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group : uk.people.support.cfs-me      view archive
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The pain of fibromyalgia is real     Sat, 30 Dec 2006 17:16:08 -0000
The pain of fibromyalgia is real, and doctors need to take patients' complaints seriously, concludes a review paper by University of Michigan Health System doctors. "It is time for us to move past the rhetoric about whether these conditions are real, and take these patients seriously as we endeavor to learn ...

Prince Charles     Sun, 24 Dec 2006 18:20:38 -0000
http://www.i-c-m.org.uk/journal/2004/feb/006.htm Forteans never prove anything; we just weigh up the evidence on the scales in our eyes. ...

fraud     Sat, 23 Dec 2006 19:05:16 -0000
Message from: Phil Corris, Police Constable/Crime Prevention Officer If you receive a phone call on your mobile from any person, saying that, he or she is a company engineer, or telling you that they're checking your mobile line, and you have to press #90 or #09 or any other number. End this call immediatel ...

Dark chocolate beats fatigue, study     Thu, 21 Dec 2006 20:50:59 -0000
http://www.nutraingredients.com/news/ng.asp?n=72894-barry-callebaut- mars-dark-chocolate 19/12/2006 - Further evidence of the health benefits of chocolate has come to light in a new study - giving manufacturers yet another route into the functional food niche. Eating a small amount of dark chocolate each ...

Foul Language     21 Dec 2006 04:00:00 -0800
Don't do it around me. If you have any intelligence at all you will not need to use foul language especially Steve what was said in the posts I received this morning. Thanks but no thanks~~Beauty ...

Hello, I have CFS/ME in Amerca, I am honored     19 Dec 2006 15:08:48 -0800
I have had this iLLness since 1998, I feel I do not have the right to post here, but to know people who have the iLLness is a wonderful support area for me as I have yet to meet anyone here in my State, City or online that has this horrible disease. I wish that America's CDC would call it ME because to me it so ...

Testosterone injection greatly improved my ME/CFS     Tue, 19 Dec 2006 15:05:10 GMT
4 years ago my ME/CFS got a lot worse, from preventing strenous exercise/bad sleep etc, to hardly able to walk. At that time I got checked by endocrinologist, who basically made a total f' balls up of it. He basically assumed that ME/CFS = whiney lazy, and thus my obesity had caused the lack of testosterone ...

Any conection between CFS and Statins     Mon, 18 Dec 2006 23:41:30 +0000
Hi Does anyone have experience of Statins affecting their CFS. My GP put me on Simvastatin about 4 months ago. At first there was possibly a beneficial effect then over the period I noticed that I was getting even worse sleep than usual, having difficulty getting asleep and staying asleep. The slightest ...

How To Solve A Problem Like ME?     Mon, 18 Dec 2006 12:37:22 -0000
PERMISSION TO REPOST > > We publish today news of the screening of the most > excellent Lyme Disease/Borreliosis documentary. > Below this piece, we also publish a short comparison > > chart of ME/CFS symptoms from the Canadian > Guidelines > and Lyme Borreliosis symptoms from the ILADS > Guidelines > on t ...

RiME Newsletter No. 8     Tue, 12 Dec 2006 19:24:01 -0000
Much has happened over the last few weeks. A quick recap: 1. Nov. 16 APPG Meeting. 2. The NICE Draft guidelines. RiME replied, condemning them by the deadline Nov. 24. It will be in the next Newsletter. 3. Other recent publications: a. The NHS sponsored, 'Occupational Aspects of the Management of CFS... ' ...


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