National MS Society
@mssociety
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We will cure multiple sclerosis while empowering people affected by MS to live their best lives.
Joined March 2009
If you had the chance to tell MS anything, what would you say? #MSAwarenessWeek #MSEndsWithUs
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Know your rights — because they matter. The ADA helps protect people with MS from discrimination and ensures equal access to jobs, transportation, public spaces and more. Understanding the law is key to self-advocacy. Learn more in our ADA Guide:
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🏁Gamers: Start your engines! Join 7X NASCAR Cup Series Champion crew chief @chadknaus and others on August 13th for the 5th annual MS Race for the Cure on the 1.5-mile-long Lime Rock Park track via @iRacing. Get started by fundraising in @DonorDrive.
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What if your voice could shape the future of MS treatments?.This fall, it can. Shaping Tomorrow Together is a chance for people with MS to share what matters most directly with the FDA, researchers and clinics. Join us online 7/29 at 1pm ET to participate:
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Your support makes programs like the clinical care fellowship possible. Our annual July Research campaign is underway, and that means 100% of donations made in July go directly to funding research. Chip in to support these vital programs at:
nationalmssociety.org
The National MS Society is the leading resource for MS research, education, and support. See how we drive progress to change the world for people affected by MS.
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What began in 2004 as a bold step to train MS specialists has become a global force in MS care. The National MS Society’s clinical care fellowship has helped close the gap in access to expert care:
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RT @MSactivist: Breaking News: U.S. House of Representatives passes budget resolution with deep cuts to healthcare coverage, food assistanc….
nationalmssociety.org
The National Multiple Sclerosis Society exists because there are people with MS. Our vision is a world free of MS.
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RT @MSactivist: 📱We need YOU to call your U.S. Representative today! This is our LAST chance as MS Activists to stop cuts to healthcare cov….
nmss.quorum.us
Contact Congress ASAP!
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This July, every dollar you give to the National MS Society will go directly to MS research. The future of MS treatment is being developed right now in labs across the globe, and your support is crucial to continuing that work. MS ends with us. Give at
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Contact your Senators TODAY — tell them “No Healthcare Cuts” on the House-passed budget bill, One Big Beautiful Bill, which includes devastating cuts to coverage! 16mil people, including people living with #MS, would be affected. Contact your Senators:
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The Society has committed over $18mil in funding to support groundbreaking research aligned with the Pathways to Cures roadmap. These projects are only part of our annual investment of over $30mil in research, support and leadership around the world. Visit
nationalmssociety.org
Learn about the new research projects funded by the National MS Society as part of their annual investment & how they align with the Pathways to Cures roadmap.
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The big day is almost here. 📅 Are you ready to Climb to the Top of @CitiField and @GilletteStadium — and help end MS while you're at it? Sign up now before it’s too late:
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Today is @WorldMSDay, a global moment to honor the courage of those living with multiple sclerosis and reaffirm our commitment to ensuring that MS ends with us. Whether you live with MS, care for someone who does, or support the cause to find a cure in your own way — thank you.🧡
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Mental health support can help people with MS move from feeling overwhelmed to taking control of their care. In a recent conversation with @NeurologyLive, Dr. Evan Smith shares how mental health support can enhance MS care. 📘 Read the full feature:
neurologylive.com
Evan L. Smith, PhD, assistant professor of Physical Medicine & Rehabilitation at University of Michigan, discussed how emotional wellbeing, motivation, and evidence-based therapies can significantly...
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An MS diagnosis can feel overwhelming and scary – many people don’t even know where to begin, like Courtney. In honor of @WorldMSDay, we want to shine a light on MS diagnoses. Tell us, what is your diagnosis story?
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What if we told you your next livestream could help fund groundbreaking research? When you @StreamToEndMS, you’re helping us get one step close to creating a world free of MS. Get started today at
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“We hear time and time again that Hike MS is more than just a fundraiser – it’s healing, empowering and deeply personal,” — Robyn M. Read more about the history of Hike MS (and get a special discount code for $10 off registration! 👀) at:
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🚨Take Action: The House just passed a bill slashing Medicaid & ACA funding — threatening care for millions, including those living with #MS. Now it’s up to the Senate. Urge your Senators to reject these cuts. Your voice matters. Act now: @MSactivist.
nmss.quorum.us
Contact your U.S. Senators today!
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Having a parent with MS can feel overwhelming. You're not alone, and you don’t have to figure it out on your own. Join our teen support program to connect with others who get it. Share what you're going through, and find tools that help:
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📣 MS ACTIVISTS: A new bill working its way through Congress will threaten healthcare coverage for 13 million Americans. The impact would be especially devastating for the MS community. We have time to stop this, but we need to act now. Find out how at:
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Eighty years ago, an ad in the New York Times sparked a movement. Sylvia Lawry, driven by her brother’s struggle with MS, refused to accept “no cure.”. Today, we honor her legacy—one that has fueled hope for generations. Read Sylvia's story:
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