FASD-CAN (Fetal Acohol Spectrum Disorder Care Action Network) is a New Zealand-based, non-profit, incorporated society made up of parents, caregivers, extended whānau and professionals. 

Most of our board members have been through the FASD journey with their own children. With lived experience, we know what you're going through and we know what you need.

Our vision is to ensure wider public knowledge of FASD, to push for more access to disability support and services, and to help understand and support individuals with FASD and their caregivers so they can live their best lives.