The ALS Association, established in 1985, is the only national nonprofit organization dedicated to fighting Amyotrophic Lateral Sclerosis (ALS) on multiple fronts. The Association leads global research efforts, provides essential assistance to individuals living with ALS through a nationwide network of chapters, and coordinates multidisciplinary care via certified clinical care centers. By fostering partnerships with government entities, the ALS Association aims to build hope and enhance the quality of life for those affected by ALS while actively pursuing new treatments and a cure.