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June 2019
Annual Meeting – Community Member Registration
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.
Highlights include: Sessions on advocacy, gene therapy, and bleeding disorders outside of hemophilia; Lyman Fisher Scholarship recognition; VHF chapter updates; on-site children and teen programming; and on-site childcare for 5 and under.
Find out more »Annual Meeting – Sponsors and Speakers Registration
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.
Find out more »July 2019
2019 Camp Youngblood
A week-long overnight camp at Camp Holiday Trails (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 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.
Find out more »August 2019
2019 HACA/VHF Teen Retreat
A weekend of fun and learning for teens that are faced with similar challenges. Join us for a chance to connect and create a strong sense of community! For teens age 13–17 who live within HACA/VHF territory and meet one of the following criteria: Have a bleeding disorder, be the sibling of someone with a bleeding disorder, or have a parent/caregiver with a bleeding disorder. If a hotel room is requested then parent/caregiver must be in attendance with registered teen(s).
Find out more »Educational Dinner – Richmond
Educational dinners are a series of educational presentations hosted at restaurants around the state. Facilitators are clinicians, national advocates, and industry experts. Educational dinners enable those affected by inherited bleeding disorders to connect with people from their local community, as well as learn about a range of relevant topics.
Find out more »
