Health : Diseases, Disorders, and Disciplines

The ALS Association, National Office

Create a world without ALS

four stars

94.62

1275 K Street, NW. Suite 250
Washington, DC 20005
tel: (888) 949-2577   Web Site
EIN: 13-3271855

Board Leadership
Doug Butcher
Chair

CEO
Barbara Newhouse
President, CEO

  Score
(out of 100)
Rating
Overall Score & Rating 94.62 four stars
  Financial 93.02 four stars
  Accountability & Transparency 97.00 four stars
This rating was published 02/01/2017 and includes data from FY2016, the most recent 990 received at that time.

Leading 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. Mission Priorities 1. Raise the level of awareness of The ALS Association as the leading voice and most trusted source of information about Lou Gehrig's Disease. 2. Lead, direct and/or collaborate on global research to understand the disease, develop treatments and ultimately find a cure. 3. Provide every person with ALS and their families access to high quality, consistent and compassionate support services. 4. Advance a nationwide advocacy program that increases funding for ALS research, improves patient services and empowers the entire ALS community. 5. Function as one organization with unity of purpose. 6. Operate within a business model designed to ensure stability and promote financial strength.

Leading 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. Mission Priorities 1. Raise the level of awareness of The ALS Association as the leading voice and most trusted source of information about Lou Gehrig's Disease. 2. Lead, direct and/or collaborate on global research to understand the disease, develop treatments and ultimately find a cure. 3. Provide every person with ALS and their families access to high quality, consistent and compassionate support services. 4. Advance a nationwide advocacy program that increases funding for ALS research, improves patient services and empowers the entire ALS community. 5. Function as one organization with unity of purpose. 6. Operate within a business model designed to ensure stability and promote financial strength.

Results Information

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This results data is current as of November 2017, when it was provided to us by GuideStar. Results information published on this organization's rating page has no effect on its rating at this time. data iconLearn More

Financial

four stars

93.02

Accountability & Transparency

four stars

97.00

This rating was published 02/01/2017 and includes data from FY2016, the most recent 990 received at that time.
Overall Rating Chart
  Program Expenses
(Percent of the charity's total expenses spent on the programs
and services it delivers)
78.1%
  Administrative Expenses 6.4%
  Fundraising Expenses 15.4%
  Fundraising Efficiency $0.08
  Working Capital Ratio (years) 3.29
  Program Expenses Growth 25.4%
  Liabilities to Assets 6.5%
All data for Financial Performance Metrics calculations was provided by The ALS Association, National Office on recent 990s filed with the IRS.
Joint Cost Allocation Adjustment applied. Learn more.
All data for Financial Performance Metrics calculations was provided by The ALS Association, National Office on recent 990s filed with the IRS.
REVENUE  
Contributions  
   Contributions, Gifts & Grants $22,568,769
   Federated Campaigns $239,873
   Membership Dues $0
   Fundraising Events $359,289
   Related Organizations $0
   Government Grants $319,397
Total Contributions $23,487,328
   Program Service Revenue $115,362
Total Primary Revenue $23,602,690
   Other Revenue $2,042,460
TOTAL REVENUE $25,645,150
   
EXPENSES (Adjusted)  
   Program Expenses $28,250,571
   Administrative Expenses $2,358,153
   Fundraising Expenses $4,853,138
TOTAL FUNCTIONAL EXPENSES $35,461,862
   
Payments to Affiliates $0
Excess (or Deficit) for the year $-9,816,712
   
Net Assets $106,041,180

Charts

Compensation % of Expenses Paid to Title
$303,429 0.85% Barbara J. Newhouse President & CEO

Mission

Leading 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. Mission Priorities 1. Raise the level of awareness of The ALS Association as the leading voice and most trusted source of information about Lou Gehrig's Disease. 2. Lead, direct and/or collaborate on global research to understand the disease, develop treatments and ultimately find a cure. 3. Provide every person with ALS and their families access to high quality, consistent and compassionate support services. 4. Advance a nationwide advocacy program that increases funding for ALS research, improves patient services and empowers the entire ALS community. 5. Function as one organization with unity of purpose. 6. Operate within a business model designed to ensure stability and promote financial strength.

Highly Rated

Charity Name & State Overall Score Overall Rating
The ALS Association, National Office (DC) 94.62 four stars
The ALS Association Florida Chapter (FL) 93.98 four stars
The ALS Association Connecticut Chapter (CT) 92.21 four stars
The ALS Association, St. Louis Chapter (MO) 95.24 four stars
The ALS Association Western Pennsylvania Chapter (PA) 92.22 four stars

Compare These Charities (Highly Rated)

Charity Contact Info

The ALS Association, National Office
1275 K Street, NW.
Suite 250
Washington, DC 20005
tel: (888) 949-2577
fax: (202) 289-6801
EIN: 13-3271855

Visit Web Site

Board Leadership

Doug Butcher
Chair

CEO

Barbara Newhouse
President, CEO