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 News – Study – Metals Debris Found in Vaccine Supply

Lead developer of HPV vaccine admits it’s a giant, deadly scam
Thursday, September 29, 2016 by: Samantha Debbie
(NaturalNews) An expert involved in the approval process for the human papilloma virus (HPV) vaccines Gardasil and Cervarix, is speaking out about the dangers and why you shouldn’t risk your child’s health in getting them.
Diane Harper, M.D., professor and chair of the department of Family and Geriatric Medicine at the University of Louisville, revealed at the 4th International Conference on Vaccination that HPV vaccines are essentially worthless, because rates of cervical cancer in the U.S. are extremely low anyway.
Her speech was intended to promote the benefits of vaccines, but she changed her mind and went in a different direction in an effort to “clean her conscience about the deadly vaccines,” according to The Daily Sheeple.
Dr. Harper, a former vaccine research scientist for Merck, said she wouldn’t be able to sleep at night unless she aired the truth about HPV vaccines. In her speech, given in Reston, Virginia, she said that 70 percent of all HPV infections resolve themselves without treatment, and 90 percent do so within two years.
Over 40 young girls reported to have died from HPV vaccines
All safety trials for HPV vaccines were done on 15-year-olds, said Dr. Harper, and not 9-year-olds, the demographic for which the immunizations are now recommended. Furthermore, there is a real risk associated with these vaccines, she added.
More than 15,000 girls have experienced adverse side effects from Gardasil, according to the Vaccine Adverse Event Reporting System (VAERS). A number likely to be far higher in reality, since many vaccine side effects go unreported.
At least 44 girls are known to have died from these vaccines. Some side effects experienced by those receiving the HPV vaccines include seizures, blood clots, brain inflammation, lupus and Guillain Barre Syndrome, a rare but serious autoimmune deficiency that causes the immune system to attack and damage nerve cells.
While the majority of those with GBS recover, the disorder may cause muscle weakness, difficulty breathing, paralysis and sometimes death.
As with most vaccines, parents are usually not made aware of the risks.
HPV vaccines work on only four of the 40 strains of the venereal disease

How Vaccinated Kids Infect The Non-Vaccinated
Posted on:Sunday, February 8th 2015 at 3:45 pm Written By: Sayer Ji, Founder
This article is copyrighted by GreenMedInfo LLC, 2015
With the thousands of mainstream media articles blaming the non-vaccinated for disease outbreaks, this article will provide a necessary counterbalance by showing the vaccinated can (and do) infect the non-vaccinated…
A groundbreaking study published in 2013 in the journal Vaccine titled, “Comparison of virus shedding after lived attenuated and pentavalent reassortant rotavirus vaccine,” referenced the fact that rotavirus vaccines contain live viruses capable of causing infection, shedding and even transmission to non-vaccinated subjects:
“In fact, transmission of these two rotavirus vaccines or vaccine-reassortment strains to unvaccinated contacts has been detected [9–13][1], even in the absence of symptoms.”
One of the five studies referenced in the passage above confirming that the vaccinated can infect the non-vaccinated, “Sibling transmission of vaccine-derived rotavirus (RotaTeq) associated with rotavirus gastroenteritis,” published in 2009, is the first report in the literature to identify the transmission of rotavirus vaccine-derived virus to unvaccinated contacts resulting in symptomatic rotavirus gastroenteritis requiring emergency medical attention:
“We document here the occurrence of vaccine-derived rotavirus (RotaTeq [Merck and Co, Whitehouse Station, NJ]) transmission from a vaccinated infant to an older, unvaccinated sibling, resulting in symptomatic rotavirus gastroenteritis that required emergency department care.”
The study also indicated that two of the five strains of rotavirus within the Rotateq reassorted to produce a more harmful virus either within the vaccinated infant or within the subsequently infected unvaccinated sibling:
“Results of our investigation suggest that reassortment between vaccine component strains of genotypes P7[5]G1 and P1A[8]G6 occurred during replication either in the vaccinated infant or in the older sibling, raising the possibility that this reassortment may have increased the virulence of the vaccine-derived virus.”
This phenomenon of Rotateq vaccine strain reassortment and subsequent gastoenteritis infection in vaccine recipients was also observed in a 2012 study in 61 infants.[2] Additionally, A Nicaraguan study published in 2012 found “the widespread use of the RotaTeq vaccine has led to the introduction of vaccine genes into circulating human RVs.,” revealing that the widespread introduction of the vaccine strain has altered the genetic makeup of wild-type rotavirus that now infects exposed populations.[3]
It has been estimated that between 80-100% of infants shed rotavirus at some point during 25-28 days after vaccination.[4] [5] This reveals that the vaccinated, contrary to widespread assumptions about the the risks represented by the non-vaccinated, pose a clear risk of infecting the non-vaccinated, and may be producing the ideal virological conditions for the recombination of diverse rotavirus strains into vaccine-resistant ‘super viruses.’
Another case study, reported on in the National Vaccine Information Center’s document on vaccine viral shedding:
“In 2010, a case report was published in Pediatrics describing a 30-month old healthy boy who had never received rotavirus vaccine and was infected with vaccine strain rotavirus. 237 He ended up in the emergency room with severe gastroenteritis 10 days after his healthy two-month old brother was given a dose of Merck’s RotaTeq vaccine. A stool sample was taken in the emergency room and came back positive for RotaTeq vaccine derived strains after RT-PCR testing.”
The authors of the case report noted that “transmission of RotaTeq strains to unvaccinated contacts was not evaluated in the pivotal [pre-licensure] clinical trials.” They added that  both RotaTeq and Rotarix [GlaxoSmithKline Biologicals] vaccines have “the potential for vaccine-virus transmission to contacts.”

