✨ 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

Today is Giving Tuesday, a global day of giving. Your donation, no matter the size, makes a significant impact on critical ALS research. Throughout the day, you'll hear from our researchers how your support makes their work possible, and what it could mean for people living with ALS. Join us in the fight against ALS: https://bit.ly/projectals24 #GivingTuesday #GivingTuesdayCountdown #ALSawareness #ALSResearch #ALS | 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

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

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Meet Brooke Eby, a Her ALS Story member, current fighter against ALS, and a new friend of Project ALS. Brooke gives us a glimpse into what her everyday life looks like living with ALS, and her optimism and bright spirit shine through. Her strength drives Project ALS to work even harder to find treatments, and a cure, for ALS. Your support helps people living with ALS, like Brooke, get closer to an ALS-free future. | Project ALS

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