National MS Society (@mssociety) header
National MS Society (@mssociety) profile picture

For 80 years the National MS Society has reshaped the story of MS. Now we intend to finish it.

Joined March 2009
Photo by National MS Society (@mssociety)Photo by National MS Society (@mssociety)Photo by National MS Society (@mssociety)Photo by National MS Society (@mssociety)Photo by National MS Society (@mssociety)Photo by National MS Society (@mssociety)Photo by National MS Society (@mssociety)Photo by National MS Society (@mssociety)Photo by National MS Society (@mssociety)Photo by National MS Society (@mssociety)
As a single mom determined to be strong for her children, Alejandra carries the weight of not knowing how MS will shape her family’s future. Learn how you can give back confidence for the future: ntlms.org/MSTakesYE
2
18
620
Join us — give to stop what MS takes: ntlms.org/MSTakesYE Your support helps fund research, connect people to critical resources and ensure no one faces MS alone. MS takes, but together we can give back.
1
9
977
National MS Society retweeted
realtalkms.com/479 Thousands of researchers and hundreds of presentations led to new questions, discoveries, and possibilities. Which of these developments deserve our attention? Dr. Bruce Bebo shares his scientific highlights from #MSToronto2026 on #RealTalkMS. 🎧 Listen now! #MultipleSclerosis @mssociety @BeboBruce
1
11
363
New research identified CFH, a protein that may help nerve cells withstand inflammation in MS. This discovery could open new paths to protecting nerve cells and stopping MS progression. Learn more: ntlms.org/NerveCellProtectio…
7
2
27
1,017
7,000 scientists. 102 countries. One shared commitment to accelerating progress against MS. Bruce Bebo, PhD, Chief Research & Medical Affairs Officer at the Society, shares key takeaways from #MSToronto2026 and the research advances generating hope for people affected by MS.
1
21
1,093
On the @AmericanBrainCo Voices for the Brain podcast, Leslie Ritter, National MS Society SVP of Advocacy and Access joins MS patient advocates Samantha Strickland and Scott Crawford to discuss the Society's patient-focused initiatives. 🎧 Listen in: ntlms.org/3UEcUZX
1
1
7
576
National MS Society retweeted
🎙️ From Day Two at #MSToronto2026, Tim Coetzee of @mssociety and Pam Valentine of @MSCanOfficial join us to talk research, collaboration – and turning scientific progress into real-world impact. 🎧 𝐋𝐢𝐬𝐭𝐞𝐧 𝐧𝐨𝐰: 🟢 𝐒𝐩𝐨𝐭𝐢𝐟𝐲: open.spotify.com/episode/04R… 🍎 𝐀𝐩𝐩𝐥𝐞: podcasts.apple.com/us/podcas… 🖥️ 𝐖𝐞𝐛𝐬𝐢𝐭𝐞: ectrims.eu/podcast/mstoronto… #ECTRIMSPodcast #MSResearch
2
10
719
Just one week left before @ECTRIMS Patient Community Day on 10/23! This free event, available in 50+ languages, connects you with MS experts, researchers and healthcare professionals and break down valuable insights for the future of MS care. Register: ectrimspatientcommunity.eu/r…
1
1
10
636
For 80 years, the National MS Society has led the global movement to confront one of the most complex neurological diseases of out time. Now we intend to finish it. Here's how we're building a future free of MS: ntlms.org/CTEMSRecap
18
670
What if MS relapse risk could be detected months before symptoms appear? New research found evidence of Epstein-Barr Virus (EBV) reactivation up to 3 months before a relapse, offering new insights into earlier monitoring and intervention. Learn more: ntlms.org/EBVResearch
5
25
958
An MS diagnosis can feel like your life hit fast-forward: new words, appointments, treatment decisions and a million questions. You don’t have to know what comes next. Take it one step at a time: ntlms.org/TakingControlOfMS
1
2
17
718
A world free of MS is within reach. The Campaign to End MS will address the challenges of MS from multiple angles: faster diagnosis, personalized care, supportive communities and, ultimately, a cure. ntlms.org/EndMS 📸 ©Rod Morata/Michael Priest Photography
1
1
24
1,356
For 80 years, we have shaped the story of MS. Now we intend to finish it. The Campaign to End MS is both an ambitious goal and 5-year plan for what's next. Learn more: ntlms.org/EndMS
3
19
1,181
For 80 years, we've led the global movement to confront one of the world's most complex neurological diseases. But our work is not finished. We are entering a new era of possibility. The question is no longer whether we can end MS. The question is how fast we can make it happen.
1
8
27
1,244
Today, leaders across sectors are coming together for a one-of-its-kind research symposium exploring opportunities that can advance progress toward ending MS. As we celebrate 80 years of breakthroughs, this moment represents both how far we've come and what's possible next.
1
22
1,092
Researchers are making strides in myelin repair, opening new avenues for MS treatment. At @ECTRIMS Patient Community Day on 10/23, you'll have the chance to learn more and ask your questions directly to MS experts. Register free: ntlms.org/4hmJ4Ss
1
3
16
1,077
A new global study estimates 3.1M people are living with MS worldwide, up from 2.8M. This increase reflects earlier diagnosis and better data collection, not higher risk. Learn more: ntlms.org/MSPrevalence
2
5
2
24
1,390
September is #FallPreventionMonth. This month, empower yourself with the skills and knowledge you need to support a lifetime of safer movement and living well. Here's how to get started: ntlms.org/FallPrevention
5
11
1,076
Your voice matters. ✅ If you're living with MS, making a voting plan and understanding the issues that impact the MS community will make sure your perspective is represented. Explore accessibility resources, check your registration and more: ntlms.org/VoterResources
1
2
8
946
If you're looking for a deep dive into what this years' legislative landscape could mean for those living with MS, join us, September 22 at 3 p.m. ET for a free webinar with special guest Nathaniel Weixel, healthcare reporter for @thehill. Register: ntlms.org/AdvocacyWebinarSep…
4
241