Established in 1948, the National Hemophilia Foundation has long been one of the nation’s leading organizations dedicated to serving patients and families living with inheritable blood and bleeding disorders such as hemophilia, von Willebrand disease, ultra-rare platelet disorders, and more.

People with blood or bleeding disorders and their family members are the heart of our work. We support research that has a measurable impact on people’s lives; deliver education that helps people with bleeding disorders and their family members thrive; and advocate for policies at the state and local level that protects access to healthcare.

Our mission is to serve those affected by all inheritable bleeding disorders. We are committed to our employees as well as those we serve. To do so, we seek and value those qualities, both visible and invisible, that makes individuals unique. We strive to be a safe place where regardless of age, color, disability, gender, gender identity, gender expression, family status, national origin, race, ethnicity, or sexual orientation, you are heard, empowered and valued. We believe that every person's unique perspective and experience helps us advance our mission.