Guest guest Posted December 16, 2004 Report Share Posted December 16, 2004 Bill, Here's 2 resources for you. First, see if you can contact Dr. Hilton-. This information might be old, and I am not sure it still works, but give it a shot. If he is elsewhere, someone else there might give you direction. Muscular Dystrophy Campaign Muscle and Nerve Centre, Department of Clinical Neurology, Radcliffe infirmary, Oxford OX2 6HE, UK. david.hilton-jones@... If you strike out there, try contacting CMT-UK email secretary@... Hope this helps. Gretchen 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.