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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 Colleen Farewell

Pānui for March 2017

31 March 2017

Check out the March issue of Pānui. Find out all about Buddy Awards, The End of an Era, Theatre time, PEP Talk, and all the Latest News from HFNZ... Check it out HERE

Read the full article and more here
Our Upcoming Events PEP Logo

Parents Empowering Parents (PEP) 2017

16 June 2017

This is an amazing parenting programme especially designed for parents with a child with a bleeding disorder. Raising a child with a genetic bleeding disorder is a challenge that impacts the...

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