Study 2014 Feb 26 – Comparison of virus shedding after lived attenuated and pentavalent reassortant rotavirus vaccine.
Transmission of rotavirus vaccine or vaccine-reassortant strains to unvaccinated contacts has been reported. Therefore, it is essential to evaluate and characterize the nature of vaccine-virus shedding among rotavirus vaccine recipients. Two groups of healthy infants who received a complete course of RotaTeq (RV5) or Rotarix (RV2) were enrolled (between March 2010 and June 2011) to compare fecal shedding for one month after each vaccine dose. Shedding was assessed using both enzyme immunoassay (EIA) and real-time reverse transcription-polymerase chain reaction (RT-PCR). Eighty-seven infants (34 girls and 53 boys) were enrolled in the study. After the first vaccine dose, the peak time of virus shedding occurred between day 4 and day 7, with positive detection rates of 80-90% by real-time RT-PCR and 20-30% by EIA. In both groups, vaccine shedding occurred as early as one day and as late as 25-28 days. Mixed effects logistic regression analysis of real-time RT-PCR data showed no significant differences between two groups when shedding rates were compared after the first vaccine dose (odds ratio [OR] 1.26; P=0.71) or after the second vaccine dose (odds ratio [OR] 1.26; P=0.99). However, infants receiving RV2 shed significantly higher viral loads than those receiving RV5 when compared after the first vaccine dose (P=0.001) and after the second dose (P=0.039). In terms of shedding rates detected by real-time RT-PCR, vaccine uptake of RV5 or RV2 among infants in Taiwan was comparable. Clinical significance of higher shedding viral loads in RV2 should be further observed.

Study 2010 Feb – Sibling transmission of vaccine-derived rotavirus (RotaTeq) associated with rotavirus gastroenteritis.
Although rotavirus vaccines are known to be shed in stools, transmission of vaccine-derived virus to unvaccinated contacts resulting in symptomatic rotavirus gastroenteritis has not been reported to our knowledge. We document here the occurrence of vaccine-derived rotavirus (RotaTeq [Merck and Co, Whitehouse Station, NJ]) transmission from a vaccinated infant to an older, unvaccinated sibling, resulting in symptomatic rotavirus gastroenteritis that required emergency department care. Results of our investigation suggest that reassortment between vaccine component strains of genotypes P7[5]G1 and P1A[8]G6 occurred during replication either in the vaccinated infant or in the older sibling, raising the possibility that this reassortment may have increased the virulence of the vaccine-derived virus. Both children remain healthy 11 months after this event and are without underlying medical conditions.

CDC – The Emerging Risks of Live Virus & Virus Vectored Vaccines: Vaccine Strain Virus Infection, Shedding & Transmission
Referenced Report from the National Vaccine Information Center
by Barbara Loe Fisher Co-founder & President
Your Health. Your Family. Your Choice.
Can People Receiving Live Virus Vaccines Transmit Vaccine Strain Virus to Others?
Public health officials say that unvaccinated children pose a big danger to those around them and even threaten the health of fully vaccinated children and adults because vaccines can fail to prevent infection in vaccinated persons.
Today, the most common argument used to justify “no exceptions” mandatory vaccination laws is that unvaccinated people pose a serious health threat to others who “cannot be vaccinated,” such as the immunocompromised.
Some parents of unvaccinated children are asking the opposite question:
Could my unvaccinated or immune compromised child get sick from coming in contact with a recently vaccinated person?
When it comes to live virus vaccines, the short answer is:
Yes.
During a viral infection, live virus is shed in the body fluids of those who are infected for varying amounts of time and can be transmitted to others. Vaccine strain live virus is also shed for varying amounts of time in the body fluids of vaccinated people and can be transmitted to others. Although public health officials maintain that live attenuated virus vaccines rarely cause complications in the vaccinated person and that vaccine strain viral shedding rarely causes disease in close contacts of the recently vaccinated, it is important to be aware that vaccine strain live virus infection can sometimes cause serious complications in vaccinated persons and vaccine strain live viruses can be shed and transmitted to others with serious or even fatal consequences

