The Hemophilia Alliance Foundation
The Hemophilia Alliance Foundation is a 501(c)(3) that receives and administers funds to enable organizations serving inherited bleeding and thrombotic disorders to build capacity and to support direct consumer financial assistance programs. The foundation awards grants and scholarships on an annual cycle and publishes grant guidance and reports on its site.
Source: Website · Mar 2026
Ideal Applicant
State or regional hemophilia/bleeding-disorder nonprofits or programs focused on capacity building and direct consumer financial assistance.
Good Fit
- • Organization serves people with inherited bleeding or thrombotic disorders.
- • Applicant is a state or local hemophilia chapter or a health charity with similar mission.
- • Requests target capacity-building or direct financial assistance programs.
- • Applicant can demonstrate prior operating history and measurable use of grant funds.
Geography
Observed grants in the latest year reached organizations in 38 states, showing a national footprint rather than a local or regional focus.
Recipient Variety
The foundation funded 68 distinct recipients in the latest year with 45 repeat grantees across the three-year window, indicating a broad and diverse recipient set for its size.
New Applicants
Direct evidence of new entrants exists (about 23 new recipients in 2024, roughly one third of grantees) and the portfolio is distributed across many independent organizations, suggesting unfamiliar applicants can realistically enter the giving pattern.
Source: Zeffy Agent · Mar 2026
