August 17, 2023
The National Hemophilia Foundation has changed their name to the National Bleeding Disorders Foundation in an effort to more reflect the people it serves. For many years the NHF, now NBDF, has helped not only patients with hemophilia, but those with von Willebrand disease, rare factor deficiencies, platelet disorders and more.
Links to articles listed may take readers to websites separate and out of the control of the CU School of Medicine and the Hemophilia and Thrombosis Center. The CU School of Medicine and the Hemophilia and Thrombosis Center are not responsible for any errors, inaccuracies or opinions that may be expressed in any of the linked articles.
Previous articles featured on our website can be found at our archive page here. Please note that links in our archive files may take readers to websites that may have changed their link. In some cases these links do not work anymore. We periodically check and remove articles that have broken links. If you have questions about these articles, please contact us at hemophilia@ucdenver.edu.