Named for George. And for yours.
A community movement for every regional family
doing it without enough support, doing it anyway.
In regional Australia, a child's postcode is determining their educational ceiling. We are building the movement, and the evidence base, to change that. Named for George, my four-year-old son who is autistic and non-verbal and one of the most joyful little people you'd ever meet.
About Us
I'm a single mum of three boys, Harry, Ollie, and George, and we live in Metung, in East Gippsland, Victoria. Our corner of the world is beautiful. It is also a long way from the services our kids need.
George is my youngest. He is autistic and non-verbal, and one of the most joyful little people you will ever meet. When we couldn't find a school placement that was right for him, I stopped waiting for someone else to fix it.
I built Do It For instead. For George. And for every family in regional Australia doing it without enough support, doing it anyway. 🫧
In November 2026, I'll be running the Lakes Entrance half marathon in George's honour, training through the early mornings, the muddy tracks, and the chaos of life with three boys.
The Run, Lakes Entrance Running Festival
Counting down to the starting line
Lakes Entrance Running Festival, 1 November 2026
Fundraising Progress
23.3% of the way there. Every dollar counts 🫧
George's Story
George is four. He's autistic, non-verbal, and one of the most joyful little people you'll ever meet. He loves being around people, he's learning to communicate in his own beautiful way, and he lights up every room he walks into.
He is also approaching school age with nowhere appropriate to go in regional Australia. George falls into a gap that doesn't have a name yet, too capable for a specialist school, too complex for mainstream.
And he is not the only one. There are families all over regional Victoria, and regional Australia, living exactly this. Do It For was named for George. But it was built for yours, too.
The Movement
Autism-specific education works. Schools like Aspect and the Mansfield Autism Statewide Services model prove it. But in regional Australia, the distance to those services is too great for most families.
Do It For is building the evidence base, the community, and the political will to change that. We are not asking for something new. We are asking for something that already works — to reach further.
Connecting regional families who are navigating the gaps, so no one does it alone.
Building the data and stories that make the case to government for change.
Taking that case directly to the people with the power to act on it.
The Run
On 1 November 2026 I'll run the Lakes Entrance Running Festival half marathon in George's honour. I am not a runner. I am a mum who is doing it anyway, because that's what this movement is about.
Every dollar raised goes directly toward the Do It For movement, building community, funding advocacy, and making noise where it matters most.
Advocacy
We have met with Federal Member for Gippsland Darren Chester. We have written to Ministers Jason Clare, Ben Carroll, and Kristy McBain. State MP Tim Bull has responded positively and flagged existing mechanisms that could help.
This is what advocacy looks like when it comes from a community, not a lobby group.
In March 2025, Lily met with Federal Member for Gippsland Darren Chester to present the Do It For case directly. A media release was published through his office following the meeting — the first formal recognition of the movement at a federal level.
Meeting with Darren Chester MP, Federal Member for Gippsland. A media release published through his office.
Tailored letters to Ministers Jason Clare (Education), Ben Carroll (Vic Education), and Kristy McBain (Regional Education).
Engagement with State MP Tim Bull, who responded positively and flagged a regional discretion mechanism worth pursuing.
The Wall of Names
These are the children behind the movement. Every name is evidence. Every family that registers makes this louder.
Children on the Wall
and growing every day 🫧
You can keep your child's name private. They'll still be counted, still matter. 🫧
🫧 You can keep your child's name private if you prefer. They'll still be counted, still be seen, still matter.
You don't have to have a child with a diagnosis to be part of this. You just have to believe that where a child is born shouldn't determine what they can access.
Add a Name to the WallYou Don't Need a Diagnosis
This movement exists because of the people who show up, not just the families living it, but the friends, teachers, neighbours, and strangers who decide it matters. Here's how you can be part of it.
Every dollar supports our advocacy work, getting regional families' stories in front of the people who can change things. No amount is too small.
Support the movement →Share our page. Talk about it at school pickup. Tag us. Post about it. The more people who know this gap exists, the harder it is to ignore. That's the whole point.
Follow @doitfor_____ →Come to Lakes Entrance on 1 November. Line the course. Make noise. Every familiar face on race day is a reminder of why this is worth doing.
About the run →Know a family affected by this? Add their child to the Wall of Names. You can keep it private. They still get counted. Every bubble on that wall is proof the need is real.
Add to the wall →You don't need to be a policy expert. A short email from a constituent matters. We can help you with what to say. Reach out and we'll point you in the right direction.
