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Louisiana Hemophilia Foundation

3636 S. Sherwood Forest Blvd.
Suite 390
Baton Rouge, LA 70816-5211
United States
(225) 291-1675
(225) 291-1679

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.


Role Email
Edgar Guedry President
Rebecca McDaniel Camp Contact
Erica Simpson Executive Director

Advocacy Efforts