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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…
Read ArticleIn May 2020 we took Archie to Sydney for his first NAPA Intensive. NAPA (Neurological…
Read ArticleThere has been a lot of recent activity in the field of PWS research in…
Read ArticleEarlier in 2020, the Prader-Willi Syndrome Association Victoria (PWSA Vic) received an Information, Linkages and…
Read ArticleFour years ago, the Prader-Willi Syndrome community was lucky enough to find themselves being supported…
Read ArticleIn 2019 PWSA Victoria successfully established various committees to ensure continuing smooth operation and delivery…
Read ArticleThe 2020 15 for 15 Challenge has raised over $28,000 and an incredible amount of…
Read ArticleDylan aged 8 lives with Prader-Willi Syndrome and against all odds has learnt to ride…
Read ArticleAfter years many years of advocating for Growth Hormone (GH) to become available under the…
Read ArticlePrader-Willi Syndrome (PWS) is a rare and complex, genetic disorder that affects Chromosome 15. So,…
Read ArticleThank you to our members for the ongoing support you’ve shown the Prader-Willi Syndrome Association…
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