Year: 2008
Language: Setswana
Author(s): World Federation of Hemophilia
Format: Document
Also Available In: English, Spanish, French, Arabic, Russian, Simplified Chinese, Japanese
This resource has also been translated into the following languages, with permission from the WFH, by NMOs: Farsi, Polish, Bengali
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 for the translation or for any errors or changes to content from the original English edition. Patient organizations interested in translating a WFH resource must first obtain permission from the WFH, available here.
This patient handbook contains basic information about the inheritance, diagnosis, symptoms and management of von Willebrand disease.
In this session from the WFH 2020 Virtual Summit, Dawn Rotellini, Paula James, Jeannette Cesta, Cody Kester & Baiba Ziemele
In this session from the WFH 2020 Virtual Summit, Jill Johnsen, Michael Laffan & Jameela Sathar discuss von Willebrand disease
Escuche este webinario de 90 minutos presentado el 1 de septiembre de 2021 para aprender cómo abogar por una mejor
Écoutez ce webinaire de 90 minutes présenté le 1er septembre 2021 pour en savoir plus sur le plaidoyer pour de
Listen to this 90-minute webinar presented on September 1, 2021 to learn about advocating for better care using the ASH
Listen to this 90-minute webinar presented on September 1, 2021 to learn about advocating for better care using the ASH