Sad link page
Sad link page
If you actually have the same kind of illness as me then mail me a tell, and we can feel sorry for ourselves (for a little while). If you are interested in finding out more, without my overt bias then follow the external links below... (however, I suppose that they are all hand selected by me...).
People suffer this illness for a very long time. Look here for a moving list of some of them. (and these are just the some of the online ones remember). Forget my site, Go here.
Providers of the above list.
A good place to start if you have the disease.
They have done some really important work for sufferers here in GB. Not least helping to force the government to recognise it as a 'serious' and 'debilitating' condition.
A great deal of useful ME information.
List of resources on the internet.
UK based support group.
Intelligent check list of symptoms for a CFS diagnosis.
"...UPSCM [uk.people.support.cfs-me] is an unmoderated group for the discussion of Myalgic Encephalomyelitis (ME) / Chronic Fatigue Syndrome (CFS), and for the mutual support of sufferers and their carers, in the U.K...".
A fantastic site, with loads of tips for sufferers.
at cfs-news.org
(Frequently Asked Questions) at cfs-news.org
Mary Schweitzer's informative and detailed pages.
UK based Website for ME/CFS and Fibromyalgia worldwide.
|
A page from James David Chapman's website.
Located at: http://www.users.globalnet.co.uk/~jchap/ Site mirrored here at: http://www.j.chap.btinternet.co.uk |
|
|
This page last updated:
My rating for the page: 
|