Camping in cabins, educational programs, campfires, songs, swimming, service projects, arts and crafts, and more! All meals provided.
In order to reserve a spot at Family Camp we are asking each family to provide a $25 deposit to hold your spot. You will have the option to leave credit card information or send a check. HFO will not charge your card, nor cash your check, if you attend the event.
The Hemophilia Foundation of Oregon enhances the quality of life for individuals with bleeding disorders and their families through advocacy, assistance, outreach, education and research support.
The goal of this effort is to create and maintain state-of-the-art guidelines on the diagnosis and management of VWD. Read more about NHF to Collaborate on Clinical Practice Guidelines for von Willebrand Disease
The update reported on a Phase 1/2 clinical trial for the company’s investigational therapy for the treatment of patients with severe hemophilia B/factor IX (FIX) deficiency. Read more about Catalyst’s Trial Update Includes Reports of Antibody Responses