Censored Study of Vaccinated vs. Unvaccinated sees Daylight
by James O. Grundvig
The study defined NDD as “Autism Spectrum Disorder, Attention Deficit Hyperactivity Disorder, and/or a learning disability.”
The Study Accepted, Released, Censored
Frontiers Journal received the study on September 17, 2016. After a two-month peer review process, published it on November 21 for its “68,000 on board editors” from institutions around the world (www.frontiersin.org), with the National Institute of Health (NIH) and Harvard University being the top two providing the science editors.
Over the course of four days, more than 80,000 views of the study found it important enough to read, going “viral” according to one familiar with its release. Then on November 28, the bottom fell out when Frontiers scrapped the publication. In one week, it went from being accepted, published, and then retracted. The abstract can still be found online.
The paper, however, wasn’t retracted; it was “unaccepted,” according to Mawson via email. That means Frontiers didn’t retract it, since it was never officially published. What’s left for a study after its accepted, reviewed 80,000 times in less than 100 hours? . . . Censorship.
Beyond that clarification, Mawson wrote: “I am not allowed to comment on the paper/work by my Dean.”
Melissa Cochrane, the communications manager for Frontiers Journal, which is headquartered in Lausanne, Switzerland, replied via email:
“As we have previously noted, this article was provisionally accepted but not published. In response to concerns raised regarding the abstract and the provisional PDF — which were made provisionally available online — Frontiers then reopened its review. Following further manuscript assessment by the Field Chief Editor of Frontiers in Public Health, in consultation with an external expert, the manuscript was subsequently rejected, not retracted as retraction can only occur once a paper has been officially published and indexed.
“The rejection was due to severe limitations in the validity of the results.”
A day later, Ms. Cochrane replied to an email seeking clarification on the “rejection” process, writing:
“The reasons for the rejection were communicated in more detail to the corresponding author but I am unable to give you the reviewer’s comments as the Frontiers’ review process involves an open and collaborative dialogue between the reviewers and the authors, all of whom participate with the understanding and security that Frontiers will keep these exchanges confidential, as explained in our terms of use. You can read more about the Frontiers peer review process here.”
Vaccines Cause Health Issues Big and Small

Metals Debris Found in Vaccine Supply
Robert F. Kennedy, Jr.
A landmark new study has found metal debris and biological contamination in every human vaccine tested. The study should have profound and immediate impact on public health policies and vaccine industry procedures around the globe.
A team of scientists used a highly sensitive technology—an Environmental Scanning Electron Microscope equipped with an x-ray microprobe—to scan for solid contaminants in 44 samples of 30 vaccines. The researchers reported their results in the International Journal of Vaccines and Vaccination. They found widespread contamination by toxic aluminum salts, red blood cells of unknown origin and inorganic, foreign particle debris in aggregates, clusters and independent particulates. The composition of those clusters, the researchers observe, are consistent with “burnt waste.”

Study – New Quality-Control Investigations on Vaccines: Micro-and Nanocontamination
International Journal of Vaccines and Vaccination
Abstract
Vaccines  are  being  under  investigation  for  the  possible  side  effects  they  can cause. In order to supply new information, an electron-microscopy investigation method was applied to the study of vaccines, aimed at verifying the presence of solid contaminants by means of an Environmental Scanning Electron Microscope equipped  with  an  X-ray  microprobe.  The  results  of  this  new  investigation  show the presence of micro- and nanosized particulate matter composed of inorganic elements in vaccines’ samples which is not declared among the components and whose unduly presence is, for the time being, inexplicable. A considerable part of  those  particulate  contaminants  have  already  been  verified  in  other  matrices and  reported  in  literature  as  non  biodegradable  and  non  biocompatible.  The evidence  collected  is  suggestive  of  some  hypotheses  correlated  to  diseases  that are mentioned and briefly discussed.

