Cystic Fibrosis Wellington Christmas Tree Festival

The Cystic Fibrosis Wellington Christmas Tree Festival lights up Wellington Airport through December, and all for a great cause. Find out how you can get involved.

Businesses and organisations sponsor and decorate a tree, and the funds raised support the valuable work of Cystic Fibrosis New Zealand. Cystic Fibrosis NZ is the only charity dedicated to supporting and improving quality of life for people with CF and their families in New Zealand.

Funds raised through the Christmas Tree Festival provides personalised support, whether it is emotional guidance, practical advice, or financial assistance, to individuals and their families throughout their journey.

It also provides medical equipment, vouchers during hospitalisations, and advocacy services to secure cutting-edge medicines such as Trikafta.

Vote for your favourite tree

We have over 60 beautifully decorated trees in the terminal for the 2024 Cystic Fibrosis NZ Christmas Tree Festival. Vote for your favourite and go in the draw to WIN $500 to spend at any store in the terminal! The People’s Choice winning tree sponsor will win a $5000 advertising package at Wellington Airport.

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Kids Design Your Own Tree competition

To celebrate the Cystic Fibrosis Wellington Christmas Tree Festival in terminal we're running our annual kids' Christmas colouring competition. Get inspired by the variety of trees in terminal, design your own tree on the entry form and be in to win one of two kids' prize packs valued at $250!

Design-your-own-tree-competition

Sponsor a tree

View the sponsors pack with all the information about sponsoring a tree for the 2024 Christmas Tree Festival. Please contact us: cfwgtnxmastrees@gmail.com with any questions.

About Cystic Fibrosis

Cystic fibrosis (CF) is a serious and ultimately terminal genetic condition affecting around 540 people in NZ. CF causes the body to produce thick, sticky mucus which damages the lungs, digestive system, liver and other parts of the body.

People with CF endure a rigorous daily treatment regime, including chest physiotherapy, oral, nebulised and occasionally intravenous antibiotics, and taking enzyme tablets with food. Some people with CF will have a feeding tube overnight. This regime can take up to three hours each day, having a huge impact on quality of life.

Progressively, CF can cause diabetes, asthma, liver disease, and permanently reduced lung function which, in many cases, requires a transplant. Life expectancy is in the 30s – less than half that of the average New Zealander.

Cystic Fibrosis NZ is the only charity dedicated to supporting and improving quality of life for people with CF and their families in New Zealand.

Funds raised through the Christmas Tree Festival provides personalised support, whether it is emotional guidance, practical advice, or financial assistance, to individuals and their families throughout their journey. It also provides medical equipment, vouchers during hospitalisations, and advocacy services to secure cutting-edge medicines such as Trikafta.