Injury Compensation Program (NVCP). The stark reality is that vaccine injured kids are rarely compensated, however. Two out of every three applicants are denied recompense. Those fortunate enough to receive compensation must wait years or even a decade or more! Despite the few parents of vaccine injured children receiving any compensation whatsoever, the NVCP paid out over $3 billion dollars in claims through 2010 (2).
Instead of withdrawing the dangerous HPV vaccines from the market or attempting to reformulate them to make them safe, vaccine manufacturers have chosen the stealth route to get parents to comply.

New Concerns about the Human Papillomavirus Vaccine
American College of Pediatricians – January 2016
It has recently come to the attention of the College that one of the recommended vaccines could possibly be associated with the very rare but serious condition of premature ovarian failure (POF), also known as premature menopause.

Cell phone radiation breast cancer link – New study raises grave concerns

Cell phone radiation breast cancer link – New study raises grave concerns

(NaturalNews) A new study raises concerns of a possible association between cell phone radiation exposure and breast cancer in young women.
The research team, led by Dr. Lisa Bailey, a former president of the American Cancer Society’s California Division and one of California’s top breast surgeons, studied four young women – aged from 21 to 39 years old – with multifocal invasive breast cancer.
The researchers observed that all the patients developed tumors in areas of their breasts next to where they carried their cell phones, often for up to 10 hours per day, for several years. None of the patients had a family history of breast cancer. They all tested negative for BRCA1 and BRCA2 – breast cancer genes linked to about one-half of breast cancer cases – and they had no other known breast cancer risks.
Imaging of the young girls’ breasts revealed a clustering of multiple tumor foci in the part of the breast directly under where their cell phones touched their body.
Tiffany Frantz, one of the young girls involved in the study, said that she had no idea of the risks involved. “I put my cellphone right in my bra,” said Miss Frantz in a TV interview that also won an Emmy. However, her mother Traci Frantz immediately made the connection right after Tiffany developed breast cancer at age 21. “We never took it seriously until after she was diagnosed.” Her tumors were exactly where her cellphone had been kept in her bra for about six years. No one ever told us that this was a very bad idea.” said Traci Frantz. Surgeons had to remove Tiffany’s left breast. Her family had no genetic or other risk factors.

Dangers of other EMF exposures

Cell phones emit a form of electromagnetic field (EMF) called radio frequency radiation. This radiation exposure has previously been linked to brain tumors, cancer, cardiovascular disease, depression and other serious illnesses.
Studies show that other EMF exposures from similar, supposedly harmless, everyday appliances and devices can also be dangerous. The recently published “BioInitiative Report 2012” concluded, “there is sufficient evidence from in vitro and animal studies, from human biomarker studies, from occupational and light-at-night studies, and a single longitudinal study with appropriate collection of urine samples to conclude that high MF (magnetic field) exposure may be a risk factor for breast cancer.” The report’s authors went on to say that “there is rather strong evidence from case-control studies that longterm, high occupational exposure (over 10 milliGauss) to ELF (Extremely low frequency) magnetic fields is a risk factor for breast cancer.”

EMF safety standards outdated

Currently, the main international guidance comes from the International Commission on Non-Ionizing Radiation Protection. These guidelines offered no protection for Traci Frantz and others who unknowingly put their health at risk by carrying their cell phone in close proximity to their body.
Nor do these guidelines protect individuals from high magnetic field exposures in the home and workplace. The existing exposure limit for magnetic fields is 904 mG in the US – some 90 times higher than the levels at which independent studies have observed adverse biological effects!
Even cell phone manufacturers suggest that users keep their cell phone at least one-half inch or more away from any body part. But these recommendations, lost in the small print in user manuals, are not heeded.
Current safety limits can no longer be said to be protective of public health, and they should be replaced.
Sources for this article include:
http://www.bioinitiative.org
http://www.sbwire.com
http://www.hindawi.com
http://science.naturalnews.com