iConquerMS

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 iConquerMS.org.

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

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: iConquerMS.org/KidsAndTeens #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. 🔗 acceleratedcure.org/every-voice-ev… #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

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: acceleratedcure.org/creative-heali… #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": acceleratedcure.org/fresh-ms-insig… #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: acceleratedcure.org/july-2025-rese… @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: iConquerMS.org #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: acceleratedcure.org/august-2025-re… @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. iConquerMS.org #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 👉 s.alchemer.com/s3/Perspective… @mssociety #MSResearch #MS

realtalkms.com/419 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

realtalkms.com/419 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 👉 acceleratedcure.org/july-2025-icon… @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