The Autism-Vaccine controversy is not going to die off any times soon. The pro-vaccine side says there are hundreds of studies debunking any link. What I find most interesting, is that all those studies are in response to one little observation with 12 children back in the late 90’s.
The controversy has been heightened in recent days due to the scheduled showing of the film Vaxxed: From Cover Up to Catastrophe.
The part that interests me is that whenever the link gets mentioned in major news media outlets, the name Dr. Andrew Wakefield is included. It’s not just his name, it’s the fact that his study of 12 children gets blamed on Dr. Wakefield starting the autism-vaccine link. Not only is he blamed, there’s an immediate statement that his study has been tarred and feathered and anyone thinking of using it as credible evidence is just as much of a quack as Wakefield.
Let’s take a look at Dr. Wakefield’s study that turned the world up side down. The study was only 12 kids. The kids were sent to Dr. Wakefield, a GI specialist, not to diagnose an MMR link with the autism, but to assess the child’s bowels. Here is a paraphrased version of it.
We investigated a consecutive series of children with chronic enterocolitis and regressive developmental disorder.
12 children (mean age 6 years [range 3–10], 11 boys) were referred to a paediatric gastroenterology unit with a history of normal development followed by loss of acquired skills, including language, together with diarrhoea and abdominal pain. Children underwent gastroenterological, neurological, and developmental assessment and review of developmental records. Ileocolonoscopy and biopsy sampling, magnetic-resonance imaging (MRI), electroencephalography (EEG), and lumbar puncture were done under sedation. Barium follow-through radiography was done where possible. Biochemical, haematological, and immunological profiles were examined.
None had neurological abnormalities on clinical examination; MRI scans, EEGs, and cerebrospinal-fluid profiles were normal; and fragile X was negative. Prospective developmental records showed satisfactory achievement of early milestones in all children. The only girl (child number eight) was noted to be a slow developer compared with her older sister. She was subsequently found to have coarctation of the aorta. After surgical repair of the aorta at the age of 14 months, she progressed rapidly, and learnt to talk. Speech was lost later. Child four was kept under review for the first year of life because of wide bridging of the nose. He was discharged from follow-up as developmentally normal at age 1 year. In eight children, the onset of behavioural problems had been linked, either by the parents or by the child’s physician, with measles, mumps, and rubella vaccination. Five had had an early adverse reaction to immunisation (rash, fever, delirium; and, in three cases, convulsions).
Asperger first recorded the link between coeliac disease and behavioural psychoses. (4) Walker-Smith and colleagues (5) detected low concentrations of alpha-1 antitrypsin in children with typical autism, and D’Eufemia and colleagues (6) identified abnormal intestinal permeability, a feature of small intestinal enteropathy, in 43% of a group of autistic children with no gastrointestinal symptoms, but not in matched controls. These studies, together with our own, including evidence of anaemia and IgA deficiency in some children, would support the hypothesis that the consequences of an inflamed or dysfunctional intestine may play a part in behavioural changes in some children.
We did not prove an association between measles, mumps, and rubella vaccine and the syndrome described. Virological studies are underway that may help to resolve this issue. If there is a causal link between measles, mumps, and rubella vaccine and this syndrome, a rising incidence might be anticipated after the introduction of this vaccine in the UK in 1988. Published evidence is inadequate to show whether there is a change in incidence (22) or a link with measles, mumps, and rubella vaccine. (23)
Urinary methylmalonic-acid concentrations were raised in most of the children, a finding indicative of a functional vitamin B12 deficiency. Although vitamin B12 concentrations were normal, serum B12 is not a good measure of functional B12 status. (25) Urinary methylmalonic-acid excretion is increased in disorders such as Crohn’s disease, in which cobalamin excreted in bile is not reabsorbed. A similar problem may have occurred in the children in our study. Vitamin B12 is essential for myelinogenesis in the developing central nervous system, a process that is not complete until around the age of 10 years. B12 deficiency may, therefore, be a contributory factor in the developmental regression. (26)
We have identified a chronic enterocolitis in children that may be related to neuropsychiatric dysfunction. In most cases, onset of symptoms was after measles, mumps, and rubella immunisation. Further investigations are needed to examine this syndrome and its possible relation to this vaccine.
The bold font is my emphasis.
And then the world lost it’s sh*t.





