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-   -   Need help finding a good/kind RSD specialist. New to the area (https://www.neurotalk.org/reflex-sympathetic-dystrophy-rsd-and-crps-/251436-help-finding-rsd-specialist.html)

eviec3 05-06-2018 10:58 AM

Need help finding a good/kind RSD specialist. New to the area
 
Hello!

I was curious if anyone had any recommendations for a RSD specialist in the Humble/Kingwood area or even as about as far as Tomball? I have had RSD after doctors failed to give me treatment for Gullian Burray so it transformed into CIPD and gained the RSD during that change. As such I have been very neglected and abused by neurologists with god complexes for a long time.

My husband and I just moved out here to the Humble/Atascocita area and while I have been pretty much RSD free (as close as RSD free as we can hope) thanks to doing a Ketamine Treatment for 4 years but now it's coming back and it's coming back strong and fast so I need to find a doctor. But I'm nervous of finding a doctor that isn't going to be compassionate, kind, or experienced with the illness. If anyone has recommendations I would really appreciate it!

CRPSbe 05-07-2018 09:57 AM

Quote:

Originally Posted by eviec3 (Post 1262297)
Hello!

I was curious if anyone had any recommendations for a RSD specialist in the Humble/Kingwood area or even as about as far as Tomball? I have had RSD after doctors failed to give me treatment for Gullian Burray so it transformed into CIPD and gained the RSD during that change. As such I have been very neglected and abused by neurologists with god complexes for a long time.

My husband and I just moved out here to the Humble/Atascocita area and while I have been pretty much RSD free (as close as RSD free as we can hope) thanks to doing a Ketamine Treatment for 4 years but now it's coming back and it's coming back strong and fast so I need to find a doctor. But I'm nervous of finding a doctor that isn't going to be compassionate, kind, or experienced with the illness. If anyone has recommendations I would really appreciate it!

Maybe try calling RSDS.org - the support group. They might have a list of doctors in your area, or at least the name of a support group local to you that you can consult.

Good luck!


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