At just six years old, Maya Konstantinou has already faced challenges many adults struggle to comprehend.
Diagnosed with type 1 diabetes at the age of two, she was introduced early to hospital rooms, needles and the daily realities of a lifelong autoimmune condition that requires constant care.
Type 1 diabetes occurs when the immune system attacks the insulin-producing cells in the pancreas, meaning the body can no longer regulate blood glucose levels on its own. There is currently no cure, and those living with the condition must monitor their blood sugar closely and rely on insulin every day to stay alive.
But rather than allowing fear to define her childhood, Maya has emerged as a courageous young advocate – one who speaks with clarity, honesty and a wisdom well beyond her years.
From standing inside Parliament House in her blue Breakthrough T1D T-shirt to meeting the Prime Minister and senior decision-makers, Maya has helped put a human face to life with type 1 diabetes, reminding adults that children living with the condition are, first and foremost, still children.
Supported by her parents and inspired by a desire to ensure no child feels alone or frightened by a diagnosis, Maya is using her voice to call for early screening, better support and, ultimately, a cure.
In her own words, Maya shares what it’s like to live with type 1 diabetes, what gives her strength on hard days, and why she believes hope – and community – can change everything.
Maya, do you remember when you found out you had type 1 diabetes, and what do you want other kids to know about living with it?
I remember going to the hospital and feeling really tired. There were lots of doctors and needles, which I didn’t like. I want other kids to know it’s scary at first, but you can still play, laugh, and be happy. You’re still you. I remember receiving Rufus and now he stays with me forever and through everything.
You’ve met the Prime Minister and spoken in Parliament House – how did that make you feel, and what do you like telling grown-ups about diabetes?
Excited, I love going to Parliament house in my blue Breakthrough T1D top. Parliament House is so big! I like telling grown-ups that kids with diabetes are just kids and we need help, talking about what we need and why. And we don’t get diabetes from eating too much sugar. The support of the people in Parliament House is really important, we get our voices heard so change can happen.
What are some of the hardest parts of having type 1 diabetes every day, and what helps you stay brave when things feel tough?
The hardest parts are finger pricks and pod changes. The worst is having to stop when playing to check my blood sugar. I stay brave by holding Mum or Dad’s hand and reminding myself I can do hard things. Mummy and my little brother like to tickle me when I do pod changes which makes it more fun than sad.
Your mum and dad say you’re a big advocate – why do you think it’s important to talk about diabetes and help other families?
Because I don’t want other kids to feel scared or lonely like I did. If we talk about it, families know they’re not alone and it makes it a little bit easier. It is really fun having other friends with type 1 because we can play and talk knowing we are like each other. That’s why Type 1 Diabetes events are important
If you could change one thing for kids who might be diagnosed with type 1 diabetes in the future, what would you hope for them?
They can be caught early and don’t have to go through the scary part. I hope it won’t be so annoying in the future, but my big hope is there’s a cure. A cure means, me, Baba, Theo, my cousin and my Papou can be cured. Plus, all the other children with Type 1.
When you’re not being a diabetes advocate, what are your favourite things to do, and what makes you feel happy and strong?
I like playing, drawing, soccer, and Greek dancing. I feel happy when I laugh and strong when I try even if things are hard. Creating new things and drawing is my favourite.
Is there anything else you’d like to say?
Kids with diabetes are brave, it’s okay to be scared – you’re still amazing.
My mummy works hard to help others with Type 1. She’s doing another gala. Last time she told me she dressed up like a princess. Daddy wore a fancy outfit too. She told me it was for me and all the children living with Type 1. She is doing it again!
Alongside President of the Greek Orthodox Community & Church of Canberra, John Loukadellis, who is also a Director at Macquarie Group, and the Konstantinou family who are hosting the gala, funds raised on the night go to Breakthrough T1D – the leading research, advocacy, and community support organisation for type 1 diabetes (T1D) globally. Striving for a brighter future for everyone living with type 1 diabetes.
Working together in 2024, the Macquarie Group Foundation supported the matching of funds raised, contributing $50,000 to the Gala. Hellenic Club Woden is also a sponsor for the second time in a row and the venue host.
Type 1 Diabetes Gala Details
- When: Saturday 16th May 2026
- Where: Hellenic Club Woden
- Details: 3 course meal drinks included, silent and live auction.Â
- Tickets on sale – tables of 10 available – https://type1diabetesgalacbr.eventbrite.com.au/Â
