Health : Diseases, Disorders, and Disciplines

The ALS Association, National Office

Create a world without ALS

three stars

88.85

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

Board Leadership
Sue Gorman
Chairman

CEO
Calaneet Balas
President, CEO

  Score
(out of 100)
Rating
Overall Score & Rating 88.85 three stars
  Financial 84.52 three stars
  Accountability & Transparency 97.00 four stars
This rating was published 11/01/2019 and includes data from FY2019, 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.

Impact Information

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This impact information is current as of September 2019, when it was provided to us by GuideStar. At this time, Impact information published on this organization's page has no effect on its rating per our methodology.

Financial

three stars

84.52

Accountability & Transparency

four stars

97.00

This rating was published 11/01/2019 and includes data from FY2019, 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)
81.4%
  Administrative Expenses 6.0%
  Fundraising Expenses 12.5%
  Fundraising Efficiency $0.16
  Working Capital Ratio (years) 2.51
  Program Expenses Growth -0.4%
  Liabilities to Assets 6.1%
All data for Financial Performance Metrics calculations was provided by The ALS Association, National Office on recent 990s filed with the IRS.
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 $27,267,200
   Federated Campaigns $153,834
   Membership Dues $0
   Fundraising Events $1,628,674
   Related Organizations $0
   Government Grants $379,992
Total Contributions $29,429,700
   Program Service Revenue $146,365
Total Primary Revenue $29,576,065
   Other Revenue $-2,510,363
TOTAL REVENUE $27,065,702
   
EXPENSES  
   Program Expenses $27,872,039
   Administrative Expenses $2,664,289
   Fundraising Expenses $4,353,885
TOTAL FUNCTIONAL EXPENSES $34,890,213
   
Payments to Affiliates $0
Excess (or Deficit) for the year $-7,824,511
   
Net Assets $90,438,715

Charts

Compensation % of Expenses Paid to Title
$300,317 0.86% Calaneet Balas 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) 88.85 three stars
The ALS Association Western Pennsylvania Chapter (PA) 90.46 four stars
The ALS Association Connecticut Chapter (CT) 88.45 three stars
The ALS Association, St. Louis Chapter (MO) 95.43 four stars
The ALS Association Greater New York Chapter (NY) 97.52 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

Sue Gorman
Chairman

CEO

Calaneet Balas
President, CEO