The ALS Association

Our Mission

To discover treatments and a cure for ALS, and to serve, advocate for, and empower people affected by ALS to live their lives to the fullest.

The ALS Association: What We Do

Established in 1985, The ALS Association is the only national non-profit organization fighting Lou Gehrig’s Disease on every front.  By leading the way in global research, providing assistance for people with ALS through a nationwide network of chapters, coordinating multidisciplinary care through certified clinical care centers, and fostering government partnerships, The Association builds hope and enhances quality of life while aggressively searching for new treatments and a cure.

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 the disease.  The Association’s nationwide network of chapters provides comprehensive patient services and support to the ALS community. The mission of The ALS Association is to lead the fight to treat and cure ALS through global research and nationwide advocacy, while also empowering people with Lou Gehrig’s Disease and their families to live fuller lives by providing them with compassionate care and support.

Office Location

National Headquarters
1275 K Street NW, Ste. 250
Washington, DC 20005
phone: 202-407-8580
fax: 202-464-8869

www.alsa.org

Kansas City area office
6950 Squibb Rd., Ste 210
Mission, KS 66202

(913) 648-2062

Central Kansas office
3450 N. Rock Rd., Ste 211
Wichita, KS 67226

(316) 612-0188

Nebraska office
900 S. 74 PLZ., Ste 106
Omaha, NE 68114

(402) 991-8788

Southern Missouri office
2209 Petrus Cir.
Ozark, MO 65721

(417) 886-5003

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