Organisation Profile

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 member of the World Federation of Haemophilia. Its aims are:

  • To provide support for people with haemophilia and their families
  • To educate families, health professionals and others
  • To secure a high standard of treatment of haemophilia throughout New Zealand
  • To represent the haemophilia population at a government level and to health services providers

    • HFNZ is dedicated to improving the lives of people with haemophilia and related bleeding disorders; but we can not 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

    Quick Links

    NEWS

    HFNZ Publications


    HFNZ 2009 Annual Report

    Donate Online



    Important information for people who received plasma-derived clotting factor in the United Kingdom between 1980 and 2001