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  1. Link to Post #81
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    Default Re: Autism

    FDA Document Reports Autism Link After Tetanus, Pertussis & Diptheria Combination Vaccine

    April 9, 2014 by Arjun Walia. 24 Comments.




    An FDA report from 2005 titled “Diphtheria and Tetanus Toxoids and Acellular Pertussis Vaccine Adsorbed Tripedia” outlines a number of adverse events reported during post-approval use of the Tripedia vaccine, and one of them is autism. (1)

    Health-care providers who administer vaccines are required to keep permanent vaccination records, they are also required to report any occurrences (adverse events such as autism) to the Secretary of the US Department of Health and Human Services following immunization of any events.

    The report also illustrates that the tripedia vaccine has not been evaluated for its carcinogenic or mutagenic potentials or impairment of fertility. This makes one wonder what other vaccines have not been properly evaluated. Furthermore, it illustrates how a review by the Institute of Medicine (IOM) found evidence for a causal relationship between tetanus toxoid and both brachial neuritis and Guillain-Barre syndrome.

    This document just adds more confusion to the topic of vaccines and autism. How can the general public be expected to believe there is no link when more evidence keeps on mounting that suggests that there could be. Why does an FDA document even mention autism and its association with vaccinations?

    There is good reason to be confused, this isn’t fear mongering.

    For example, a recently published study in the peer-reviewed journal Translational Neurodegeneration provided epidemiological evidence supporting an association between increasing organic-Hg exposure from thimerosal-containing childhood vaccines and the risk of ASD diagnosis. (2)

    On the other hand, a study published in March of 2013 determined that “Increasing exposure to Antibody-Stimulating Proteins and Polysaccharides (antigens) in Vaccines is Not Associated with Risk of Autism.” You can view that study here.

    Back the other way, there are a number of court cases where families have been compensated for vaccine related injuries. Courts have ruled (in multiple cases) that vaccines did indeed cause autism. How could a court of law rule this to be so if there is no scientific link (as claimed by governing health authorities) between vaccines and autism? Courts have compensated over 80 families linking vaccines to autism. Here is one example, you can learn more about that process by watching this video.

    I think it’s important to keep an open mind with regards to health authorities covering up information involving the risks associated with vaccines. Proof is already in the public domain. Researchers at the University of British Colombia have uncovered evidence showing that health authorities, pharmaceutical companies and vaccine manufactures have known about the dangers associated with multiple vaccines, but have withheld them from public knowledge in order to maintain “herd immunity.” (3)

    There have also been reports that the CDC has been hiding data showing that mercury in vaccines is linked to autism, you can read more about that here.

    The link between vaccines and autism is still speculative. With all the information available in the public domain, I do not see how anybody can say with certainty that there is no possibility of a link. The studies below demonstrate that this has been the subject of rigorous investigation by researchers all over the world, and the investigations continue until this day.

    Sure, there are doctors that support and trust vaccinations, but just as valid are the arguments of those that don’t support them. They should not be ignored. The point I’m trying to make is that there is no definite answer, that the debate has not been settled as so many governing health authorities claim it to be.


    Besides the vaccine autism controversy, vaccines have been linked to a number of other health ailments,

    A paper published in the peer reviewed International Journal of Environmental Research and Public Health titledThimerosal Exposure and the Role of Sulfation Chemistry and Thiol Availability in Autism concluded:

    “With the rate of children diagnosed with an ASD in the US now exceeding 1 in 50 children and the rate of children with neurodevelopment/behavioural disorders in the US now exceeding 1 in 6 children, and the preceding evidence showing that there is vulnerability to ™ that would not be known without extensive testing, the preponderance of the evidence indicates that ™ should be removed from all vaccines”

    A paper published in the Journal of Toxicology titled B-Lymphocytes from a population of Children with Autism Spectrum Disorder and Their Unaffected Siblings Exhibit Hypersensitivity to Thimerosal clearly demonstrates that certain individuals with a mild mitochondrial defect may be highly susceptible to mitochondrial specific toxins like thimerosal.

    A study published in the Journal Annals of Epidemiology has shown that giving the Hepatitis B vaccine to newborn baby boys could triple the risk of developing an autism spectrum disorder compared to boys who were not vaccinated as neonates. The research was conducted at Stony Brook University Medical Centre, NY.

    A study published in the Journal of Inorganic Biochemistry by researchers at the Neural Dynamics Group, Department of Ophthalmology and Visual Sciences at the University of British Columbia determined that Aluminum, a highly neurotoxic metal and the most commonly used vaccine adjuvant may be a significant contributing factor to the rising prevalence of ASD in the Western World. They showed that the correlation between ASD prevalence and the Aluminum adjuvant exposure appears to be the highest at 3-4 months of age. The studies also show that children from countries with the highest ASD appear to have a much higher exposure to Aluminum from vaccines. The study points out that several prominent milestones of brain development coincide with major vaccination periods for infants. These include the onset of synaptogenesis (birth), maximal growth velocity of the hippocampus and the onset of amygdala maturation. Furthermore, major developmental transition in many bio-behavioural symptoms such as sleep, temperature regulation, respiration and brain wave patterns, all of which are regulated by the neuroendocrine network. Many of these aspects of brain function are known to be impaired in autism, such as sleeping and brain wave patterns.
    According to the FDA, vaccines represent a special category of drugs as they are generally given to healthy individuals. Further according to the FDA, “this places significant emphasis on their vaccine safety.” While the FDA does set an upper limit for Aluminum in vaccines at no more that 850/mg/dose, it is important to note that this amount was selected empirically from data showing that Aluminum in such amounts enhanced the antigenicity of the vaccine, rather than from existing safety. Given that the scientific evidence appears to indicate that vaccine safety is not as firmly established as often believed, it would seem ill advised to exclude paediatric vaccinations as a possible cause of adverse long-term neurodevelopment outcomes, including those associated with autism.
    A study published in the Journal of Toxicology and Environmental Health, Part A: Current Issues by the Department of Economics and Finance at the University of New York shows how researchers suspect one or more environmental triggers are needed to develop autism, regardless of whether individuals have a genetic predisposition or not. They determined that one of those triggers might be the “battery of vaccinations that young children receive.” Researchers found a positive and statistically significant relationship between autism and vaccinations. They determined that the higher the proportion of children receiving recommended vaccinations, the higher the prevalence of autism. A 1 % increase in vaccination was associated with an additional 680 children having autism. The results suggest that vaccines may be linked to autism and encourages more in depth study before continually administering these vaccines.

    A study published in the Journal of Toxicology by the Department of Neurosurgery at The Methodist Neurological Institute in Houston has shown that ASD is a disorder caused by a problem in brain development. They looked at B-cells and their sensitivity levels to thimerosal, a commonly used additive in many vaccines. They determined that ASD patients have a heightened sensitivity to thimerosal which would restrict cell proliferation that is typically found after vaccination. The research shows that individuals who have this hypersensitivity to thimerosal could make them highly susceptible to toxins like thimerosal, and that individuals with a mild mitochondrial defect may be affected by thimerosal. The fact that ASD patients’ B cells exhibit hypersensitivity to thimerosal tells us something.

    A study published in the Journal of Biomedical Sciencesdetermined that the autoimmunity to the central nervous system may play a causal role in autism. Researchers discovered that because many autistic children harbour elevated levels of measles antibodies, they should conduct a serological study of measles-mumps-rubella (MMR) and myelin basic protein (MBP) autoantibodies. They used serum samples of 125 autistic children and 92 controlled children. Their analysis showed a significant increase in the level of MMR antibodies in autistic children. The study concludes that the autistic children had an inappropriate or abnormal antibody response to MMR. The study determined that autism could be a result from an atypical measles infection that produces neurological symptoms in some children. The source of this virus could be a variant of MV, or it could be the MMR vaccine.

    Study published in the Annals of Clinical Psychiatry suggests that Autism is likely triggered by a virus, and that measles virus (MV and/or MMR vaccine) might be a very good candidate. It supports the hypothesis that a virus-dincued autoimmune response may play a causal role in autism.

    A study published in the American Journal of Clinical Nutrition determined that an increased vulnerability to oxidative stress and decreased capacity for methylation may contribute to the development and clinical manifestation of autism. It’s well known that viral infections cause increased oxidative stress. Research suggests that metals, including those found in many vaccines are directly involved in increasing oxidative stress.

    A study published by the Department of Pharmaceutical Sciences at Northeastern University, Boston determined that a novel growth factor signalling pathway that regulates methionine synthase(MS) activity and thereby modulates methylation reactions. The potent inhibition of this pathway by ethanol, lead, mercury, aluminum and thimerosal suggests that it may be an important target of neurodevelopmental toxins. You can read more about this here, and here. You can read more about the MS/autism link here

    A study published in the Journal of Child Neurologyexamined the question of what is leading to the apparent increase in autism. They expressed that if there is any link between autism and mercury, it is crucial that the first reports of the question are not falsely stating that no link occurs. Researchers determined that a significant relation does exist between the blood levels of mercury and the diagnosis of an autism spectrum disorder.

    A study published in the Journal of Child Neurology noted that autistic spectrum disorders can be associated with mitochondrial dysfunction. Researchers determined that children who have mitochondrial-related dysfunctional cellular energy metabolism might be more prone to undergo autistic regression between 18 and 30 months of age if they also have infections or immunizations at the same time.

    A study conducted by Massachusetts General Hospital at the Centre for Morphometric Analysis by the department of Paediatric Neurology illustrates how autistic brains have a growth spurt shortly after birth and then slow in growth a few short years later. Researchers have determined that neuroinflammation appears to be present in autistic brain tissue from childhood through adulthood. The study excerpt reads:
    Oxidative stress, brain inflammation and microgliosis have been much documented in association with toxic exposures including various heavy metals. The awareness that the brain as well as medical conditions of children with autism may be conditioned by chronic biomedical abnormalities such as inflammation opens the possibility that meaningful biomedical interventions may be possible well past the window of maximal neuroplasticity in early childhood because the basis for assuming that all deficits can be attributed to fixed early developmental alterations in net
    A study conducted by the Department of Paediatrics at the University of Arkansas determined that thimerosal-induced cytotoxicity was associated with the depletion of intracellular glutathione (GSH) in both cell lines. The study outlines how many vaccines have been neurotoxic, especially to the developing brain. Depletion of GSH is commonly associated with autism. Although thimerosal has been removed from most children’s vaccines, it is still present in flu vaccines given to pregnant women, the elderly and to children in developing countries.

    A study published in the Public Library of Science (PLOS) determined that elevation in peripheral oxidative stress is consistent with, and may contribute to more severe functional impairments in the ASD group. We know that oxidative stress is triggered by heavy metals, like the ones contained in multiple vaccines.

    A study conducted by the University of Texas Health Science Centre by the Department of Family and Community Medicine determined that for each 1,000 Ib of environmentally released mercury, there was a 43% increase in the rate of special education services and a 61% increase in the rate of autism. Researchers emphasized that further research was needed regarding the association between environmentally released mercury and developmental disorders such as autism.

    A study published in the International Journal of Toxicology determined that in light of the biological plausibility of mercury’s role in neurodevelopment disorders, the present study provides further insight into one possible mechanism by which early mercury exposures could increase the risk of autism.

    A study published in the Journal of Toxicology and Environmental Health determined that mercury exposure can induce immune, sensory, neurological, motor and behavioural dysfunctions similar to traits defining or associated with ASDs. Based upon differential diagnoses, 8 of 9 patients examined were exposed to significant mercury from Thimerosal-containing vaccine preparations during their fetal/infant developmental periods. These previously normal developing children suffered mercury encephalopathies that manifested with clinical symptoms consistent with regressive ASDs. Evidence for mercury intoxication should be considered in the differential diagnosis as contributing to some regressive ASDs.

    A study published by the US National Library of Medicine conducted by the University of Texas Health Science Centre suspected that persistent low-dose exposures to various environmental toxicants including mercury, that occur during critical windows of neural development among genetically susceptible children, may increase the risk for developmental disorders such as autism.

    A study conducted by the Department of Obstetrics and Gynaecology at University of Pittsburgh’s School of Medicine showed that Macaques are commonly used in pre-clinical vaccine safety testing. Collective Evolution does not support animal testing, we feel there is a large amount of evidence and research that already indicated the links to vaccines in which some animals have been used to illustrate. The objective of this study was to compare early infant cognition and behaviour with amygdala size and opioid binding in rhesus macaques receiving the recommended childhood vaccines. The animal model, which examines for the first time, behavioural, functional and neuromorphometric consequences of the childhood vaccine regimen, mimics certain neurological abnormalities of autism. These findings raise important safety issues while providing a potential model for examining aspects of causation and disease pathogenesis in acquired disorders of behaviour and development.

    A study conducted by The George Washington University School of Public Health from the Department of Epidemiology and Biostatistics determined that significantly increased rate ratios were observed for autism and autism spectrum disorders as a result of exposure to mercury from Thimerosal-containing vaccines.

    A study published in the Journal Cell Biology and Toxicology by Kinki University in Osaka, Japan determined that in combination with the brain pathology observed in patients diagnosed with autism, the present study helps to support the possible biological plausability for how low-dose exposure to mercury from thimerosal-containing vaccines may be associated with autism.

    A study published by the Journal Lab Medicine determined that vaccinations may be one of the triggers for autism. Researchers discovered that substantial data demonstrates immune abnormality in many autistic children consistent with impaired resistance to infection, activation of inflammatory responses and autoimmunity. Impaired resistance may predispose to vaccine injury in autism.

    A study published in the Journal Neurochemical Research determined that since excessive accumulation of extracellular glutamate is linked with excitotoxicity, data implies that neonatal exposure to thimerosal-containing vaccines might induce excitotoxic brain injuries, leading to neurodevelopmental disorders.


    Sources:

    (1) http://www.fda.gov/downloads/biologicsbloodvaccines/vaccines/approvedproducts/ucm101580.pdf

    (2) http://www.ncbi.nlm.nih.gov/pubmed/24354891

    (3) http://nsnbc.me/wp-content/uploads/2013/05/BSEM-2011.pdf
    Last edited by Hervé; 24th April 2014 at 15:03.

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    Default Re: Autism

    thank you so much for taking the trouble to compile and post that.
    sometimes i let the "wrong side" beat me, convince me we're crazy here,

    but we're not -

  4. Link to Post #83
    France Honored, Retired Member. Hervé passed on 13 November 2024.
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    Default Re: Autism

    Quote Posted by Tesla_WTC_Solution (here)
    thank you so much for taking the trouble to compile and post that.
    sometimes i let the "wrong side" beat me, convince me we're crazy here,

    but we're not -
    ... errrr...

    I didn't compile the whole thing, Arjun Walia did and posted it at: http://www.collective-evolution.com/...ation-vaccine/

    ...where the hyperlink under the title (blue highlight) would have led you: FDA Document Reports Autism Link After Tetanus, Pertussis & Diptheria Combination Vaccine (<--- click )

    In any, case thank you for appreciating it!

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    Default Re: Autism

    http://www.ncbi.nlm.nih.gov/pubmed/23318464

    Behav Brain Res. 2013 Apr 15;243:138-45. doi: 10.1016/j.bbr.2012.12.062. Epub 2013 Jan 11.

    Heparan sulfate deficiency in autistic postmortem brain tissue from the subventricular zone of the lateral ventricles.

    Pearson BL1, Corley MJ, Vasconcellos A, Blanchard DC, Blanchard RJ.
    Author information
    Abstract

    Abnormal cellular growth and organization have been characterized in postmortem tissue from brains of autistic individuals, suggestive of pathology in a critical neurogenic niche, the subventricular zone (SVZ) of the brain lateral ventricles (LV). We examined cellular organization, cell proliferation, and constituents of the extracellular matrix such as N-sulfated heparan sulfate (HS) and laminin (LAM) in postmortem brain tissue from the LV-SVZ of young to elderly individuals with autism (n=4) and age-matched typically developing (TD) individuals (n=4) using immunofluorescence techniques. Strong and systematic reductions in HS immunofluorescence were observed in the LV-SVZ of the TD individuals with increasing age. For young through mature, but not elderly, autistic pair members, HS was reduced compared to their matched TDs. Cellular proliferation (Ki67+) was higher in the autistic individual of the youngest age-matched pair. These preliminary data suggesting that HS may be reduced in young to mature autistic individuals are in agreement with previous findings from the BTBR T+tf/J mouse, an animal model of autism; from mice with genetic modifications reducing HS; and with genetic variants in HS-related genes in autism. They suggest that aberrant extracellular matrix glycosaminoglycan function localized to the subventricular zone of the lateral ventricles may be a biomarker for autism, and potentially involved in the etiology of the disorder.

    Copyright © 2013 Elsevier B.V. All rights reserved.

    PMID: 23318464 [PubMed - indexed for MEDLINE] PMCID: PMC3594061 Free PMC Article

    Quote Powerpoint Slides - People.csail.mit.edu
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    Mar 26, 2014 - Heparan sulfate in the lysosomes is critical for recycling cellular debris. Heparan sulfate deficiency leads to autism. Pineal gland delivers sulfate to cerebral ...

