About Hemophilia Alliance Foundation
The Hemophilia Alliance Foundation is dedicated to receiving and administering funds to enable eligible organizations in the inherited bleeding and thrombotic disorders community to build capacity in order to achieve their mission and to support direct consumer financial assistance programs.
Focus Areas
HemophiliaInherited bleeding disordersInherited thrombotic disordersPatient financial assistanceEducation and scholarshipsCapacity building for community organizations
Who They Fund
people with hemophiliaindividuals with other bleeding disordersfamilies and caregivers of people with hemophilia
Funding Style
disease-specific program funding
About Hemophilia Alliance Foundation
The Hemophilia Alliance Foundation channels most of its recent giving into a single pattern: $24,000 grants to hemophilia and bleeding-disorders organizations for “PROMOTE HEMOPHILIA.” That repeated award level shows a funder built around steady support for community groups rather than one-off, highly varied gifts. Recent recipients include the Hemophilia Foundation of Michigan, the Western Pennsylvania Bleeding Disorders Foundation, and the Hemophilia Foundation of Southern California. Its stated mission centers on helping eligible organizations in the inherited bleeding and thrombotic disorders community build capacity and on supporting direct consumer financial assistance programs. That combination appears across multiple grant programs, including support for organizational strengthening, patient assistance, and regional hemophilia treatment center activity. The foundation also makes scholarships for individuals with inherited bleeding or thrombotic disorders who are active patients in a federally funded Hemophilia Treatment Center. Recent grantmaking reaches local and regional affiliates as well as treatment centers and community organizations. Awards in the current set include grants to Orlando Health Arnold Palmer Hospital for Children and the University of Colorado Hemophilia and Thrombosis Center, alongside state and regional bleeding-disorders groups.
What Hemophilia Alliance Foundation Funds
Capacity building is a core theme. The HAF Impact Grant supports eligible organizations in the inherited bleeding and clotting disorders community to build capacity and achieve their mission, with grants ranging from $10,000 to $50,000. A related Project Grant can support organizational strengthening projects and patient or consumer financial assistance. Education and convening also appear in the funding pattern. The Regional Core Centers Grant includes support for regional hemophilia treatment center annual meetings, and the Patient Assistance Grant can fund projects that strengthen organizational ability to better serve constituents. Scholarship support is a separate track. The Joe Pugliese Educational Award Scholarship provides $12,500 for individuals diagnosed with an inherited bleeding or inherited thrombotic disorder who are active patients in a federally funded Hemophilia Treatment Center, supporting post-secondary educational pursuits. Consumer assistance is another recurring use of funds, including direct consumer financial assistance programs within the foundation’s active grant portfolio.
Financial Snapshot
Annual Giving
$805K
Total Assets
$71K
Total Revenue
$1M
Total Expenses
$1M
Typical Grant Size
Most grants fall between $8K and $10K, with a median of $8K.
25th Percentile
$8K
Median
$8K
75th Percentile
$10K
Geographic Reach
National40 states funded
About 5% of grants go to recipients in NY.
Funding intensity
LowHigh
Headquarters
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