Hi Lynn, my name is Christine. This group, while good to have as
another source, isn't that active. I would suggest the following:

MySpace has a few RSD/CRPS Groups

& Neurotalk - I hope the link comes through.

"http://neurotalk.psychcentral.com/index.php?s=c9d8dd1d2b7e5d3b248aa1b5bb70b6dd"

Hugs. There are quite a few who have the SCS and can answer or provide
insight to your question, I cannot. I get mine on Aug. 6 this year.

Christine
--- In RSD_LINKS@yahoogroups.com, "lynntoast" <lynntoast@...> wrote:
>
> Hi My name is Lynn and I also have RSD. I was injured in Feb. 2004. I
> have had 7 surgerys since then. I had a Spinal Cord Stimulator
> permently Inplanted in Feb 2006. I got quite a bit of relief from it
> the first 6 months but now not as much. Anyone else have this problem
> with a stimulator?
>