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 | ||
|
|||
Junior Member
|
I had an SCS Implant surgery for RSD for my legs (with full success) & was wondering if anyone has heard of, or experienced, RSD starting in the incision site if their implant??? Please help???? Really concerned
![]() ![]() |
||
![]() |
![]() |
![]() |
#2 | ||
|
|||
Magnate
|
I have heard of people have issues with the surgery from the scs. I would call the doctor who did this surgery asap.
|
||
![]() |
![]() |
"Thanks for this!" says: | renhenne (03-07-2011) |
![]() |
#3 | ||
|
|||
Junior Member
|
Quote:
![]() ![]() |
||
![]() |
![]() |
![]() |
#4 | ||
|
|||
Magnate
|
I am sorry and can understand your fears. I hope your doctor can give you some answers. I will say some pains and symptoms I have had thru this I thought was an rsd spread cause the pain was so high and for so long but it did go away with time. I am a slow healer that is for sure so maybe that could be what is going on with you. I hope regardless you get relief and answers
|
||
![]() |
![]() |
"Thanks for this!" says: | renhenne (03-08-2011) |
![]() |
#5 | |||
|
||||
Member
|
Hi renhenne,
I had a SCS implanted to help with the RSD in my right leg and foot. After my 2nd surgery for this in Dec of 2010, I began to experience symptoms of RSD in my back, arms, neck shoulders and fingers. I am now being told that the due to the surgery, the RSD has "flared" into those areas. If they told me before the surgery (or if I had read on my own) that surgery increases the flaring of RSD, I would not have agreed to the surgery. Right now, I am still having trouble getting my stim to work and cover the correct areas, I have had 2 additional blocks to try and help with the "new area". Nothing seems to be working. I am not sure what to do next, but I do know that surgery WILL NOT be an option. Best of luck to you, continue to talk to your doctors - ask questions, and do not be afraid to insist or see someone else. |
|||
![]() |
![]() |
"Thanks for this!" says: | renhenne (03-08-2011) |
![]() |
#6 | |||
|
||||
Elder
|
Redhenne...
Here is the link to our SCS and Pain Pump Forum.... http://neurotalk.psychcentral.com/forum118.html There may be someone there with similar situation as yours.... ![]() Abbie
__________________
My avatar pic is my beautiful niece Ashley! . Rest in Peace 3/8/90 ~~ 4/2/12
|
|||
![]() |
![]() |
Reply |
|
|