Harry Potter Tri-Wizard Tournament Party

Harry Potter Tri-wizard Tournament 

Hogwarts Houses Cake

Gold changer and clear glass plate with Hogwarts decal added.

Names for the goblet of fire.

Goblet of Fire 

The games were rolling toilet paper with no hands, eating

 a doughnut off a stick with out hands, and picking up 

marbles with their feet.

The argument

The argument 

Measles - The illness is worse than the vaccine injury or is it.  

For developed countries like America where we have proper nutrition and medical supplies.
450 (American deaths prior to 1963) / 3,500,000(Infected) = .00013 
1.3/10,000  
This number is likely to be even smaller in light of medical advancements made since 1963.
Even with recent outbreaks there has not been a single death contributed to measles since 2003 in America. 
Chance of death from measles pre vaccine in America was 2.5/1,000,000 or .0000025%

Vaccine Adverse Events Reporting System (VAERS) database, as of December 14, 2014 there have been 6,962 serious adverse events reported in connection with measles vaccine since 1990, with over half of those occurring in children three years old and under. Of these events 329 were death

Unvaccinated causing Measle outbreaks
 Even vaccinating 100% of the population wouldn’t be enough, say scientists at the Mayo Clinic’s Vaccine Research Group, because the measles vaccine is a dud with some people, offering no protection at all, and its effectiveness wanes with others, even if they get boosters. According to Tetyana Obukhanych of Stanford University’s School of Medicine, the measles vaccine works as planned with only 25% of the population, leaving the majority of adults who have been vaccinated as children with little or no protection. Up to half of today’s cases involve adults.


The Argument that science has proven no link with vaccines and autism.

 Only 2 of 36 shots have been studied for Autism. The 68 shot vaccine schedule has never been studied. Do not post that being against 68 shots given to a kid under 5yrs old is against science when there has been no science test done to prove that it is safe to give that much that soon. And no test done that wasn't by the CDC with 3 out of 5 members having stock in pharm companies. The head of the CDC owns the most pharm stock than any other stock holder.  
Instead of trying to prove that the measles vaccine does harm I think that people should ask their doctors these questions. Why do autistic kids have measles strain in their intestine and in their bone marrow?  Why are the symptoms of mercury poisoning the same as autism symptoms?  Why does treating autism with detoxing from mercury poisoning cause kids to start talking and have less gut problems?  Here is a link for you http://www.jpands.org/vol9no2/bradstreet.pdf


-Recent peer-reviewed scientific/medical studies by Nataf et al. (2006) and by Geier and Geier  leave little doubt that many autistic children are indeed mercury poisoned. These studies utilized urinary porphyrin profile analysis to assess the body-burden and magnitude of physiological effects of mercury in children.

Vaccines are proven to be safe and cause no harm

Whether vaccines can, and do, cause severe, irreparable damage is not up for debate. The CDC stated that 1% of people that get a vaccine will have a side effect or injury.  4,000,000 million kids got vaccines last years so that is 40,000 vaccine injuries. The U.S. government’s table of recognized vaccine injuries includes anaphylaxis, a severe, whole-body reaction to vaccine ingredients; encephalopathy, brain damage; brachial neuritis, a degree of loss of sensation to the shoulders, arms, hands, and chest, which can be accompanied by chronic pain, lasting years; chronic arthritis; Thrombocytopenic purpura, a loss of blood platelets resulting in “increased tendency to bleed”, an autoimmune disorder caused by the production of antibodies against platelet antigens - See more at: http://www.vaccinationcouncil.org/2014/11/18/the-greater-harm-by-shawn-siegel/#sthash.T19VYWED.dpuf

Serious side effect from vaccines do happen  according to the Vaccine Adverse Event Reporting System. We should be able to choose if we want to take the change on a side effect that could be deadly or the illness. I already have a vaccine injured kid I will take the illness. You may think that every illness causes death but they do not and can be just fine after a few weeks.  However vaccines can also cause death.  Educate before you vaccinate.

Science or Vaccine deniers
A mother is not a vaccine denier if she questions the safety of a vaccine containing mercury, aluminum, MSG, antibiotics, eggs, or formaldehyde. Or Beta HCG hormone. Or the urabi virus . She is not a denier if her child is frail or has already had an adverse vaccine reaction and she chooses to opt her child out. She is not a denier if she questions giving children 49 injections of 14 vaccines by age six, including a vaccine at birth for hepatitis B, a disease usually infecting IV drug users. Nor is she a denier if she declines the CDC recommendation that she take the flu vaccine (containing mercury) when she is pregnant, even though the flu vaccine is not tested for safety for pregnant women and fetuses and the FDA advises it be used “only if clearly needed”.

Get a Tetanus shot for every cut that needs medical treatment
Tetanus shot after the fact is pointless if it does work. It does not cure tetanus. If a kid has tetanus they can take an antibiotic that does cure tetanus not a shot that is suppose to prevent it before it happens.  So if you have a non bleeding puncher wonder it could be tetanus but treating it with a tetanus shot is pointless you would need an antibiotic.  And if you have a bleeding wound it is not tetanus and does not need a tetanus shot. 

Got Whooping Cough -Thanks Anti vaxers 
You didn't get whooping cough from health vaccinated people .  National Academy of Sciences, offers another explanation of why so many out breaks of whooping cough. Using baboons, the researchers found that recently vaccinated animals continued to carry the infection in their throats. Even though those baboons did not get sick from it, they spread the infection to others that were not vaccinated. “When you’re newly vaccinated you are an asymptomatic carrier, which is good for you, but not for the population,” said Tod J. Merkel, the lead author of the study, who is a researcher in the Office of Vaccines Research and Review in the Food and Drug Administration.
http://www.nytimes.com/2013/11/26/health/study-finds-vaccinated-baboons-can-still-carry-whooping-cough.html?_r=0 

Polio vaccine saved lives
CDC reported that 87% of the cases of polio in the us between 1973-1983 were caused by the vaccine. Jonas Salk, inventor of polio vax testified before a Senate subcommittee that nearly all polio outbreaks since 1961 were caused by the oral polio vaccine.
6 states reported increase in polio one year after the vaccine was introduced, ranging from more than doubling in Vermont to Massachusetts' astounding increase of 642%. Utah actually halted vaccination due to the increased incidence and death rate.

The polio vaccine of the 1950’s and 60’s was contaminated by the SV40 virus which is now confirmed to have caused cancer in many people who had received the vaccine.

In 1976, Dr. Jonas Salk, creator of the Polio vaccine used in the 1950s, testified that the live-virus vaccine was the ‘principal if not sole cause’ of all reported polio cases in the U.S.  In fact, according to CDC figures, every case of polio in the U.S. since 1979 was caused by the oral polio vaccine. Authorities claim the vaccine was responsible for about eight cases of polio every year. However,  the government’s own vaccine database during a recent period of less than five years uncovered 13,641 reports of adverse events following use of the oral polio vaccine. These reports included 6,364 emergency room visits and 540 deaths.

People say vaccine saved us from small poxs-
 "It is pathetic and ludicrous to say we ever vanquished smallpox with vaccines, when only 10% of the population was ever vaccinated." Dr Glen Dettman.

Even their chief smallpox expert admitted as much recently:

"If people are worried about endemic smallpox, it disappeared from this country not because of our mass herd immunity. It disappeared because of our economic development. And that's why it disappeared from Europe and many other countries, and it will not be sustained here, even if there were several importations, I'm sure. It's not from universal vaccination."----Dr. Mack

Immunology

When you do not vaccinate people often say "You just don't understand Immunology"  Well, lets hear from the doctors with a PhD in Immunology.

Immunity is an ancient concept that refers to the observation that many acute infectious diseases occur only once in a person’s life, usually in childhood. The examples of such diseases would be measles, mumps, rubella, or whooping cough, to name a few.

Natural immunity is, in a way, a tautological expression because immunity can only be acquired naturally at this point, only through the exposure to an infected individual, although occasionally such exposure would go asymptomatic while still establishing immunity. Nevertheless, because there is a common misconception that vaccines also confer immunity, it is sometimes necessary to use a qualifier “natural,” when referring to immunity, to distinguish it from vaccine-based protection.

Dr Tetyana Obukhanych, author of the book “Vaccine Illusion” has studied immunology in some of the world’s most prestigious medical institutions. She earned her PhD in Immunology at the Rockefeller University in New York and did postdoctoral training at Harvard Medical School, Boston, MA. and Stanford University in California. 

