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About us

Founded in 1958, HNZ is a registered charity that supports and advocates for people affected by haemophilia, von Willebrands Disorder, and other inherited bleeding disorders.             

Improving the lives and long-term outcomes of people affected by bleeding disorders since 1958

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Promoting excellence in haemophilia 
care, education, advocacy and support.

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About Us

Annual reports

Read our Annual Reports for a snapshot of HNZ as an organisation.

Each year Haemophilia New Zealand produces an Annual Report to highlight our activities, programmes and provide financial information on our organisation.

In 2013, our financial year changed from ending in December to ending in June.

 

2023/24 HNZ Annual report

2022/23 HNZ Annual report

2021/22 HNZ Annual Report

2020/21 HNZ Annual Report

2019/20 HNZ Annual Report

2018/19 HNZ Annual Report

2017/18 HNZ Annual Report

2016/17 HNZ Annual Report

2015/16 HNZ Annual Report

2014/15 HNZ Annual Report

2013/14 HNZ Annual Report

2012 HNZ Annual Report

2011 HNZ Annual Report

2010 HNZ Annual Report

2009 HNZ Annual Report

2008 HNZ Annual Report