Cystic Fibrosis Association of New Zealand

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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. 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 register for our Community Forum?

Important Dates Coming Up

August 4th - 10th   National Awareness Week - Look out for collectors in your area 

August 23rd, Winter Caeli (Scottish Ball) - Intercontinental Hotel Wellington

September 27/ 28 - Reuters Charity Golf Classic - Wairakei Resort, Taupo

December 7th - Crusaders Charity Cricket Match - Hagley Oval Christchurch

November 1st - January 9th - Emma's Walk for a Cure - support Emma Daken as she walks the length of NZ for CF Research!

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:

  • Providing an information service about CF, publishing brochures and other printed material.
  • Promoting public awareness of CF.
  • Providing support for people with CF and their families,e.g. conference travel grants, welfare assistance.
  • Providing educational opportunities for people with CF, e.g. tertiary study grants and scholarships, and achievers awards.
  • Communication and co-ordination through newsletters and conferences.
  • Providing a voice to Government and agencies on behalf of the CF community.
  • Encouragement and funding for CF research.

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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Cystic Fibrosis Association of New Zealand © 2008
PO Box 8241, Riccarton Christchurch New Zealand - Phone: +64 3 341-8024
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