The National Multiple Sclerosis Society provides excellent resources for education, support, and research. Use their publications and website to locate community resources, counseling, information, self-help groups (both online and in person), and the latest on research and treatments.
The most important recommendation I have to give to newly-diagnosed patients and their loved ones -
YOU are not your MS!! MS has not replaced your LOVED ONE. She/he is the same person you have known and loved, who now just happens to have MS.
Stay strong through the ups and downs and put your relationship first.
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