
Overcoming Challenges in Hemophilia Care
This booklet contains basic information about psychosocial aspects of rare coagulation factor deficiencies. This resource was developed by members of
Year: 2022
Language: English
Author(s): World Federation of Hemophilia
Format: Congress recordings
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In this session from the WFH 2022 World Congress, Susan Cutter (United States), Patricia Cabré (Spain) and Sarah Whitaker (United Kingdom), will discuss the impact of anxiety and stress on parents and caregivers, couples, young adults, and people with inherited bleeding disorders, as well as possibly interventions.
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.
The WFH does not promote any particular pharmaceutical product and any mention of any commercial brand in this presentation is strictly for educational purposes.

This booklet contains basic information about psychosocial aspects of rare coagulation factor deficiencies. This resource was developed by members of

This booklet contains basic information about psychosocial aspects of rare coagulation factor deficiencies. This resource was developed by members of

This booklet contains basic information about psychosocial aspects of rare coagulation factor deficiencies. This resource was developed by members of

Welcome to this exciting project, a collaborative effort between the Nurses Committees of the European Association for Haemophilia and Allied

Welcome to this exciting webinar, a collaborative effort between the Nurses Committees of the European Association for Haemophilia and Allied

Psychosocial support is an important part of comprehensive care for people with hemophilia. The aim of this monograph is to