We invite all current Prader-Willi Syndrome Association of Victoria (PWSA Victoria) members to our upcoming Annual General Meeting (AGM).
This is a great opportunity for us to showcase all that we have achieved over the past 12 months and more importantly hear from our community on items that matter to them.
Details of the AGM will be emailed to current members shortly. If you still haven’t registered your 2021/2022 membership, please do so by clicking on the link below the follwing video.
Renee enjoys working with organisations to improve business outcomes by implementing and reviewing procedures to assist organisations to work more efficiently, effectively and strategically. Renee is mother to 3 children, the youngest of whom was diagnosed with Prader-Willi Syndrome not long after birth. Renee now spends her days caring for her son and volunteering full time as President of the Prader-Willi Syndrome Association of Victoria, helping to build on the supports and services provided by the Association since 1979.
