Joined March 2014
AnswerALS retweeted
Rebel was nominated by Steve Gleason to take the Ice Bucket Challenge Follow Rebel on Instagram: instagram.com/rebeltanea?igs… ALS Support Organization, Lou Gehrig's Disease & ALS Resources Washington DC - I AM ALS share.google/y6fG2oldxoOwWnj…
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Sponsor Spotlight: @AnswerALS . Through the Neuromine platform (the world’s largest open-access ALS resource) @AnswerALS provides advanced iPSC lines from 1,000+ participants, paired w/deep multi-omics data, to model disease, uncover subtypes, and identify therapeutic targets.
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AnswerALS retweeted
ALS TDI is launching Champion Insights with @AnswerALS & @AugiesQuest to uncover why elite athletes & military members face higher ALS risk — and how this can lead to better treatments. Former NFL player Steve Gleason will be participant #1. Learn more: als.net/news/united-for-answ…
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Replying to @AnswerALS
@AnswerALS executive director Clare Durrett says, “This is more than a research partnership, it’s a strategic investment in the future of ALS discovery.” See how: bit.ly/4ocPe8M #ALS #ALSResearch #ALSNews #ALSCommunity #ALSTreatment #AIinHealthcare
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#LongitudePrizeOnALS The £7.5 million (~$10 million) Longitude Prize on ALS incentivises the use of artificial intelligence-AI-based approaches to transform drug discovery for amyotrophic lateral sclerosis, the most common form of motor neurone disease-MND linkedin.com/posts/krzysztof…
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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 joy carved from pain. Every story echoed how Team Gleason has helped and inspired them. I’m grateful for their words and for the state’s support for the ALS community and in efforts to end the disease through Answer ALS. No White Flags.
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The Longitude Prize on #ALS launches June 25th! Ahead of that launch, join @trisdyson & @Rothstein_Lab at #BioITExpo to learn more about #AI for ALS/#MND. The Prize will support global innovation with access to the largest datasets in ALS #openinnovation #drugdiscovery #biotech #pharma #neurodegeneration #BioIT2025
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I encourage everyone to listen to today's opening comments today from @DrTedros. He outlines exactly what U.S. abdication of global health leadership will mean for the world, and for Americans too. The WHO needs the U.S. And the U.S. needs the WHO. xitter.cf/i/broadcasts/1LyxBWmvR…
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Guys, pls have a look at the Neuromine Data Portal, Answer ALS’s most comprehensive clinical, genetic, molecular, and biochemical assessment of ALS. These are the data bricks for a fully operational StemVAULT™️ application at Prepaire LAM. Using IPSC and organs-organs-on-a-chip for disease modeling. Opening summer 2025’ @Prepaire_labs This groundbreaking resource not only sheds light on the disease's complexity but also: •Offers an unprecedented understanding of ALS progression and its various forms. •Equips researchers with data to uncover new therapeutic approaches. •Bridges the gap between raw scientific data and actionable insights for patients and caregivers. •Empowers public awareness and education, helping demystify this challenging disease. @moldev @alsassociation @AnswerALS dataportal.answerals.org/hom…
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ALS is missing from the headlines today about roberta flack. she lived with the disease for the past two/three years, and it cruelly stole her voice first. rip, queen.
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The Steve Gleason Game Changer Gala 🎭 Saints Legend @SteveGleason, @TeamGleason, and @AnswerALS hosted the Game Changer Gala to raise funds for ALS research and patient empowerment 💛 📸 neworlns.co/3WQbNUJ
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There is still time to register for our upcoming live webinar on Nov. 21! Moderated by an ALS advocate and volunteer, join two people living with ALS as they share their personal ALS experiences. Register now: bit.ly/4dzYvBq
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Interesting presentation from @DGateLab of @NUFeinbergMed using data from @AnswerALS looking at cell type changes in #ALS spinal cords.
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I went to see Steve Gleason while in New Orleans today. He’s home from the hospital (following an infection) and was outside basking in the beautiful day. After our story aired on @CBSMornings, Steve’s book shot up from 10,000, on the Amazon list, to nearly 100. Here’s the full interview: youtu.be/aflvYUOMgic?si=MaRy…
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13 years ago, former @Saints player @SteveGleason was diagnosed with ALS — & now, he’s detailing his death-defying journey in a memoir. “This body may be a prison, but my mind is free,” Gleason told @davidbegnaud in what David describes as one of the most moving interviews he’s ever done. Cc: @TeamGleason @CBSMornings @CBSNews
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Through adversity, we find our Heroes. Some of our care crew have been with me since 2011. They’ve been with us through the darkness and the light. They were with me in the ambulance Wednesday as we navigated the precipice. They changed their daily schedules to stay with me at the hospital, and because of their service, I am the luckiest man on the face of the earth. Infinite Gratitude & Love
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Former @Saints player @SteveGleason and his wife Michel inspire others through their work supporting ALS research with @TeamGleason. Gleason was diagnosed with ALS in 2011. Monday, @DavidBegnaud shares their conversation on living, dying and mindfulness around it all.
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