LEADING scientist Raymond Perrin believes he has proof that chronic fatigue syndrome - once dubbed yuppie flu - has a physical cause.
For years sufferers of CFS - which includes ME - have lived under the stigma of being diagnosed with a condition that many dismissed as being in the mind.
But Manchester osteopath Dr Perrin believes he has proved that the debilitating syndrome is the physical result of the way the body deals with toxins.
He believes a picture of varicose lymphatic vessels taken during a research project at Salford University shows for the first time the "backflow" of lymphatic drainage that he believes is the cause of toxin build-up.
And it is this accumulation of toxins in the central nervous system, which Dr Perrin believes is the cause of conditions such as chronic fatigue syndrome and ME.
Valves
Dr Perrin, who runs clinics in Prestwich, central Manchester and London, said: "Normally these vessels are the size of the thinnest pencil line and you can't usually see them without a magnifying glass, but the fact they are swollen like this is significant. There is a backflow against the valves.
"Very rarely can you see these, but with every person I have seen in the last 16 years with chronic fatigue syndrome you can feel them under the surface. It means this person has had ME for a number of years."
Until now experts have believed that valves in the lymphatic vessels only allowed the flow of fluids in one direction. But Dr Perrin says these varicose lymphatic vessels - which resemble varicose veins but are the same colour of the skin instead of a bluish colour - are the proof that the backflow exists, when vessels are damaged, allowing toxins to concentrate in the central nervous system.
He revealed the picture at a seminar at Salford University.
He hopes to publish it in a respected medical journal later in the year.
Margaret Cannon, who had to give up work because of the condition, said: "After about three months of Raymond's treatment my concentration was restored and the symptoms improved greatly."
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Caroline Ellis, Rochdale (03/08/2005 at 17:54)
Dragging up the phrase 'Yuppie Flu' in newspaper headlines continues to promote prejudice against ME sufferers. There are around 8,000 ME sufferers in Greater Manchester many of whom read the MEN.
Denise, Pa, United States (04/08/2005 at 04:34)
Ros Melrose, Market Harborough (04/08/2005 at 14:14)
Judith Meagher, Hampshire (04/08/2005 at 19:21)
I am in no doubt that there is a physical cause for this as I get 'aches' and 'pressure' build up in my neck and back which appears very 'nervy' and makes me feel irritable. It subsides after rest which would tie in with the swollen aspect of your findings.
I would be interested to see how you propose to treat this.
debbie price, newark, notts (04/08/2005 at 19:32)
M Lynch, Herts (04/08/2005 at 21:51)
It is frustating however, that after decades of research that ALREADY prove that ME is physical, that this should still even be a matter of debate.
The World Health Organisation has classified ME as a neurological disorder (code ICD-10 G93.3) since 1969!
A whole host of tests have already highlighted abnormalities in ME sufferers. I refer readers to the 'Canadian Criteria' which contains the most up to date information on ME/CFS diagnostics:
http://tinyurl.com/br8oa
Cardiovascular, endocrine and immunological abnormalities are well noted. The potential dangers of certain 'treatments' including graded exercise are well documented. Why therefore does the UK insist on following a psychosocial approach? In Canada and Belgium anti-viral therapies are licensed for treatment of ME. How can such a difference in treatment approaches from one nation to the next be accounted for?
The treatment of ME sufferers in the UK needs an urgent public enquiry to establish why sufferers (including children) are being coerced into dangerous therapies, and denied medicines available elsewhere.
Surely in the year 2005 we should be able to move on from Freudian notions of hysteria when it comes to severely ill sufferers of neurological conditions?
Steven Du Pre, Calif. (04/08/2005 at 22:05)
Angel, Liverpool (04/08/2005 at 22:08)
e.g medications, therapy etc
Tracey Fielding, Cannock, Staffs (05/08/2005 at 09:16)
Rob, Essex (10/08/2005 at 14:13)
B. Taylor, Madison, AL USA (10/08/2005 at 14:48)
Shary Gard, Tallahassee, FL (10/08/2005 at 15:16)
Kathryn, Winnipeg, Manitoba, Canada (10/08/2005 at 19:38)
What is this treatment??
I've had this life-destroying illness for 15 years, my daughter for ten.
Medical help is mediocre; I feel lucky to have a doctor who believes in the illness.
But no treatment to offer.
Kathryn
Paul, hertford (11/08/2005 at 16:44)
Neil, Scotland (11/08/2005 at 17:27)
Margaret Hursh, Valdez, Alaska (15/08/2005 at 13:21)
Cheryl, Tacoma,WA USA (17/08/2005 at 02:12)
Send me any and all information on this research. I am interested in any treatment that is available. I will travel any where in the world for a possible treatment plan that is effective. I want my life back! Desperate in the US
Margaret again, Valdez, Alaska (17/08/2005 at 11:31)
Check bottom of this page:
www.valdezlink.com/acute.htm
Recovered CFS Sufferer, Altrincham (17/08/2005 at 16:58)
Kay, US (18/08/2005 at 01:03)
Tracy Bloom, LMT, Ct, USA (29/08/2005 at 00:05)
Cheryl, Houston, TX (01/09/2005 at 14:24)
Vics, Swinton, Salford (02/09/2005 at 02:18)
Diane Fiebelkorn, Kenmore, NY (06/09/2005 at 13:02)
Evon Johnson, USA (New York (09/10/2005 at 04:02)