Hi all,

I was wondering if there's any chance that any other MGers are dealing with Stiff Person Syndrome. Probably not as its so rare, but as autoimmune diseases go together, I thought I'd ask.

My doctor finally got back in touch with me (she's been in a conference in Jamaca with really bad Internet. She thought she had responded to me, but it never came through). Anyway, she confirmed I do have SPS and is starting me on treatment for it. I was just wondering what other people's experience with this might be.

Jeff