Scientists Hoped To Increase Vaccine Rates by Publicizing Side Eeffects; Instead People Chose NOT To Vaccinate

Vaccines
Source: NaturalNews.com
David Gutierrez
June 27, 2016

In a recent study published in the journal Vaccine, researchers from the University of Missouri had hypothesized that directing people to information on vaccine side effect reports would reassure people that reported side effects are rare and may have nothing to do with vaccination at all. This would then make people more likely to get the vaccine in question.

“One of the issues in vaccine acceptance is trust,” researcher Laura Scherer said. “Individuals, parents and vaccine opponents lack trust that doctors and the government have done sufficient research to validate the safety of vaccines. By educating participants about the VAERS system, we thought that this might increase trust that the Centers for Disease Control [and Prevention (CDC)] are doing everything that they can to research and document vaccine harms.”

Instead, the researchers found that letting people read the side effect reports made them less trustful of vaccines and the CDC, and less likely to get vaccinated.

Are more informed patients less likely to vaccinate?

The study was conducted on more than 1,200 people who were eligible to receive the Human Papillomavirus (HPV) vaccine. One-third of the participants were provided with the standard vaccine statement that all patients are supposed to receive before getting the HPV shot. Another third were provided with the vaccine statement, plus information on the Vaccine Adverse Event Reporting System (VAERS) and a summary showing that in 2013, there were 31 serious adverse events reported among 10 million HPV vaccinations: 24 reports of disability and 7 reports of death. The final third received everything the second group received, plus detailed accounts of the 31 cases.

The VAERS is a safety reporting system developed by the CDC. It allows anyone to report any adverse event that happens following a vaccination, without needing to prove that the vaccine caused the effect. The database is available online for anyone to view.

“Since anyone can report anything to VAERS for any reason, the VAERS reports contain incidents of serious adverse events that may not have anything to do with the vaccine,” Scherer said. “We thought that by having people read the actual reports, they would see that there are very few reported serious events, and that the vaccine may not have even caused the event. Taken together, we felt this might make participants feel more assured that vaccines are safe—but in fact, what we found was the opposite.”

Participants who received the VAERS report summary reported being slightly more likely to get the HPV vaccine than those who only received the vaccine statement. But participants who read the adverse event reports were less likely to vaccinate, and reported decreased trust in CDC promises of vaccine safety.

Mistrust in health agencies fuels vaccine refusal

Notably, vaccine mistrust increased even among participants who didn’t think the HPV vaccine had even caused the adverse events they read about.

“When participants read the incident reports, there was a marked reduction in their willingness to vaccinate—even though most participants believed the vaccines caused few or even none of the deaths,” Scherer said. “Stories about vaccine harms can influence vaccine acceptance even when people don’t completely believe them.”

The findings build on prior research showing that people become less likely to vaccinate when they think public health agencies are exaggerating the safety of vaccines. A 2014 study in the Journal of Risk Research found that during Israel’s 2013 polio outbreak, many parents who normally complied with all vaccine recommendations refused to give their children the extra course of polio vaccine recommended by the government.

The most common reasons cited for refusal were concerns about vaccine safety and a feeling that the government had not really explained the need for the extra vaccine. Parents were particularly turned off by assurances that there were “zero side effects,” interpreting such blanket statements as patently false and condescending.

Sources for this article include:
http://medicalxpress.com/news/2016-06-vaccines-adherence.html
https://www.sciencedaily.com/releases/2014/12/141218081121.htm

Read More At: NaturalNews.com

Vaccines’ Dark Inferno: What Is Not on Insert Labels?

Vaccines' Dark Inferno: What Is Not on Insert Labels?
Source: GreenMedInfo.com
By: Gary Null, PhD and Richard Gale

Originally published on Townsendletter.com

The vast majority of scientists, physicians, nurses, and public health educators trust that the ingredients in a vaccine have been individually and synergistically proven safe and effective. The public believes that these vaccines, aside from their specified virus(es), are sterile solutions, free from undesirable contaminants not listed on the manufacturers’ package inserts. When the pediatrician injects a vaccine into the muscle of a child, the parents’ unquestioning faith is that this is the case. In other words, we want to believe that vaccines have been generated under perfect conditions for the safety of children and ourselves.

What Is Not on Insert Labels?

Our investigation shows that most people do not know what is actually in a vaccine: the active ingredients listed on product labels, the inert ingredients, and, most important, the hidden ingredients. Even more remote is taking the time to actually study the subject matter, review the scientific literature, and discover the truth for oneself. To our amazement, that truth was easy to find. But it is a truth that will scare the hell out of you.

