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A little about us
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 nonprofit organization serving the bleeding disorder community since 1976.
Louisiana Hemophilia Foundation provides networking opportunities, access to care, summer camp for children, educational programs, scholarships, & MedicAlert Services.
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Be a part of this incredible community!
It's so easy to join! Simply fill out this form & be on the list to find out fun things first.
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