Camp Youngblood

Kids enjoy a week of fun and learning with others who face similar challenges and life experiences. » LEARN MORE

Annual meeting

An opportunity for the inherited bleeding disorder community to network and to share information on a variety of topics.

Dedicated to serving and supporting the needs of those impacted by a bleeding disorder through education, advocacy and community.

Education

Giving Hands

VHF provides many opportunities for education through meetings, newsletters and scholarships.

Advocacy

Giving Hands

VHF participates in national and federal advocacy initiatives.

Community

Giving Hands

VHF builds community by strengthening relationships and offering support through numerous programs.

News & Events

Happy 50th Anniversary VHF!

Celebrating 50 Years of the Virginia Hemophilia Foundation Honoring Our Past, Embracing Our Future Fifty years ago, a small but determined group of advocates came together with a shared mission: to support individuals and families affected by bleeding disorders in...

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Advocacy Update: 2025 General Assembly Session

In the 2025 session, VHF and HACA monitored bills related to school health policies, health insurance, medical debt, drug affordability, and the budget bill, including threats to Medicaid. During the 2025 session, a few measures passed, while others failed. The school...

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Von Willebrand Disease and Me

Von Willebrand Disease and Me

By Giselle Washington When I was three years old, I was diagnosed with a bleeding disorder VWD [von Willebrand disease] that means when I get a cut or a bruise it will bleed longer than most kids. Sometimes I get a nosebleed at school, and I must see the nurse. People...

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CSL Behring - Biotherapies for Life
CSL Behring - Biotherapies for Life