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    Quote Roundup: The “Nontoxic” Chemical that May Be Destroying our Health PDF Print E-mail
    Written by Stephanie Seneff, PhD
    Wednesday, 30 October 2013 18:09
    According to Monsanto, producer of Roundup®, the most popular herbicide used on the planet, the product is nearly nontoxic for humans. The usage of Roundup to kill weeds has skyrocketed around the world since the year 2000, in part because it went off patent that year, but also because of the enormous increase (especially in the U.S.) in the appearance of “Roundup-Ready” GMO crops.4
    Glyphosate, the active ingredient in Roundup, kills weeds by interfering with what is called the shikimate pathway. This pathway is essential in plants for the synthesis of a class of amino acids called the “aromatics.” But this pathway is nonexistent in any mammalian cell. By simple logic, the fact that our cells don’t have this pathway means that glyphosate cannot harm us. Is there a fallacy in this argument?
    GLYPHOSATE CONNECTION TO DISEASE

    While mammals don’t possess the shikimate pathway, all of the microbes that take up residence in our digestive tract do have this pathway, and exposure to glyphosate, the active ingredient in Roundup, will cause them serious stress as a consequence. Studies have shown that glyphosate disrupts the gut bacteria in chickens, 54 cows,29 and pigs,10 causing inflammation in the gut along with an overgrowth of pathogenic forms and concurrent loss of beneficial bacteria. It is now becoming apparent that our gut bacteria, which outnumber our own cells by a factor of ten to one, play many important roles in supplying nutrients and protecting us from toxins.19 There’s also an intricate connection between the gut and the brain, such that an unhealthy digestive system translates into pathologies in the brain.35
    Together with Anthony Samsel, I recently published a paper arguing that Roundup® could plausibly be the most important factor in the observed increase in a number of diseases and conditions like obesity and autism over the past two decades in the U.S.47 Despite spending nearly two and a half times as much on health care as our peer nations,36 the U.S. lags behind many of these other nations in basic metrics like infant mortality and life expectancy.34 The most recent figures for infant mortality place the U.S. at number forty-six, behind Cuba and Guam. Clearly we are doing something wrong, and our wholesale embrace of GMOs is an obvious candidate.
    Ninety percent of the GMO crops (GMO corn, soy, cotton, sugar beets, and canola) are engineered to be “Roundup Ready,” which means that they can be sprayed with Roundup and they will happily soak it up into their tissues. The practice of “desiccating” crops like wheat and sugar cane just before the harvest by spraying them with Roundup is also becoming more and more popular as a way to reduce the amount of vegetation that needs to be cleared in preparation for planting next year’s crop. These two changes in agricultural practices almost certainly mean that Roundup is entering our food supply in record amounts. And most homeowners are likely careless in their use of Roundup to fight weeds on the lawn, due to a misconception that it is nearly nontoxic. A recent study involved sampling glyphosate in the urine of city-dwellers in eighteen European countries.23 Measurable amounts of glyphosate were found in 44 percent of these people, despite the fact that Europe has a much more conservative view towards GMOs than does the U.S.
    So, why is the shikimate pathway so important? Plants and microbes use the shikimate pathway to produce the aromatic amino acids, tryptophan, tyrosine and phenylalanine.22 Because they don’t have this pathway, mammals can’t produce these essential nutrients, and therefore we depend on plants and microbes to provide them for us. So it is logical that glyphosate, by interfering with this pathway, would lead to a deficiency in these nutrients. Tryptophan is the sole precursor to serotonin, and serotonin deficiency is implicated in a litany of diseases and conditions that are prevalent today, including autism, obesity, Alzheimer’s disease, depression, suicide, and homicidal behavior.47 Serotonin is an appetite suppressant8 so it’s hard not to overeat when it is in short supply. If you are disciplined to resist these urges, then you run the risk of depression and Alzheimer’s disease, or autism in your children. Serotonin is the precursor to melatonin, the neurotransmitter that regulates the wake-sleep cycle, and melatonin deficiency is also implicated in autism.2,39 Tyrosine is the precursor to dopamine,41 and impaired dopamine supply is the key defect associated with Parkinson’s disease. Glyphosate activates an enzyme called phenylalanine ammonia lyase (PAL), which breaks down phenylalanine and releases ammonia as a by-product.33 Excess ammonia in the blood stream can trigger a cascade leading to encephalitis and seizures.30

    AUTISM EPIDEMIC AND ROUNDUP USAGE

    Autism is a condition characterized by cognitive and social deficits, which has been alarmingly on the rise in the last decade. Some children seem to be born with the condition, while others develop normally up to a certain point and then begin regressing into autism.55 Autism is associated with two comorbidities that may yield hints as to its underlying etiology: disrupted gut bacteria and impaired sulfur metabolism.57 A characteristic feature of children with autism is an overgrowth of pathogenic bacteria in the gut, which can lead to neurological defects arising from exposure of the brain to toxins produced by these bacteria.24,56,58
    I have been studying autism for many years, trying to understand the environmental factors that might be causal in the current epidemic in this complex condition. Autism used to be rare, affecting one in ten thousand children. The latest numbers put out by the CDC in March 2013, show one in fifty.6 This is an alarming number, and, what is even more alarming is how quickly the number has been rising in recent years. Figure 1 shows a plot of autism rates over the past twenty years alongside a plot of total Roundup usage on corn and soy in the U.S., the two core crops of the processed food industry. It is remarkable how well these two plots line up. The Pearson correlation coefficient is 0.985 (1.0 would be perfect alignment). This plot also demonstrates the alarming increases in glyphosate application that have followed the insertion of the Roundup Ready GMO bacterial gene into the seeds.
    Correlation does not necessarily mean causation, but if you can explain logically how A might lead to B, then the likelihood of causation goes way up. It took a long time before I thought of glyphosate as a possible factor in autism, probably because I believed Monsanto’s claims that it is relatively nontoxic. This all changed when I heard a lecture given by Professor Don Huber at the 2012 Indianapolis WAPF chapter conference. His explanation of the effects of glyphosate on biological systems filled in important gaps in the theory I was developing to explain the underlying pathologies in autism.

    Most striking, of course, is the disruption of gut bacteria, something that Natasha Campbell McBride has been speaking about for many years at WAPF conferences and in her books.9 A recent study involving nearly three thousand children with autism spectrum disorder (ASD) found that a quarter of them suffered from chronic GI problems like constipation, diarrhea, and bloating.37 This subset had significantly higher rates of both anxiety and over-sensitivity to sensory stimulation.
    AUTISM, PATHOGENS, AND SULFATE

    As Anthony Samsel and I gathered information about glyphosate, we began to see a striking pattern linking glyphosate to specific pathogens like Clostridia difficile (C. diff ) and Pseudomonas aeruginosa, which are currently causing a major crisis in hospitals in the U.S. and elsewhere due to their increased prevalence and multiple antibiotic resistance.12, 28 Pseudomonas is among the very few bacterial forms that can metabolize glyphosate. A breakdown product is formaldehyde, a known carcinogen and neurotoxin.43 Formaldehyde may however be preferred over glyphosate as the lesser of two evils. So we surmise that this bacterium is allowed to survive in the gut precisely because it can dispose of glyphosate, but then you have to suffer the consequences of formaldehyde toxicity.



    Figure 1: Autism rates in the U.S. school system and of the amount of glyphosate used on corn and soy acreage in the U.S. Figure generously provided by Nancy Swanson: http://www.examiner.com/article/data...eases-and-gmos.
    Explaining the overgrowth of C. diff requires a digression. My extensive research has led me to believe that systemic sulfate deficiency may be the most important factor in many of the health issues facing us today.21, 48 Certainly it is a factor in autism. Autistic children have been found to have only one third as much free sulfate in the blood as their normal peers.57 The essential sulfur-containing amino acid, methionine, is a source of both sulfur and methyl groups to the body, both of which are crucial for normal brain development.17,21,26 Heparan sulfate is a sulfated molecule derived from sugar which plays remarkable roles in regulating ion and nutrient transport as well as molecular signaling cascades, for most of the body’s cells.5 It’s also crucial in brain development of the fetus.12 A loss of heparan sulfate in the gut lining results in protein leaks into the blood,7 which can then induce gluten and casein intolerance, which are common among autistic children. Mice engineered to be impaired in heparan sulfate synthesis in the brain exhibit all of the features of autism.27
    C. diff produces a toxic phenol called p- Cresol, which has been identified as a factor present in the urine in association with autism.1 In fact, as we gathered more data on glyphosate and its effects on plants, we noticed that phenolic compounds, more generally, are produced by both plants and microbes upon exposure to glyphosate, along with the over-production of other compounds with carbon rings called flavonoids. You may be aware that flavonoids in coffee, tea, and brightly colored vegetables and polyphenolic compounds like resveratrol and curcumin are considered to be beneficial for their antioxidant properties. I believe that their beneficial effect may actually be due to their ability to safely transport sulfate, a feature they all possess, and a feature they share with the toxic phenols such as those produced by the pathogen C. diff.
    SULFATE TRANSPORT AND CARBON RINGS

    Extensive prior research has led me to a hypothesis that sulfate transport in the blood poses a special challenge to the body, and that this may be the main reason why there is a plethora of biologically interesting molecules that are typically sulfated when they are transported in the blood, as well as a huge number of sulfotransferases that can attach these sulfates15 and transfer them from one molecule to another. I suspect that one of the important but heretofore overlooked consequences is that they transport sulfate from a source site in the body such as the gut to a delivery site such as the liver, the pancreas, or the brain, and that this is a crucial part of their function in biology.
    Two major classes of these biologically active sulfate-transporting molecules are the sterols (cholesterol, vitamin D3, DHEA, estrone) and the monoamine neurotransmitters (dopamine, serotonin, norepinephrine). All of these molecules have the interesting property that their biological effects are inactivated when they are sulfated. This is of course beneficial so that they are inert during transport, an attractive feature. But I believe that, more important than this, is the fact that the sulfate that is attached to these molecules is also inactive while being transported. And it might even be the case that one of the most important functions these molecules perform is to transport sulfate! All of these molecules share the property that the sulfate anion is attached to a carbon ring, and the ring distributes the negative charge on the sulfate, changing its biophysical properties in important ways.
    What are these biophysical properties? Sulfate is a member of a class of anions called anionic kosmotropes. Other biologically important members of this class are phosphates and carbonates, both of which are also pervasive in biological systems. These three anions are essential for maintaining the water in the immediate vicinity of the cells’ plasma membranes in the tissues and of particles suspended in the blood in a structured almost crystal-like “liquid ice” configuration, creating a protective “exclusion zone” (the glycocalyx).45 Gelatin desserts are a familiar version of this structured water—it’s mainly carbonate that structures the water in this case. Water is by far the most common molecule in our bodies, yet this is hard to imagine given how firm our bodies are. With 99 percent of our molecules being water, it’s surprising that we don’t just collapse into a puddle! Pollack believes that the main reason our tissues are not liquid is that nearly all the water is maintained in a gelled state by these kosmotropes.45
    However, the one big exception to this model is the blood. The blood that courses through our veins is definitely a liquid, and if it were to become gelled it would lead to a no-flow situation and a major catastrophe. This, to me, is the key reason why all these biologically active molecules travel through the blood stream in a sulfated form.



    Figure 2: The molecular structure of glyphosate.
    Now let’s consider what happens when glyphosate enters the picture. Glyphosate is almost certainly an anionic kosmotrope as well. As shown in Figure 2, it contains a carbonyl group and a phosphonyl group, and it doesn’t have any carbon rings. When a person takes an overdose of glyphosate in an attempt to commit suicide, a blood pathology called “disseminated intravascular coagulation” (DIC) ensues59 and this can easily be fatal. So glyphosate causes an increase in blood viscosity and competes with free sulfate, which also has this effect, for a limited load capacity. This problem would be especially acute in the hepatic portal vein carrying nutrients from the gut to the liver. The liver desperately depends on sulfate to make cholesterol sulfate, which is essential in the synthesis of bile acids, and bile acids in turn are essential for digesting fats. Cholesterol sulfate also plays an important role in the outer shell of LDL and HDL particles, to protect them from reactive agents in the blood (e.g., oxidizing and glycating agents). The “small dense LDL particles” that are most damaging in heart disease arise because of oxidation and glycation damage that disrupts the lock-and-key mechanism during reuptake in the liver after they have delivered their goods, and therefore prevents them from being recycled. So, insufficient sulfate leads to LDL and HDL particles that are more susceptible to such damage, a key factor in heart disease.
    In addition to “jamming the waterways” in blood vessels, glyphosate also interferes with the supply of sulfate carrier molecules that depend on the shikimate pathway. Dopamine, serotonin and norepinephrine are all derived from the aromatic amino acids whose synthesis is blocked by glyphosate. Worse than this, glyphosate also interferes with a class of enzymes called cytochrome P450 enzymes (CYP enzymes for short),31 which play many different roles in the body, especially in the liver and the reproductive system.42 Certain members of this class are essential for bile acid synthesis. These enzymes are also involved in cholesterol homeostasis and vitamin D activation in the liver, whose disruption will further interfere with sulfate transport, among other problems.
    In our recent paper on glyphosate47 we argued that the toxic phenolic compounds like p-Cresol that are produced by pathogenic bacteria like C. diff actually perform an important service by transporting sulfate from the gut to the liver and pancreas. According to this hypothesis, toxic phenolic compounds are produced because the sterols and monoamine neurotransmitters are impaired in their ability to perform this much-needed service. However, once the phenol drops off its sulfate, it becomes a highly reactive molecule, capable of doing damage to the lipids and DNA in the liver and pancreas, as well as in the gut, as a single phenol is likely cycled around again and again to deliver multiple sulfates to the liver and pancreas, and, whenever it’s not sulfated, it’s toxic.
    SUMMARY

    In this paper, I have developed an argument that, contrary to Monsanto’s assurances, glyphosate is not a safe chemical for human exposure. On the contrary, glyphosate’s well established effects in biological systems can plausibly explain many of the diseases and conditions we are experiencing today in epidemic form. These include autism, Alzheimer’s, obesity, depression, excessive violence, colitis, inflammatory bowel disease, heart disease and diabetes. I now believe that, while several environmental toxicants, including mercury, aluminum, lead, fluoride, nitrates, insecticides and fungicides, are likely implicated in autism, glyphosate may be the single most important factor in the autism epidemic. I believe this not only because glyphosate usage has gone up in step with autism rates, but also because many of the pathologies associated with autism can be explained through glyphosate’s disruptive mechanisms.
    I also would argue that Alzheimer’s disease arises from similar pathologies as does autism, and it might be characterized as “autism for the elderly.” Therefore, its recent alarming increases may also be due predominantly to glyphosate.
    Glyphosate can also easily explain the obesity epidemic and depression through its disruption of the supply of tryptophan, the sole precursor to serotonin. I have shown how glyphosate disrupts both sulfate synthesis and sulfate transport, and my research has led me to believe that impaired sulfate supply to all the tissues is a common underlying pathology in most modern diseases.
    The best way to minimize glyphosate exposure is to adhere strictly to a completely organic diet. Most important is to avoid all the Roundup-Ready GMO crops: corn, soy, sugar beets, canola oil, and cottonseed oil, as well as wheat and sugar cane, due to desiccation practices. Any use of Roundup to kill weeds in lawn maintenance should be abandoned.
    SIDEBARS

    OTHER HEALTH TROUBLES RELATED TO GLYPHOSATE

    As if it weren’t enough already that glyphosate causes an overgrowth of pathogenic bacteria in the gut, interferes with the supply of critical neurotransmitters to the brain and nervous system, and likely disrupts vitamin D activation, bile acid synthesis, cholesterol homeostasis, and sulfate synthesis and transport, there are several other ways in which glyphosate could do harm. Here I will touch upon four topics: endocrine disruption, liver damage, abdominal obesity, and breast cancer. Additional topics are discussed in our original paper.47 For example, glyphosate also chelates important micronutrients like zinc and cobalt.14

    ENDOCRINE DISRUPTION: Glyphosate is an established endocrine disruptor16 and studies have shown it inhibits aromatase, a CYP enzyme that converts testosterone to estrogen.46 Aromatase is synthesized in the testes,32 and this may explain why autism is far more prevalent in males than in females. Autism is associated with aromatase deficiency, and some have attempted to explain autism as a “super male” syndrome on the basis of overproduction of testosterone and insufficient estrogen.3 Retinoic acid is intimately involved in embryonic development. Low doses of glyphosate caused many deformities in frog and chick embryos44 due to overexpression of retinoic acid. The enzyme that breaks down retinoic acid is a CYP enzyme, so its disruption would explain glyphosate’s effects. One can expect similar effects in humans. Fertility rates have been declining sharply in many countries where glyphosate usage is increasing. Most striking are countries in South America such as Argentina and Brazil. Women in Brazil used to have six children on average, but now the fertility rate is less than that of the U.S. Argentina’s fertility rate has been declining ever since 1978. Both Brazil and Argentina produce a significant amount of the world’s supply of soybeans—most of which are engineered to be “Roundup® Ready.” While it’s difficult to sort out the role played by social pressure, it is possible that glyphosate’s disruption of aromatase and retinoic acid could be a factor in declining fertility rates.

    LIVER DAMAGE : According to our hypothesis, phenols are sulfated in the gut and transported through the hepatic portal vein to the liver in this sulfated form. In the liver, the sulfate is detached and most likely transferred to cholesterol to produce bile acids. Once freed from sulfate, phenolic compounds become fat-soluble and highly reactive, and they can readily cross cell membranes and do damage to cell contents. Phenols have been shown to cause damage to the kidneys, liver, muscles, and eyes.40 They induce the formation of organic radicals and reactive oxygen species that can damage lipids and DNA, which explains their ability to induce cancer. However, a much worse problem in the liver is the disruption of CYP enzymes, because the liver contains many CYP enzymes that are involved in detoxifying xenobiotics—both drugs and environmental toxins. With impaired CYP function, these other toxic chemicals linger longer, causing much more damage than they would otherwise. In fact, an inability to break down acetaminophen (Tylenol) has been proposed as a possible factor in autism.49 This can easily be explained by glyphosate’s potential disruption of the CYP enzyme that detoxifies Tylenol. The inflammation associated with the overgrowth of pathogens in the gut leads to the production of cytokines like TNF-∂ by macrophages, brought in to keep the pathogens in check. Cytokines induce inflammation, which damages the gut, liver and pancreas. TNF-∂ has been identified as a key factor in fatty liver disease, which has emerged as a growing public health problem worldwide.11 In the extreme case, liver pathology develops into nonalcoholic steatohepatitis (NASH), which can lead to cirrhosis and liver failure.
    ABDOMINAL OBESITY : It is easy to imagine a possible role for fat cells in protecting the liver from damage caused by the toxic phenols. Abdominal obesity can be viewed as providing a way station where sulfate can be transferred from one carrier molecule to another. The toxic phenols can thus deliver sulfate to fat cells in the belly, which then transfer it to a sterol to produce estrone sulfate, a well established “export” molecule from fat cells.52 Thus estrone then carries the sulfate to the liver, and the phenol never reaches the liver or the pancreas, where it could have damaged the DNA of cells with important roles. The liver and pancreas are never exposed to the toxic phenolic compound, and are therefore safeguarded from damage. Thus, abdominal obesity becomes a defense mechanism to deflect the phenols towards a tissue where damage is more forgivable, since the fat cells do not perform the kinds of critical metabolic roles that liver or pancreatic cells perform.

    BREAST CANCER : One in eight women in the U.S. is now expected to develop breast cancer at some point in their lives. A study on rats that were administered food that had been treated with Roundup throughout their lives showed an alarming incidence of massive mammary tumors in the female rats50 along with liver and kidney disease in the males, and premature death for both males and females. After our paper was published, a study came out showing that glyphosate, even in trace amounts (parts per trillion) could induce breast cancer cells to proliferate; that is, it promotes tumor growth.53

    GLYPHOSATE USAGE AND DISEASE RATES









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    This article appeared in Wise Traditions in Food, Farming and the Healing Arts, the quarterly journal of the Weston A. Price Foundation, Fall 2013.



    I think one of my greatest journalistic accomplishments was helping link Heparan Sulfate to autism spectrum disorder.

    I felt so tired afterward too, like I had aged a year in a week.
    More like a day actually.

    http://nuclearnuttery.wordpress.com/...paran-sulfate/



    Quote Hepatitis B virus infection initiates with a large surface protein-dependent binding to heparan sulfate proteoglycans.
    Schulze A, Gripon P, Urban S.
    Source

    Department of Molecular Virology, Otto-Meyerhof-Zentrum (OMZ), University of Heidelberg, Heidelberg, Germany.
    Abstract

    Contrary to many other viruses, the initial steps of the hepatitis B virus (HBV) infection, including attachment to hepatocytes, specific receptor interactions, and membrane fusion, are unsolved. Using HepaRG cells as an in vitro cell culture system, we here report that HBV entry into hepatocytes depends on the interaction with the glycosaminoglycan (GAG) side chains of cell-surface-associated heparan sulfate proteoglycans. Binding to GAGs requires the integrity of the pre-S domain as a part of the large (L-) viral envelope protein. HBV infection was abrogated by incubation of virions with heparin, but not the structurally related GAGs chondroitin sulfate A, B, and C. Infection was also abolished by suramin, a known inhibitor of duck hepatitis B virus infection or highly sulfated dextran sulfate. Polycationic substances such as poly-L-lysine, polybrene, and protamine also prevented infection, however, by addressing cellular components. Enzymatic removal of defined acidic carbohydrate structures from the cell surface using heparinase I/III or the obstruction of GAG synthesis by sodium chlorate inhibited HBV infection of HepaRG cells and, moreover, led to a reduction of HBV cell surface binding sites. The biochemical analysis showed selective binding of L-protein-enriched viral particles (virions or filaments) to heparin. GAG-dependent binding of HBV was improved by polyethylene glycol, a substance that specifically enhances HBV infection. Conclusion: HBV infection requires the initial attachment to the carbohydrate side chains of hepatocyte-associated heparan sulfate proteoglycans as attachment receptors. This interaction initializes the multistep entry process of HBV and cannot be bypassed by alternative routes.

