Michelle, thank you so much for taking the time with me. I'm hoping to put a name to this one, not that my "care" will be much different and my world won't come to an end. I just don't want to let these new symptoms go and then loose the use of my leg, and I would like to get rid of the nerve pain in my face. So how do you know what is AS and what is MS? and, if a person has AS and MS, they can't use the Biologics????
I hope you aren't over doing it out there. I watch the news everyday and just cry at the inevitable devastation. You remain in my prayers sweetie.
Cindy
