The most comprehensive lab focused on ALS/Lou Gehrig's Disease. We are the Drug Discovery Engine discovering & inventing effective treatments for ALS. #EndALS
Joined September 2010
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Before an ALS therapy reaches a clinical trial, years of research come first.
We're expanding our team and building out a new 33k sq. ft. laboratory to help test more therapies and accelerate progress toward effective treatments.
Thank you for helping make this work possible.
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Join us June 18 at 3 PM ET for an ALS TDI Town Hall featuring David Meissner of Your ALS Guide.
Get a first look at the new ALS Research Guide, designed to help people with ALS and families better understand research and participation opportunities.
🔗 als.net/als-town-hall/
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"There is still a lot of living to be done with the disease."
In a new blog, ALS 100 Chief Inspiration Officer Zach shares how living with ALS led him to the ALS 100 and why he's committed to raising awareness and funds for research.
Read the full blog: als.net/news/l-i-v-i-n-with-…
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Looking for a way to make an impact this June? 💙
Join us at one of our upcoming events, including community fundraisers, educational programs, Kids Quest to Cure ALS, The ALS 100, and the Tri-State Trek.
Check out what's happening this month: als.net/als-events/upcoming/
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As ALS Awareness Month comes to a close, thank you to everyone who shared, advocated, fundraised, & supported ALS research.
Awareness Month may be ending, but the work continues. Every day, our community comes together with one goal: ending ALS.
Thank you for driving progress.
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Why do certain populations face a higher risk of ALS?
Champion Insights is studying elite athletes, veterans, and first responders to better understand how genetics, environment, and lifestyle may influence ALS risk and progression.
Watch more: youtube.com/watch?v=crtIacXX…
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Yesterday, Stuart Chapin began a 3,000 mile ride across the country in honor of his father, who passed away from ALS.
Now through August, he’ll ride from NYC to San Francisco to raise funds for ALS research at ALS TDI.
Read his story: als.net/news/going-the-dista…
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ALS progression looks different for every person living with it. Through the ARC Study, ALS TDI is collecting clinical, biological, and digital data over time to better understand how ALS changes in individuals.
Better data can help guide better trials: als.net/arc/
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Step up to the plate for Lou Gehrig Day âš¾
Our limited-edition ALS TDI baseball shirt is available now for $30. Order soon to receive yours before June 2!
🛒 alstdi.88blue.com/
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ALS research has reached a turning point.
ALS TDI is expanding our scientific team and building a new 33,000 sq. ft. lab to test more ideas, move faster, and help advance more potential treatments toward clinical trials.
Follow along for updates on this landmark expansion.
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Honored to announce Team ALS TDI / @Google Co-Scientist received a #LongitudePrizeOnALS Discovery Award! We'll use advanced AI to find new drug targets and move closer to real treatments.
@mndassociation @ChallengeWorks
Learn more: als.longitudeprize.org/
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ALS is a progressive disease that damages nerve cells that send signals from the brain to muscles. As communication breaks down, people experience muscle weakness, loss of movement, & paralysis.
Our team is working to understand these breakdowns & move research forward faster.
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May is ALS Awareness Month, and we’ve got a great lineup of events to support ALS research. Join us and be part of what moves research forward → als.net/als-events/upcoming/
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Our Fight ALS Film Fest returns for year 5—kicking off ALS Awareness Month.
5 powerful films special guests from each story. Sunny of Sunnystrong and Her ALS Story returns as emcee.
Learn more & register: als.net/als-film-fest/
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