MS Assoc. of America

"In our MS community, advocacy empowers change... At its heart, advocacy is about connecting people with resources, connecting stories to audiences, and connecting needs to solutions." Read more from Dr. Eva Jackson by visiting Blog.MyMSAA.org

Every fundraiser, big or small, makes a difference for the #multiplesclerosis community. 💙 There are endless ways to fundraise and support MSAA’s free programs and services – check out our DIY fundraising toolkit and our A- Z idea guide by visiting MyMSAA.org/DIY

Learn strategies on how to effectively advocate for yourself within your community and healthcare settings, by watching “Advocacy Starts with You” featuring lived experience advocate Anita Williams and #multiplesclerosis specialist Dr. Erica Rivas. mymsaa.org/videos/advocac…

Team MSAA is coming up on our 10th year of being an official Charity Partner with @runDisney and we want to extend our thanks to every one of you who continue to help us make a difference in the MS community, one mile at a time. #MSassociation #rundisney #MSawareness

"The idea of self-advocacy is something that becomes incredibly important when you live with #multiplesclerosis… One area that often gets overlooked, however, is how we advocate for our time.” Read more from Samuel Fitch by visiting MS Conversations: blog.mymsaa.org/its-national-m…

Part 2 of #MSassociation's podcast series Beyond the Chart: Strengthening Self-Advocacy Through Communication is available now!🎙️ Listen now on your favorite podcast streaming platform. MyMSAA.org/podcasts #multiplesclerosis #MSawareness #MSawarenessmonth

To commemorate MS Awareness Month, give a gift that makes a meaningful difference in the lives of those affected by #multiplesclerosis when you make a tribute donation in honor or in memory of someone you care about.🎁 MyMSAA.org/Tribute

"#Multiplesclerosis does not follow a universal script. Because of that, self-advocacy is not a skill I can master and check off a list. It is an ongoing practice that requires me to ebb and flow." Read Kate Durack's article now on #MSconversations blog.mymsaa.org/the-ongoing-pr…

The first part of MSAA’s podcast episode Beyond the Chart: Strengthening Self-Advocacy Through Communication is available now!🎙️ Listen now on your favorite podcast streaming service or by visiting: mymsaa.org/msaa-podcasts/… #MSassociation #MSawareness #multiplesclerosis

We are proud to announce the 2026-2027 MSAA Art Showcase, featuring the work of many talented artists living with #multiplesclerosis. This March, we feature “Uneasy Shockwave” by Leidy Burgos as our Artist of the Month. #MSawarenessmonth #MSassociation #MSartshowcase

Often the first symptom of MS, visual disorders are common in #multiplesclerosis and ultimately affect the majority of people with MS at some time in their lives. Learn more by reading MSAA’s latest Ask the Expert:: blog.mymsaa.org/ask-the-expert…

March is MS Awareness Month and this year, MSAA is proud to provide programs and resources focusing on the theme “Your MS, Your Voice: The Power of Self-Advocacy.” Check out resources from MSAA all month long…and beyond! For more information visit: mymsaa.org/about-msaa/ms-…

"Lifestyle medicine can have a profound impact on quality of life in those of us with #multiplesclerosis.” Watch Dr. Lisa Doggett (@lisadoggettmd) in MSAA’s recent webinar “The Long Game: Lifestyle Medicine and MS” mymsaa.org/videos/the-lon…

Get text updates from MSAA on your phone by joining our texting program! Text MSAA to 75101 and you will receive: ✅ Important information ⏰ Timely research updates 🙋 Opportunities to get involved ❗ and more! On a mobile phone? Click here to join: go.txting.io/wna4sm

MSAA is proud to announce our Improving Lives Benefit Honorees!🏆 MS advocate, best-selling author, and inspirational speaker Tyler Campbell (@tcspeaks32) is the #MSassociation Mission Honoree, and @icometrix, a global leader in AI-driven neuroimaging, is our Corporate Honoree!

Join MSAA, along with Dr. Heidi Crayton, Neurologist and MS Specialist, and Dawn Morgan, MS and Women’s Health Researcher, for a conversation that centers on the lived experiences of Black women with MS. This webinar takes place on February 24th at 8:00 PM Eastern.

Episode 20 of MSAA's podcast is out now! In this episode we explore both clinical insights and real-world strategies to foster communication and support in the face of #multiplesclerosis Listen on your favorite podcast streaming app or MyMSAA.org/podcasts #MSassociation

“Traditional goal setting has never resonated with me. I tend to set ambitious goals but frequently find myself unable to achieve them. In contrast, setting intentions feels more aligned...and offers a more individualized approach.” -Dr. Eva Jackson blog.mymsaa.org/the-power-of-i…

"Unable to hold a paintbrush because of my MS, I created my own unique way of painting – using only my fingers and knuckles." MSAA's FINAL artist of the month for the 2025-2026 season is Shana Stern with her work titled "Feels Like Lightning."🎨 #MSawareness #MSartshowcase

The latest "What's New in MS Research" is out now!🔬 🔎 Stay updated on advances in understanding, diagnosing, and managing #multiplesclerosis by visiting mymsaa.org/news #MSassociation #MSresearch #multiplesclerosis