Thanks for the link Ballerina, it's the most informative I've read so far.

Hi Nick,

Very curious to know how your treatments for tinnitus is coming. I know how miserable it can be. I also know how incredible it was to have it gone. Please keep us posted.

Hi Ballerina

Still in the process of gathering equipment & parts. When I've received everything I'll give you a blow-by-blow account of my inevitably good progress. I've met some pretty smart people like yourself that have told me any kind of tinnitus is curable, so that's reassuring. Mine is due to a sudden acoustic trauma/loud sound shock. I am so happy your own tinnitus is gone.I would shed tears of joy if mine went. I used to have a milder form and thought it couldn't possibly get worse, but now it's total agony, a concept I'm sure you can relate to. By the way, what caused your tinnitus (CRPS-related?), how long did you endure it, and what was it like to live with?

Mine was one of the many symptoms of progressive CRPS. The tinnitus lasted for about two years. It began with other autonomic issues. First just annoying, would come and go, but then it was ever present. Sadly, the other symptoms, especially the pain, were even worse.

I hope you are successful with tDCS. Please don't give up if the first protocol does not work.

Hoping there are better days ahead for you!