Imagine sitting down to eat veal parmigiana, and a video is placed on your table and used as a living reality recipe instead of the actual meal. This video displays every step in the calf’s life, from its birth to the parmigiana on your plate. You witness how the little creature was starved of its natural nutrients, kept in a tiny stall, grossly malnourished and deformed, filled with antibiotics, diseased and suffering complete privation until finally slaughtered, cooked, and served on your plate. Would your appetite be the same? Would you still desire the parmigiana?

Conveniently, we rarely ask, where does our food come from? How and where was it grown? What was sprayed on it prior to our consumption? Thus we are going to re-record something that even most top health educators and opinion leaders on vaccines are unaware of: what goes into the making of vaccines, and what is hidden from you that should give you pause? Afterward, ask yourself: do you want vaccines in your body?

For the most in-depth, honest, scholarly, and objective examination of the methods by which vaccines and their hidden ingredients are prepared, we turn to award-winning British investigative medical journalist Janine Roberts, who paints an entirely different picture of the darker inferno in vaccines that does not appear on product labels. This is the same Janine Roberts who brought to the world’s attention blood diamonds, genocide in the Congo, and the destruction of aboriginal cultures by the Australian government.

Roberts’s account of conversations between high-level members from the World Health Organization (WHO), federal health agencies, and expert vaccine scientists who determine whether a certain vaccine will be approved, is horrid. Her investigations are based on official meeting documents and her attendance at emergency vaccine meetings, and confirm that our world’s vaccine and health experts agree that there is no solution in sight to resolve the potential threats posed by these hidden ingredients.1

The story begins with the vaccine industrial complex’s attempt to reduce manufacturing costs by seeking government approval to use cancerous cell lines in the development of vaccines. The industry’s rationale is that cancerous cells are “immortal.” Current vaccine methodology relies on animal cells, such as fertilized hen embryos and monkey kidneys, that die quickly in culture. Using cancerous cell lines is also much cheaper than relying on the purchase of animals, especially monkeys, that need to be sacrificed for vaccine substrates.

Roberts records two separate meetings – a meeting of the Vaccine and Related Biological Products Advisory Committee on November 9, 1998, and a subsequent gathering of the Evolving Scientific and Regulatory Perspective Workshop less than a year later. The conversations were conducted at a scientific level between top officials and expert scientists from the FDA, Center for Biologics Evaluation and Research (CBER), the National Institute of Allergies and Infectious Diseases (NIAID), the WHO, and others, each providing evidence and/or confirmation that all vaccines are dangerously contaminated.

Conversations focused primarily on the influenza, MMR, and yellow fever vaccines, which rely on fertilized chicken eggs for their culturing viruses. Fertilized chicken eggs, while ideally suited for culturing certain viruses for vaccines, such as the influenza and MMR vaccines, are also living incubators for large numbers of known and unknown viruses in the animal kingdom. While these do not transmit from their animal host to humans naturally, they nevertheless are sequential genetic codes that, when injected into the human body, have the potential for any number of unpredictable adverse effects by interfering or merging with the codes of human cells.

Vaccine research is at best a primitive science, because it involves injecting into the bloodstream foreign substances, chemical and genetic, that would not otherwise naturally enter the body. When we bring into the equation the enormous amount of known and unknown genetic material and foreign proteins that vaccines introduce into the body, and then consider the rapid increase in epidemics raging through the American population – adult diabetes in children, large numbers of various inflammatory and immune deficiency diseases, asthma and new allergies, severe gastrointestinal disorders (e.g., leaky gut syndrome and Crohn’s disease), chronic fatigue syndrome, and many different neurological disorders (e.g., autism, ADD and ADHD, Parkinson’s, Alzheimer’s) – we must step back and reconsider their causes. We should avoid the kind of faith that the vaccine industrial complex has in its determinist, reductionist perspective of genetic materialism to find these answers without taking into account the bombardment of toxic chemicals such as vaccine adjuvants and preservatives, extraneous genetic material, pathogenic organisms, and foreign genetic fragments that assault our bodies from shortly after birth into old age.

For some time, it was known that the enzyme reverse transcriptase (RT) was present in final vaccine solutions. RT has been used to this day as an indicator that there is a presence of a retrovirus. During the meeting’s proceedings, the WHO decided to withhold public announcement of such genetic contamination, in this case concerning the MMR vaccine; not to remove it from the market; and, in the meantime, continue safety studies at various laboratories.

Roberts reports that Dr. Arifa Khan from the FDA confirmed:

The RT activity in the vaccine was associated with retrovirus particles from two separate viral strains: Avian Leuokosis Virus (ALV) and Equine Arteritis Virus (EAV). The former was especially disturbing because ALV is a leukemia cancer, and Dr. Khan stated: “There was a theoretical possibility that the virus [ALV] could … infect the [human] cell.”

