Guest guest Posted March 31, 2008 Report Share Posted March 31, 2008 MMR & Bowel Inflammation & Autism This is a very complicated subject to cover as there has been so much since the early 1990's when the ideas started to develop................. I will try to put this in a linear way. A. The first inkling that MMR may be associated with inflammatory bowel disease - Crohns, etc. B. That many autistic children now have inflammatory bowel disease C. MMR may be implicated as a cause of autism in children also with inflammatory bowel disease Wakefield has been in the crosshairs here, especially since 1998, and it has gotten very complicated. Wakefield is a well respected gastroenterologist who has become the victim of harrassment and persecutation. When all this started he was at The Royal Free Hospital in the UK There is research done by him and his colleagues showing possible links, but nothing definitive. And there have been all sorts coming out and using epidemiological studies (using numbers and population) to 'prove' that MMR is not related to inflammatory bowel disease and autism. And then there have been the rebuttals showing that those epidemiological studies prove nothing - you can prove anything you want with those type of studies. What is needed is indepth examination of children and adults with inflammatory bowel disease (and/or autism) - physical examination, laboratory examination, true research, looking for honest answers. There have been many drug company funded studies showing no link. I will try to summarize this all here, but it is a monumental task. Some of the progression of this is shown on my mmr webpages http://www.nccn.net/~wwithin/mmr.htm starting with further down the page and working up (earliest to latest) There has been much back and forth and it continues today. I will share research papers, Dr. Wakefield's website with info and all info up until to day. There will be a lot of information There are a lot of questions, as you know, surrounding autism and its cause(s). Mercury is one idea, drugs during pregnancy and labor are others, amalgams in teeth, MMR vaccine and other environmental toxins, as well as susceptibility of certain children in certain families with auto-immune history. Here I will present the possible connections of MMR to autism and why. Is the problem with MMR and not measles vaccine itself alone - is it the combination of 3 live vaccines or something else? Is it what tips the scales after an infant has received mercury-laden vaccines? We just don't know. Sheri Summary of some of the issues with MMR since the early days through the MMR/Inflammatory Bowel/Austism issue http://www.909shot.com/Diseases/mmr.htm excerpt MMR VACCINE The most frequent reactions reported to occur following MMR vaccine include brief burning and stinging at the injection site; fatigue, sore throat, cough, runny nose, headache, dizziness, fever, rash, nausea, vomiting or diarrhea, and sore lymph glands. Other reported reactions include anaphylaxis, convulsions, encephalopathy, otitis media, conjunctivitis, nerve deafness, thrombocytopenia purpura, optic neuritis, retinitis, arthritis, Guillain-Barre syndrome, and subacute sclerosing panencephalitis. In 1981, the British National Childhood Encephalopathy Study concluded that there was a statistically significant association between measles vaccination and the onset of a serious neurological disorder within 14 days of receiving measles vaccine. The risk for previously normal children was estimated to be 1 in 87,000 measles vaccinations. In 1991, the Institute of Medicine concluded that there is compelling scientific evidence that the rubella vaccine portion of the MMR shot can cause acute arthritis, with the highest incidence occurring in adult women who receive rubella vaccine (up to 15 percent) and that some individuals go on to develop chronic arthritis. Because either no studies or too few scientific studies have ever been conducted to investigate rubella vaccine reactions, a determination could not be made as to whether rubella vaccine causes other serious health problems which have been reported following rubella vaccination including thrombocytopenia purpura, radiculoneuritis (spinal nerve pain) or other neuropathies such as carpal tunnel syndrome. In 1994, the Institute of Medicine concluded that there is compelling scientific evidence that the measles vaccine can cause anaphylaxis that can end in death and that the MMR vaccine can cause thrombocytopenia (a decrease in the number of platelets, the cells involved in blood clotting) that can end in death. The incidence of thrombocytopenia was estimated to be 1 case per 30,000 to 40,000 vaccinated children. The IOM also concluded that the measles vaccine portion of the MMR vaccine can cause vaccine-strain measles