I was diagnosed with CRPS about 10 days ago. I've seen a pain specialist and he's given me all sorts of tablets and says we have to experiment until we find the right doses of everything. Does anyone have any experience of CRPS, and any idea of how to relieve the horrible constant pain and muscle spasms.
Until I was diagnosed with it I'd never heard of CRPS, don't know anyone else with it. My consultant says it's a rare illness, and I was just unlucky to get it. 