    PMID:
    18046710
    [PubMed - indexed for MEDLINE]

    Heparan sulfate and syndecan-1 are essential
    in maintaining murine and human intestinal
    epithelial barrier function
    Lars Bode,1 Camilla Salvestrini,2 Pyong Woo Park,3 Jin-Ping Li,4 Jeffrey D. Esko,5
    Yu Yamaguchi,1 Simon Murch,6 and Hudson H. Freeze1
    1Burnham Institute for Medical Research, La Jolla, California, USA. 2Centre for Pediatric Gastroenterology, Royal Free Hospital, London, United Kingdom.
    3Department of Medicine, Baylor College of Medicine, Houston, Texas, USA. 4Department of Medical Biochemistry and Microbiology, Biomedical Center,
    Uppsala University, Uppsala, Sweden. 5Department of Cellular and Molecular Medicine, UCSD, La Jolla, California, USA.
    6Clinical Sciences Research Institute, Warwick Medical School, Coventry, United Kingdom.

    Patients with protein-losing enteropathy (PLE) fail to maintain intestinal epithelial barrier function and develop
    an excessive and potentially fatal efflux of plasma proteins. PLE occurs in ostensibly unrelated diseases, but
    emerging commonalities in clinical observations recently led us to identify key players in PLE pathogenesis.
    These include elevated IFN-γ, TNF-α, venous hypertension, and the specific loss of heparan sulfate proteoglycans
    from the basolateral surface of intestinal epithelial cells during PLE episodes. Here we show that heparan
    sulfate and syndecan-1, the predominant intestinal epithelial heparan sulfate proteoglycan, are essential in
    maintaining intestinal epithelial barrier function. Heparan sulfate– or syndecan-1–deficient mice and mice
    with intestinal-specific loss of heparan sulfate had increased basal protein leakage and were far more susceptible
    to protein loss induced by combinations of IFN-γ, TNF-α, and increased venous pressure. Similarly,
    knockdown of syndecan-1 in human epithelial cells resulted in increased basal and cytokine-induced protein
    leakage. Clinical application of heparin has been known to alleviate PLE in some patients but its unknown
    mechanism and severe side effects due to its anticoagulant activity limit its usefulness. We demonstrate here
    that non-anticoagulant 2,3-de-O-sulfated heparin could prevent intestinal protein leakage in syndecan-deficient
    mice, suggesting that this may be a safe and effective therapy for PLE patients.

    Autism: Oxidative Stress, Inflammation, and Immune Abnormalities
    By Abha Chauhan, Ved Chauhan, Ted Brown

    Leaky gut is a name used to describe intestinal or bowel hyperpermeability. Tight junctions (TJs) represent the major barrier within the pathway between intestinal epithelial cells that line the digestion tract. Disruption of TJs leads to intestinal hyperpermeability (the so-called “leaky gut”) which has been proposed by some researchers to involve a relationship with acute and chronic diseases such as systemic inflammatory response syndrome (SIRS), inflammatory bowel disease, type 1 diabetes, allergies, asthma, and autism.[1]

    from wiki: A trio of factors including an aberrant intestinal microbiota, a “leaky” intestinal mucosal barrier, and altered intestinal immune responsiveness are hypothesised to play a role in the failure to form tolerance, resulting in the autoimmunity that underlies type 1 diabetes. [2]

    A lack of mucosal integrity (leaky gut) with consecutive local and systemic inflammation and dysfunction of transport proteins may worsen the clinical symptoms of chronic heart failure. A ‘leaky’ bowel wall may lead to translocation of bacteria and/or endotoxin, which may be an important stimulus for inflammatory cytokine activation. Although it remains unclear whether increased adherent bacteria in patients with chronic heart failure are a primary or secondary event and whether they contribute to systemic inflammation. Further studies are needed to address the pathophysiology of the intestinal barrier whose reactivity seems to be crucial for heart function.[3][4]

    Primary sclerosing cholangitis (PSC) and autoimmune hepatitis (AIH) are enigmatic chronic inflammatory diseases of the liver, which can be associated with chronic inflammatory bowel diseases. Cross-recognition between microbial antigens in the gut and host components by the immune system along with stimulation of pattern recognition receptors might give rise to chronic hepatic inflammatory disorders with features of autoimmunity.[5]

    SURFACE PROTEIN OF VIRUS CAUSES PROTEIN DEPLETION OF THE GUT AND ABNORMAL FLORA

    AUTISM AND AIDS

    Aisha Nazli, a researcher in Kaushic’s laboratory, noticed every time she put HIV on epithelial cells their resistance went down significantly. Repeated tests confirmed this.

    Kaushic said the surface protein of the virus causes the epithelial barrier to break. “The surface protein signals to the inside of the epithelial cells by binding to it,” she said. “The epithelial cells start making inflammatory proteins which cause these cells to go on their self-destructive pathway.”

    http://www.microbialinfluence.com/

    We have collected many research articles to show that the toxins found in microorganisms play an important role in the suspected causes of ASD, in particular, lipopolysaccharide ( LPS) the bacterial toxins from gram negative bacteria that inhabit the guts of autistic children. LPS toxicity works synergistically with mercury and other heavy metal poisonings to expand damage. These heavy metals increase harm from LPS.[1] In addition, LPS decreases glutathione levels making it even more difficult for the body to detoxify heavy metals.[2]

    One explanation for why symptoms of mercury are so similar to the symptoms of LPS could be the fact that mercury inhibits carbohydrate absorption in the gut. Unabsorbed food does not get into the blood stream quickly; when it remains in the gut, it becomes available as a food supply for bacteria. Consequently, gram negative bacteria multiply and produce LPS. [3] This raises a strong suspicion that some of the symptoms commonly attributed to mercury could be directly caused by LPS and only indirectly by mercury.

    LPS also renders toxins from Candida Albicans more damaging.[4] The poisonous effects of LPS are so potent that they produce symptoms of autism even without the help of Candida Albicans and heavy metals. All collected experiments on the following website involve laboratory mice injected with only LPS and exhibiting the same symptoms as those in ASD.

    LPS induces a depressive syndrome, characterized by anhedonia, anorexia, body weight loss, and reduced locomotor, exploratory, and social behavior. This result has been replicated so many times by different research studies that the names, “Sickness Behavior” and “Endotoxemia” are now applied to this condition. [5][6][7]

    The mission of this website is to collect and display links to some of the available research articles from PubMed, a service from the National Library of Medicine and the National Institute of Health, that link LPS to the varied and diverse symptoms of ASD. We were able to find and collect experiments for almost every possible neurological and biological symptom of ASD in order to prove that most symptoms of ASD, have a corresponding experiment on Medline that proves each is a symptom of LPS toxicity.

    The articles on this website are just a tiny fraction of the available research The amount of evidence is overwhelmoing, for example, performing a search for “hippocampus lps”, in PubMed will retrieve 222 citations.

    The number of similarities between ASD and LPS toxicity is sufficiently impressive to demand attention and cannot be ignored. The following are symptoms of LPS poisoning; these symptoms are also found in children with autism:
    Last edited by Tesla_WTC_Solution; 24th April 2014 at 20:08.

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    Default Re: Autism

    p.s. got cut off
    Quote BRAIN

    Reductions in oligodendrocyte or myelin markers
    A marked cerebral cytokine response
    White matter injury
    Changes in amygdala
    Change in dopamine and serotonin levels
    Reduction of blood flow to the brain
    Changes in blood-brain barrier permeability for large (protein) molecules
    Increased the number of pyramidal and granular cells in the hippo-campus

    EMOTIONS AND BEHAVIOR

    Anxiety
    Depression
    Reduction in social behavior
    Lack of social interaction
    Increase in addiction
    Lack of exploratory behavior

    DIGESTIVE

    Weight loss
    Breakage and depletion of microvilli
    The tight junctions widen and become disrupted.
    IBS and IBD
    Gut inflamation
    Leaky Gut
    Digestive symptoms
    Disrupted Intestinal Transit
    LPS is linked to the problems of gluten,soy and dairy in ASD children

    IMMUNE FUNCTION

    Increase in TNF alpha.
    Increases in certain NK cells and monocytes
    Increases in lymphocytes

    OTHER

    Low Levels of Thyroid
    Low Levels of Glutathione
    Low Levels of Amino Acids
    Impairment of Bile Flow
    Increasing the Number of Viable Candida Albicans
    An increase in pain sensitivity

    Researchers at the UC Davis M.I.N.D. Institute found clear differences in cellular responses between autistic children and neurotypical children following exposure to LPS, bean lectin and bacterial agents. At the Institute this was discovered to be a major and important difference between children with ASD and typical children.[8]
    HEPARAN SULFATE IN BRAIN DEVELOPMENT



    Quote Sci. STKE, 11 November 2003
    Vol. 2003, Issue 208, p. tw436
    [DOI: 10.1126/stke.2003.208.tw436]

    EDITORS’ CHOICE
    DEVELOPMENTAL BIOLOGY Heparan Sulfate in Brain Development
    Heparan sulfate binds to a number of growth factors and morphogens and is highly expressed in the developing mammalian central nervous system (CNS). In order to elucidate heparan sulfate’s role in brain development, Inataniet al. selectively knocked out heparan sulfate synthesis in the developing mouse CNS. Mutant mice exhibited malformations in specific regions of the brain that corresponded to disrupted distribution of fibroblast growth factor and decreased cell proliferation. Axon pathfinding in the brain and retina was also disrupted, pointing to additional regulatory functions of heparan sulfate.

    M. Inatani, F. Irie, A. S. Plump, M. Tessier-Lavigne, Y. Yamaguchi, Mammalian brain morphogenesis and midline axon guidance require heparan sulfate. Science 302, 1044-1046 (2003). [Abstract] [Full Text]

    Citation: Heparan Sulfate in Brain Development. Sci. STKE 2003, tw436 (2003).

    “ASK NOT WHAT YOUR COUNTRY CAN DO FOR YOU…”
    _________________________________________________________

    Heparan sulfate
    From Wikipedia, the free encyclopedia
    Heparan sulfate (HS) is a linear polysaccharide found in all animal tissues. It occurs as a proteoglycan (HSPG) in which two or three HS chains are attached in close proximity to cell surface or extracellular matrix proteins.[1][2] It is in this form that HS binds to a variety of protein ligands and regulates a wide variety of biological activities, including developmental processes, angiogenesis,blood coagulation and tumour metastasis. HS has been shown to serve as cellular receptor for a number of viruses including the respiratory syncytial virus (Hallak et al. 2000)

    _________________________________________________

    “…BUT WHAT YOU CAN DO FOR YOUR COUNTRY.”
    ___________________________________________________

    The Heparan Sulfate-Fibroblast Growth Factor Family: Diversity of Structure and Function
    Wallace L. McKeehan,
    Fen Wang,
    Mikio Kan
    Center for Cancer Biology and Nutrition Albert B. Alkek Institute of Biosciences and Technology, Department of Biochemistry and Biophysics, Texas A & M University Houston, Texas 77030
    Available online 14 May 2008.
    The fibroblast growth factor (FGF) receptor complex is a ubiquitous regulator of development and adult tissue homeostasis that bridges the peri-cellular matrix and the intracellular environment. Diverse members of the FGF polypeptide family, the FGF receptor tyrosine kinase (FGFRTK) family and the FGF receptor heparan sulfate proteoglycan (FGFRHS) family combine to result in active and specific FGFR signal transduction complexes. Regulated alternate splicing and combination of variant subdomains give rise to diversity of FGFRTK monomers. Divalent cations cooperate with the FGFRHS to conformationally restrict FGFRTKtrans-phosphorylation, which causes depression of kinase activity and facilitates appropriate activation of the FGFR complex by FGF. Diffusional and conformational molecular models of the oligomeric FGFR complex are presented to explain how different point mutations in the FGFRTK commonly cause craniofacial and skeletal abnormalities of graded severity by graded increases in FGF-independent activity of total FGFR complexes. The role of the FGF family in liver growth and function and in prostate tumor progression is discussed.

    Copyright © 1998 Academic Press. Published by Elsevier Inc. All rights reserved.

    _________________________________________________________

    Performing your original search, “heparan sulfate” glutamate, in PubMed will retrieve 33 records.
    Proc Natl Acad Sci U S A. 2012 Mar 27;109(13):5052-6. Epub 2012 Mar 12.
    Autism-like socio-communicative deficits and stereotypies in mice lacking heparan sulfate.
    Irie F, Badie-Mahdavi H, Yamaguchi Y.
    Source
    Genetic Disease Program, Sanford Children’s Health Research Center, Sanford-Burnham Medical Research Institute, La Jolla, CA 92037, USA.

    Abstract
    Heparan sulfate regulates diverse cell-surface signaling events, and its roles in the development of the nervous system recently have been increasingly uncovered by studies using genetic models carrying mutations of genes encoding enzymes for its synthesis. On the other hand, the role of heparan sulfate in the physiological function of the adult brain has been poorly characterized, despite several pieces of evidence suggesting its role in the regulation of synaptic function. To address this issue, we eliminated heparan sulfate from postnatal neurons by conditionally inactivating Ext1, the gene encoding an enzyme essential for heparan sulfate synthesis. Resultant conditional mutant mice show no detectable morphological defects in the cytoarchitecture of the brain. Remarkably, these mutant mice recapitulate almost the full range of autistic symptoms, including impairments in social interaction, expression of stereotyped, repetitive behavior, and impairments in ultrasonic vocalization, as well as some associated features. Mapping of neuronal activation by c-Fos immunohistochemistry demonstrates that neuronal activation in response to social stimulation is attenuated in the amygdala in these mice. Electrophysiology in amygdala pyramidal neurons shows an attenuation of excitatory synaptic transmission, presumably because of the reduction in the level of synaptically localized AMPA-type glutamate receptors. Our results demonstrate that heparan sulfate is critical for normal functioning of glutamatergic synapses and that its deficiency mediates socio-communicative deficits and stereotypies characteristic for autism.

    PMID:
    22411800

    [PubMed - indexed for MEDLINE] PMCID:

    PMC3323986 [Available on 2012/9/27]

    ____________________________________________________________

    The role of heparan sulfate and TLR2 in cytokine induction by hepatitis B virus capsids
    Vanlandschoot P, Leroux-Roels G.

    Bron: J Immunol. 2005 Nov 15;175(10):6253; author reply 6253-5.

    http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342043/

    Front Immunol. 2012; 3: 79.
    Published online 2012 April 18. doi: 10.3389/fimmu.2012.00079
    PMCID: PMC3342043
    The Role of TLR2 in Infection and Immunity
    Laura Oliveira-Nascimento,1,2 Paola Massari,1 and Lee M. Wetzler1,*
    Author information ► Article notes ► Copyright and License information ►
    Go to:
    Abstract
    Toll-like receptors (TLRs) are recognition molecules for multiple pathogens, including bacteria, viruses, fungi, and parasites. TLR2 forms heterodimers with TLR1 and TLR6, which is the initial step in a cascade of events leading to significant innate immune responses, development of adaptive immunity to pathogens and protection from immune sequelae related to infection with these pathogens. This review will discuss the current status of TLR2 mediated immune responses by recognition of pathogen-associated molecular patterns (PAMPS) on these organisms. We will emphasize both canonical and non-canonical responses to TLR2 ligands with emphasis on whether the inflammation induced by these responses contributes to the disease state or to protection from diseases.

    Keywords: TLR2, TLR1, TLR6, TLR2 ligands, polymorphisms, co-receptors
    __________________________________________

    Talent hits a target no one else can hit; Genius hits a target no one else can see.

    —Arthur Schopenhauer
    .


    Genius is a talent for producing something for which no determinate rule can be given,
    not a predisposition consisting of a skill for something that can be learned by following some rule or other.

    —Immanuel Kant
    Last edited by Tesla_WTC_Solution; 24th April 2014 at 20:11.

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    Default Re: Autism

    Another scam to add on top of the scams' pyramid:

    THE GOVERNMENT’S DEMONIC STRATEGY AGAINST PARENTS OF AUTISTIC CHILDREN
    by Jon Rappoport September 13, 2012

    Let me start with this controversial statement: The worst thing parents can do is obtain a diagnosis of autism for their vaccine-damaged child.

    The primary fact to keep in mind is: the government must deny any link between vaccines and autism, because to admit the connection would force it to pay out gigantic sums of money to parents, under its Vaccine Injury Compensation Program (VICP).

    VICP was created in 1988, through an agreement between the US government and pharmaceutical companies, to funnel all law suits for damage away from those companies, and into a bureaucratic maze of government madness, where the parents’ chances of compensation are minimal, where the deck is most assuredly stacked against them.

    National Vaccine Injury Compensation Program

    Vaccine Adverse Event Reporting System (VAERS)

    Once parents enter the maze, hoping to gain funds to care for their children, they are immediately confronted with a list of disorders and diseases. This list essentially tells them:

    “If your vaccine-damaged child has been diagnosed with any of the following medical conditions, you may be able to win financial support. If not, you’re out of luck.”

    Autism isn’t on the list. Here is the list:

    Vaccine Injury Table

    Can things be any clearer than that? A diagnosis of autism is a trap.

    One: a young child receives a vaccine.

    Two: he suddenly withdraws from life.

    Three: a doctor makes a diagnosis of autism.

    Four: the parents want to sue the company that makes the vaccine, but they can’t; they must apply to the VICP for funds to care for their child for the rest of his life.

    Five: as soon as they enter the VICP system, they learn that the label “autism” is the very thing that will keep them from the funds they desperately need.

    That is the long and short of it.

    Forget about the fact that the parents never wanted to involve themselves with a federal government program. They wanted to sue the vaccine maker. They wanted a court award. But they were barred from suing.

    At this point, you might say, “But if their child really does have autism and it was obviously caused by a vaccine, then they should be able to find justice somehow.”

    You don’t understand how deep this deception goes. You don’t understand how criminally insane it is.

    Because, you see, the label of “autism,” the very label that keeps parents from getting help for their children, is an arbitrary word that means nothing.

    A deviously designed word that means nothing is keeping parents in a lifelong state of desperation, as they go bankrupt trying to care for their vaccine-damaged child.

    We begin here: all 297 official mental disorders, listed in the (DSM) publication of the American Psychiatric Association, are defined and approved by committees of psychiatrists. Whether it is schizophrenia or autism or ADHD or clinical depression or bipolar disease, the definitions consist wholly of described behaviors. That’s all.

    Psychiatrists will tell you these symptomatic behaviors are signs of underlying chemical imbalances or genetic aberrations, but they have no tests to back up this assertion. Therefore, all they are left with are the behaviors, their own menu-like clusters of those behaviors, and the “mental disorder” label they place on each cluster.

    If they had more, if they had blood tests or brain scans or genetic assays, they would publish those tests and claim they are definitive for diagnoses of mental disorders. But they don’t.

