The ALS Association is the only national not-for-profit health organization dedicated solely to the fight against ALS. ALSA covers all the bases — research, patient and community services, public education, and advocacy — in providing help and hope to those facing the disease. The ALS Association's mission is to empower people with Lou Gehrig's disease and their families to live fuller lives by providing them with compassionate care and support, and to lead the fight to cure and treat ALS through global, cutting-edge research. We work together to accomplish our mission. The Evergreen 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 and materials.
