Cystic Fibrosis Wellington Christmas Tree Festival
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 Christmas Tree
This year we have over 60 beautifully decorated trees in the terminal as part of our annual Cystic Fibrosis NZ Christmas Tree Festival. Vote for your favourite tree and automatically go in the draw to WIN a $500 shopping spree at Wellington Airport! Click ‘Vote Now’ to view the trees and make a vote. Terms & conditions apply.
Design your own Christmas Tree competition for kids
It's time for our annual kids' Christmas colouring competition with the chance to win one of two kids' prize packs valued at $250! To enter, get your kids to design their own special Christmas tree and send it to us by 9am Friday 9 January 2026. Print an entry form via the link below or grab one at the airport. Submit the finished artwork via the online entry form below. T&Cs apply. Good luck!
Tree Sponsorship queries
2025 Tree Sponsorship Information Pack
If you have any questions, please contact the Festival Coordinator: cfwgtnxmastrees@gmail.com
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.