Established in 1985, The ALS Association (Amyotrophic Lateral Sclerosis Assn) is the only national nonprofit organization fighting ALS on every front.
Advocacy Partners
We are honored to partner with nonprofit advocacy organizations to amplify their missions, share helpful resources, and ensure patients and families have access to information that supports everyday decision-making. The information featured below was provided by our advocacy partners as part of this collaboration.
Muscular Dystrophy Association (MDA) is the #1 voluntary health organization in the United States for people living with muscular dystrophy, ALS, and over 300 related neuromuscular conditions.
The ALS Network – Your connection to care, research, and advocacy. We connect need with support, questions with answers, thought leaders with new ideas, research to funding, and advocates to challenge the status quo.