These FAQs may be updated as more information becomes known. This guide was developed using information from the New Zealand Ministry of Health, the Haemophilia Foundation Australia, and the...
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The Haemophilia Foundation of New Zealand (HFNZ) is a charitable organisation supporting people and their family and whānau living with haemophilia and related bleeding disorders across New ...
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This new edition of the World Federation of Hemophilia (WFH) guidelines for the management of hemophilia comes at an exciting time in the evolution of the diagnosis and treatment of this con...
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Kia ora koutou, At the next HFNZ AGM, on 8 November 2020, a special resolution will be put to members related to amendments to the HFNZ constitution. The current constitution was enacted in ...
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Kia ora koutou, It is with deep sadness that we advise of the passing of Dr. Mark Smith, haematologist and Clinical Director of Haematology at Canterbury Health Laboratories in Christchurch....
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The World Federation of Hemophilia Research and Education Department is happy to announce that the WBDR 2019 Data Report is now published and available online. The WBDR is a web-based data e...
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Haemophilia Foundation of New Zealand Inc. (HFNZ) is dedicated to improving the lives of people with haemophilia and related bleeding disorders, and their families/whānau, by providing support, care, education and advocacy.
Find out more about usHaemophilia and related bleeding disorders such as von Willebrand's Disorder are lifelong chronic conditions for which there are no cures.
As a charity, your donation to HFNZ means that you can help us ensure that people with bleeding disorders have the tools to live the best life they can.