Camp Youngblood Application Process and Pre-Screening Survey Link - Camp Youngblood is a week-long overnight camp at 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 VHF or HACA coverage area. Kids enjoy a week of fun and learning with others that are faced with similar challenges and life experiences.
RSVP Deadline: Monday, March 18, 2024. 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.
We appreciate your interest and support of our 2024 Annual Meeting, contact Kelly Waters at kelly@vahemophilia.org or 804-740-8643 for more information about sponsorship. Closer to the date of the event we will send a detailed email to all registered industry supporters and presenters. This email will include the agenda, booth set up times, what to bring, how many people to expect, etc.
The VHF Bleeding Disorders Awareness Education Celebration is an exciting new event that was designed to raise awareness, increase education, honor the hard work and dedication in the bleeding disorders community, and best of all CELEBRATE and enjoy time with friends and family in a unique setting!
Join VHF and HTC staff for a program for new families! This program is designed to support families of infants and young children who have been diagnosed within the last 7 years with hemophilia and other inherited bleeding disorders with community connection and education. This program is designed for VHF constituents (and their immediate family and/or household members only) lunch and admission to the museum will be provided and there is no fee to attend. What to Expect: Education, time for Q&A, lunch, networking with other parents and children, and free admission to the Virginia Living Museum.