Dr. Andy Wakefield
[Dr
Wakefield was caught up in the vaccine damage fallout from MMR when parents
brought him, and his team, their vaccine bowel damaged children. Supported by
his hospital, he then said in a public meeting that single vaccines would be a
good idea over MMR. When the shit hit the fan he was thrown to the wolves
(by the likes of
Professor Zuckerman), and is a perfect
example of what happens when you criticise vaccines. They are now trying to
break him (take away his licence and stop him being an expert witness for the
vaccine damaged) with a medical kangaroo court. You can see why medical industry
people keep their heads below the parapet, unless they fancy a new job in
Australia or the USA.
He was the perfect man in the right place at the right time
as regards truth and the welfare of children. The vaccine industry
couldn't care less about children as their actions demonstrate here, and
historically (eg suppressing Vitamin C cure for infections:
see). Read (mostly) Martin Walker's GMC reporting
here, especially this recent
Interview
of Martin Walker. You won't see a better example of
medical psychopathy in action. Historically it reminds one of how they
tried to break Dr Hadwen with a
manslaughter charge, and you can see the long history of persecuted (mostly
cancer) doctors here. A recent escapee from GMC vaccine tyranny was Dr Jayne Donegan.
Notice also how the media,
especially the BBC, just spews anti-Wakefield
propaganda.]
Articles about Dr
Wakefield Letters Interviews Media stories Dr Wakefield articles/papers |
Web: http://www.thoughtfulhouse.org/
See: Autism & vaccines Smearing of Dr Wakefield Whistleblowers MMR vaccines
See: Dr Arthur Krigsman Bryan Jepson, MD
[2009 Aug] How Thoughtful House and Drs. Wakefield, Krigsman and Jepson Helped My Son
[2009 June] Dr. Andrew Wakefield on The Poisoning of Young Minds
Petition for Wakefield - From Carmel Wakefield (wife)
[2009 Feb] Dr Andrew Wakefield Demolishes Ignorant US Vaccine Lobby
Lancet - Statements by all on Dr Wakefield's study
"Prof Denis McDevitt,.....attended meetings that discussed warnings from other countries about an early form of the triple jab, using the Urabe strain of mumps virus, which caused encephalitis and meningitis. Despite warnings and the fact that this vaccine had already been withdrawn in Canada, the Urabe-containing jab was introduced in the UK in 1988. Some of the 12 children whose medical history featured in the controversial 1998 Lancet paper, drawn up by Dr Wakefield and his colleagues and which suggested a possible link between the jab and bowel disease and regressive autism, had received the Urabe-strain vaccine - as indeed had some of those children in the high court litigation with manufacturers." [June 2007 Private Eye] MMR Conflict of Interest Zone
[2008 Oct] Dr Andrew Wakefield On MMR Vaccine In Sunday Express
[June 2007 Private Eye] MMR Conflict of
Interest Zone
[May 2007] MMR judge faces probe over
brother's link to vaccine firm
[May 2007] GMC Challenged On MMR Inquiry Chief's
Vaccine Firm Links
[May 2007]
MMR JUDGE FAILED TO DISCLOSE HE WAS BROTHER
OF Glaxo SmithKline DIRECTOR AND LANCET BOSS
Articles about Dr
Wakefield
[Media Oct 2006 Wakefield] VILIFED by the MMR
zealots
MMR - SCIENCE AND FICTION": the Richard Horton
story 25 September 2004 ------John Stone
[May 2007] GMC Challenged On MMR Inquiry Chief's Vaccine Firm Links
Letters & statements by
Dr Wakefield
[Dec 2006] Response by Dr Andy Wakefield
to enquiries about expert fees.
[Nov 2002] Letter to NEJM from Dr Andrew J Wakefield MB.,BS FRCS FRCPath
[Oct 2004] Press Release: Thoughtful House scientists make important breakthrough in autism
[Sept 2004]
Dr. Wakefield Responds To British Study Clearing MMR
Vaccines
MMR Studies that Count, Studies that Don't - F.E. Yazbak,
MD, FAAP
[April 6, 2000] Autism -
Present Challenges, Future Needs - Why the Increased Rates?
Testimony pdf
HTML
(text only)
Rebuttals
[Jan
2001 MMR] Rebuttal to Wakefield
Called 'Weak' with 'Distortions': Shattock
Interviews
CBS News – Research Links Kids Vaccines & Brain Damage Posted
on October 9, 2009 by childhealthsafety . A new scientific safety study by
British researcher Dr Laura Hewitson shows US children’s vaccines are linked to
brain damage. CBS interviews Dr Andrew Wakefield on this new study and also the
controversy over the MMR vaccine and autism.
