Succession Planning
Through the eyes of a parent Most of you, like me, have probably thought about your children’s…
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Interactive Story Time
Calling for expressions of interest Living with Prader-Willi Syndrome is challenging for the individuals but can be…
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Discovering the artist within
Hayley, our 35-year-old daughter, was born before genetic testing for Prader-Willi Syndrome (PWS) existed and…
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PWSA Vic Time Out Camp 2021
Camp Toolangi, September 25th 10am (Saturday) to September 28th (Tuesday) It seems like a lifetime since…
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State Wide Care Plan
For the past 12 months, the PWSA Victoria has been working closely with Monash University, Monash…
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Who Cares for the carers? Carer Gateway!
The Prader-Willi Syndrome Association of Victoria asked Carers Victoria to provide some information that we…
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A Tribute to Michael Andrews
I am very honoured to be invited to share with you all a tribute for…
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PWSA Victoria Face Masks – Now Available
Australian made, washable and lined with non woven fabric to filter out the unwanted nasties.…
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EAP Assist
The EAP Assist counselling service is still open and taking calls from PWSAV Families and…
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I can… because I am Archie
In May 2020 we took Archie to Sydney for his first NAPA Intensive. NAPA (Neurological…
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