HFNZ Profile

Asia-Pacific Haemophilia Camp

Win a trip to the Asia-Pacific Haemophilia Camp in Qingdao, China from 16-18 August. Applicants aged 11-17 years will be judged on a drawing and essay competition.
Click here to download the entry form.
Applications Close 20th June, 2013

The Haemophilia Foundation of New Zealand Inc. (HFNZ) was established in 1958 to serve the needs of people with haemophilia and other related bleeding disorders. It is a National Member Organisation of the World Federation of Haemophilia. Its aims are:

To provide support for people with haemophilia and related bleeding disorders and their families/whanau
To educate families, health professionals and other key stakeholders
To maintain a high standard of treatment of haemophilia and related bleeding disorders throughout New Zealand
To be a representative of the haemophilia population at a government level and to health services providers
To be a responsible member of the global haemophilia community
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 our dreams come true.
Be sure to check out our Events and News Sections – or download the latest edition of our newsletter Bloodline for the latest information from the HFNZ.

Role of HFNZ

Promote the personal interest, treatment, rehabilitation, lifetime care, and advancement in life, of all people with haemophilia and related genetic bleeding diseases
Offer information and guidance, which promotes effective measures of care
Promote full participation and equal opportunity for all in community activities, education, recreation, and employment
Provide or seek individual assistance welfare, participation, opportunity, and advocacy
Provide representation, at a regional and national level, to ensure that adequate and safe supplies of treatment products, and other treatments or cares are available
Advocate for adequate services to meet the needs of people with haemophilia
Provide up-to-date information
Act as a consultative body to Government