Raising a child with a rare disorder

A guide for parents and caregivers living in Aotearoa New Zealand

This booklet has been created by Rare Disorders New Zealand to help parents and caregivers navigate the path in caring for a child with a rare disorder in New Zealand.

By gathering insights and advice from parents and caregivers who share this journey, as well as information and resources that may help along the way, we hope to provide a guide of sorts – to help you find what works best for your whānau.

Download Caregiver Guide

While we do not have all the answers, we hope this guide provides reassurance that there are many others going through a similar journey and that support is available.

The guide was launched on 28 February 2023, Rare Disease Day, at Government House, by our patron Her Excellency, The Right Honourable Dame Cindy Kiro, GNZM, QSO, Governor-General of New Zealand.

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Our Collective

Rare Disorders NZ is the collective voice of all people living with a rare disorder and their whānau. Our rare collective is made up of more than 150 disorder-specific support groups. Our work is informed by the issues important to our collective, and we work together to improve healthcare and wellbeing for everyone living with a rare health condition in New Zealand.

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