National MS Society

While the exact cause of MS is unknown, research is narrowing in on factors like medical history, exposure, and prior illnesses that may increase risk. More from Bruce Bebo, EVP and Chief Research & Medical Affairs Officer at the Society on Real Talk MS: ntlms.org/4bkaZPQ

Maximize coziness, arrange for meals and rides, and expect the unexpected. Brett, a yoga therapist living with MS, shares her top tips for infusion days.

Cutting-edge research from Dr. Arman Eshaghi uses pathophysiology, or functional changes in the body, to categorize different sub-types of MS, providing insights on which treatments might work best for which people. 🎧 More on Real Talk MS with Jon Strum: ntlms.org/40Oo51E

"I want people to know that the journey may be tough, but you're going to be okay." — Orlando P. 7 years after his MS diagnosis, Orlando opened his first restaurant. Last year, he received his first Michelin Star. Photos: Ryan Belk/Wild Common, Easton Porter Group

Living with MS can bring challenges others may never face — sacrificing plans to get rest, having patience when your body doesn't cooperate, and knowing that others won't always understand. We see the strength needed to keep showing up, regardless of what that looks like today.

In a disease like MS that so disproportionately affects women, female voices in research aren’t just important — they’re essential. This Women's History Month, we're celebrating the women scientists changing the landscape of MS research and mentorship for future leaders.

For too many people, managing MS means managing tradeoffs others may never think about. Work and rest, independence and support, hope and fear. While the effects of MS are not always visible, support is. Let’s end MS together. ntlms.org/msawAnnsStory

Just like the effects of MS aren't always visible, progress might not be either. We're teaming up with MS-specialized physical therapist Dr. Gretchen Hawley to talk about the small neural wins that lead to big transformations.

Progress in the care and treatment of MS has led to advancements that make daily life more manageable for the 1+ million people living with it. But with MS, what you see is rarely the whole story. This #MSAwarenessWeek, see MS for what it is. ntlms.org/msawxraiseawar…

Understanding the nervous system's response to inflammation can be as important to slowing MS progression as knowing how and why the immune system targets nerves. Dr. Manuel Friese discusses his research into neural behavior on RealTalkMS with Jon Strum:. ntlms.org/4cdcJLA

MS Activists are champions for change who advance our mission with federal and state policymakers. This month, they're convening on Capitol Hill to make their voices heard and move us closer to a world free of MS. Feeling fired up? Get involved: ntlms.org/becomemsactivi…

Awareness and understanding matter. DIY fundraisers are a way for anyone to turn their passion into extraordinary impact for those living with MS. From karaoke nights to car shows, there's no limit to the ways to get involved. Learn how to get started: ntlms.org/DIY-Fundraising

The impacts of MS extend far beyond what's visible. This #MSAwarenessMonth, we're shining a light on the daily realities that don't show up on the outside. Awareness isn't just knowing MS exists, it's understanding what living with MS truly means.

Did you know some meds can affect how people with MS think and process information? New research found links to improved cognition and others to slower thinking, especially when a few meds are involved: ntlms.org/medsandcogniti… That’s why conversations with your care team matter.

Research shows MS affects the Black community more than previously thought, with unique challenges like delayed diagnosis and limited access to care impacting their support throughout the MS journey. Learn more about how MS affects the Black community at: ntlms.org/msaftsbhmonth

Over the weekend, some of the smartest minds in MS research convened at the ACTRIMS Forum 2026 to exchange knowledge and tackle challenges in MS care and treatment. We're incredibly grateful and proud to partner with those committed to improving outcomes for the MS community.

Migraines and MS share similarities, often starting between ages 20 and 40 and affecting women more than men. Both overlap in symptoms like fatigue and mood changes, as well as in common triggers such as stress. Learn more at: ntlms.org/migrainesandms

"Resilience is my best feature. 🧡 Fifteen years ago, I was battling the news of my MS diagnosis. Since then, I've traveled to 36 countries and embraced my journey. I may not have written this story, but I'm the main character." — Nafisa (@globallistictravel)

“Getting involved in patient advocacy work, I began to speak with Black women and heard the same story over and over again — they had never met another Black person with MS.” — Victoria Learn more at: ntlms.org/victoriaps

"I was blind to MS until the National MS Society." Diagnosed in 2008, Vickie found support, community, and guidance. Now an MS Ambassador, she raises awareness and shows how one story can inspire many.