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Date Posted: 17:49:35 06/15/00 Thu
Author: Sharron
Subject: Re: I finally got an answer
In reply to: Joan 's message, "Re: I finally got an answer" on 04:57:23 06/15/00 Thu

> Hi Heidi
Yes it was a neuro I went to. He was recommended by the MS society here in Boise. He did his exam and the pressure points etc. I think he based it on the exam and also from the negative brain/spine mri. He said that I do not have any nerve involvement which is good.

I have to investigate to see how they do diagnose FM but now at least I have a starting point and know what direction to go.

you know it is funny that so many people think that if you can't put a name to how you are feeling and why you can't always walk well and fall down/trip etc that you must be making it up for attention. For a while my husband got that look on his face like he didn't believe me or when he would just touch my arm or leg that it really hurt(to the point where I would cry) from the pressure of it and he barely touched me. When I came home and told him what the doc said I had he seemed relieved that now we have a name for it.

sorry this is so long...hope you are doing ok...
(((HUGS)))) Sharron

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