Library & Education Programs

The Ask an Expert weekly program series is an opportunity to learn more about multiple sclerosis from top MS experts. Each week’s edition will focus on a topic related to the MS community and feature a presentation followed by the opportunity to ask the expert your questions live.

Being Black and living with multiple sclerosis brings unique challenges and experiences. From scientific and clinical differences in the disease itself to stark inequities in the healthcare system and beyond. The Black MS Experience Summit is an opportunity to connect with others who understand the distinct experience of life with MS as a Black person. Throughout this interactive, three-day virtual event, we will forge powerful connections, learn from leading scientific and healthcare experts and give voice to the unique needs of our community.

The Webinar Series brings together a collaboration of MS experts — to help you learn strategies to live your best life with MS. Each free webinar program features two presenters, with time for Q&A.

Momentum, the award-winning quarterly magazine of the National MS Society, is the largest MS-related publication in the world.

National MS Society's online educational webcast series. Transcripts (.pdf format) are available for most programs.

Knowledge Is Power is a free, at-home educational series for people newly diagnosed with multiple sclerosis and their families. The program provides up-to-date facts about many aspects of MS.

Managing your health and wellness is an integral part of "living well" with MS. Live Fully, Live Well is a comprehensive wellness program from the National MS Society and Can Do MS, designed for people living with MS and their support partners.

The National MS Society’s Everyday Matters, supported by Genzyme, a Sanofi company, was an interactive national project that uncovered stories of real people facing the everyday challenges that MS can bring on the path to one’s best life.

View a list of upcoming and recorded webcasts with leading MS researchers and clinicians.

These books have been approved by a review committee and align with the Society’s organizational values.

Keep S’myelin is a colorful, engaging, informative, and reassuring newsletter to help children and their parents talk and learn about MS together.

Bienvenidos a este su centro de información sobre la esclerosis múltiple (EM). Aquí hallará información sobre diagnóstico y tratamientos, manejo de síntomas y asuntos laborales, así como información para cuidadores y niños.

The National Multiple Sclerosis Society provides free downloadable resources for people affected by MS and others. For help navigating the online library, contact an MS Navigator.