Vaccine News – Mother-of-two dies from flu despite being vaccinated

World Renowned Genetics Doctor Sees Relationship Between Fetal Cells Used in Vaccines and Increasing Autism Rates
Health Impact News
Dr. Theresa Deisher recently granted an interview with the VAXXED team to discuss, among other things, vaccines and autism.
Theresa Deisher, Ph.D., is the president of Sound Choice Pharmaceutical Institute (SCPI), a cutting edge biomedical research organization.
Dr. Deisher is a genetic engineer with over 20 years experience in the pharmaceutical industry, from basic human biology through clinical trials.
Dr. Deisher obtained her Ph.D. in Molecular and Cellular Physiology from Stanford University and has spent over 20 years in commercial biotechnology. Prior to founding AVM Biotechnology and Sound Choice Pharmaceutical Institute (SCPI), she worked with leading biotechnology companies, including Genentech, Repligen, ZymoGenetics, Immunex and Amgen.
Dr. Deisher is an inventor on 23 issued U.S. patents, and her discoveries have led to clinical trials of FGF18 for osteoarthritis and cartilage repair, and for Factor XIII for surgical bleeding. Dr. Deisher was the first person to discover adult cardiac derived stem cells, and has been a champion of adult stem cell research, both professionally and privately, for two decades. Dr. Deisher was a plaintiff in the U.S. federal lawsuit to prohibit use of federal tax payer dollars for embryo destructive research, which was instrumental in steering science towards adult stem cell research, which has led to 14 U.S. FDA approved adult stem cell products and the Washington Post Dec 2013 headline “Scientists Go Ethical in 2013.”
AVM Biotechnology is the marquee prolife biotech company worldwide, certifying that it does not use morally illicit material in any process. SCPI’s mission is to end human trafficking in biomedical research.
Discovering the Link Between Fetal Tissue in Vaccines and Autism
Dr. Deisher states in her VAXXED interview that she looked at the rise in autism rates in the U.K. and its link to the MMR vaccine, originally discovered and published by Dr. Andrew Wakefield, and how the medical establishment tried to discredit Dr. Wakefield’s research.
She notes that one reason given to try and discredit Dr. Wakefield’s research was that MMR vaccination rates remained steady both prior to and after the spike in autism rates in 1988.
However, what she discovered that was not reported was that the manufacturer of the MMR vaccine switched from animal cells to develop cultures to human fetal cells from aborted babies in 1988.

Infant Twins Die Simultaneously After Vaccines, Medical Board Rules ‘Just a Coincidence’
By Erin Elizabeth – February 1, 2017
Given that the sudden and simultaneous deaths of twins rarely occur, you would think- especially given the fact that they had been recently vaccinated– that it would receive quite a bit of attention. However, this story went largely unreported. (In order for twins to meet the criteria for simultaneous SIDS both babies must have died independently and within the same 24 hour time period.)
PubMed reports that identical twin girls, aged 3.5-months and delivered via c-section, were found dead (by their poor momma) in their crib, both laying face up. Not surprisingly, both babies were healthy will no serious medical history. Two days before their death, both of the girls had received their second dose of oral polio, DPT, and their first dose of hepatitis B vaccines. They had a fever the day after the vaccines and were given a teaspoon of acetaminophen.
All that and yet, “the death scene investigation, judicial investigation, parental assessment, macroscopic and microscopic autopsy findings and the toxicological analysis didn’t yield any specific cause of death.” Because the case was so rare it was referred to a board of multidisciplinary medical professionals at the Institute of Forensic Medicine, in the Ministry of Justice, in Istanbul. And yet, the Board still decided that the data they had was consistent with SIDS.

Babys werden mit gedrosseltem Immunsystem geboren
Datum: 02.05.2017
Das Immunsystem von Säuglingen arbeitet augenscheinlich im ersten Jahr nach der Geburt absichtlich auf Sparflamme. Das zeigt eine Studie der Medizinischen Hochschule Hannover sowie der Universitäten Bonn und Münster. Dadurch verhindert die Natur vermutlich, dass die Immunabwehr nach der Geburt zu stark auf Bakterien und Fremdstoffe außerhalb des Mutterleibs reagiert. Die Ergebnisse könnten auch neue therapeutische Ansätze ermöglichen, um Säuglinge vor einer so genannten Sepsis zu schützen. Dabei handelt es sich um eine lebensgefährliche Entzündungsreaktion, die besonders häufig Frühgeborene trifft. Die Arbeit ist in der renommierten Fachzeitschrift „Nature Immunology“ erschienen.
Dass die Immunzellen von Neugeborenen nur in sehr geringem Maße Entzündungen auslösen, ist schon lange bekannt. Bislang dachte man, das Immunsystem sei bei Säuglingen noch nicht ganz ausgereift und daher nicht besonders schlagkräftig. Die Ergebnisse der neuen Studie werfen an dieser Deutung Zweifel auf: „Wir vermuten, dass dieser verminderten Entzündungsantwort eine spezifische und sinnvolle Programmierung zugrunde liegt“, erklärt Dr. Thomas Ulas vom LIMES-Institut der Universität Bonn.
Sobald das Neugeborene den Mutterleib verlässt, kommt es schlagartig mit zahllosen unbekannten Bakterien und Fremdstoffen in Kontakt. „Das »Spar-Programm« verhindert vermutlich, dass die körpereigenen Abwehrtruppen in unzählige Scharmützel verwickelt werden“, sagt Dr. Sabine Pirr von der Medizinischen Hochschule Hannover. Folge könnte sonst nämlich eine lebensgefährliche starke Entzündungsreaktion sein, eine Sepsis. Zudem sind viele der unbekannten Mikroorganismen gar keine Krankheitserreger. So funktioniert der Darm nur dann so, wie er soll, wenn er mit bestimmten Bakterien besiedelt wurde. Auch aus diesem Grund muss sich das Immunsystem zurückhalten.

Mother-of-two dies from flu despite being vaccinated
3:51pm Sep 26, 2017
A touching tribute to a Canberra mother who died of influenza has been posted online after she became the latest victim of Australia’s horror flu season.
Mother-of-two Jennifer Thew spent a week suffering from bad influenza symptoms before she died at Calvary Hospital on Saturday.
It’s understood her daughter Estella, aged 7, has also been sick with the virus.
Thew, who moved to Australia from Germany, was a medical receptionist who had reportedly been vaccinated.
A Go Fund Me page has been set up for the Thew Family by her daughter’s dance school.

Vaccines Produce Homosexuality, Says Italian Scientist Gian Paolo Vanoli
An Italian scientist is arguing that vaccinations produce homosexuality.
Gian Paolo Vanoli, a 70-year-old scientist, journalist and opponent of vaccinations, says that vaccines make people gay.
Vanoli, who’s a proponent of alternative medicine, recently spoke with Vice Italy’s Matteo Lenardon about his ideals.
Via a Huffington Post translation of the Vice interview:

The vaccine is introduced into the child, the child then grows and tries to find its own personality, and if this is inhibited by mercury or other substances present in the vaccine which enter the brain, the child becomes gay. The problem will especially be present in the next generations, because when gays have children, the children will carry along with them the DNA of their parent’s illness. Because homosexuality is a disease, even though the WHO has decided that it is not. Who cares! The reality is that it is so. Each vaccination produces homosexuality, because it prevents the formation of one’s personality. It is a microform of autism, if you will. You will see how many gays there will be in the next generation, it will be a disaster.

Despite these views, Vanoli insists he supports same-sex marriage and gay adoption. He doesn’t “blame” gay people for their “illness,” just as he wouldn’t blame someone who “suffers from cancer or a heart attack,” he told GayStarNews.

“My Family Was Devastated By Vaccines” Tasha Dāvid, AVN President
Tasha has 6 vaccine injured kids and 2 healthy vaccine free kids. Her 6 vaccine injured kids include diagnoses of Autism, ADHD, severe mood swings and severe language disorder, as well as gastrointestinal issues, skin problems, chronic ear infections, chemical sensitivities, and many other health issues. However, her vaccine free kids are very healthy. Her 6 kids who were vaccinated always had more health issues after vaccination, but Tasha never understood that the vaccines were destroying her children because the doctors never told her. Tasha Dāvid is President of Australian Vaccination-skeptics Network Inc. and advocates that parents have complete choice over whether or not to vaccinate. She believes that a vaccine free lifestyle is a healthy lifestyle. Tasha Dāvid suggests that parents do their own research into vaccines and vaccination. Australian Vaccination-skeptics Network Inc. A video production. Copyright © 2017 Larry Cook

Former Merck Rep Says Mandatory Vaccination Is For Profit and Not Public Health – Brandy Vaughan is a former sales rep for Merck & Co. – a vaccine maker – and she details how vaccine companies are using vaccines as a vehicle for massive profit and not public health. Brandy researched the safety of vaccines and found that not only do vaccines contain known toxins that can cause neurological damage, but that vaccine makers do not create the same safety studies for vaccines as they do for other drugs. This lack of true safety research of vaccines combined with the known adverse reactions to vaccination has helped Brandy to decide to never vaccinate her own child. Brandy says giving children a vaccine is like playing Russian roulette with our children and that mandatory vaccination is simply a way for vaccine makers to profit off of our children. Don’t be fooled: we do not need mandatory vaccination.
Stop Mandatory Vaccination
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Vaccine News – Almost 650 girls needed medical intervention after HPV vaccine




PROOF: Flu shots are the greatest medical fraud in the history of the world
Saturday, September 16, 2017

(Natural News) As one of the very few independent voices willing to stand up against the scientific dogma of our modern medical regime, I’ve long felt a need to communicate the dangers of flu shots to the public so that people can have better information to prevent vaccine injuries and save lives.
This doesn’t mean I’m opposed to the theory of vaccination, by the way. In fact, I’m the author of A Blueprint for Safer Vaccines, an audio guide to saving lives and preventing vaccine injuries and deaths.
To my knowledge, I’m the only independent journalist in the world who is scientifically trained to run an atomic mass spectrometry laboratory, which I’ve been running for over three years now and testing the heavy metals content of organic superfoods like cacao, common vaccines as well as the ability of water filters to remove toxic heavy metals. I’m the creator of the Low Heavy Metals Verified standard and I’m the inventor of patented nutritional formulas for capturing heavy metals during digestion and binding with the radioactive isotopes of cesium (such as Cesium-137) to eliminate them from the digestive tract. Click here to see my Cesium Eliminator patent that was recently approved by the U.S. government.
My independent atomic elemental analysis of flu vaccines, published in the summer of 2014, proved that flu vaccines contain over 50 ppm mercury, an extremely toxic heavy metal linked to kidney failure, birth defects, spontaneous abortions and neurological damage. This finding has never been refuted by anyone. In fact, it was affirmed by vaccine proponents who insisted that it is perfectly safe to inject pregnant women, young children and senior citizens with mercury even though the flu vaccine insert itself readily admits there is no scientific evidence whatsoever to support the safety and efficacy of the vaccine in such groups.


