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1st Visit to Pain Doc

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Hi all --

Some might remember that I wrote in a few weeks ago to introduce

myself -- I've had pain from psoriatic arthritis and ankylosing

spondilitis for more than 15 years, and recently I'd been referred to

a pain doctor. I had my first meeting with him today --

After an inspection he suggested that I had fibromylagia. Honestly

I'd always thought that FMS was a made-up disease (and please all you

FMSers, please don't write in with indignant objections -- after all,

what do I know?!). I even asked him directly, I said: " Isn't FMS

just a catch-all term meaning 'I don't know why you are in pain'? " --

He seems to think FMS is a real thing, so maybe it is, who knows.

His solution was to prescribe a full-spine MRI and some medication

called Neurontin. I did a search on Neurontin on both the Internet

and this list but didn't really find anything useful. Can anyone

tell me about Neurtontin?

He also suggested that he'd likely send me to a place that does bio-

feedback and acupunture. Does anyone have experience with either of

those?

Finally, I recently bought a book on accupressure. Does anyone have

any experience with _that_?

I know there are a lot of questions and more than just a little

cynicism layered in this email, but please understand that I am

sincere in both my own well being and my concern for everyone on this

list -- cheers --

RA

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