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.
National Bleeding Disorders Foundation (NBDF): The NBDF, formerly known as the National Hemophilia Foundation (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.
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.
Hope for Hemophilia (HOPE): HOPE is a national not-for profit organization that helps people living with hemophilia and their families with financial, emotional, and practical support.