Almost 650 girls needed medical intervention after HPV vaccine
Almost 650 girls in Ireland reported requiring medical intervention or treatment after receiving the HPV vaccine, according to data collected by the State’s medicines watchdog.
The Health Products Regulatory Authority has received 1,099 reports of adverse reactions and events associated with the use of the vaccine, but it said that this should not be taken as evidence of a causal link and that the benefits continue to outweigh the potential risks.

Resurgence of Whooping Cough May Owe to Vaccine’s Inability to Prevent Infections
Posted on: September 21, 2017
The startling global resurgence of pertussis, or whooping cough, in recent years can largely be attributed to the immunological failures of acellular vaccines, School of Public Health researchers argue in a new journal article.
The article, published in F1000 Research, points to the differences in mucosal immunity between whole-cell pertussis (wP) vaccines and the newer acellular pertussis (aP) vaccines, first introduced in the 1990s, as playing a pivotal role in the resurgence of the disease.
“This disease is back because we didn’t really understand how our immune defenses against whooping cough worked, and did not understand how the vaccines needed to work to prevent it,” said Christopher J. Gill, associate professor of global health and lead author of the article. “Instead we layered assumptions upon assumptions, and now find ourselves in the uncomfortable position of admitting that we may made some crucial errors. This is definitely not where we thought we’d be in 2017.”
Up until the 1950s, there were millions of cases of whooping cough around the globe each year, with numerous fatal cases in infants. The introduction of whole-cell pertussis (wP) vaccines led to a 99 percent reduction in cases. Later, as wP vaccines raised concerns of possible rare neurologic adverse events, aP vaccines were licensed and used in a number of countries starting in the early 1990s. Since then, cases of whooping cough have risen sharply. In 2014, there were more than 32,000 cases reported in the US.
“The resurgence of pertussis in the US to its highest levels since the 1940s emphasizes the need for answers to these questions,” the authors wrote.
The researchers examined mathematical models of pertussis transmission, data derived from the aP and wP vaccines responses in animals, and recent insight into the immunology of pertussis and pertussis vaccines. They found that, contrary to existing assumptions, although both vaccines blocked symptomatic disease, wP vaccines blocked also infections in animals while aP vaccines did not. Other differences included wP vaccines’ ability to induce a stronger herd immunity and robust TH17 responses, which confer mucosal immunity, while aP vaccines only induced TH2 responses.


Vaccine News – BREAKING: Robert F. Kennedy Jr. calls for extradition of CDC vaccine criminal mastermind Poul Thorsen to face charges of criminal scientific misconduct

Deep sequencing reveals persistence of cell-associated mumps vaccine virus in chronic encephalitis
Routine childhood vaccination against measles, mumps and rubella has virtually abolished virus-related morbidity and mortality. Notwithstanding this, we describe here devastating neurological complications associated with the detection of live-attenuated mumps virus Jeryl Lynn (MuVJL5) in the brain of a child who had undergone successful allogeneic transplantation for severe combined immunodeficiency (SCID). This is the first confirmed report of MuVJL5 associated with chronic encephalitis and highlights the need to exclude immunodeficient individuals from immunisation with live-attenuated vaccines. The diagnosis was only possible by deep sequencing of the brain biopsy. Sequence comparison of the vaccine batch to the MuVJL5 isolated from brain identified biased hypermutation, particularly in the matrix gene, similar to those found in measles from cases of SSPE. The findings provide unique insights into the pathogenesis of paramyxovirus brain infections

To my friends in Australia: the vaccine war deepens
by Jon Rappoport
September 20, 2017
The string of abuses laid on citizens of Australia by their government grows almost week by week.
Now, parental rights to raise children, without interference from the State, is under a new form of attack. This must be resisted.
Schools are bringing doctors on board, as a permanent feature. Young children will be subjected to medical diagnoses and treatment, without consent or approval from parents, even if those parents actively object. The State is stealing the role of guardian.
The Herald Sun reports. Read carefully:
“DOCTORS will have the power to treat students as young as 12 in schools even if parents refuse their consent.”
“GPs will consult at 100 Victoria high schools for up to one day a week as part of a $43.8 million program.”
“Guidelines released on Thursday show that even if a parent ‘expressly states’ that a doctor should not [examine] their child, the GP can if they deem the teen mature enough.”
“’Any student who wants to see the GP will be permitted to make an appointment,’ the policy said.”
“The GP will decide if the young person is mature enough to provide consent to any medical treatment for the prevailing issue.”
A young child “giving consent?” This is supposed to be “informed consent” when facing off with an adult doctor?


Australian Medical Association: Class Action against the AMA for Vaccine Injury
Why this is important
The health and well being of our beautiful and innocent Australian children are paramount to all Australians.
It’s obvious to anyone with intelligence that there is an epidemic of ill health occurring with children around the World and particularly, with our Australian children which can be traced to Vaccine Injury through multiplying forced application of a large and growing number of untested combined vaccines riddled with known carcinogens and poisons being directly administered into the blood streams of our Australian babies and children.
Modern medical, psychological, health and nutritional sciences have grave questions as to the efficacy of these vaccines and in fact clearly, illustrate that these vaccines are in general unnecessary and poisonous and in fact interfere with the natural immune system of the human being.
We call for a moratorium of forced vaccination of Australian children and the initiation of major testing initiatives in Australia and elsewhere to prove any efficacy of injecting these poisons into our Children.
We are appalled at the support of the Australian Medical Association of these unscientific and abusive injurious procedures causing epidemic harm to our beautiful and innocent

Australian Children and demand:
1. The AMA stop all support for these appalling procedures.
2. Pay full and appropriate damages to the Australian Parents and Children injured by these AMA supported procedures.
3. Instigate a full review of these appalling procedures, based particularly on the evidence presented in the film ‘VAXXED’ and the documentation series ‘The Truth about Vaccines’, ‘Vaccines Revealed’, ‘Trace Amounts’, and ‘Vaccine Syndrome’.
4. Place the health and well‐being of our Australian children as paramount before commercial gain by Pharmaceutical and Medical industries and professionals

Deep sequencing reveals persistence of cell-associated mumps vaccine virus in chronic encephalitis
Routine childhood vaccination against measles, mumps and rubella has virtually abolished virus-related morbidity and mortality. Notwithstanding this, we describe here devastating neurological complications associated with the detection of live-attenuated mumps virus Jeryl Lynn (MuVJL5) in the brain of a child who had undergone successful allogeneic transplantation for severe combined immunodeficiency (SCID). This is the first confirmed report of MuVJL5 associated with chronic encephalitis and highlights the need to exclude immunodeficient individuals from immunisation with live-attenuated vaccines. The diagnosis was only possible by deep sequencing of the brain biopsy. Sequence comparison of the vaccine batch to the MuVJL5 isolated from brain identified biased hypermutation, particularly in the matrix gene, similar to those found in measles from cases of SSPE. The findings provide unique insights into the pathogenesis of paramyxovirus brain infections


BOMBSHELL: Flu vaccines don’t work in the elderly, new science shows … U.S. media

Tuesday, September 19, 2017
(Natural News) The Centers for Disease Control and Prevention (CDC), the same authority that determines the national vaccination schedule, notes that those most at risk of complications from the flu virus are children younger than 5, but particularly those under the age of 2; pregnant women; people in nursing homes; and adults over the age of 65. The elderly are therefore among the most vulnerable members of society when it comes to influenza. It makes sense, therefore, to believe that the flu vaccination would need to be especially effective for that demographic.
A recent report by Public Health England (PHE), however, has revealed that though it seems to have been slightly more effective at preventing influenza among children than in previous years, last year’s flu shot was totally ineffective for the elderly.
Experts believe that the shot was ineffective because it did not protect against the most common circulating strain – the H3 strain. This is because the flu shot is essentially a game of chance each year; experts have to try to predict in advance which three strains of the virus will be in circulation in the coming winter. Even in a good year, their strike rate is only 50 percent.
Of course, instead of admitting the uselessness of the vaccine, health professionals are blaming the elderly themselves.

BREAKING: Robert F. Kennedy Jr. calls for extradition of CDC vaccine criminal mastermind Poul Thorsen to face charges of criminal scientific misconduct
Thursday, September 21, 2017
(Natural News) Robert F. Kennedy Jr. (RFK Jr.) and his team at World Mercury Project have drafted up a new report that reveals the criminal conduct of CDC consultant and vaccine cultist Poul Thorsen. With an overwhelming body of evidence, RFK Jr is calling for Attorney General Jeff Sessions to take action and extradite Poul Thorsen so he can face up to his numerous crimes. In a statement, RFK Jr declared, “World Mercury Project calls upon Attorney General Jeff Sessions to extradite Thorsen back to the U.S. to face prosecution. We also call upon Secretary of Health and Human Services Dr. Tom Price to retract the Thorsen-affiliated autism research papers that are the fruit of illegally conducted research.”
What has World Mercury Project (WMP) uncovered? In addition to evidence of criminal activity, new findings by WMP show that Thorsen and his team never obtained permission from the Institutional Review Board (IRB) to do their studies, published in 2002 by the New England Journal of Medicine and in 2003 by the journal Pediatrics. As WMP explains, this alone detracts from the validity of their research, but to make matters worse, records indicate that the CDC was complicit in covering up this little “mistake.” According to the WMP report, CDC staff realized that no IRB approval had ever been granted for Thorsen’s research, but the error was simply ignored and the studies were never retracted. Freedom of Information Act documents show that supervisors at the CDC looked the other way and actively tried to conceal what transpired.

Criminal Conduct – Poul Thorsen
Robert F. Kennedy, Jr. and World Mercury Project Issue Report Regarding New Evidence of Ongoing Corruption and Scientific Misconduct at CDC
Kennedy hopes new evidence and a fresh look at criminal misconduct will result in law enforcement action, rigorous and transparent vaccine safety science, and safer vaccines.
In a new report released September 18, 2017, Robert F. Kennedy, Jr. and his team outlined various criminal acts on the part of employees and consultants for the Centers for Disease Control and Prevention (CDC) whose questionable ethics and scientific fraud have resulted in untrustworthy vaccine safety science.

PDF – Poul Thorsen Fugitive Researcher

HighWire with Del Bigtree – Jimmy Kimmel the Hypocrite. Vaccine Risk Now Mainstream!

