Not sure about anyone else, but I never knew about RSD or CRPS Type II until I actually got it and have had to endure it.

There must be a way to educate our local areas about this? I find so few support groups, local information, etc.

Seems like most people (especially around me, hopefully NOT around you!) would prefer to either not know or ignore and not care.

Not a clue on how to raise awareness here, nut one thought I had I expanded on an idea of something I have wanted to do for years any how:

I want to get a full back tattoo of a phoenix spread-winged rising up and out of flames and ashes holding a sword in each claw to sort of signify our daily battle and the successes many have had.

Comments, suggestions, am I just going out of my mind??