Join VHF and the Hemophilia Association of the Capital Area (HACA) for an opportunity to advocate for policies that improve access to care, support, and resources for those living with bleeding disorders. Your voice can directly impact legislation that affects the lives of individuals with bleeding disorders by meeting with your state legislators. Open to all community members.

SAVE THE DATE - RSVP COMING SOON! Annual Education Meeting: Celebrating Community and Connection. VHF’s Annual Meeting brings together individuals and families affected by inherited bleeding disorders for a weekend of education, support, and connection. This special event offers opportunities to learn about the latest in treatment and care, share experiences, and strengthen our community through networking and collaboration.

Camp Youngblood is a week-long overnight camp at CHT for children ages 7-17 with inherited bleeding disorders, their siblings, and children of members of the inherited bleeding disorder community that reside within the VHF or HACA coverage area. Kids enjoy a week of fun and learning with others that are faced with similar challenges and life experiences.