Multiple Sclerosis Foundation

Be part of an exciting virtual Q&A session featuring Dr. Ben Thrower, the Andrew C. Carlos MS Institute Medical Director at Shepherd Center. Scheduled for Tuesday, April 8th at 4:30 pm EST, this is a fantastic opportunity to tap into Dr. Thrower's wealth of knowledge on multiple sclerosis. Make sure you don't miss it—register today! 🧠 msfocus.us/Thrower0425

For #National DoctorsDay, we’re proud to honor two visionary leaders in MS care: Dr. Ben Thrower from the Shepherd Center and Dr. Aaron Boster from The Boster Center for Multiple Sclerosis. Their work goes beyond the clinic — driving research, building support networks, and inspiring hope for many living with multiple sclerosis. We asked them what inspires their work, what advances give them the most hope, and how patient-centered nonprofits like MS Focus help bridge the gap. Their insights remind us why we do what we do. ➡️ Swipe through to read their reflections, and join us in thanking all MS care professionals for their dedication.

We’re proud to partner with Sharecare this National MS Education and Awareness Month to raise awareness and advocate for those impacted by multiple sclerosis. MS is the most common progressive neurological disease in young adults, affecting nearly four times as many women as men. Thank you, Sharecare, for helping us spotlight how mindfulness, exercise, and proper nutrition can empower people with MS to manage symptoms and improve quality of life.

All MS is progressive MS. Even if someone experiences relapsing-remitting MS (RRMS), unseen progression is likely happening. Primary progressive MS (PPMS) is a distinct form of the disease, affecting about 10-15% of people with MS from the start, without relapses but with steady worsening of symptoms. While treatment options for PPMS are limited, research is ongoing, and new treatments bring hope for slowing progression in all forms of MS. Let's raise awareness today on #ProgressiveMSDay and beyond and push for more breakthroughs

A new study presented at #ACTRIMS2025 highlights a promising MS risk score model that could help with early screening and diagnosis. Researchers stress the need for more research in underserved communities to ensure better accuracy for everyone. #MSNews Read our full report: msfocus.us/model

Join us for a live session on Wednesday, April 2nd, at 3:00 pm EST with Cherie Binns, RN, MSCN, as she shares valuable insights and tips on managing MS symptoms. Cherie will address fatigue, pain, cognitive issues, and more. Don't miss this opportunity to learn from our experienced Health Liaison. Secure your spot today at msfocus.us/Binns0425

"The results of your neck MRI are fine. But your brain MRI shows lesions… You have MS." "It was October 2017, and those words changed everything. I had been called into the office early that morning, and when my nurse practitioner asked if I was angry, my response was simple: "No, I'm relieved." After years of unexplained aches and pains, I finally had an answer. From that moment, things moved quickly. I had to retire from my career—I could no longer give 100% like I used to. But instead of letting MS stop me, I chose to learn everything I could. I researched, joined a support group, and when the pandemic hit, I created my own online community for people with MS. It gave those of us who couldn't get out often a place to connect. Through advocacy, MS walks, and online exercise groups, I've met some of the most incredible people—people who get it. We may all have the same diagnosis, but we experience MS in different ways. Still, we understand each other in a way few others can. MS changed my life, but it didn't take it away. If something doesn't get done today, it will happen tomorrow. If today isn't great, tomorrow will be better. Rest is no longer something to feel guilty about—it's something I embrace. MS isn't just a game changer—it's a life changer. And I'm still living mine." ~ Deborah Hynes, Diagnosed 2017 #MYMSStory #NMSEAM2025 #TheWholePicture

Life with MS means learning to adapt, not giving up. Whether it's a mobility aid, a tech tool, or a simple routine change, the right adaptation can make all the difference. What’s one tool or adjustment that’s helped you navigate daily life with MS? Share your experience! #NMSEAM2025 #TheWholePIcture

Are you caring for a loved one living with MS? In this week's Real Talk, find out how the Caregiver Help Desk connects families with life-changing support. 📆 Tuesday, March 25 -- 1:00 p.m. EST 💡 Topic: Caregiving & MS ❇️ Featuring: Kasey Minnis, Executive Director, Multiple Sclerosis Foundation with Real Talk Host Nichole Goble, CAN’s Director of Community Initiatives ***** Real Talk is a weekly Facebook Live session exclusively for Caregiver Action Network Community members. It offers valuable insights on caregiving topics. If you’re not yet a member, join us here: https://lnkd.in/eiw2kqTW

🌸 Spring is here! As the season changes, it’s the perfect time to step outside, breathe in fresh air, and embrace self-care. Whether it’s a short walk, gentle stretching in the sunshine, or simply enjoying nature, small moments outdoors can help manage MS symptoms and boost your well-being. How do you practice self-care in the spring? Drop your favorite tips in the comments! #NMSEAM2025 #TheWholePicture