Vaccine News – Dr. Suzanne Humphries, M.D. – Vaccine Strain of Measles Virus Found in Measles

Dirty Vaccines: Every Human Vaccine Tested Was Contaminated With Metals and Debris in New Study
Researchers examining 44 samples of 30 different vaccines found dangerous contaminants, including red blood cells in one vaccine and metal toxicants in every single sample tested – except in one animal vaccine.
Using extremely sensitive new technologies not used in vaccine manufacturing, Italian scientists reported they were “baffled” by their discoveries which included single particles and aggregates of organic debris including red cells of human or possibly animal origin and metals including lead, tungsten, gold, and chromium, that have been linked to autoimmune disease and leukemia.
In the study, published this week in the International Journal of Vaccines and Vaccination, the researchers led by Antoinetta Gatti, of the National Council of Research of Italy and the Scientific Director of Nanodiagnostics, say their results “show the presence of micro- and nano-sized particulate matter composed of inorganic elements in vaccine samples” not declared in the products’ ingredients lists.
Lead particles were found in the cervical cancer vaccines, Gardasil and Cevarix, for example, and in the seasonal flu vaccine Aggripal manufactured by Novartis as well as in the Meningetec vaccine meant to protect against meningitis C.
Samples of an infant vaccine called Infarix Hexa (against diphtheria, tetanus, pertussis, hepatitis B, poliomyelitis and haemophilus influenzae type B) manufactured by GlaxoSmithKline was found to contain stainless steel, tungsten and a gold-zinc aggregate.
Other metal contaminants included platinum, silver, bismuth, iron, and chromium. Chromium (alone or in alloy with iron and nickel) was identified in 25 of the human vaccines from Italy and France that were tested.
GSK’s Fluarix vaccine for children three years and older contained 11 metals and aggregates of metals. Similar aggregates to those identified in the vaccines have been shown to be prevalent in cases of leukemia, the researchers noted.
Many of the vaccines contained iron and iron alloys which, according to the researchers, “can corrode and the corrosion products exert a toxicity affecting the tissues”.
The researchers supply an image of an area in a drop of Sanofi Pasteur MSD’s Repevax (diphtheria, pertussis, tetanus, polio) vaccine “where the morphology of red cells – we cannot tell whether they are human or animal- is clearly visible” along with the presence of “debris” composed of aluminum, bromine, silicon, potassium and titanium.
Feligen, the only veterinary vaccine tested in the 44 total vaccines sampled, proved to be the only sample free from inorganic contamination.

Dirty Vaccines: New Study Reveals Prevalence of Contaminants
Posted by Celeste McGovern on Jan 30, 2017 5:31:20 PM
Every Human Vaccine Tested Was Contaminated by Unsafe Levels of Metals and Debris Linked to Cancer and Autoimmune Disease, New Study Reports
Researchers examining 44 samples of 30 different vaccines found dangerous contaminants, including red blood cells in one vaccine and metal toxicants in every single sample tested – except in one animal vaccine.
Using extremely sensitive new technologies not used in vaccine manufacturing, Italian scientists reported they were “baffled” by their discoveries which included single particles and aggregates of organic debris including red cells of human or possibly animal origin and metals including lead, tungsten, gold, and chromium, that have been linked to autoimmune disease and leukemia.
In the study, published this week in the International Journal of Vaccines and Vaccination, the researchers led by Antonietta Gatti, of the National Council of Research of Italy and the Scientific Director of Nanodiagnostics, say their results “show the presence of micro- and nano-sized particulate matter composed of inorganic elements in vaccine samples” not declared in the products’ ingredients lists.
Lead particles were found in the cervical cancer vaccines, Gardasil and Cervarix, for example, and in the seasonal flu vaccine Aggripal manufactured by Novartis as well as in the Meningetec vaccine meant to protect against meningitis C.
Samples of an infant vaccine called Infarix Hexa (against diphtheria, tetanus, pertussis, hepatitis B, poliomyelitis and haemophilus influenzae type B) manufactured by GlaxoSmithKline was found to contain stainless steel, tungsten and a gold-zinc aggregate.

PDF source: http://medcraveonline.com/IJVV/IJVV-04-00072.pdf
Study – New Quality-Control Investigations on Vaccines: Micro-and Nanocontamination
International Journal of Vaccines and Vaccination
Abstract
Vaccines  are  being  under  investigation  for  the  possible  side  effects  they  can cause. In order to supply new information, an electron-microscopy investigation method was applied to the study of vaccines, aimed at verifying the presence of solid contaminants by means of an Environmental Scanning Electron Microscope equipped  with  an  X-ray  microprobe.  The  results  of  this  new  investigation  show the presence of micro- and nanosized particulate matter composed of inorganic elements in vaccines’ samples which is not declared among the components and whose unduly presence is, for the time being, inexplicable. A considerable part of  those  particulate  contaminants  have  already  been  verified  in  other  matrices and  reported  in  literature  as  non  biodegradable  and  non  biocompatible.  The evidence  collected  is  suggestive  of  some  hypotheses  correlated  to  diseases  that are mentioned and briefly discussed.