One vaccine injection could carry many doses
Microparticles created by new 3-D fabrication method could release drugs or vaccines long after injection.
Anne Trafton | MIT News Office
September 14, 2017
MIT engineers have invented a new 3-D fabrication method that can generate a novel type of drug-carrying particle that could allow multiple doses of a drug or vaccine to be delivered over an extended time period with just one injection.
The new microparticles resemble tiny coffee cups that can be filled with a drug or vaccine and then sealed with a lid. The particles are made of a biocompatible, FDA-approved polymer that can be designed to degrade at specific times, spilling out the contents of the “cup.”
“We are very excited about this work because, for the first time, we can create a library of tiny, encased vaccine particles, each programmed to release at a precise, predictable time, so that people could potentially receive a single injection that, in effect, would have multiple boosters already built into it. This could have a significant impact on patients everywhere, especially in the developing world where patient compliance is particularly poor,” says Robert Langer, the David H. Koch Institute Professor at MIT.
Langer and Ana Jaklenec, a research scientist at MIT’s Koch Institute for Integrative Cancer Research, are the senior authors of the paper, which appears online in Science on Sept. 14. The paper’s lead authors are postdoc Kevin McHugh and former postdoc Thanh D. Nguyen, now an assistant professor of mechanical engineering at the University of Connecticut.


Vaccine News – The Alex Jones Channel – Nurse Ratchet Cranks Up Medical Tyranny

Apart from the racism of the white doctor saying “kill all the white people” because they’re “refusers”, Jon Rappoport breaks down the medical tyranny that would mandate some medical treatments, prohibit others and threaten to kill those who “refuse”. Follow David Knight On Twitter: Follow Real News On Twitter: Like Real News On Facebook: Watch At: Help us spread the word about the liberty movement, we’re reaching millions help us reach millions more. Share the free live video feed link with your friends & family: Follow Alex on TWITTER – Like Alex on FACEBOOK –… Infowars on G+ – :Web:

