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Haemophilia Advocacy

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 Lauren Nyhan FB DP

Pānui for June 2016

6 July 2016

Check out the June issue of Pānui. Hear about what our Youth Committee are up to, find out more about Family Camp, get ready for the Piritoto Noho Marae, and more... Check it out HERE

Read the full article and more here
Our Upcoming Events 2016 NFC promo

National Family Camp 2016 - Rotorua

30 September 2016

The National Family Educational Camp is an educational weekend for those families who have a child with a bleeding disorder aged between 0 to 10 years – with a fair bit of fun and relaxation...

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