ALS Association

Highly Engaged Employees

The ALS Association, founded in 1985, is a leading American nonprofit dedicated to combating amyotrophic lateral sclerosis (ALS), or Lou Gehrig's disease. Operating in the Charitable Organizations & Foundations and Organizations sectors, its mission focuses on funding global ALS research, providing care services through a nationwide network, and advocating for policies benefiting those affected by the disease. The organization is committed to driving progress towards a cure and enhancing the lives of ALS patients.

The ALS Association maintains a significant operational presence with 31 chapters across the United States, each serving distinct geographic areas. This extensive network ensures comprehensive support and program delivery. Employing between 500 and 1,000 individuals, the organization leverages its team to offer patient advocacy, public education, and community support. Further insights into their personnel and leadership can be found at Meet ALS Association's team. Their operations are vital for patient empowerment and care.

With an annual revenue of $72.9 million, the ALS Association strategically allocates funds to cutting-edge research for understanding, treating, and curing ALS, alongside essential patient support programs. Through advocacy, the organization champions state and federal policies to improve access to care and resources. Their comprehensive approach includes providing informational brochures, guiding patient journeys, and fostering community engagement, all contributing to their ultimate goal of eradicating the disease.