Hello fellow RSD'ers, I have been working really hard trying to get the best doctors and treatment for the past month or so. This has pretty hard to do for some reason. Half the pain doctors and head shrinkers here don't know what RSD is. One of my doctors thinks I might have MS on top of my RSD. I am having an MRI of my brain tomorrow morning. I was wondering if anyone else has had their doctor ask them to have a brain MRI because of some of your symptoms and voice concern that you may have MS on top of your RSD? I sure hope everyone is doing well. It's really good to be back on here...I've missed you guys. Karen