virus infection that can end in death. Because either no studies or too few studies have ever been conducted to investigate MMR vaccine reactions, a determination could not be made as to whether measles or mumps vaccine causes encephalitis or encephalopathy (brain disease); sensorineural deafness, or insulin dependent diabetes mellitus; whether the mumps vaccine causes aseptic meningitis, orchitis (inflammation of the testis) or sterility; or whether the measles vaccine causes subacute sclerosing panencephalitis, residual seizure disorders, optic neuritis, transverse myelitis, or Guillain-Barre syndrome. In 1995, a British study concluded that adults who were vaccinated with measles vaccine as children were at much higher risk of developing inflammatory bowel disease such as Crohn's disease and ulcerative colitis, as adults. Several researchers are looking into the possible link between inflammatory bowel disease and measles vaccine as well as other vaccines. The vaccine manufacturer's product insert for MMR vaccine states " It is also not known whether [the vaccine] can cause fetal harm when administered to pregnant women or can affect reproduction capacity " and " it is not known whether measles or mumps vaccine virus is secreted in human milk. Recent studies have shown that lactating postpartum women immunized with live attenuated rubella vaccine may secrete the virus in breast milk and transmit it to breast-fed infants. " An MMR vaccine manufacturer states that in a study of 279 children 11 months to 7 years of age, MMR vaccine was shown to be 95 to 99 percent effective. Protection is estimated to persist for up to 11 years. In a measles outbreak in the U.S. in the late 1980's and early 1990's, it was found that there were a significant number of vaccine failures in older children, teenagers and adults, when the disease can be more severe. The government proceeded to recommend that a second MMR shot be given to boost immunity either before entrance to kindergarten or before entrance to junior high school. In the national outbreak of measles during the late 1980's and early 1990's, it also became apparent that children who had been vaccinated before 15 months of age were also at risk for vaccine failure, especially if their mothers had recovered naturally from measles disease as children. An MMR vaccine manufacturer states " Infants who are less than 15 months of age may fail to respond to the measles component of the vaccine due to presence in the circulation of residual measles antibody of maternal origin, the younger the infant, the lower the likelihood of seroconversion. " The manufacturer goes on to advise that infants vaccinated at less than 12 months of age will have to be revaccinated after 15 months of age even though " there is some evidence to suggest that infants immunized at less than one year of age may not develop sustained antibody levels when later immunized. " The measles outbreaks in the late 1980's and early 1990's in the U.S. also demonstrated that babies, whose young vaccinated mothers had never naturally recovered from measles infection as children, were vulnerable to measles infection from birth. The young vaccinated mothers did not have natural maternal antibodies to transfer to their newborns to protect them from measles in the first year of life. In the 1989-91 measles outbreak in the U.S., the largest increase in measles cases was in infants under one year old. In 1995, there were 309 cases of measles reported in the U.S. Out of 219 cases where vaccination status was known, 123 (56 percent) had been vaccinated with at least one dose. Of 285 measles cases where age was known, 38 percent were under 5 years old and 39% were more than 20 years old. In the mid-1990's, reports of an association between autism and vaccination (specifically suggesting a possible link with MMR vaccine) were published. Although the U.S. Institute of Medicine (IOM) acknowledged the hypothesis was biologically plausible, IOM concluded there was not enough evidence establishing a causal relationship. Nevertheless, in light of persistent reports by parents that their children are regressing into autism after MMR vaccination, there is an on-going scientific investigation by independent scientific researchers, such as British gastroenterologist Wakefield, M.D., into clinical and laboratory evidence that MMR vaccination may cause autism in biologically vulnerable children. ********** http://www.909shot.com/Diseases/autismsp.htm excerpt Measles, MMR, The Gut and Autism Considering the mounting scientific evidence that viral and bacterial infections and the vaccines used to prevent them are capable of producing a wide range of immune and neurological dysfunction, it is somewhat strange from a scientific (although not a political) standpoint