NBDF’s BDC features educational sessions, industry symposia, networking and social events, and exhibits. A lineup of dynamic speakers who provide essential information and insights on the evolving landscape in this exciting new era of treatment for hemophilia, von Willebrand disease, and rare bleeding disorders. Meeting Dates: August 21 – 23, 2025; Meeting Location: Aurora-Denver, CO
SAVE THE DATE! Location details and registration coming soon! Join VHF for a special program designed to support families of infants and young children diagnosed with hemophilia and other inherited bleeding disorders. This event offers an opportunity to connect with the bleeding disorders community and gain valuable education and resources.
The Virginia Hemophilia Foundation (VHF) Lyman Fisher Scholarship was established to honor Dr. Lyman Fisher, a teacher, researcher, and clinician in hemostasis. For many years, he directed the adult hemophilia program for Virginia. He will be remembered for his steadfast commitment to his patients and students, his respect for those who served under him, his community service and his affection for his family.
SAVE THE DATE - Registration coming soon! Join VHF for an unforgettable Family Camp experience at Camp Holiday Trails! This weekend retreat is designed for families impacted by inherited bleeding disorders, offering a unique blend of education, support, and traditional camp fun in a beautiful, relaxing environment.
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.