Association for Creatine Deficiencies
Data sourced from IRS 990 public filings
Association for Creatine Deficiencies To promote and fund medial research for treatments and cures, provide patient, family, and public education, and advocate for early intervention through newborn screening for Cerebral Creatine Deficiency Syndromes (CCDS).
Annual Revenue
$411,288
Known Funders
9
Grants Received
12
Financial History
| Year | Revenue | Expenses | Assets |
|---|---|---|---|
| 2024 | $411,288 | $653,844 | $418,617 |
| 2023 | $588,192 | $602,613 | $674,679 |
| 2022 | $699,129 | $599,640 | $685,374 |
| 2021 | $322,273 | $474,054 | $574,512 |
| 2020 | $638,614 | $95,949 | $714,167 |
Top Funders
ALEXANDRIA, VA
Washington, DC
LONG BEACH, CA
LONG BEACH, CA
HOUSTON, TX
DEERFIELD, IL
NEW YORK, NY
NEW YORK, NY
Rolling Meadows, IL
Key Personnel
From 2024 IRS 990 filing
Heidi Wallis
Executive Director
Erin Coller
Director of Comm
Kim Tuminello
Director of Advocacy
Mikelle Law
Director of Compliance
Daniel Coller
Board Chair
Celeste Graham
Director of Education
Randy Allen
Vice Chair
Frequently Asked Questions
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