"As an immunologist, I have a concern that the practice of manufacturing vaccines using yeast, egg, animal, or even human fetal cells implies that vaccines by necessity include some small amount of protein or other products from these cells or media, in which these cells are being cultured. I would really want to know whether and how well vaccine manufacturers test their final vaccine products for such unspecified vaccine “ingredients” and how much contamination they discover.

The reason I am concerned about such contamination is because I believe that the exposure to yeast, egg, animal, or human proteins in the context of immunogenic (antibody producing) stimuli has the potential to result in sensitization to these proteins or even to break human immunologic tolerance to “self.” The latter is especially relevant to infants, since their immune system is only starting to make the distinction between “self” and “foreign.” Setting this distinction the wrong way from the start, in my view, is likely to pave the road to allergic or autoimmune manifestations.

We would expect that vaccinated individuals would not be involved (or very minimally involved) in any outbreak of an infectious disease for which they have been vaccinated. Yet, when outbreaks are analyzed, it becomes apparent that most often this is not the case. Vaccinated individuals are indeed very frequently involved and constitute a high proportion of disease cases.

I think this is happening because vaccination does not engage the genuine mechanism of immunity. Vaccination typically engages the immune response—that is, everything that immunologists would theoretically “want” to see being engaged in the immune system. But apparently this is not enough to confer robust protection that matches natural immunity. Our knowledge of the immune system is far from being complete.

Immunology does not study immunity. Immunology studies how the immune system responds to immunization—that is, to the injection of a “foreign” protein or particle (virus, bacteria). Immunologic research focuses mainly on the long-term changes that occur in immunologic organs and bodily fluids following immunization. Such changes are collectively referred to as “immunologic memory.”

But the question is: what makes immunologists think, as they surely do, that immunologic memory is the basis of immunity? I see no evidence in immunologic research to allow me to conclude that this is the case. If anything, I see immunologic memory as being the basis for sensitization rather than for immunity. I am starting to doubt that immunologic memory is beneficial to us."

When asked"If you were a betting person, where would you place your wager: on vaccines or on natural immunity? Why?" 
She answered
"Betting on vaccines versus natural immunity to achieve what? Could you please specify the effect you are asking me about? If it’s about making the human race unfit for survival, then I bet on vaccines."






What Happens When the Brain’s Immune System is Activated?

The brain’s immune system cells, once activated, begin to move about the nervous system, secreting numerous immune chemicals (called cytokines and chemokines) and pouring out an enormous amount of free radicals in an effort to kill invading organisms. The problem is–there are no invading organisms. It has been tricked by the vaccine into believing there are.

Unlike the body’s immune system, the microglia also secrete two other chemicals that are very destructive of brain cells and their connecting processes. These chemicals, glutamate and quinolinic acid, are called excitotoxins. They also dramatically increase free radical generation in the brain. Studies of patients have shown that levels of these two excitotoxins can rise to very dangerous levels in the brain following viral and bacterial infections of the brain. High quinolinic acid levels in the brain are thought to be the cause of the dementia seen with HIV infection.

The problem with our present vaccine policy is that so many vaccines are being given so close together and over such a long period that the brain’s immune system is constantly activated. This has been shown experimentally in numerous studies. This means that the brain will be exposed to large amounts of the excitotoxins as well as the immune cytokines over the same period.

Studies on all of these disorders, even in autism, have shown high levels of immune cytokines and excitotoxins in the nervous system. These destructive chemicals, as well as the free radicals they generate, are diffused throughout the nervous system doing damage, a process called bystander injury. It’s sort of like throwing a bomb in a crowd. Not only will some be killed directly by the blast, but those far out into the radius of the explosion will be killed by shrapnel.
Normally, the brain’s immune system, like the body’s, activates quickly and then promptly shuts off to minimize the bystander damage. Vaccination won’t let the microglia shut down. In the developing brain, this can lead to language problems, behavioral dysfunction, and even dementia. In the adult, it can lead to the Gulf War Syndrome or one of the more common neurodegenerative diseases, such as Parkinson’s disease, Alzheimer’s dementia, or Lou Gehrig’s disease (ALS).
http://thedailyresistance.com/doctors-against-vaccines-hear-from-those-who-have-done-the-research/

What I will tell my kids about how to treat family

I want my kids to know that people are wrong.  People will often say that their family fight like cats and dogs but are always there for each other and that is what counts.  But this is wrong.  

Your family; you should never fight with like cats and dogs.  They will be with you on every good day you have and every bad day you have.  They deserve respect and kindness.  They have earned the right to be treated nicely. Save your best behavior for family and learn to sometimes bite your tongue and say how you feel politly and learn to listen to what the other says and show compassion when talking over problems.  Listen more, give more, and share more.

Always be the first to forgive and the first to say you are sorry.  If both sides are doing this then it is a win win.  Act on your feelings don't just say sorry but show the person you are sorry with your actions and kindness.  Use your best behavior on your family and you will never have to fight like cats and dogs.  Because someone fighting with you at holidays but showning up during the bad times does not mean love. Treating someone with love every time you are with them means love.  And asking for forgiveness when you fail to treat them right. 

Love is in the kindness.

10 commandments- If I was a god my list of ten who be like this.

10 commandments- If I was a god my list of ten who be like this.

1 - thou shall not hurt a child, no abuse sexually
 or physically

2 - thou shall not rape

3 - thou shall not kill

4 - thou shall not raise a hand to hurt others 
except to save a life

5 - thou shall not own a slave

6 - thou will treat all people equal no matter 
the color, gender or sexual orientation

7 - thou shall let no person be homeless or 
go without food

8 - thou shall not tell others what to do with 
their own bodies

9 - thou shall not steal

10- thou shall not bare false witness

MiB Party

DNA Fetal Cells used in Vaccines

Why could human DNA potentially cause brain damage? The way Ratajczak explained it  "Because it's human DNA and recipients are humans, there's homologous recombinaltion tiniker. That DNA is incorporated into the host DNA. Now it's changed, altered self and body kills it. Where is this most expressed? The neurons of the brain. Now you have body killing the brain cells and it's an ongoing inflammation. It doesn't stop, it continues through the life of that individual."   Journal of Immunotoxicology is entitled "Theoretical aspects of autism: Causes--A review." The author is Helen Ratajczak, surprisingly herself a former senior scientist at a pharmaceutical firm
A number of independent scientists have said they've been subjected to orchestrated campaigns to discredit them when their research exposed vaccine safety issues, especially if it veered into the topic of autism. We asked Ratajczak how she came to research the controversial topic. She told us that for years while working in the pharmaceutical industry, she was restricted as to what she was allowed to publish. "I'm retired now," she told CBS News. "I can write what I want."

How might the human DNA contaminated vaccines contribute to human disease? First, there is the potential for the contaminating DNA to be mixed with our own genes by a process called homologous recombination. Homologous recombination is an established biologic phenomenon in which a segment of a cell’s DNA is substituted by another segment of DNA that is similar. This can occur during cell division or DNA repair. Homologous recombination occurs naturally to create genetic diversity in our offspring, and is also conveniently harnessed by scientists to introduce experimental DNA into cells or animals. We
do not yet know if this occurs with the contaminating human DNA found in some of our vaccines, and if so, to what extent. Imagine the potential consequences of human DNA from a vaccine, a vaccine that is given to children at an average age of 15 months, being incorporated into a child’s developing brain. Dr. Theresa Diesher  
Dr. Theresa Deisher, a PhD in Molecular and Cellular Physiology from Stanford University, the first person to discover adult cardiac derived stem cells, determined that residual human fetal DNA fragments in vaccines may be one of the causes of autism in children through vaccination.

