Reflex Sympathetic Dystrophy

[madjack]

I have RSD, anyone else out there ?? It`s rare and painful

[headlesspets]

hi there MJ... i confess to looking at your post out of curiosity (having no idea what RSD is) and then did a quick search for info.. I don't know if you have already done so but there is a network called RSD Uk : www.rsd-crps.co.uk/ who offer support, education etc for sufferers. hope its of small help, and best wishes to you