Gut bacteria linked to autism#ASD#iBelieve#Vaccines

By Dr Flannery  

The digestive tract is home to more than 100 trillion microorganisms. That’s ten times the number of cells in the human body! Although humans can survive without these tiny guests, they perform a host of useful functions, such as fermenting unused food, preventing growth of harmful bacteria, producing vitamins, and training the immune system. But did you know the bacteria in your gut can affect your brain, too? In fact, recent research on the gut has found some interesting links between the gut microbiome – the complex and unique microbiological community within the gut –- and autistic behavior in children.

As parents well know, children with autism have a high rate of problems with gastrointestinal (GI) disorders. The resulting discomfort can worsen behaviors and interfere with their ability to participate in, and benefit from, activities of daily life, education, and therapeutic activities.

On a related note, it has been known for some time that children with autism tend to have abnormal and less diverse communities of gut bacteria than children without autism. Recent research on children with autism has revealed these interesting facts:

Their intestinal cells show abnormalities in how they break down and transport carbohydrates, which can affect the amount and type of nutrients these cells provide to intestinal bacteria. This in turn may alter the makeup of the intestine’s normal community of digestive bacteria — with ill result.
Their intestines are home to abnormal amounts of certain digestive bacteria that contribute to digestive problems, intestinal inflammation, and more severe autism symptoms.
There are lower levels of three important gut bacteria; Prevotella, Coprococcus, and Veillonellaceae.
Theory has it that the community of bacteria in the gut affects the immune system, which then sends messages to the brain. This may explain why parents of children with autism report that special diets and probiotics (nutritional supplements containing “good” bacteria) improve their children’s digestion as well as their behavior.

The Gut-to-Brain Connection
The most recent research on the connection between the gut and autism explores how the gut microbiome affects the autistic brain. Researchers at Arizona State University found that concentrations of metabolites (byproducts) from seven specific bacteria are more prevalent in autistic children’s fecal samples. According to study author Dae-Wook Kang, “Most of the seven metabolites could play a role in the brain … We suspect that gut microbes may … affect gut-to-brain communication and/or alter brain function.”

Of the seven metabolites that were noticed, three warrant special note for their apparent relation to brain function, thereby behavior:

Homovanillate was present at lower levels in children with autism; it is normally produced when dopamine (an important brain neurotransmitter involved in many aspects of mood and behavior) is broken down.
N,N-dimethylglycine was found at lower levels; it has been used before to decrease autism symptoms.
The ratio of glutamine to glutamate was higher: these are metabolized into GABA, a vital inhibitory neurotransmitter associated with relaxation. An imbalance between glutamate and GABA transmission has been associated with autistic-spectrum type behaviors such as hyper-excitation.
These connections offer insight into possible link between the gut biome and the behaviors seen in autistic children. Researchers say they would like to conduct a clinical study using fecal transplants from healthy donors to see if normalizing an individual’s community of gut bacteria would reduce autism symptoms.

Although the study was small, it adds to the growing body of research that tells us the gut is closely tied to the brain.

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Frank B. Engley, Jr., PhD – A Pioneer in the research of Thimerosal Efficacy and Toxicity#Vaccines#ASD#IBelieve

“Apparently the medical profession does not read the safety data sheets provided by Lilly and other chemical manufacturers made available to physicians, pharmacies, hospitals and health departments. It states for thimerosal: toxic, mutagen, allergen, hypersensitivity, alters genetic materials, may cause mild to severe mental retardation, may cause mild to severe motor coordination, all sounds a lot like autism.”

Frank B. Engley, Jr., PhD, by Eric Gladen and David Ayoub, MD

How to Lie to a Generation of Families – Malfeasance in the CDCs Vaccine Safety Program – Dr. Brian Hooker#Flu shot#ASD#Vaccines

If you receive a Thimerosal (mercury) containing flu shot when pregnant, then you are 37% more likely to have a child with autism.

Find the details, and much more within the clip below. This talk was given at AutismOne from Dr. Brian Hooker, who is a PhD, PE, biochemist, researcher, investigator, vaccine industry watchdog, and father of an autistic child.

You can gather additional details to educate yourself in the link below.  Often a practitioner will say there is no mercury, but sometimes that is what they are told, and they do not know for certain.

There are many more harmful ingredients, but if you determine to take the shot, for work purposes, then protect yourself, and your family by insuring you read the package inserts, to insure no Thimerosal is contained within the shot.

  You Have A Choice!  🙂

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Study Links Vaccine Induced Immune Overload to Autism, Diabetes, Obesity#Vaccines#Health#ASD

Written By: Sayer Ji, Founder

A new vaccine study published in Molecular and Genetic Medicine is bringing to the forefront the disturbing connection between the dramatic expansion in the quantity of routine childhood vaccines administered and a corresponding increase in inflammation-associated disorders.

