For a person newly diagnosed, an old hand just wanting to keep updated, a caregiver, a friend, or someone who is still doing the "MS Limbo", I have found these links to be great reference points. This is just a small example of what is available for research.
(Note: Links will open in a new window)
Multiple Sclerosis International Federation
Multiple Sclerosis Association of America
Multiple Sclerosis Society of Canada National Office
Multiple Sclerosis Society United Kingdom
Deutsche Multiple Sklerose Gesellschaft Germany
MS World Hollandse Dutch
MS World Down Under Australian & New Zealand
Suomen MS-Liitto The Finnish MS Society
Americans with Disabilities Act
All About Multiple Sclerosis Paul Jones' MS Page
Cowboy's Multiple Sclerosis News
Multiple Sclerosis Web Forum (A forum to discuss and comment on Multiple Sclerosis.)
Multiple Sclerosis - The First Step (Formally "Crutch's Corner On Multiple Sclerosis")
National Multiple Sclerosis Society
MS Newsgroup (alt.support.mult-sclerosis) You can join MSLIST-L also by email. Send LISTSERV@techunix.technion.ac.il (new address!) a message with no subject, one line in the message, "subscribe MSLIST-L your name" (without the quotes).
The Myelin Project. (Thank you Jon for submitting this link)
Claude The Cartoon Pooch with Multiple Sclerosis
Tee
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