Ma te kaha o te kaha, te aratohu me te whakaaro nui, ka tupu te tipu me te whakatutuki i te hunga ki te FASD.
With shared strength, guidance and wisdom, those with FASD can grow and achieve.
Tēnā koutou! Nau mai haere mai ki a FASD-CAN.
Hello! Welcome to FASD-CAN.
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.
Ko ā mātou mahi
What we do
We provide general information, help with diagnosis, funding, the justice system, housing and more on your FASD journey.
There's so much to know about FASD – we have info for educators, employers, health professionals and the justice sector.
We have tips and strategies, webinars, crisis support, contacts and educational material for caregivers and whānau.
We advocate for the rights, interests, welfare and inclusion of people with FASD in Aotearoa New Zealand, including the right to have their disability recognised.
We coordinate and run whānau and caregiver support groups nationwide and partner with other disability groups, carers and inclusive education groups.
ka whakaaraara mōhiotanga
we raise awareness
We aim to increase awareness and understanding of FASD, reduce stigma and increase knowledge of this neurodisability in Aotearoa New Zealand.
Tō Mātou Pūrākau Matua
See all stories
Leanne and Dennis: The Caregivers
We know that many of our tamariki who are fostered or adopted are affected by FASD. Those initial contacts with new caregivers can make a world of difference to children who may have been traumatised in their birth homes.
Ko mātou tēnei
Who we are
He kōrero anō e pā ana ki a FASD
More about FASD
Alcohol is a 'teratogen' – a substance that reaches the baby in utero and can change the structure and function of developing organs. Fetal Alcohol Spectrum Disorder is a lifelong brain injury that will not 'get better'. But if diagnosed early enough, the effects can be mitigated.
E pā ana ki a mātou
We're a group of committed caregivers and whānau, service providers and health professionals. We meet regularly to discuss current issues relating to FASD in New Zealand, and how our organisation can grow public awareness and support families working through their FASD challenges.
Ko ō mātou kaitautoko
FASD-CAN is grateful for support from the Rātā Foundation, the Nikau Foundation, Foundation North, Te Whatu Ora and Oranga Tamariki.
For information on becoming a funder or sponsor please contact us at [email protected]
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