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What is the HFO?

The Hemophilia Foundation of Oregon (HFO) was founded in Portland in 1963 by a small group of parents of children with hemophilia. Its goal has always been to improve the quality of life of those living with bleeding disorders and related diseases, and those who care for them. It serves individuals, their families and friends living in Oregon and Clark County, Washington.

HFO is a volunteer organization dedicated to providing education and support to families affected by hemophilia and other bleeding disorders. Nationally, there are approximately 20,000 individuals with hemophilia; 400 with bleeding disorders in the Foundation's service area alone. Including family, friends and caregivers, many thousands of people are touched by hemophilia.

Our Mission

The Hemophilia Foundation of Oregon serves as an active force to enhance the quality of life for the genetic bleeding disorders community through advocacy, support, outreach, education, research and promotion of excellence in medical care.

Board of Directors - Officers and Trustees