Lou Gehrig’s Disease
Jan 10-31, 2026 | Anywhere in the world The Running Bitcoin Challenge brings together Hal Finney’s love of running and Bitcoin to raise funds and awareness for ALS research in his…
11/20/25 – FOR IMMEDIATE RELEASE LOS ANGELES – The ALS Network, in partnership with 12 ALS United member organizations, announces the selection of its 2025 Research Innovation Grantees—an accomplished group…
Mark your calendars for Giving Tuesday – December 2, 2025. Giving Tuesday is a global generosity movement unleashing the power of radical generosity and a great time to support the ALS…
DALLAS–(BUSINESS WIRE)–The Impossible Dream Machine, an initiative founded by Broadway actor, Grammy-nominated singer, and ALS patient and advocate Aaron Lazar, has announced a groundbreaking collaboration with the Parkland Center for…
Every ticket sold, every cup brewed, and every item worn helps raise vital funds that bring care and hope to the ALS community. Our partners help turn everyday purchases into…
Texas voters Tuesday approved Proposition 14, which creates a state-funded dementia research facility and sets aside money aimed at prevention of the disease. SJR 3 authorizes the state comptroller to set…
Nohea Nakaahiki shares her ALS journey and invites you to the 13th Hawaii Walk & Roll, Oct 11, Kapiolani Park.
Hosted by Aaron Lazar, Actor, Health Advocate, Grammy Nominee, Impossible Dreams Shares Journeys of Hope and Determination LOS ANGELES — October 7, 2025 — Hosted by acclaimed actor, Grammy nominated singer,…
The ALS Network is honored to announce its role as Charity Champion for the inaugural season of the Impossible Dreams podcast, launching on Tuesday, October 7, 2025. Hosted by acclaimed…
LOS ANGELES — September 23, 2025 — The ALS Network is proud to announce that acclaimed actor, Eric Dane, has been named the recipient of the Advocate of the Year…