Kim has a strong background in the not-for-profit sector and a passion for helping people living with chronic conditions. This includes as a volunteer and past board member of Cystic Fibrosis New Zealand. She has successfully built strong sustainable relationships with clinical and non-clinical stakeholders to help deliver a wide range of projects and events that make a difference to patient’s lives.

Kim McGuinness

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. We work together to improve healthcare and wellbeing for everyone living with a rare health condition in New Zealand.

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