Even more alarming, Dr Theresa Deisher, lead scientist and SCPI founder noted that, “Not only are the human fetal contaminated vaccines associated with autistic disorder throughout the world, but also with epidemic childhood leukemia and lymphomas.”

http://soundchoice.org/autism/autism-research/

New Study in Journal of Public Health and Epidemiology Correlates Autism Disorder Increase and Human Fetal DNA, Retroviral Agents in Vaccines

http://nevadagovernor2014.com/new-study-vaccines-cause-autism-leukemia-lymphomas-journal-of-public-health-and-epidemiology-nevada-governor-2014-david-lory-vanderbeek/

Vaccine Info - Autism - Resources, Studies, Articles, and General Info

Vaccine Info - Autism - Resources, Studies, Articles, and General Info
    

The autism epidemic that began in the late 1980’s is likely due primarily to toxins adversely affecting fetus and infants during development.  Autism is closely correlated with a lessened ability to excrete toxins.
Mercury is likely a major contributor to this toxin-induced autism, whether the source of the mercury is from vaccines or environmental mercury exposure
Other toxins, whether from vaccines or environmental exposure, can also contribute to toxin-induced autism.
When mercury is present in the body either from recent acute exposure or long-term chronic exposure, it can exponentially increase the adverse affect of other toxins 10-fold to 100-fold in a process known as “synergistic toxicity.”  Why do autistic kid not have mercury in their hair from their first hair cut when non autistic kid do (that is how the body should get rid of the toxins) 
http://www.ncbi.nlm.nih.gov/pubmed/12933322.  
Why do autistic kids have measles strain in their intestine and in their bone marrow? http://www.jpands.org/vol9no2/bradstreet.pdf  Why are the symptoms of mercury poisoning the same as autism symptoms.  Why is mercury in baby teeth 2x higher in autistic children? http://www.tandfonline.com/doi/abs/10.1080/15287390601172080#.VQTp9Y54rpU . These are the questions that the doctors and scientist are looking into in the many links below.

-Recent peer-reviewed scientific/medical studies by Nataf et al. (2006) and by Geier and Geier (2006) leave little doubt that many autistic children are indeed mercury poisoned. These studies utilized urinary porphyrin profile analysis (UPPA) to assess the body-burden and magnitude of physiological effects of mercury in children.
-Mercury poisoning and autism have nearly identical symptoms, and a single day’s vaccination regimen may inject 41 times the level of mercury known to cause harm. California’s autism rate has mushroomed 1000% over the past 20 years, with dramatic increases following the introduction of the MMR vaccine in the early 1980’s. England had dramatic autism increases beginning in the 1990’s, following the introduction of the MMR vaccine there. Some infants receive 100 times the EPA’s maximum allowable amount of mercury through vaccines.

In January, 2000, the Journal of Adverse Drug Reactions reported that the MMR vaccine was not adequately tested and should not have been licensed. Further reinforcing the suspected vaccine-autism connection is the fact that many physicians using a systematic mercury-detoxification regimen with autistic patients have seen dramatic improvements in the health and behavior of their patients.
-Los Angeles Times, Merck & Co., the makers of several vaccines, knew in 1991 that the cumulative amount of mercury in vaccines given to infants by six months of age was about 87 times the level then thought to be safe
-"However, in 2001, the vaccine was found to cause a serious, frequently fatal, multisystemic illness, called yellow fever vaccine–associated viscerotropic disease (YEL-AVD), which resembles the illness it was designed to prevent."
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3310656/

Mercury in the body
- study of children with developmental delay found that 75 of 91 patients with autism and inflamed bowels had live measles virus detected in samples of their intestinal tissues. Only 7 of the 70 normal patients (or controls) were found to have the measles virus in their gut. Vaccine measles strains have been isolated from the spinal fluid of autistic children. http://www.jpands.org/vol9no2/bradstreet.pdf
-A case control study of 221 children with autism and 18 controls found that after a DMSA challenge test, vaccinated autistic children had THREE times the level of mercury in their urine compared to controls
Biopsy samples found 22,000 times the level of mercury in people with heart failure from unknown causes compared to controls whose heart failure was caused by virus, heart attacks, or high blood pressure
-Research proves that even very low levels of exposure have adverse effects on language, attention, and memory, making children less able to think and learn. When you read this list of symptoms, it is easy for even the layperson to correlate that this environmental toxin has caused havoc with our children’s development starting in the late 80’s when the numbers of vaccines containing thimerosal and the epidemic of developmental disorders began to increase
-Monkey studies have shown that the mercury in thimerosal does indeed cross the blood brain barrier and results in significant deposition of inorganic mercury in the brain. Research has documented that inorganic mercury becomes trapped in the brain (the estimated half-life is over 700 days).
-A review by Dr. Paul G. King has proven otherwise, showing that ethylmercury is first metabolized by the body into toxic methylmercury, which is then metabolized into inorganic mercury.
The abstract from that study states the following:
"In the rat study, which Dr. King cites, the lab rats were raised for the purpose of this study and had no reported mercury levels in their blood before the experiment.
There were three groups in the study:
1. A test group of Thimerosal-(ethylymercury)-treated rats;
2. A test group of methylmercury-chloride-treated rats; and
3. A control group of rats treated with a 'water' placebo.
At the end of the experiment, as expected, the water-treated control group had no reported levels of mercury in their blood or organs.
The group treated with methylmercury chloride (which vaccine purveyors routinely "sound bite" as the harmful organic mercury as compared to the "safe" Thimerosal, ethylmercury), as expected, had both methylmercury and inorganic mercury in their blood and organs."
And goes on to conclude:
"In layman's terms, these studies, as brought to light by Dr. King, establish that ethylmercury (Thimerosal), a "supposedly harmless" compound of mercury according to the vaccine establishment, is converted in the rat and apparently in the human infant into "methylmercury" which, the establishment admits is a harmful form of mercury. It is then further reduced to the long-term most harmful, "inorganic mercury" that bioaccumulates in the tissues and organs.
Based on these findings, we can conclude that injecting the Thimerosal (ethylmercury), found in flu shots, into pregnant women (exposing the in utero fetus to mercury [see Table I on page 15 of Dr.King's posting http://dr king.com/docs/110915_PGKReviewOfUSSubmissionToUNEP_b.pdf
5) "There is no mercury in vaccines. It has all been phased out."
Oh, but it hasn't! In fact, it's still regularly added to the influenza vaccine, and is active in other vaccines, hidden under other titles.
The FDA themselves have gone on to say the following:
"While the use of mercury-containing preservatives has declined in recent years with the development of new products formulated with alternative or no preservatives, thimerosal has been used in some immune globulin preparations, anti-venins, skin test antigens, and ophthalmic and nasal products, in addition to certain vaccines," right on its "Thimerosal in Vaccines" page which can be found here:
http://www.fda.gov/BiologicsBloodVaccines/SafetyAvailability/VaccineSafety/UCM096228
http://pediatrics.aappublications.org/content/121/2/e208.full?sid=9a37d1db-5082-4a07-abdb-4807dd9e61d0
6) "The mercury is vaccines is good for you, since it produces an immune response."
There are absolutely no studies that show that mercury, a toxic substance, is good for you. In fact, just the opposite is true. The study cited in the post above goes on to say:

"The antibacterial activity of thimerosal (sodium ethyl mercury thiosalicylate) is attributed to the ethyl mercury cation that dissociates from the thimerosal molecule. By 1999, expanding recommendations for infant vaccination meant that US children who received a complete series of vaccines that contained thimerosal potentially received up to 187.5 μg of ethyl mercury during the first 6 months of life.1-3 This cumulative exposure could exceed the US Environmental Protection Agency's recommended safe intake level, estimated in 1997 to be no more than 0.1 μg of mercury per kg of body weight per day.4 This observation led to a recommendation by the American Academy of Pediatrics that thimerosal be removed from all vaccines that are administered to infants in the United States."
Yet, it has not been removed. The EPA themselves acknowledge the toxic effects of mercury:
http://www.epa.gov/hg/effects.htm

Vaccines cause encephalitis.
Vaccines cause seizures.
Vaccines cause immune system deficiencies.
Vaccines cause gastrointestinal problems.
Encephalitis causes mood swings.
Encephalitis causes extreme pain.
Encephalitis causes inattention  and impulsivity.
Encephalitis causes aggression.
Encephalitis causes balance problems and difficulty relating to one's environment.
Seizures cause mood swings.
Seizures cause inattention and impulsivity.
Seizures cause alterations in conciousness.
Immune system deficiencies cause children to have more frequent bacterial infections, such as ear infections, upper respiratory infections (URIs), sinusutis, and strep infections.
Immune system deficiencies cause childrn to have more frequent viral infections, such as stomatitis, "fevers of unknown origin," "viral rashes," hives, conjunctivitis, and gastrointestinal viruses that cause vomiting and diarrhea.
Immune system deficiencies cause children to be more vulnerable to "everything that's going around" and to have a tougher time getting over things than their peers.
Gastrointestinal damage from vaccines causes diarrhea.
Gastrointestinal damage from vaccines causes nausea, reflux, vomiting, and the recently discovered "disease" now known as GERD (Gastro-Esophageal Reflux Disease).  Gatrointestinal damage from vaccines causes increased vulnerability to viruses and bacteria, which leads to increased administration of antibiotics, which leads to overgrowth of pathogenic yeast.  Pathogenic yeast overgrowth leads to intestinal hyperpermeability ("leaky gut syndrome").
Pathogenic yeast overgrowth leads to constipation. Pathogenic yeast overgrowth leads to food allergies.  Pathogenic yeast overgrowth leads to skin eruptions, "drunken, silly behavior," inattention and impulsivity, and cravings for bread, sugar, ice cream, milk, and carbohydrates.  Technically, vaccines do not cause autism because techincally there is no such thing as AUTISM. 


