The ALS Association is the only national not-for-profit health organization dedicated solely to the fight against ALS. As the preeminent ALS organization, The Association leads the way in research, care services, public education, and public policy — giving help and hope to those facing this devastating disease.

Together, our Chapter and the National Office operates under a shared mission to serve people living with Amyotrophic Lateral Sclerosis in Tennessee and relentlessly pursue the search for a cure.

The Tennessee Chapter focuses primarily on helping local patients and families live with ALS while the National Office focuses primarily on research and advocacy. The Chapter supports the National Office through revenue sharing and research contributions. The National Office supports the Chapters by providing up-to-date information, national conferences, and professional development.