The ALS Association led the advocacy effort behind The Chris Larkin Act, working alongside legislative champion Rep. Ryan Guillen and advocates across the state to push for this life-changing ...

In this hour of Live at 9: A local couple shares their ALS journey, plus insights from the ALS Association. Midsouth students talk about their award-winning documentaries, and election officials ...

The Walk to Defeat ALS is the ALS Association’s signature event, with funds raised directly supporting innovative research, care services, and advocacy efforts.

LOS ANGELES, May 6, 2025 /PRNewswire/ -- May is ALS Awareness Month, and the ALS Network is committed to raising awareness and understanding of the devastating disease that has no known cure. This ...

Answer ALS is proud to announce the launch of a groundbreaking collaborative initiative aimed at accelerating AI-powered drug discovery for ALS and other neurodegenerative diseases. This effort, known ...

But Brian Wallach and Sandra Abrevaya, the founders of the advocacy group I Am ALS, don’t see it as a particularly difficult balancing act. “We know that these treatments are not cures, ...

Patient advocacy is often visible during FDA advisory committee meetings. The agency usually allows an hour, sometimes more, for members of the public to express support or concerns about the ...

Buffalo Sabres Hall of Famer Danny Gare is joining Buffalo’s Walk to Defeat ALS. On August 3, The ALS Foundation is hosting a walk to support Western New Yorkers living with ALS. The event takes place ...