Your MS, Your Voice: The Power of Self-Advocacy — MS Awareness Month Highlights & Resources

MS Awareness Month 2026 badge to signify that March is Multiple Sclerosis Awareness Month

MSAA proudly recognizes March as Multiple Sclerosis Awareness Month and is pleased to present the MS community with helpful and encouraging resources and programs throughout the month.

Our MS Awareness Month theme in 2026 – Your MS, Your Voice: The Power of Self-Advocacy – focuses on what advocating for oneself really looks like in everyday life. Throughout March, explore self-advocacy from both the clinician and lived-experience perspective as we share practical tools to help the MS community. Please join us for the following free MS Awareness Month activities:

Podcast Mini-Series “Beyond the Chart: Meaningful Communication Between Patients & Providers”

Tune in and discover how meaningful communication helps people living with MS and healthcare providers build trust and work together more effectively. You can subscribe to the MSAA Podcast wherever you listen to podcasts.

Educational Video “Advocacy Starts with You”

Explore how people can effectively advocate for themselves within their families, communities, and healthcare teams.

Ongoing Blog Posts on MS Conversations

Focusing on the theme of self-advocacy, read new posts each week from MSAA and our guest bloggers.

Launch of MSAA’s 2026-2027 Art Showcase

The debut of our latest Art Showcase spotlights inspiring works from artists with MS. For more details, please check out the Program Highlight section further down in this edition of My MSAA Today.

To learn more about MSAA’s exciting MS Awareness Month initiatives, please visit mymsaa.org/MS-awareness-month.

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About MSAA

The Multiple Sclerosis Association of America (MSAA) is a national nonprofit organization and leading resource for the entire MS community, improving lives today through vital services and support. MSAA provides free programs and services, such as: a Helpline with trained specialists; award-winning publications, including, The Motivator; MSAA’s nationally recognized website, featuring educational videos, webinars, and research updates; a mobile phone app, My MS Manager™; safety and mobility equipment products; cooling accessories for heat-sensitive individuals; MRI funding; My MSAA Community, a peer-to-peer online support forum; MS Conversations blog; a clinical trial search tool; podcasts; and more. For additional information, please visit www.mymsaa.org or call (800) 532-7667.

Comments

  • Zoe says:

    thank you for the tips and tales of resilience …. this is a marathon fight not just a quick duel!

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