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April 2019
VHF/HACA Family Bleeding Disorders Camp
Join Virginia Hemophilia Foundation (VHF) & Hemophilia Association of the Capital Area (HACA) at Camp Holiday Trails (CHT) for a weekend camp for families impacted by an inherited bleeding disorder. This program is designed for families with at least one child living at home who is between the ages of 5 – 17, whose children are camp ready and/or are looking to attend camp in the next two years. Eligible families are those impacted by an inherited bleeding disorder who live in the territorial jurisdiction of VHF & HACA.
Find out more »Application Due: 2019 Camp Youngblood
All parts of the online application for Camp Youngblood must be complete by April 30th
CAMP YOUNGBLOOD | July 7 – July 12 at Camp Holiday Trails
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.
May 2019
Scholarship Applications Due: Lyman Fisher and NHF Bleeding Disorders Conference
All parts of the applications must be emailed to VHF by midnight, May 1st. LYMAN FISHER:The VHF Lyman Fisher Scholarship was established to honor Dr. Lyman Fisher; a teacher, researcher, and clinician in hemostasis who for many years directed the adult hemophilia program in Virginia. Award: One-year award in the amount of $2,000 for a full academic year Eligibility: The scholarship was designed for individuals living with an inherited bleeding disorder, their sibling(s) or their parents and may be used at any accredited non…
Find out more »Educational Dinner – Roanoke
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 »First Step Program For New Families
Program is designed to support families of infants and young children with hemophilia and other inherited bleeding disorders with community connection and education. This program is for families with children who have been diagnosed with an inherited bleeding disorder in the last 7 years.
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