The Cure Autism Conspiracy of Parents and the M.I.N.D. Institute (Wakefield & Rollens interview)
Media stories
[Media March 2002] Expert says MMR autism link will be
proved this year
[Media 3 Feb 2002] PANORAMA MMR Every Parent's
Choice
[Media Feb 2002] MMR: Dr Maverick sticks to his guns
[Media 2/12/2001] Anti-MMR doctor is forced out
[Media UK, Dec 2001] Scientists: MMR Vaccine Should Not Have Been
Licensed
[Media UK, Jan 2001] Study claims MMR vaccine trials were inadequate
[Media] 'Triple Jag Autism Could Be Next BSE'
170 Cases of Autism Linked to Vaccine in UK
So What's Not to Like About Andrew Wakefield?
http://www.autism-spectrum.com/vaccine.htm
Dr Wakefield articles/papers
[Nov 2005]
The Seat of the Soul; The Origins of the Autism Epidemic
by ANDREW WAKEFIELD, MB, BS, FRCS, FRCPath
Andrew J. Wakefielda, FRCS FRCPath; Carol Stottb,
PhD; and Kirsten Limbc, BSc
Gastrointestinal comorbidity, autistic regression and Measles-containing
vaccines: positive re-challenge and biological gradient
Article-in-press; Medical Veritas: The Journal of Medical Truth; Volume 3, Issue
1, April 2006.
Medical Veritas is the journal of Medical Veritas International (MVI);
www.MedicalVeritas.com.
[Jan 2001] Measles, Mumps, Rubella Vaccine: Through a Glass, Darkly.
[Oct 2004] Press Release: Thoughtful House scientists make important breakthrough in autism
Measles-containing vaccines and IBD-----Andrew Wakefield, 02 January 2002
Torrente
F, Ashwood P, Day R, Machado N, Furlano RI, Anthony A, Davies SE, Wakefield AJ, Thomson
MA, Walker-Smith JA, Murch SH.Small intestinal enteropathy with
epithelial IgG and complement deposition in children with regressive autism.Mol Psychiatry. 2002;7(4):375-82.PMID: 11986981 [PubMed - in process]
We have reported lymphocytic colitis in children with regressive autism, with epithelial
damage prominent. We now compare duodenal biopsies in 25 children with regressive autism
to 11 with coeliac disease, five with cerebral palsy and mental retardation and 18
histologically normal controls. Immunohistochemistry was performed for lymphocyte and
epithelial lineage and functional markers. We determined the density of intraepithelial
and lamina propria lymphocyte populations, and studied mucosal immunoglobulin and
complement C1q localisation. Standard histopathology showed increased enterocyte and
Paneth cell numbers in the autistic children. Immunohistochemistry demonstrated increased
lymphocyte infiltration in both epithelium and lamina propria with upregulated crypt cell
proliferation, compared to normal and cerebral palsy controls. Intraepithelial lymphocytes
and lamina propria plasma cells were lower than in coeliac disease, but lamina propria T
cell populations were higher and crypt proliferation similar. Most strikingly, IgG
deposition was seen on the basolateral epithelial surface in 23/25 autistic children,
co-localising with complement C1q. This was not seen in the other conditions. These
findings demonstrate a novel form of enteropathy in autistic children, in which increases
in mucosal lymphocyte density and crypt cell proliferation occur with epithelial IgG
deposition. The features are suggestive of an autoimmune lesion.PMID: 11986981 [PubMed -
in process]
Uhlmann V, Martin CM, Sheils O, Pilkington L, Silva I, Killalea A, Murch SB, Walker-Smith J, Thomson M, Wakefield AJ, O'Leary JJ. Potential viral pathogenic mechanism for new variant inflammatory bowel disease.Mol Pathol. 2002 Apr;55(2):84-90.PMID: 11950955 [PubMed - in process]
AIMS: A new form of inflammatory bowel disease (ileocolonic lymphonodular hyperplasia) has been described in a cohort of children with developmental disorder. This study investigates the presence of persistent measles virus in the intestinal tissue of these patients (new variant inflammatory bowel disease) and a series of controls by molecular analysis. METHODS: Formalin fixed, paraffin wax embedded and fresh frozen biopsies from the terminal ileum were examined from affected children and histological normal controls. The measles virus Fusion (F) and Haemagglutinin (H) genes were detected by TaqMan reverse transcription polymerase chain reaction (RT-PCR) and the Nucleocapsid (N) gene by RT in situ PCR. Localisation of the mRNA signal was performed using a specific follicular dendritic cell antibody. RESULTS: Seventy five of 91 patients with a histologically confirmed diagnosis of ileal lymphonodular hyperplasia and enterocolitis were positive for measles virus in their intestinal tissue compared with five of 70 control patients. Measles virus was identified within the follicular dendritic cells and some lymphocytes in foci of reactive follicular hyperplasia. The copy number of measles virus ranged from one to 300,00 copies/ng total RNA. CONCLUSIONS: The data confirm an association between the presence of measles virus and gut pathology in children with developmental disorder.
