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Join us virtually on October 20 and 21, 2026, for the fifth edition of the WFH Global Policy and Access Summit (GPAS). This free, two-day global event is a unique opportunity to learn, discuss, and exchange knowledge on navigating the evolving treatment landscape and addressing existing gaps in access to care and treatment for people with bleeding disorders.
August 20
In Lebanon, refugees and non-Lebanese people with inherited bleeding disorders (PWBDs) can’t access treatment products because they aren’t nationals. Staying true to its mission to support every patient within Lebanese borders who needs care, the Lebanese Association for Hemophilia (LAH)—the World Federation of Hemophilia (WFH) national member organization (NMO)—has been stepping in to provide access to treatment regardless of nationality or legal status.
August 21
For years, Tanvirul Haq’s childhood was shaped by pain, limited mobility, and the constant disruption caused by severe bleeding episodes. Diagnosed with hemophilia as an infant, the Bangladeshi youth struggled to participate in everyday activities that many healthy children take for granted. Today, thanks to access to non-factor replacement therapy provided by the World Federation of Hemophilia (WFH), he can attend school regularly, play with his friends, and enjoy a far more active and independent life.
August 10
National member organizations (NMOs) are the heartbeat of the World Federation of Hemophilia (WFH). The WFH works in close collaboration with NMOs to provide them with support tailored to their realities to help them increase the level of care for the people with bleeding disorders (PWBDs) in their countries. Every few weeks we will be profiling an NMO on the WFH News page, showcasing the work that they are doing, the challenges they are facing, and the difference they are making in their communities. Today, we look at the NMO in the Ivory Coast, the Hémophilie et autres maladies du sang de Cote d’Ivoire (ONG IHMS-CI).
August 5

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Disclaimer

The information on the WFH website is provided for general information purposes only. The WFH does not engage in the practice of medicine and under no circumstances recommends particular treatment for specific individuals. For diagnosis or consultation on a specific medical problem, the WFH recommends that you contact your physician or local treatment centre. Before administering any products, the WFH urges patients to check dosages with a physician or hemophilia centre staff, and to consult the pharmaceutical company’s printed instructions.

While every effort has been made to ensure the accuracy of the information on this site, the WFH does not guarantee the information is accurate, and is not responsible in any way whatsoever for damages arising out of the use of this website or any of the information contained herein.

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References and links to other websites or references to other organizations, products, services, or publications do not constitute endorsement or approval by the WFH. The WFH is not responsible and assumes no liability for the content of any linked websites.

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Unauthorized solicitations – Warning

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If you receive a suspicious solicitation, exercise extreme caution. In the case of an email, look at the email address to see if it looks suspicious (for example, all WFH emails come from @wfh.org).

We are asking you to remain vigilant, and if you have any doubts about the correspondence, please forward the email to the WFH at [email protected] or call +1 514-875-7944.

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Use of links

Throughout our website, we provide links to other servers which may contain information of interest to our readers. We take no responsibility for, and exercise no control over, the organizations, views, or accuracy of the information contained on other servers. When linking to the WFH USA, we request that you ensure that there are no associated connections for commercial purposes. Any official use of the name WFH USA or the use of its logo needs to be approved by the WFH USA. If you have a link you’d like us to consider adding to our website, please send an email to [email protected] with the subject “Link request.”

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Functional Scales

The outcomes of interest collected by the WBDR include demographic characteristics, clinical and treatment-related outcomes, burden of disease outcomes, and patient-reported outcomes.

The WBDR includes five functional scales as part of its extended data set:

WBDR hemophilia data sets

WBDR Minimal Data Set

The WBDR Minimal Data Set (MDS) is a set of data on demographics, diagnosis, symptoms and treatment which are collected on patients participating in the WBDR.

WBDR Extended Data Set

The WBDR Extended Data Set (EDS) is a larger set of data, with more details than the MDS, which includes questions on patient demographics, diagnosis, symptoms, treatment and burden of disease. The EDS can be used by hemophilia treatment centers to collect data on patients participating in the WBDR. The WBDR Extended Data Set (EDS), was added to the database in March 2019.