ALS Association

The ALS Association is a prominent American nonprofit organization committed to combating amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease. Established in 1985, it operates a comprehensive nationwide network of chapters, delivering vital care services and programs to individuals impacted by ALS. A significant portion of its efforts is dedicated to funding global ALS research, with the ultimate goal of discovering effective treatments and a cure. The organization actively engages in advocacy, collaborating with state and federal policymakers to advance policies that benefit those living with ALS.

With 31 locations and an employee range of 500 - 1,000, The ALS Association maintains a substantial operational presence. Its annual revenue of $72.9M enables extensive research initiatives and robust patient support programs. The organization focuses on empowering patients and their families through accessible resources and community engagement. Meet The ALS Association's team to learn more about the individuals driving its critical mission.

The ALS Association prioritizes public education and awareness campaigns to highlight the impact of ALS. It fosters collaboration with diverse stakeholders to achieve its objectives, serving as a central resource for ALS information and support. Its offerings include patient advocacy, compassionate care, public service announcements, and the dissemination of research findings via periodicals and newsletters. The organization operates within a competitive landscape of health foundations, striving for maximum impact in its specialized medical field.