Vaccine News – Study – Gender-selective toxicity of thimerosal – Mar.2009
A recent report shows a correlation of the historical use of thimerosal in therapeutic immunizations with the subsequent development of autism; however, this association remains controversial. Autism occurs approximately four times more frequently in males compared to females; thus, studies of thimerosal toxicity should take into consideration gender-selective effects. The present study was originally undertaken to determine the maximum tolerated dose (MTD) of thimersosal in male and female CD1 mice. However, during the limited MTD studies, it became apparent that thimerosal has a differential MTD that depends on whether the mouse is male or female. At doses of 38.4-76.8mg/kg using 10% DMSO as diluent, seven of seven male mice compared to zero of seven female mice tested succumbed to thimerosal. Although the thimerosal levels used were very high, as we were originally only trying to determine MTD, it was completely unexpected to observe a difference of the MTD between male and female mice. Thus, our studies, although not directly addressing the controversy surrounding thimerosal and autism, and still preliminary due to small numbers of mice examined, provide, nevertheless, the first report of gender-selective toxicity of thimerosal and indicate that any future studies of thimerosal toxicity should take into consideration gender-specific differences. – 15.Mar.2010
Mercury (Hg) exposure from dental amalgam fillings and thimerosal in vaccines is not a major health hazard, but adverse health effects cannot be ruled out in a small and more susceptible part of the exposed population. Individual differences in toxicokinetics may explain susceptibility to mercury. Inbred, H-2-congenic A.SW and B10.S mice and their F1- and F2-hybrids were given HgCl2 with 2.0 mg Hg/L drinking water and traces of (203)Hg. Whole-body retention (WBR) was monitored until steady state after 5 weeks, when the organ Hg content was assessed. Despite similar Hg intake, A.SW males attained a 20-30% significantly higher WBR and 2- to 5-fold higher total renal Hg retention/concentration than A.SW females and B10.S mice. A selective renal Hg accumulation but of lower magnitude was seen also in B10.S males compared with females. Differences in WBR and organ Hg accumulation are therefore regulated by non-H-2 genes and gender. Lymph nodes lacked the strain- and gender-dependent Hg accumulation profile of kidney, liver and spleen. After 15 days without Hg A.SW mice showed a 4-fold higher WBR and liver Hg concentration, but 11-fold higher renal Hg concentration, showing the key role for the kidneys in explaining the slower Hg elimination in A.SW mice. The trait causing higher mercury accumulation was not dominantly inherited in the F1 hybrids. F2 mice showed a large inter-individual variation in Hg accumulation, showing that multiple genetic factors influence the Hg toxicokinetics in the mouse. The genetically heterogeneous human population may therefore show a large variation in mercury toxicokinetics.
US National Library of Medicine – National Institutes of Health – Feb.2015
Developmental Domain: ASD Diagnostic Criteria
Social Communication/Social Interaction
Deficits in social communication and social interaction are core factors in the diagnostic criteria of ASD. Impairments in social communication may present as abnormalities in eye contact, poor integration of verbal and nonverbal behaviors, and difficulties understanding the nonverbal communication of others (American Psychiatric Association, 2013). In some cases, persons with ASD may not participate in conversation or struggle with pragmatic language (American Psychiatric Association, 2013). Impairments in social interaction include difficulties with social-emotional reciprocity, failure to develop peer relationships, and reduced empathetic understanding and/or response (American Psychiatric Association, 2013).
There were 21 articles reviewed on social communication and social interaction in persons with ASD published between 1993 and 2013: 13 case-control studies, 7 cross-sectional studies, and 1 surveillance study. Nine studies were conducted in the United States and 12 studies were conducted at outside of the US. Of these 21 articles, 14 address social communication or other language abilities. In samples of children with varying cognitive abilities, some studies showed no significant differences in communication, conversational deficits, and language levels between males and females with ASD (Andersson et al., 2013; Dawson et al., 2007; Nicholas et al., 2008; Pilowsky et al., 1998; Park et al., 2012a, 2012b; Mayes and Calhoun, 2011; Mandy et al., 2012; Sipes et al., 2011; Solomon et al., 2012; Amr et al., 2011). One study found that males with ASD had greater expressive and receptive language skills than females with ASD (Carter et al., 2007) and another study found that females with ASD had more impaired social communication skills than males with ASD (Hartley and Sikora, 2009). Conversely, Park et al. (2012b) found that females with ASD had stronger non-verbal communication abilities than males with ASD. The majority of the literature reviewed on social communication found no difference between males and females with ASD, but there is some inconsistency.
The literature on sex differences in social interaction among persons with ASD (13 of 21 articles reviewed) is also inconsistent but generally suggests no significant sex differences in social interaction skills (Andersson et al., 2013; Dawson et al., 2007; Nicholas et al., 2008; Pilowsky et al., 1998; Mayes and Calhoun, 2011; Park et al. 2012b; Mandy et al., 2012; Sipes et al., 2011; Solomon et al., 2012). In population-level surveillance of eight-year olds, 80 % of children with ASD had poor social-emotional reciprocity with no significant difference between males and females (Nicholas et al., 2008). Szatmari et al. (2012) also found no sex differences in social-emotional reciprocity for children with varying cognitive abilities in a study from the Autism Genome Project. Oppositely, in an age and IQ matched case–control study, female adults with ASD were found to have fewer socio-communication difficulties during interpersonal interaction than male adults with ASD (Lai et al., 2013). Lastly, no sex differences have been noted in emotional reactiveness or being withdrawn (Hartley and Sikora, 2009) and in empathetic understanding and responses (Auyeung et al., 2009).
Cognitive functioning is likely to play a role in these social processes. Lower intellectual abilities are often linked with greater social impairment regardless of sex (Dawson et al., 2007). Among children with high functioning autism (IQ≥70), social skills have been found to be more impaired in female children than male children (Holtmann et al., 2007) and more severe as children aged (McLennan et al., 1993). In contrast, other studies found adult females with high functioning autism to have less socio-communication issues compared to males (Lai et al., 2011) or there were no sex differences in socio-communication skills in older children and adolescents (Holtmann et al., 2007; Kopp and Gillberg, 2011).
Overall, the 21 articles reviewed suggest no difference in social interaction between males and females with ASD and inconsistent differences in social communication between males and females with ASD, although both social interaction and social communication may be influenced by intellectual ability and age.
Restricted, Repetitive Patterns of Behavior, Interests, or Activities
There were 18 articles reviewed on restricted and repetitive patterns of behaviors and interests (RRBI) published between 1993 and 2013: nine cross-sectional studies, seven case–control studies, one cohort study, and one surveillance study. Eleven studies were conducted in the United States and seven studies were conducted in other countries. Based on this review, the literature suggests that males with ASD have more RRBI than females with ASD (Hattier et al., 2011; Carter et al., 2007). When assessing individual facets of RRBI, restricted interests are seen more often in males with ASD than females with ASD independent of cognitive ability (Kohane et al., 2012; May et al., 2012; Mandy et al., 2012; Szatmari et al., 2012). Males with ASD are also more likely to have more routines, rituals, and fascination with parts of objects than females with ASD (Nicholas et al., 2008; Park, et al., 2012b; Beuker et al., 2013). The literature on repetitive motor movements is less consistent: adult males with high functioning autism or Asperger’s syndrome had more repetitive motor movements than adult females with high functioning autism or Asperger’s syndrome in one case-control study (May et al., 2012), but there were no sex differences in repetitive motor movements among persons with autism in two other case-control studies (McLennan et al., 1993; Worley and Matson, 2011), one cross-sectional study (Auyeung et al., 2009), and one population-based cross-sectional study (Nicholas et al., 2008).
Age may influence the presentation of RRBI in males and females with ASD. One study found no sex difference among RRBI in toddlers (Sipes et al., 2011), whereas a different study found significantly more RRBI among adult males with ASD compared to females with ASD (Hattier et al., 2011). In summation, most studies reviewed suggested that males with ASD are likely to have more RRBI than females with ASD across levels of cognitive ability, although RRBI may be influenced by age.
Sensory issues are prevalent among persons with ASD (Nicholas et al., 2008) and are included as a RRBI in the DSM 5 (American Psychiatric Association, 2013). Common issues are oversensitivity to touch, sound, smell, taste, and attraction to certain tactile stimuli (American Psychiatric Association, 2013; Baranek et al., 2006; Rogers et al., 2003). Abnormal sensory reactions have been reported to occur in up to 47 % of persons with ASD, which is a rate ten times higher than reported in the general population (Nicholas et al., 2008). Additionally, there is a significant correlation between sensory issues in each of the individual senses (Kern et al., 2007); therefore, impairment is compounded for persons with ASD and sensory abnormalities.
Cross-sectional studies found no observed differences between males and females in sensitivity to sound (Mandy et al., 2012) or sensory sensitivity in general (Louisa et al., 2012; Mayes and Calhoun, 2011; Baranek et al., 2006). Mandy et al. (2012) examined RRBI in children and adolescents 3 to 18 years of age and found that age did not influence the presentation of RRBI. However, Lai et al. (2011) found that adult females with high functioning autism had more lifetime sensory issues than males with ASD. Overall, the majority of articles reviewed that addressed sensory issues in ASD do not suggest a sex difference, although aging may be a factor and should be further explored.
Developmental Domain: other Developmental Endophenotypes
Attention Deficit Hyperactivity Disorder
Attention deficit hyperactivity disorder (ADHD) and corresponding symptoms are common in children with ASD (Bradley and Isaacs, 2006; Nicholas et al., 2008). Previous studies show that 50 % to 83 % of children and teenagers with ASD had hyperactivity and attention problems (Nicholas et al., 2008; Bradley and Isaacs, 2006). There were seven articles that met search criteria and addressed ADHD. These seven articles were published between 2008 and 2012 with five cross-sectional studies and two cohort studies. Two studies were conducted in the United States and five were conducted in other countries.
A study of 7 to 12 year-olds with varying cognitive abilities found that males with ASD had higher levels of hyperactivity and impulsivity than females with ASD and this difference was more pronounced at younger ages (May et al., 2012). Males with high functioning autism from middle childhood to adolescence had higher levels of hyper-activity and inattention in teacher reports as compared to female peers, but there was no difference in parental reports (Mandy et al., 2012). A study of children and young adults aged 5 to 20 with high functioning autism found females had more attention problems (Bryson et al., 2008). A majority of studies found no difference in ADHD co-occurrence between males and females with ASD (Simonoff et al., 2008; Sinzig et al., 2009; Mayes and Calhoun, 2011; Horovitz et al., 2011). In summary, the current literature leans toward no sex differences in the co-occurrence of ADHD and ASD, but there is still inconsistency in the literature and thus, the sex difference is largely inconclusive
Challenging Behavior (Aggressiveness/Temper Tantrums/Oppositional Tendencies)
Challenging behavior is a common associated feature of ASD and includes aggression expressed toward other people, temper tantrums, and oppositional and defiant tendencies. Aggression expressed toward other people and temper tantrums are found in 50 % and 54 % of children with ASD compared to only 28 % and 23 % of children without ASD (Nicholas et al., 2008). The 12 articles in this review that met search criteria and addressed challenging behaviors were published between 2005 and 2012 and included six cross-sectional studies, four case–control studies, one clinical trial, and one surveillance study. Six studies were conducted in the United States and six were conducted in other countries. In general, there were no differences in aggression, temper tantrums, or anger between child sexes, regardless of age or cognitive ability (Kozlowski et al., 2012; Worley and Matson, 2011; Carter et al., 2007; Murphy et al., 2009; Mandy et al., 2012; Quek et al., 2012; Mayes and Calhoun, 2011; Horovitz et al., 2011). One study found that females with ASD had more “challenging behaviors” than males with ASD, although challenging behaviors were not explicitly defined (Dworzynski et al., 2012). Delinquent behavior (Park et al., 2012b) and oppositional defiance (Gadow et al., 2005) were more prevalent in males than in females with ASD in two studies reviewed.
Cognitive Skills and Intellectual Disability
In a review from 1966 to 2001, Fombonne (2003) found that the median prevalence of intellectual impairment in persons with ASD was 70 % in the studies evaluated. More recent population-based studies have found lower rates of ID in persons with ASD, with a range from 18 % to 55 % (Charman et al., 2011). The National Health Interview Study found 0.71 % of all children aged 3 to 17 from 1998 to 2007 had an ID (Boyle et al., 2011). Our review found 12 articles that met the search criteria and addressed ID or specific cognitive skills. These 12 articles were published between 1983 and 2011, and included seven cross-sectional studies, four case–control studies, and one-surveillance study. Four studies were conducted in the United States and eight were conducted in other countries.
The 12 articles reviewed support a relationship between child sex and co-occurring ID in children with ASD. The sex ratio between males and females without ID is greater than the sex ratio for all levels of cognitive ability combined (Nicholas et al., 2008; Hartley and Sikora, 2009). Consequently, the male to female ratio is lower when there is co-occurring ID compared to when there is no co-occurring ID (Hartley and Sikora, 2009; Nicholas et al., 2008; Yeargin-Allsopp et al., 2003). The ratio of males to females with ASD and co-occurring ID has been seen to range from 1.3:1 (Tsai and Beisler, 1983) to 2.8:1 (Bryson et al., 2008) with a trend toward fewer sex differences as ID becomes more severe (Yeargin-Allsopp et al., 2003). This differential sex difference in ID results in females with ASD, on average, having lower intelligence test scores than males with ASD (Banach et al., 2009; Volkmar et al., 1993).
Specific cognitive skills posited to vary between males and females with ASD include cognitive flexibility, response inhibition, working memory, and attention to detail (Geurts et al., 2004). Female adolescents with high functioning autism were seen to have superior information processing, multiple conceptual tracking, divided attention, and cognitive flexibility compared to male adolescents with high functioning autism (Bolte et al., 2011). In contrast, studies show males with ASD have superior attention to detail, visuo-spatial skills (Auyeung et al., 2009), and inhibitory control (Lemon et al., 2011) compared to females with ASD. There were no sex differences between adults with ASD in the “eyes test” which measures ability to infer mental states through the eyes (Lai et al., 2011). In summary, the 12 journal articles reviewed in this section suggest that females with ASD generally have lower intelligence test scores than males with ASD and that specific cognitive skills may vary by sex.
Developmental Regression
Parents of some children with ASD report a period of typical development followed by a loss in language, social, motor, self-help, imaginative play, or other skills. This developmental regression is usually reported to occur between 15 and 24 months of age (Meilleur and Fombonne, 2009). Our review found six articles that met search criteria and addressed developmental regression. These six articles were published between 2007 and 2013 and comprised two cohort studies, three cross-sectional studies, and one surveillance study. In a population-based surveillance study of children with ASD, 17 % of children had documented developmental regression and that percentage rose if the child had a previous ASD diagnosis (Wiggins et al., 2009). Males had significantly more regression than females and were more likely to regress at a younger age (Wiggins et al., 2009). This higher risk of regression in males was also seen in smaller, non-population based studies (n=4, 8, and 17 female children) (Bernabei et al., 2007; Ekinci et al., 2012; Zhang et al., 2012). In contrast, a cross-sectional study found that females aged 18 months to 15 years had significantly higher occurrence of regression as compared to males (30 % vs. 19 %) (Ben-Itzchak et al., 2013). No difference in the presence of developmental regression between males and females with ASD was observed in a small clinical sample of 20 females (Meilleur and Fombonne, 2009). In sum, the review of sex differences of developmental regression is contradictory and thus inconclusive.
Excess/Absence of Fear
Excess or absence of fear is more common in children with ASD than other children (Evans et al. 2005; Nicholas et al., 2008). In a population-based surveillance of eight-year olds, Nicholas et al. (2008) found that 32 % of children with ASD had atypical fear noted in service records compared to 6 % of children with ASD symptoms but no ASD diagnosis. Three articles met search criteria and addressed excess or absence of fear. All three of these articles were published in the United States between 1990 and 2011 and were two cross-sectional studies and one case–control study. In these studies, females with ASD had more specific phobias than males with ASD (Gadow and DeVincent, 2012; Matson and Love, 1990) and more unusual fears (Mayes et al., 2013). One study conducted by Matson and Love (1990) found more fear in typically developing female children compared to male children and no significant difference in fear between typically developing female children and female children with ASD. Given the sparse amount of research on this topic, further exploration is warranted to understand sex differences in fear among persons with ASD.
Safety Issues (Self-Injury/Elopement)
About 50 % of children with ASD engage in self-injurious behavior (Richards et al., 2012; Baghdadli et al., 2003; Duerden et al., 2012). Four studies met search criteria and three pertained to self-injurious behavior. All three of these studies were cross-sectional designs with two being conducted in Europe and one in the United States. No difference in self-injurious behavior was found between males and females with ASD (Richards et al., 2012; Baghdadli et al., 2003; Duerden et al., 2012).
Elopement, also known as wandering off, is a rising concern among parents of children with ASD. One online survey addressing elopement met our search criteria. This survey was conducted in the United States in 2013 and found that 49 % of parents reported that their child with an ASD wandered off at least once after the age of four years (Anderson et al., 2012). Results also found that sex did not influence the prevalence of elopement, although children with more intellectual impairment were more likely to elope (Anderson et al., 2012). Few conclusions can be drawn since there is little research on elopement and other safety issues in children with ASD and associated sex differences.
Psychiatric Domain
Anxiety/Mood Disorders
Symptoms of anxiety and mood disorders are more prevalent in children with ASD than in typically developing children (Worley and Matson, 2011; Nicholas et al., 2008). Among children who met a surveillance definition for an ASD, 55 % had abnormal mood or affect compared to 26 % of children with at least one symptom of an ASD but no ASD diagnosis (Schendel et al., 2009). The Special Needs Autism Project in the UK found 44 cases of emotional disorder per 100 children with ASD (Simonoff et al., 2008). Moreover, among eight-year-old children who met a surveillance definition for an ASD, 3 % had anxiety, 2 % had emotional disorder, 2 % had mood disorder, and less than 2 % had obsessive-compulsive disorder (OCD), depression, bipolar, or oppositional defiant disorder (Levy et al., 2010). Nine studies were found that met search criteria and addressed anxiety or mood disorders. These nine studies were published between 2005 and 2012 and included five cross-sectional studies and four case–control studies. Four of the studies were conducted in the United States and five were conducted in other countries.
The literature on sex differences in co-occurring anxiety or mood disorders and ASD is mixed and dependent on cognitive abilities. In some studies, females with high functioning autism were at greater risk for internalizing psychopathology than both male children with ASD and typically developing female children (Solomon et al., 2012; Mandy et al., 2012). These studies are supported by a Finnish report that found female children with ASD had lower scores on a test associated with major depressive disorder compared to male children with ASD (Mattila et al., 2010). Other studies found no sex differences in the of co-occurrence of anxiety or depression in children with ASD and varying cognitive abilities (Quek et al., 2012; Gadow et al., 2005; Park et al., 2012b; Simonoff et al., 2008; Mayes and Calhoun, 2011; Lai et al., 2011). In the general population, females have more panic attacks, generalized anxiety disorders and males have more social anxiety (American Psychiatric Association, 2013). Based on this review, the current literature is inconclusive on whether a sex difference in children with ASD and co-occurring anxiety or mood disorders exists, although a few studies suggest more anxiety and mood disorders in females than males with ASD.
Schizophrenia is a mental disorder that involves delusions, disorganized behavior, disorganized speech, hallucinations, and restrictions in the range and intensity of emotions (American Psychiatric Association, 2013). Schizophrenia typically presents between 18 and 30 years of age with earlier onset associated with male sex. Lifetime prevalence of schizophrenia is near 0.2 % (American Psychiatric Association, 2013) The prevalence of schizophrenia in eight-year olds with ASD is less than 1 % (Levy et al., 2010). Two articles met search criteria and addressed schizophrenia. These two articles were published in 2005 and 2010 and were both case–control studies. Review of the two studies found conflicting results on sex differences and the co-occurrence of ASD and schizophrenia or schizophrenia spectrum traits. A parental survey of 6 to 12 year olds with ASD found schizophrenia spectrum traits to be twice as prevalent in females compared to males (57 %: 28 %) independent of ID (Gadow and DeVincent, 2012). Conversely, in a group of 6 to 12 year olds with ASD and ID, schizophrenia was more common in males than females (Tsakanikos et al., 2011). Again, the literature is relatively sparse due to the late onset of schizophrenia and the rarity of co-occurring schizophrenia: future research is warranted.
Medical Domain
Birth defects/Chromosomal Disorders /Genetic Disorders
Population-based surveillance data from the 2008 ADDM report found that among children with ASD, less than 1 % had a co-occurrence of fragile X syndrome, Down syndrome, chromosomal disorders, or other genetic and congenital diagnoses (Levy et al., 2010). It is likely that these rates are under-reported because investigation of ASD co-occurring conditions was not the focus of the ADDM surveillance effort. However, a cohort study of children in Georgia found a similar prevalence of chromosomal disorders and Down syndrome in persons with ASD (Schendel et al., 2009).
There were four studies reviewed that met search criteria and addressed ASD sex differences in birth defects, chromosomal disorders, and genetic disorders: two systematic reviews, one case–control study, and one surveillance study. Co-occurring birth defects, such as impairments to the central nervous system, cardiovascular system, genitourinary system, or musculoskeletal system, appear more often in males than females with ASD. Among children with ASD, the male to female ratio was 9:1 if a child had a co-occurring birth defect and 3.6:1 if the child did not have a co-occurring birth defect (Schendel et al., 2009).
A review conducted by Reilly (2009) found that males with ASD have more co-occurring Down syndrome than females with ASD and the male to female ratio among children with both ASD and Down syndrome may be near the overall ASD prevalence ratio of 4:1. A review conducted by Wiznitzer (2004) found no difference between males and females with ASD and the co-occurrence of tuberous sclerosis. Clifford et al. (2007) found that about 70 % of males aged 5 to 80 with fragile X syndrome had co-occurring ASD while 23 % of females in the same age range with fragile X had co-occurring ASD. The difference in co-occurrence of ASD between males and females may suggest a greater association between the two conditions in males as compared to females.
It is important to note that birth defects, chromosomal disorders, and genetic disorders are rare and seldom studied. Therefore, the results on sex differences for co-occurring ASD and chromosomal and genetic conditions are inconclusive.
Head Size / Encephalopathy
Head size, specifically an enlarged head circumference or macrocephaly, has been associated with ASD (Wallace and Treffert, 2004). Three articles were reviewed that examined differences in head size between males and females with ASD. Studies include two case–control studies and one cross-sectional study. Two studies were conducted in the US and one study was conducted in Italy. A cross-sectional study by Fombonne et al. (1999) found no difference in head size between males and females aged 2 to 16 with ASD. Sacco et al. (2007) also found no difference in head size between males and females aged 3 to 16 with ASD. In contrast, Aylward et al. (2002) found larger head sizes in male adults and children compared to female adults and children with ASD, but the female sample size was low (n=9).
Abnormal Eating and Gastrointestinal Issues
In a population-based study conducted by Nicholas et al. (2008), about 54 % of children with ASD had an abnormality in eating, drinking, or sleeping, which is nearly 40 % higher than that of children with at least one symptom of ASD but no diagnosis (Nicholas et al., 2008). Some studies have shown an increase in certain gastrointestinal symptoms among persons with ASD, including constipation (Ibrahim et al., 2009) and diarrhea (Wang et al., 2006), while other studies found no significant increase in overall gastrointestinal symptoms or symptoms such as esophageal reflux, vomiting, and abdominal discomfort (Ibrahim et al., 2009; Wang et al., 2006; Valicenti-McDermott et al., 2007). However, little research on gastrointestinal issues has been conducted at a population level and no studies were found that compared males to females on gastrointestinal response. More research is needed to determine if there is an association between gastrointestinal symptoms and ASD and whether the association differs between the sexes.
Four studies were found that compared the sexes and addressed food selectivity. These four studies were conducted in the United States between 2006 and 2010 and included one case–control and three cross-sectional designs. In general, review of these studies found food selectivity and feeding issues to be more frequent in children with ASD than children without ASD (Valicenti-McDermott et al., 2007; Ibrahim et al., 2009), although limited research is available in this area. There was no difference between child sexes in over or under-eating in a study of children with high functioning autism (Worley and Matson, 2011) and no differences between the sexes in eating abnormalities in two studies conducted in children with ASD and varying cognitive abilities (Mayes and Calhoun, 2011; Horovitz et al., 2011). Based on this limited review, it appears unlikely that there is a difference in eating habits between males and females with ASD.
Seizures/ Epilepsy
Epilepsy and other seizure disorders co-occur in 5 % to 40 % of children with ASD and there is differential prevalence based on ID (Baird et al., 2008; Nicholas et al., 2008). This review found three articles that met search criteria and addressed seizures or epilepsy. These three articles were published between 2008 and 2013 and consist of a cohort study, one cross-sectional study, and one meta-analysis. Females with ASD were found to have more epilepsy than males with ASD; the male to female ratio drops to near 2:1 in children with ASD and co-occurring epilepsy, but this may be partly due to differential ID (Amiet et al., 2008; Bolton et al., 2011; Ben-Itzchak et al., 2013). There may be an increased likeliness in females with ASD to have co-occurring epilepsy or seizure disorder; however, the literature is sparse so a conclusion cannot be drawn. Further research is needed to enhance current knowledge of sex differences in children with ASD and epilepsy or seizure disorder.
Sleep Disturbances
In a systematic review of parental sleep surveys, sleep problems were present in 50 % to 80 % of children with ASD compared to 9 % to 50 % in matched typically developing children (Kotagal and Broomall, 2012). There were six articles reviewed that met search criteria and addressed sleep disturbances. These six articles were published between 2004 and 2012 and included two case–control studies, two cohort studies, and two cross-sectional studies. Four were conducted in the United States and three were conducted in other countries. Based on this review, some studies found no sex differences in sleep problems among persons with ASD (Liu et al., 2006; Wiggs and Stores, 2004; Mayes and Calhoun, 2011; Horovitz et al., 2011), one study found that female children with ASD have less sleep problems than male children with ASD (Sivertsen et al., 2012), and one study found female children with ASD have more sleep problems than male children with ASD (Hartley and Sikora, 2009). The minimal amount of research in this area leads to inconsistent results and prevents definitive conclusions on whether a sex difference exists in sleep disturbance.

