Patient Medical Resources
On this page, you can find resources to learn more about emicizumab or hemophilia A from Genentech and patient advocacy groups.
[RECENTLY ADDED] Comprehensive Assessment Tool of Challenges in Hemophilia (CATCH) Survey
The CATCH survey is a tool for people with hemophilia to use throughout their lives. You can use the CATCH survey to assess how hemophilia impacts different parts of your life and what activities you find risky. Each time you take the CATCH survey you receive a score. The CATCH survey and results are provided for educational purposes only and are not intended for the purposes of diagnosis or making any treatment related decisions. The survey and results are not a substitute for the clinical judgment of trained healthcare providers.
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 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.
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.