It amazes me how many people are coming here on a daily basis asking about the SCS/Pain Pumps ! And for those who don't know, a new forum specific to SCS/PP discussion has been created. Here's the direct link to get there
Click on:

http://neurotalk.psychcentral.com/fo...prune=-1&f=118

It is listed in the main menu as a subforum in the "Medications" section

Lots of new testimonies there and lots of questions being asked......
So much support is needed!
I get tears in my eyes when I read of these battles with RSD, and the ones who get the SCS and end up with RSD spreading.....

All I can do is pray.....
I'll never understand RSD and why so many wonderful people have to be plagued by it.....