
Could a Natural Supplement be the answer to ‘correcting’ the hunger in PWS Patients?
My name is Joanne Griggs, and for those, I don’t know, especially those with younger…
Read ArticleMy name is Joanne Griggs, and for those, I don’t know, especially those with younger…
Read ArticleThe 2020 15 for 15 Challenge has raised over $28,000 and an incredible amount of…
Read ArticleEach year we host the PWSA Victoria Time Out Camp. This four-day event encourages those living…
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…
Read ArticlePhysiotherapy for children with Prader Willi Syndrome (PWS) primarily focusses on the child’s low muscle…
Read ArticleJamal’s recent achievement in his swimming will see him compete at the 2021 Special Olympics…
Read ArticleWith all the talk of vaccines for the coronavirus many of us are getting more…
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