Parents of children with autistic spectrum disorder report extreme fatigue
Pamela Cowan, Regina Leader-Post
Published on: January 13, 2017
For more than two years, Sarah Elizabeth Ivens was fascinated to work one-on-one with children who have autism spectrum disorder.
“It’s amazing how the mind can work differently,” she said.
As she got to know the childrens’ families, Ivens was struck by the many challenges they juggled and their high level of fatigue.
“Fatigue is a sense of exhaustion that cannot be resolved by getting rest,” she said. “It’s not just being tired. If you’re tired, then you can go to bed early, sleep in and the next day you’re feeling better. That’s not the case with fatigue.”
Fatigue impacts a person’s physical and mental capacities.
Ivens completed her honours degree in psychology at the University of Victoria, and is now a PhD student in clinical psychology at the University of Regina.
Her Victoria experience spurred her to take a closer look at parents’ experiences for her master’s thesis, titled Fatigue in parents of children with Autism Spectrum Disorders: The role of parental and child factors for mothers and fathers.
“We do know from other research that fatigue is problematic for parents in general and that it can really have a big impact on their well-being and their child rearing, which results in less-effective parenting,” Ivens said.
Past research focused on mothers. For her thesis, Ivens surveyed 112 parents of children with autism between the ages of two and 12 years, with the average age being seven.
“The kids had been diagnosed three years prior, so this was not families going through the transition of learning to deal with the diagnosis,” Ivens said. “These were parents who were doing it for a few years.”
Of those answering the online questionnaires for her 2015 study, 78 were mothers and 34 were fathers.
Getting dads involved was important. In many studies, only 10 per cent are fathers, she said.
“I think their answers and experiences are really getting lost in the noise,” Ivens said.
According to existing literature, mothers report being more fatigued than fathers, the 31-year-old said.
Her survey echoed that finding.

Merck Created Hit List to “Destroy,” “Neutralize” or “Discredit” Dissenting Doctors
By Jim Edwards May 6, 2009
Merck made a “hit list” of doctors who criticized Vioxx, according to testimony in a Vioxx class action case in Australia. The list, emailed between Merck employees, contained doctors’ names with the labels “neutralise,” “neutralised” or “discredit” next to them.
According to The Australian, Merck emails from 1999 showed company execs complaining about doctors who disliked using Vioxx. One email said:
We may need to seek them out and destroy them where they live …
The plaintiffs’ lawyer gave this assessment:
It gives you the dark side of the use of key opinion leaders and thought leaders … if (they) say things you don’t like to hear, you have to neutralise them … It does suggest a certain culture within the organisation about how to deal with your opponents and those who disagree with you.
The Australian:
The court was told that James Fries, professor of medicine at Stanford University, wrote to the then Merck head Ray Gilmartin in October 2000 to complain about the treatment of some of his researchers who had criticised the drug.
“Even worse were allegations of Merck damage control by intimidation,” he wrote, … “This has happened to at least eight (clinical) investigators … I suppose I was mildly threatened myself but I never have spoken or written on these issues.”
The allegations come on the heels of revelations that Merck created a fake medical journal — the Australasian Journal of Bone and Joint Medicine — in which to publish studies about Vioxx; had pop songs commissioned about Vioxx to inspire its staff, and paid ghostwriters to draft articles about the drug.

New Merck Allegations: A Fake Journal; Ghostwritten Studies; Vioxx Pop Songs; PR Execs Harass Reporters
By Jim Edwards April 23, 2009
Federal prosecutors in the U.S. will be reading with amusement the Australian press’s coverage of a class action trial down under for patients who took Merck’s now-withdrawn painkiller Vioxx.
Details emerging in Oz make some of the antics that Merck’s American counterparts got up to look tame by comparison. For example, in Australia, Merck allegedly:
Had a doctor sign his name to an entirely ghostwritten journal article even though a Merck staffer had complained that the data within it was based on “wishful thinking.”
Created a fake “peer-reviewed” journal, the “Australasian Journal of Bone and Joint Medicine,” in which to publicize pro-Vioxx articles.
Created a Ricky Martin-style pop song to get Merck sales reps all jazzed up about Vioxx (lyrics below!).
During the trial, Merck has employed an unusually aggressive set of PR consultants, some of whom have even followed reporters into the bathroom to make sure they got the story “right.”
Hatched a Blackadder-style “cunning plan” to seed seminars with speakers who were sympathetic to Vioxx but under instructions not to mention the brand name too often.
Regarding the “wishful thinking” study, The Age reports on these emails turned over in the trial:
Email from Merck senior researcher Briggs Morrison, August 2001:
“That seems wishful thinking, not a critical interpretation of the data … The data appears to have been interpreted to support a preconceived hypothesis.”
The claim was nonetheless included in the final version of the article, which Merck employees sent to US cardiologist Dr Marv Konstam for approval.
Dr Konstam was named as the article’s lead author when it was published in the medical journal Circulation in October 2001
The Australian describes the fake journal. And The Age notes that the journal was “designed to resemble a peer-reviewed publication and reprinted previously published articles.”

