About Our Chapter
The ALS Association - DC/MD/VA Chapter was founded in 1991 to serve the needs of those living with ALS (Amyotrophic Lateral Sclerosis) and their families throughout Washington, D.C., Maryland and Virginia.
The ALS Association is the only national not-for-profit health organization dedicated solely to the fight against ALS and battling the disease on every front. The ALS Association 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 (National Office and the DC/MD/VA Chapter) operates under a shared mission: to help people living with Amyotrophic Lateral Sclerosis and to leave no stone unturned in search for the cure. On a daily basis staff and volunteers are working diligently to develop programs to make sure that our ALS family can count on the caring, compassionate support of people who understand the daily challenges of living with this disease.
We work together to accomplish our mission. The ALS Association - DC/MD/VA Chapter focuses primarily on providing services and support to those currently living with the disease and their families. 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, support and materials.