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Quote:
Originally Posted by Rrae
VERY good questions! And you are so wise to be asking around before making any decisions.....
Getting an SCS is a big deal!
It's a very individualized form of therapy/treatment......so don't take any ONE person's word as gold.....
Here is the direct link to our SCS forum....click on
http://neurotalk.psychcentral.com/fo...ysprune=&f=118
Lots of folks willing to share their experiences.
I'd recommend starting your own new thread and others will join in
I've had mine for almost a month.....it's working for my lower extremity peripheral neuropathy burning pain (nerve damage)...but you'll soon find out that, like you mentioned, other's w/RSD have encountered their's to cause the RSD to spread.....
I'll be in touch.....I'm anxious to see the feedback you get.
Everybody truly cares here!
Best wishes,
Rae |
Rae,
Thanks for the info and directing me to the SCS forum where I have posted a new thread. I'm new to all of this and don't totally understand how it all works. I'm not a youngster and am posting on behalf of my son (33 yrs). To complicate matters his CRPS is the direct result of a work related injury, therefore another layer of #$%^&*%#@ to deal with. Again, thanks for the info and hope things work out well for you.
Al