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Huge thanks to Microsoft for empowering Neuromine’s open data sharing! You’re helping break barriers to accelerate treatments. Let’s keep revolutionizing collaboration. Read more in the link below! #GAAD #Together to #AnswerALS

Breakthroughs happen because of people like Terri Thompson, Director of Data Management and Program Manager for Multi-Omics at Answer ALS. Discover how Terri’s work is shaping the future of ALS research at 👉 pxl.to/BehindTheMissi…

Is there a connection between ALS and Lyme disease? It’s a common myth. Early symptoms can look similar, which makes it easy to misread. That’s why clinical evaluation and testing by medical professionals are key to getting the right diagnosis. #AnswerALS #LymeDisease

International Clinical Trials Day. The future of medicine is being written in clinical trials today. From life-saving therapies to pioneering discoveries, research paves the way for a future without ALS. Learn more at answerals.org #InternationalClinicalTrialsDay

ALS research needs YOU!  During National ALS Awareness Month help us spread the word, support research, and be part of the movement for answers. Every share, donation, and conversation fuels the fight against ALS.  Donate at: interland3.donorperfect.net/weblink/weblin…

Most research hides behind walls. Not at Answer ALS. The Neuromine Data Portal gives researchers, clinicians, and specialists access to one of the largest ALS datasets ever assembled. Over 2,000 participants and growing. Endless potential for new insights. dataportal.answerals.org/home

Yesterday at the Louisiana State Capitol was a special day. Representatives John Illg and Paula Davis presented House Resolution 160, declaring May as ALS Awareness Month. We met many with friends and family members who have experienced ALS, each sharing stories of resilience and

Solving ALS will not come from doing the same thing, and expecting different results. It takes fresh thinking, better tools, and a lot more data. That’s what Answer ALS is building—and what you can help drive forward. Curious minds welcome: answerals.org #AnswerALS

Today, we remember the heroes who fought for freedom and those who fight ALS with unwavering strength. #MemorialDay #AnswerALS #EndALS

ALS is a complex disease. Understanding it demands coordination, commitment, and action. At Answer ALS, we are calling on new participants, researchers, and collaborators to help uncover critical insights and push research forward. Join the fight at answerals.org

ALS research is driving forward. Not slowly. Not hypothetically. We’re changing what we know and what we can do. Every advancement brings us closer to treatments that can actually make a difference. See what’s happening at answerals.org #ALSResearch #AnswerALS #EndALS

Lou Gehrig. A legend lost to ALS at 37. 82 years later, no cure. No end in sight. On June 3 at T-Mobile Park, Steve Gleason - "Live Impossible" (#37) will throw the first pitch with his son, River. Let’s push for a cure. Learn more: answerals.org #LouGehrigDay #mlb Team Gleason

The clock doesn’t stop. Neither do we. Yesterday afternoon, Steve Gleason and his son Rivers took the mound for #LouGehrigDay in Seattle.  A reminder of what we’re fighting for. Join the movement at answerals.org

Meet NeuroMine. The portal that helps researchers crack ALS. It has opened the door to more than 450 unique research projects thus far, using stem cell data, clinical profiles, and the largest, most diverse ALS dataset ever assembled.  dataportal.answerals.org

ALS doesn’t wait. Neither can we. Every breakthrough in research pushes us closer to real treatments. See how at answerals.org. #EndALS #AnswerALS #NeurodegenerativeDiseases #ALSResearch

Every person living with ALS teaches us something new. Every conversation moves the work forward. Together, we get closer to the answers that matter. #EndALS #AnswerALS

Subscribe to our email list and stay connected to the latest breakthroughs and updates in ALS research. Your support fuels progress, helping to make a difference. Sign up now at answerals.org #EndALS #AnswerALS #ALSResearch

On Father’s Day, we honor the strength, love, and courage of dads, and especially those living with ALS. Even in the face of an unimaginable fight, they continue to show up with resilience, hope, and heart.   Join us in seeking answers to ALS at answerals.org

As our data grows, so does our potential to unlock breakthroughs in ALS research and care. Every new data point brings us closer to understanding the disease, identifying patterns, and developing more effective treatments. answerals.org #EndALS #AnswerALS

Calling all #Neurotech and #BrainHealth startups: Apply now for the 2025 BioChallenge Pitch Competition from @NewOrleansBio. $100K+ in non-dilutive awards. Backed by Answer ALS. Live pitch in New Orleans on Oct 30. Apps close Aug 1. 🔗 neworleansbio.com/save-the-date-…