Who created the ALS Association?
Who created the ALS Association?
Robert Lotz
Robert Lotz, a Founder of The ALS Association, Remembered.
What does ALS Association do?
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 ALS and their families to live fuller lives by providing them with compassionate care and support.
How can I help find a cure for ALS?
The ALS Association leads the way in global research and helps 20,000 Americans living with ALS. Your gift today will help find a cure for ALS, while providing care and support to families right here in your community. For your convenience, you can also give by mail or by calling us at 888-949-2577.
Where is ALS Association located?
Washington, D.C.
ALS Association
| Abbreviation | The ALS Association |
|---|---|
| Focus | advocacy and patient services |
| Location | Washington, D.C., U.S. |
| Area served | United States |
| President and CEO | Calaneet Balas |
What percentage of donations go to ALS?
80.3%
| Element | Percentage |
|---|---|
| Administrative | 6.60% |
| Fundraising | 12.90% |
| Program | 80.30% |
Who are the leaders of the ALS Association?
The ALS Association commits over 80% of its annual budget to delivering program services, including research. We have a senior leadership team at the national office that includes individuals with expertise in chapter management, communications and marketing, care services, public policy and finance.
Where to find the ALS Association Greater Philadelphia chapter?
Visit www.ALSmonthlygift.org today! A heartfelt Thank You to the Chapter’s invaluable volunteers who enable us to give help and hope to those whose lives have been touched by ALS. Each month one outstanding volunteer who goes above and beyond is recognized for this honor.
What does the ALS Association evergreen chapter do?
The Evergreen Chapter supports people living with ALS and their loved ones through services and education. We leave no stone unturned in search for the cure of this progressive neurodegenerative disease. 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.
Is there an ALS chapter in Nebraska or Kansas?
The Mid-America Chapter supports people living with ALS and their loved ones through services and education in Kansas, Nebraska and Western Missouri. We leave no stone unturned in search for the cure of this progressive neurodegenerative disease.