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Old 04-15-2008, 09:56 AM #31
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Brain, I haven't ruled anything out at this point including a pain clinic and thank you for the extra information about them

I really am just waiting to see my original neuro May 6th and get his opinion and insight - I really adore him and in my opinion he is very good at what he does, Although he is not a MS specialist his professor wrote a book on MS many years ago and was the first book I had ever read on MS.
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Old 04-15-2008, 10:41 PM #32
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Hi Snoopy
I was just thinking about you and your pain. Back earlier in my MS career, I was using Wellbutrin to help with the sensory pain, mostly in my hands. It was the only med to bring me any sense of relief.

I had to stop after I developed a siezure disorder, relating to my MS, not the med.

Just a thought. Throwing it out in the universe.

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"Thanks for this!" says:
Snoopy (04-16-2008)
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