Get in touch →Sometimes the most important thing is simply believing this matters, and saying so out loud. That's where movements start.
Where your support goes
Every dollar raised goes directly to regional families doing it without enough support. Here is exactly where your contribution lands.
Filling what NDIS no longer covers
The NDIS provides just $200 a year for sensory equipment on any plan. A weighted blanket alone can cost that. The Gap Fund steps in where the system steps out, covering sensory and regulation equipment, AAC devices and communication aids, therapy top-ups when plans run out mid-year, and travel costs to reach specialists hours away.
Because you can't pour from an empty cup
80% of NDIS families are single-parent households. The Carer Recharge Program exists for the person holding everything together. A funded break with no strings attached, emergency respite when formal respite falls through, counselling and mental health support for the carer, and peer connection for isolated regional carers.
The kids who hold it all together, quietly
Siblings of neurodivergent children often move to the back seat without being asked. They adapt. They wait. They grow up fast. The Sibling Circle funds experiences that are entirely theirs, connection groups for regional kids who understand, mentoring programs, and school holiday activities designed just for them.
Because geography shouldn't determine destiny
In regional Australia, a child's postcode is determining their ceiling. This pillar funds transport subsidies to Melbourne-based services, telehealth setup for families without reliable tech, bringing specialists into the region, and school holiday intensive programs delivered locally so families don't have to choose between distance and support.
The infrastructure that makes everything else possible
Staff and coordination, grant writing, legal and compliance costs, communications, and technology. The work that keeps this foundation running so the other four pillars can keep changing lives.
Like every sustainable charity, Do It For carries operational costs. We believe in full transparency, so you always know exactly where your support goes.
A foundation that can't sustain itself can't sustain families.
Get support
Do It For exists to support the whole family. The child, the carer, the siblings, and everyone holding it all together. Below you will find the different ways we can help and how to apply.
For when NDIS doesn't cover what your child needs
Weighted blankets, sensory swings, communication devices, therapy top-ups, travel costs to see specialists. If NDIS has left a gap, we want to help fill it.
Who can apply: Families of neurodivergent children in regional Australia where NDIS funding does not cover the item or service needed.
Because you can't pour from an empty cup
A funded break, emergency respite, counselling support or simply something just for you. If you are the person holding everything together, this one is for you.
Who can apply: Carers and parents of neurodivergent children in regional Australia who need rest, respite or mental health support.
So siblings are seen too
An experience, an outing, a program or simply something that is entirely theirs. If you have a sibling who has quietly moved to the back seat, we see them.
Who can apply: Siblings of neurodivergent children aged 18 and under, or still living at home, in regional Australia. Applications are welcomed from parents or guardians on their sibling's behalf.
Because geography shouldn't determine destiny
Travel subsidies, telehealth setup support or help accessing services that simply don't exist in your town. Living regionally should not mean going without.
Who can apply: Families in regional or remote Australia who face barriers to accessing services due to their location.
Every month we celebrate a carer who is doing it anyway
Being a carer is one of the hardest and most invisible jobs in the world. Every month Do It For selects one carer, a parent, grandparent, guardian or support person, and gives them something just for them. A funded experience, a break, a gift, something that says we see you and we are grateful.
Nominate yourself or someone you know. You do not need to explain or justify. You just need to show up.
Any carer, parent, grandparent or guardian of a neurodivergent child in regional Australia. You can nominate yourself or someone else.
A funded experience chosen for them, whether that is a weekend away, a spa day, a meal, or something else entirely. Plus a celebration of their story across the Do It For community.
Selected monthly by the Do It For Foundation based on nominations received. All nominations are treated with care and confidentiality.
How to apply
Tell us a little about yourself and what you are applying for. There are no wrong answers and no hoops to jump through. We read every single application and respond to every one.
Applications are assessed monthly. You will hear back from us within two weeks of submitting. If we cannot help right now, we will tell you honestly and keep your details on file for when we can.
Everything you share with us is treated with complete care and confidentiality. We will never share your story without your permission. This is a safe space. 🫧
Our Sponsors
These incredible East Gippsland businesses have come on board to support the Do It For Foundation half marathon run. We are deeply grateful for every single one of them.
Support the Movement
All contributions go directly to neurodivergent children and their families in regional Australia — because where you live should never determine the support you receive.
Choose an amount
Have a question about donating, or want to get involved in another way? Reach out directly — we'd love to hear from you.
All contributions gratefully received. DGR status pending — we'll update when confirmed. 🫧