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Programs and Services for Your Patients


Patient Programs 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.

Newly Diagnosed

  • Knowledge is Power - Knowledge Is Power is a free, in-home 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.)


  • Brochures - More than 60 booklets and brochures are available to people with MS and their families. Categories include General Information, Newly Diagnosed, Employment Issues, Staying Well, Managing Specific Problems, Managing Major Changes, and For Children & Teenagers. Publications, including many in Spanish, are available online.

Connection Programs

  • Connection Programs - The Society helps people living with MS connect with others to share experiences and provide support. Connection programs include traditional, in-person self-help groups, peer-to-peer support, online communities and other means of bringing people together.
  • MS Connection Online Community - is an online community that provides the opportunity to connect with people involved in the MS movement with valuable content, activities and resources.
Financial Planning
  • Financial Planning - The Financial Education Partners program provides pro bono financial planning and education to individuals with special health or financial circumstances.
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.
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
© 2020 The National Multiple Sclerosis Society is a tax exempt 501(c)3 nonprofit organization and our Identification Number (EIN) is 13-5661935.