Vaccines cause the underlying physical conditions that result in the pain, neurological damage, immune system disorders, gastrointestinal damage, and yeast overgrowth - all of which combine to produce the behavioral symptoms that result in the "autism" diagnosis.  Gastrointestinal damage is the most obvious result of vaccine damage. On this page I have listed on this page lots of links to show studies, peer reviews and doctors personal studies showing autism and vaccine link.
     

*86 Research Papers Supporting the Vaccine/Autism Link
http://www.scribd.com/doc/220807175/86-Research-Papers-Supporting-the-Vaccine-Autism-Link?
*Metals, Environmental Toxin & Autism 6 links
http://vaccinechoicecanada.com/science-supporting-vaccine-risk/autism/#metals

*Peer reviews and papers
Mito Action – Autism and Mitochondrial Disease   http://www.mitoaction.org/about-autism-and-mito

Vaccine Autoimmune Project for Research and Education
http://www.vaclib.org/sites/vap/mmr-briefing-20070430.htm

Thimerosal-Derived Ethylmercury Is a Mitochondrial Toxin in Human Astrocytes: Possible Role of Fenton Chemistry in the Oxidation and Breakage of mtDNA
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3395253/

Increased risk of developmental neurologic impairment after high exposure to thimerosal-containing vaccine in first month of life. http://mercury-freedrugs.org/docs/00mmdd_EISAbstractSubmission_IncreasedRiskOfDevelopmentalNeurologicImpairmentAfterHighExposureToThimerosal-containingVaccine_.pdf

Aluminum-Induced Entropy in Biological Systems: Implications for Neurological Disease
http://omsj.org/reports/tomljenovic%202011.pdf

Blood Levels of Mercury Are Related to Diagnosis of Autism
http://jcn.sagepub.com/content/22/11/1308.abstract

Metabolic biomarkers of increased oxidative stress and impaired methylation capacity in children with autism
http://ajcn.nutrition.org/content/80/6/1611.full

Neuroglial activation and neuroinflammation in the brain of patients with autism
http://www.ncbi.nlm.nih.gov/pubmed/15546155

Serological association of measles virus and human herpesvirus-6 with brain autoantibodies in autism
http://www.ncbi.nlm.nih.gov/pubmed/9756729

Reduced levels of mercury in first baby haircuts of autistic children
http://www.ncbi.nlm.nih.gov/pubmed/12933322

Evidence of toxicity, oxidative stress, and neuronal insult in autism
http://www.ncbi.nlm.nih.gov/pubmed/17090484

A case series of children with apparent mercury toxic encephalopathies manifesting with clinical symptoms of regressive autistic disorders.
http://www.ncbi.nlm.nih.gov/pubmed/17454560

Heavy-Metal Toxicity—With Emphasis on Mercury
http://adventuresinautism.blogspot.ca/2007/06/no-evidence-of-any-link.html?m=1

Epidemiology of autism spectrum disorder in Portugal:
http://adventuresinautism.com/images/VivaPortugal.pdf

Thimerosal exposure in infants and neurodevelopmental disorders: an assessment of computerized medical records in the Vaccine Safety Datalink
http://www.ncbi.nlm.nih.gov/pubmed/18482737

Hepatitis B triple series vaccine and developmental disability in US children aged 1–9 years
http://www.tandfonline.com/doi/abs/10.1080/02772240701806501#.VNW12Z3F-3h

Induction of metallothionein in mouse cerebellum and cerebrum with low-dose thimerosal injection
http://www.ncbi.nlm.nih.gov/pubmed/19357975

Mercury induces inflammatory mediator releasefrom human mast cells
http://www.jneuroinflammation.com/content/pdf/1742-2094-7-20.pdf

Urinary porphyrin excretion in neurotypical and autistic children
http://www.ncbi.nlm.nih.gov/pubmed/20576582

Vaccines and Autism
http://labmed.ascpjournals.org/content/33/9/708.full.pdf

Theoretical aspects of autism: Causes—A review
http://informahealthcare.com/doi/abs/10.3109/1547691X.2010.545086

Ancestry of pink disease (infantile acrodynia) identified as a risk factor for autism spectrum disorders
http://www.ncbi.nlm.nih.gov/pubmed/21797771

MMR vaccination and febrile seizures: evaluation of susceptible subgroups and long-term prognosis
http://www.ncbi.nlm.nih.gov/pubmed/15265850

Adverse Events following 12 and 18 Month Vaccinations: a Population-Based, Self-Controlled Case Series Analysis
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0027897

Administration of Thimerosal to Infant Rats Increases Overflow of Glutamate and Aspartate in the Prefrontal Cortex: Protective Role of Dehydroepiandrosterone Sulfate
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3264864/?tool=pubmed

Environmental mercury release, special education rates, and autism disorder: an ecological study of Texas.
http://www.ncbi.nlm.nih.gov/pubmed/16338635

Empirical Data Confirm Autism Symptoms Related to Aluminum and Acetaminophen Exposure
http://www.mdpi.com/1099-4300/14/11/2227

Aluminum-Induced Entropy in Biological Systems: Implications for Neurological Disease
http://www.hindawi.com/journals/jt/2014/491316/

Abnormal measles-mumps-rubella antibodies and CNS autoimmunity in children with autism
http://www.ncbi.nlm.nih.gov/pubmed/12145534

Infection, vaccines and other environmental triggers of autoimmunity
http://www.ncbi.nlm.nih.gov/pubmed/16126512

Unanswered Questions
A Review of Compensated Cases of Vaccine-Induced Brain Injury
http://www.ebcala.org/unanswered-questions

Thimerosal and autism? A plausible hypothesis that should not be dismissed.
http://www.ncbi.nlm.nih.gov/pubmed/15082108

Detection and sequencing of measles virus from peripheral mononuclear cells from patients with inflammatory bowel disease and autism.
http://www.ncbi.nlm.nih.gov/pubmed/10759242

The spectrum of ASIA: ‘Autoimmune (Auto-inflammatory) Syndrome induced by Adjuvants’
http://lup.sagepub.com/content/21/2/118.full

Aluminum in the central nervous system (CNS): toxicity in humans and animals, vaccine adjuvants, and autoimmunity
http://link.springer.com/article/10.1007%2Fs12026-013-8403-1#page-1

Hepatitis B vaccination of male neonates and autism diagnosis, NHIS 1997-2002.
http://www.ncbi.nlm.nih.gov/m/pubmed/21058170/

Vaccines and Brain Inflammation

http://www.vaccinationcouncil.org/2011/06/01/vaccines-and-brain-inflammation/

Impact of enviromental factors on the prevalence of autistic disorder after 1979
http://www.ms.academicjournals.org/article/article1409245960_Deisher%20et%20al.pdf

A positive association found between autism prevalence and childhood vaccination uptake across the U.S. population.
http://www.ncbi.nlm.nih.gov/pubmed/21623535

Neonatal administration of a vaccine preservative, thimerosal, produces lasting impairment of nociception and apparent activation of opioid system in rats.
http://www.ncbi.nlm.nih.gov/pubmed/19747466?

