Come Celebrate Summer with your bleeding disorders community! Join us for a fun filled educational picnic for individuals with inherited bleeding disorders and their immediate family and/or household members at First Landing State Park on Cape Henry in North Virginia Beach.
Advocacy, Education, and Community Building in the Nation’s Capitol! A unique opportunity to spend time at the Hemophilia Federation of America (HFA) office, meet one-on-one with legislative staff and young professionals in the public sector, and take a guided tour of the capitol. Go behind the scenes of the political process and learn that YOUR voice matters.
A week-long overnight camp at Camp Holiday Trails (CHT) for children with inherited bleeding disorders, their siblings, and children of members of the inherited bleeding disorder community that reside within the Virginia Hemophilia Foundation (VHF) or Hemophilia Association of the Capital Area (HACA) coverage area. Kids enjoy a week of fun and learning with others that are faced with similar challenges and life experiences.
VHF’s Annual Meeting brings together the inherited bleeding disorder community to share information on a wide variety of topics, from the basics of diagnosis to the most relevant developments in treatment. It is a great opportunity for networking and support for individuals and families.
An evening of education and community building in memory of Terry Lamb, VHF Board Member, friend, advocate and all around amazing man. Dinner, educational presentation, networking with other families, tickets to see the Norfolk Tides, and a post-game fireworks extravaganza. Dinner attendance required to receive tickets. This event is for individuals with an inherited bleeding disorder and their immediate family/household members only. There is no cost for VHF members and their families.