Program areas at ALS
Patient and community services: The Association is committed to providing fully developed, managed and evaluated programs and services to people living with Als, families, caregivers and professionals across The united states. Programs incorporate The perspectives from key stakeholders including people living with The disease, subject matter experts, clinical best practice, caregivers, technology, academicians and research. Activities address current needs and explore future services, creating a foundation for innovative and advanced program development based on specific community needs and knowledge advancements. Specific activities include 1) developing and implementing clinical and professional education programs based on ongoing needs assessments and best practice; 2) implementing certified care center certification and recertification programs based on nationally-recognized standards of practice, including grants to support centers of excellence; 3) developing strategies and actualizing plans to deliver care through other than certified centers; 4) providing current information, resources and referrals to The communities we serve; and 5) developing and implementing comprehensive, consistent programs and services that address individual, family, and caregiver needs based on 'best practice and available resources.
Public and professional education: The Association's public policy department develops awareness and understanding of Als and The work of The Association among The general public, healthcare professionals, The scientific community, and elected and other government officials. For The year ending january 31, 2023, The Association worked with congress to continue funding for The national Als registry and The Als research program at The department of defense as well as funding for Als research at The national institutes of health. In addition, The advocacy department secured funding from state governments for care and support of people living with Als.
Research programs - The Association funds scientific research grants to doctors/scientists to find The cause and cure of Amyotrophic Lateral Sclerosis (Als).
Who funds ALS Association (ALS)
Grants from foundations and other nonprofits
Personnel at ALS
Name | Title | Compensation | Date of data |
---|
Calaneet Balas | President and Chief Executive Officer | $456,666 | 2024-09-22 |
Greg Mitchell | Chief Financial Officer | $306,968 | 2024-09-22 |
Tina Zeff | Chief Operations Officer / Executive Vice President , Development | $308,028 | 2023-01-31 |
Gregory Mitchell | Chief Financial Officer | $218,987 | 2023-12-13 |
Brian Frederick | Chief Marketing and Communications Officer | $224,926 | 2024-09-22 |
...and 21 more key personnel |
Financials for ALS
Revenues | FYE 01/2023 | FYE 01/2022 | % Change |
---|
Total grants, contributions, etc. | $53,676,289 | $37,557,524 | 42.9% |
Program services | $0 | $0 | - |
Investment income and dividends | $1,849,992 | $2,158,934 | -14.3% |
Tax-exempt bond proceeds | $0 | $0 | - |
Royalty revenue | $83 | $0 | 999% |
Net rental income | $0 | $0 | - |
Net gain from sale of non-inventory assets | $-78,455 | $54,926 | -242.8% |
Net income from fundraising events | $0 | $0 | - |
Net income from gaming activities | $0 | $0 | - |
Net income from sales of inventory | $0 | $0 | - |
Miscellaneous revenues | $119,699 | $21,419 | 458.8% |
Total revenues | $55,567,608 | $39,792,803 | 39.6% |
Organizations like ALS
Organization | Type | Location | Revenue |
---|
National Multiple Sclerosis Society | 501(c)(3) | New York, NY | $149,451,246 |
Epilepsy Foundation | 501(c)(3) | Bowie, MD | $17,841,214 |
Arthritis Foundation | 501(c)(3) | Atlanta, GA | $68,319,013 |
Parkinsons Disease Foundation Incorporated (PDF) | 501(c)(3) | New York, NY | $48,333,484 |
Muscular Dystrophy Association | 501(c)(3) | Chicago, IL | $59,437,892 |
Autism Speaks | 501(c)(3) | Washington, DC | $36,262,685 |
National Bleeding Disorders Foundation | 501(c)(3) | New York, NY | $19,047,848 |
Susan G Komen | 501(c)(3) | Dallas, TX | $107,597,705 |
Cystic Fibrosis Foundation | 501(c)(3) | Bethesda, MD | $248,630,352 |
Lupus Research Alliance (ALR) | 501(c)(3) | New York, NY | $50,861,497 |
Data update history
September 22, 2024
Updated personnel
Identified 5 new personnel
February 4, 2024
Posted financials
Added Form 990 for fiscal year 2023
Nonprofit Types
Grantmaking organizationsDisease research fundraisersDisease-focused nonprofitsHeadquarter / parent organizationsCharities
Issues
HealthDiseases and disorders
Characteristics
Political advocacyConducts researchLobbyingFundraising eventsPeer-to-peer fundraisingOperates internationallyNational levelReceives government fundingEndowed supportFundraising races, competitions, and tournamentsTax deductible donationsAccepts online donations
General information
- Address
- 1300 Wilson Blvd 600
- Arlington, VA 22209
- Metro area
- Washington-Arlington-Alexandria, DC-VA-MD-WV
- County
- Arlington County, VA
- Website URL
- als.org/Â
- Phone
- (202) 407-8580
- Facebook page
- alsassociationÂ
- Twitter profile
- @alsassociationÂ
IRS details
- EIN
- 13-3271855
- Fiscal year end
- January
- Taxreturn type
- Form 990
- Year formed
- 1985
- Eligible to receive tax-deductible contributions (Pub 78)
- Yes
Categorization
- NTEE code, primary
- G50: Nerve, Muscle, and Bone Diseases
- NAICS code, primary
- 813212: Health and Disease Research Fundraising Organizations
- Parent/child status
- Parent of group exemption
California AB-488 details
- AB 488 status
- May Operate or Solicit for Charitable Purposes
- Charity Registration status
- Current - Awaiting Reporting
- FTB status revoked
- Not revoked
- AG Registration Number
- 059513
- FTB Entity ID
- 1368689
- AB 488 data last updated ("as-of") date
- 2024-11-20
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