National MS Society

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

[National MS Society @mssociety]

@AndreaMHutchins Hi Andrea! Unfortunately we can't provide health recommendations. We recommend speaking with your health care team about the best options for you.

[National MS Society @mssociety]

If you're one of the roughly 25% of people living with both MS and migraines, medication and lifestyle changes can help limit disruptions to your daily life. Read more to explore the relationship between the two and discover tips for managing both: https://t.co/yNoCKPHOCm

[National MS Society @mssociety]

For many LGBTQ+ people living with MS, navigating healthcare and finding affirming support can bring added challenges. No one should face them alone. MS Navigators are here to connect you with resources, support and community: https://t.co/lOp3o79bRX

[National MS Society @mssociety]

Irisin—a hormone released during exercise—may help protect nerve cells and improve recovery for people living with MS. A new Society-funded study explores how irisin could play a role in new treatments that prevent nerve cell damage.

Here's how: https://t.co/I6FaYiOKAj

[National MS Society @mssociety]

Together, MS ends with us. 🤝

On #TogetherTuesday, people unite to strengthen their communities through shared generosity. Your support accelerates life-changing research, creates access to resources and brings us closer to a world free of MS. Give now: https://t.co/TVnnnK6jlj

[National MS Society @mssociety]

Understanding both the emotional and biological drivers of depression is key to empathic care, reducing stigma around mental health challenges and more effective support for people living with MS.

More on RealTalk MS: https://t.co/XKoP0pwJbW

[National MS Society @mssociety]

When brain fog hits, pushing through it can feel like the only option.

Pushing through may help you focus today, but it often comes at the cost of clarity tomorrow. Sometimes the most productive thing you can do is let your brain rest. Learn more: https://t.co/WkhwplSNe4

[National MS Society @mssociety]

Real strength isn't pushing through at all costs. It's knowing when to rest, ask for help and honor your limits. Self-care may not look heroic, but listening to your body often takes the most courage: https://t.co/6IxPAcB4Qj

[National MS Society @mssociety]

Many men are taught to "man up," push through and tackle life's struggles alone. When MS makes that impossible, guilt can follow.

Real strength comes from respecting your limits and accepting support when you need it.

[National MS Society @mssociety]

Today is #WorldMSDay, a moment to recognize the estimated 2.9 million people globally who live with MS and countless others dedicated to research, support, advocacy and care.

With @MSIntFederation, we're making sure the realities of MS don't go unseen.
https://t.co/9oLAh5DRPo

[National MS Society @mssociety]

The newly released Voice of the Patient Report highlights insights from nearly 3,000 people affected by MS to inform the future of MS research and treatment.

Real-world MS data, ready to use. Download the report today: https://t.co/7UxizcOB05

#ThisIsMS

[National MS Society @mssociety]

Starting at 8 p.m., @DystopiaTonight is going live for 24 hours to support everyone living with MS.

A special thanks to Ray Romano for helping spread the word, and to @JohnPoveromo for creating an event that's hilarious and impactful.

Tune in: https://t.co/7dMxh9KOPP

[National MS Society @mssociety]

24 hours. One stream. For a really good cause.

We’ve got comedians, actors and some people who definitely shouldn’t be awake for 24 hours. Come hang out May 27-28, donate and watch things spiral in real time on @DystopiaTonight.

📆: May 27-28
🔗: https://t.co/7dMxh9KOPP

[National MS Society @mssociety]

Mobility changes with MS don’t mean life stops moving. From mobility aids and workplace accommodations to vehicle modifications and rehab support, there are many ways to stay safe, active and independent while navigating MS.

Learn how to get started: https://t.co/ciZmuGmQCi

[National MS Society @mssociety]

Women are diagnosed with MS 3x more often than men, yet research guiding their care remains limited. The National MS Society is funding 11 new studies focused on menopause, pregnancy, immune response and more to help close critical gaps in women’s MS care. https://t.co/yo1lPEuCBk

[National MS Society @mssociety]

"Strength is showing up with hope every single day." — Elsa Mendoza

To all moms and mother figures living with MS:
Your quiet, steady strength can often go unnoticed. This Mother's Day and every day, we honor that strength. Learn more: https://t.co/LysyvFCMKo

[National MS Society @mssociety]

Pain today might feel like a moment of discomfort to finish one last thing, avoid canceling plans or stay longer at work.

Tomorrow, it might return as a flare-up, stiffness or lost mobility. Pain isn't something to defeat, it's a sign to rest, slow down and ask for support.

[National MS Society @mssociety]

"I never believed that motherhood and MS could coexist. But now, I see how beautifully they can — and how much strength, joy, and clarity this chapter of life has brought me."
— Myra Q.

[National MS Society @mssociety]

On May 14 at 12:00 p.m. ET, the National MS Society will host its next MS Activist Webinar. You'll learn more about the Society's advocacy efforts to protect funding across the federal budget.

Register now and to learn how you can help fuel progress: https://t.co/uPv4O9Y4lK

[National MS Society @mssociety]

Fernando Mendoza knows what really matters.

As the #1 draft pick, he skipped the live ceremony to celebrate at home with his mom, Elsa, whose MS makes travel difficult.

The biggest moments are about who you share them with. Watch the full story from @NBCNews: