Snapshot: ASH ISTH NHF WFH Guideline Recommendations for the Diagnosis of von Willebrand Disease (VWD)
This one-page summary presents the highlights of the ASH ISTH NHF WFH Guidelines on the Diagnosis of von Willebrand Disease (VWD). It outlines what is covered in the guidelines, why they matter and who they affect. Click here to access the full ASH ISTH NHF WFH VWD Guidelines.
Report on the Annual Global Survey 2019
The Report on the Annual Global Survey (AGS) includes demographic and treatment data, providing a global snapshot of people with hemophilia, von Willebrand disease, other rare factor deficiencies, and inherited platelet disorders around the world.
Exercises for People with Hemophilia – Amharic
Also Available In: English, Spanish, French, Arabic, Russian, Simplified Chinese This is not an official WFH translation. This resource has been translated with permission by a WFH National Member Organization (NMO), and is shared here with their kind permission. Translating organizations are encouraged to have translations reviewed by local experts, the WFH is not responsible […]
What is Hemophilia? – Amharic
The 2023 edition is available in: English, Spanish, French, Arabic, Russian, Simplified Chinese This edition is also available in: Japanese This edition of the resource has also been translated into the following language, with permission from the WFH, by NMOs: Setswana This is not an official WFH translation. This resource has been translated with permission […]
WBDR 2019 Data Report
The World Bleeding Disorders Registry (WBDR) 2019 Data Report provides aggregate data on more than 4,000 people with hemophilia around the globe who are registered in the WBDR.
Abstracts of the World Federation of Hemophilia Virtual Summit
The freely available special Haemophilia Journal supplement dedicated to the WFH Virtual Summit – Connecting the Global Bleeding Disorders Community (June 2020, Vol 26, Issue Supplement S4 Pages 1–149) features abstracts of many of the iPosters presented at the Virtual Summit.
What is von Willebrand Disease – Bengali
The 2023 edition is available in: English, Spanish, French This edition is also available in: Arabic, Russian, Simplified Chinese, Japanese This edition of the resource has also been translated into the following language, with permission from the WFH, by NMOs: Polish, Farsi, Setswana This patient handbook contains basic information about the inheritance, diagnosis, symptoms and […]
An international survey to inform priorities for new guidelines on von Willebrand disease
As part of their international collaboration to develop guidelines for the diagnosis and management of von Willebrand disease (VWD), the American Society of Hematology (ASH), the International Society on Thrombosis and Haemostasis (ISTH), the National Hemophilia Foundation (NHF) and the World Federation of Hemophilia (WFH), along with the guidelines methods team, conducted a stakeholder survey […]
Report on the Annual Global Survey 2018
This report celebrates the 20th anniversary of the Annual Global Survey (AGS). It includes demographic and treatment data, providing a global snapshot of people with hemophilia, von Willebrand disease, other rare factor deficiencies, and inherited platelet disorders around the world.
ePosters of the XXXI International Congress of the World Federation of Hemophilia
This interactive carousel features over 500 posters presented at the WFH 2014 World Congress in Melbourne, which can be searched by title, author, poster number, or topic. Via the Options tab on the right of each poster, viewers may download, print, or email posters; email poster authors directly; or participate in an online discussion. Please […]
ePosters of the XXX International Congress of the World Federation of Hemophilia
This interactive carousel features over 400 posters presented at the WFH 2012 World Congress in Paris, which can be searched by title, author, poster number, or topic. Via the Options tab on the right of each poster, viewers may download, print, or email posters; email poster authors directly; or participate in an online discussion. Please […]
WBDR 2018 Data Report
The World Bleeding Disorders Registry (WBDR) 2018 Data Report provides aggregate data on more than 1100 people with hemophilia around the globe who are registered in the WBDR.