In summary, this means the ALV genetic code could integrate with human DNA, hence causing some kind of cancer.

The FDA’s reassurance that the ALV RT activity was safe is based on laboratory observations that there was no viral–human DNA merger activity for “a full 48 hours.” This kind of assurance is almost nonsensical and flies in the face of scientific reasoning, since cancers can take years to develop!

As a side note, RT activity is one of the stalwarts of the HIV/AIDS hypothesis. An article, “Influenza & Nursing Home Deaths” published by Canada’s Vaccine Risk Awareness Network, reports that some studies, and even some vaccine package inserts, “indicate that vaccinations increase HIV viral replication.”2 This means that all vaccines stimulate a strong suppressive effect on the immune system. Under stress conditions, viruses turn hyperactive and increase their ability to replicate.

The other risk stated by the FDA official was the possibility of the ALV sequence’s merging with the measles virus, hence creating a completely new, mutant, and dangerous virus. (This could also apply equally to the H1N1 swine flu and any other flu vaccines). As an aside, the world-renowned British geneticist Dr. Mae-Wan Ho from the Institute of Science in Society wrote:

“Vaccines themselves can be dangerous, especially live, attenuated viral vaccines or the new recombinant nucleic acid vaccines, they have the potential to generate virulent viruses by recombination and the recombinant nucleic acids could cause autoimmune disease.”3

During the meeting, Dr. Andrew Lewis, then head of the DNA Virus Laboratory in the Division of Viral Products, confirmed: “All the egg-based vaccines are contaminated. … These fertilized chicken eggs are susceptible to a wide variety of viruses.” The participants also realized that only a very small fraction of these small contaminants have been identified and there are likely hundreds more to be discovered.

Roberts found a 2001 CDC report showing that RT investigative studies for both the ALV and EAV retroviruses were conducted in 100 patients receiving the MMR vaccine. They found undesirable “RT activity in all measles vaccine lots from different manufacturers tested.” Their conclusion is that “this occurrence is not sporadic and that vaccine recipients may be universally exposed to these [chicken] retroviral particles.”

In a separate National Institutes of Health transcript of a meeting, Dr. Conroy of the World Health Organization stated that EAV viruses are found in all fertilized chicken eggs. There appears to be little change in the scientific protocol for making the influenza, MMR, and yellow fever vaccines. The current release of intramuscular H1N1 vaccines for the global market relies on the use of fertilized chicken embryos. This includes each of the approved vaccines by CSL, Medimmune, Novartis, and Sanofi-Pasteur, as well as GlaxoSmithKline’s, if and when it is approved in the US.

A later meeting of the FDA’s Scientific and Regulatory Perspective Workshop, without the press, was convened on September 7, 1999, in Washington, DC, and attended by “representatives from all the largest public health institutions in the West.” The following are summaries of key points and statements raised during this meeting as recorded in Janine Roberts’s invaluable book Fear of the Invisible.