    Here is an exchange between a respected psychiatrist and a PBS interviewer, which occurred during a Frontline report titled, “Does ADHD Exist?”

    PBS FRONTLINE INTERVIEWER: Skeptics say that there’s no biological marker—that it [ADHD] is the one condition out there where there is no blood test, and that no one knows what causes it.

    BARKLEY (Dr. Russell Barkley, professor of psychiatry and neurology at the University of Massachusetts Medical Center): That’s tremendously naïve, and it shows a great deal of illiteracy about science and about the mental health professions. A disorder doesn’t have to have a blood test to be valid. If that were the case, all mental disorders would be invalid…There is no lab test for any mental disorder right now in our science. That doesn’t make them invalid. [Emphasis added]

    Yes, it actually DOES make all those disorders invalid, unless “science” suddenly means “the opinions of psychiatrists sitting in a room, collecting together various human behaviors, and labeling them.”

    Here is a link to the official psychiatric definition of autism disorder. It’s worth reading:

    https://www.firstsigns.org/screening/DSM4.htm

    Notice that all the criteria for an autism diagnosis are behavioral. There is no mention of laboratory tests or test results. There is no mention of chemical imbalance or genetic factors.

    Despite public-relations statements issued by doctors and researchers, they have no laboratory findings to establish or confirm an autism diagnosis.

    But, people say, this makes no sense, because children do, in fact, withdraw from the world, stop speaking, throw sudden tantrums. Common sense dictates that these behaviors stem from serious neurological problems.

    What could cause the behaviors listed in the official definition of autism disorder?

    Vaccine injury; a toxic medical drug; a head injury; ingestion of a poison; an environmental chemical; a severe nutritional deficit; oxygen deprivation at birth; perhaps the emotional devastation accompanying the death of a parent…

    There are many possible causes of the behaviors arbitrarily called autism.

    However, then, why bother to say “autism?” Why not just say vaccine injury or head injury? Why not try to find the crucial event that brought on a specific child’s sudden and unique withdrawal from the world?

    The answer should be clear. By establishing a label like autism, medical drugs can be sold. Studies can be funded. An industry can be created.

    Something more can be done, too. The government can reject vaccine injury as a defining event in a child’s life, and reject the need to pay out compensation for it.

    The government can say, “Since we know that some children who are diagnosed with autism have not received vaccines, or have not received vaccines containing a neurological poison (mercury), we do not compensate parents whose children are vaccine-injured on the basis that they have autism.”

    Poof. It all goes away. Did you catch the sleight-of-hand trick?

    Let me expose it. A child is given a vaccine. The child goes into a massive withdrawal from life and communication. A doctor, assessing the child’s behaviors, connects them with the official menu of behaviors labeled “autism.” The doctor then says, “This child has autism.”

    Then the parents try to obtain government compensation through the VICP, the Vaccine Injury Compensation Program.

    The parents, who now have alarmingly high expenses for ongoing care of their vaccine-damaged child, go to the VICP and say, “Our child has been diagnosed with autism, and we want to collect funds for the vaccine-injury he sustained.”

    The government replies, “This is impossible. You see, we know that autism isn’t caused by vaccine injury. We know it because many children who are diagnosed with autism have never been injured by vaccines. Some autistic children have never had vaccines.”

    Do you see what is going on here? The parents stepped into a fatal trap. They said “autism” and the government said “vaccine injury does not cause autism.”

    You might think the parents could back up and regroup. They could say, “We don’t care what you call it, we just know our child was severely damaged by a vaccine, and we need funds.”

    But it’s not as easy as that. The government has no category called “vaccine damage.” The government demands some disease or disorder that is diagnosed and officially attributed to a vaccine injury. As I established earlier, the government has a specific list of diseases or disorders that it will allow—to even begin thinking about financial compensation.

    But, you say, this is an evil word game. Of course it’s a word game. The whole notion of “autism” based on no definitive tests was a word game to begin with.

    What is called autism (merely a label) is not one condition caused by one factor. It is a loose collection of behaviors that can be caused by various traumas.

    Parents say, “My child’s life was stolen away from him. He must have autism.”

    A label provides some measure of relief for the parents. It doesn’t prove that the label actually means something. In fact, the label can be a diversion from knowledge that would actually help the child. Suppose, for example, after receiving the DPT vaccine, the child went into a screaming fit and then withdrew from the world. Calling that autism tends to put the parents and the child in the medical system, where there is no definitive effective treatment. Outside that system, there might be some hope with, say, hyperbaric oxygen treatments, or other strategies.

    If all this creates a sense of outrage in you, you are not alone.

    If a hundred thousand parents of children who have been devastated by vaccines traveled to the headquarters of the Vaccine Injury Compensation Program, at the Parklawn Building, 5600 Fishers Lane, Rockville, Maryland, and if they stayed there and Occupied the area, and if they had a unified position that cut through the word game and the purposeful official delusion, perhaps this criminal insanity would end.

    A doctor’s diagnosis of autism most assuredly does not end the insanity. It adds to it.

    I once had a conversation with a parent whose child was vaccine-injured and then diagnosed with autism. She spent years trying to obtain compensation from the VICP and failed. Here is a paraphrase of how our conversation went:

    “I found out my child wasn’t the point of the VICP proceeding at all. The government’s attorney was doing everything possible to deny us compensation. I felt I was up against a monster.”

    “They denied you benefits because your son had been diagnosed with autism?”

    “Yes. They said there was no established connection between the vaccine-damage and autism, so they rejected my claim.”

    “So you see that the the label ‘autism’ was the very thing they used to reject your claim.”

    “I know it now. I didn’t know it then.”

    “You also know there is no reason to use the ‘autism’ label. It’s an arbitrary word.”
    “It’s a word that is ruining us.”

    “Do you realize that, if your doctor had diagnosed your son with a different catch-all label, you would have stood a better chance of gaining compensation?”

    “What label?”

    “Encephalopathy, for example.”

    “So you’re telling me it was all a game, and if I could have gotten the doctor to understand that, he might have written a different diagnosis in my son’s chart, and my chances [of compensation] might have improved.”

    “That’s right. A different word.”

    In a just world, a parent whose child is damaged by a vaccine would be permitted to sue the vaccine maker. In a less just world, the parent would be able to enter the VICP system and claim a right to compensation based on the simple stand-alone fact that her child was damaged by a vaccine.

    In the world we live in, that parent has to prove her child was diagnosed with a condition that the government admits could be caused by a vaccine.

    And if the doctor wrote down the word “autism,” the chances of compensation are suddenly very, very remote. They’re zero, unless the parent was able to obtain an accompanying word like “encephalopathy.”

    Finally, people will insist that researchers are getting closer to discovering the true and basic cause of autism. This is just more arbitrary verbiage. The “symptoms” listed as definitive for autism are just a collection of behaviors. I could put together a list, and so could you:

    “Fatigue, eye flutters, sadness, lack of desire to participate in school, loss of appetite, halting communication…” I could give these behaviors a name, “Remoteness Syndrome,” and call it a disorder, and then I could raise a few billion dollars to search for the underlying cause…but there would be no underlying single cause, because the list was a non-starter. It was just an arbitrary collection of behaviors.

    “Autism” is nothing more than a catch-all phrase that indicates a variety of possible unconnected neurological insults. Each patient should be examined by a health practitioner who can really find the cause in that case. Then, perhaps, a treatment plan can be devised for that child.

    Meanwhile, the government and its VICP program embroils parents and works them over and tortures them for years, and dumps most of them out on the street with no compensation.

    Jon Rappoport

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  10. Link to Post #87
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    Default Re: Autism

    Thanks for posting this. Very sad but necessary.

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    Default Re: Autism

    Are Genetically Engineered Foods Promoting Autism?



    Follow the discussion on Twitter using hashtag #gmoautism

    By Jeffrey M. Smith

    International bestselling author and filmmaker Jeffrey M. Smith is the executive director of the Institute for Responsible Technology www.ResponsibleTechnology.org and a leading spokesperson on the health dangers of GMOs. His books include Seeds of Deception and Genetic Roulette, and his films include Hidden Dangers in Kids’ Meals, Your Milk on Drugs—Just Say No!. For a list of thousands of products that have been verified as non-GMO, go to www.NonGMOShoppingGuide.com, or download the iPhone app ShopNoGMO.

    Download the Autism booklet Click here
    The Autism booklet can be read below, followed by full references:

    Are Genetically Engineered Foods Promoting Autism?

    “It appears there is a direct correlation between GMOs and autism.” --Arden Anderson, MD, PhD, MPH

    Physician Jennifer Armstrong admits, “Twenty years ago, I didn’t even know what the word autism meant. It was rare.” But then something shifted. Whether it was the food, medicine, environment, or some combination, by 2008, an astounding 1 in 54 boys suffered from autism spectrum disorder (ASD) in the US [1]. What is it that is damaging the health and well-being of so many of our children? Don Huber, PhD, professor emeritus from Purdue University, has an idea.

    In October 2011, Dr. Huber gave a talk in Germany about the physiological, neurological, and behavioral symptoms of pigs, cows, and rats fed genetically modified (GM) feed. After his lecture, a physician and autism specialist approached him and said, “The symptoms you describe are exactly what we are finding in our autistic children.”

    The animals in those studies were fed the same GM soy and corn eaten by children and adults in the US. Both crops are outfitted with bacterial genes that allow them to survive being sprayed with herbicide, which kills plants. As a result, higher residues of toxic weed killer end up inside our food. In addition, some GM corn varieties have an even more unsettling characteristic: their inserted genes produce an insect-killing poison called Bacillus thuringiensis (Bt) toxin in every cell—and in every bite. Although the biotech seed companies like Monsanto claim that their genetically modified organisms (GMOs) are harmless, that’s not what the independent scientists are finding.

    Agitated, antisocial animals
    When Dr. Huber visited an ongoing research project utilizing rats, he said those animals fed non-GMO feed were “as passive as can be. You can take them out. You can put them on your lap. Treat them almost like a pet cat.” Not so with the rats eating genetically engineered food: “You can hardly catch the rats that have received the GMO feed for a month and a half to two months,” he said. “They go off by themselves. They’re irritated. Crawl up the cage. . . . [They] don’t get along with each other.”

    Farmers are reporting the same thing with pigs raised on GMO corn. According to Dr. Huber, a farmer told him that “his pigs just seem to be always irritated. They can’t get along with the other pigs.” Veterinarian Don Skow described similar odd behavior in the pigs of his client. “They would get cannibalistic. They would consume each other—ear biting and tail biting.” And when put in nurseries after weaning, he says, some “would get a condition like Alzheimer’s. They would lose the ability to know where the feed was. A lot of them would die.” Although many of these odd behaviors had been dismissed as normal stress responses for confined animals, when farmers switched to non-GMO feed and the problems went away, the real cause became obvious.

    Similar antisocial patterns that Huber described were observed by a Dutch college student more than a decade ago when comparing mice fed GMO or non-GMO soy and corn. He wrote, “The mice fed on GM food seemed less active while in their cages. The differences in activity between the two cages grew as the experiment progressed.” The differences were most striking when he moved the mice to weigh them: “The mice from the GM cage were noticeably more distressed by the occurrence than the other mice. Many were running round and round the basket, scrabbling desperately in the sawdust, and even frantically jumping up the sides, something I’d never seen before. They were clearly more nervous. . . . For me this was the most disconcerting evidence that GM food is not quite normal.”[2]



    Dr. Irina Ermakova, PhD, a senior researcher at the Russian Academy of Sciences, reported to the European Congress of Psychiatry in March 2006 that male rats fed GM soy exhibited anxiety and aggression, while those fed non-GMO soy did not [3]. Ermakova reported the same behavior in GM soy-fed female rats and their offspring in her study published in Ecosinform. The animals “attacked and bit each other and the worker."[4]

    (Far more shocking, however, was that more than 50% of the offspring from the GMO-fed group died within three weeks when compared with a 10% death rate among the group fed natural soy. The GM group also had high rates of infertility and had smaller members.)

    Autism and gastrointestinal problems
    A disproportionate number of autistic children have digestive ailments, suggesting that it plays a significant role in the disease [5]. A Harvard study in 2010, for example, stated that “Gastrointestinal disorders and associated symptoms are commonly reported.”[6] An earlier Harvard and Mass General Hospital study [7] found that most autistic children whom they examined had some type of GI symptom, food allergy, or absorption problem. A 2006 study found that “A history of GI symptoms was elicited in 70% of children with ASD compared with 28% of children with typical development.”[8]

    The relationship between digestive health and autism is controversial. What is undeniable, however, is that numerous healthcare practitioners report greater success when they address the gastrointestinal disorder as part of their autism treatment protocol. For some, gastrointestinal intervention is their primary intervention.

    Distressed intestines
    The many GI disorders in autistic kids [9] include inflammation, intestinal permeability, [10] and imbalances in the intestinal bacteria. [11] These also appear to plague animals fed GMOs. According to Dr. Huber, for example, “When you look at the intestine on those pigs fed the GMO feed, the lining is deteriorated and the critical microbial balance is drastically changed.”

    We’ll first examine the damage to the gastrointestinal tract.

    According to some butchers who’ve done the comparison, the small intestines in GMO-fed livestock are typically thin and can tear easily as they’re removed from the carcass. The same organ from a non-GMO fed animal, they say, is much stronger. In fact, meat processors in the US typically import intestinal sausage casings from New Zealand, since the quality of the intestines in US livestock is too poor.

    Dan Skow, who has treated farm animals for more than 40 years, confirms that after GMOs were introduced in the mid-1990s, he saw a much higher incidence of ileitis, which is inflammation or infection in the ileum (lower part of the small intestine). “Looking at microscopic slides of the intestinal tract,” he says, “there’s definitely something [that] has changed. Whether or not we can actually pinpoint that to the GMO grain thing, I personally think it is.”

    Howard Vlieger, an Iowa agricultural consultant, also discovered problems. He asked a slaughterhouse to set aside the stomachs of two sets of pigs he sent for slaughter—one group was fed GMOs and the other non-GMOs. The stomachs of the GMO-fed group were inflamed and ulcerated.

    Danish farmer Ib Borup Pedersen also found dramatic changes in his 450-pig operation after switching from GMO soy to non-GMO soy in April 2011. In the previous two years, he had lost 36 sows from ulcers and bloat. Since non-GMO soy was introduced, he had no deaths from these digestive ailments. In the previous year, two pigs died of loss of appetite. None died since the change. And within two days of switching to non-GMO soy, his massive problems with diarrhea virtually disappeared. Both diarrhea and bloat are common symptoms of autistic children.

    (In addition to improved digestion, the overall health of Pedersen’s pigs improved, antibiotic use dropped by more than half, milk production increased, conception rate was significantly higher, and average litter size was up.)

    One of the earliest indications that GMOs might cause GI tract distress was a 1999 study published in the Lancet. After rats were fed experimental GMO potatoes for just 10 days, the cells of the stomach lining and intestines were significantly altered.[12]



    When California pediatrician Michelle Perro reviewed the study in 2011 and saw the photos of the increased cellular growth and abnormal architecture, she thought to herself, “Uh oh -- we’ve got some problems.” Based on her experience treating children for 30 years, she said, “You can extrapolate that the same thing may be occurring in babies clinically. They are not digesting their food. They are malabsorbing. . . . And I’m seeing that commonly now.” Digestive issues are skyrocketing among her patients.

    She’s not alone. According to US hospital discharges and ambulatory admissions records data, inflammatory bowel disease in the US population skyrocketed by 40% since the introduction of GMOs. Dr. Perro strongly suspects that GMOs are a major contributor.

    Family practitioner Myrto Ashe agrees: “We know food allergies are on the rise and also diseases related to common foods, like celiac disease. Patients report that dairy products make them wheeze, or tomatoes give them joint pains. It’s as though our food is harming us,” she says. “Something is happening. And if the intestines are playing a big role, and I’m getting the sense they are, then any change in our diet becomes a suspect.”

    Holes in our gut
    A connection to GMOs became an increasing concern when Dr. Ashe was asked to give a presentation on the health risks of GMOs to a mothers’ group in California. “To prepare for this,” she said, “I reviewed a lot of literature and tried to see what mechanisms are supported by the most solid scientific research. And to me, it was this intestinal permeability.”

    Dr. Ashe explains: “Once intestinal permeability increases, then it’s possible for larger bits of food to go though—bits that really should have been digested fully before getting assimilated. Once these go into the bloodstream, the body can react to them, and this reaction is an immune reaction. . . . I think anything that can increase intestinal permeability is a huge danger. The same diseases that research suggests are connected to intestinal permeability are the diseases that seem to be on the rise.”

    Numerous doctors point to holes in the gut walls as responsible for a long list of diseases and disorders. Although this notion is not yet at the forefront of mainstream medical understanding for these diseases, there have been books, medical conferences, and professional practices all devoted to the concept.

    Physician Gary Gordon puts it simply: “If you buy a brand new car and it says that it’s meant to run on gas and you go and put diesel in it, you could expect it won’t go very far. . . By making your intestine leaky, we are permitting building blocks to go into our body that are the wrong fuel.”

    Pesticide-producing corn may be the culprit
    When considering intestinal permeability, concern about the Bt-toxin in GMO crops looms large. This poison is designed to create holes (pores) in the digestive tract of insects. That is how it kills them.[13]

    The Environmental Protection Agency (EPA), which labels Bt corn and Bt cotton plants as registered pesticides, insists that Bt-toxin will have absolutely no influence on human or mammalian cells. But research published in the Journal of Applied Toxicology [14] this past February proves them wrong. Researchers “documented that modified Bt toxins [from GM plants] are not inert on human cells, but can exert toxicity.” In high concentrations (generally higher than that produced in average Bt corn), Bt-toxin disrupts the membrane in just 24 hours, causing certain fluid to leak through the cell walls. The authors specifically note, “This may be due to pore formation like in insect cells.” Thus, Bt-toxin may indeed create small holes in our intestines.

    Dr. Gordon warns, “If [Bt-toxin] is causing an increased propensity for our intestine to become permeable or leaky and for foods to be presented to our bloodstream in a premature fashion, the havoc that it will cause will be across the entire spectrum of disease, from premature aging and Alzheimer’s to Parkinson’s to autism to cancer to asthma.”

    Numerous professionals believe that Bt toxin produced in corn is already accelerating many diseases in the US. Arden Andersen, DO, PhD, MPH, believes Bt toxin is specifically implicated in the development of autism.

    Compromised flora
    In addition to structural deformities in the digestive tract of autistic kids, many also point to intestinal flora that’s gone wild. The bacteria living inside us play an important role in digestion, immunity, detoxification, and even the production of nutrients. In fact, the number of these bacterial cells in our digestive system is about 10 times the number of cells in our entire body. There’s an emerging health field dedicated to restoring the proper balance of intestinal microorganisms.

    There is also growing evidence that animals fed GMOs have an improper balance. Dr. Huber says the pigs fed GMOs have a “very dramatic difference in the microflora.” He says it “has a terrible odor to it compared to the normal microflora because of that changed bio environment.” Some farmers that butcher their own livestock also report that GMO-fed pigs and cows have a horrible stench and discolored organs.

    Dan Skow says that the balance of the good bacteria inside livestock has been thrown way off. “Now what set this off and why these disruptions of the balance to the microscopic flora in the intestinal tract? I’m personally suspicious—there’s a lot of impact from the GMOs.” Dr. Skow, like many others, is not willing to make an ironclad determination that GMOs are the causative factor. “There needs to be a lot more work to verify this,” he says. But that hasn’t stopped him from strongly urging his clients to switch to non-GMO animal feed. And when they do, he sees a difference in both the health and behavior of their livestock.