Titled, “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 Prediabetes and other Immune Mediated Diseases,” the study argues that vaccine-induced immune overload is a driving factor in a number of rapidly accelerating childhood epidemics including:

  • Autism
  • Type 1 diabetes
  • Asthma
  • Food allergies
  • Many autoimmune diseases
  • Obesity
  • Type 2 diabetes
  • Non-alcoholic fatty liver disease (NAFL)
  • Metabolic disease.

The paper sought to provide a theory of vaccine induced immune overload to explain many observations about the changes in the epidemics.  The fundamental problem, according to the study, is that vaccinology assumes a ‘one size fits all’ approach that results in the majority of the vaccine recipients having overstimulated immune systems:

“One major problem with vaccines is the concept of one size fits all. Package inserts of almost all vaccines recommend a dose based on age. In order for a vaccine to be a commercial success it is expected to induce a protective immune response in well over 90% of children. In order for this to happen a dose, based on age, must stimulate a protective immune response in those with the weakest immune system. In the process of doing this, the other 90% or more of children have their immune system over stimulated. The process of over stimulating the immune system time and time again increases the risk of inflammatory diseases like autoimmune diseases, and allergies which cause even more inflammation.”…

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Should Premature Babies Be Included In The One-Size-Fits-All Vaccination Policy?#premature#Health#vaccines

by Christina England       

According to a fact sheet published by the University of Auckland, premature babies weighing as little as seventeen ounces are supposed to be vaccinated with same dose of vaccines given to an adult. The vaccination schedule is not being adjusted in any way and does not take into consideration a premature baby’s fragility or their weight.

Their decision has left many professionals questioning whether or not the “one-size-fits-all” vaccination policy is really suitable for premature babies, given the fact that many of them are not yet medically stable.

The University of Auckland believes that no changes are needed and recommends that the vaccination schedule should not be adjusted. They insist that these fragile babies should be vaccinated according to their chronological age, rather than their due date, and that they should be vaccinated in line with the vaccination schedule set by the government.

Is The One-Size-Fits-All Policy Right For Premature Babies?

In the USA, approximately 500,000 babies are born prematurely each year. These are babies born before 37 weeks of completed pregnancy. According to the Centers for Disease Control and Prevention (CDC), the earlier a baby is born, the more likely they are to suffer from severe health problems. Many of these babies die, while others may be severely disabled with learning disabilities, cerebral palsy, respiratory disorders, visual complications, hearing loss and feeding and digestive problems.

The CDC states:

“Although most babies born just a few weeks early do well and have no health issues, some do have more health problems than full term babies. For example, a baby born at 35 weeks is more likely to have—

  • jaundice
  • breathing problems
  • longer hospital stay” [1]

Many of these babies spend weeks, if not months, in incubators, while their lives hang in the balance. Is it really appropriate to vaccinate such fragile babies, regardless of their state of health?

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CDC’s Vaccine Safety Research is Exposed as Flawed and Falsified in Peer-Reviewed Scientific Journal#Vaccines#ASD#Health

CDC’s Vaccine Safety Research is Exposed as Flawed and Falsified in Peer-Reviewed Scientific Journal

PRNewswire-iReach/ — Just months after U.S. Congressman Bill Posey compared the Center for Disease Control (CDC)’s vaccine safety studies to the SEC’s Bernie Madoff scandal, malfeasance in the CDC’s studies of thimerosal-containing vaccines has, for the first time, been documented in peer-reviewed scientific literature. While the CDC states on its website that “low doses of thimerosal in vaccines do not cause harm, and are only associated with minor local injection site reactions like redness and swelling at the injection site,” the journal BioMed Research International now provides direct evidence that the CDC’s safety assurances about the mercury-containing preservative are not fact-based, according to the article’s lead author, Brian Hooker, PhD.

The paper opens by citing over 165 studies that have found Thimerosal to be harmful, including 16 studies that had reported outcomes in human infants and children of death, acrodynia, poisoning, allergic reaction, malformations, auto-immune reaction, Well’s syndrome, developmental delay and neurodevelopmental disorders including tics, speech delay, language delay, ADHD and autism. These findings by multiple independent research groups over the past 75+ years have consistently found thimerosal to be harmful. “Substantial scientific evidence exists and has existed for many years that the vaccine ingredient thimerosal is a developmental neurotoxin” says George Lucier, former Associate Director of the National Toxicology Program.

Studies showing harm from thimerosal sharply contradict published outcomes of six CDC coauthored and sponsored papers – the very studies that CDC relies upon to declare that thimerosal is “safe” for use in infant and maternal vaccines. Dr. Hooker, biochemist and vaccine industry watchdog, said of the six CDC studies, “Each of these papers is fatally flawed from a statistics standpoint and several of the papers represent issues of scientific malfeasance.  For example, important data showing a relationship between thimerosal exposure and autism are withheld from three of the publications (Price et al. 2010, Verstraeten et al. 2003 and Madsen et al. 2003).  This type of cherry-picking of data by the CDC in order to change the results of important research studies to support flawed and dangerous vaccination policies should not be tolerated.”

