World Federation of Hemophilia

World Federation of Hemophilia The WFH has been a member of the World Health Organization since 1969 and has national member organization (NMOs) in 147 countries.

The World Federation of Hemophilia (WFH) is a not-for-profit organization working to improve and sustain treatment of people with hemophilia and other inherited bleeding disorders. Our vision of Treatment for All is that, one day, all people with a bleeding disorder will enjoy a more certain future filled with promise, no matter where they live.

For 13-year-old Mohammad Hussein, access to treatment means fewer bleeds, greater confidence, and being able to attend s...
08/21/2026

For 13-year-old Mohammad Hussein, access to treatment means fewer bleeds, greater confidence, and being able to attend school without fear of physical activity.

In , refugees and other non-Lebanese people with inherited cannot access treatment products. The Lebanese Association for is helping bridge this gap.

In 2025, the association supported 53 non-Lebanese patients with treatment donated through the WFH Humanitarian Aid Program, along with consultations, physiotherapy, follow-up care, and home infusion training.

Read how this support is helping vulnerable families access care and regain hope: https://bit.ly/4c2xxEI

🧪Inhibitors are a serious complication that may occur when people with have an immune response to treatment with clott...
08/19/2026

🧪Inhibitors are a serious complication that may occur when people with have an immune response to treatment with clotting factor concentrates. Learn more about inhibitors: https://bit.ly/4cFlKdj

🌍 “Access to treatment shouldn’t depend on where you live.” — Nathan Connell, WFH Global Champion. Join Nathan and our c...
08/18/2026

🌍 “Access to treatment shouldn’t depend on where you live.” — Nathan Connell, WFH Global Champion.

Join Nathan and our community of supporters to help expand access to life-saving care for people with worldwide.
💙 Donate now: https://give.wfh.org/

Congratulations to Mark W. Skinner, WFH USA Board Member and former WFH President, on receiving the Lifetime Achievement...
08/16/2026

Congratulations to Mark W. Skinner, WFH USA Board Member and former WFH President, on receiving the Lifetime Achievement Award at the National Bleeding Disorders Foundation’s 78th Annual Bleeding Disorders Conference in .

For more than three decades, Mark has been a leading advocate, scholar, and statesman in the community, helping shape systems of care and policies worldwide. This well-deserved recognition celebrates his remarkable leadership and lasting contributions to the global community.

Please join us in congratulating Mark on this outstanding achievement! 👏

The severity of describes how serious the condition is. The level of severity depends on the amount of clotting factor...
08/13/2026

The severity of describes how serious the condition is. The level of severity depends on the amount of clotting factor that is missing from a person’s blood.

🔗 Learn more about hemophilia on the WFH eLearning Platform: https://bit.ly/3EAFO4H

In the , the WFH partnered with the Association Congo Democratic de l’Hémophilie (ACDH) to strengthen the identificatio...
08/11/2026

In the , the WFH partnered with the Association Congo Democratic de l’Hémophilie (ACDH) to strengthen the identification and diagnosis of bleeding disorders through training for healthcare professionals in Kinshasa.

The visit also included governance and volunteer engagement training for national member organization (NMO) leaders, helping build local capacity to improve care for people with .

08/10/2026

For years, severe bleeding episodes made everyday life incredibly difficult for Tanvirul Haq. He attended school exams in a wheelchair, relied on crutches to walk, and found a way to express his pain and experiences through art.

His story is a powerful reminder of how inherited can affect every aspect of a young person's life, and why access to care matters.

Read more about Tanvirul's journey: https://bit.ly/4hq79Io

During a recent visit to the , the WFH and the Association Congolaise de l’Hémophilie (ACH) brought together health aut...
08/07/2026

During a recent visit to the , the WFH and the Association Congolaise de l’Hémophilie (ACH) brought together health authorities, health care professionals, NMO leaders, patients, and families to help strengthen care in the country.

Alongside a meeting with the Deputy Minister of Health, the visit included bleeding disorders management training for 30 health care professionals, governance and volunteer engagement sessions for six ACH board members, and therapeutic education for 35 patients and parents.

Together, these efforts support stronger local capacity and improved care for people with and other bleeding disorders.

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