Explore a growing catalog of publications on a broad range topics including rare bleeding disorders, von Willebrand disease, and more.
Explore this page for NBDF's HEDI related efforts including the white papers detailing the findings from our past two Health Equity Summits.
Access NBDF’s interactive directory to search the chapter network, stretching across the U.S. from east to west!
Searching for information, resources, or answers to frequently asked questions? Connect with HANDI today!
Frequently Asked Questions
Are you living with inheritable bleeding disorders or suspect you may have one? Find the answers to frequently asked questions!
Do you care for someone with an inheritable bleeding disorder? No doubt you have questions! Explore this section to find some of those answers.
Read synopses of articles published in peer-reviewed journals covering a wide range of topics.
Community Voices in Research
Learn more about this community-powered registry and how your voice and experiences can inform the future of inherited bleeding disorders research.
The T.H.R.I.V.E. initiative educates individuals with bleeding disorders and their support networks about six key steps for leading a healthy life with a bleeding disorder.
Take control of your health care with the Own Your Path program! If you are an adult (18+) and on a prophylaxis treatment plan for VWD or hemophilia A or B, we would love to have you join.