Merck target of Vioxx federal grand jury probe
Mon Mar 23, 2009
Merck & Co said on Monday that it has been advised it is a target of a U.S. grand jury investigation involving its withdrawn pain drug Vioxx.
The company had previously disclosed the government probe, which has been ongoing since 2004. But it only last week received a letter from the U.S. Attorney’s office for the District of Massachusetts informing the drugmaker it is a target of the grand jury investigation, Merck said.
The probe involves Merck’s research, marketing and selling activities regarding Vioxx, the once $2.5 billion a year drug that was pulled from the market in September 2004 after a study showed it doubled the risk of heart attack and stroke in long-term users.
Merck said it has responded and will continue to respond to requests from the U.S. Attorney for documents and information in connection with the probe. The investigation includes subpoenas for witnesses to appear before a grand jury, the company has said in securities filings.
The New Jersey-based drugmaker was sued by tens of thousands of former Vioxx users who claimed to have been injured by the arthritis medicine.
After winning the majority of product liability trials that reached a jury, Merck agreed to pay $4.85 billion to settle personal injury claims from former users who had suffered heart attacks and strokes.

Study – Investigating Viruses in Cells Used to Make Vaccines; and Evaluating the Potential Threat Posed by Transmission of Viruses to Humans
Principal Investigator: Arifa S. Khan, PhD
General Overview
The emergence of pathogenic virus infections like influenza and HIV have created an urgent need for new vaccines.
Virus-based vaccines are made in living cells (cell substrates). Some manufacturers are investigating the use of new cell lines to make vaccines. The continual growth of cell lines ensures that there is a consistent supply of the same cells that can yield high quantities of the vaccine.
In some cases the cell lines that are used might be tumorigenic, that is, they form tumors when injected into rodents. Some of these tumor-forming cell lines may contain cancer-causing viruses that are not actively reproducing. Such viruses are hard to detect using standard methods. These latent, or “quiet,” viruses pose a potential threat, since they might become active under vaccine manufacturing conditions. Therefore, to ensure the safety of vaccines, our laboratory is investigating ways to activate latent viruses in cell lines and to detect the activated viruses, as well as other unknown viruses, using new technologies. We will then adapt our findings to detect viruses in the same types of cell substrates that are used to produce vaccines. We are also trying to identify specific biological processes that reflect virus activity.
These methods will enable FDA scientists to help manufacturers to determine whether their specific cell substrate is safe to use for vaccine production. The methods our laboratory are developing and testing will help to ensure the production of safe and effective vaccines in two ways: 1) FDA will be able to develop testing guidelines for manufacturers who use new cell substrates for producing vaccines; and 2) FDA will publish the new methods it develops in peer-reviewed scientific journals, thus making them readily accessible to all manufacturers.
We are also evaluating the risk of retrovirus infections in humans. (Retroviruses are RNA viruses that use an enzyme called reverse transcriptase (RT) to replicate; RNA is the de-coded form of DNA). Simian foamy virus (SFV) can be transmitted from nonhuman primates (e.g., monkeys) to humans. Although there is no evidence that SFV causes disease, the virus can remain in a lifelong quiet state in the DNA after infection. Moreover, two individuals in Africa were recently found to be infected with both HIV-1 and SFV. Therefore, it is important to determine if SFV poses a threat to human health and to understand how the virus spreads in order to create strategies for controlling human infections. Such work will also help FDA to develop a new policy regarding blood donation by individuals working with nonhuman primates and implementing formal safety guidelines for people working with SFV-infected animals. We are also investigating the consequences of dual SFV and HIV-1 infection in the monkey model.

#RFKcommission – Great video! Dartmouth-educated and Portland, OR-based Pediatrician Dr. Paul Thomas responds to Dr. Peter Hotez’s ridiculous Op-Ed in the NY Times trying to talk President Trump out of having a Vaccine Safety Commission. Oregon proud!

