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Thanks and everyone who contacted me about ra and neuropathy. I got in

with a new rheumatologist today. He evidently really really dislikes my old

rheumatologist, but I do also. He thinks I have vasculitus. So something

should show up in the nerve study / emg done? (BTW is the nerve conduction

test supposed to hurt? It hurt some places, but I did not feel it in

others?) He also says I will probably need a nerve biopsy. He also told me

that my nerve damage is probably permanent, so we need to stop future

problems. I am on a lovely dose of 60 mg prednisone daily tapering weekly

by 10 mg unless I get worse. I was totally shocked when I left his office.

I guess I still want to be in denial about all of this. That tomorrow I

will wake up and this will be gone.

I have been in touch with a dr birnbaum at s Hopkins. He is a

rheumatologist / neurologist. You can read all about him and his clinic at

http://www.sjogrensworld.org/forums/ . Look in the cns discuss group. Dr

Birnbaum is seeing rheumatic patients with neurological complications. He

contacted me today, and I have an appointment next week!!!! I hope and pray

that I can get some real answers. Not more of the blame the last stupid dr

I saw or well, it's just postpartum and we just don't know.

My neighbor is a really sweet man. He is a family doc. He thinks most of

this is stress. <big sigh> Does he really know how much stress that adds?

I just can't believe the really stupid comments I get, even from drs.

Friday I get a lumbar puncture. This is my final test to prove it is not

MS. I am looking forward to having that done, as in already done! It will

be great to here it really really is not ms.

Thanks for letting me vent!

G

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