Jasmine's story

Families like Jasmine's are why we're here this evening. We're working to accelerate type 1 diabetes (T1D) research to make the condition a thing of the past. 

Hear Jasmine's speak at Night of Champ1ons

Every single person and family impacted by type 1 diabetes (T1D) is why Breakthrough T1D exists. Because the 135,000+ Australians living with T1D and the 8 more who are diagnosed every day – as well as the countless more who are impacted by the condition – desperately need breakthroughs to transform their lives.    

Jasmine and her family are just some of those Australians counting on us to create a world without T1D. 

"Let me tell you a little about how I feel about type 1 diabetes. It’s not just a diagnosis – it’s an invisible shadow that never leaves. It’s relentless. It’s there when I wake up, when I eat, when I sleep. It’s there when I’m laughing with friends or just trying to be a normal teenager..."

– Jasmine, 15, diagnosed with T1D at 5

The words above are a sneak peek at the story Jasmine will be sharing at Night of Champ1ons. You'll hear the brutal reality of living with T1D as a young person who knows there's currently no cure for this relentless condition. You'll learn about what goes into trying to stay healthy as someone living with T1D, and also the emotional toll it brings – not just for the person living with the condition, but for their family and loved ones, too. 

We are committed to driving cures and improving lives for those living with T1D. But we will not get there alone. We need you to stand with us.

With your support, we will change lives and move closer to cures for T1D – for Jasmine, and the 135,000+ Australians just like her.   

Help create a world without type 1 diabetes for 135,000+ Australians just like Jasmine – and their families