Louisiana's trusted resource and supportive community for individuals & families affected by bleeding disorders
Together, we make a difference in the lives of our community
Committed to improving lives by supporting Louisiana
people, families, and communities with bleeding disorders,
through impactful programs.
Our Mission
To improve the quality of life for people affected by bleeding disorders through education, advocacy, support services, and research.
About Us
Founded in 1976, the Louisiana Hemophilia Foundation (LHF) is a 501(c)(3) nonprofit organization serving individuals and families affected by hemophilia,
von Willebrand disease, and other bleeding disorders throughout Louisiana.
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Education & Resources – Providing medical updates, educational materials, newsletters, and resources to help families stay informed.
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Support & Connection – Offering programs, services, and opportunities that connect and support our bleeding disorders community.
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Advocacy – Helping ensure the needs and voices of people affected by bleeding disorders are heard.
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Community Resources – Connecting families with treatment centers and state, local, and national resources.
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Local Leadership – Based in Baton Rouge and guided by a Board of Directors with extensive experience in the bleeding disorders community.
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Community Supported – Funded through individual donations, fundraising, grants, and support from industry and community partners
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For 50 years, we have been committed to helping Louisiana’s bleeding disorders community live healthier, fuller lives.