Vaccine News – This is the Best Explanation of the Vaccine/Autism Connection I’ve Ever Heard!

The Only Vaccine Guide a New Parent Will Ever Need
First, a disclaimer: I’m not a doctor, and the final decision about vaccinating your child should take place between you and your healthcare provider. I’m not giving you medical advice; I’m stating my opinion.
I am a dad. And, I write this without benefitting in anyway from what is said here. I have no book to peddle, no profits to protect, and there’s no doubt that writing this will result in some amount of hate directed in my general direction for challenging a popular narrative that vaccines are only safe and effective and should be administered the same way to all children without consideration for the unique biology of each and every child. So be it.
Do your own research. Understand the risks and benefits of everything you are putting into your child.
Find a healthcare provider who doesn’t believe “one size fits all” when it comes to vaccines

The Vaccine Studies That Have Never Been Done.
1. Study Proving the Existing Vaccine Schedule Is Safe – NEVER DONE
2. Study Proving Safety of Childhood Vaccines For Children – NEVER DONE
3. Study Proving Safety of Infant Vaccines For Infants – NEVER DONE
4. Study Proving Vaccines Safe for Pregnant Women – NEVER DONE
5. Study Proving Vaccines Safe For Unborn Fetus – NEVER DONE
6. Study Comparing the Health of Vaccinated vs Un-Vaccinated – NEVER DONE
7. Study to Prove Combining Several Vaccines at One Doctor’s Visit Is Safe – NEVER DONE
8. Study That Exposes Vaccinated People to Targeted Virus (to see if they get sick or not) – NEVER DONE
9. Study That Proves Vaccinated People Don’t Acquire the Targeted Disease – NEVER DONE
10. Study Proving Thimerosal (mercury) or Aluminum Are Safe to Inject Into Children – NEVER DONE
Read # 8 again and then read it again…….and then think about that.
These are the studies the average person assumes were already done decades ago and they have NEVER been done. If you’re not concerned, you’re not paying attention.
~ Chris Kirckof

Disturbing tape-recording of an immunologist having a laugh over the numerous and useless vaccines they inject for a child’s first year of life, in order to keep parents compliant and unquestioning of what is being done to their baby. Research is KEY and education is empowerment

Pro-Vaccine Immunologist Admits a Shocking Truth About Vaccines
For several years, until April of this year, I had been lecturing nationally to health professionals about the great vaccine hoax. Attending one such seminar was a board member of an association of health professionals, who invited me to speak on this subject at their national conference. I did, and had 90 minutes to present the most salient points from my 7-hour seminar. It caused quite a stir, and several clinicians thanked me for having the courage to speak the truth about this controversial subject.
Later that day, I sat on a panel of four experts to answer questions from conference attendees. Many of the questions were directed at the PhD immunologist on the panel, asking if the statements I had made in the morning presentation were true. To my surprise, the immunologist confirmed every assertion I had made.
The first was that it is pointless to administer drugs intended to stimulate antibody production to babies who are too young to produce antibodies. Infants in their first year mostly depend on generalized, non-specific immunity, including (hopefully) immunoglobulins from breast milk, to protect their young bodies from infection. They do not produce antibodies of their own until about age one. Despite this basic fact, the medical establishment insists administering a total of 19 shots, containing 24 vaccines, to infants on the 2, 4 and 6 month pediatric visits (Source: Somehow, the basic facts of human physiology and development do not apply to vaccines.
You can listen to an audio file of an exchange between an attendee and the immunologist about this question. She declined to be identified in my presentations, including this post, perhaps because she knows that anyone who speaks the truth about vaccines is savaged by the medical establishment and their compliant lapdogs in the mainstream media. It is professional suicide for anyone in conventional medicine to question the unquestionable (yet unproven) assumptions about vaccines: that they are effective, safe and necessary. I have stopped lecturing publicly on this subject for the same reason, because the attacks in recent years have become particularly vicious; and because my main message in my teachings is about personal responsibility, innate wholeness and opening to the largeness of who we are, not just vaccines.

