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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 H alone trans sml

HFNZ Covid-19 update: 06 April

6 April 2020

Kia ora koutou, As of today all of New Zealand is on day twelve of alert level four - a full lockdown for at least four weeks. That means only essential services remain open and movement is ...

Read the full article and more here
Our Upcoming Events Teramwork at 2017 Youth Camp

Youth Camp 2020

10 July 2020

On July 10 - 12 2020 HFNZ are running a Youth Camp at an as-yet undetermined venue in Auckland. Growing up is exciting, challenging, and often very confusing. When a bleeding disorder is add...

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