Join us Tuesday, March 25, at 8 p.m. ET for the livestream debut of ALS Matters—a new series of conversations led by the ALS community, for the ALS community. Hosted by Cory Mosley, who is living with a genetic form of ALS, this powerful first episode dives into how ALS has impacted Cory, his cousins, and the game-changing role of new ALS treatments. Why tune in? Because these conversations matter. Because ALS Matters. Don’t miss it—join us for part one of the first conversation tomorrow night!

ALS is 100% fatal and there is no cure…yet. People living with living ALS need your help now—for care, for research, for hope. Give today to help make ALS livable for everyone, everywhere, until there is a cure. | The ALS Association

2.1K views · 97 reactions | An ALS diagnosis is life changing. Steve from Massachusetts is an ALS advocate and is sharing his experience of what it's like to live with the disease. | The ALS Association | Facebook

Progress takes commitment. In 2007, the ALS Association helped establish the Amyotrophic Lateral Sclerosis Research Program (ALSRP) at the Department of Defense. It is programs like these that are strengthening the fight against ALS through dedicated research and innovation. | The ALS Association