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Cystic Fibrosis NZ

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Vote for Cystic Fibrosis NZ to share $110,000 this Grants Round.

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Cystic Fibrosis NZ
#960 Rank6 Votes27 Days to vote
Cystic Fibrosis NZ

About us

“I remember it being very overwhelming in the beginning. I struggled to accept that my tiny baby Amber had this life-limiting, progressive illness without a cure,” Claire explains. Amber, now aged 13, is one of the 530 New Zealanders currently living with cystic fibrosis, a genetic condition that causes a build-up of thick sticky mucus in the lungs, digestive system and other organs, causing a wide range of challenging symptoms affecting the entire body. Cystic Fibrosis NZ is the only charity in New Zealand dedicated to supporting and improving the quality of life for people with CF and their families. Established in 1968 as a volunteer support group for parents with a newly diagnosed child, we dedicate ourselves to shaping a brighter future for everyone with cystic fibrosis. We receive less than 4% government funding and rely on the generosity of everyday New Zealanders to meet the ongoing needs of our community. With their help (and yours!) people with CF and their families receive personalised support from our team of CF Social Workers, financial assistance during hospitalisations and hardship, mobile medical equipment and more. We also contribute to promising CF research projects and advocate on behalf of the community for better access to treatment and care.
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Sept 2025 Grants Round

Grant Closes: September 30th

This grant round we are giving $31,000 to the Top #10 Australia and NZ Charities. Vote and support the Charities you love today and help them share in grants on 30 Sep 2025 10:01AM.

1st Place:
$8,000
#2:
$5,000
#3:
$3,000
#4-#10:
$2,000 each