Program areas at Solve Me CFS Initiative
Research programs - the organization has developed and operates the database platform registry and biobank, an open-sourced research tool it developed that is designed to help advance the research and development of diagnostics and treatments for me/cfs. The organization provided curated research updates by email to approximately 35,000 constituents and continued to expand the database platform registry creating the worlds largest longitudinal me/cfs and long covid database, with nearly 7,000 participants enrolled. Initiated transition to Solve together, state-of-the-art, patient-driven data platform to enable recruitment for clinical studies. Database platform enrolled participants for 2 biomarker studies with external collaborators. The organization also provides scientific research grants for scientists and doctors to find causes and ways to treat and cure post infection diseases like me/cfs and long covid. During the year ended june 30, 2023, the organization awarded ramsay research grants to 6 scientists at organizations in the us, netherlands, and the uk, cont. On sch. O
Advocacy and communication. The organization works with the us congress to increase funding for me/cfs research by the national institute of health nih, center for disease control cdc and the department of defense. During the year ended june 30, 2023, more than 350 advocates participated in over 220 virtual meetings with members of congress and their staff and over 6,300 virtual connections were made in support of the organizations advocacy goals. In addition, the organization launched a major national awareness campaign. Developed a tv and radio public service announcement psa describing long covid symptoms. With support from the entertainment business foundation eif and donated air time, the psa segment was broadcasted 173,000 times in 2,200 media outlets during the year, to a total audience exposure of 1 billion people. The organization also continued to lead the long covid alliance that the organization co-founded, delivering monthly meetings to a coalition of approximately 1,000 long covid and associated conditions organizations and individuals from cont on sch. O
Grants made by Solve Me CFS Initiative
Who funds Solve Me CFS Initiative
Grants from foundations and other nonprofits
Personnel at Solve Me CFS Initiative
Name | Title | Compensation | Date of data |
---|
Emily Taylor | President , Chief Executive Officer | $123,912 | 2024-10-02 |
Oved Amitay | Chief Executive Officer | $185,393 | 2023-10-12 |
Takeisha Walker | Chief Operating Officer | $75,214 | 2023-06-30 |
Sadie Whittaker | Chief Scientific Officer | $100,481 | 2022-06-30 |
Maryellen Gleason | Director of Development / Interim President and Chief Executive Officer | $135,061 | 2022-06-30 |
...and 7 more key personnel |
Financials for Solve Me CFS Initiative
Revenues | FYE 06/2023 | FYE 06/2022 | % Change |
---|
Total grants, contributions, etc. | $1,989,833 | $5,519,863 | -64% |
Program services | $0 | $0 | - |
Investment income and dividends | $48,048 | $620 | 7649.7% |
Tax-exempt bond proceeds | $0 | $0 | - |
Royalty revenue | $0 | $0 | - |
Net rental income | $0 | $0 | - |
Net gain from sale of non-inventory assets | $0 | $0 | - |
Net income from fundraising events | $0 | $0 | - |
Net income from gaming activities | $0 | $0 | - |
Net income from sales of inventory | $0 | $0 | - |
Miscellaneous revenues | $0 | $0 | - |
Total revenues | $2,037,881 | $5,520,483 | -63.1% |
Organizations like Solve Me CFS Initiative
Organization | Type | Location | Revenue |
---|
TSC Alliance | 501(c)(3) | Silver Spring, MD | $10,016,383 |
National MPS Society | 501(c)(3) | Durham, NC | $2,296,659 |
Beyond Celiac | 501(c)(3) | Ambler, PA | $3,093,277 |
National Pku Alliance | 501(c)(3) | New York, NY | $1,305,823 |
Prader-Willi Syndrome Association | USA (PWSA) | 501(c)(3) | Brandon, FL | $1,577,352 |
National Center for Learning Disabilities | 501(c)(3) | Washington, DC | $1,255,350 |
Foundation for Ichthyosis and Related Skin Types (FIRST) | 501(c)(3) | Lansdale, PA | $734,946 |
Schizophrenia & Psychosis Acti | 501(c)(3) | Alexandria, VA | $1,546,410 |
International Dyslexia Association (IDA) | 501(c)(3) | Pikesville, MD | $2,207,902 |
Lupus Foundation of America Philadelphia Tri-State Chapter | 501(c)(3) | King of Prussia, PA | $715,394 |
Data update history
October 2, 2024
Updated personnel
Identified 1 new personnel
August 9, 2024
Updated personnel
Identified 1 new personnel
July 23, 2024
Received grants
Identified 2 new grant, including a grant for $201,847 from Eddema Foundation July 15, 2024
Used new vendors
Identified 2 new vendors, including , and
July 11, 2024
Posted financials
Added Form 990 for fiscal year 2023
Nonprofit Types
Grantmaking organizationsDisease research fundraisersDisease-focused nonprofitsMedia and communications organizationsCharities
Issues
HealthDiseases and disorders
Characteristics
Political advocacyConducts researchLobbyingOperates internationallyNational levelEndowed supportTax deductible donationsAccepts online donations
General information
- Address
- 350 N Glendale Blvd Ste 368
- Glendale, CA 91206
- Metro area
- Los Angeles-Long Beach-Anaheim, CA
- County
- Los Angeles County, CA
- Website URL
- solvecfs.org/Â
- Phone
- (704) 364-0016
IRS details
- EIN
- 56-1683450
- Fiscal year end
- June
- Taxreturn type
- Form 990
- Year formed
- 1987
- Eligible to receive tax-deductible contributions (Pub 78)
- Yes
Categorization
- NTEE code, primary
- G80: Specifically Named Diseases
- NAICS code, primary
- 813212: Health and Disease Research Fundraising Organizations
- Parent/child status
- Independent
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
- CT0223243
- FTB Entity ID
- 3750193
- AB 488 data last updated ("as-of") date
- 2025-02-05
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