Hemophilia Federation of America is a national nonprofit organization that assists, educates, and advocates for the bleeding disorders community.
We’re excited to bring back TEACH Immersion (Together we Empower, Advocate, and Collaborate for Hemophilia and other Bleeding Disorders) for 2018! TEACH brings together 16 men, women, moms and dads for three days of educational programming and advocacy training in Washington, D.C., designed to educate participants about the legacy of advocacy efforts in the bleeding disorders community.
Interested in becoming a member of HFA? Follow the link to find out how to become an individual, family, or corporate member!
Moving to the next stage in life for any young person can be exhilarating, terrifying and confusing. When you factor in the added complexities of living with hemophilia and an inhibitor, it can be downright overwhelming. This new workshop aims to help.
Don’t wait and sign-up for the HFA Community Research Portal! The HFA Community Research Portal is a platform HFA uses to collect data for research on the bleeding disorders community to more effectively serve the needs of bleeding disorder patients and their families.
Sign up for E-mails, Dateline Magazine, and other ways to stay connected.