    The German physician who approached Dr. Huber is also convinced enough to make changes in his autistic patients. When he understood the connection with altered gut bacteria, he responded: “I now know exactly where I have to look, and why when I could modify the diet of an autistic child 10 years ago and have a very excellent response for remediation and recovery, why I’m not getting that response now. We are no longer able to change that microflora back—because we’re continuing to feed GMO-contaminated food to our children.”

    Botulism
    There are several ways that GMOs might be causing problems in our gut bacteria, all of which are unsettling. The first is that most of the genetically engineered crops are “herbicide tolerant"; they end up with much higher levels of poisonous weed killer concentrated in the food portion of the plant. The two main weed killers, Roundup and Liberty, both have antibacterial properties. In other words, they can kill bacteria. According to Dr. Huber, the active ingredient in Roundup (glyphosate) is even patented as a microbiocide to kill intestinal microorganisms. This can have serious consequences.

    Dr. Huber describes German research demonstrating that even tiny amounts of Roundup in a cow’s diet can kill beneficial bacteria that normally control the growth of botulism. He and others believe that the overuse of Roundup, especially on Roundup Ready crops, is the likely reason for an apparent rise in botulism poisoning in livestock -- and possibly humans.[15] (And low levels of botulism are also implicated as a possible contributor to sudden infant death syndrome.) [16]

    Dead sheep, buffalo, and cows
    A second reason why GMO crops may interfere with gut bacteria has been proposed by renowned Indian biologist P. M. Bhargava, PhD. In India, farmers allow sheep, goats, and buffalo to graze on cotton plants after harvest. While the animals had no negative reactions year after year, when genetically engineered Bt cotton was introduced into the country, the results were tragic. Thousands of animals died. Numerous others suffer from a variety of disorders.[17]

    These animals are called ruminants. They all have a compartment in their digestive tract where specialized bacteria break down the cellulose before it travels on to be digested and assimilated.

    Dr. Bhargava believes that the Bt-toxin produced in every cell of the cotton plant kills the cellulose-digesting bacteria normally found in the rumen. This would explain why autopsies of the dead sheep revealed shriveled intestines. According to Bhargava, since the cellulose was never broken down, the food never made it into the intestines.

    Similar evidence was found in a village near Warangal, India. All 13 of their buffaloes died after grazing for just a single day on Bt cotton plants. When I interviewed the villager who assisted with the autopsy of one of the animals, he reported that there was still undigested food in the rumen—three to four days after consumption.

    US agriculture consultant Marc Tainio reports another story that might be related. His client was raising miniature cattle, only three feet high. When the client switched to GMO corn feed, the animals “weren’t able to process the food correctly, and they would bloat up and die.” The farmer quickly lost about 90% of his herd. He was able to save the rest by switching back to non-GMO corn.

    If Bt-toxin kills rumen bacteria, it may not be a problem for us humans since we don’t have rumens. On the other hand, we do have gut bacteria, and the Bt toxin may interact with those bacteria in some way to cause harm. This appears to be the case in insects: a study demonstrated that Bt-toxin only killed certain insects when their gut bacteria were present. When the bacteria were removed by administering antibiotics, the toxin was no longer lethal. The authors suggest that Bt-toxin can cause “otherwise benign gut bacteria to exert pathogenic effects.”[18] The mechanics of how this happens, and whether it also impacts humans, is not known.

    GMOs “stick to the ribs”
    The only human GMO feeding study ever published does show interactions with our intestinal flora. The implications of this research are quite serious. British scientists found that part of the DNA inserted into GMO crops can actually transfer into the DNA of our gut bacteria.[19] Specifically, part of the Roundup Ready gene normally found in Monsanto’s soybeans had taken up residence within the intestinal flora of three out of seven subjects tested. The transfer did not occur in the lab. It had apparently taken place after consuming GM soy in some previous meal(s). And these subjects lived in the UK, where the intake of GM soy is a small fraction of what is eaten in the US.

    The study was published in Nature Biotechnology in 2004. It was condensed from a larger, more detailed study. The published version left out a significant fact: the gut bacteria that contained part of the Roundup Ready gene was not killed when exposed to Roundup’s active ingredient, glyphosate. These people had Roundup Ready gut bacteria! This suggests that the transferred genes may continue to function inside us. In other words, we may have GM proteins continuously produced inside our intestines long after we stop eating GMOs.

    There are insufficient studies on the GMO soybeans’ Roundup Ready protein to know what exactly its impacts might be on our health. One study, recommended by the World Health Organization (WHO) as part of its recommended allergen screening protocol for GMOs, looks to see if any portion of the protein’s amino acid sequence is similar to a sequence that is known to elicit an allergic response. Unfortunately, Roundup Ready soybeans fail the WHO* test. The protein has a section that is quite similar to that of a dust mite allergen. Therefore, if people who are allergic to dust are also reactive to the Roundup Ready protein, their immune system may be continuously triggered if that protein is produced within their intestines. *Since the WHO criteria were just suggestions, Monsanto chose not to remove their soy after this risk was discovered.

    Living Pesticide Factories Inside Us
    A more dangerous scenario would be if the Bt-gene produced in Monsanto’s corn were to transfer to our gut bacteria. If so, it might convert our intestinal flora into living pesticide factories. With the inside of our intestines continuously exposed, Bt-toxin might erode the integrity of our GI tract, leading to widespread gut permeability and dysfunction.

    In addition, many studies implicate Bt-toxin as an allergen. In its natural state derived from soil bacteria, Bt-toxin has triggered immune responses in farm workers [20] and allergic- and flu-like symptoms in hundreds of exposed citizens.[21] It also evoked immune responses [22] (and intestinal tissue damage) [23] in mice. Similarly, an Italian government study showed that mice fed Bt-corn had dramatic immune responses.[24] And thousands of Indian farm workers who harvest Bt cotton are also experiencing allergic- and flu-like symptoms.[25]

    Thus, Bt-toxin production within our intestines might simultaneously trigger immune responses, compromise our digestive tract, and expose the blood to undigested food (which may further trigger immune responses).



    And now the bad news:

    a 2011 Canadian study conducted at Sherbrooke Hospital discovered that 93% of the pregnant women they tested had Bt-toxin from Monsanto’s corn in their blood. And so did 80% of their unborn fetuses.[26]

    The toxin is likely to wash out of our blood fairly quickly. If that is the case, how can we explain why more than 9 out of 10 women had it circulating? It must be that the intake of Bt-toxin must be very frequent. But Canadians don’t eat that many corn chips and tortillas. They do eat lots of corn derivatives like corn syrup, but these highly processed foods no longer have the Bt-toxin present.

    The authors of the study speculate that the source of the Bt-toxin in the blood must have been the meat and dairy of animals fed Bt corn. This assumes that the Bt-toxin protein remains intact through the animals’ entire digestive process and then again through the humans’ digestive process after they eat the meat or dairy.

    A more plausible explanation may be that Bt-toxin genes transfer from corn chips or tortillas into our gut bacteria. The active genes then produce the poison on a continuous basis inside the intestinal tract, which then gets into our blood. And for pregnant mothers, the toxin then travels through the placenta into their fetuses.

    Precaution
    There are numerous theories about autism. Many blame vaccines, others say it’s genetic. The theories are not necessarily mutually exclusive as autism may be caused by several factors.

    The link between autism and GMO consumption is by no means verified. Numerous studies would be required to confirm or disprove such a connection. But those won’t happen anytime soon.

    Scientists who discover adverse health dangers are routinely attacked and often gagged or fired. The journal Nature describes these “strikes . . . launched from within the scientific community” as sometimes “emotional and personal,” and which can even “accuse scientists of misconduct.”[27] And according to insiders around the world, they successfully suppress the much needed research.

    But that hasn’t stopped numerous healthcare professionals from prescribing non-GMO diets to their patients. Indeed, the American Academy of Environmental Medicine urges all doctors to do so. And they also recommend that practitioners distribute educational materials that describe the risks and suggest ways to avoid GMOs.[28]
    The LIA (Lyme Induced Autism) Foundation, which looks at Lyme disease and autism, has similarly urged the elimination of 100% of all GMOs from the diets of those suffering from these diseases.[29] Numerous autism education programs also caution against GMOs.

    Whether or not GMOs are ultimately linked to autism, animal feeding studies already implicate them in numerous other disorders. Under the sway of the biotech industry, most governments ignore these findings. And no government yet monitors the health impacts of GMO consumption on the health of their citizens.

    There are nine GM food crops: soy, corn, cotton (used for cottonseed oil), canola, sugar beets (used in most US sugar), Hawaiian and Chinese papaya, some zucchini and yellow crook neck squash, and alfalfa (used for hay). To make it easier to avoid GMOs, the Institute for Responsible Technology (IRT) offers a list of thousands of products that have been verified as non-GMO at www.NonGMOShoppingGuide.com or via a free iPhone app ShopNoGMO. To avoid GMOs, you can use the guide, look for non-GMO labels, buy organic products, or avoid any of the at-risk crops or their derivatives (which are also listed in the Guide).

    To better understand the impacts of GMOs on health, the Institute is collecting case studies of humans, livestock, and pets taken off (or put on) a GMO diet. The stories collected so far are compelling. Please share yours by emailing healthy@responsibletechnology.org.

    The first case study related to autism is summarized below, and it provides some good news. Safe eating.

    Case Study
    Laura’s son Phillip is autistic. And her experience tells her that dietary interventions—including avoiding GMOs—are the key to recovery. She first noticed a huge improvement when she took her son off of gluten (a protein in wheat and other grains) and casein (a protein in milk). Then she started converting his diet to organic. “Once we moved to organics,” she said, “I really believe that it helped him . . . it’s like another layer was removed that prevented him from really being interested in other children and connecting with other children — playing.”

    By introducing organic foods, not only did Laura start using foods that were free of synthetic chemicals, but organic producers are also prohibited from using GMOs. After switching to a mostly organic diet, she estimated that her son was 80% recovered.

    “For the longest time, we were stuck in kind of a plateau,” she said, “where he had about an 80 percent recovery.” When people asked her what she did to bring that about, she would respond, “Well, he’s gluten free, he’s casein free, and we are 80 percent organic.” After about the third or fourth time she used those same words, she made the connection. “I’m using the same number . . . like 80 percent recovered, 80 percent organic.” At that point, she realized she needed to go 100% organic.

    “It made a huge difference.” She said that in just six months “he has become much more social, much more caring, empathetic, [and] plays with other children.” And his recovery rate? “We call it pretty darn close to 100%. . . . We know that it has to do with what he is eating and what he is not eating.” Laura is now careful to never feed him any GMOs. And she and her husband also follow a non-GMO diet.

    It is clear that this single experience is not sufficient to draw wider conclusions. Please share yours. Email healthy@responsibletechnology.org.


    References

    Special thanks to Andrea Lalama for her pioneering investigations into the link between Bt-toxin and autism.

    [1] Morbidity and Mortality Weekly Report (MMWR), Prevalence of Autism Spectrum Disorders — Autism and Developmental Disabilities Monitoring Network, 14 Sites, United States, 2008, March 30, 2012 / 61(SS03);1-19

    [2] Hogendoorn H. Genetically Modified Corn (Zea mays) and Soya (Glycine soja) or Their Natural Varieties - Do Mice Have a Preference?

    [3] Ermakova IV. Diet with the Soya Modified by Gene EPSPS CP4 Leads to Anxiety and Aggression in Rats. 14th European Congress of Psychiatry. Nice, France, March 4-8, 2006.

    [4] Ermakova IV. Genetically modified soy leads to the decrease of weight and high mortality of rat pups of the first generation. Preliminary studies. Ecosinform. 2006;1:4–9.

    [5] http://www.autismbiomed.com/gut-diet.html

    [6] Buie T et al. Evaluation, diagnosis, and treatment of gastrointestinal disorders in individuals with ASDs: a consensus report. Pediatrics. 2010 Jan;125 Suppl 1:S1-18.

    [7] Buie T, Winter H, Kushak R. Preliminary findings in gastrointestinal investigation of autistic patients. 2002. Summary: Harvard University and Mass General Hospital

    [8] Valicenti-McDermott M, McVicar K, Rapin I, Wershil BK, Cohen H, Shinnar S. Frequency of gastrointestinal symptoms in children with autism spectrum disorders and association with family history of autoimmune disease. J Dev Behav Pediatr. 2006 Apr;27(2 Suppl):S128-36.

    [9] Wasilewska J, Jarocka-Cyrta E, Kaczmarski M. [Gastrointestinal abnormalities in children with autism] [Article in Polish]. Pol Merkur Lekarski. 2009 Jul;27(157):40-3.

    [10] de Magistris L, Familiari V, Pascotto A, Sapone A, Frolli A, Iardino P, Carteni M, De Rosa M, Francavilla R, Riegler G, Militerni R, Bravaccio C. Alterations of the Intestinal Barrier in Patients With Autism Spectrum Disorders and in Their First-degree Relatives. J Pediatr Gastroenterol Nutr. 2010 Oct;51(4):418-24.

    [11] Wasilewska J, Jarocka-Cyrta E, Kaczmarski M. [Gastrointestinal abnormalities in children with autism] [Article in Polish]. Pol Merkur Lekarski. 2009 Jul;27(157):40-3.

    [12] Ewen SW, Pusztai A. Effects of diets containing genetically modified potatoes expressing Galanthus nivalis lectin on rat small intestine. Lancet, 1999;354:1353-1354.

    [13] http://www.bt.ucsd.edu/how_bt_work.html

    [14] Mesnage R, Clair E, Gress S, Then C, Székács A, Séralini, GE. (2012). Cytotoxicity on human cells of Cry1Ab and Cry1Ac Bt insecticidal toxins alone or with a glyphosate-based herbicide. J. Appl. Toxicol. doi: 10.1002/jat.2712

    [15] Krüger M, Große-Herrenthey A, Schrödl W, Gerlach A, Rodloff A. Visceral botulism at dairy farms in Schleswig Holstein, Germany e Prevalence of Clostridium botulinum in feces of cows, in animal feeds, in feces of the farmers, and in house dust. Anaerobe, in press.

    [16] Böhnel H, Behrens S, Loch P, Lube K, Gessler F. Is there a link between infant botulism and sudden infant death? Bacteriological results obtained in central Germany. Eur J Pediatr. 2001 Oct;160(10):623-8. Arnon SS, Midura TF, Damus K, Wood RM, Chin J. Intestinal infection and toxin production by Clostridium botulinum as one cause of sudden infant death syndrome. Lancet. 1978 Jun 17;1(8077):1273-7.

    [17] See for example, Mortality in Sheep Flocks after Grazing on Bt Cotton Fields—Warangal District, Andhra Pradesh. Report of thePreliminary Assessment, April 2006. http://www.gmfreecymru.org/pivotal_papers/mortality.htm .

    [18] Broderick NA et al.. Midgut bacteria required for Bacillus thuringiensis insecticidal activity. Proc Natl Acad Sci USA. 2006, 103:15196-15199. Broderick NA et al. Contributions of gut bacteria to Bacillus thuringiensis-induced mortality vary across a range of Lepidoptera. BMC Biology 2009;7:11. http://www.biomedcentral.com/1741-7007/7/11 . Mason KL, Stepien TA, Blum JE, et al. 2011. From Commensal to Pathogen: Translocation of Enterococcus faecalis from the Midgut to the Hemocoel of Manduca sexta. mBio 2(3): doi:10.1128/mBio.00065-11.

    [19] Netherwood T et al. Assessing the survival of transgenic plant DNA in the human gastrointestinal tract. Nat Biotech. 2004;22:204-209.

    [20] Bernstein IL et al. Immune responses in farm workers after exposure to Bacillus thuringiensis pesticides. Environmental Health Perspectives. 1999;107(7):575–582.

    [21] Green M et al. Public health implications of the microbial pesticide Bacillus thuringiensis: An epidemiological study, Oregon, 1985-86, Amer J Public Health. 1990;80(7):848–852. Noble MA, Riben PD, and Cook GJ. Microbiological and epidemiological surveillance program to monitor the health effects of Foray 48B BTK spray (Vancouver, BC: Ministry of Forests, Province of British Columbi, Sep. 30, 1992)

    [22] Vazquez et al. Intragastric and intraperitoneal administration of Cry1Ac protoxin from Bacillus thuringiensis induces systemic and mucosal antibody responses in mice. 1897–1912. Vazquez et al. Characterization of the mucosal and systemic immune response induced by Cry1Ac protein from Bacillus thuringiensis HD 73 in mice. Brazilian Journal of Medical and Biological Research. 2000;33:147–155. Vazquez et al. Bacillus thuringiensis Cry1Ac protoxin is a potent systemic and mucosal adjuvant. Scandanavian Journal of Immunology. 1999;49:578–584. See also Vazquez-Padron et al. 147 (2000b).

    [23] Fares NH, El-Sayed AK. Fine Structural Changes in the Ileum of Mice Fed on Endotoxin Treated Potatoes and Transgenic Potatoes. Natural Toxins. 1998;6:219–233.

    [24] Finamore A et al. Intestinal and Peripheral Immune Response to MON810 Maize Ingestion in Weaning and Old Mice. J Agric Food Chem. 2008;56:11533-11539.

    [25] Gupta A et al. Impact of Bt Cotton on Farmers’ Health (in Barwani and Dhar District of Madhya Pradesh). Investigation Report, Oct–Dec 2005. Also, "Bt cotton causing allergic reaction in MP; cattle dead," Bhopal, Nov. 23, 2005.

    [26] Aris A, Leblanc S. Maternal and fetal exposure to pesticides associated to genetically modified foods in Eastern Townships of Quebec, Canada. Reprod Toxicol. 2011 May;31(4):528-33. Epub 2011 Feb 18.

    [27] Biotech proponents aggressively attack independent research papers: GM crops: Battlefield. Waltz, E., Nature 461, 2009, 27–32; see also Under wraps – Are the crop industry’s strong-arm tactics and close-fisted attitude to sharing seeds holding back independent research and undermining public acceptance of transgenic crops? Waltz, E., Nature Biotechnology, Vol. 27, No. 10, October 2009.

    [28] http://www.aaemonline.org/gmopost.html

    [29] http://www.lymeinducedautism.com/gmopositionpaper.html

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    Default Re: Autism

    ...Superb, mindblowing, heartbreaking.

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    Default Re: Autism

    http://edition.cnn.com/2014/04/29/he...tml?hpt=hp_bn8

    How Bobby Smith learned to talk at 9, and other autism success stories
    Join the conversation
    iReport CNN iReport
    By Daphne Sashin, CNN
    April 29, 2014 -- Updated 1236 GMT (2036 HKT)

    Editor's note: April is National Autism Awareness Month. Journalist Ron Suskind's emotional essay in The New York Times Magazine about reaching his son using dialogue from scenes in Disney movies inspired CNN iReport to ask families for their communication strategies.

    (CNN) -- Bobby Smith's mother, like all parents, looked forward to the day when her baby could use words to tell her what was wrong. What hurts? Why are you sad?

    By the time Bobby turned 7, Cheri Smith was still wondering if that day would ever come.

