National MS Society (@mssociety) 's Twitter Profile
National MS Society

@mssociety

We will cure multiple sclerosis while empowering people affected by MS to live their best lives.

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linkhttp://www.nationalmssociety.org calendar_today06-03-2009 22:13:04

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Hear how Brandon (Coupleanerdz on Twitch) uses his platform to educate and raise awareness about MS. Then head to ntlms.org/MarchTogether25 to learn how you can join us for #MarchTogether before time runs out!

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There's only a few more days to make your #MarchTogether donation! Don’t take an L, support those affected by MS today at ntlms.org/MarchTogether25 🧡 Stream to End MS

There's only a few more days to make your #MarchTogether donation! Don’t take an L, support those affected by MS today at ntlms.org/MarchTogether25 🧡 <a href="/StreamToEndMS/">Stream to End MS</a>
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📅 Tax Day is almost here—have you considered these three ways to give? Make a lasting impact and take advantage of tax savings by giving through a stock gift, donor-advised fund, or qualified charitable distribution. Learn more at: ntlms.org/TaxDay

📅 Tax Day is almost here—have you considered these three ways to give? 

Make a lasting impact and take advantage of tax savings by giving through a stock gift, donor-advised fund, or qualified charitable distribution. Learn more at: ntlms.org/TaxDay
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We are BEYOND grateful to everyone who came together for #MarchTogether! From the incredible streamers to the generous donors, we are so glad to have you as a part of the Stream to End MS family. 🧡

We are BEYOND grateful to everyone who came together for #MarchTogether! From the incredible streamers to the generous donors, we are so glad to have you as a part of the <a href="/StreamToEndMS/">Stream to End MS</a> family. 🧡
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Connect one-on-one with someone else who understands life with MS through MSFriends – a program that welcomes adults living with MS, carepartners, friends, family, and those who have lost someone who lived with MS. Find your friend at: ntlms.org/MS_Friends

Connect one-on-one with someone else who understands life with MS through MSFriends – a program that welcomes adults living with MS, carepartners, friends, family, and those who have lost someone who lived with MS. Find your friend at: ntlms.org/MS_Friends
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While there’s no cure for MS yet, there are strategies to help manage symptoms, delay disability, and modify the course of the disease. Managing MS can feel like a full-time job, but we’re here to help. Visit here for the full list of treatment options: ntlms.org/ManageMS

While there’s no cure for MS yet, there are strategies to help manage symptoms, delay disability, and modify the course of the disease. 

Managing MS can feel like a full-time job, but we’re here to help. Visit here for the full list of treatment options: ntlms.org/ManageMS
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🚨 Action needed – RSVP today! Last month, we learned the MS Research Program would receive 0 funding in FY 2025 — a devastating blow to all who live with MS. Join us Tuesday, April 29 at 2 p.m. ET to help restore this critical funding. RSVP: ntlms.org/SaveTheMSRP

🚨 Action needed – RSVP today!

Last month, we learned the MS Research Program would receive 0 funding in FY 2025 — a devastating blow to all who live with MS.

Join us Tuesday, April 29 at 2 p.m. ET to help restore this critical funding. RSVP: ntlms.org/SaveTheMSRP
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Hope for people with MS depends on strong research funding and right now, that hope is under threat because Congress has cut all funding for the MS Research Program in 2025. Join us on April 29 at 2:00 p.m. ET to hear how you can make a difference. RSVP: ntlms.org/SaveTheMSRP

Hope for people with MS depends on strong research funding and right now, that hope is under threat because Congress has cut all funding for the MS Research Program in 2025.

Join us on April 29 at 2:00 p.m. ET to hear how you can make a difference. RSVP: ntlms.org/SaveTheMSRP
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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: ntlms.org/80Years

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
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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: nmss.quorum.us/campaign/12481…

📣 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…
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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: ntlms.org/TeenSupport

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
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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: ntlms.org/3Ft3hWf MS Activist

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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: ntlms.org/15YearsOfHikeMS

“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
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What if we told you your next livestream could help fund groundbreaking research? When you Stream to End MS, you’re helping us get one step close to creating a world free of MS. Get started today at ntlms.org/Stream25.

What if we told you your next livestream could help fund groundbreaking research? When you <a href="/StreamToEndMS/">Stream to End MS</a>, you’re helping us get one step close to creating a world free of MS. Get started today at ntlms.org/Stream25.
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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 World MS Day, we want to shine a light on MS diagnoses. Tell us, what is your diagnosis story?

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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: ntlms.org/43EqIFk

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Today is World MS Day, 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.🧡

Today is <a href="/WorldMSDay/">World MS Day</a>, 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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The big day is almost here... 📅 Are you ready to Climb to the Top of Citi Field and Gillette Stadium — and help end MS while you're at it? Sign up now before it’s too late: ntlms.org/Climb25

The big day is almost here... 📅 Are you ready to Climb to the Top of <a href="/CitiField/">Citi Field</a> and <a href="/GilletteStadium/">Gillette Stadium</a> — and help end MS while you're at it? Sign up now before it’s too late: ntlms.org/Climb25
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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 ntlms.org/18millionforre…

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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: nmss.quorum.us/campaign/12776….

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….