Study – A modified self-controlled case series method to examine association between multidose vaccinations and death
The self-controlled case series method (SCCS) was developed to analyze the association between a time-varying exposure and an outcome event. We consider penta- or hexavalent vaccination as the exposure and unexplained sudden unexpected death (uSUD) as the event. The special situation of multiple exposures and a terminal event requires adaptation of the standard SCCS method. This paper proposes a new adaptation, in which observation periods are truncated according to the vaccination schedule. The new method exploits known minimum spacings between successive vaccine doses. Its advantage is that it is very much simpler to apply than the method for censored, perturbed or curtailed post-event exposures recently introduced. This paper presents a comparison of these two SCCS methods by simulation studies and an application to a real data set. In the simulation studies, the age distribution and the assumed vaccination schedule were based on real data. Only small differences between the two SCCS methods were observed, although 50 per cent of cases could not be included in the analysis with the SCCS method with truncated observation periods. By means of a study including 300 uSUD, a 16-fold risk increase after the 4th dose could be detected with a power of at least 90 per cent. A general 2-fold risk increase after vaccination could be detected with a power of 80 per cent. Reanalysis of data from cases of the German case-control study on sudden infant death (GeSID) resulted in slightly higher point estimates using the SCCS methods than the odds ratio obtained by the case-control analysis.

The Top 10 Reasons To Never Take A Vaccine
There are many, many good reasons to never take a vaccine. Whether you want to protect yourself against carcinogenic hidden ingredients, disallow toxic adjuvants into your body, defend your immune system against a chemical onslaught or refuse to be part of any sinister schemes of sterilization-depopulation agenda, this information is vitally important.
More and more, we are learning the truth about vaccines, what they are really composed of and what they really do to the human body – and the more we learn about them, the more we see just how dangerous and harmful they are. Whatever they may have been or could be, as it stands, they are a weapon of medical destruction that makes billions of dollars for the Rockefeller Medicine Big Pharma cartel. Here is my list of the top 10 reasons for an ordinary person to never take a vaccine, unless they were in a life-threatening situation where somehow the benefit outweighed the risk.

Reason #1 to Never Take a Vaccine: Toxic Ingredients – Formaldehyde, MSG, Antibiotics, GMOs, Polysorbate, Mercury, Squalene and More
Reason #2 to Never Take a Vaccine: Toxic Adjuvants – Aluminum
Reason #3 to Never Take a Vaccine: Hidden Ingredients – Immunity-Destroying Nagalese
Reason #4 to Never Take a Vaccine: Injection of Human and Animal Cells
Reason #5 to Never Take a Vaccine: Blood Sludge, Hypoxia, Ischemia and Localized “Strokes” in Your Body
Reason #6 to Never Take a Vaccine: The Herd Immunity Myth Busted
Reason #7 to Never Take a Vaccine: Viral Shedding
Reason #8 to Never Take a Vaccine: Possible Side Effects of Paralysis and Death
Reason #9 to Never Take a Vaccine: Insufficient Legal Recourse
Reason #10 to Never Take a Vaccine: The Vaccine-Sterilization-Depopulation Connection

Remember that Bill Gates himself, point man for the NWO agenda, has slipped up and admitted there is a vaccine-depopulation link on at least 2 occasions:

“… if we do a really great job on new vaccines … we could lower that (i.e. population growth) perhaps by 10-15% …”
“… the benefits (of vaccines) are there in terms of reducing sickness, reducing population growth …”

Zeit für einen Shitstorm gegen die Impfstoffhersteller! In deren Prospekten stimmt kein einziger Satz, schwere Nebenwirkungen werden mit Hilfe einer Armada von Lobbyisten verschwiegen, damit der Rubel rollt. Es ist Zeit, den Verletzungen an Körper, Geist und Seele, die von Impfungen verursacht werden, ein Ende zu bereiten!
Impfungen haben keine einzige Seuche ausgerottet – das zeigen Statistiken des Bundes. Jede Seuche war aufgrund des wachsenden Wohlstands nach dem 2. WK schon so gut wie verschwunden, BEVOR die entsprechende Impfung auf den Markt kam!
Schluss mit den Lügen der Pharma-Industrie und staatlich organisierten Subventionen wie bei den “Schweinegrippe-Impfstoffen”!
Konkret sind im ersten Lebensjahr von der Lobbygruppe “StIKo” empfohlen:4 x 6-fach-Impfung, 4 x Pneumokokken, 1 x MMRV (4-fach), dazu kommen optionale Impfungen wie gegen “Rotaviren” oder Influenza, die viele Ärzte zusätzlich verimpfen. Macht maximal 34 Impfungen im ersten Lebensjahr. Und im 2. Lebensjahr wird dann munter weitergeimpft…

Study – What is regressive autism and why does it occur? Is it the consequence of multi-systemic dysfunction affecting the elimination of heavy metals and the ability to regulate neural temperature?
There is a compelling argument that the occurrence of regressive autism is attributable to genetic and chromosomal abnormalities, arising from the overuse of vaccines, which subsequently affects the stability and function of the autonomic nervous system and physiological systems. That sense perception is linked to the autonomic nervous system and the function of the physiological systems enables us to examine the significance of autistic symptoms from a systemic perspective. Failure of the excretory system influences elimination of heavy metals and facilitates their accumulation and subsequent manifestation as neurotoxins: the long-term consequences of which would lead to neurodegeneration, cognitive and developmental problems. It may also influence regulation of neural hyperthermia. This article explores the issues and concludes that sensory dysfunction and systemic failure, manifested as autism, is the inevitable consequence arising from subtle DNA alteration and consequently from the overuse of vaccines.

Study – A two-phase study evaluating the relationship between Thimerosal-containing vaccine administration and the risk for an autism spectrum disorder diagnosis in the United States
Autism spectrum disorder (ASD) is defined by standardized criteria of qualitative impairments in social interaction, qualitative impairments in communication, and restricted and stereotyped patterns of behavior, interests, and activities. A significant number of children diagnosed with ASD suffer a loss of previously-acquired skills, which is suggestive of neurodegeneration or a type of progressive encephalopathy with an etiological pathogenic basis occurring after birth. To date, the etiology of ASD remains under debate, however, many studies suggest toxicity, especially from mercury (Hg), in individuals diagnosed with an ASD. The present study evaluated concerns about the toxic effects of organic-Hg exposure from Thimerosal (49.55% Hg by weight) in childhood vaccines by conducting a two-phased (hypothesis generating/hypothesis testing) study with documented exposure to varying levels of Thimerosal from vaccinations.
A hypothesis generating cohort study was undertaken to evaluate the relationship between exposure to organic-Hg from a Thimerosal-containing Diphtheria-Tetanus-acellular-Pertussis (DTaP) vaccine in comparison to a Thimerosal-free DTaP vaccine administered, from 1998 through 2000, for the risk of ASD as reported in the Vaccine Adverse Event Reporting System (VAERS) database (phase I). A hypothesis testing case–control study was undertaken to evaluate the relationship between organic-Hg exposure from Thimerosal-containing hepatitis B vaccines administered at specific intervals in the first six months of life among cases diagnosed with an ASD and controls born between 1991 through 1999 in the Vaccine Safety Datalink (VSD) database (phase II).
In phase I, it was observed that there was a significantly increased risk ratio for the incidence of ASD reported following the Thimerosal-containing DTaP vaccine in comparison to the Thimerosal-free DTaP vaccine. In phase II, it was observed that cases diagnosed with an ASD were significantly more likely than controls to receive increased organic-Hg from Thimerosal-containing hepatitis B vaccine administered within the first, second, and sixth month of life.
Routine childhood vaccination is an important public health tool to reduce the morbidity and mortality associated with infectious diseases, but the present study provides new epidemiological evidence supporting an association between increasing organic-Hg exposure from Thimerosal-containing childhood vaccines and the subsequent risk of an ASD diagnosis.

#VaxXed #medical #Oregon
Dr Paul Thomas interview with Polly Tommey
June 17, 2017

The Shift Episode 8: Del Bigtree
Join host Doug McKenty as he discusses the controversial movie Vaxxed with producer Del Bigtree. Listen in as the conversation includes the real story behind Dr. Andrew Wakefield’s study of the MMR vaccine that started it all, the realization that regulatory agencies have been corrupted at the highest levels, as well as the real reasons behind the mainstream media’s complicity in covering up the actual science behind vaccine safety. Find out more about it at, and as always help out at or visit for more information about making The Shift.

Billy D Live with Del Bigtree
Watch Billy D and Del Bigtree talk about vaccines
Go to to watch Jeremy’s Stretch video series.

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Vaccine’s Safety: A Crime Against Humanity
Dr. Sherri J Tenpenny warns about the perils of vaccination

This is the Best Explanation of the Vaccine/Autism Connection I’ve Ever Heard!
Dr. Stephanie Seneff discusses the potential connection between vaccines and autism. It’s a hotly-debated topic. Here she gets specific into what ingredient in the vaccine may be linked to autism and other conditions. Find out what her research has found. You may think differently after watching this!

Trace Amounts: Ethyl Mercury | Educational Documentary
Has Ethyl Mercury Caused One of the Worst Health Crises in American History? During the past 20 years, the frequency of autism occurring in children has .
This video shares facts about the devastating mercury based preservative, thimerosal, used in vaccines. .
For this EP of Zero Doubt Zone, host Dane Sorenson, circles back to the subject of vaccines. On the heels of viewing the documentary, ‘Trace Amounts’, .
Courtesy of AAE tv Documentary filmmaker and researcher, Eric Gladen. Ethann and Eric discuss his new film “Trace Amounts”. They talk about the scientific .