that a young British gastroenterologist would have been subjected to personal attacks by the medical community when he and 13 colleagues at Royal Free Hospital in London presented evidence in 1998 (The Lancet, Feb. 27, http://www.thelancet.com ) that measles infection and measles vaccine may be linked to the development of inflammatory bowel disease and autism in previously healthy, normally developing children. Wakefield, M.D. and his team had inadvertently stumbled upon the connection while studying Crohn's disease and other inflammatory bowel disease (IBD) in children. The mother of one of Wakefield's young patients, Rosemary Kessick, urged him to look for the biological mechanism for simultaneous development of IBD and autistic behavior in previously normal children. The Wakefield report reviewed the medical factors common to eight out of 12 previously normal children who simultaneously developed severe intestinal disorders and autistic behaviors. Previously, five of those eight children had reacted adversely to vaccinations. All reported onset of symptoms of IBD and autism after MMR vaccination. In their discussion of the interaction between the immune, nervous and gastrointestinal systems of the body, Wakefield and his associates remarked that Asperger in 1961 had observed that there was a high rate of gastrointestinal (celiac) disease in those suffering with autism. (In 1944, Asperger had identified a subgroup of high functioning " borderline " autistics.) The authors hypothesized that persistent viral infection, either from natural disease or live virus vaccines, can cause chronic inflammation of the bowel and damage to the central nervous system development in some children. They pointed to the " opioid excess " theory of autism, first suggested by Panksepp in 1979 and then by Shattock (1991) and Reichelt (1993) that autistic disorders result from the incomplete breakdown and excessive absorption of gut-derived peptides from foods, including barley, rye, oats and casein from milk and dairy products leading to disruption of normal brain functioning and development. As these gut-derived peptides get into the blood and cross the blood brain barrier, where they are not supposed to be, they negatively affect the ability of the body to maintain appropriate endorphin, serotonin and dopamine levels in the brain. Science Meets Politics The study authors emphasized that they had not proved a cause and effect relationship and simply called for more studies to explore the hypothesis. Their report was immediately met with charges by CDC officials that " vaccine safety concerns such as that reported by Wakefield and colleagues may snowball " when the public and the media " confuse association with causality and shun immunization. " A Reuters newswire story quoted Neal Halsey, M.D., of 's Hopkins and chair of the American Academy of Pediatrics Committee on Infectious Diseases, as saying it was " highly inappropriate " for Wakefield and his colleagues to discuss a possible connection between the children's health problems and measles or MMR vaccines. British government health officials were also displeased and, in 1999, published a small retrospective cases series analysis ( et al, The Lancet) that they said proved MMR vaccine is not associated with regressive autism but British and U.S. parent groups and independent physicians have criticized the study as methodologically flawed. (http://www.909shot/autismto.htm) Digging In and Speaking Out However, Wakefield and his associates have pressed on, continuing research into several hundred cases of normal children who suddenly develop gastrointestinal disease and developmental regression. At the First International Public Conference on Vaccination sponsored by the National Vaccine Information Center in September, 1997, Wakefield spoke about his concerns that most of the original studies in the 1960's and 1970's evaluating the safety of live measles and MMR vaccines only included a three week follow-up. And at the Second International Autism Conference sponsored by Allergy in Autism (AIA) in London in March, 1999, Wakefield commented that children with a pre-existing immune abnormality may be predisposed to sequestering the measles virus in the gut and the MMR vaccine prompts them to develop autoimmunity leading to immune mediated CNS damage. One of the most compelling regressive autism cases he had recently reviewed in his practice was reminiscent of the days when autism was thought to be " early-onset " schizophrenia: it was that of a normal, healthy 14 year old boy who got an MMR shot and, within one week, developed bizarre behavior that was diagnosed as schizophrenia. Quote Link to comment Share on other sites More sharing options...
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