Linked Resources

Clinical Practice Guidelines 

World Federation of Hemophilia (WFH) Guidelines for the Management of Hemophilia. 3rd Edition.

Srivastava A, et al. Hemophilia. 2020;26(suppl 6):1-158. 

Patient Advocacy Organizations and Resources 

Hemophilia Federation of America (HFA)

The HFA is a patient advocacy organization serving the rare bleeding disorders community. It is a community-based, patient-centered organization committed to championing the needs of families living with debilitating bleeding disorders. It advocates for safe and effective therapies and quality, affordable health coverage.

National Bleeding Disorders Foundations (NBDF)

The NBDF (formerly the National Hemophilia Foundation) is dedicated to finding cures for inheritable blood and bleeding disorders and to addressing and preventing the complications of these disorders through research, education, and advocacy enabling people and families to thrive.

WFH

The WFH is a non-profit organization dedicated to improving and sustaining care for people with inherited bleeding disorders around the world.  

Related activities
Webcast Series 
0.50 AMA PRA

Hemophilia and the Coagulation Cascade

Module 1

Faculty: Stacy E. Croteau, MD, MMS; Guy Young, MD
Release: 08/28/2025
Expiration: 08/28/2026
Webcast Series 
0.75 AMA PRA

Individualized Nonfactor Therapy for Hemophilia

Module 2

Faculty: Stacy E. Croteau, MD, MMS; Guy Young, MD
Release: 08/28/2025
Expiration: 08/28/2026