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 2023/2024 membership, please do so by clicking on the link below.
Renee excels in enhancing business operations by refining processes, ensuring organisations function with greater efficiency, effectiveness, and strategic insight. Beyond her professional expertise, Renee is a mother to four children. Her life took a poignant turn when her second youngest child was diagnosed with Prader-Willi Syndrome shortly after birth. Embracing this challenge with grace, Renee now dedicates her time to caring for her son while also committing herself wholeheartedly to her role as President of the Prader-Willi Syndrome Association of Victoria.
Ever since her son Harvey’s diagnosis, Renee has been a force of change, initiating and steering innovative programs and services designed to empower individuals with Prader-Willi Syndrome. Renee is deeply invested in the tenets of social justice and inclusion, driven by the conviction that individuals with disabilities deserve equitable access to support and resources necessary for a full and inclusive life. Her profound dedication to her work and her family reflects an overarching mission to ensure that every individual with disabilities can thrive in a supportive and inclusive society.