Shots In The Dark: Silence on Vaccine
Following the increase in cases of autism and other immune disorders among some particularly vulnerable people, several recognized specialists are questioning the safety of large-scale vaccination. Despite the serious side effects, pharmaceutical companies, the medical profession and government authorities continue to bury their heads in the sand, refusing to see a serious problem. In Quebec, the United States and France, as in most industrialized countries, victims are almost without recourse despite the high toxicity of substances such as mercury and aluminum contained in vaccines. With this hard-hitting documentary, Lina B. Moreco highlights a very worrying public health problem.
Since they were introduced in the early 20th century, vaccines have been a tremendous medical and scientific success. Today perceived as a necessity, they are so familiar to us that their potential risks are rarely mentioned.
However, the stakes are significant. Based on recommendations of health agencies, North American children receive about 48 doses of 14 different vaccines before the age of 6 — double the amount prescribed 25 years earlier. Despite this extraordinary increase, few studies independent of the pharmaceutical industry have been conducted into their long-term side effects. This is a disturbing situation given the numerous toxins, including mercury and aluminum, contained in some commonly administered vaccines.
Several worried pediatricians and scientists are sounding the alarm. Some of the research underway indicates that vaccination is directly responsible for immune or neurological disorders among certain people genetically or neurologically predisposed to react badly to vaccine components. Cases of autism, multiple sclerosis, Guillain-Barré syndrome, macrophagic myofasciitis, encephalitis, paralysis and neuropathies indicate the seriousness of the situation.
Despite these findings, the pharmaceutical industry and government authorities deny there is a serious problem. Relying on perfunctory studies, some of which date back to the late 1920s, they reject out of hand any cause-and-effect relationship. Given the known fact that adding preservatives such as thimerosal (mercury) helps reduce production costs, the reaction of the pharmaceutical industry is at the very least puzzling. Preferring not to question a system that has proved its worth, a majority of the medical profession’s members reject any potential toxicity in vaccines.
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The truth about vaccines and Big Pharma, and info on GMO foods

Se cere demisia ministrului Sănătăţii. Motivul – legea care prevede vaccinarea obligatorie
In nicio țară din Uniunea Europeană nu sunt obligatorii 8 vaccinuri!
In Germania, Austria, Olanda, Spania, Portugalia, Marea Britanie, Luxemburg, Suedia, Danemarca, Italia, Irlanda, Finlanda, Suedia, Croația, Cipru, Estonia și Lituania, părinții decid dacă își vaccinează copiii!
Vaccinul este un medicament, dar poate fi și o armă biologică!
Peste 180.000 de copii vor fi obligați, in primul an de viață, să primească 26 de vaccinuri!
in cazul unui copil contraindicația definitivă la un vaccin sau mai multe se acordă numai la București de către GTCAV!
Pana la varsta de 6 ani un copil trebuie să primească 33 de vaccinuri!
Vaccinurile provoacă boli autoimune: un copil din patru suferă de o boală alergică, iar un copil din zece suferă de astm bronșic!
Asociația Pro Consumatori are o activitate de peste 27 de ani in domeniul apărării drepturilor și intereselor economice ale consumatorilor.


Vaccine News – Biopersistence in the Brain of Aluminum Nanoparticles from Vaccines

Dr. Brownstein on CDC Corruption: “I am Tired of Writing About This – I See Patients Damaged by Vaccines”
CDC Whistleblower Case Three Years Later: Nothing Happening
by Dr. Brownstein’s
Holistic Medicine
I honestly cannot believe I am still writing about this. It was three years ago that a senior CDC scientist, Dr. William Thompson, claimed whistleblower protection after he issued a statement that he and his fellow colleagues altered, hid, and threw out data that showed a direct association between the MMR vaccine and autism.

CDC Whistleblower Case Three Years Later: Nothing Happening
I honestly cannot believe I am still writing about this. It was three years ago that a senior CDC scientist, Dr. William Thompson, claimed whistleblower protection after he issued a statement that he and his fellow colleagues altered, hid, and threw out data that showed a direct association between the MMR vaccine and autism. In August, 2014, I wrote in a blog post, “Now, there may be proof that the CDC not only knew about the link between the MMR vaccine and autism but they changed the data in a landmark 2004 study to hide the damning data. What did the heads of the CDC do? They altered the data and reported in 2004 (1) that there was no association between autism and the MMR vaccine. Who wrote this article? William Thompson, PhD, the whistleblower, was one of the authors of that 2004 study. He is reported to be suffering with regret and remorse over the damage that has been done to our children over the last ten years.”
The data that was altered showed a whopping 240% increase in autism cases among African American males who received the MMR vaccine before 36 months of age. Furthermore, there was a 69% increase risk in any male injected with MMR before 36 months of age. Guess which racial group has the highest incidence of autism? If you guessed African American males, you win the prize. Guess who suffers with more autism, boys or girls? If you guessed boys, you win again.

‘I would rather be dead than like this’: Teenager’s agony as she is left wheelchair-bound and feeling like an ’80-year-old’ as her parents claim controversial HPV vaccine is to blame
Zara Beattie, from Wigton, Cumbria was once a promising football player
Now the teenager struggles to stand up on her own and is largely bed bound
Her parents believe her symptoms started after she had the HPV vaccine
Since the jab, Zara suffers heart palpitations and severe pain all over her body
Experts say there is no link between the HPV vaccine and chronic illness
By Daisy Dunne For Mailonline

Mia, left paralyzed from the neck down after suffering a reaction to the HPV vaccine, has no feeling in her arms or legs and is unable to lift her head. Her Mother, Gini Blesky, says the symptoms of her debilitating illness all began after being given Gardasil. Parents! Please BE INFORMED now and share this crucial information with everyone you love. View this newly available docu-series right now and protect your beloved children:
#Gardasil #Cervarix #RevolutionForChoice #HearThisWell #VaccineInjury #VAXXED #INFORMEDconsent

Johns Hopkins Researcher Releases Shocking Report On Flu Vaccines
In 2015, a whole new slew of flu vaccines found themselves getting approved by the Federal Drug Administration. This isn’t an uncommon practice; most flu vaccines pass inspection every year. It’s well known advice that has been passed down from doctor to patient that the flu vaccine is something that we all should get, but it has been quickly surfacing that what’s in the vaccines–especially those from 2015 and after–might actually be more damaging then simply rolling the dice on getting the flu.
The ingredient that is getting the most flack is called an adjuvant. The particular one involved is called Squalene, and it has been linked to auto-immune disease side effects. In fact, it may have been used during chemical attacks in the Gulf War. Symptoms include chronic fatigue, muscle aches, and neurologic damage.
While it may be a contested subject, it remains that we aren’t really sure what’s going into these vaccines we’re being convinced should be used. A scientist who has been working at the Johns Hopkins School of Medicine, released a report sharing his views on the subject. And they aren’t pretty.
Here is an excerpt from that summarizes aspects of Peter Doshi’s report. You can find the original report at the British Medical Journal’s site. Determine for yourself if the evidence he presents is credible or not…

WATCH NOW: – Watch this free 7-part miniseries featuring over 60 vaccine experts to hear both sides of the vaccine debate. Playing through August 23rd. WATCH NOW:

INFERTILITY – DISEASE – DEATH … Laura Hayes, Mother of vaccine-injured children, on a mission to end the vaccine holocaust! Share this LIFE-SAVING information with your loved ones and stay informed with this groundbreaking docu-series happening now:
“Would you allow something that could cause infertility, such as nonstick chemicals and solvents, to be injected into your child? Of course not. You know that you would never want to destroy your child’s future reproductive capabilities. However, millions of mothers across America are allowing doctors to inject their children with polysorbate 80, known to adversely affect fertility. And who knows what propylene glycol (antifreeze), Triton X100 (detergent), aluminum, mercury, foreign DNA fragments, and the myriad other vaccine ingredients do to one’s future reproductive ability, especially when injected in conjunction with polysorbate 80.
We know that the HPV vaccine has caused Primary Ovarian Failure (which is premature menopause) and amenorrhea (the prolonged cessation of a female’s menstrual cycle) in girls and young women, rendering them infertile, and possibly sterile for life. We know that tetanus vaccines given to girls and women in Kenya were laced with Human Chorionic Gonadotropin (HCG), rendering them sterile. How? Administering HCG via vaccination stimulates the production of antibodies to HCG, and these antibodies then cause the woman’s body to reject embryos, effectively sterilizing her. Such an HCG-laced tetanus vaccine is in actuality a contraception vaccine.
Do you think any of these Kenyan women was told that prior to vaccination? To add to the evilness and deception, the Kenyan women were given a 5-dose tetanus program spread over a number of years, versus the 2-3 dose norm. Clearly, those vaccines were being used for induced sterility and birth control without the girls’ and women’s knowledge or consent.
Does any parent or vaccine recipient really know what is in the vaccines being injected into their child or themselves? It’s no wonder pharmaceutical companies don’t test to see whether or not their vaccine products cause infertility, they already know the answer. Instead, they simply write “not tested for impairment of fertility” on their package inserts, and our unethical government regulators let them get away with that. Interestingly, we are seeing record numbers of couples struggling with infertility issues. Coincidence?
Would you allow something that could kill your baby to be injected into your otherwise healthy child? Of course not! Mothers would lay down their lives for their children, they don’t purposefully put them in harm’s way. However, millions of mothers across America are allowing doctors to inject their children with more and more vaccines, not knowing that each and every one carries the risk of death, even more so when combined, as they most often are.
Interestingly, we are seeing record numbers of babies who are dying before their 1st birthday in the U.S., including many of “SIDS” and “SBS” (the labels that unethical doctors and unethical medical examiners use for vaccine-induced deaths instead of calling them what they are…i.e. vaccine-induced deaths). Coincidence?
Now that we have discussed what is actually in vaccines, let’s talk once more about how parental instincts have been demeaned, grossly manipulated, and obliterated, specifically, about how parents have been grievously lied to and misled, to the point where parents are now allowing things that simply do not make sense.
Imagine looking from the outside in, and seeing a tiny newborn, small infant, or trusting toddler, being held down, painfully stuck with a needle multiple times, screaming so that its face is beet red with tears, all while the child’s parents not only watch, but due to being lied to and coerced, they participate in this atrocity! What must this do to the psyche and stress hormones of a child to have this happen, time and again, while the person he trusts most is not only allowing it, but participating in it?
What would you say if you walked by the window to my house, peered in, and saw my husband and me holding down our tiny baby on the dining room table, then roughly jabbing and injecting it multiple times with toxic cocktails and true witches’ brews of ingredients…all while our baby, or child of any age, screamed bloody murder, trying to escape our grip and savagery? I imagine you would whip out your cell phone, call the police, then try to barge into our home to stop the abuse! How is what I just described any different than what goes on every minute of every day in doctors’ offices and hospitals in our country and across the world? To be very clear, it isn’t.
To state it very plainly, vaccination is child abuse in the form of medical assault and battery. With regard to adults, when vaccination is carried out against one’s will or wishes, say for school admittance, job requirements, elder care and housing, or military admission, or when carried out with one who is hesitant, or with one who is unsuccessful in resisting and refusing, it also meets the legal definition for assault and battery.
We must begin to label these vaccine atrocities for what they are: blatant and inexcusable child abuse; medical assault and battery; and when death is the result for the vaccine recipient, involuntary manslaughter. These vaccine-induced injuries, illnesses, and deaths are iatrogenic in nature, meaning they are caused by doctors and nurses. Vaccinations are crimes against humanity, and there is no time to mince words about this fact.”
This is a MUST SEE docu-series – totally free!
#RevolutionForChoice #VaccineInjury #TheTruthAboutVaccines #VAXXED #Infertility

