Each year VHF’s Annual Education Meeting brings together the inherited bleeding disorders community to share information on a wide variety of topics including advocacy, general health and wellness, and recent treatment developments. This year, in order to keep...
A HUGE THANK YOU to our amazing community for supporting #GivingTuesdayNow by donating toward the VHF Scholarship Program. Together we raised $1,180 from 30 wonderful supporters. We are so grateful for your generosity during a challenging time, and we know our...
VHF is proud to spotlight Krista Davidson as a nominee for VHF Volunteer of the Year in 2020. Krista has been actively involved with VHF since 2015 and is the co-chair of the VHF/HACA Advocacy Committee, has volunteered her time creating and facilitating numerous...
Growing up in a family of hemophiliacs had its challenges, but Soren, 18, still felt empowered to lead a normal life. “My brother and I are both severe hemophiliacs and we both play basketball, baseball, swim, golf, and I personally have run track so there is no limit...
VHF continues to support the bleeding disorders community with reliable information, programs and services. This support includes advocacy webinars, patient financial assistance, scholarships and updates on COVID-19 and how it specifically impacts the bleeding...
March 30 2020, From National Hemophilia Foundation’s (NHF’s) Medical and Scientific Advisory Council (MASAC) Supplemental MASAC Statement Regarding Home Delivery and Refill Under State of Emergency Declaration Patients on home therapy receive regular shipments...