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The ALS Association

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The ALS Association was founded in 1985 to serve the needs of those living with Amyotrophic Lateral Sclerosis and their caregivers. The mission of The ALS Association is to discover treatments and a cure for ALS, and to serve, advocate for, and empower people affected by ALS to live their lives to the fullest.

The ALS Association is the only national not-for-profit health organization dedicated solely to the fight against ALS. ALSA covers all the bases — patient and community services, research, public education, and advocacy — in providing help and hope to those facing the disease. Our vision is to create a world without ALS.

The ALS Association focuses on helping patients and families live with ALS while supporting research and advocacy programs.

Individuals

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Recent donors

Recent donors
Date Name Amount
Dec 15 Anonymous Undisclosed amount
Nov 12 Kelly Clymer Undisclosed amount
Sep 08 Anonymous Undisclosed amount