The arrival of a child is an exciting time. Receiving a diagnosis of Prader-Willi syndrome (PWS) can be very daunting. You are not alone! These brochures can help in understanding what PWS might mean for your child’s future and what you can do.
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She is smiley, cuddly and about the happiest little girl you could ever meet! Evie is living with PWS. There a many things parents and care givers can do to support Evie to have her best life. Evie will develop and grow and thrive when those supporting her, from family to health professionals and others in the community know about PWS. The following articles will help with educating yourself and others on journeys like Evie’s.
All babies and toddlers thrive on games, love and fun. This is a crucial development phase. This series of articles about the health and development of birth to 2 year olds living with PWS provides ideas and guidance for families and professionals.
We welcome enquiries about anything related to PWS. This could be about the changes through the life stage of living with PWS, individual needs, services, getting help or interacting with the NDIS, the Quality and Safeguards Commission or the AAT.