iConquerMS

iConquerMS: Empowering the #MS community to drive #MultipleSclerosis research. Join the online platform dedicated to fighting MS. Together, we can conquer MS!

[iConquerMS @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 https://t.co/8vaf492z35.

[iConquerMS @iConquerMS]

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

[iConquerMS @iConquerMS]

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

[iConquerMS @iConquerMS]

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

[iConquerMS @iConquerMS]

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

[iConquerMS @iConquerMS]

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

[iConquerMS @iConquerMS]

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

[iConquerMS @iConquerMS]

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

[iConquerMS @iConquerMS]

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

[iConquerMS @iConquerMS]

What’s a common misconception about MS that you wish more people understood?

🧡 Share in the comments!

#MSAwareness #MSCommunity

[iConquerMS @iConquerMS]

😴 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

[iConquerMS @iConquerMS]

🦠 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

[iConquerMS @iConquerMS]

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

[iConquerMS @iConquerMS]

📢 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

[iConquerMS @iConquerMS]

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

[iConquerMS @iConquerMS]

🧩 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

[iConquerMS @iConquerMS]

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

[Jon Strum @RealTalkMS_jon]

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

[Jon Strum @RealTalkMS_jon]

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

[iConquerMS @iConquerMS]

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

[iConquerMS @iConquerMS]

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