Cystic Fibrosis is NZ's most common life-threatening inherited disease and the CF Association is the only national organisation dedicated to all aspects of the condition.

Important Dates

 

Reuters Charity Golf Classic

September 27/ 28

Wairakei Resort, Taupo.

 

Crusaders Charity Cricket Match

December 7th

Hagley Oval Christchurch.

 

Emma's Walk for a Cure

November 1st - January 9th

Support Emma Daken as she walks the length of NZ for CF Research! 

Welcome to the

Cystic Fibrosis New Zealand website

Take some time to navigate around our information pages. If you have an interest in CF-related matters, why not sign up for our newsletter or post a question on our message board.

 

The Cystic Fibrosis Association is an incorporated society providing membership for regional groups, businesses and individuals who wish to work together in support of people with cystic fibrosis and their families. There are branches in most regions to provide local support.


» Our Goal

The goal of the Association is to ensure increased life expectancy for people with cystic fibrosis and improved quality of life for them and their families; and through research to achieve better control and ultimate cure for the illness. Currently there are funds available for CF Research; applications should be made through Child Health Research (Cure Kids). An application form is available online at www.childhealth.org.nz

» Our Activities

The Cystic Fibrosis Association's activities include:

 

» Your Support

The Cystic Fibrosis Association needs your help to conduct its vital family support, education, information
and research services .

Options include:

  • A personal donation or business sponsorship
  • Approaching your local service club, community group, workplace or other organisation to donate urgently needed funds
  • Leaving a legacy or bequest in your will.
  • Volunteering for fundraising or other activities. 

 

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