National MS Society

If you had the chance to tell MS anything, what would you say? #MSAwarenessWeek #MSEndsWithUs

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: ntlms.org/44PW6QG

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 ntlms.org/Stream25.

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: ntlms.org/adaguide

🏁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. ntlms.org/iRacing_Charit…

Breaking News: U.S. House of Representatives passes budget resolution with deep cuts to healthcare coverage, food assistance and more - learn more about the work of MS Activists and the impact of HR 1 at: nationalmssociety.org/news-and-magaz…

📱We need YOU to call your U.S. Representative today! This is our LAST chance as MS Activists to stop cuts to healthcare coverage and food (SNAP) for millions of people across the country – call ASAP: nmss.quorum.us/campaign/13237…

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 ntlms.org/4lCogFL

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: nmss.quorum.us/campaign/12776….

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 ntlms.org/18millionforre…

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: ntlms.org/Climb25

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.🧡

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: ntlms.org/43EqIFk

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?

“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: ntlms.org/15YearsOfHikeMS

🚨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: ntlms.org/3Ft3hWf @MSactivist

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: ntlms.org/TeenSupport

📣 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: nmss.quorum.us/campaign/12481…

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: ntlms.org/80Years