iConquerMS @iConquerMS

iConquerMS: Empowering the #MS community to drive #MultipleSclerosis research. Join the online platform dedicated to fighting MS. Together, we can conquer MS! iconquerms.org Waltham, MA Joined March 2014

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iConquerMS @iConquerMS

10 hours ago

✨ What gives you the most hope when it comes to MS research? New treatments? Innovative technologies? Patient-driven studies? Drop your thoughts below—we want to hear from you! #MultipleSclerosis #MSResearch

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iConquerMS @iConquerMS

2 days ago

The gut is home to trillions of microbes — and some may hold keys to treating MS. Explore how gut bacteria like Prevotella histicola could change the way we approach immune balance in MS. Read more: acceleratedcure.org/bugs-that-heal/ #MultipleSclerosis #MSResearch @AcceleratedCure

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iConquerMS @iConquerMS

3 days ago

Too many groups are left out of MS research — older adults, people with disabilities, LGBTQ+ folks, and racial minorities. This limits what we know. The August @AcceleratedCure newsletter snapshot looks at how to change that: acceleratedcure.org/august-newslet… #ms #msResearch

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iConquerMS @iConquerMS

a week ago

When people with MS, caregivers, & researchers work together, the science changes. iConquerMS creates a direct line between lived experience & lab research — making sure studies address real challenges faced every day. Join: iConquerMS.org #MultipleSclerosisResearch #MS

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iConquerMS @iConquerMS

2 weeks ago

The latest iConquerMS Spotlight explores the vital role of caregivers and ways we can better meet their needs. What’s one thing YOU think could make a caregiver’s day easier? acceleratedcure.org/july-2025-icon… #MultipleSclerosis #MSCare @AcceleratedCure

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iConquerMS @iConquerMS

2 weeks ago

When you join iConquerMS, the data you share — through surveys or study participation — is combined with thousands of others’ experiences. Researchers use it to spot patterns, identify urgent needs, & design studies that answer your questions about MS. #MSresearch #MS

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iConquerMS @iConquerMS

2 weeks ago

Trials and Triumphs reflects on lessons from history and how they can guide a more inclusive, transparent future for MS research. What do YOU think helps build trust between researchers and participants? acceleratedcure.org/trials-and-tri… #MultipleSclerosis #MSResearch @AcceleratedCure

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iConquerMS @iConquerMS

2 weeks ago

MS research needs your perspective. Joining iConquerMS means contributing through surveys and studies that reflect the real experiences of people living with #MultipleSclerosis. Get started at iConquerMS.org #MSresearch @AcceleratedCure

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iConquerMS @iConquerMS

2 weeks ago

A Patient-Powered Research Network means YOU help set the research agenda. In iConquerMS, people living with MS suggest research questions, review study ideas, & share data that drives discoveries. iConquerMS.org #MultipleSclerosisResearch #MS

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Jon Strum @RealTalkMS_jon

3 weeks ago

realtalkms.com/415 What are the first steps someone living with MS should take in their financial planning journey? We’re sharing the details on RealTalk MS. #MultipleSclerosis

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iConquerMS @iConquerMS

3 weeks ago

Want to join #MultipleSclerosis research from home? This month’s Research Spotlight features studies on fatigue, exercise, mobility, and mood — many you can do remotely. Your voice matters in shaping the future of MS care. acceleratedcure.org/july-2025-rese… #MSResearch @AcceleratedCure

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iConquerMS @iConquerMS

3 weeks ago

Accessibility matters everywhere — from how we move through public spaces to how we access information. If you could make ONE accessibility change universal, what would it be? Reply below ⬇️ #Accessibility #MultipleSclerosis

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iConquerMS @iConquerMS

3 weeks ago

Decentralized clinical trials (DCTs) are making #MS research more accessible than ever — reducing barriers like travel, mobility, and time so more people can participate. Your voice matters in shaping the future of care. acceleratedcure.org/every-voice-ev… @AcceleratedCure #MSResearch

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iConquerMS @iConquerMS

4 weeks ago

Critical data = critical progress. 🧡 When people with MS share their experiences through iConquerMS, researchers gain the insights they need to accelerate discoveries and improve treatments. Be part of the change: iConquerMS.org #MultipleSclerosisResearch #MS

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iConquerMS @iConquerMS

4 weeks ago

In 1951, Henrietta Lacks’ cells were taken without consent — yet became the foundation for medical breakthroughs. Her story shows why ethics, trust, and diverse voices matter in MS research. acceleratedcure.org/trials-and-tri… #MultipleSclerosis #MSResearch @AcceleratedCure

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iConquerMS @iConquerMS

4 weeks ago

What’s one way you think makes the biggest impact in supporting the MS community? Vote and share your thoughts below ⬇️ #MultipleSclerosis #MSCommunity

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iConquerMS @iConquerMS

4 weeks ago

When you participate, the info you share—about symptoms, daily life, treatments—goes into a secure research database. Researchers use this data to: • identify unmet needs • design better studies • improve MS care for everyone iConquerMS.org #MS #MSResearch

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iConquerMS @iConquerMS

a month ago

Travel. Mobility. Time. These shouldn’t be barriers to MS research. iConquerMS is expanding decentralized clinical trials (DCTs) — making it easier for more people to participate from home. acceleratedcure.org/every-voice-ev… @AcceleratedCure #MultipleSclerosis #MSResearch

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iConquerMS @iConquerMS

a month ago

Too many people are left out of MS research. Older adults, rural communities, people with disabilities, LGBTQ+ folks, and many racial minorities are often missing from trials—limiting what we truly know. acceleratedcure.org/july-newslette… @AcceleratedCure #MultipleSclerosis #MSResearch

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iConquerMS @iConquerMS

a month ago

What drains your energy the most with MS? 💡 Physical activity 🌡️ Heat 😵 Stress 🧠 Cognitive effort Something else? Let us know in the comments! #MSFatigue #MultipleSclerosis