    Her son had been diagnosed on the moderate-to-severe end of the autism spectrum as a toddler. He had ways of conveying his needs -- he'd give Smith or her husband the remote control if he wanted to watch TV, or hand his mom her purse if he wanted to go out -- but there were so many things he couldn't communicate.

    He "cannot tell us if something hurts, why he is upset or happy, where he would like to go, what happened at school today, what he would like to do for his birthday, what he would like Santa to bring him for Christmas," Smith wrote on CNN iReport in March 2012. The older he grew, the worse Bobby's behavior was getting. He would fly into rages, which Smith believed were in part the result of his inability to effectively communicate his feelings and to understand what others were telling him.

    esperate for help, in April 2012, Smith found a behavioral therapist who would change their family's life. Bobby turns 10 next month and is a totally different boy now, she said.

    "She knew that Bobby had the ability to talk," Smith said in a recent update. "She pushed Bobby like none of us had before."

    Wherever they fall on the spectrum, people with autism often struggle with communication. They can have trouble developing language skills or fail to understand nonverbal communication through things like eye contact and facial expressions.

    Parents, therapists and those with autism themselves described a gamut of communication techniques that have helped. Besides working on actual talking, some have found success with picture card systems, sign language or printed words; others speak through stuffed animals or video game characters.

    'Learn to speak our language'

    Kat Muir, 26, works as a speech-language pathologist in Indianapolis, bridging the communication gap. Most of the children she works with have Autism Spectrum Disorder -- like herself. Muir was diagnosed with Asperger's Syndrome at age 22 when she was in graduate school and still not making friends.

    She was always adept at using words, but was challenged by social communication. It was particularly hard in junior high.

    "Girls are expected to know instinctively how to be social, and when they don't, it is very obvious," she said.

    For years, she thought of a conversation "as a contest to see who could say the most interesting thing." She remembers one time when some girls were talking about Britney Spears; she jumped in with her own contribution, saying something like, "Planes in World War I had synchronized guns so the gunmen didn't shoot their own propellers off."

    No one cared. And they told her so.

    It got better when she moved to a big public high school, where students seemed more tolerant of differences. Now she reminds herself to talk about what other people like, not just what she finds interesting.

    She said it helps to find an activity "that encourages communication but doesn't force it." For her, that's dance class.

    "It's reassuring to know that I will see familiar faces for an hour at the same time every week. I may socialize by starting a conversation about favorite dance moves, or I may exchange smiles with someone because we're doing what we love. The more structured a social interaction is, the more comfortable it is."

    To those without autism, said Muir, "Everyone with autism has something to say. Learn to speak our language, and we will learn to speak yours."

    Power of a pig

    California speech-language pathologist Lois Jean Brady agrees. As a certified autism specialist, she advises parents to use their child's special interests -- animals, music, technology or cars, for instance -- to build their language.

    "Go into their world and slowly lead them to yours," she said.

    With students who love animals, Brady uses a potbellied pig named Buttercup to communicate. She has found many children feel comfortable talking with an animal and some have said their first words to Buttercup.

    She tells the story of a junior high school student who desperately wanted friends. She rehearsed a few answers to "common pig questions" such as "What does he eat?" and "How much does he weigh?" then sent the young man into the school hallway with Buttercup on a leash.

    "It was not long before he was surrounded by other students, mostly girls, answering questions with a smile from ear to ear. A couple of the students remained friends," she said.

    Brady's own son is on the autism spectrum. He is now 20 years old, goes to college and works with other special needs children. When he was younger, he and his mother would spend hours in the living room, lining up toy cars.

    "I kept the cars in a large bucket and if he wanted one he had to ask for it," Brady said. "Initially it was just 'car,' then 'blue car,' then 'shiny blue car,' building language one car at a time."

    More cookies?

    It has taken about two years for Emily Ferguson's son Sammy to learn to use cards with pictures to communicate. The 8-year-old has severe autism, and speaks about three to seven words a month. He can't tell his mother when he's in pain, and she would give anything to have a conversation with him. But she celebrates that he is able to communicate about 30 food requests and 16 nonfood requests (play, go outside, etc.) through pictures.

    "I was tickled when Sammy realized he had no limit to the amount of times he could request cookies. For the first time, I felt like a 'normal' mother, because I had a child who was asking for something he wanted repeatedly, and he was getting the same answer ('No.')," Ferguson wrote in an e-mail.

    "It has been an amazing experience to see Sammy go from just crying to using pointing to giving others picture cards on sentence strips."

    Ferguson prays Sammy will find the communication tools that work best for him, "and that he will be able to share his thoughts and emotions with those around him. Until that day, I want the world to understand that my child is worth respecting, loving and cherishing."

    Talking at 9

    Cheri Smith's son, Bobby, knew about 50 words by the time he was 9, but his main form of communication was taking his parents by the hand to what he wanted. A behavioral therapist near their West Virginia home helped Smith understand that their son was physically capable of speaking more, with practice.

    For the first six months, therapist Sharon Holbert worked with Bobby on sitting properly in his seat, keeping his hands folded on the table (instead of hitting her) and his feet in front of him (instead of kicking her). There was a close link between behavior and talking: As he learned how to stay calm, he was able to learn more; as he became better at communicating, he grew more relaxed, Holbert said.

    "If you have a student who's hitting and screaming and kicking, you can't teach them anything. Once you get them to a place where they're ready to learn, then bam, you can do something," said Holbert, a board-certified behavior analyst. "His ability to learn was there. I think he figured out 'if I hit people, they probably will leave me alone.'"

    As they worked on identifying colors, numbers or letters, Holbert wouldn't acknowledge his response as correct unless he said it verbally.

    Smith copied the model at home.

    "If he wanted any food items, if he wanted a particular TV show that he liked, if he wanted to go outside, he had to ask verbally or he didn't get his want," Smith said. "Quickly it was just easier for him to say the word than it was to throw a fit."

    He can now verbally identify letters, colors, animals and some shapes, count up to 20 and say about 100 vocabulary words. He can answer simple questions and has gone from using single words to short sentences like, "I want rice cakes please," or mostly complete sentences like, "I want swim at the beach."

    "We went from being a family where our child was physically aggressive and having constant meltdowns to one that is enjoying experiencing the world through Bobby's eyes."

    He also has his own unique language, which his parents have come to appreciate, too.

    Bobby loves to go for car rides. When he wants his mom to turn down a particular road, "he will put on his own turn signal. He clicks his tongue and makes it sound exactly like a car's turn signal, and that is how I have known where he wants to go."

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    Default Re: Autism

    http://www.activistpost.com/2014/05/...tra-first.html

    Thursday, May 1, 2014
    Interview With Arnold Hoekstra, First Canadian To Be Fired For Vaccine Refusal
    Brandon Turbeville
    Activist Post

    In my recent article entitled, “First Canadian Fired For Refusing Vaccine,” I wrote about the case of Arnold Hoekstra, the first man in Canada to be fired for refusing to submit to a flu vaccination at his place of employment, the Boundary Hospital in British Columbia.

    Hoekstra, who is 49, held a permanent part-time position at the hospital as an adult day program worker. However, when he was instructed to submit to a flu vaccination, he refused to be injected with the toxic cocktail of chemicals and viruses that have been demonstrated to cause a number of adverse health effects in both children and adults. Short of agreeing to be injected with a vaccine that has been shown to be ineffective at preventing the flu (at best), Hoekstra’s only other option was to wear a face mask at all times while at work.

    Hoekstra refused this option as well because he claims that wearing a mask all day makes him feel like he is suffocating. Thus, Hoekstra was terminated from his job as a result of his decision.

    In my article, I used quotes from Hoekstra as they were presented in other media outlets as well as those that he provided me with in an email interview. Below is the entirety of the email interview between myself and Arnold Hoekstra.

    As I wrote previously, social approval and disapproval is often used to enforce a number of tragic policies by using the force of the people who themselves will be further enslaved by them. The recent propaganda push by the pharmaceutical companies and their media mouthpieces is simply the gearing up for a major battle in the future that will inevitably lead to the universal mandate of vaccination applicable to all people with no exemptions.

    For now, Arnold Hoekstra stands as one of the first victims of this quiet war.

    Brandon: How long had you worked for the Boundary Hospital?

    Arnold Hoekstra: 5 yrs

    Brandon: How many times had the hospital asked that employees submit to vaccination in the past?

    Arnold Hoekstra: Once before in 2012. The ruling was overturned because of union intervention.

    Brandon: What was the process used by the hospital in order to encourage employees to vaccinate? What was the language used by management in this regard?

    Arnold Hoekstra: They used notices throughout the hospital giving their reasoning for getting the shot [and] posted notices in the office, [brought]gifts, br[ought]the vaccine to the work site and personally ask[ed] me if I was going to have the shot on more than one occasion. And advertising on [the] work site online.

    Brandon: What are your reasons for refusing to vaccinate?

    Arnold Hoekstra: The ingredients [and] Principle. When a choice comes to do or not to do I must trust the true way rather than the way the majority is going. When the masses flock to something, it is, in most cases, the wrong way. Few exceptions.

    Brandon: What are some specific issues you have with the vaccine? Does your skepticism extend to vaccinations in general or only the flu vaccine?

    Arnold Hoekstra: I believe all vaccinations are harmful. It also puts people in a false sense of security. They try to shortcut their health, deceiving themselves to believe that the professionals know better and that they could not possibly know for themselves.

    Brandon: Obviously, your resistance to the dictate to vaccinate was based on the potential adverse health effects that vaccines have demonstrated to produce. But what about the idea that individuals should be free to choose what they put in their bodies? Did that concept influence your decision as well?

    Arnold Hoekstra: Yes it did. To my understanding when someone attempts to invade that sacred place (my body) it is a violation.

    Brandon: Why did you refuse to even wear the face mask?

    Arnold Hoekstra: The main reason I did not wear the mask is because I did not want to exhibit fear. I did not want anyone to think I agreed in any way with this policy. I believe the only reason people wore the masks wasn't because they believed it was going to be affective or that the policy in general was right but that they would be disciplined for not doing so.

    Also, I believe that it was used to label those who didn't get the shot as uncooperative. And l believe it was coercive in the way that those who wouldn't have taken the flu shot, did so in order to avoid wearing it for 4 months of the "flu season."

    Brandon: Do you plan to take any legal action against the hospital?

    Arnold Hoekstra: That is a hard question to answer. The hospital is run by a governing authority (Interior Health) B.C. They are responsible for firing me.

    Who is ultimately responsible? You have to work your way up the ladder. Follow the money. It doesn't take a genius to figure out the rest.

    To answer the question about what to do legally ... My main goal is for health professionals or, for that matter, anyone to be able to choose for themselves what they want in this matter and [to] not to be put in this position.

    If legal action will stop the madness then my answer is yes.

    Do I believe I should be compensated? Yes. They forced me into this position. I could not go against my conscience. They did not consider me as an individual or listen to the reason for my decision to not comply.

    Brandon: Do you regret your decision?

    Arnold Hoekstra: I do not regret my decision. I regret that the powers that be made this awful choice.

    Brandon: Do you think your case is indicative of what is to come? Do you think we will see more people lose their jobs as a result of their refusal to submit to vaccinations?

    Arnold Hoekstra: I believe the screws will continue to tighten until the whole nation is on board. They have said in the media that they want the percentage of health care workers taking the shot to go much higher than 80 percent.

    As far as people losing their jobs ... well I hate to say it but most people tend to do what they’re told, regardless of the fact that they are putting their health at risk. Many I talked to disagreed with the policy but because of fear of discipline and losing their jobs. They just complied.

    Brandon: If you could say one thing to the people who may be hearing about your case for the first time, what would it be?

    Arnold Hoekstra: Think for yourself. Don't allow others - no matter how many degrees they have to the right of their name - to think for you. And always remember that you always have a choice.


    Brandon Turbeville is an author out of Florence, South Carolina. He has a Bachelor's Degree from Francis Marion University and is the author of six books, Codex Alimentarius -- The End of Health Freedom, 7 Real Conspiracies, Five Sense Solutions and Dispatches From a Dissident, volume 1 and volume 2, and The Road to Damascus: The Anglo-American Assault on Syria. Turbeville has published over 300 articles dealing on a wide variety of subjects including health, economics, government corruption, and civil liberties. Brandon Turbeville's podcast Truth on The Tracks can be found every Monday night 9 pm EST at UCYTV. He is available for radio and TV interviews. Please contact activistpost (at) gmail.com.

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    Default Re: Autism

    Hi Tesla and other contributors,

    I must confess, I'm struggling to find the time to be able to carry out sufficient research to gain a sufficient grasp of the vaccination Autism spectrum debate.

    I'm a recent dad, I'm doing a masters degree whilst working full time and my wife is also studying full time…so we're pretty time poor.

    I've seen enough evidence in a whole range of high level conspiracies to establish that people in high places don't necessarily have the publics best interests at heart. I see it as highly conceivable that vaccinations may indeed be causing some nasty autoimmune/neurological/who knows what reactions, temporary and permanent in children and that the government/transnationals/whoever stands to gain/lose from this issue is not revealing all that is known re the consequences of vaccinations.

    With my young child approaching her first hit of the MMR vaccine, I'd like to know more, but just can't wade through mass of papers, blogs, videos etc.

    Could I ask a big favour to those who have dedicated some serious hours in this issue and point me towards the strongest high level empirical evidence that indicates a link between vaccinations and autism and the like. Any particularly powerful documentaries etc would be great also.

    Based on all of the evidence, are the consequence of not vaccinating i.e. infectious disease outbreaks still too severe to consider not maintaining herd immunity. In other words, if the odds are say 1 in 100 (extremely high odds) for a bad reaction to vaccinations, on the whole, is it still a necessary evil to vaccinate?

    For what it's worth, my current stance is that there are characteristics amongst a minority of individuals who appear to react poorly to vaccinations for host of different reasons. I think that this number is still relatively low, but is still there, despite denial from government and health groups for fear of litigation and fear of loss of herd immunity. I believe more needs to be done to identify a subset of characteristics that make individuals vulnerable to a bad reaction to vaccinations with measures put in place for a safe alternative or to simply not vaccinate those individuals.

    This stance is based on a fraction of the knowledge you guys have acquired, so I'd be keen to hear your opinion and the key data to back those opinions up.

    Apologies if this has already been done previously - happy to be redirected.

    Cheers,

    Napping

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    Default Re: Autism

    Since there is a link to allergies, we need to be looking at the mechanism of the proteins on cell surfaces, for starters, when looking at autism.
    People think they are going to find a "gene" for it, some factor other than vaccination allowing them to use the word "because" -- but science is coming up empty.


    I read two or three years ago that scientists still do not fully understand the mechanism behind the interactions between Hepatitis B and the substance Heparan Sulfate, for example. How can scientists say that a certain vaccine is harmless, when they don't even understand what happens between the body and the germ itself in the first place?
    Quote http://www.ncbi.nlm.nih.gov/pubmed/18046710

    Hepatitis B virus infection initiates with a large surface protein-dependent binding to heparan sulfate proteoglycans.
    Contrary to many other viruses, the initial steps of the hepatitis B virus (HBV) infection, including attachment to hepatocytes, specific receptor interactions, and membrane fusion, are unsolved.


    HBV infection requires the initial attachment to the carbohydrate side chains of hepatocyte-associated heparan sulfate proteoglycans as attachment receptors. This interaction initializes the multistep entry process of HBV and cannot be bypassed by alternative routes.
    Simulated autism symptoms in mice by affecting Heparan Sulfate:

    Quote http://www.ncbi.nlm.nih.gov/pubmed/22411800
    Autism-like socio-communicative deficits and stereotypies in mice lacking heparan sulfate.

    Heparan sulfate regulates diverse cell-surface signaling events, and its roles in the development of the nervous system recently have been increasingly uncovered by studies using genetic models carrying mutations of genes encoding enzymes for its synthesis. On the other hand, the role of heparan sulfate in the physiological function of the adult brain has been poorly characterized, despite several pieces of evidence suggesting its role in the regulation of synaptic function. To address this issue, we eliminated heparan sulfate from postnatal neurons by conditionally inactivating Ext1, the gene encoding an enzyme essential for heparan sulfate synthesis. Resultant conditional mutant mice show no detectable morphological defects in the cytoarchitecture of the brain. Remarkably, these mutant mice recapitulate almost the full range of autistic symptoms, including impairments in social interaction, expression of stereotyped, repetitive behavior, and impairments in ultrasonic vocalization, as well as some associated features. Mapping of neuronal activation by c-Fos immunohistochemistry demonstrates that neuronal activation in response to social stimulation is attenuated in the amygdala in these mice. Electrophysiology in amygdala pyramidal neurons shows an attenuation of excitatory synaptic transmission, presumably because of the reduction in the level of synaptically localized AMPA-type glutamate receptors. Our results demonstrate that heparan sulfate is critical for normal functioning of glutamatergic synapses and that its deficiency mediates socio-communicative deficits and stereotypies characteristic for autism.

    We know that Y Pestis, the black plague of the tales, works against the human body by affecting Cell Signaling.

    Well, having problems with Heparan Sulfate in the body, also affects cell signaling.

    Many stress disorders and diseases, and even autism, share the common factor of faulty cell signaling.



    _______________


    Cell signaling adulterations


    http://www.thedogplace.org/VACCINES/...an-DVM-107.asp

    How Vaccines Dysregulate The Immune System and
    Impact Genetic Control Over Disease Expression


    5th Annual Joint American Homeopathic Conference Poster Session 2010

    presented by Patricia Jordan, DVM, CVA, CTCVH, & Herbology http://dr-jordan.com

    Mucosal Immunity



    Quote Cell mediated responses (Th1) Lymphocytes, (CD1, CD 2, CD3, CD4, CD8) monocytes- macrophages and natural killer (NK) cells (principal components) Cytokines

    Humoral responses (Th2) involve soluble components including immunoglobulins (antibodies) [Igs-IgG, IgM, IgA, IgE, IgD], class switching, antibody gamma globulins and complement proteins.

    Immune System Components Genetic Major histocompatibility complex (MHC) system Chromosome, gene, haplotype, and polymorphism and super gene family molecules.9 MHC genes and include [HLA-A, HLA-B, HLA-C, HLA-DPA 1, HLADPB1, HLA-DQA1, HLA-DQB1, HLA-DRA and HLADRBI.] MHC region divided into three regions Class I (HLA-A, B and C) Class II (HLADP, DQ and DR) and Class III genes encode complement components (C2, C4 and Factor B), cytokines (TNF-α) MHC genes display high levels of allelic diversity


    Activation of Adaptive Immunity Innate immunity may trigger adaptive immune responses thru Antigen processing and presentation by macrophages and dendritic cells .The evolution of the immune system is a direct consequence of pathogen-exerted selection pressure. It is particularly those qualities like progressive development of humoral and cellular adoptive immunity, Major Histocompatibility Complex (MHC), variable class I and class II genes, precise mechanisms of immune recognition and long-term immune memory that reflect the fundamental evolutionary advancement of the vertebrate immune system. In evolution the survival advantage imposed by an extremely reactive immune system is jeopardized if that system turns against the host and causes "self" destruction.

