Year: 2020
Language: English
Author(s): World Federation of Hemophilia
Patient Education is a core function of the work of any national member organization (NMO). It plays a vital role in enhancing patient care and outcomes. An educated patient is not only better able to manage their condition, but they are also better placed to support NMO efforts in advocating for improved access to care and treatment.
Listen to this 75-minute webinar that took place on 18th September 2020, chaired by Magdy El-Ekiaby, MD, Regional Advisor for the Middle East. Speakers include David Page (Canada), Brian O’Mahony (Ireland), Solange Sakr El-Hage (Lebanon) and Masood Malik (Pakistan). The objectives of this session are to underline the importance of patient education as part of the NMO’s core functions; share international and regional lessons learnt through years of designing and implementing patient education programs; and discuss the challenges faced and the strategies that can be used to cope with changing country and regional contexts.
The Report on Annual Global Survey (AGS) includes demographic and treatment data, providing a global snapshot of people with hemophilia,
This patient handbook contains basic information about the inheritance, diagnosis, symptoms and management of fibrinogen disorders, including afibrinogenemia, hypofibrinogenemia, dysfibrinogenemia
Publishing in Haemophilia—the official journal of the WFH—presents both opportunities and challenges for researchers and practitioners in the field. While
The WFH Shared Decision Making (SDM) Workbook is for people with hemophilia A or B and their healthcare team. It
The World Bleeding Disorders Registry (WBDR) 2023 Data Report provides aggregate data on more than 14,000 people with hemophilia &
In celebration of International Women’s Day, the WFH hosted an educational webinar. The event centered around reproductive tract bleeding, pregnancy,
