U of Michigan
 

Just wondering if anyone here has had any dealings with the University of Michigan neurology department in regards to RSD? Thinking of asking for a referral for a second opinion to U of M and just curious. Thank you for any replies!!

Hello! I also suffer from RSD/CRPS in Michigan. Wondering if you ended up seeing a neurologist at U of M and how it went? I hope u r having a low pain day!

The post you have found and responded to is over 4 years old and that poster hasn't been active on the site for years - I've been around for about 8.5 years so I've seen people come and go.

I only mention it in case you hadn't realised - I know some folk post in the hope that the person still reads the site and will reply but often people just don't spot how old posts are.