Reconnecting with our community after COVID
After close to a year of lockdown and restrictions, we are eager to reconnect with…
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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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Time Out Camp Postponed until September 2021
It is with our deepest regret that the 2021 PWSA Victoria Time Out Camp will…
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Cheerful Monster
If you could pick the worst candidates for ‘parents of a PWS child’ – I…
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Santa Claus says “Christmas will not be cancelled this year”
The Prader-Willi Syndrome Association of Victoria (PWSA Victoria) recognises that our families have felt the…
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Filling the void in Information available for Siblings living with Prader-Willi Syndrome
The Prader-Willi Syndrome Association of Victoria (PWSA Vic) would like to thank the Rotary Club…
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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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At home learning strategies for people with PWS during COVID-19
A summary of a presentation to the Foundation for Prader Willi Research by Elizabeth Roof,…
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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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Research and Clinical trials news
There has been a lot of recent activity in the field of PWS research in…
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