Our mission is to improve the quality of life and assist persons affected by inherited bleeding disorders by providing education, advocacy, support services and by promoting research.
The Louisiana Hemophilia Foundation was established in 1976 to help Louisiana residents with hemophilia, von Willebrand disease, and other bleeding disorders, lead normal and productive lives. We are a 501 (C) 3 Organization.
While we support research for a cure to bleeding disorders, and look forward to the cure, our families continue to need the services that we offer to increase the quality of their lives. Our programs are designed to meet the needs of the community.
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