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Pws

Prader-Willi Syndrome (PWS) is a rare and complex neurodevelopmental disorder occurring in 1 in 16000 births, affecting approx 200 New Zealanders.
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Conditions We Support

Central Nervous System

  • Cognitive Impairment

Genetic Disorders

  • Prader-Willi Syndrome (PWS)

Hormonal Disorders

  • Growth Hormone Deficiency

Nutritional Disorders

    Rare

    • Other Rare Disease

    Mental Health

      If you've been diagnosed with any of these conditions, we're here to help.

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      Link to this page on PatientGroups.ai