Lasting neuropathological changes in rat brain after intermittent neonatal administration of thimerosal
http://www.termedia.pl/Original-paper-Lasting-neuropathological-changes-in-rat-brain-after-intermittent-neonatal-administration-of-thimerosal,20,15811,1,1.html

Persistent behavioral impairments and alterations of brain dopamine system after early postnatal administration of thimerosal in rats.
http://www.ncbi.nlm.nih.gov/pubmed/21549155

B-lymphocytes from a population of children with autism spectrum disorder and their unaffected siblings exhibit hypersensitivity to thimerosal.
http://www.ncbi.nlm.nih.gov/pubmed/23843785

Thimerosal-Derived Ethylmercury Is a Mitochondrial Toxin in Human Astrocytes: Possible Role of Fenton Chemistry in the Oxidation and Breakage of mtDNA
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3395253/

Thioredoxin: A novel, independent diagnosis marker in children with autism
http://www.ncbi.nlm.nih.gov/pubmed/25433158

Inhibition of the human thioredoxin system. A molecular mechanism of mercury toxicity.
http://www.ncbi.nlm.nih.gov/pubmed/18321861

Effects of selenite and chelating agents on mammalian thioredoxin reductase inhibited by mercury: implications for treatment of mercury poisoning.
http://www.ncbi.nlm.nih.gov/pubmed/20810785

Porphyrinuria in childhood autistic disorder: Implications for environmental toxicity
http://www.sciencedirect.com/science/article/pii/S0041008X06001335

Activation of methionine synthase by insulin-like growth factor-1 and dopamine: a target for neurodevelopmental toxins and thimerosal.
http://www.ncbi.nlm.nih.gov/pubmed/14745455


Vaccine, Neurological disorders study 
http://www.iom.edu/~/media/Files/Activity%20Files/PublicHealth/ImmunizationSafety/Bradstreet.pdf

Interview with Dr. Maurice Hilleman, Merck Pharmaceutical’s Chief developer of Vaccines for over 45 years.
http://truthalerts.com/medical-evidence-that-vaccines-cause-cancer-autism-narcolepsy-developmental-disorders-and-death/

Measles RNA in spinal fluid of children with regressive autism 
http://www.jpands.org/vol9no2/bradstreet.pdf

Detection and sequencing of measles virus from peripheral mononuclear cells from patients with inflammatory bowel disease and autism.
http://www.ncbi.nlm.nih.gov/pubmed/10759242

Medline Plus- Government Website Explains Encephalitis
http://www.nlm.nih.gov/medlineplus/ency/article/001415.htm

MMR Vaccine as a cause of encephalitis
http://vaccinechoicecanada.com/in-the-news/measles-mumps-rubella-mmr-vaccine-as-a-potential-cause-of-encephalitis-brain-inflammation-in-children/

The Merck Manual on Encephalitis (one of the side effects of vaccines written by the maker of the vaccines)
http://www.merckmanuals.com/home/brain_spinal_cord_and_nerve_disorders/brain_infections/encephalitis.html

Merck Medical Textbook of a Vaccine Adverse Reaction Brain Infection
http://therefusers.com/refusers-newsroom/the-medical-textbook-definition-of-a-vaccine-adverse-reaction-brain-infection-merck-manual/#.VMxR42jF_pd

Vaccine Induced Enchephalitis
http://www.vaccinationnews.org/DailyNews/May2002/MechEncephDamVax.htm  

Vaccine Adjutants and Autism (Thimerosal, Mercury and Aluminum)
Changes in Vaccines Making them more Damaging (sources at bottom of article)
Dr. Stephanie Seneff, senior scientist at MIT           http://nourishingplot.com/2014/06/27/recent-changes-in-vaccines/

Aluminum and Autism
http://omsj.org/reports/tomljenovic%202011.pdf

Data linking aluminum, acetomenophen and autism
http://www.mdpi.com/1099-4300/14/11/2227   
full study here
 http://groups.csail.mit.edu/sls/publications/2012/entropy-14-02227.pdf

Aluminum and neurological symptoms
http://www.ncbi.nlm.nih.gov/pubmed/19568732   

Aluminum vaccine adjuvants- are they safe?
http://www.meerwetenoverfreek.nl/images/stories/Tomljenovic_Shaw-CMC-published.pdf

Autism Symptoms Related to Aluminum and Acetaminophen Exposure        
 http://www.mdpi.com/1099-4300/14/11/2227

Aluminum hydroxide injections lead to motor deficits and motor neuron degeneration
http://www.ncbi.nlm.nih.gov/pubmed/19740540

Thimerosal Timeline and Autism
http://www.ashotoftruth.org/history

Trace Amounts of Thimerosal in vaccines 
http://www.thedoctorwithin.com/newsletters/mercury-thimerosal-hib-vaccine-injury/

Symptom Comparison of Mercury Poisoning and Autism
http://www.vaccinationnews.org/Scandals/feb_15_02/comparison_symptoms.htm

Effect of mercury on developing fetus study
Is there a safe amount?  Flu shots given to pregnant women contain extremely dangerous high levels of mercury
http://www.tandfonline.com/doi/abs/10.1080/02772248.2012.724574?journalCode=gtec20#.VIHlszHF_pc

Thimerosal autism connection
http://www.ncbi.nlm.nih.gov/pubmed/17454560

A Case Series of Children with Apparent Mercury Toxic Encephalopathies Manifesting with Clinical Symptoms of Regressive Autistic Disorders
Journal of Toxicology and Environmentsl Health
http://www.tandfonline.com/doi/abs/10.1080/15287390701212141?url_ver=Z39.88-2003&rfr_id=ori%3Arid%3Acrossref.org&rfr_dat=cr_pub%3Dpubmed.VMGedEfF_pd

Children with mercury toxic enchephalopathies and regressive autism
http://www.ncbi.nlm.nih.gov/pubmed/17454560

A Dose-Response Relationship between Organic Mercury Exposure from Thimerosal-Containing Vaccines and Neurodevelopmental Disorders          http://www.mdpi.com/1660-4601/11/9/9156

Methodological Issues and Evidence of Malfeasance in Research Purporting to Show Thimerosal in Vaccines Is Safe (a study by the CDC)    http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4065774/
Mercury in vaccines exceeded safety guidelines and is still in several vaccines as an ingredient
http://www.ncbi.nlm.nih.gov/pubmed/11339848   

Monkey study 1990s connecting thimerosal with damage to brain structure and function
http://www.ane.pl/pdf/7020.pdf  

 Mercury and autism- accelerating evidence
http://www.ncbi.nlm.nih.gov/pubmed/16264412     

Administration of thimerosal to infant rats increases overflow of glutamate and aspartate in the prefrontal cortex
http://www.ncbi.nlm.nih.gov/pubmed/22015977   

Rats studied with amounts consistent with infant vaccines developed neurodevelopmental disorders.
http://www.ncbi.nlm.nih.gov/pubmed/21225508

MMR as a potential cause of encephalitis brain inflammation in children
http://vran.org/about-vaccines/specific-vaccines/measles-mumps-rubella-vaccine/measles-mumps-rubella-mmr-vaccine-as-a-potential-cause-of-encephalitis-brain-inflammation-in-children/

Autism Symptoms are Identical to Encephalomyopthy listed on vaccine package inserts
http://therefusers.com/refusers-newsroom/autism-symptoms-are-identical-to-encephalomyopathy-listed-on-vaccine-package-inserts/#.VMPvj_54rAG

Thimerosal and adverse events
http://www.najms.org/article.asp?issn=1947-2714%3Byear%3D2014%3Bvolume%3D6%3Bissue%3D10%3Bspage%3D519%3Bepage%3D531%3Baulast%3DGeier

Heavy Metals in Hair Samples from Severely Autistic Children
http://www.mdpi.com/1660-4601/9/12/4486

Toxicity of Thimerosal
http://toxnet.nlm.nih.gov/cgi-bin/sis/search2/r?dbs+hsdb:@term+@rn+54-64-8 

Regressive Autism and Heavy Metals
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3364648/

Genetic heritability and shared environmental factors among twin pairs with Autism http://www.ncbi.nlm.nih.gov/pubmed/21727249

Causal link between MMR and autism
An inappropriate antibody response to MMR, specifically the measles component thereof, might be related to pathogenesis of autism
http://www.ncbi.nlm.nih.gov/pubmed/12145534   

MMR and Autism-  article in Journal of Biomedical Science
http://vran.org/wp-content/documents/VRAN-Abnormal%20Measles-Mumps-Rubella-Antibodies-CNS-Autoimmunity-Children-Autism-Singh-Lin-Newell-Nelson.pdf

Conjugate Vaccines may predispose children to autism disorders
http://www.ncbi.nlm.nih.gov/pubmed/23576057    