STUDY: Reality Trumping Establishment Vaccine “Facts”
The past week has offered glimpses of hope for the growing number of people who know they are being lied to by the mainstream medical establishment about vaccine safety. More people are now aware that the kind of rigorous testing required for drugs to be put on the market does not apply to vaccines, or that vaccines like the HPV shot were not properly tested against a saline placebo before approval by the US Food and Drug Administration (FDA).
Yet, the medical establishment continues to omit these facts and instead focuses on why vaccine hesitancy is on the rise. Studies are being done in an attempt to understand vaccine hesitancy and come up with solutions to the “problem” of poor vaccine uptake. In 2014, the Boston Globe ran the headline Doctors Still Hesitant to Urge HPV Vaccine for Teenagers, highlighting a survey from the US Centers for Disease Control and Prevention (CDC), in which the agency stated that the inoculation rate is ‘unacceptably low.’ In 2015, NPR ran the story titled Doctors, Not Parents, Are the Biggest Obstacle to the HPV Vaccine in response to a study published in the journal Cancer Epidemiology, Biomarkers & Prevention, which found that more than a quarter of pediatricians and family doctors do not strongly endorse the HPV vaccine.
A new study in the journal PLOS One titled Misinformation Lingers in Memory: Failure of Three Pro-vaccination Strategies is an eye-opener at how clueless the medical establishment appears to be as to why its vaccine propaganda is being rejected. In this study, the researchers compared three strategies in vaccine promotion: a) contrasting myths vs. “facts,” b) employing “fact” and icon boxes, and c) showing images of non-vaccinated sick children. It should be noted that when the study’s authors refer to “facts,” they are using the term to mean vaccine propaganda. Beliefs in the autism-vaccine link and in vaccines side effects, along with intention to vaccinate a future child, were evaluated both immediately after the “correction intervention” and after a 7-day delay to reveal possible backfire effects. The study concluded the following:
“Results show that existing strategies to correct vaccine misinformation are ineffective and often backfire, resulting in the unintended opposite effect…”

Study – The Introduction of Diphtheria-Tetanus-Pertussis and Oral Polio Vaccine Among Young Infants in an Urban African Community: A Natural Experiment
•When DTP and OPV were introduced in Guinea-Bissau in 1981, allocation by birthday resulted in a natural experiment of being vaccinated early or late.
•Between 3 and 5 months of age, children who received DTP and OPV early had 5-fold higher mortality than still unvaccinated children.
•In the only two studies of the introduction of DTP and OPV, co-administration of OPV with DTP may have reduced the negative effects of DTP.
Few studies have examined what happened to child survival when DTP and OPV were introduced in low-income countries. These vaccines were introduced in 1981 in an urban community in Guinea-Bissau from 3 months of age in connection with 3-monthly weighing sessions. Children were therefore allocated by birthday to receive vaccines early or late between 3 and 5 months of age. In this natural experiment vaccinated children had 5-fold higher mortality than not-yet-DTP-vaccinated children. DTP-only vaccinations were associated with higher mortality than DTP + OPV vaccinations. Hence, DTP may be associated with a negative effect on child survival.
Among 3–5-month-old children, having received DTP (±OPV) was associated with a mortality hazard ratio (HR) of 5.00 (95% CI 1.53–16.3) compared with not-yet-DTP-vaccinated children. Differences in background factors did not explain the effect. The negative effect was particularly strong for children who had received DTP-only and no OPV (HR = 10.0 (2.61–38.6)). All-cause infant mortality after 3 months of age increased after the introduction of these vaccines (HR = 2.12 (1.07–4.19)).
DTP was associated with increased mortality; OPV may modify the effect of DTP.

Dr. Buchwald testimony before the Quebec College of Physicians Medical Board:
Dr. Gerhard Buchwald takes the stand
A physician from Germany, Dr. Buchwald testifies through an interpreter. Dr. Lanctot tables his credentials as well as a copy of his book entitled “Vaccination: Business Based on Fear”. He is recognized as an expert on vaccination by the Committee.
Dr. Buchwald testifies that his experience includes being a medical counselor to an association of parents whose children have been injured or killed by vaccinations. He adds that he is aware of a thousand vaccination related injury cases and has had personal contact with 350 cases. In 150 of these cases, he wrote the medical opinion and acted as an advisor during the legal proceedings.
Dr Lanctot (L).: If you take this stand in your country, have you been reprimanded by the medical authorities?
B.: I wrote a paper entitled, “Vaccinations: A Crime Against our Children”. I received written reprimands from the College of Physicians… In Germany, we have a law called “Kronegesetz” in the Civil Code, which stipulates that everyone has the right to freely voice his or her opinion. When I was fed up with this nonsense with the College, I drew their attention to the fact that their responses were actually a breach of those sections of the law. German judges, who deal with these issues, are very touchy on this issue… It is impossible to suppress the free speech of a physician in a free country which is why the College knew that it would lose. They also knew that the press would really have a field day. Since then I’ve heard nothing more…
L.: You mentioned earlier that the first criterion in medicine is to do no harm… And you referred to these ethics in
He continues with a brief history of his experiences in general and describes how he got interested in the whole question of immunization. He recalls that after graduating from medical school, he was a supporter of vaccination policies, as was everyone else he knew. Then he relates to the Committee the story of the eldest of his three children, born in 1957, who at eighteen months received a smallpox vaccination and who, eight days later was no longer able to stand up in his crib. Until then, his son’s development had been absolutely normal:
“He fell sick with a post-vaccination encephalitis, and ever since, I have a completely destroyed human being at home.”
It was at that time that someone approached him to become a member of a protective association in Germany. It was through this group that he got to know other vaccination damage cases.

Study – Human papillomavirus vaccination and risk of autoimmune diseases: A large cohort study of over 2million young girls in France.
Among 2,252,716 girls, 37% received HPV vaccine and 4,096 AID occurred during a mean follow-up time of 33months. The incidence of AID was not increased after exposure to HPV vaccination, except for Guillain-Barré syndrome (GBS) (incidence rate of 1.4 among exposed [20 cases] versus 0.4 per 100,000 PY among unexposed [23 cases]; adjusted HR: 3.78 [1.79-7.98]). This association persisted across numerous sensitivity analyses and was particularly marked in the first months following vaccination. Under the hypothesis of a causal relationship, this would result in 1-2 GBS cases attributable to HPV vaccine per 100,000 girls vaccinated.
Our study provides reassuring results regarding the risk of AID after HPV vaccination, but an apparently increased risk of GBS was detected. Further studies are warranted to confirm this finding.

Study – Detection of contaminants in cell cultures, sera and trypsin.
The aim of this study was standardization and application of polymerase chain reaction (PCR) for the detection of contaminants in cell cultures, sera and trypsin. Five PCR protocols were standardized to assess the presence of genetic material from mycoplasma, porcine circovirus 1 (PCV1), bovine leukemia virus (BLV) or bovine viral diarrhea virus (BVDV) in cell culture samples. PCR reactions for the genes GAPDH and beta-actin were used to evaluate the efficiency of nucleic acid extraction. The PCR protocols were applied to 88 cell culture samples from eight laboratories. The tests were also used to assess potential contamination in 10 trypsin samples and 13 fetal calf serum samples from different lots from five of the laboratories. The results showed the occurrence of the following as DNA cell culture contaminants: 34.1% for mycoplasma, 35.2% for PCV1, 23.9% for BVDV RNA and 2.3% for BLV. In fetal calf sera and trypsin samples BVDV RNA and PCV1 DNA was detected. The results demonstrated that cell culture, sera and trypsin used by different laboratories show a high rate of contaminants. The results highlight the need for monitoring cell cultures and controlling for biological contaminants in laboratories and cell banks working with these materials.

C-Span – April 6, 2000
Autism and Childhood Vaccines Witnesses testified about a theory that routine vaccinations may cause autism in a growing number of children. Parents spoke about their experiences with their own autistic children. Medical experts and researchers then testified about the scientific evidence of a link between vaccines and autism, often disagreeing on whether a causal link existed.

Alfred Lambremont Webre – EXPERT PANEL Forced Adult vaccinations are component of extermination program Refuse all vaccines

Vaccines-The True Weapons Of Mass Destruction
Dr.Rebecca Carley.
ADVERSE REACTIONS to immunizations are more common than many people realize.
Please visit her website:

Biopersistence in the Brain of Aluminum Nanoparticles from Vaccines
Posted by Merinda Teller, Ph.D, MPH on Aug 14, 2017
In the 1990s, French clinicians and researchers began noticing and reporting on a mysterious inflammatory muscle disorder with a distinctive pathological pattern that later earned the name “macrophagic myofasciitis” or MMF.1 Myofasciitis refers to inflammation of muscles and their connective tissue (fascia).
Initially, the cause and features of MMF were unknown. Subsequent research by French investigators elucidated that the deltoid muscle lesions characteristic of MMF were secondary to intramuscular injection with vaccines containing aluminum hydroxide adjuvants.2 The lesions revealed both an ongoing local immune reaction along with long-term persistence of aluminum hydroxide at the injection site.2
An ongoing series of admirably methodical studies also have confirmed a number of other post-vaccination clinical symptoms associated with MMF.3 These disabling health problems include not just muscle pain but joint pain, chronic fatigue, autonomic nervous system dysfunction, autoimmunity, and cognitive dysfunction.4 The cognitive deficiencies experienced by MMF patients mirror the cognitive impairments that have been observed to result from chronic exposure to aluminum particles.5 Together, all of these dysfunctions are “paradigmatic” of an emerging aluminum-adjuvant-related syndrome that has come to be known as ASIA (autoimmune/inflammatory syndrome induced by adjuvants).

Finally! I’ve teased around the real reason polio began to paralyze people in the late 1800s and in this video, I explain it completely. It’s a crazy simple answer that’s so obvious, most people have looked right past it.
Watch Part 1:
Watch Part 2:
Watch Part 3:
Watch Part 4:
Watch Part 5:
Watch Part 6:

#VaxXed #Tennessee #flu #medical
chiropractor fed up with vaccine harm!
Dr Humphries outs flu shot fail:

#VaxXed #NorthCarolina #Nebraska