Contact

3084 Westfork Drive

Suite A

Baton Rouge, LA 70816

​​

Tel: 225.291.1675

Fax: 225.291.1679

contact@lahemo.org

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The mission of Louisiana Hemophilia Foundation 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.

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.

Louisiana Hemophilia Foundation 2017

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

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