Become A Member

HFO is a volunteer organization dedicated to providing education and support to families affected by bleeding disorders.  Fill out the member information form online or fill out the paper pdf form and become part of this dynamic foundation.  By supplying your information you will be notified of upcoming events, programs specific to your diagnosis, and support services.  Join our community!

HFO serves people living with Hemophilia, von Willebrand Disease, and other rare bleeding disorders. Our service area includes all counties in Oregon. We provide education, advocacy, and many other services to help our members manage their disease and improve their quality of life.

Members with Bleeding Disorders
Membership is FREE for people with bleeding disorders and their immediate family members. To qualify for free membership, you or an immediate family member (i.e., spouse, child, or parent who lives in the same household) must have a documented, qualifying diagnosis* and live in the region we serve. To register with the Chapter, please fill out the online form and submit it to us, or for those who prefer paper, download and complete the Membership Registration Form and mail it to the Chapter.

*Please note: If you have not been referred to HFO by the Hemophilia Center at OHSU, or have not been a previous member of HFO, proof of diagnosis may be required to receive some of our free services and participate in some of our activities.

Friends of HFO
Extended family members, friends, and medical professionals are welcome to join HFO and receive our information by completing a Mailing List Registration Form and paying a nominal, yearly membership fee. The annual membership fee is $15 for an individual and $30 for a family.