  • It was reconfirmed that vaccines are “widely contaminated by viral and DNA genetic code fragments, many viruses and proteins.” There was expressed concern that these may also contain prions (tiny proteins responsible for incurable diseases and neurological disorders in both humans and animals) and oncogenes (a gene that turns normal cells into cancerous ones). One attendee, Dr. Goldberg, stated, “There are countless thousands of undiscovered viruses, proteins and similar particles. We have only identified a very small part of the microbial world – and we can only test for those we have identified. Thus the vaccine cultures could contain many unknown particles.”
  • Dr. Andrew Lewis of the FDA said that a brand-new monkey-human mutant virus was created during the course of developing an adenovirus vaccine with adenvovirus-SV40 hybrid viruses. Dr. Lewis also worried that “foreign cellular DNA” common in childhood vaccines could include “viral oncogenes” capable of causing cancer.
  • The scientists presented a question to themselves as to whether an attenuated vaccine strain could revert into a variant virus capable of replicating so fast that it would cause AIDS. They agreed that they were unable to answer this question.
  • On the question of whether mutation events could occur in children after vaccination, the answer was: “Recombination among a variety of viruses [contaminant viruses] and cells co-infected in tissue culture is not uncommon.” What this basically means is that because it is “not uncommon” for genetic codes of both contaminant viruses and living cells to recombine and create mutations in laboratory cultures, this can certainly occur in a child’s body after vaccination.
  • Dr. Hana Golding, chief of CBER’s Laboratory of Retrovirus Research, raised the fear that although DNA fragment contaminants in vaccines may be thought dead, they could remain active and dangerous. This meant that the codes of these contaminants could combine in vaccines and create new mutant strains of pathogens.
  • Dr. Leonard Hayflick, a virologist at both Stanford and the University of California, San Francisco, raised a concern that the common primary culture used for making vaccines with animals and bird embryos has created a situation where it is “apparent that these cells contained many unwanted viruses, some of which were lethal to humans.” This was especially worrisome of those vaccines, such as polio, which still rely on monkey kidney cells that have contributed to widespread death and illness.
  • One of the UK’s leading vaccine experts, Dr. Phil Minor from the National Institute of Biological Standards and Control, noted that some cases of polio vaccine are polluted with more monkey virus, SV40, than actual poliovirus. Although the uninitiated who are not informed about closed-door vaccine science have been led to assume that SV40 was no longer in polio vaccines at the time of this meeting, the conversations confirmed that it was still in use. This is another example of conspiracy at high levels among the vaccine industrial complex and government health officials to withhold information that directly affects the citzens’ well-being.
  • Dr. Rebecca Sheets, from the CBER’s laboratory responsible for monitoring vaccine safety, stated that the national health organi­zations had no control over how vaccines were made. In short, they could make recommenda­tions, but the vaccine industrial complex was free to act as it chooses.
  • It is impossible to remove DNA contaminants from vaccines. Although weight limits for contaminating DNA were set by the FDA as far back as 1986, vaccine makers have never been able to reach that goal. The CDC decided to limit its weight recommendation to cancerous cell lines and then increase the other DNA contamination allowance 100-fold. However, these limits are only “recommendations,” and therefore the FDA cannot enforce them. Vaccine manufacturers are still free to choose whether to take scientific measures to reduce contaminants.
    Remember, this contamination limit (10 nanograms) only applies to a single vaccine. Children today are inoculated with many vaccines before entering school, each with unique DNA and viral contaminants due to the specific cell substrates used for a given vaccine. This toxic genetic soup is what then flows through a vaccinated person’s body.
  • One government health official stated: “I chaired the committee that licensed the chickenpox vaccine, and it [residual DNA] was actually an issue that we considered at that time. We looked among recipients of the vaccine for evidence of an autoimmune response associated with the DNA included in that vaccine. … Actually, we didn’t look, we asked the company to look and they did not find one.” Well, of course, only such assurances can be convincing if in fact the company conducted the study, for which there was no compulsory reason to. Clearly, what the official is saying is that health authorities may not possess any documents that such a study actually exists.
  • Can vaccine DNA contamination cause cancer or autoimmune disease? A meeting participant responded: “When you consider that almost every one of these vaccines is injected right into the tissue … I think you couldn’t do much more to get the DNA expressed [to get contaminating DNA taken up by human cells] than to inject it into a muscle in the way it’s being done.”
  • Again, CBER’s Dr. Sheets: “I think that the vast majority of licensed vaccines, US licensed vaccines, have not been tested for residual DNA.”
  • A more frightening question was raised as to whether there has been any presence of foamy virus. Foamy virus (HFV in human form and its more widespread parent SFV from monkeys), although not infectious, is a deadly carcinogen. To the participants’ knowledge, no laboratory has ever searched for it in vaccine preparations.
  • The meeting confirmed that a particular cell, “which under many conditions is neoplastic [tumor causing],” has been licensed for the production of both injectible and oral polio vaccines in the US, Thailand, Belgium, and France. Therefore, these vaccines carry the high risk of containing cancer-causing oncogenes.

    Continue Reading At: GreenMedInfo.com

80+ Studies Outlining Some Of The Dangers Of Vaccinations

Image Source: RevolutionOfTheMind.org

TheBreakaway
By: Zy Marquiez
December 14, 2015

[Editor’s Note]

Below follow a diverse set of studies that detail some of the dangers in vaccinations.

The information was found at LearnTheRisk.org

Although most of the links as of this date are currently working, a handful of links below do not work.  The links that do not work have strikethroughs running through them.  In many cases, was able to find another link that provides the same information, and that particular link is shown below the one that didn’t work.   This is so any person gathering data is still able to find said information and sift through it as needed.

If the title of the study has a strikethrough through it, then the information is not provided any longer.  The link/data is still shown in order to show the educated reader that there was at one point data in said link, but it has been erased/moved for whatever reason.  Hope that helps.
————————————————————–

Studies on the Dangers of Vaccine Ingredients:

Adverse events following immunization with vaccines containing adjuvants. Immunol Res, 2013

http://www.ncbi.nlm.nih.gov/pubmed/23576057

Investigating Viruses in Cells Used to Make Vaccines; and Evaluating the Potential Threat Posed by Transmission of Viruses to Humans FDA.gov

http://www.fda.gov/biologicsbloodvaccines/scienceresearch/biologicsresearchareas/ucm127327.htm

Dangers of Aluminum Studies:

Administration of aluminium to neonatal mice in vaccine relevant amounts is associated with adverse long term neurological outcomes. Journal of Inorganic Biochemistry, 2013

http://www.ncbi.nlm.nih.gov/pubmed/23932735

Aluminum adjuvant linked to gulf war illness induces motor neuron death in mice. Neuromolecular Medicine, 2007

http://www.ncbi.nlm.nih.gov/pubmed/17114826

Aluminum and Alzheimer’s disease: after a century of controversy, is there a plausible link? Journal of Alzheimer’s Disease, 2011

http://www.ncbi.nlm.nih.gov/pubmed/21157018

Aluminium and breast cancer: Sources of exposure, tissue measurements and mechanisms of toxicological actions on breast biology Journal of Inorganic Biochemistry, 2013

http://www.sciencedirect.com/science/article/pii/S0162013413001608%20

Aluminum hydroxide injections lead to motor deficits and motor neuron degeneration Journal of Inorganic Biochemistry, 2010

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2819810/?tool=pubmed

Aluminum Vaccine Adjuvants: Are They Safe? Current Medical Chemistry, 2011

http://www.ncbi.nlm.nih.gov/m/pubmed/21568886/

Elevated brain aluminium and early onset Alzheimer’s disease in an individual occupationally exposed to aluminium: a case report. Journal of Medical Case Reports, 2014

http://www.jmedicalcasereports.com/content/8/1/41

Mechanisms of aluminum adjuvant toxicity and autoimmunity in pediatric populations. Lupus. 2012

http://www.ncbi.nlm.nih.gov/pubmed/22235057

Dangers of Aborted Fetal Tissue Studies:

Danger of Fetal Tissue in Vaccines. Sound Choice Pharmaceutical Institute, September 2014

http://s3.amazonaws.com/soundchoice/soundchoice/wpcontent/uploads/SCPIADvaccinewebsite.pdf

Dangers of Polio Vaccine and Cancer Studies:

Medulloblastoma in childhood: an epidemiological study. Journal of Neurosurgery, 1984

http://www.ncbi.nlm.nih.gov/pubmed/6470775?dopt=Abstract

Poliovirus Vaccination during Pregnancy, Maternal Seroconversion to Simian Virus 40, and Risk of Childhood Cancer. Oxford Journals Medicine & Health American Journal of Epidemiology

http://aje.oxfordjournals.org/content/160/4/306.abstract

Simian Virus 40 Infection of Humans. Journal of Virology

http://jvi.asm.org/content/77/9/5039.full

Dangers of Chickenpox Vaccine:

Review of the United States universal varicella vaccination program: Herpes zoster incidence rates, costeffectiveness, and vaccine efficacy based primarily on the Antelope Valley Varicella Active Surveillance Project data. Vaccine, 2013

http://www.ncbi.nlm.nih.gov/pubmed/22659447

Dangers of Hepatitis B Vaccine:

Autoimmune hazards of hepatitis B vaccine. Autoimmun Rev, 2005

http://www.ncbi.nlm.nih.gov/pubmed/15722255

Hepatitis B triple series vaccine and developmental disability in US children aged 19 years. Journal Toxicological & Environmental Chemistry, 2008

http://www.tandfonline.com/doi/abs/10.1080/02772240701806501#preview

Hepatitis B vaccine induces apoptotic death in Hepa16 cells. Apoptosis, 2012

http://www.ncbi.nlm.nih.gov/pubmed/22249285

Recombinant hepatitis B vaccine and the risk of multiple sclerosis. Neurology Journal of the American Academy of Neurology, 2004

http://www.neurology.org/content/63/5/838.abstract

Rheumatic disorders developed after hepatitis B vaccination. Oxford Journals Medicine & Health Rheumatology, 1999

http://rheumatology.oxfordjournals.org/content/38/10/978.long

Dangers of Haemophilus B (HIB) Vaccine:

A causal association between Haemophilus influenzae type b (Hib) vaccine and diabetes. Autoimmunity, 2003

http://www.ncbi.nlm.nih.gov/pubmed/12911277

Association between type 1 diabetes and Hib vaccine. British Medical Journal, 1999

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1116914/

Dangers of Thimerosal Studies:

