Peer Support


MyTime is a free virtual peer group discussion for parents and carers raising a child with a delay or disability. It’s a place to share and learn from other families and talk about your experiences. It’s a world away from appointments and therapy. It’s support for you.

Our peer groups are run by trained and knowledgeable parent facilitators who understand what it’s like to have a child with disability and have experience navigating the different services and systems, including NDIS.

These virtual sessions are run regularly, with sessions in the day and night. Each MyTime is a topic-based discussion, meaning you are able to attend the discussions which are most relevant to your child, and the stage in your parenting journey. We regularly have guest speakers, including parents, professionals, as well as services who share information about the support available to families. You can find out more and register for a free MyTime peer group via our EVENTS page

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Kindred Community is our private Facebook group which you can come to at any time. It is a moderated community for families raising a child with disability to come together to share and learn with each other.

Our community is a safe space to get help with everyday life. It’s a trusted place to come to find helpful information based on the lived experience of other families. Connect with other parents and caregivers who understand the unique joys and challenges of the journey. Come to share your concerns, celebrate the wins, no matter how big or small, and step back to look at the big picture.

Search on Facebook – Kindred Community or CLICK HERE.

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Don’t worry, we’re not here to overload your inbox. What you’ll get from us will be inspiring stories, details of upcoming events, helpful resources and other opportunities to be part of our community. From our family to yours, every fortnight or so.

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Join our community facebook group

To connect, celebrate and learn with parents and carers on their own beautiful journeys. Ours is a safe space where you can come to ask advice and share experiences on anything from your child's diagnosis to navigating the NDIS.

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