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.
Mark your calendars! The Virginia Hemophilia Foundation (VHF) is turning the big 50, and we want to celebrate this incredible milestone with YOU! For five decades, VHF has been a beacon of support and advocacy for our bleeding disorders community. Join us as we reflect on the progress we've made together and look forward to an even brighter future. We're planning a special event filled with fun, inspiration, and a chance to connect with fellow community members. Stay tuned for more details, and in the meantime, save the date – we can't wait to celebrate with you!
REGISTRATION IS NOW OPEN! 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.