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Resources and Services for Your Patients


Patient Resources and Services

Finding answers and making sound decisions relies on having the right information at the right time. The National MS Society provides answers to questions and access to information about all of the options available. Our MS Navigators are highly-skilled professionals — equipped to respond to patient needs. Contact the National MS Society to learn more or request copies of the resources listed.

Ask an MS Navigator®

  • Ask an MS Navigator - MS Navigators connect people living with MS, their family members and caregivers to the information, resources and support needed to move their lives forward.
Edward M. Dowd Personal Advocate Program

Newly Diagnosed

  • Knowledge is Power - Knowledge Is Power is a free, online educational series for people newly diagnosed with MS and their families. This comprehensive program provides upto-date facts about many aspects of MS. (Available in Spanish.)

Diet, Lifestyle and Wellness


  • Brochures - More than 60 booklets and brochures in multiple categories are available to people with MS and their families. Publications, including many in Spanish, are available online.

Educational Programs

  • The National MS Society maintains a library of educational programs for the MS community, including a weekly Ask an MS Expert webinar, The Black MS Experience Summit, access to videos, brochures and more.

Connection Programs

  • Connection Programs - The Society helps people living with MS connect with others to share experiences and provide support. Connection programs include traditional self-help groups, peer-to-peer support, online communities and other means of bringing people together.
Insurance and Financial Information Pediatric MS Resources Veterans - The National MS Society is collaborating with the Department of Veteran’s Affairs (VA) MS Centers of Excellence to improve care and support services for Veterans with multiple sclerosis and their families through:
  • Ensuring benefits available from “Service Connected” status.
  • Referring to VA MS Centers of Excellence.
  • Department of Veterans Affairs monthly conference calls for care partners of Veterans with MS.
  • Veteran specific community referrals.
Information for Specific Populations Resources For Families


Become a Research Champion

An MS Research Revolution

Support MS Research

Understanding and ending MS can’t come fast enough – it will take all of us working together. It’s easy to be a champion for MS Research – join us and proudly let everyone know that you’re helping to lead the MS Research Revolution.

Become a Research Champion

Become a Research Champion
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