    Vaccination is an abnormal pathogen presented in an abnormal route (injection) and influences the entire immune system in an unnatural way, leading to unnatural evolutionary selection where the results are dys regulation of the immune system, disruption of TH1 bias, atrophy of mucosal, increased inflammation, loss of specification and control. Vaccination dysregulates the immune system and genetically impacts the HLA (MHC) leading to an abnormal expression of disease susceptibility. The vaccine is no more a reflection of the actual environmental challenges faced by those vaccinated than the now dysregulated immune system is a reflection of intelligent design or natural selection. Vaccines are genotoxic; corrupted genomes are leading to the loss of the organic self. Vaccines are responsible for autoimmune, cancer, Type I-IV reactions, allergies, asthma, atopy anaphylaxis, eczema, organ failure, neurological, behavioral disease and death.[List is not complete]





    Anything that affects gene coding affects genetic expression of disease



    The evolution of the immune system is a direct consequence of the pathogens the immune system was exposed to from the environment. The pathogens exert an evolutionary selection pressure which was in part responsible for the genotypes of the MHC (major histocompatibility complexes) that developed in tandem to handle the pathogens. The MHC determines the host’s immunopathology impact from the antigen and is responsible for the expression of clinical disease. The immune system is very complex and developed to handle an enormous variety of pathogens, the genetic ability to respond to a large number of pathogens was necessary in order to survive to live another day.



    The MHC tissue markers are one of the major routes of tapping into the possible needs for survival via the immune response. Although not the only way, besides the MHC we have the major loci, minor loci and many other locations for gene expression to effect disease expression. We now see the complexity of immune system response pathways and still there are many factors that remain unknown. The MHC and the HLA and DLA (yes, dogs also have MHC sites like the humans) in fact all vertebrates have this important link of genetic expression of antigen reception and engagement. The groups of receptor sites not only engage with the pathogens, they are also responsible for a cascade of events that have evolved over time to express the organism’s impact with a pathogen, reflecting in dis ease susceptibility and genetic expression.



    There is a great variability in how any one individual will react to any pathogen and it is the individual’s genetic variability that is the marvel of individual and species survival .Not everyone would respond the same way to each pathogenic impact. The immune system, like a virus has great reach with incredible mutation ability through gene expression and this brings an organism forward to survive another day.



    Vaccines lead to genetic mutations. Genetic impact on MHC (HLA) is what dictates genetic expression of disease susceptibility. Vaccines rob the individual of natural evolutionary selection pressures based on natural antigen risks. Vaccines are altering gene sequences, inserting genes, affecting genome and destroying the organic immunologically determined susceptibility that evolved with natural selection. Determined susceptibility is genetically impacted ahead of disease expression by the antigens presented to or encountered by the individual. The immune system has evolved naturally to promote life and what is happening with unnatural antigen environment delivered in unnatural route to dysregulate the immune system is resulting in unnatural selection, immune system corruption and species distortion.



    The genetic basis for susceptibility to disease is complex but well before man understood anything about the immune system and how it worked, he intruded on the evolved design with a hubris that is having collateral damage and unintended consequences of species de evolution.

    A little immunology review;

    The innate immune system was developed to provide the organism with an immediate response. The natural immune system is composed of three portions; the first line of defense is the mucosal immunity and works with the cell mediated immune system (Th1) to deal with the great majority of pathogens. Entry sites to the body via the skin, mucosal sites of the nasal/respiratory, oral/rectal, ocular, aural and urogenital is where the majority of trials for the immune system would have started. The mucosal immunity has antiseptic patches of secretory immunoglobulins (IgA) to respond first. If the mucosal surfaces were actually penetrated than the IgE immunoglobulins came forth for the defense.



    The cell mediated responders have evolved to provide the acute inflammation response which is necessary in properly maturing the body’s immune system. Without the majority of pathogens entering from these sites, the immune system does not reach maturity and therefore is unable to respond competently. The childhood xanthamatic diseases fulfill this purpose of immune system maturation. Denied the ability to “mature” the immune system, the organism is left with a dysfunctional immune response and genetic disease expression is altered.



    Acute inflammation in the mature immune system can process and effectively clear the intruder. The hypothesis on how this takes place is via the dendritic cells instructions to TH1 polarity. Of course if the dendritic cells are damaged from the vaccine or the aluminum or the mercury in the vaccines, this is one way the vaccines dysregulate the polarity of the immune response. The body needs to be able to focus on the correct form of response as the body deals with the pathogen. Later, after the invasion by pathogen has been cleared, the body then engages the humoral immunity (Th2) to recognize the pathogen and produces antibody against it. This form of the immune system is the acquired immune response which vaccinations were meant to augment. The humoral immunity makes the specific recognizing antibody after the body is over the acute inflammation so as not to exhaust the individual and prevent recovery.



    Humoral immunity (Th2) unskewed system is a much different system designed to deal with pathogens or agents that might penetrate the skin bypassing the mucosal immunity ex; venoms from snakebites, poisons or toxins from bites, stings or deep punctures and microbial injection into areas of low oxygenation .The humoral system is capable of handling toxin inactivation and antigen opsonization, dealing with intracellular pathogens and direction of recognition via antibody production. The natural immune system never evolved to see immune challenges enter the body like this. Rarely would a pathogen come into the immune system’s pristine internal environment of the blood. Humoral immunity was not designed to handle a myriad of pathogens this route, rather the humoral immunity is an internal deeper acting immune system for a lesser number of directly injected pathogens. Parental presentation of the pathogens via vaccination was not “good shepherding” practice and instead has been responsible for the improper wiring, signaling and biochemical pathway disruptions that make up many disorders today. Again, the wrench thrown into the dynamics of an evolutionarily successful system by manual manipulations not based on evolutionary pressure but by medical hubris. Although pleased with this intervention, man has remained incapable of understanding the chaos they have created.

    The complex immune system with the spread of genetic variability has served us well through the beginning of time. Unfortunately, about 300 years ago an adulteration and violation of the natural workings of the immune system took place. This adulteration was the unnatural injection of unnatural pathogens that were not from the natural environment but rather a concoction of ingredients made artificially and mixed with toxic chemicals. Early on the recipe included embalming agents, later with heavy and light metals, and eventually with genetically engineered chimeras, man made monsters of unnatural origin. Many of the viruses being injected into the bodies are genetically engineered and certainly not organic. The vaccine has never been a natural pathogen of the natural environment and never a natural route of introduction and penetration of the host immune system. Why would we not foresee the dys regulation, dysfunction and the accompanied corresponding genetic compromises and hybridization that explain the growing number of health issues that have run parallel with the rise in vaccine number and use?



    The many ways the vaccines dysregulate the immune system and de construct health. First imposition of the vaccine is to affect genetic expression of disease by affording the unnatural engagement of the MHC, the major HLA then minor loci; cytokine genes, CD-encoding genes, T cell receptor genes, growth hormone and immunoglobulin genes any of the polygenes that cascade down to the intricacies of our many possible gene responses.



    Second imposition of the vaccine is to skew the immune system and remove the balance of Th1 and Th2 between cell mediated immunity and humoral immunity. Total dysregulation, shifting of the poles of immunity which will include a combination of mutations, gene expression, biochemical pathway alterations, enzyme disruptions, hijacking the system dys regulation by up regulation of the IgE expression and a down regulation of the IgA, disruption of the cytokine profile and many, many other routes depending on the nature of the pathogen and toxins in the vaccine and the variable gene response of the individual.



    Expression of disease now, is a function of the unnatural exposure to unnatural pathogens and toxins and the expression of disease as varied as behavioral, Type I-IV Hypersensitivity; allergies, asthma, anaphylaxis, atopy, eczema, cancer, autoimmune, bacterial, viral, yeast, fungal, internal and external parasites and genetic diseases. The genetic expression of disease is predated by the link up of the pathogen and the individual’s gene which are pathogen impact impressionable. The unnatural selection pressure on the species by the use of vaccines is unnaturally evolving or de evolving the species through genotoxicity and genetic disease increase. The genetic damage or “genetic susceptibility” is transferable to the next generation. The next generation when vaccinated, expresses easily the adverse events that vaccines are selecting for.

    The type of immune response that occurs after pathogen binding is determined by cytokine messengers that are triggered by certain elements of the pathogen. The vaccine contains a multiple number of ways to affect this: contamination with unknown viruses and microbial components, unnatural pathogens, chimeras and other genetically engineered products, unfiltered genetic pieces like virions, prions, viruses from other species, aluminum, mercury which can directly lead to abnormal cytokine messengers being produced via pathogen alterations/adulterations/mutations. Modified live viruses or “attenuated viruses” allow live cells to migrate to and replicate onto the host’s tissues. Another act of hubris has occurred because playing with viruses all of these last 300 years, it was only recently that science has now discovered that viruses are not dead, they are not live, they are packets of genetic material that when in the presence of a susceptible and permissive living cell that has the necessary receptor can replicate and infect .We have to remember, the virus affects the appearance of antigen recognition sites in our MHC system which evolved as a type of ANTIVIRUS SOFTWEAR SYSTEM.



    Sometimes, virus contamination in a vaccine can activate viruses in the human body 30-40 years after inoculation. The presence of unknown viruses, the contamination of viruses, the recombination and reassortment of viral genes and the introduction of xenotropic viruses, infective DNA viruses have all again - due to the hubris of man - introduced disease and pathology into organisms receiving the jab. The process of injecting unnatural substances into the body started well before the identification of the fist virus! The contamination continues today with the filtering process not finding virions and prions and other smaller genetic impacting contaminants. [Rotavirus vaccine for children found to contain pig virus]. The viral and even microbial antigens are all players in the genetic expression of disease and disease susceptibility to every genome via the MHC and other still unidentified pathways.



    Adjuvants additionally adulterate the intelligence of the innate immune response. Adjuvants “add” inflammation and pathogen distortion and therefore cell signaling adulterations, impingement upon the evolutionarily perfected system and result in a loss of order. In 1988, Dr. Ron Schultz spoke out in a roundtable discussion over his concerns of the random addition to anything into vaccines without understanding in the least the impact that the addition of for example interleukins into the vaccines. He framed the impact of the whole body or even just the immune system as a complete unknown yet the cavalier attitude from vaccine makers was that no caution was necessary.



    We know now that including interleukin in the vaccines in the 1980’s has now produced children born to vaccinated populations with the genetic disease of missing interleukins! The “new” auto inflammatory syndrome DIRA deficiency of interleukin 1 receptor agonist where children display a constellation of serious and potentially fatal systemic symptoms from birth are inherited mutations in IL IRN - a gene that encodes a protein known as interleukin 1 receptor antagonist. The irony that Dr. Ian Tizzard would compare the ability to add ingredients like alum to vaccines used since 1926 and still in l988 not having any idea how it worked, is little comfort to the many parents of children suffering the highest rate of cancer, brain cancer. In 1999 theWHO through the IARC listed the aluminum in vaccines as a grade 3 out of 4 carcinogens. It doesn’t help either to understand now that aluminum will increase the permeability of the blood brain barrier and allow viruses (viruses that have an affinity for the central nervous system like measles) into the brain along with the mercury and aluminum - both metals that can act synergistically to mutate. Seriously, they still don’t see where the rise in childhood brain cancer is coming from?



    Aluminum in the vaccines is also up regulating the IgE and compromising the IgA, therefore the presence of aluminum in the vaccines is a much involved gene impactor which causes vaccines to result in allergies, atopy, anaphylaxis, asthma and eczema expression. The natural immune system has a variety of defense tools to use in the protection of the organism however these systems are dys regulated when damaged pathways result from damaged pathogens or genetically engineered pathogens are artificially introduced.

    The effects of alum were never known even though the toxin has enjoyed a hierarchical rise in use and success. The amount used in vaccines is not a “safe” amount, it is only the amount they found necessary to exert its inflammatory effect as an adjuvant! The lack of safety studies, lack of teratogenicity or carcinogenic studies or any long term effects signaling genetic defects from vaccines were never done. For any agency from the HHS, CDC, FDA, USDA,WHO, UN, UNICEF, and GAVI to endorse or project vaccines as safe is criminal and investigations should be called for.



    Liability waivers put in force for the drug companies to escape prosecutorial litigation will not be upheld in the face of gross criminal action for failure to perform due diligence in the safety study or even of the efficacy studies that are lacking for vaccine use in the first place. The question as to what exactly was known as FDA-licensed products are unleashed upon the public gives rise to another question: why is it that the drug companies that makes vaccines and promotes their use, are the same drug companies that make the drug for the VACCINE DISEASE that follows the vaccine use? What exactly are the revelations that are bound behind “proprietary confidentiality clauses” and is this the way drug companies are pleading the Fifth Amendment for protection from self incrimination? Would this be the reason the governments remove vaccine liability from the manufacturers of the experimental guise under which health care is purported?



    The highly polymorphic HLA/DLA antigen systems which are involved in antigen presentation clearly affects responses to vaccination and therefore this impact is unknown in any organism receiving the jab. This lack of knowing makes every vaccination: “experimentation under the guise of health care delivery.” Effects of vaccines on any individual are variable and therefore any expected result incalculable, the risk to any organism is therefore unknown.



    Administering a jab is not synonymous with conveying immunity. Antibody production is not equated to immunity and vaccination does not mean immunization. Damage from vaccines are cumulative, cell mediated immune suppression increases significantly with every jab. Multivalent vaccines are particularly damaging and immune disrupting.



    Only vaccinated individuals were found to develop auto antibodies in a landmark study done at Perdue University. Auto antibodies are made with the vaccines from the viruses, from the microbial antigens, from the aluminum and mercury and other ingredients that would mutate or disrupt the pathogen. The increase of molecular mimicry increases with vaccines and these examples of pathways to increase the number of auto antibodies formed the trigger necessary to promote genetic expression of autoimmune disease. Certainly, autoimmune disease expression is one step closer to genetic disease and that handicap will transfer vertically to the next generation in many instances. The important understanding is that the adulteration of the genome came in via the injection of vaccine.

    Since not even a very heavy book could contain all the pathways to disease expression from genetic effects of the vaccine (the great immune adulterant), let us at least end this with the following understanding; vaccines have no environmental epidemiological studies to support the benefits over risks of vaccine administration, they are not safe nor innocuous and have not even been proven effective in conveying immunity which is the only reason one would consider their use in the first place. Vaccination use fits the definition of “a medical assumption” and according to Dr. Stephen Blake is certainly the biggest medical assumption ever made in the history of mankind and is directly responsible for more disease, death and disability than any other medical procedure or act.



    Not surprisingly, with the safety of vaccination questioned and autism, autoimmune diseases and cancer linked in hospitals to vaccinations, only now is the NIH announcing research grants for the purpose of addressing vaccine safety. The Research to Advance Vaccine Safety (R21) is just now in 2010 being initiated to research vaccines:



    “research that will contribute to the overall understanding of vaccine safety such as physiological and immunological responses to vaccines and vaccine components, how genetic variations affect immune/physiological responses that may impact vaccine safety and identification of risk factors and biological markers that may be used to access whether there is a relationship between certain diseases or disorders and licensed vaccines and the application of genomic/molecular technologies to improve knowledge of vaccine safety”



    The problem is that this “scientific study is too late”. For three centuries genotoxicity, immune dysregulation and immune dysfunctioning - even to immune deficiency and annihilation - has been de evolving the genomes of man and animals.



    Dr. Harris Coulter would consider the vaccination as medical hubris and the many diseases spawned from its use the “unintended consequences and collateral damage”. The National Childhood Vaccination Program is a program in which any parent should have the right to protect their child. The mandatory vaccine programs are genetic assaults and project a form of invalid federal medicine which is tyranny. The promotion of the vaccine programs are fraudulent and criminal acts which no taxpayer should be made to support as the effect in many cases, cases rising with the rise in vaccine use, are genetic and constitute genotoxicity.



    This attempt to violate the natural laws of evolution is impacting the species in a de-evolutionary format leading to increased genetic expression of disease and forcing those jabbed into a cycle of chronic disease management if not death first. Of course the same drug companies that make vaccines are usually the same ones that sell the medications to palliate and suppress said disease expression. This system of making disease and then making the medications to suppress and palliate the disease puts into the hands of the drug companies all the federal funds that sponsored the vaccines and then the money from the manipulated health care system treating the disease. Soon the allocation of funds for the drug companies will shift the power from the democratic state to the hands of the drug companies that have full impunity from liability, this benefit legislated for them by the members of the democratic legislature elected to represent those being vaccinated into disease and harmed in the first place!


    Dr. Harris Coulter stated that” medicine” had a lot more to do with “politics” than it did with “science”. Dr. Patricia Jordan noted that it took a Doctor of Political Science to point out to the medical profession what they did not seem capable of recognizing right in front of their face, that medicine is politics and politics is about money, no science necessary.



    Any NIH research done under the Research to Advance Vaccine Safety (R21) must have independent, nonconflict oversight with participation of those harmed by vaccines to ensure that the real measure of vaccine damage is properly addressed. That is, unless the disease, disability and deaths from vaccines were to be immediately stopped in accordance with the Precautionary Principle.



    The precautionary principle is a moral and political principle which states that if an action or policy might cause severe or irreversible harm to the public or to the environment, in the absence of a scientific consensus that harm would not ensue, the burden of proof falls on those who would advocate taking the action. The principle aims to provide guidance for protecting public health and the environment in the face of uncertain risks, stating that the absence of full scientific certainty shall not be used as a reason to postpone measures where there is a risk of serious or irreversible harm to public health or the environment.



    It is obvious that the unnatural vaccine has unnaturally selected for genes that do not reflect a natural exposure from the real environment and thusly resulted in unnatural selection of genes that have dys regulated the immune system and disrupted the inflammatory pathway and distorted the populations genetically. Unnatural gene selection is then leading to resistance and susceptibility to disease which is unnatural and not the real picture of the antigen state within our external environment for which an immune system is geared to provide survivability against encounter. Vaccination is resulting in abnormal disease expression and the making of disease previously not encountered. Although it is popular to blame our external environment, this is not the main environment our immune system is being pressured by. In the madness, the species are being distorted and genomes are being corrupted. The rise of genetic susceptibility and genetic disease is a reflection of this distortion. Most of what we see today is Vaccine Disease, in that the dysregulation of the immune system by vaccines have altered the genetic susceptibility and expression of disease and is not evolving a better immune system and health but deconstructing the immune system and the genome towards doom.
    it even ties in with diseases like arthritis and lupus




    http://arthritis-research.com/content/14/6/R243
    Quote Modulating proximal cell signaling by targeting Btk ameliorates humoral autoimmunity and end-organ disease in murine lupus

    Systemic lupus erythematosus is a chronic autoimmune disease characterized by an abundance of autoantibodies against nuclear antigens. Bruton's tyrosine kinase (Btk) is a proximal transducer of the BCR signal that allows for B-cell activation and differentiation. Recently, selective inhibition of Btk by PCI-32765 has shown promise in limiting activity of multiple cells types in various models of cancer and autoimmunity. The aim of this study was to determine the effect of Btk inhibition by PCI-32765 on the development of lupus in lupus-prone B6.Sle1 and B6.Sle1.Sle3 mice.
    what is an antigen
    http://en.wikipedia.org/wiki/Antigen
    Quote In immunology, an antigen (Ag), or antibody generator, is any substance which provokes an adaptive immune response.[1] An antigen is often foreign or toxic to the body (for example, a bacterium) which, once in the body, attracts and is bound to a respective and specific antibody.
    what is nuclear antigen
    http://en.wikipedia.org/wiki/Prolife...uclear_antigen
    Quote Proliferating cell nuclear antigen (PCNA) is a protein that acts as a processivity factor for DNA polymerase δ in eukaryotic cells. It achieves this processivity by encircling the DNA, thus creating a topological link to the genome. It is an example of a DNA clamp.