Administration of thimerosal to infant rats increases overflow of glutamate and aspartate in the prefrontal cortex: protective role of dehydroepiandrosterone sulfate. Neurochem Res. 2012

http://www.ncbi.nlm.nih.gov/pubmed/22015977

Comparison of Blood and Brain Mercury Levels in Infant Monkeys Exposed to Methylmercury or Vaccines Containing Thimerosal. Environmental Health Perspectives, August 2005

http://www.ncbi.nlm.nih.gov/pubmed/16079072

Integrating experimental (in vitro and in vivo) neurotoxicity studies of lowdose thimerosal relevant to vaccines. Neurochem Res. 2011

http://www.ncbi.nlm.nih.gov/pubmed/21350943

Lasting neuropathological changes in rat brain after intermittent neonatal administration of thimerosal. Folia Neuropathology, 2010

http://www.ncbi.nlm.nih.gov/pubmed/21225508

Maternal thimerosal exposure results in aberrant cerebellar oxidative stress, thyroid hormone metabolism, and motor behavior in rat pups; sex and strain dependent effects. Cerebellum. 2012

http://www.ncbi.nlm.nih.gov/pubmed/22015705

Neonatal administration of thimerosal causes persistent changes in mu opioid receptors in the rat brain. Neurochem Res. 2010

http://www.ncbi.nlm.nih.gov/pubmed/20803069

Neurodevelopmental disorders following thimerosal containing childhood immunizations: a followup analysis International Journal of Toxicology, 2004

http://www.ncbi.nlm.nih.gov/pubmed/15764492

Persistent behavioral impairments and alterations of brain dopamine system after early postnatal administration of thimerosal in rats. Behav Brain Res, 2011

http://www.ncbi.nlm.nih.gov/pubmed/21549155

Thimerosal induces neuronal cell apoptosis by causing cytochrome c and apoptosisinducing factor release from mitochondria. International Journal of Molecular Medicine, 2006

http://www.ncbi.nlm.nih.gov/pubmed/16273274

Thimerosal Exposure and the Role of Sulfation Chemistry and Thiol Availability in Autism Int. J. Environ. Res. Public Health 2013

www.mdpi.com/journal/ijerph

Dangers of Measles, Mumps, Rubella (MMR) Vaccine:

Nonfebrile Seizures after Mumps, Measles, Rubella, and Varicella Zoster Virus Combination Vaccination with Detection of Measles Virus RNA in Serum, Throat, and Urine.  Clinical and Vaccine Immuniology, 2013

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3697452/

Two successive outbreaks of mumps in Nova Scotia among vaccinated adolescents and young adults. CMAJ, 2006

http://www.ncbi.nlm.nih.gov/pubmed/16940266

Waning of Maternal Antibodies Against Measles, Mumps, Rubella, and Varicella in Communities With Contrasting Vaccination Coverage. Oxford Journals Medicine & Health The Journal of Infectious Diseases, 2013

http://jid.oxfordjournals.org/content/early/2013/04/29/infdis.jit143.full

Mumps vaccination coverage and vaccine effectiveness in a large outbreak among college students–Iowa, 2006. Vaccine 2008

http://www.ncbi.nlm.nih.gov/pubmed/18539365

Dangers of Pertussis (Whooping Cough) Vaccine:

FDA study helps provide an understanding of rising rates of whooping cough and response to vaccination. FDA Press Release, November 2013

http://www.fda.gov/newsevents/newsroom/pressannouncements/ucm376937.htm

Acellular pertussis vaccines protect against disease but fail to prevent infection and transmission in a nonhuman primate model. Proceeding of the National Academy of Sciences, 2013

http://www.pnas.org/content/111/2/787.abstract

Effectiveness of pertussis vaccines for adolescents and adults: case control study British Medical Journal, 2013

http://www.bmj.com/content/347/bmj.f4249

Unexpectedly Limited Durability of Immunity Following Acellular Pertussis Vaccination in PreAdolescents in a North American Outbreak.  Oxford Journals Medicine & Health Clinical Infectious Diseases, 2012

http://cid.oxfordjournals.org/content/early/2012/03/13/cid.cis287.short

Author Insights: Protection From Pertussis Vaccine Wanes Over Time Journal of the American Medical Association, 2012

http://newsatjama.jama.com/2012/11/27/authorinsightsprotectionfrompertussisvaccinewanesovertime/
http://healthland.time.com/2012/11/29/protection-from-whooping-cough-vaccine-wanes-over-time/

Whooping Cough Outbreaks Among Fully Vaccinated. Office of Medical and Scientific Justice, 2012

http://www.omsj.org/blogs/historicwhoopingcoughoutbreakhappeningamongthefullyvaccinated

Autoimmune Issues from Vaccines:

Evidence that Food Proteins in Vaccines Cause the Development of Food Allergies and It’s Implications for Vaccine Policy. Journal of Developing Drugs, 2015

http://www.omicsgroup.org/journals/evidence-that-food-proteins-in-vaccines-cause-the-development-of-foodallergies-and-its-implications-for-vaccine-policy
http://vaccinechoicecanada.com/in-the-news/evidence-that-food-proteins-in-vaccines-cause-the-development-of-food-allergies/
http://www.omicsgroup.org/journals/evidence-that-food-proteins-in-vaccines-cause-the-development-of-foodallergies-and-its-implications-for-vaccine-policy-2329-6631-1000137.pdf

