Episode 40: Diagnosed at 10 Months: Eli's Type 1 Diabetes Story

Episode 40: Diagnosed at 10 Months: Eli's Type 1 Diabetes Story

In this episode of The Type 1 Club, Jacqui speaks with Hannah, a fellow Type 1 mum whose son Eli was diagnosed at just 10 months old. Hannah shares the early signs they missed, the terrifying moment that led to calling an ambulance and Eli’s time in intensive care with severe diabetic ketoacidosis. What began as months of an unsettled baby quickly turned into a life-changing diagnosis just days before Christmas. Together, Jacqui and Hannah talk about navigating life with a very young child with type 1 diabetes – from learning injections and managing unpredictable blood sugars to the relief of moving onto insulin pump therapy with diluted insulin. They also discuss: * The challenges of managing diabetes in babies and toddlers * Food aversions and the realities of dosing insulin for little eaters * Sibling dynamics when one child needs extra care * The role of technology * How the type 1 community often becomes an invaluable source of support and practical advice * Preparing a child with type 1 diabetes for kinder and school Hannah also shares her perspective on protecting children from the emotional weight of diabetes for as long as possible while still helping them grow into confident young people living with the condition. A thoughtful and honest conversation about parenting, advocacy and finding your people in the “worst best club.” Further Resources:             Type 1 Foundation Website [https://www.type1foundation.com.au/] Follow us on Instagram [https://www.instagram.com/thetype1foundation/] Join the Facebook Group [https://www.facebook.com/share/g/1Agrpd2YbW/] If you'd like to share your story with our podcast listeners, please email: podcast@type1foundation.com.au

Episode 39: Living With Type 1 Together

In this episode of the Type 1 Club Podcast, Jacqui speaks with Himanshu, who shares his experience of living with type 1 diabetes and later supporting his son through the same diagnosis. They discuss the realities of managing diabetes across different generations, the role of technology and how families learn to adapt, support each other and keep life moving forward. Himanshu shares the importance of family support, managing parental anxiety and helping his son see diabetes not as a limitation but simply as part of their lifestyle. It’s an honest and thoughtful conversation about parenting, resilience and learning to live with type 1 together. Further Resources:            Type 1 Foundation Website [https://www.type1foundation.com.au/] Follow us on Instagram [https://www.instagram.com/thetype1foundation/] Join the Facebook Group [https://www.facebook.com/share/g/1Agrpd2YbW/] If you'd like to share your story with our podcast listeners, please email: podcast@type1foundation.com.au

Episode 38: Teen Life with Type 1

In this episode, Jacqui chats with Emily Mason, a teenager from Tasmania who shares her experience of being diagnosed with type 1 diabetes at 13. Emily speaks openly about becoming critically unwell before diagnosis, returning to school just days later and navigating life as the only person she knew with type 1. Now using pump therapy and playing football, she reflects on growing confidence, managing diabetes alongside sport and finding connection with others living with the condition. It’s an honest and hopeful conversation about growing up with type 1 and learning to thrive. Further Resources:           Type 1 Foundation Website [https://www.type1foundation.com.au/] Follow us on Instagram [https://www.instagram.com/thetype1foundation/] Join the Facebook Group [https://www.facebook.com/share/g/1Agrpd2YbW/] If you'd like to share your story with our podcast listeners, please email: podcast@type1foundation.com.au

Episode 37: Chris Roome, Adventures With Type 1

In this episode, Jacqui chats with Chris Roome, who has spent much of his life proving that type 1 diabetes doesn’t have to define what’s possible. Diagnosed at 12, Chris quickly adopted the mindset of being child first, diabetic second. Since then, he’s taken on endurance races, extreme outdoor adventures and even dog sledding in the Arctic, all while managing the constant decisions that come with type 1 diabetes. Chris also shares the inspiration behind Project InsulNation, a community designed to bring people with type 1 together through outdoor adventure and shared experience. This episode is a reminder that with preparation, resilience and the right support, life with type 1 diabetes can still be bold, adventurous and full of possibility. Connect further with our guest: Instagram:  @project_insulnation [https://www.instagram.com/project_insulnation/] Facebook: Chris Roome [https://www.facebook.com/chris.roome.2025] Website: www.projectinsulnation.com [http://www.projectinsulnation.com/] Further Resources:          Type 1 Foundation Website [https://www.type1foundation.com.au/] Follow us on Instagram [https://www.instagram.com/thetype1foundation/] Join the Facebook Group [https://www.facebook.com/share/g/1Agrpd2YbW/] If you'd like to share your story with our podcast listeners, please email: podcast@type1foundation.com.au

Episode 36: From Diagnosis to the Unexpected: Ellen's Story

In this episode, Jacqui is joined by Ellen Chaplin, a type 1 mum who shares her family’s experience of diagnosis, diabetes technology and resilience. Ellen’s daughter Charlotte was diagnosed with type 1 diabetes at six years old, just days before Christmas. What began as a routine appointment quickly became a life-changing hospital admission, marking the start of an intense and emotional learning curve. Ellen reflects on navigating diagnosis in a rural area, learning to trust diabetes technology and finding balance around food, independence and school life. She also shares the impact of an unexpected brain tumour diagnosis of her own and what it meant to hand over her daughter’s diabetes care while facing major surgery. This episode is a powerful reminder that life with type 1 diabetes unfolds alongside real life, messy, unpredictable and deeply human. Further Resources:         Type 1 Foundation Website [https://www.type1foundation.com.au/] Follow us on Instagram [https://www.instagram.com/thetype1foundation/] Join the Facebook Group [https://www.facebook.com/share/g/1Agrpd2YbW/] If you'd like to share your story with our podcast listeners, please email: podcast@type1foundation.com.au