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Old 12-23-2008, 05:06 PM #13
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ewizabeth ewizabeth is offline
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Join Date: Sep 2006
Location: northern Illinois
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ewizabeth ewizabeth is offline
Elder
ewizabeth's Avatar
 
Join Date: Sep 2006
Location: northern Illinois
Posts: 5,258
15 yr Member
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Quote:
Originally Posted by jmiller View Post
It has never gone away, and gets worse when its hot or during stress. Ive seen several neuros and all say the same thing, theres nothing they can do.

So even though its been very annoying, somehow I have learned to ignore it and try to adjust. Some of us can do it and some cant, its just like anything else this stupid MS decides to throw our way.
I pretty much agree with JMiller. I've had numbness on and off for years now. It's currently better (knock on wood-like surface) but it gets worse with heat or if I overdo it. The only way I'll take steroids is if I get a knock down, drag out flare up that affects my bladder, bowels, legs or eyes or something akin to that. (Can you tell I don't like them?)

I just ignore it but I also take it as a sign, since it always gets worse if I do too much or don't get enough sleep, etc...

I'm sorry you have to deal with this danged disease anyway.
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RRMS DX 01/28/03 Started Copaxone again on 12/09/09
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