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Position Papers & Policies

Our MS activism and government affairs efforts focus on five priorities for people living with MS:

In addition, the National MS Society and MS activists nationwide also are involved throughout the federal budget process (.pdf) to ensure that programs and activities that benefit individuals living with MS and their families receive the funding they deserve. Many members of Congress have joined the Congressional Multiple Sclerosis Caucus. Find out how your Senators or Representative can join (.pdf).

Click here for updates on recent federal legislation and key votes on MS issues.

Increased MS research

We actively pursue public funding for MS-related biomedical, rehabilitative, and stem cell research. That includes securing increased funding for the National Institutes of Health (NIH) and finding new avenues for MS research funding, such as the Department of Defense.

Disability rights

For people living with MS and other disabilities, many obstacles can inhibit quality of life and community participation. We work to remove barriers to physical accessibility, prevent discrimination, and sustain independence.

Access to quality health care

Quality health care has no benefit to people with MS, if it is not affordable. We seek policies and programs that can make healthcare services, including the cost of prescription MS therapies, more affordable.

Long-term care resources

We help ensure the highest possible quality of life by providing quality, affordable alternatives for long-term care and more resources for caregivers.

Accessible, affordable health insurance

We pursue access to health insurance coverage for more people at a more affordable price, including Medicare and Social Security disability benefits.