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Haemophilia Foundation of New Zealand

Improving the lives and long-term outcomes of people impacted by bleeding disorders

Established in 1958, Haemophilia Foundation of New Zealand Inc. (HFNZ) supports and represents people with haemophilia and other related bleeding disorders in New Zealand.

Haemophilia and related bleeding disorders such as von Willebrand Disorder are lifelong chronic conditions for which there are no cures. HFNZ aims to ensure that affected people and their families in New Zealand receive the best possible treatment, care and support.

Haemophilia and other bleeding disorders are rare. Our members are all unique but they have this one rare thing in common – being part of the bleeding disorder community. HFNZ creates ways to unify this community and assist those affected by bleeding disorder.

HFNZ is dedicated to improving the lives of people with haemophilia and related bleeding disorders; but we cannot do it alone. Only with the generous financial support of caring New Zealanders can we make difference.

Find out more about haemophilia or check out our Events and News Sections – or download the latest edition of our newsletter Bloodline.

HFNZ Latest News Catriona 2

10th WFH Global Forum

28 November 2017

At the beginning of November HFNZ Vice-President Catriona Gordon attended the 10th WFH Global Forum on Treatment Products for Bleeding Disorders. These are always full of interesting informa...

Read the full article and more here
Our Upcoming Events IMG 0018

2018 Women's Wellness Weekend

14 September 2018

If you're an HFNZ woman with a diagnosed bleeding disorder, or who carries the haemophilia gene, then this is the fab weekend for you. Over the weekend of September 14 -16, women aged 18 plu...

Read about the event and more here
Give a little today

HFNZ are here to support people with haemophilia and other bleeding disorders, their families/whanau.
For as little as $20 you can help the cause.

Make a donation today