Hi Ballerina,

Just wanted to send a quick thanks for sharing your experience in the tDCS thread. I don't post very often because I don't have CRPS but my husband does, although he's been in remission for two years. He is forbidden from reading anything on the internet regarding CRPS (I call him 'Eeyore' for a reason) but I check this forum nearly daily to keep up with current treatments and the progress of members.

I believe that if he were to ever relapse, tDCS is probably the first thing he would want to try since it's cheap and non-invasive. It's something we would never have even known about if you hadn't posted on it, so thank you for that. I have the thread bookmarked for future reference, should the need ever arise.

Thanks again, and best wishes for continued healing.

Merle