Resources » Psychosocial Support for Families at the Child’s Diagnosis Stage
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Year: 2026

Language: English

Author(s): World Federation of Hemophilia

Format: Document

Psychosocial Support for Families at the Child’s Diagnosis Stage

ADDITIONAL INFORMATION

This booklet contains basic information about psychosocial aspects of rare coagulation factor deficiencies.

This resource was developed by members of the WFH Psychosocial Committee: Patricia Cabré and Silvina Graña

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.

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