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Any experiences with Chronic Fatigue Syndrome? More options

Question:
I hope that since this syndrome frequently strikes grad students (and since this group doesn't get much traffic), I won't be flamed for not putting this in whatever med groups exist in the internet.

Anyway, has anyone been diagnosed with CFS? What were/are your symptoms, and how was it detected?

Or for that matter, has anyone experienced unusual fatigue which was attributed to another cause?


Answer:
For you tired grad students out there (I guess that is redundant): CFS == Chronic Fatigue Syndrome CFIDS == Chronic Fatigue Immune Deficiency Syndrome

There is a website that is primarily a support group for CFIDS sufferers, alt.med.cfs, and a lot of the people seem to be grad students. Lots of good advice and support for coping. There is also a listserv which has some references; the moderator of the list, Roger Burns, follows the news group, which also posts to the listserver. There are some "official" ways of diagnosing CFS (as in eliminating everything else), but since fatigue is a symptom of so many other things it is tricky, and a lot of doctors apparently just "don't believe in" CFS. My sister has had CFS since she was 15 (now in 30's). Initially diagnosed as "some sort of mononucleosis," finally got the CFS diagnosis in the early 80's, just after she finished her Ph.D. It comes and goes for her, with the most obvious symptoms other than debilitating fatigue being swollen lymph glands, swollen liver, & impaired liver function. But the symptoms vary so much from one person to another that it's really tricky. For almost all CFS sufferers, stress triggers it, and physical stress is the most drastic trigger; whereas exercise is suggested for depression and other conditions that can cause fatigue, it is *not* recommended for CFS patients. Many people with CFS that have started feeling better and tried to resume their previous level of activity have had relapses.

There's a lot of misinformation out there about CFS, so following the alt.med.cfs group for a while is a good idea if you think you might have it....they are a nice bunch of people. Flames are actively suppressed, and support is freely given. There is talk of re-naming the group, but I haven't followed it for a while; the alt. name is still in my .newsrc. Depression is not a cause of "official" CFS, though it may be caused *by* the condition, so that awful malaise that grad students seem to feel may not be CFS after all....


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