Dr. Suzanne Humphries, M.D. – Vaccine Strain of Measles Virus Found in Measles Outbreaks
February 21, 2017
Health Impact News Editor Comments
Dr. Suzanne Humphries is a practicing nephrologist (kidney physician). In this lecture (video below), she addresses a study done in Croatia [1] where a child who was vaccinated with the MMR vaccine was tested positive for the measles vaccine strain Schwarz eight days after vaccination.
This was a significant finding, because the child’s symptoms were thought to be similar to rubella, and without testing, the sickness would have been possibly mis-diagnosed as rubella, or the wild-type strain of measles the vaccine is designed to protect against.
This concept of “shedding,” where the child comes down with the disease from the virus in the vaccine itself, surprised the researchers:
Virus excretion in vaccinees has been reported before, but to our knowledge, this is documented for the first time for the Schwarz vaccine strain. [1]
Since 2010, this phenomena of vaccine shedding with measles in the MMR vaccine has been observed in at least two other studies:
Differentiating the wild from the attenuated during a measles outbreak. Paediatrcis and Child Health, 2012:
In the midst of a local measles outbreak, a recently immunized child was investigated for a new-onset measles-type rash. Nucleic acid testing identified that a vaccine-type measles virus was being shed in the urine. Clinically differentiating measles from a nonmeasles rash is challenging, but can be supported by a thorough medical history evaluation. Rashes are expected to occur after immunization; nucleic acid testing can be used when it is difficult to differentiate between wild and attenuated strains. [2]
Case of vaccine-associated measles five weeks post-immunisation, British Columbia, Canada, Eurosurveillance, 2013:
We describe a case of vaccine-associated measles in a two-year-old patient from British Columbia, Canada, in October 2013, who received her first dose of measles-containing vaccine 37 days prior to onset of prodromal symptoms. Identification of this delayed vaccine-associated case occurred in the context of an outbreak investigation of a measles cluster. [3]
Are health officials testing cases of measles in the current outbreak in the United States, to determine if the measles strain is the wild strain of the vaccine strain?
Not likely, and it is not likely that the mainstream media “TV doctors” will even discuss this as they falsely vilify parents who choose not to administer the MMR vaccine to their children as the cause of these outbreaks. Some of these cases are confirmed to be among those who have received the MMR vaccine, and for those who have not been vaccinated, is it possible they were infected from those recently vaccinated when the vaccine was still “shedding,” and that the vaccine-strain of measles was passed on from the vaccinated child to the unvaccinated child?

The euthanasia of Nancy Fitzmaurice, a severely disabled child who was not dying, has made international waves with disability advocates especially outraged

The euthanasia of Nancy Fitzmaurice, a severely disabled child who was not dying, has made international waves with disability advocates especially outraged. Nancy’s mother had requested that her daughter be killed and was granted approval by the British legal system. While the 12-year-old Nancy had significant disabilities, she was able to breathe on her own and did not require life support.
Image result for Killing of disabled girl “wholly inappropriate” and “extremely troubling” says Autism group
Following the starving of Nancy through the withholding of fluids, the Autism Self Advocacy Network [ASAN] has released a statement slamming this decision, calling it “troubling” and “concerning”.

Gardasil Vaccine Becomes International Scandal: Deceptive Emails by Health Officials Exposed to Public

by Brian Shilhavy
Editor, Health Impact News

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.

This statement was made in April of 2014 by French medical doctor Bernard Dalbergue, a former pharmaceutical industry physician with Merck, the manufacturer of the HPV vaccine Gardasil. (Story here.)

This past week, Dr. Sin Hang Lee, M.D., F.R.C.P. (C), FCAP, director of the Milford Molecular Diagnostics Laboratory in Connecticut, proved Dr. Dalbergue’s prediction correct, when he published a letter sent to the U.S. CDC, the World Health Organization, the Ministry of Health in Japan, and others, documenting “scientific misconduct” among the world’s leading health organizations tasked with providing vaccine safety, by deliberately misleading Japanese health authorities on the safety of the HPV vaccine.

Japanese health authorities had halted their recommendation of the HPV vaccines in 2013 due to safety concerns. Japanese officials began a full investigation into the HPV vaccines at that time.

Dr. Sin Hang Lee has allegedly discovered that at a public hearing on HPV vaccine safety which was held in Tokyo, Japan on February 26, 2014, members of the Global Advisory Committee on Vaccine Safety (GACVS), the World Health Organization, the CDC and other scientific/health professionals:

deliberately set out to mislead Japanese authorities regarding the safety of the human papillomavirus (HPV) vaccines, Gardasil® and Cervarix®, which were being promoted at that time.

