Rare Disease Day media
Our CE, Lisa Foster, was interviewed four times for Rare Disease Day along with two mums of children living with a rare disease.
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Our CE, Lisa Foster, was interviewed four times for Rare Disease Day along with two mums of children living with a rare disease.
Last Friday Rare Disorders NZ launched a campaign calling for the development of a National Rare Disorder Framework.
In 2012, my brother Andrew became very unwell.
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Here are some resources created for people living with a rare disorder and their family by Rare Disorders NZ and our expert advisers.
Rare Disorders NZ (RDNZ) welcomes the recommendations within the New Zealand Health and Disability System Review.
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A time of change, challenge and new ways of living face us all.