Guest guest Posted January 2, 2001 Report Share Posted January 2, 2001 My name is but I go by MJ because there are so many 's. I've had FMS since 1995 and probably before. I'm always looking and reading to see what I can find. I'm wondering now if FMS could have something to do with my difficulty in walking. I have other weird things too but will start wish that. My doctor did Botox shots on my neck and that worked wonders, If you are unfamiliar with Botox I can send some papers on it. Mostly I want to be listened to. I own a pain group but try to be strong there.Hopefully we'll be able too help each other and become friends. Hugs, MJ Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.