Has anyone been referred to the University of Michigan for their Fibromyalgia/Pain? If so, what was your experience?
It was very helpful. IDE try there if it's closer? It's also FREE😊
Thanks, were they able to help you with any treatment options or things you didn't know prior to going? I'm thinking about going to a workshop/retreat at a clinic on the west coast, Michigan would be WAY closer ;)
I found out the only doctors who see you there are the Rhemotologist. They do have a good Fibro./pain workshop. I went and it was very good.