HEALEY ALS Platform Trial

Join the Project ALS family and support critical research. Chris Combs, husband, father of 3, and former pitcher for the North Carolina State Wolfpack and Pittsburgh Pirates, was diagnosed with ALS in 2016. Watch his story and donate to Project ALS research now to bring us closer to a cure. | Project ALS

✨ NEW SEATS ADDED ✨ A night to push ALS research forward while enjoying unique performances from Broadway legends such as Aaron Lazar, Andrew Rannells, Sara Bareilles, Kate Baldwin, Norm Lewis, Adam Pascal, Anthony Rapp and a guest appearance from Muniba Mazari. Mark your calendars for October 22nd at City Winery in New York City and be a part of creating a future free of ALS. Doors open at 6:30 PM. Join the experience today with tickets starting at $200: https://bit.ly/3ZdmnXY ALS is an aggress

ALS drugs are near. Project ALS has built a Pre-Clinical Core at Columbia University, an ALS drug-testing initiative, that utilizes 20 years of research breakthroughs to create and test drugs more accurately, and deliver the most promising of them to clinical trial. Read about the Core at projectals.org/our-research and help us bring drugs to clinical trial in 2019. Give today: https://fundraise.projectals.org/give/211906/#!/donation/checkout | Project ALS

Last month we shared an article outlining the results of the first-in-human study of jacifusen, which showed a halt in FUS-ALS disease progression. This month, we’re breaking down the science so that everyone can understand just how exciting this development is and its implications on the broader ALS community. Thank you to those who made this possible: Project ALS researchers, especially Dr. Neil Shneider, co-director of the Project ALS Therapeutics Core at Columbia; Ionis; Charles River; and,

Jenifer Estess was a 35-year-old New York theater and film producer who was diagnosed—out of nowhere--with ALS. Her doctors told her to max out her credit cards and eat junk food—because they had no medicine to give her for ALS, a fatal brain disease. Jenifer made another choice. With her sisters, family and friends, she founded the non-profit Project ALS. Jenifer’s vision was to unite competing scientists to work together toward the first effective treatments. Project ALS built the world’s firs

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SoulCycle goddess and Project ALS board member Stacey Griffith is taking a vow of silence for #DontTalkAThon2017 — are you? Join us for the Don’t Talk-a-Thon on Sunday, May 21 and help us raise vital funds for ALS research. Register at DontTalkAThon.org and pledge to take a one-hour (or more!) vow of silence to honor those who are robbed of their speech by this devastating disease. Ask friends, family, colleagues, and online/offline supporters to sponsor you. 100% of funds raised through the Don

This holiday season marks twenty years since Project ALS founder Jenifer Estess died from ALS. Those closest to her always—and will forever—believe that we can solve the ALS puzzle together. Simon Halls, Jenifer's dearest friend, and member of the Project ALS board of directors, asks for your partnership at year's end. Let's finish this. Give today: https://bit.ly/3FOKuRy | Project ALS