A Positive Association found between Autism Prevalence and Childhood Vaccination http://www.ingentaconnect.com/content/tandf/uteh/2011/00000074/00000014/art00002?token=004c170388ee06a6e5865462431636f5720415d23763c247b5e4e26634a492f2530332976261 

 Biological Evidence of Significant Vaccine Related Side-effects Resulting in Neurodevelopmental Disorders
Dr. Jeff Bradstreet MD FAAFP Director of Clinical Programs, ICDRC Visiting Professor of Pediatrics, SCNM Adjunct Professor of Neurosciences, Stetson 
http://www.iom.edu/~/media/Files/Activity%20Files/PublicHealth/ImmunizationSafety/Bradstreet.pdf                  https://www.scribd.com/doc/220807175/86-

Research-Papers-Supporting-the-Vaccine-Autism-Link A positive association found between autism prevalence and childhood vaccination uptake across the U.S.
http://www.ncbi.nlm.nih.gov/pubmed/21623535   

Causal relationship between vaccine induced immunity and autism
http://www.ncbi.nlm.nih.gov/pubmed/12849883

Autism and mercury poisoning
http://www.ncbi.nlm.nih.gov/pubmed/11339848

Hypothesis: conjugate vaccines may predispose children to autism spectrum disorders
http://www.ncbi.nlm.nih.gov/pubmed/21993250

Rise in autism coincides with rise in vaccines
http://www.ncbi.nlm.nih.gov/pubmed/21623535

Subtle DNA changes and the overuse of vaccines in autism
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3364648/

Vaccine and Autism- a New Scientific Review
http://www.cbsnews.com/news/vaccines-and-autism-a-new-scientific-review/  
summary of previous Journal of Immunology
http://danmurphydc.com/wordpress/wp-content/uploads/2011/01/AR-10-12-rata-AUTISM-VACCINE.pdf

Autism and Resulting Medical Conditions:  
http://www.tacanow.org/wp-content/uploads/2011/09/autism-studies-april-2008.pdf 

Mercury toxic encephalopathy  manifesting with clinical symptoms of regressive autistic disorders.  http://www.ncbi.nlm.nih.gov/pubmed/17454560
Relation of mercury to high autism rates in boys
http://www.ncbi.nlm.nih.gov/pubmed/16264412

Elevated levels of measles in children with Autism
http://www.ncbi.nlm.nih.gov/pubmed/12849883

Abnormal MMR antibodies in children with autism
http://www.ncbi.nlm.nih.gov/pubmed/12145534

Detection of Measles Virus Genomic RNA in Cerebrospinal Fluid of Children with Regressive Autism
http://www.jpands.org/vol9no2/bradstreet.pdf

3 fold increase in autism in boys injected as neonates
(greater risk in non white children)
http://www.ncbi.nlm.nih.gov/pubmed/21058170

Hepatitis vaccination male neonates and Autism diagnosis 1997- 2002
http://www.ncbi.nlm.nih.gov/m/pubmed/21058170/

Fraud and Deception and the Whistleblower

Congressman Bill Posey in possession of 100,000+ documents
http://benswann.com/update-congressmans-office-in-possession-of-100000-cdc-whistleblower-documents/


Whistleblower at CDC goes public
http://www.naturalnews.com/046552_MMR_vaccine_autism_CDC_whistleblower.html

Manipulation of Studies has flawed Data on vaccines and autism
http://www.marketwired.com/press-release/study-focus-autism-foundation-finds-cdc-whistleblower-reveals-widespread-manipulation-1939179.htm


Merck’s Director says MMR causes autism
https://childhealthsafety.wordpress.com/2010/06/30/vaccination-causes-autism-%E2%80%93-say-us-government-merck%E2%80%99s-director-of%C2%A0vaccines/

The Hooker info gotten by the freedom of info act.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4128611/        

Brian Hooker refutes studies on autism by the pharmaceutical companies
http://www.ageofautism.com/2012/04/revisiting-denmark-more-rotten-than-ever.html

Correspondence between HRSA and Sharyl Atkinson reporter
(US Health Resources Administration)
https://childhealthsafety.wordpress.com/2010/06/30/vaccination-causes-autism-%E2%80%93-say-us-government-merck%E2%80%99s-director-of%C2%A0vaccines/


Studies data on autism and African American boys
Look at the conclusion
http://www.ncbi.nlm.nih.gov/pubmed/25114790

Dr. Kenneth P. Stoller, MD, FACHM
Speaks on the American Academy of Pediatrics and fraud
https://www.youtube.com/watch?v=36_qz2beMaE

Videos

http://earthweareone.com/mit-researchers-new-warning-at-todays-rate-half-of-all-u-s-children-will-be-autistic-by-2025/

Dr Russel Blaylock videos on vaccines and cancer http://cancervortex.com/vaccinedangers1.htm

Aluminum Autism Connection
Dr Chris Shaw Neuroscientist At University of British Columbia
https://www.youtube.com/watch?v=FfTo35UrFPA
 Profile of Dr Chris Shaw    http://www.neuraldynamicsubc.ca/profiles/shaw.html

Theresa Deisher, Ph.D. (President, Sound Choice Pharmaceutical Institute , CEO andManaging Member, AVM Biotechnology). Dr. Deisher, an expert in the field of adult stem cell therapies and regenerative medicine, brings 18 years of experience in scientific and corporate leadership positions involving research, discovery, production and commercialization of human therapeutics. Dr. Deisher’s penchant for ground breaking scientific discovery and her distinguished scientific research has resulted in 23 patents issued in her name. She has published numerous scientific manuscripts and is a frequent invited lecturer and guest speaker in the area of stem cell technology and regenerative medicine. Throughout her career, Dr. Deisher has been recruited by some of the country’s top biotechnology companies, including Genentech, Repligen, ZymoGenetics, Immunex and Amgen. She has managed and mentored undergraduate honors students, post-doctoral fellows, scientific executives and over 20 research assistants/scientists at all levels of responsibility.Dr. Deisher graduated with honors and distinction from Stanford University, and obtained her Ph.D. in Molecular and Cellular Physiology from the Department of Molecular and Cellular Physiology, Stanford University.

Dr Theresa Deisher on  Worldwide Autism Epidemic & Human Fetal Manufactured
Contaminated Vaccines
https://www.youtube.com/watch?v=6Bc6WX33SuE

Dr Theresa Deisher Series with 4 Parts on Autism 
https://www.youtube.com/watch?v=ZsCAUKUTb20&feature=youtu.be     part 1

https://www.youtube.com/watchv=I5b9xsGZs1E  

https://www.youtube.com/watch?v=UVZSs9vgYQ    

https://www.youtube.com/watch?v=M5y9mYQQmt4    

Dr. Stephanie Seneff discusses the potential connection between vaccines and autism
Senior scientist at MIT                    
https://www.youtube.com/watch?v=o3P6wVUH0pc&utm_content=buffer058b6&utm_medium=social&utm_source=facebook.com&utm_campaign=buffer

The history of thimerosal and autism. Excellent
https://www.youtube.com/watch?v=KiT7Y233404&feature=youtu.be



Vaccine Overload and Autism Link

Children receive 80 vaccinations throughout childhood- autism linked to vaccine overload
http://www.collective-evolution.com/2014/06/05/children-receive-80-vaccinations-throughout-childhood-new-study-links-vaccine-induced-overload-to-autism/

Study on Vaccine Induced Immune Overload  in Molecular and Genetic Medicine Journal
Review of Vaccine Induced Immune Overload and the Resulting Epidemics of Type 1 Diabetes and Metabolic Syndrome, Emphasis on Explaining the Recent Accelerations in the Risk of Pre diabetes and other Immune Mediated Diseases        
J. Barthelow  Classen MD*
http://www.vaccines.net/vaccine-induced-immune-overload.pdf

Subtle DNA changes and the overuse of vaccines in autism
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3364648/

Autism Symptoms Related to Aluminum and Acetaminophen Exposure                                       http://www.mdpi.com/1099-4300/14/11/2227


Fetal DNA and Autism
Autism And Cancer Related To Human Fetal DNA In Vaccines                                                     Journal of Public Health                                           http://www.globalresearch.ca/new-study-in-journal-of-public-health-finds-autism-and-cancer-related-to-human-fetal-dna-in-vaccines/5402912

Vaccine and GMO converge to fuel Autism
http://kinseimindbody.com/synergistic-destruction-how-vaccines-and-gmos-converge-to-fuel-autism-and-neurodegenerative-conditions/

