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Post 1

Quill

I am constantly amazed by the lack of information about ME/CFS - especially in Britain. My GP, for example, has never heard of it - I had to explain it to him!

I want to write an entry gathering together all that I have been able to find out about the condition - and I would welcome your help. Let me know if you are interested.

I was diagnosed in 1997, and I think I'm almost out of the woods but not sure yet.


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Post 2

Quill

OK - just found Lighthousegirl's entry. Now I'm feeling VERY SILLY, so please ignore the last post.

smiley - footinmouth


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Post 3

Bubble

Hi Outasync!

Sorry for the delay in reply!

It is a good article that Lighthouse wrote, and is a great way to understand what ME is really about. It was easily one of the many mountains to climb, having to explain to those around you what it really meant. I still suffer with ME, but life is getting closer to normal, whatever normal now is, touch wood!

If you ever need to refer somebody to reading matter, of what ME is, this is another really good article posted on wikipedia:
http://en.wikipedia.org/wiki/Myalgic_encephalomyelitis

If you ever fancy a chat, I usually call in to hootoo now and then smiley - biggrin it would be good to hear that a fellow sufferor is doing ok.

smiley - bubblysmiley - magic


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