i see a pain management doc that is also a neurosurgeon .. and i also see a reg. neurosurgeon for my pump.. you key is finding someone that knows a great deal about RSD and the correct treatments..

wlecome to our group. im sorry that we had to meet like this ever. im happy to see that people are gettin DX sooner tho it took a couple years to DX my RSD as i was a teenager when this happend 11 yrs ago. and kids having it then was rare to say the least.. well i gues not rare but docs knowing how to treat a kid with rsd is what was rare. it took alot of differnt docs to find the one that was knowledge able. but by this time my rsd spread to all of my limbs face and neck and back. now its basicly head to toe and internal.


i really hope that you are able to find the right doctor to help you..

welcome again

carrie