The ALS Association is the only national not-for-profit health organization dedicated solely to lead the fight against ALS. The 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 mission of The ALS Association is to lead the fight to cure and treat ALS through global, cutting-edge research, and to empower people with Lou Gehrig's disease and their families to live fuller lives by providing them with compassionate care and support.
The ALS Advocacy Support Community connects patients, families, friends and caregivers for support and inspiration. The ALS Advocacy Support Community is sponsored by The ALS Association in partnership with Inspire.
The ALS Association
601 Pennsylvania Avenue, NW
Suite 900, South Building
Washington, DC 20004
Phone: (877) 444-ALSA
Fax: (202) 638-6316
advocacy@alsa-national.org
www.alsa.org
Inspire connects patients, families, friends, caregivers and health professionals for health and wellness support. Inspire works with trusted health partners to build safe and secure health and wellness groups.
"We believe no one should have to go it alone, we all need a safe place to talk, and we can help one another." More about our work.