Dr. Boyd Haley, international expert in mercury toxicity and a co-author of the recently published paper said “There is no doubt that authorities in the CDC have initiated and participated in a cover-up of vaccine-induced damage from thimerosal to our children—-and this I consider criminal.” The paper, “Methodological Issues and Evidence of Malfeasance in Research Purporting to Show Thimerosal in Vaccines is Safe,” was published on June 6 and contains eight pages of evidence that the CDC has had knowledge of the vaccine preservative’s neurological risks, yet continues to cover them up.

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Herd Immunity: Myth or Reality?#Vaccines#Health#ASD

Written By: Tetyana Obukhanych, PhD 

Tetyana Obukhanych (Ph.D. in immunology from Rockefeller University, New York, NY) is the author of Vaccine Illusion. The book is available in pdf e-book form for immediate download here.  

Even though endemic outbreaks of common childhood diseases, such as measles, have been eliminated in some regions after prolonged mass-vaccination efforts, we are still being constantly reminded that reducing vaccination coverage of children in a community poses the risk of a reimported disease outbreak with potentially dire consequences to infants and immuno-compromised individuals.  We are also being persuaded that implementing strict vaccination compliance will prevent an outbreak and protect vaccine-ineligible infants via the herd-immunity effect.

There is no question that a disease outbreak can happen in a non-immune community, if a virus gets there.  The real question is, how well can high-vaccination compliance ensure herd immunity and protect a community from an outbreak?

Herd Immunity, a Key Principle

Herd immunity is not an immunologic idea, but rather an epidemiologic construct, which theoretically predicts successful disease control when a certain pre-calculated percentage of people in the population are immune from disease.  A scholarly article on herd immunity states:

“Along with the growth of interest in herd immunity, there has been a proliferation of views of what it means or even of whether it exists at all. Several authors have written of data on measles, which “challenge” the principle of herd immunity and others cite widely divergent estimates (from 70 to 95 percent) of the magnitude of the herd immunity threshold required for measles eradication.”[1]

Herd immunity has been deemed instrumental in rapid disease eradication.  Relying upon the meticulous work of Dr. A. W. Hedrich, who documented annual measles attack rates in relation to the proportion of naturally immune people in the 1900s-1930s, the United States Public Health Service had confidently announced in 1967 its intent to swiftly eradicate measles in the USA over the Winter by vaccinating a sufficient number of still susceptible children.[2] Mass vaccination was implemented, but the expected herd-immunity effect did not materialize and measles epidemics did not stop in 1967.

The concept of herd immunity has been used to justify the idea of vaccinating children against a mild disease, who do not personally benefit from such vaccination, to protect a vulnerable but vaccine-ineligible segment of the population.  For example, rubella is not dangerous for children.  However, for pregnant women who have not become immune from rubella prior to pregnancy, a rubella infection poses a danger during the first trimester by increasing the risk of fetal developmental abnormalities (congenital rubella).  Obviously, vaccination with a live-attenuated viral vaccine, such as the rubella vaccine, is contraindicated during pregnancy….

Herd Immunity, a Flawed Concept…

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Dr. David Lewis at AutismOne: An Insider’s View of Scientific Integrity in a State of Crisis#Vaccines#ASD#Health

On Friday, May 23, Dr. David Lewis delivered a powerful talk entitled: Science For Sale: How the U.S. Government Controls Science to Support its Policies. Dr. Lewis is an internationally recognized research microbiologist, formerly with the EPA’s Office of Research and Development. Now retired from government service, Dr. Lewis has written of his research and the ensuing change in policies at the EPA and other federal agencies in the last 30 years that have led to a mass exodus of microbiologists, engineers, and scientists from government agencies.  Dr. Lewis has chronicled this in his newly released book,Science for Sale: How the US Government Uses Powerful Corporations and Leading Universities to Support Government Policies, Silence Top Scientists, Jeopardize Our Health, and Protect Corporate Profit.Sold..

Dr. Lewis points out that many books have been written on corporate influence on scientific and academic integrity.  However, he states that corporate influence is just a subset of a much larger problem – the government’s own agenda and policies which dictate and even predetermine research outcomes.  Advocates have observed this phenomenon time and again in the government’s study of autism causation.  Government-sponsored scientists have focused on genetic and environmental factors linked to autism and chronic disease while publishing studies with flawed statistical analyses and other deceptive tactics to obscure any connections with vaccines recommended by the CDC.

Who is Causing Viral Epidemics? Consumers or the Medical Industry Designed to Protect Us?…

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