Peer reviewed study on fetal cell contamination with retro virus associated with autism and cancer
http://www.globalresearch.ca/new-study-in-journal-of-public-health-finds-autism-and-cancer-related-to-human-fetal-dna-in-vaccines/5402912
Study documentation- Dr Deisher        http://www.ms.academicjournals.org/article/article1409245960_Deisher%20et%20al.pdf


Data linking aluminum, acetomenophen and autism
http://www.mdpi.com/1099-4300/14/11/2227   
full study here
http://groups.csail.mit.edu/sls/publications/2012/entropy-14-02227.pdf 

Autism Cancer and Human DNA  References in body of article 
http://soundchoice.org/research/  

Subtle DNA changes and the overuse of vaccines in autism
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3364648/

Connection between brain damage and human DNA  documentation at bottom
http://www.cbsnews.com/news/vaccines-and-autism-a-new-scientific-review/

Fetal cells that are tumorgenic can contaminate healthy cell DNA
http://www.fda.gov/biologicsbloodvaccines/scienceresearch/biologicsresearchareas/ucm127327.htm

New Study in Journal of Public Health and Epidemiology Correlates Autism Disorder Increase and Human Fetal DNA, Retroviral Agents in Vaccines
http://www.standardnewswire.com/news/965249574.html   

Gut Issues in Autistic Children

Analysis of the Use of Antibiotics on Gut Flora
http://www.sciencedaily.com/releases/2013/01/130109081145.htm

MMR and gut issues
http://www.vaclib.org/basic/mmr.htm


A blog with a huge number of studies
http://adventuresinautism.blogspot.com/2007/06/no-evidence-of-any-link.html?m=1

Parents with autistic kids do lots of research http://www.regardingcaroline.com/pubmed

If Vaccines Don’t Cause Autism, What do they Cause?
http://vaxtruth.org/2011/08/vaccines-do-not-cause-autism/

Vaccines Induce Autistic Disorders
Numerous credible, medical journals over the past decade or so have found significant correlations between certain vaccines and autism.

“Using regression analysis and controlling for family income and ethnicity, the relationship between the proportion of children who received the recommended vaccines by age 2 years and the prevalence of autism (AUT) or speech or language impairment (SLI) in each U.S. state from 2001 and 2007 was determined. A positive and statistically significant relationship was found: The higher the proportion of children receiving recommended vaccinations, the higher was the prevalence of AUT or SLI.” – Journal of Toxicology and Environmental Health, 2011

“Further, linear regression revealed that Varicella (chickenpox) and Hepatitis A immunization coverage was significantly correlated to autistic disorder cases…Autistic disorder change points years are coincident with introduction of vaccines manufactured using human fetal cell lines, containing fetal and retroviral contaminants, into childhood vaccine regimens.” – Journal of Public Health and Epidemiology, 2014

“Implicated vaccines: MMR, Varicella, and Hepatitis A using data from the U.S. government, United Kingdom, Denmark, and Western Australia, researchers found a spike in autism around the world after vaccines using animal cells were replaced by vaccines using aborted fetal cells.” – Journal of Public Health and Epidemiology, 2014

“Thus autistic children have a hyper-immune response to measles virus, which in the absence of a wild-type measles infection might be a sign of an abnormal immune reaction to the vaccine strain or virus reactivation.” – Pediatric Neurology, 2003

“Measles might be etiologically linked to autism because measles and MMR antibodies (a viral marker) correlated positively to brain autoantibodies (an autoimmune marker)—salient features that characterize autoimmune pathology in autism.” – Journal of Child Neurology, 2009

“Although the committee has concluded that the evidence favors rejection of the causal relationship at the population level between MMR vaccine and autistic spectrum disorders, the committee nevertheless recommends that this issue receive continued attention. It does so in recognition that its conclusion does not exclude the possibility that MMR vaccine could contribute to ASD in a small number of children.” – Institute of Medicine (US) Immunization Safety Review Committee, 2001

“Thus the MMR antibody in autistic sera detected measles HA protein, which is unique to the measles subunit of the vaccine. Furthermore, over 90% of MMR antibody-positive autistic sera were also positive for MBP (myelin basic protein) autoantibodies, suggesting a strong association between MMR and CNS (central nervous system) autoimmunity in autism. Stemming from this evidence, we suggest that an inappropriate antibody response to MMR, specifically the measles component thereof, might be related to pathogenesis of autism.” – Journal of Biomedical Science, 2002

Studies and Science Show the Statistical Relationship
“The number of dose relationships is linear and statistically significant. You can play with this all you want. They are linear. They are statistically significant.” – Dr. Weil from Association of American Physicians and Surgeons, Inc, 2003

“From a cellular perspective, it would appear that the existing scientific literature supports the biological plausibility of a Hg-based (mercury) autism pathogenesis…Nevertheless, research studies identifying Hg’s effects on glial cells and mitochondria that are consistent with findings in autistic patients, lend further support to the Hg-autism hypothesis.” – PubMed – National Center for Biotechnology Information, 2011

 “In phase I, it was observed that there was a significantly increased risk ratio for the incidence of ASD (Autism Spectrum Disorder) 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.” – PubMed – National Center for Biotechnology Information, 2013


“There was a significant dose-response relationship between the severity of the regressive ASDs (Autism Spectrum Disorder) observed and the total mercury dose children received from Thimerosal-containing vaccines/Rho (D)-immune globulin preparations. Based upon differential diagnoses, 8 of 9 patients examined were exposed to significant mercury from Thimerosal-containing biologic/vaccine preparations during their fetal/infant developmental periods, and subsequently, between 12 and 24 mo of age, these previously normally developing children suffered mercury toxic encephalopathies that manifested with clinical symptoms consistent with regressive ASDs.” –  Journal of Toxicology and Environmental Health, 2007



Lawsuits and Compensation in the Vaccine Courts

US govt compensates children for autism caused by vaccines
http://www.wesupportorganic.com/2014/11/u-s-government-compensates-83-autistic-children-for-vaccine-injury.html

Autism Law and Advocacy and the Vaers Court
A review of brain injury cases
http://www.ebcala.org/unanswered-questions

 A Review of Compensated Cases of Vaccine-Induced Brain Injury
http://www.ebcala.org/unanswered-questions

