Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS)


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Old 11-15-2008, 12:16 PM #9
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Quote:
Originally Posted by Summertime View Post
Hi Rita

Glad to hear your husband is doing ok!!!!

I have a couple questions if you don't mind me asking???

Did your husband have to see a neuropsychologist prior to his SCS trial/implant? (if anyone else has an answer please let me know)

I am told I need to see a neuropsychologist but no one is telling what for.
I do not understand what is going on.

Did they tell you and your husband that he will be able to go off all his medications once the SCS is working to where he needs it?

Thanks
Summer
Hi Summer,
Yes , Reed did have to see a psych. Every prospective SCS patient has to see one and have an evaluation. From what the psych told Reed, they want to make sure you are emotionally able to handle having a device implanted in your body and they want to gauge your anxiety and depression. Reed said it wasn't bad at all. He was asked alot of questions and had to fill out one of those silly tests that ask if you ever hear voices in your head and so forth.
As far as meds, Reed's doc said he wasn't going to lie, that Reed will probably always be on meds. But the hope is to be able to discontinue narcotics someday, since they are the most dangerous as far as addiction. The biggest thing for Reed is to be able to walk again, without debilitating pain. hope this helps!
Rita
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