[voner]

hi:

I do not officially have crsd, but I have body wide chronic pain.

I am looking to talk to ballerina and/or fmicheal about tDCS etc. I am especially interested in a discussion on the devices.

To start out, I did find this nice website:

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please excuse me being a bit blunt -- because one of the most nasty pain inducers for me is touch (mechanical allodynia), so I use voice dictation -- but and up using the keyboard a bit -- and I cannot use a keyboard very much before it is too painful.....