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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2021 PWS 15 for 15 Challenge Highlights
Thank you 🧡 Thank you 🧡 Thank you 🧡 We have been blown away by the incredible generosity…
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Putting the CARE in Childcare
We know all too well how hard it is to hand your little one over to childcare. But to hand over a child with special needs, as…
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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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‘Summer Days’ – Katia’s Song
As we watched our daughter, Katia, perform her song, ‘Summer Days’ on ABC Radio on…
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The History of Prader-Willi Syndrome Awareness Month
During the month of May Community organisations, Associations and Foundations, Families and Supporters of people…
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PWSA Victoria working effectively in a COVID world
While many parts of the country have opened into the post COVID-19 world, Victoria and in particular Melbourne are still…
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