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National Multiple Sclerosis Society 2020 Policy Survey

July 23, 2020

MS Activists drive change for people affected by MS at the federal, state and local level. The National Multiple Sclerosis Society conducts a biennial survey to seek input on our public policy priorities. Through this survey, MS Activists and other constituents help us identify and confirm which issues are of greatest importance for people affected by MS.

The results of this survey will be shared with the Society's leadership and Activism Advisory Committee, a national advisory committee comprised of staff and volunteer leaders that recommends the policy priorities the Society will pursue.

The survey should take approximately 10 minutes or less to complete. Click here to complete the survey today. Thank you for taking the time to provide your input and guide our work.

About Multiple Sclerosis

Multiple sclerosis is an unpredictable, often disabling disease of the central nervous system. There is currently no cure for MS. Symptoms vary from person to person and range from numbness and tingling, to mobility challenges, blindness and paralysis. An estimated 1 million people live with MS in the United States. Most people are diagnosed between the ages of 20 and 50, and it affects women three times more than men.

About the National Multiple Sclerosis Society

The National MS Society, founded in 1946, funds cutting-edge research, drives change through advocacy, and provides programs and services to help people affected by MS live their best lives. Connect to learn more and get involved: nationalMSsociety.org, Facebook, Twitter, Instagram, YouTube or 1-800-344-4867.

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© 2021 The National Multiple Sclerosis Society is a tax exempt 501(c)3 nonprofit organization. Its Identification Number (EIN) is 13-5661935.