Louisiana Hemophilia Foundation

Louisiana Hemophilia Foundation Welcomes You!

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.





Louisiana Hemophilia Foundation Lunch

Joined by Consumer Speaker Dylan Young and Baxter Educator Kim Spencer. Saturday, March 7, 2015 12:00pm Mike Anderson’s Seafood Restaurant 1031 W. Lee Drive Baton Rouge, LA 70820 RSVP to Erica by Wednesday, 3/4/15 Louisiana Hemophilia Foundation:(225) 291-1675 or admin@lahemo.org

  • Mike Anderson's Seafood Restaurant: 1031 W. Lee Drive, Baton Rouge, Louisiana, 70820
  • March 7, 2015

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Latest Blog Posts

  • Louisiana Hemophilia Foundation March 2015

     On Friday, March 6th, The Louisiana Hemophilia Foundation will be having an educational program followed by dinner at the Michabelle Inn. The program is sponsored by Pfizer and features CNE speaker, Daysi Fardales. Arrive at 6:30 PM for registration. Michabelle Inn is located on 1106 South Holly street in Hammond, Louisiana. We ask that you […]

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