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Patient Medical Resources

On this page, you can find resources to learn more about emicizumab or hemophilia A from patient advocacy groups.

Patient Advocacy Organizations

Hemophilia Federation of America (HFA): The HFA is a national nonprofit organization that assists, educates, and advocates for the bleeding disorders community.

Visit the HFA website

National Hemophilia Foundation (NHF): The NHF is a national nonprofit organization dedicated to finding better treatments and cures for inheritable bleeding disorders and to preventing the complications of these disorders though education, advocacy, and research.

Visit the NHF website

World Federation of Hemophilia (WFH): The WFH is a worldwide not-for-profit organization working to improve and sustain treatment of people with hemophilia and other inherited bleeding disorders. The WFH has been a member of the World Health Organization since 1969 and has national member organizations in more than 100 countries. 

Visit the WFH website

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Link to Healthcare Professionals Site

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Link to Healthcare Professionals Site

The information contained in this section of the site is intended for U.S. healthcare professionals only. Click "OK" if you are a healthcare professional.

Link to Third Party Site

The link you have selected will take you away from this site to one that is not owned or controlled by Genentech, Inc. Genentech, Inc. makes no representation as to the accuracy of the information contained on sites we do not own or control. Genentech does not recommend and does not endorse the content on any third-party websites. Your use of third-party websites is at your own risk and subject to the terms and conditions of use for such sites.