Wakefield AJ. MMR vaccination and autism. Lancet. 1999 Sep 11;354(9182):949-50. No abstract available.PMID: 10489978; UI: 99418510.
(Adverse Drug Reactions 2000,19(4) 1-19. Authors: Andrew J Wakefield FRCS, Scott M Montgomery PhD.)
A J Wakefield,
S H Murch, A Anthony, J Linnell, D M Casson, M Malik,
M Berelowitz, A P Dhillon, M A Thomson, P Harvey, A
Valentine, S E Davies, J A Walker-SmithVolume 351, Number 9103 28 February 1998
Ileal-lymphoid-nodular hyperplasia, non-specific colitis, and
pervasive developmental disorder in children
American Journal of Gastroenterology, September, 2000
Original Contribution
September 2000
Volume 95, Number 9
Pages 2285-2295
A. J. Wakefield, F.R.C.S.,a,b A. Anthony, M.Sc., Ph.D., M.B.B.S.,b S. H.
Murch, Ph.D., F.R.C.P., F.R.C.P.C.H.,b M. Thomson, MB.ChB., M.R.C.P.,
F.R.C.P.C.H.,c S. M. Montgomery, Ph.D.,c S. Davies, M.R.C.Path.,b J. J.
O'Leary, M.D., D.Phil., M.R.C.Path.,b M. Berelowitz, F.R.C.Psych.,e and J.
A. Walker-Smith, M.D., F.R.C.P., F.R.A.C.P., F.R.C.P.C.H.d
OBJECTIVE: Intestinal pathology, i.e., ileocolonic lymphoid nodular
hyperplasia (LNH) and mucosal inflammation, has been described in children
with developmental disorders. This study describes some of the endoscopic
and pathological characteristics in a group of children with developmental
disorders (affected children) that are associated with behavioral regression
and bowel symptoms, and compares them with pediatric controls.
METHODS: Ileocolonoscopy and biopsy were performed on 60 affected children
(median age 6 yr, range 3-16; 53 male). Developmental diagnoses were autism
(50 patients), Asperger's syndrome (five), disintegrative disorder (two),
attention deficit hyperactivity disorder (ADHD) (one), schizophrenia (one),
and dyslexia (one). Severity of ileal LNH was graded (0-3) in both affected
children and 37 developmentally normal controls (median age 11 yr, range
2-13 yr) who were investigated for possible inflammatory bowel disease
(IBD). Tissue sections were reviewed by three pathologists and scored on a
standard proforma. Data were compared with ileocolonic biopsies from 22
histologically normal children (controls) and 20 children with ulcerative
colitis (UC), scored in an identical manner. Gut pathogens were sought
routinely.
RESULTS: Ileal LNH was present in 54 of 58 (93%) affected children and in
five of 35 (14.3%) controls (p < 0.001). Colonic LNH was present in 18 of 60
(30%) affected children and in two of 37 (5.4%) controls (p < 0.01).
Histologically, reactive follicular hyperplasia was present in 46 of 52
(88.5%) ileal biopsies from affected children and in four of 14 (29%) with
UC, but not in non-IBD controls (p < 0.01). Active ileitis was present in
four of 51 (8%) affected children but not in controls. Chronic colitis was
identified in 53 of 60 (88%) affected children compared with one of 22
(4.5%) controls and in 20 of 20 (100%) with UC. Scores of frequency and
severity of inflammation were significantly greater in both affected
children and those with UC, compared with controls (p < 0.001).
CONCLUSIONS: A new variant of inflammatory bowel disease is present in this
group of children with developmental disorders.
Cite this article as: . Wakefield AJ, Anthony A, Murch SH, Thomson M,
Montgomery SM, Davies S, O'Leary JJ, Phil D, Berelowitz M and Walker-Smith
JA. Enterocolitis in Children With Developmental Disorders. Am J
Gastroenterol September;95:2285-2295.
aUniversity Departments of Medicine, bHistopathology, cPaediatric
Gastroenterology, and dPaediatric Psychiatry, Royal Free and eUniversity
College Medical School, Royal Free Campus, London, United Kingdom, and
University Department of Pathology, Coombe Women's Hospital and Trinity
College, Dublin, Eire