    The protein encoded by this gene is found in the nucleus and is a cofactor of DNA polymerase delta. The encoded protein acts as a homotrimer and helps increase the processivity of leading strand synthesis during DNA replication. In response to DNA damage, this protein is ubiquitinated and is involved in the RAD6-dependent DNA repair pathway. Two transcript variants encoding the same protein have been found for this gene. Pseudogenes of this gene have been described on chromosome 4 and on the X chromosome.[1]
    what is a DNA clamp

    http://en.wikipedia.org/wiki/DNA_clamp
    Quote A DNA clamp, also known as a sliding clamp, is a protein fold that serves as a processivity-promoting factor in DNA replication. As a critical component of the DNA polymerase III holoenzyme, the clamp protein binds DNA polymerase and prevents this enzyme from dissociating from the template DNA strand. The clamp-polymerase protein–protein interactions are stronger and more specific than the direct interactions between the polymerase and the template DNA strand; because one of the rate-limiting steps in the DNA synthesis reaction is the association of the polymerase with the DNA template, the presence of the sliding clamp dramatically increases the number of nucleotides that the polymerase can add to the growing strand per association event. The presence of the DNA clamp can increase the rate of DNA synthesis up to 1,000-fold compared with a nonprocessive polymerase.[2]
    what is antibody to nuclear antigen
    http://en.wikipedia.org/wiki/Anti-nuclear_antibody
    Quote Antinuclear antibodies (ANAs, also known as antinuclear factor or ANF)[1] are autoantibodies that bind to contents of the cell nucleus. In normal individuals, the immune system produces antibodies to foreign proteins (antigens) but not to human proteins (autoantigens). In some individuals, antibodies to human antigens are produced.[2]




    maternal antibodies and autism

    http://www.medscape.com/viewarticle/807760

    Maternal Antibodies May Trigger up to 25% of Autism Cases

    Megan Brooks
    July 12, 2013

    Quote Maternal antibodies that interfere with fetal brain proteins during pregnancy may be responsible for roughly one quarter of cases of autism spectrum disorder (ASD), a new study suggests.

    Lead researcher Judy Van de Water, PhD, and colleagues have coined the term "maternal autoantibody–related," or MAR, autism for these cases.
    maternal antibodies and autism

    http://cat.inist.fr/?aModele=afficheN&cpsidt=14998996
    Mechanisms by which maternal antibodies influence infant vaccine responses: review of hypotheses and definition of main determinants

    Quote Résumé / Abstract
    Several mechanisms have been suggested as mediating the inhibitory influence of maternal antibodies (MatAb) on infant responses. This inhibition is B cell determinant-specific, depends on the ratio between MatAb titers at the time of immunization and the dose of vaccine antigen, and leaves infant T cell responses largely unaffected. Neutralization of vaccine replication or FcγRIIB-mediated inhibitory signalling to infant B cells would not account for these characteristics. In contrast, determinant-specific masking of B cell epitopes and APC uptake of MatAb:vaccine antigen immune complexes, followed by antigen processing and presentation, explain the pattern of pre-clinical and clinical responses to infant vaccines. This allows the definition of the main determinants of the influence of MatAb on infant immunity.
    passive immunity

    http://en.wikipedia.org/wiki/Passive_immunity
    Quote Maternal passive immunity is a type of naturally acquired passive immunity, and refers to antibody-mediated immunity conveyed to a fetus by its mother during pregnancy. Maternal antibodies (MatAb) are passed through the placenta to the fetus by an FcRn receptor on placental cells. This occurs around the third month of gestation.[2] Immunoglobulin G is the only antibody isotype that can pass through the placenta.[2] Immunization is often required shortly following birth to prevent diseases such as tuberculosis, hepatitis B, polio, and pertussis, however, maternal antibodies can inhibit the induction of protective vaccine responses throughout the first year of life. This effect is usually overcome by secondary responses to booster immunization.[3]

    Passive immunity is also provided through the transfer of IgA antibodies found in breast milk that are transferred to the gut of the infant, protecting against bacterial infections, until the newborn can synthesize its own antibodies.[4]

    Artificially acquired passive immunity is a short-term immunization achieved by the transfer of antibodies, which can be administered in several forms; as human or animal blood plasma or serum, as pooled human immunoglobulin for intravenous (IVIG) or intramuscular (IG) use, as high-titer human IVIG or IG from immunized donors or from donors recovering from the disease, and as monoclonal antibodies (MAb). Passive transfer is used prophylactically in the case of immunodeficiency diseases, such as hypogammaglobulinemia.[5] It is also used in the treatment of several types of acute infection, and to treat poisoning.[1] Immunity derived from passive immunization lasts for only a short period of time, and there is also a potential risk for hypersensitivity reactions, and serum sickness, especially from gamma globulin of non-human origin.[4] Passive immunity provides immediate protection, but the body does not develop memory, therefore the patient is at risk of being infected by the same pathogen later.[4]


    The one exception to passive humoral immunity is the passive transfer of cell-mediated immunity, also called adoptive immunization which involves the transfer of mature circulating lymphocytes. It is rarely used in humans, and requires histocompatible (matched) donors, which are often difficult to find, and carries severe risks of graft-versus-host disease.[1] This technique has been used in humans to treat certain diseases including some types of cancer and immunodeficiency. However, this specialized form of passive immunity is most often used in a laboratory setting in the field of immunology, to transfer immunity between "congenic", or deliberately inbred mouse strains which are histocompatible.
    vaccines make you likelier to catch diseases:

    http://jid.oxfordjournals.org/conten...is.jit143.long

    Waning of Maternal Antibodies Against Measles, Mumps, Rubella, and Varicella in Communities With Contrasting Vaccination Coverage

    Quote Conclusions. Children of mothers vaccinated against measles and, possibly, rubella have lower concentrations of maternal antibodies and lose protection by maternal antibodies at an earlier age than children of mothers in communities that oppose vaccination. This increases the risk of disease transmission in highly vaccinated populations.
    so they don't even work. might as well not buy them.

    vaccines might damage human cells:

    http://www.ncbi.nlm.nih.gov/pubmed/12612250

    Pediatrics. 2003 Mar;111(3):653-9.
    Addressing parents' concerns: do vaccines cause allergic or autoimmune diseases?
    Offit PA1, Hackett CJ.
    Author information
    Abstract

    Quote Anecdotal case reports and uncontrolled observational studies in the medical literature claim that vaccines cause chronic diseases such as asthma, multiple sclerosis, chronic arthritis, and diabetes. Several biological mechanisms have been proposed to explain how vaccines might cause allergic or autoimmune diseases. For example, allergic diseases might be caused by prevention of early childhood infections (the "hygiene hypothesis"), causing a prolongation of immunoglobulin E-promoting T-helper cell type 2-type responses. However, vaccines do not prevent most common childhood infections, and large well-controlled epidemiologic studies do not support the hypothesis that vaccines cause allergies. Autoimmune diseases might occur after immunization because proteins on microbial pathogens are similar to human proteins ("molecular mimicry") and could induce immune responses that damage human cells. However, wild-type viruses and bacteria are much better adapted to growth in humans than vaccines and much more likely to stimulate potentially damaging self-reactive lymphocytes. Consistent with critical differences between natural infection and immunization, well-controlled epidemiologic studies do not support the hypothesis that vaccines cause autoimmunity. Flaws in proposed biological mechanisms that explain how vaccines might cause chronic diseases are consistent with the findings of many well-controlled large epidemiologic studies that fail to show a causal relationship.

    PMID:
    12612250
    [PubMed - indexed for MEDLINE]





    this is what you need to remember from this post:

    Quote because proteins on microbial pathogens are similar to human proteins ("molecular mimicry") and could induce immune responses that damage human cells

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    Plenty of info, but I guess my only issue is that the majority of it is anecdotal, or non controlled observational studies that can be heavily influenced by bias. There's enough there to make me think that vaccines do some really bad stuff to the minority of children exposed, but if that minority is really small, even 1 in 1000, don't the consequences of not having people vaccinated far out weigh the minority of people children effected?
    Not enough time and money is put towards making vaccines safer. I suppose that would be an admission of guilt so that's not going to happen.

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    Straight from the horse's mouth: Vaccines can't prevent measles outbreaks

    Lawrence Solomon
    Financial Post
    Thu, 01 May 2014 00:50 CDT

    Measles in highly immunized societies occurs primarily among those previously immunized.

    Because different people have different genetic makeups, the vaccine is simply a dud in many, failing to provide the protection they think they’ve acquired.

    The recent outbreaks of measles in Canada and the United States came as a shock to many public health experts but they wouldn't have to Dr. Gregory Poland, one of the world's most admired, most advanced thinkers in the field of vaccinology.

    The measles vaccine has failed, he explained two years ago in a prescient paper, "The re-emergence of measles in developed countries." In that paper, he warned that due to factors that most haven't noticed, measles has come back to be a serious public health threat. Thankfully, in that paper and elsewhere he also spelled out in no-nonsense fashion what now needs to be done.

    Dr. Poland is no vaccine denier. Not only is he among the harshest and most outspoken critics of the "irrationality of the antivaccinationists," he is also one of the strongest proponents for vaccines and the good that they can do. As Professor of Medicine and founder and leader of Mayo Clinic's Vaccine Research Group, one of the world's largest vaccine research organizations; as editor-in-chief of the peer-reviewed scientific journal, Vaccine; as recipient of numerous awards; as chair of vaccine data monitoring committees for pharmaceutical giant Merck; as patent holder in various vaccines processes; as someone who enjoys special employee status with the Centers for Disease Control and the U.S. Department of Defense and as someone who has sat on every federal committee that has dealt with vaccines, no one can accuse him of seeing vaccines from a narrow perspective.

    And he sees the need for a major rethink, after concluding that the current measles vaccine is unlikely to ever live up to the job expected of it: "outbreaks are occurring even in highly developed countries where vaccine access, public health infrastructure, and health literacy are not significant issues. This is unexpected and a worrisome harbinger - measles outbreaks are occurring where they are least expected," he wrote in his 2012 paper, listing the "surprising numbers of cases occurring in persons who previously received one or even two documented doses of measles-containing vaccine." During the 1989-1991 U.S. outbreaks, 20% to 40% of those affected had received one to two doses. In a 2011 outbreak in Canada, "over 50% of the 98 individuals had received two doses of measles vaccine."

    Dr. Poland noted 15 U.S. outbreaks between 2005 and 2011 and 33 in Europe in 2011 alone, involving more than 30,000 known cases. Meanwhile, the "UK has declared measles once again endemic.... such outbreaks result from both failure to vaccinate, and vaccine failure."

    People's failure to get vaccinated is deplorable, Dr. Poland often stresses. But the more fundamental problem stems from the vaccine being less effective in real life than predicted, with a too-high failure rate - between 2% and 10% don't develop expected antibodies after receiving the recommended two shots. Because different people have different genetic makeups, the vaccine is simply a dud in many, failing to provide the protection they think they've acquired.

    To make matters worse, even when the vaccine takes, the protection quickly wanes, making it unrealistic to achieve the 95%-plus level of immunity in the general population thought necessary to protect public health. For example, 9% of children having two doses of the vaccine, as public health authorities now recommend, will have lost their immunity after just seven and a half years. As more time passes, more lose their immunity. "This leads to a paradoxical situation whereby measles in highly immunized societies occurs primarily among those previously immunized," Dr. Poland stated.

    The measles vaccine's inadequacy doesn't end there, however. It "cannot be administered to those who are immunocompromised, who have allergies to vaccine components, or who are pregnant [among other limitations, leaving] a large enough segment of the population susceptible and unprotected from measles such that cases will continue to occur."

    The answer, according to Dr. Poland, lies in our genes. Because of their genetic predisposition, some people will not respond to the current measles vaccine, even with additional boosters. By the same token, the genetic predisposition of others makes them susceptible to harm from the measles vaccine, leading to public wariness, including among the well educated. What is needed, suggests Dr. Poland, is for the public health establishment to accept that the current measles vaccine has so many drawbacks as to make it unworkable, and get on with the job of developing next-generation vaccines.

    This next generation vaccine technology, which his Mayo Clinic group is helping pioneer, marries vaccinology with genomics to create personalized, rather than one-size-fits-all, vaccines. Through this new medical discipline of "vaccinomics," a term he dubbed, medical science will not only have the wherewithal to finally achieve the decades-long dream of eradicating measles and other diseases, he believes, but will also do so at lower cost while addressing the concerns of the educated public.

    As I will discuss in part two of this series next week, vaccinomics is no pie-in-the-sky fantasy but possibly the next big coming thing, well worth pursuing, and well worth the investment in its development that will be required.
    Quote SOTT.net Comment: Take a look at just ONE of Poland's disclosures:
    Dr. Gregory Poland wishes to disclose receiving honoraria from Merck for serving as Chair - eDMC and receiving honoraria from Avianax, Dynavax, Liquidia Technologies, Inc., Novartis Vaccines and Diagnostics, PaxVax Inc., and Theraclone Sciences for consulting services.
    Obviously he is in deep with Big Pharma and they are having a lot of trouble keeping up the vaccine farse [sic]. See also:

    -Measles: A rash of misinformation
    -Vaccines Have Serious Side Effects - The Institute of Medicine Says So!
    -Courts quietly confirm MMR Vaccine causes Autism
    -Herd immunity: Myth or reality?
    -FDA document reports autism link after tetanus, pertussis & diptheria vaccine
    --------------------------------------------------------------------------------

    Quote Because different people have different genetic makeups, the vaccine is simply a dud in many, failing to provide the protection they think they’ve acquired.
    ... thare ya gau!

    ... blame it on genetics!

    Since they have no clue if it's genetics or not, their "Because" is only an authoritative arbitrary that may have nothing to do with the price of fish but, more likely, the latter may be related to "Follow the $$" into Fat Pharma.

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    Default Re: Autism

    Quote Posted by Napping (here)
    Plenty of info, but I guess my only issue is that the majority of it is anecdotal, or non controlled observational studies that can be heavily influenced by bias. There's enough there to make me think that vaccines do some really bad stuff to the minority of children exposed, but if that minority is really small, even 1 in 1000, don't the consequences of not having people vaccinated far out weigh the minority of people children effected?
    Not enough time and money is put towards making vaccines safer. I suppose that would be an admission of guilt so that's not going to happen.
    If you
    want more
    info maybe
    help me
    find it.

    ....

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    Default Re: Autism

    Quote Posted by Napping (here)
    Plenty of info, but I guess my only issue is that the majority of it is anecdotal, or non controlled observational studies that can be heavily influenced by bias. There's enough there to make me think that vaccines do some really bad stuff to the minority of children exposed, but if that minority is really small, even 1 in 1000, don't the consequences of not having people vaccinated far out weigh the minority of people children effected?
    Not enough time and money is put towards making vaccines safer. I suppose that would be an admission of guilt so that's not going to happen.
    1 in 1000 does not reflect the current autism rate.
    what on earth is this crap lol


    and how did i miss that part.
    you're trying to pull the wool over my eyes or someone has done so to you

    autism rate in the USA is like 1 in 100.

    Which means, if it's vaccine related, gosh -- at least 1 in 100 are affected.

    in some towns/states, it's more like 1 in 50.

    if you were a school teacher, and 1 in 50 students had a disability so severe they couldn't even wipe their butts or work at Burger King,
    wouldn't you want to find out what was happening, even if it meant accepting some "anecdotal" (PC buzzword) or "observational" information as a starting point?




    i am SO TIRED of people without kids, people without autistic kids, and people who have never even seen a Measles Mumps or even Rubella case in their whole lives,
    telling ME, who has a disabled/retarded child, that the group I belong to (parents with damaged kids) is WRONG.



    i am deviating from the research and articles here to engage in petty squabbling, but 1 in 1000??


    gifted and talented kids have 10-30 percent more allergies.
    meaning gifted children, noble children, children of high intelligence, MORE LIKELY to be damaged by vaccines.



    that's Genocide.
    and yes I oppose it.

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    Tesla and amza, I sincerely appreciate your efforts, but you've basically come up with all I have in my limited searching which is primarily opinion pieces and low level observational studies and anecdotal evidence.

    Interesting to note that the mmr is potentially not as full proof as one would like, but it's not overly surprising. The potential of any of these diseases at pandemic levels again is too horrific to risk doing nothing at all imo.

    For the record Tesla, I'm not suggesting that autism prevalence is 1 in 1000, a quick search can substantiate that.....I threw that speculative stat out there as a random suggestion of a rate of autism caused by vaccines. That's very different to the overall prevalence of autism. If it was something like 1 in 1000 and it prevented pandemics....I'll have to say i will still take the risk.

    What needs to happen though is more research on identifying high risk outliers and safer vaccines.

    Personally, I can't see it happening, so at this stage for the sake of "the greater good" I'm leaning towards taking the risk.

    Can I also say that I'm truely sorry you've had to go through what you have with your own child and I admire your passion and commitment for answers.
    Last edited by Napping; 6th May 2014 at 12:37.

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    Default Re: Autism

    Quote Posted by Napping (here)
    Tesla and amza, I sincerely appreciate your efforts, but you've basically come up with all I have in my limited searching which is primarily opinion pieces and low level observational studies and anecdotal evidence.

    Interesting to note that the mmr is potentially not as full proof as one would like, but it's not overly surprising. The potential of any of these diseases at pandemic levels again is too horrific to risk doing nothing at all imo.

    For the record Tesla, I'm not suggesting that autism prevalence is 1 in 1000, a quick search can substantiate that.....I threw that speculative stat out there as a random suggestion of a rate of autism caused by vaccines. That's very different to the overall prevalence of autism. If it was something like 1 in 1000 and it prevented pandemics....I'll have to say i will still take the risk.

    What needs to happen though is more research on identifying high risk outliers and safer vaccines.

    Personally, I can't see it happening, so at this stage for the sake of "the greater good" I'm leaning towards taking the risk.

    Can I also say that I'm truely sorry you've had to go through what you have with your own child and I admire your passion and commitment for answers.
    Thanks, I guess

    Feel free to post some research data along with your opinion.
    I see lots of questions and absolutism in your statements but no fact.

    Rachel



    p.s. who is going to fund the objective studies? the people who damage our kids? LOL the government?

    it's easy for people like you to feel like they are "winning" the argument when a crowd of other crooks did it for ya



    If you really care about my kid you will care about the truth more than political correctness.


    When America found out about Nazi concentration camps, was it through a German scientific research paper?

    GET IT?

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    I'm not the type of person who would gain any enjoyment from "winning" an argument against a fellow parent who has suffered the way you have with your child, but you don't know me and you're probably used to having to defend your stance against people who argue for the sake of arguing with no sense of empathy..

    I'm genuinely concerned about vaccinating my child, but simply can't find anything comclusive re causation between vaccines and adverse effects on a large scale. I've got little doubt it does occur to vulnerable individuals which worries me a lot.

    I agree that high level research won't be funded for this issue because of what it may find and that is horrible.

    Your last point suggests a new trajectory regarding our covnersation thus far all together and that is that this is being purposefully done by nefarious individuals. I don't believe that is the case. I believe vaccines were introduced with good intensiond, but perhaps I'm naive.

    You're right I should hold up my end of the argument with all the evidence that refutes what you're implying, but right now I'm under the pump, which is why I asked you guys in the first place.

    Thanks for the chat.

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