The Heather Jones Community Award celebrates the otherwise unsung heroes of the FASD community – advocates, carers, people living with FASD, and others whose passion and dedication lead to improved awareness and understanding of FASD, and positive impacts to those living with this lifelong disability.
Meet Natasha and Maree. In this video they share their experience navigating the assessment and diagnosis process for FASD, and what a diagnosis of FASD has meant for their family.
Join Jazpa and his mum Sam to learn more about their journey living with FASD
Going through an assessment and learning your child has FASD is a very challenging process, but parents & carers also report benefits from finally understanding the cause of the difficulties.
At the 2018 Australasian FASD Conference, Counsellor Kath Thomas offered personal insight into her own struggles while caring for two children living with FASD.
Our thanks go to the remarkable families who gave their time and invited us into their homes, school and life. Their stories are testament to their hardwork, dedication, love and resilience in bringing up these children and young people.
We also acknowledge the expertise and professionalism of the health professionals who gave us their time to film in their clinics and offices.
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FASD Hub Australia acknowledges Aboriginal and Torres Strait Islander peoples as the Traditional Custodians of Country throughout Australia, and we recognise their connections to land, water and community. We pay our respect to their elders past and present, and extend that respect to all Aboriginal and Torres Strait Islander peoples.