Autoimmunity following hepatitis B vaccine as part of the spectrum of ‘Autoimmune (Auto-inflammatory) Syndrome induced by Adjuvants’ (ASIA): Analysis of 93 cases. NCBI, February 2012

http://www.ncbi.nlm.nih.gov/pubmed/22235045

 

Vaccine Shedding Studies:

Cause of vaccine associated measles five weeks post immunization. British Columbia, Canada, 2013

http://www.eurosurveillance.org/images/dynamic/EE/V18N49/art20649.pdf

Detection of measles virus RNA in urine specimens from vaccine recipients. Journal of Clinical Microbiology, 1995

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC228449/

Failure to reach the goal of measles elimination. Apparent paradox of measles infections in immunized persons. Arch Intern Med, 1994

http://www.ncbi.nlm.nih.gov/pubmed/8053748

Outbreak of Measles Among Persons With Prior Evidence of Immunity, New York City. Oxford Journals, 2010

http://cid.oxfordjournals.org/content/early/2014/02/27/cid.ciu105

Horizontal transmission of the Leningrad3 live attenuated mumps vaccine virus. Vaccine, 2006

http://www.ncbi.nlm.nih.gov/pubmed/16266774

Transmission of mumps virus from mumps vaccinated individuals to close contacts Vaccine, 2011

http://www.ncbi.nlm.nih.gov/pubmed/21983359

Mumps vaccine virus transmission. Vopr Virusol, 2013

http://www.ncbi.nlm.nih.gov/pubmed/24772647

Comparison of the Safety, Vaccine Virus Shedding, and Immunogenicity of Influenza Virus Vaccine, Trivalent, Types A and B, Live ColdAdapted, Administered to Human Immunodeficiency Virus (HIV) Infected and NonHIVInfected. Adults Oxford Journals Medicine & Health The Journal of Infectious Diseases, 2000

http://jid.oxfordjournals.org/content/181/2/725.full

Detection of fecal shedding of rotavirus vaccine in infants following their first dose of pentavalent rotavirus vaccine. Vaccine. 2011

http://www.ncbi.nlm.nih.gov/pubmed/21477676

Rotavirus vaccines: viral shedding and risk of transmission. Lancet Infect Dis. 2008

http://www.ncbi.nlm.nih.gov/pubmed/18922486

Sibling Transmission of VaccineDerived Rotavirus (RotaTeq) Associated With Rotavirus Gastroenteritis. Pediatrics, 2010

http://pediatrics.aappublications.org/content/125/2/e438

Pertussis Infection in Fully Vaccinated Children in DayCare Centers, Israel. Emerging Infectious Diseases, 2000

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2627963/pdf/10998384.pdf

The Case against Universal Varicella Vaccination International Journal of Toxicology, 2006

http://www.whale.to/vaccines/goldman.pdf

Outbreak in Vaccinated NBC 4 New York, April 2014

http://www.nbcnewyork.com/news/local/HobokenCollegeCampusMumpsOutbreakFraternityMembers255738021.html

Link Between Vaccines and Autism Studies and News Stories:

Study: A Positive Association found between Autism Prevalence and Childhood Vaccination uptake across the U.S. Population. Journal of Toxicology and Environmental Health, 2011

http://www.ncbi.nlm.nih.gov/pubmed/21623535

Abnormal measlesmumpsrubella antibodies and CNS autoimmunity in children with autism. Journal of Biomedical Science, 2002

http://www.ncbi.nlm.nih.gov/pubmed/12145534

Autism: A Brain Disorder, or A Disorder That Affects the Brain? Clinical Neuropsychiatry, 2005

http://www.clinicalneuropsychiatry.org/pdf/04_herbert.pdf

Blymphocytes from a Population of Children with Autism Spectrum Disorder and Their Unaffected Siblings Exhibit Hypersensitivity to Thimerosal Journal of Toxicology, 2013

http://www.hindawi.com/journals/jt/2013/801517/

Blood Levels of Mercury Are Related to Diagnosis of Autism: A Reanalysis of an Important Data Set Journal of Child Neurology, 2007

http://www.ncbi.nlm.nih.gov/pubmed/18006963

California’s Autism Increase Not Due to Better Counting, Diagnosis Journal of Epidemiology, 2009 UC Davis Health System

http://www.ucdmc.ucdavis.edu/welcome/features/20090218_autism_environment/

Detection and sequencing of measles virus from peripheral mononuclear cells from patients with inflammatory bowel disease and autism. Dig Dis Science, 2000

