
Our mission is to connect with as many kids and families as possible during their initial Type 1 Diabetes diagnosis, offering reassurance that they are not alone and that T1D does not define their future or limit their potential. We are committed to empowering kids and their families through ongoing support, resources, and encouragement—especially for those navigating life with T1D while pursuing their passion for sports.
As you can see on my face I was scared. I had just asked the doctor if I was going to be able to play hockey again. When the doctor said "Yes in time" that’s when I decided T1D will not define me and I was playing on 19 May in the Tournament no matter what I had to do.
From the moment I learned I could still play hockey, I have not let my diagnoses STOP me. This is only possible because of the incredible village of family, friends, coaches, and teammates—who support me every single day.
Embrace T1D! Embrace the support! Never let T1D define you!
Every day, we face a battle the world rarely sees—one that unfolds with every meal, every snack, every sip. Life with Type 1 Diabetes is a constant calculation, a relentless need to plan ahead, where every choice matters. And yet… We rise. We laugh. We fight. We work. We play. We dream. T1D may shape our path, but it will never define our end goals.
To every kid living with Type 1 Diabetes, and to every family standing behind them; I see you! I honor you! I believe in you!
I pledge to stand with you not just today but every day. I understand the daily battle — the hidden and continuous alarms, the hidden fears, the brave smiles. But most of all, I understand the behind the scenes ups and downs of the daily fight that no one knows about nor do we tell anyone about because we do not want to be defined by T1D. Only WE know the whole story.
But hear this:
Diabetes does not define us! It will not break us! It will never stop us! We are more resilient than our highs and lows. We are bigger than any diagnosis! We are unstoppable and we — ALL OF US — are STRONGER as ONE.
Dear Fellow T1D Parents,
We know the whirlwind you are in right now — the fear, the confusion, the sheer weight of learning how to keep your child safe when everything feels so unfamiliar.
We are Dave and Kristy, parents of Kade, who was diagnosed with Type 1 Diabetes at age 11. We remember exactly where you are. One moment, life was normal — the next, we were in a hospital room learning a brand new language: insulin, carbs, ketones, glucagon. In just a few hours, we were handed the tools to keep our child alive and sent home to do exactly that. It was terrifying. Overwhelming. And, at times, paralyzing but here’s what we want you to know: You are not alone.
Those first days feel impossible — we’ve been there. But step by step, it gets better. You begin to understand. You learn what works for your child. You build routines. You make mistakes, and you recover from them. You get stronger. So does your child. We’re reaching out to tell you: we are here for you. Whether you need someone to listen, to answer questions, or just to say “you’re doing great,” we want to be that support. We’ve navigated school days, sports, blood sugar crashes, and burnout. We don’t have all the answers, but we have experience — and we’re more than willing to share it.
Every child with T1D is different, but there is strength in community. There is comfort in knowing others have walked this path — and are still walking it, right alongside you. If you need anything — a tip, a vent, or just a voice that gets it — please reach out. Email us in the Contact Us section below and we can communicate with you in any way that works for you and your family.
With compassion and strength,
Kristy and Dave
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