As investigational hemophilia gene therapies move closer to regulatory authorization, community stakeholders have recognized the acute need for people with hemophilia (PWH) and healthcare professionals (HCPs) to be fully engaged in shared decision making (SDM). While...
The board of directors is the governing body of VHF. Board members meet periodically to discuss and vote on the affairs of the organization, to support the work of VHF, and to provide mission-based leadership and strategic governance. Board terms align with our fiscal...
This past June the Virginia Hemophilia Foundation was thrilled to award six deserving applicants with a Lyman Fisher Scholarship. Recipients were honored in-person at our Annual Education Meeting. Congratulations to each of these scholarship winners, they have...
Eileen Bunn, VHF Member “I feel a sense of belonging participating in Family Camp at Camp Holiday Trails. CHT is a special place where families can have fun together and share stories, resources, and experiences with other families impacted by hemophilia, building a...
REGISTER AND FUNDRAISE TODAY! In partnership with CVS Specialty Pharmacy and the National Hemophilia Foundation (NHF) VHF is participating in the first ever National Unite for Bleeding Disorders Registration Drive. From July 1st until July 31st, we have a few...
Posted NHF News Page June 7, 2022. The hemophilia data for this study was drawn from deidentified medical records from four North American hemophilia treatment centers. The U.S. diabetes epidemic and its impact on the health of tens of millions of Americans has been...