What is @iConquerMS? How does it work? How can you be part of #MS research and help researchers work towards cures for multiple sclerosis? WATCH this short video to find out how you can help us #EndMS. You can also learn more or join by visiting https://t.co/8vaf492z35.

MS research is moving forward every day — from new therapies to better understanding of the immune system. 💬 What gives you the most hope about where MS research is headed? #MSResearch #MultipleSclerosis #MSCommunity

Stir up the group chat with a "let’s go to Florida this weekend 😎”

Kids and teens can have MS too — and their experiences matter. iConquerMS makes sure young voices are represented in research shaping tomorrow’s treatments. 🔗 Learn more: https://t.co/kegBoNNLPs #MSResearch #MultipleSclerosis

Too many voices are still missing from MS research — people of color, older adults, rural residents, and those with diverse gender identities. The MS Minority Research Engagement Partnership Network is changing that. 🔗 https://t.co/mSwEzymiAc #MSResearch #HealthEquity #MS

Accessibility shouldn’t depend on where you live. What’s one change you wish you could see everywhere — ramps, captions, quiet spaces, better signage, or something else? ♿️ Reply and share your ideas ⬇️ #Accessibility #MultipleSclerosis #DisabilityInclusion

There's a spirit of revival stirring in America. Dinesh D'Souza's new film, The Dragon's Prophecy, is part of that movement. Based on Jonathan Cahn's No.1 bestseller, the film reveals how war, politics and the Bible converge in a way that we need to make a choice. Watch on GJW+.

Not all MS symptoms are visible. Fatigue, cognitive fog, pain, mood changes — these challenges can be hard to explain but deeply affect daily life. 💬 What’s one invisible symptom you wish more people understood? #MultipleSclerosis #InvisibleIllness #MSAwareness

MS can affect people at any age — but most are diagnosed between 20 and 40, when life is full of work, family, and responsibilities. How old were you when you were diagnosed? #MultipleSclerosis #MSResearch

People from minority communities are often left out of MS clinical trials. When studies lack diversity, results can miss how treatments work across different groups — making care less effective for everyone. Inclusion makes research stronger. #MultipleSclerosis #MSResearch

Creative expression isn’t just art — it’s therapy. Studies show that painting, music, and dance can reduce fatigue, boost mood, and help people with #MS manage symptoms. Read about how creativity supports healing: https://t.co/HvjDs91Evc #MSResearch @AcceleratedCure

What’s a common misconception about MS that you wish more people understood? 🧡 Share in the comments! #MSAwareness #MSCommunity

😴 Nearly 80% of people with MS experience fatigue — but it’s more than being tired. It can strike suddenly, drain energy unpredictably, and disrupt daily life. Read ACP’s "Fresh MS Insights": https://t.co/Eipvi4F8ed #MultipleSclerosis #MS @AcceleratedCure

🦠 Did you know the microbes in your gut may play a role in MS? Researchers are studying how the microbiome could unlock new ways to manage symptoms — and even improve treatments. Read more: https://t.co/HGkitKhqw1 @AcceleratedCure #MSResearch #MultipleSclerosis

For many people, MS is diagnosed in their 20s or 30s — right when careers, families, and responsibilities are taking shape. Research must reflect these real-life challenges. ➡️ Learn how you can take part: https://t.co/F7yFNCPNP7 #MSResearch #MultipleSclerosis

📢 Here’s your chance to tell the FDA what matters most in MS treatment. Take the Shaping Tomorrow Together survey 📝 and share your experience — your voice will help shape future therapies. 👉 Learn More: https://t.co/IxkFygI2RF @AcceleratedCure @mssociety #MSResearch

MS affects people of all backgrounds, but clinical trials often lack diversity. When minority groups are left out, results miss differences in symptoms, treatment response, and access to care — making research less accurate. https://t.co/F7yFNCPNP7 #MSResearch #MultipleSclerosis

🧩 Trust, diversity, transparency — what would give you the most confidence in MS research? Let’s compare our experiences and ideas — your perspective could help others see research in a new way. Share YOUR thoughts in the comments! 👇 #MultipleSclerosis #MSResearch

Fatigue, mobility, quality of life — these priorities often don’t appear in trial data. The Shaping Tomorrow Together survey brings your perspective to the FDA this fall as they discuss future therapies. Share your voice 👉 https://t.co/le48MTbJ4w @mssociety #MSResearch #MS

https://t.co/G5TYSwaJKV Tomorrow: The National MS Society’s New to MS: Navigating Your Journey program! We’re telling you how to register on RealTalk MS. #MultipleSclerosis @nmss

https://t.co/G5TYSwaJKV Just 2 days away: The National MS Society’s New to MS: Navigating Your Journey program. We’ve got all the details on RealTalk MS. #MultipleSclerosis @nmss

Fatigue is one of the most disabling MS symptoms. The CAFE-MS study is testing an online program to ease fatigue & improve life for people with MS. Learn more 👉 https://t.co/dbVBfwBlvm @AcceleratedCure #MSResearch #MultipleSclerosis

Did you know heat can temporarily worsen MS symptoms? This reaction, called Uhthoff’s phenomenon, can make fatigue, vision, or mobility issues flare when body temperature rises. #MultipleSclerosis #MSResearch