Our Mission: To improve the quality of life and assist persons affected by inherited bleeding disorders by providing education, advocacy, support services, and by promoting research
We offer the following services to the bleeding disorders community:
EDUCATION
We host programs across the state that are open to all
PATIENT ASSISTANCE
To help during those tough times
ACCESS TO CARE
For needs that arise from receiving medical care, such as gas & lodging
MEDIC ALERT SCHOLARSHIPS
To provide life-saving services in case of emergency
EDUCATIONAL SCHOLARSHIPS
To help better lives through higher education
SUMMER CAMP
To grow and empower our youth into leaders
ANNUAL MEETING
To build our community and strengthen through knowledge
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 Organization.
Our mission is to improve the
quality of life and assist persons affected by hemophilia and other inherited bleeding disorders by providing education, advocacy, support services, and by promoting research.
Founded in 1976
