Wednesday, 14 November 2012

Professor Simon Wessely’s award of the inaugural John Maddox Prize for his courage in the field of ME and Gulf War Syndrome

This is a new article by Professor Malcolm Hooper (with members of the ME community).  It is long, but I would recommend reading it – it is certainly an eye opener!  To read the article, please click here.

I am not going to reproduce the whole article here, but the following is a small section from it -
Expressing his opposition to Wessely’s model of ME/CFS, Dr Harvey Alter, Chief of Clinical Studies and distinguished investigator at the US National Institutes of Health (one of the world’s foremost medical research centres) said in 2010 at an FDA Blood Products Advisory Committee meeting: “I’m absolutely convinced that when you define this disease by proper criteria, this is a very serious and significant medical disease, and not a psychological disease. It has the characteristics of a viral disease”.

Moreover, Professor Luc Montagnier (who in 2008 won the Nobel prize for discovering the AIDS virus), Honorary Member of the European Society for ME, is on record thus: “Scientists have already uncovered a lot about ME, but this information does not reach professional healthcare personnel, and the disease is not taken seriously. It is about time this changes” (http://esme-eu.com/home/experts-launch-think-tank-for-mystery-disease-article37-6.html).

This is an important point: it is not that accurate information and knowledge are unavailable; it is that in the UK, the information and knowledge are being systematically blocked by the extremely efficient and effective networking of the Wessely School who ensure that the gap between bench and bed is filled with their own views about “CFS/ME”.

Additionally, Professor Ian Lipkin, Director, Centre for Infection and Immunity, Columbia University, said on the record that patients with ME have a particular pattern of immunoreactivity, indicating a persistent disease process: “Back in the mid to late 1990s…I looked at these Chronic Fatigue Syndrome patients, many of them coming out of a clinic that was run in the Karolinska, which at that point was one of the best clinics for CFS in the world…..I said these patients are clearly sick in some way. They have some kind of immunological activation…I am convinced, after working in this field for a very long time, that this is a bona fide syndrome”. ME/CFS was described as “this crippling disease” (transcript of podcast with Professors Vincent Racaniello and Ian Lipkin, 18th September 2012, This Week in Virology).

Please see also: 

Ruffled feathers? (18th November 2012)
Margaret Williams
http://www.meactionuk.org.uk/Ruffled-feathers.htm


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