http://www.ncbi.nlm.nih.gov/pubmed/10759242

Developmental Regression and Mitochondrial Dysfunction in a Child With Autism Journal of Child Neurology, 2006

http://www.ncbi.nlm.nih.gov/pubmed/16566887

Do aluminum vaccine adjuvants contribute to the rising prevalence of autism? Journal of Inorganic Biochemistry, 2011

http://www.ncbi.nlm.nih.gov/pubmed/22099159

Elevated levels of measles antibodies in children with autism. Pediatric Neurology, 2003

http://www.ncbi.nlm.nih.gov/pubmed/12849883

Emperical Data Confirms Autism Symptoms Related to Aluminum and Acetominophen Exposure Entropy, 2012

http://www.mdpi.com/10994300/
http://www.mdpi.com/1099-4300/14/11/2227

Environmental mercury release, special education rates, and autism disorder: an ecological study of Texas Health Place, 2006

http://www.ncbi.nlm.nih.gov/pubmed/16338635

Evidence of Toxicity, Oxidative Stress, and Neuronal Insult in Autism Journal of Toxicology and Environmental Health, 2006

http://www.ncbi.nlm.nih.gov/pubmed/17090484

Hepatitis B vaccination of male neonates and autism diagnosis, NHIS 19972002. Journal of Toxicology and Environmental Health, 2010

http://www.ncbi.nlm.nih.gov/pubmed/21058170

Hypothesis: conjugate vaccines may predispose children to autism spectrum disorders. Medical Hypotheses, 2011

http://www.ncbi.nlm.nih.gov/pubmed/21993250

Study: Impact of environmental factors on the prevalence of autistic disorder after 1979 Journal of Public Health and Epidemiology, July 2014

http://www.ms.academicjournals.org/article/article1409245960_Deisher%20et%20al.pdf
http://www.academicjournals.org/journal/JPHE/article-abstract/C98151247042

Study: Measlesmumpsrubella vaccination timing and autism among young African American boys: a reanalysis of CDC data. Transl Neurodegener, 2014

http://www.ncbi.nlm.nih.gov/pubmed/25114790

Study: Metabolic biomarkers of increased oxidative stress and impaired methylation capacity in children with autism American Journal of Clinical Nutrition, December 2004

http://www.ncbi.nlm.nih.gov/pubmed/15585776

Study: Neuroglial Activation and Neuroinflammation in the Brain of Patients with Autism Annals of Neurology, Feb 2005

http://www.ncbi.nlm.nih.gov/pubmed/15546155

Study: Oxidative Stress in Autism: Elevated Cerebellar 3nitrotyrosine Levels American Journal of Biochemistry and Biotechnology, 2008

http://thescipub.com/PDF/ajbbsp.2008.73.84.pdf

Study: Porphyrinuria in childhood autistic disorder: Implications for environmental toxicity Toxicology and Applied Pharmacology, 2006

http://www.ncbi.nlm.nih.gov/pubmed/16782144

Study: Possible Immunological Disorders in Autism: Concomitant Autoimmunity and Immune Tolerance The Egyptian Journal of Immunology, 2006

http://www.ncbi.nlm.nih.gov/pubmed/17974154

Study: Reduced levels of mercury in first baby haircuts of autistic children. International Journal of Toxicology, 2003

http://www.ncbi.nlm.nih.gov/pubmed/12933322

Study: Serological association of measles virus and human herpesvirus6 with brain autoantibodies in autism. Clin Immunol Immunopathol, 1998

http://www.ncbi.nlm.nih.gov/pubmed/9756729

Study: Sorting out the spinning of autism: heavy metals and the question of incidence Acta Neurobiol Exp, 2010

http://www.ncbi.nlm.nih.gov/pubmed/20628440

Study: Vaccines and Regressive Autism North American Journal of Medical Sciences, July 2009

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3364648/#!po=4.09836

Study: Validation of the Phenomenon of Autistic Regression Using Home Videotapes Archives of General Psychiatry, 2005

http://www.ncbi.nlm.nih.gov/pubmed/16061766

Study: What’s going on? The question of time trends in autism. Public Health Rep. 2004

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1497666/

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? North American Journal of Medical Science, 2009

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3364648/

News Report: CDC Admits Vaccines Can in Some Cases Trigger Autism

http://sharylattkisson.com/cdcpossibilitythatvaccinesrarelytriggerautism
https://sharylattkisson.com/cdc-possibility-that-vaccines-rarely-trigger-autism/

News Report: Where are The Autistic Amish? CBS Reporter Sharyl Attkisson, July 2014

http://sharylattkisson.com/wherearetheautisticamish/
https://sharylattkisson.com/where-are-the-autistic-amish/

Source: http://www.learntherisk.org/