Join constituents, advocacy committee members, and community stakeholders from across Virginia for a virtual education meeting. Stay informed with the latest state and federal advocacy news, connect with fellow Virginians, and collaborate on improving the lives of those affected by bleeding disorders. Share experiences, gain knowledge, and build a stronger community.

REGISTRATION IS FULL - email heather@vahemophilia.org if you would like to be placed on the waiting list.

Join VHF and the Hemophilia Association of the Capital Area (HACA) for a virtual advocacy education training program that will focus on the 2025 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.

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! VHF’s Annual Meeting brings together the inherited bleeding disorder community to share information on a wide variety of topics and it is a great opportunity for networking and support for individuals and families.