Dr. Lee discovered the alleged deception by obtaining a series of emails via a Freedom of Information request submitted in New Zealand.

According to Dr. Lee, these emails reveal:

that Dr. Robert Pless, the chairperson of the Global Advisory Committee on Vaccine Safety (GACVS), Dr. Nabae Koji of the Ministry of Health of Japan, Dr. Melinda Wharton of the CDC, Dr. Helen Petousis-Harris of Auckland University, New Zealand, and others (including WHO officials) may have been actively involved in a scheme to deliberately mislead the Japanese Expert Inquiry on human papillomavirus (HPV) vaccine safety before, during and after the February 26, 2014 public hearing in Tokyo. (Source.)

Dr. Lee issues a very stern statement at the conclusion of his letter:

It is my opinion that Dr Pless, those whose names appeared in the emails attached to this complaint, and all who blindly dismiss the potential toxicity of the newly created HPV L1 gene DNA/AAHS compound in order to continue to promote HPV vaccinations should be held accountable for their actions. There is no excuse for intentionally ignoring the scientific evidence. There is no excuse for misleading global vaccination policy makers at the expense of public interest.

It is my contention these people have not only violated the Terms of Reference of the WHO Global Advisory Committee on Vaccine Safety (GACVS); they have violated the public trust. Immediate, independent and thorough investigations into their actions with appropriate disciplinary action is the only option available that might restore the public’s confidence in worldwide health authorities.

Who is Dr. Sin Hang Lee?

Sin Hang Lee, M.D. graduated from Wuhan Medical College in China. After a residency-fellowship at Cornell-New York Hospital and Memorial Hospital for Cancer, Dr. Lee was certified by the American Board of Pathology and obtained the F.R.C.P. (C) degree by examination in 1966. He was on the faculty of McGill University and Yale University from 1968-2004 while practicing hospital-based pathology.

Dr. Lee has been a practicing pathologist for more than 50 years, and is currently the director of Milford Molecular Diagnostics, Milford, Connecticut. In the past 10 years, Dr. Lee has developed Sanger sequencing-based testing methods for HPV, Neisseria gonorrhoeae, Chlamydia trachomatis, Lyme disease borreliae and Ebolavirus implementable in community hospitals.

In 2012 Dr. Lee was called in to examine the death of Jasmine Renata in New Zealand, who died 6 months after receiving the Gardasil vaccine.

Dr. Lee’s testimony stated:

The finding of these foreign DNA fragments in the post-mortem samples six months after vaccination indicates that some of the residual DNA fragments from the viral gene or plasmid injected with Gardasil® have been protected from degradation in the form of DNA-aluminum complexes in the macrophages; or via integration into the human genome.

Undegraded viral and plasmid DNA fragments are known to activate macrophages, causing them to release tumor necrosis factor, a myocardial depressant which can induce lethal shock in animals and humans. (Source.)

– See more at: http://healthimpactnews.com/2016/gardasil-vaccine-becomes-international-scandal-deceptive-emails-by-health-officials-exposed-to-public/#sthash.4s6EXa52.dpuf

Read more at:

http://healthimpactnews.com/2016/gardasil-vaccine-becomes-international-scandal-deceptive-emails-by-health-officials-exposed-to-public/

Mondelez International May Use Microsoft Kinect to Track Your Snack Buying Habits

Mondelez International May Use Microsoft Kinect to Track Your Snack Buying Habits

It’s a dance many of us have experienced in the grocery store: You grab a package of cookies, weigh the consequences of eating them, hesitantly put them back on the shelf and slowly walk away.

 Yet you still stare longingly at those cookies, thinking about a snack relationship that could have been.

 The ritual may now be video-recorded for quality assurance, thanks to a new Mondelez International program called Smart Shelf. The program uses Kinect for Windows, a Microsoft program available for other developers to use its motion-tracking technology. Mondelez is using it to track shoppers as they look at various Mondelez-associated brands, such as Triscuit, Ritz and Oreo.

 “Our goal is to understand how shoppers see, scan, spot, show interest and select products from the shelf in the store,” said a spokeswoman for Mondelez. “We can also engage and influence the purchase decision by delivering a targeted shopper experience. For example, we can deliver audio or play a video based on demographics, distance and even the time of the day.”

 Mondelez isn’t the first company to experiment with targeted advertising. The EyeSee Mannequin, released by Almax last year, used both cameras and microphones to track how people behaved in department stores. They were also capable of sending data to department stores and retail brands, similar to how Smart Shelf is capable of sending data back to Mondelez.

 Richard Buino, another spokesman for Mondelez, said that a customer’s privacy is a big concern for the company, and that Smart Shelf would not infringe upon it.