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New Member (Rach/CFS)

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Dear Rach

I have had ME/CFS and fibromyalgia for seventeen years and I hear what you are

saying. I have reached the point where I assume that people do not understand

and perceive me as being a whiner. I find it so offensive when I am told how

good I look!

I hope you have a doctor who is knowledgeable about ME/CFS. There is no cure

but they can help with your comfort -- IF they care to do so.

Learn about the " syndrome " you have. The best place to start is Google

Canadian Definition of ME/CFS (Myalgic Encephalomyelitis/Chronic Fatigue

Syndrome and print out the short version. This will give you an excellent

overall definition and more besides. If you are ever up to it, print out the

whole 30-page version.

Sorry, losing it right now. Email me directly if you wish.

Nina in Maine

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