Here is a list of studies from around the world that support Dr. Wakefield’s research
The following peer-reviewed papers support the findings of the original work by Wakefield and colleagues at the Royal Free Hospital in the UK:
1) Furlano R, Anthony A, Day R, Brown A, Mc Garvey L, Thomson M, et al. Colonic CD8 and T cell filtration with epithelial damage in children with autism. J Pediatr 2001;138:366-72.
 2) Torrente F., Machado N., Perez-Machado M., Furlano R., Thomson M., Davies S., Wakefield AJ, Walker-Smith JA, Murch SH. Enteropathy with T cell infiltration and epithelial IgG deposition in autism. Molecular Psychiatry. 2002;7:375-382.
 3) Ashwood P, Murch SH, Anthony A, Hayes C, Machado MP, Torrente F, Thomson MA, Heuschkel R, Wakefield AJ., Mucosal and peripheral blood lymphocyte cytokine profiles in children with regressive autism and gastrointestinal symptoms: Mucosal immune activation and reduced counter regulatory interleukin-10. Gastroenterol. 2002;122 (Suppl):A617
4) Ashwood P, Anthony A, Torrente F, Wakefield AJ. Spontaneous mucosal lymphocyte cytokine profiles in children with autism and gastrointestinal symptoms: mucosal immune activation and reduced counter regulatory interleukin-10. J Clin Immunol. 2004;24(6):664-73.
5) Wakefield AJ., Puleston J. Montgomery SM., Anthony A., O’Leary J.J., Murch SH Entero-colonic encephalopathy, autism and opioid receptor ligands. Alimentary Pharmacology & Therapeutics. 2002;16:663-674
6) Wakefield AJ. The Gut-Brain Axis in Childhood developmental Disorders. Journal of Pediatric Gastroenterology and Nutrition. 2002;34:S14-S17
7) Uhlmann V, Martin CM, Sheils O, Pilkington L, Silva I, Killalea A, Murch SH, Wakefield AJ, O’Leary JJ., Potential viral pathogenic mechanism for new variant inflammatory bowel disease. Molecular Pathology 2002;55:84-90
 8) Ashwood P, Anthony A, Pellicer AA, Torrente F, Wakefield AJ. Intestinal lymphocyte populations in children with regressive autism: evidence for extensive mucosal immunopathology. Journal of Clinical Immunology, 2003;23:504-517.
9) Torrente F, Anthony A, Heuschkel RB, Thomson MA, Ashwood P, Murch SH. Focal-enhanced gastritis in regressive autism with features distinct from Crohn's and Helicobacter pylori gastritis. Am J Gastroenterol. 2004;99:598-605
10) Ashwood P, Wakefield AJ. Immune activation of peripheral blood and mucosal CD3+ lymphocyte cytokine profiles in children with autism and gastrointestinal symptoms. J Neuroimmunol. 2006;173(1-2):126-34.
11) Wakefield AJ, Ashwood P, Limb K, Anthony A. The significance of ileo-colonic lymphoid nodular hyperplasia in children with autistic spectrum disorder. Eur J Gastroenterol Hepatol. 2005 Aug;17(8):827-36.
The following two peer-reviewed papers from the Royal Free Hospital in the UK were withdrawn for political reasons, but the science remains valid and relevant
1) Wakefield AJ, Murch SM, Anthony A et al., Ileal- lymphoid- nodular Hyperplasia, Non- specific Colitis, and Pervasive Developmental Disorder in Children, The Lancet, 1998, 351(9103): 637– 41.
2) Wakefield AJ, Anthony A, Murch SH, Thomson M, Montgomery SM, Davies S, Walker-Smith JA. Enterocolitis in children with developmental disorder. American Journal of Gastroenterology 2000;95:2285-2295.
The following peer-reviewed papers duplicate Dr. Wakefield’s original findings in five additional countries, including the US, Italy, Venezuela, Canada and Poland:
 1) Gonzalez, L. et al., Endoscopic and Histological Characteristics of the Digestive Mucosa in Autistic Children with gastro-Intestinal Symptoms. Arch Venez Pueric Pediatr, 2005;69:19-25.
 2) Balzola, F., et al., Panenteric IBD-like disease in a patient with regressive autism shown for the first time by wireless capsule enteroscopy: Another piece in the jig-saw of the gut-brain syndrome? American Journal of Gastroenterology, 2005. 100(4): p. 979- 981.
 3) Balzola F et al . Autistic enterocolitis: confirmation of a new inflammatory bowel disease in an Italian cohort of patients. Gastroenterology 2005;128(Suppl. 2);A-303.
4) Krigsman A, Boris M, Goldblatt A, Stott C. Clinical Presentation and Histologic Findings at Ileocolonoscopy in Children with Autistic Spectrum Disorder and Chronic Gastrointestinal Symptoms. Autism Insights. 2009;1:1–11.
5) Horvath K., Papadimitriou J.C., Rabsztyn A., Drachenberg C., Tildon J.T. 1999. Gastrointestinal abnormalities in children with autism. J. Pediatrics 135: 559-563.
6) Sabra S, Bellanti JA, Colon AR. Ileal lymphoid hyperplasia, non-specific colitis and pervasive developmental disorder in children. The Lancet 1998;352:234-5.
7) Sabra A, Hartman D, Zeligs BJ et al., Linkage of ileal-lymphoid-nodular hyperplasia (ILNH), food allergy and CNS developmental abnormalities: evidence for a non-IgE association, Ann Allergy Asthma Immunol, 1999;82:8
8) Galiatsatos P, Gologan A, Lamoureux E, Autistic enterocolitis: Fact or fiction? Can J Gastroenterol. 2009:23:95-98
9) Jarocka-Cyrta et al. Brief report: eosinophilic esophagitis as a cause of feeding problems in an autistic boy. The first reported case.J. Aut. Dev. Disord. Online July 10, 2010
The following articles support the importance of recognizing and treating gastrointestinal symptoms in autistic children:
 1)    Buie T, et al. Pediatrics. 2010 Jan;125 Suppl 1:S19-29.  Recommendations for evaluation and treatment of common gastrointestinal problems in children with ASDs.
 2)    Buie T, et al.  Pediatrics.  2010 Jan;125 Suppl 1:S1-18.  Evaluation, diagnosis, and treatment of gastrointestinal disorders in individuals with ASDs: a consensus report. 
"Autism may be a disorder linked to the disruption of the G-alpha protein, affecting retinoid receptors in the brain. A study of sixty autistic children suggests that autism may be caused by inserting a G-alpha protein defect, the pertussis toxin found in the D.P.T. vaccine, into genetically at-risk children." Mary N. Megson, M.D.

The following peer-reviewed papers provide further support for gastrointestinal disturbances involving the immune system in autism. 
1) Jyonouchi H., Sun S., Lee H. 2001. Proinflammatory and regulatory cytokine production associated with innate and adaptive immune responses in children with autism spectrum disorders and developmental regression. J. Neuroimmunol. 120(1-2):170-9
2) Jyonouchi H, Geng L, Ruby A, Zimmerman-Bier B. Dysregulated Innate Immune Responses in Young Children with Autism Spectrum Disorders: Their Relationship to Gastrointestinal Symptoms and Dietary Intervention. Neuropsychobiology. 2005;28:5177-85
3) Jyonouchi H, Geng L, Ruby A, Reddy C, Zimmerman-Bier B. Evaluation of an association between gastrointestinal symptoms and cytokine production against common dietary proteins in children with autism spectrum disorders. J Pediatr.2005;146(5):605-10.
4) Jyonouchi H, Sun S, Itokazu N. Innate immunity associated with inflammatory responses and cytokine production against common dietary proteins in patients with autism spectrum disorder. Neuropsychobiology. 2002;46(2):76-84.
5) Vojdani A, O'Bryan T, Green JA, McCandless J, Woeller KN, Vojdani E, Nourian AA, Cooper EL. Immune response to dietary proteins, gliadin and cerebellar peptides in children with autism. Nutr. Neurosci. 2004;7:151-61.
6) Whiteley P, Haracopos D, Knivsberg AM, Reichelt KL, Parlar S, Jacobsen J, Seim A, Pedersen L, Schondel M, Shattock P. The ScanBrit randomised, controlled, single-blind study of a gluten- and casein-free dietary intervention for children with autism spectrum disorders. Nutr Neurosci. 2010;13(2):87-100.
7) Knivsberg AM, Reichelt KL, Høien T, Nødland M. A randomised, controlled study  of dietary intervention in autistic syndromes. Nutr Neurosci. 2002;5(4):251-61.
8) Balzola F, et al. Beneficial behavioural effects of IBD therapy and gluten/casein-free diet in an Italian cohort of patients with autistic enterocolitis followed over one year. Gastroenterology 2008;4:S1364.
9) Valicenti-McDermott M., McVicar K., Rapin I., et al., Frequency of Gastrointestinal Symptoms in Children with Autistic Spectrum Disorders and Association with Family History of Autoimmune Disease. Developmental and Behavioral Pediatrics. 2006;27:128-136
10) Chen B, Girgis S, El-Matary W. Childhood Autism and Eosinophilic Colitis. Digestion 2010;18:127-129
11) Sandler R, Finegold SM., Bolte ER., et al. Short-term benefit from oral vancomycin treatment of regressive-onset autism. J Child Neurol. 2000;15:429-435

http://mercola.fileburst.com/PDF/4.Horvath%201.pdf 
http://mercola.fileburst.com/PDF/Singh%20autoimmune%20autism.pdf  
http://mercola.fileburst.com/PDF/celaic%20and%20autism.pdf 

http://mercola.fileburst.com/PDF/5.Furlano.pdf

http://mercola.fileburst.com/PDF/9.lymphocytes%20in%20autism.pdf

http://mercola.fileburst.com/PDF/Singh%20Elevated%20MV%20antibody%20titers%202003.pdf

http://mercola.fileburst.com/PDF/Neuropsych%20--%20Jyonouchi.pdf

http://mercola.fileburst.com/PDF/Jyonouchi%202005.pdf
http://mercola.fileburst.com/PDF/Singh.pdf

http://mercola.fileburst.com/PDF/Cdn%20journal%20of%20Gstrto%20-Autistic%20Entercolitis%20Fact%20ot%20Fiction%20Fed%202009.pdf

http://mercola.fileburst.com/PDF/Krigsman%20proof.pdf 
http://mercola.fileburst.com/PDF/GI%20symptoms%20in%20PDD%20Yale.pdf 

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