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  • VIRTUAL – 2026 Advocacy Education Training

    Join VHF and the Hemophilia Association of the Capital Area (HACA) for a virtual advocacy education training program that will focus on the 2026 Virginia General Assembly. Join in and hear details about proposed legislation and state policy issues that focus on access to quality healthcare.This training will be in preparation for Richmond Days but you do not have to be registered for Richmond Days to participate. Open to all community members.

  • Richmond Days

    General Assembly Building 201 North 9th St., Richmond, United States

    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.

  • VIRTUAL BRANDED EDUCATION – Learn About HYMPAVZI™ (marstacimab-hncq)

    Zoom

    Join us for a virtual educational session with Pfizer where we will explore a rebalancing treatment option for hemophilia. This session is intended for people living with hemophilia, parents, partners, and caregivers, and anyone interested in learning more about treatment options and shared decision-making with a health care provider.

  • VIRTUAL – VHF/HACA Camp Youngblood Information Session

    Zoom

    Are you thinking about sending your child to Camp Youngblood at Camp Holiday Trails (CHT) for the first time in 2026, have questions, or would you just like a refresher on the camp experience? Join the Hemophilia Association of the Capital Area (HACA), CHT, and VHF for a virtual information session via Zoom to learn more about Camp Youngblood – even if you aren’t quite ready to send your kids this year.

  • STAUNTON – Annual Education Meeting

    Hotel 24 South 24 S Market St, Staunton, Virginia

    REGISTRATION IS NOW OPEN! 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.