The Hemophilia Foundation of Michigan strives to improve the quality of life for all people affected by hemophilia, von Willebrand disease, other coagulation disorders and related complications, including HIV/AIDS and hepatitis.
| Year | Grants | Total Giving | Avg Grant | New | Repeat |
|---|---|---|---|---|---|
| 2024 | 18 | $929K | $52K | 0 | 18 |
| 2023 | 18 | $840K | $47K | 0 | 18 |
| 2022 | 18 | $862K | $48K | 3 | 15 |
| 2020 | 17 | $856K | $50K | 1 | 16 |
| 2018 | 17 | $793K | $47K | 17 | 0 |
| Year | Revenue | Expenses | Net Assets |
|---|---|---|---|
| 2024 Form 990 | $4,808,942 ↑ | $4,389,054 | $3,012,871 |
| 2023 Form 990 | $3,941,132 ↑ | $4,264,936 | $2,521,143 |
| 2022 Form 990 | $3,850,387 ↑ | $3,690,739 | $2,761,625 |
| 2020 Form 990 | $3,729,383 ↑ | $3,204,927 | $2,364,152 |
| 2018 Form 990 | $3,349,964 | $3,247,148 | $1,647,913 |
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