11 Multiple Sclerosis Organizations You Should Know About

2. Multiple Sclerosis Association of America (MSAA)

The national, non-profit organization Multiple Sclerosis Association of America was founded in 1970 with a mission to be a “leading resource for the entire MS community, (and) improving lives today through vital services and support,” according to the MSAA. The organization provides support and services to MS patients and their loved ones through programs such as a Helpline with trained specialists, award-winning educational videos and publications, safety and mobility equipment distribution, cooling accessories for heat-sensitive individuals, and a lending library.

Discover more here.

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3 comments

  1. Caroline says:

    Where is NARCOMS? It should be first on the list, I think.

    “NARCOMS is a global registry for Multiple Sclerosis research, treatment, and patient education. The Registry is an active database of over 38,000 persons with Multiple Sclerosis.”

    This organization is linked to the Consortium of Multiple Sclerosis Centers.

    These sites are where the serious work is reflected.

  2. Dennis says:

    Why no mention of Can Do MS, an exceptionally intelligent source of MS education? (MSCanDo.org)

    Why no mention of the MS Cure Fund? (MSCureFund.org)

    Why no mention of MS news and views?

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