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 | ||
|
|||
New Member
|
My name is Zamfira ,i have R.S .D on my right hand due to a dog bite .For 2 years i am in terible pain .I take Neurontin ,Amitriptilin ,go to physical therapy .I had 2 stelite black ganglion and did not healp .The pain is worst ,the R.S.D had spread .My Neurologist recomand me Spinal Cord Neurostimulation .I do not know what to do ,i am very scare .Please can somebody tell me if is worth to do the spinal cord neurostimulation .Thank you very much.God bless you all.
|
||
![]() |
![]() |
![]() |
#2 | |||
|
||||
Administrator
Community Support Team
|
Hi Zamfira
I have copied your post on the New Forum over here to RSD so that our members here can help with your question
__________________
~Chemar~ * . * . These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here. |
|||
![]() |
![]() |
![]() |
#3 | |||
|
||||
Senior Member
|
Hi zamfira!
Welcome to the best place for a comforting word, or information. I dont know too much about that, but there is some here that do. I would think your doing the best thing, and that is researching it. Be well informed before you decide. ![]()
__________________
. Gone Squatchin |
|||
![]() |
![]() |
![]() |
#4 | ||
|
|||
Member
|
Hello, Zamfira,
I agree that the Spinal Cord Stimulator (SCS) should be very carefully considered before going ahead. Not only is it very expensive, there are some drawbacks as well. I got mine in 2003 and I loved it for a while. It still is doing what it intended, reducing the pain in my left leg by about 40% - 50% at best. However, the RSD has now spread and the SCS does nothing for that since it is a localized treatment, not systemic like medications. Also, I have great discomfort at the surgical sites, where the scars are. Both the anchor for the electrodes and the generator were not buried deep enough, which are always uncomfortable, poking at the skin from the inside. A different neurosurgeon remarked that he would have installed it all differently. If you plan to do this, ask the surgeon for the names of several patients who have had this done and interview them. I wish I had. I would have shopped around more and possibly had better results. Don't get me wrong -- all in all it is a good treatment for the right candidate when all other tries have failed. I am still glad I got it. But be sure to ask lots of questions of the surgeon. I wish you better days ahead. Keep the hope. Mike |
||
![]() |
![]() |
Reply |
|
|