FAQ/Help |
Calendar |
Search |
Today's Posts |
![]() |
|
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) |
Reply |
|
Thread Tools | Display Modes |
|
![]() |
#1 | ||
|
|||
Member
|
I have a quick question. What Doctors (meaning what type of Dr) are you working with for your RSD? I have heard of people working with a neurologist, pain management and a rhuetmatoid Dr..
Currently I am working with a pain management Dr. and was wondering if a neurologist would be better? ![]() Please tell me who you have had the best results/ help with. Thanks. |
||
![]() |
![]() |
![]() |
#2 | ||
|
|||
Junior Member
|
Hi Vanessa,
I have CRPS type II in my arm, and work with a neurologist. I also see an OT and saw a psychologist this spring, who helped with depression and biofeedback techniquest. Whatever specialist you work with, make sure it's someone you can communicate well with. Good luck! Annie |
||
![]() |
![]() |
![]() |
#3 | |||
|
||||
Member
|
I see a Pain Management doctor. They have a Psychiatrist in their office he works with for his patients also. He also sends me to another type of PM doctor who does my procedures such as SGB's & LSB's. The only neurologist I have seen was an IME who didn't know jack crap. But then do they ever??? *LOL* IME's that is. I have also done PT in a pool & am planning on going back to that.
Make sure that whoever you see knows as much as possible about RSD or is atleast willing to learn about it. DebbyV |
|||
![]() |
![]() |
![]() |
#4 | |||
|
||||
Member
|
Hey
I am under a rheumatologist (who specialises in RSD), a pain management dr, a neurologist, wheelchair clinic and orthotics. Been under loads of other clinics as well. Most important thing is to research things and to find a dr that is used to treating it and who will utilise physio etc as well.. neurologists are either awesome with RSD or totally horrendously awful - my first one was dreadful but my new one is brilliant! Good Luck! ! ! Rosie xxx
__________________
It's always darkest just before dawn... but smile and the world smiles with you, cry and you cry alone |
|||
![]() |
![]() |
![]() |
#5 | ||
|
|||
Member
|
Thanks for the responses. I think I am going to see a neurologist from Hahnamonn, since they are great and deal with RSD. As others have said, what Dr. doesn't matter so much as their experience in RSD. I need someone who knows what they are doing, and who will listen to me and work with me. I agree Annie Poo, I need to be able to communicate well with him/ her. That's the trouble with some Drs.
Thanks again! ![]() Last edited by InHisHands; 01-01-2007 at 09:23 AM. |
||
![]() |
![]() |
![]() |
#6 | |||
|
||||
Junior Member
|
I am under the care of a Doctor of Osteopathic Medicine (A rehabilitation medicine doctor/physiatrist). I am now almost 21 but during my teen years (from about 14-18 I was under a pediatric neurologist and then up until this past summer i have gone without a neurologist.
I just recently found an adult neurologist which is wonderful to work with the DO on pain control although at this point I only go about once every 4-6 six months. |
|||
![]() |
![]() |
Reply |
|
|
![]() |
||||
Thread | Forum | |||
Working a lot but checking in... | Bipolar Disorder | |||
Working on SSDI | Social Security Disability | |||
Oh, God...He's already working on being a... | Autism | |||
SCS is working!! | Thoracic Outlet Syndrome | |||
how do you know if meds are working? | Epilepsy |