Women and Girls with Bleeding Disorders and Reproductive Health: Disparities in treatment and care | March 8, 2023
This 60-minute webinar explores the theme of “Women and Girls with Bleeding Disorders and Reproductive Health: Disparities in Treatment and Care” and covers topics like fertility challenges faced by WGBD, overlooked issues that have significant health impact for WGBDs and management of WGBDs in a multidisciplinary setting. Speakers included Dawn Rotellini (U.S.A), Maureen Baldwin, MD […]
Women and girls with hemophilia
The previous edition is also available in: Japanese The previous edition of this resource has also been translated into the following languages, with permission from the WFH, by NMOs: Setswana, Traditional Chinese Hemophilia is a rare bleeding disorder. For many years, people believed that only men and boys could have symptoms of hemophilia. We now know […]
WFH Gene Therapy Registry – User guide for people with hemophilia – Italian
This document is an introductory guide for people with hemophilia who wish to join the World Federation of Hemophilia (WFH) Gene Therapy Registry (GTR). It answers basic questions about the registry, its purpose, and what participants can expect. Please reach out to WFH with questions regarding participation in the registry at [email protected]. This guide is […]
WFH Gene Therapy Registry – User guide for people with hemophilia – German
This document is an introductory guide for people with hemophilia who wish to join the World Federation of Hemophilia (WFH) Gene Therapy Registry (GTR). It answers basic questions about the registry, its purpose, and what participants can expect. Please reach out to WFH with questions regarding participation in the registry at [email protected]. This guide is […]
WFH Gene Therapy Registry – User guide for hemophilia treatment centres – Italian
The World Federation of Hemophilia (WFH) Gene Therapy Registry (GTR) welcomes the participation of all Hemophilia Treatment Centres (HTCs) involved in gene therapy. This includes HTCs that administer gene therapy and those that manage or follow-up with patients who have received gene therapy at other centres. This user guide will orient HTCs to the WFH […]
WFH Gene Therapy Registry – User guide for hemophilia treatment centres – German
The World Federation of Hemophilia (WFH) Gene Therapy Registry (GTR) welcomes the participation of all Hemophilia Treatment Centres (HTCs) involved in gene therapy. This includes HTCs that administer gene therapy and those that manage or follow-up with patients who have received gene therapy at other centres. This user guide will orient HTCs to the WFH […]
WFH Gene Therapy Registry – Basics of hemophilia, gene therapy, and long-term data collection – German
This document is an introductory guide to the World Federation of Hemophilia (WFH) Gene Therapy Registry (GTR). It answers basic questions about the registry, its purpose, and what participants can expect. The guide is designed to help those who receive gene therapy for hemophilia and their care teams to decide if they should participate in […]
WFH Gene Therapy Registry – Basics of hemophilia, gene therapy, and long-term data collection – Italian
This document is an introductory guide to the World Federation of Hemophilia (WFH) Gene Therapy Registry (GTR). It answers basic questions about the registry, its purpose, and what participants can expect. The guide is designed to help those who receive gene therapy for hemophilia and their care teams to decide if they should participate in […]
Practical Education on Bleeding Disorders: Knowledge for All | WFH webinar series | December 15 2022
Listen to this 2-hour webinar presented on December 15, 2022, to learn about global topics related to bleeding disorders, with a focus on comorbidities associated with hemophilia. Patricia Cabré (Spain), Adolfo Llinas (Colombia), Luigi Solimeno (Italy), Radoslaw Kaczmarek (U.S.A.), Catherine Hayward (Canada), and Andra James (U.S.A.) presented practical information on bleeding disorders, including resilience and […]
Report on the Annual Global Survey 2021
The Report on 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.
Barriers to Accessing Care for Women and Girls with Bleeding Disorders | September 22 2022
Listen to this 90-minute webinar presented on September 22, 2022, to learn about how to address challenges faced by Women and Girls with Bleeding Disorders in accessing care and treatment and potential solutions. Issues like late diagnosis, lack of data, cultural taboos, and sexism has been discussed as part of the program and a diverse […]
WFH highlight sessions and general plenaries | WFH World Congress 2022
In these sessions from the WFH 2022 World Congress, listen to Cesar Garrido, Glenn Pierce, Mark Kay, Alain Baumann, Dawn Rotellini, Cesar Garrido, Megan Adediran, Dejan Petrovic, Robed Amin, Declan Noone, Durhane Wong-Rieger, Yuyun Maryuningsih, Margarita Elizabeth Garcia Gonzalez, Assad Haffar, Kibet Shikuku, Barun Khakurel, Donna Coffin, Margareth Ozelo, Novie Amelia Chozie and Tahira Zafar […]