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Old 12-22-2008, 06:59 PM #11
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Quote:
Originally Posted by Lady View Post
BTW, Also the drug you take at night Amitriptyline, may be causing the numbness, keeping it with you or to increase it. See below:
That was one of the big reasons I quit the Amitriptyline that I was taking for insomnia, other than the fact that it quit working for me, was that I had increased numbness...which went away after I quit it. Mostly it was making me very weird. Went off it cold turkey and gosh, that was not fun.

Too bad I've got the numbness back, but I'm pretty sure that's due to the UTI I had last week, and possibly the mild dental infection that I had at the same time. (yay! the antibiotics I was taking for the UTI did a great job on the dental infection)

My left hand feels like I'm still wearing my winter gloves I just took off. At least it's not horrible right now, but it would be nice if it went away. It's not as annoying as numb legs tho...and I can still crochet and knit with numb/tingly fingers.
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Old 12-22-2008, 09:21 PM #12
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i have a lot of numbness in my feet. i've got neuropathic pain too.
i've taken neurontin, then switched to lyrica. it's still there but if i'm late with a dose i can tell the difference.

i hope you get to feeling better.
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Old 12-23-2008, 05:06 PM #13
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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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