The Foundation monitors legislation that affects the bleeding disorders community and advocates for changes in policy when needed. We work hard to keep up to date ...
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Summer Camp: The Hemophilia Foundation of Oregon began its summer camp program in 1970, and today over 50 youngsters from Oregon and SW Washington regularly attend ...
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HFO works hard to provide opportunities for peer support and education in a small group setting where families and individuals with bleeding disorders can come ...
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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.
Progress made by Baxter during clinical trial assessing the safety and optimal dosing level of BAX 335, an investigational factor IX (FIX) gene therapy. Read more about Baxter Reports Gene Therapy Program Updates Log in to post comments
NHF is excited to partner with chapters to deliver six Collaborating in Care educational modules, some of which are now available. Read more about Collaborating in Care Educational Modules Available Now
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