Hi, I’m back to moan again. I’m confused Neuro told me I had MS Dec.2009 saw him April 2010 and again May 2011 when he said problems I was having with my feet were’nt typical MS and threw RSD into the works? I had been going to my Drs. for 6/7 years but they didn’t pick up on it. Now learn this isn’t unusual for Drs. not to know about it. I did ask one doctor if she’d ever heard of it she said she had but didnt know much about it. I saw another doctor who specialised in ortho muscular etc and he has referred me to a hospital that specialises with it in Bath 250 miles away. I understand there are only four centres in the country. Ive heard that its linked to MS and osteo arthritis and suffer from them both I just wondered if anyone else has sufferd with RSD and can give me any advice and tell me what to expect.