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) |
|
Thread Tools | Display Modes |
![]() |
#2 | ||
|
|||
Member
|
Hi Jim.
I've had rsd for almost two years now. My new PM gives me epidurals with Lidocane. He gives them right over my tail-bone as my rsd is in my leg. I get about a week of relief. Very good relief. I am unable to walk for a day or so right after the injections and I feel like I have the flu (all sore and just crappy feeling). But, I do get relief, which is just incredible. My old PM gave them to me in the L5 area and I got no relief. Just the flu symptoms. My new PM said that if I had been given those in the begining, I would be cured. I agree with you and your wife about the invasive procedures, but I am just desperate enough to get ANY relief that I was willing to try them. I know this is not very helpful, but I wanted to share my experiences. Hope you get the answers you are looking for. BTW - thanks for the info on the attorney. Kim
__________________
. . |
||
![]() |
![]() |
|
|
![]() |
||||
Thread | Forum | |||
sympathetic nerve block | Reflex Sympathetic Dystrophy (RSD and CRPS) | |||
Lumbar sympathetic block? | Reflex Sympathetic Dystrophy (RSD and CRPS) | |||
sympathetic nerve block | Reflex Sympathetic Dystrophy (RSD and CRPS) | |||
sympathetic nerve block | Reflex Sympathetic Dystrophy (RSD and CRPS) | |||
Sympathetic nerve block markedly enhances tissue oxygen delivery during HBOT | Reflex Sympathetic Dystrophy (RSD and CRPS) |