Your Voice Drives Change
When people living with type 1 diabetes share their experiences, those insights help shape research, improve care, and strengthen outcomes across the community.
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The T1D Exchange Registry makes it easy to share your perspectives through surveys and take part in research that expands what we know about living with type 1 diabetes.
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Take part in a simple way to share what life with T1D looks like. Each question focuses on your everyday decisions, challenges, and experiences — turning everyday moments into meaningful insights.
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Latest Articles
Beyond A1C: Why Time in Range Matters for T1D
For decades, hemoglobin A1C (A1C) has been the gold standard for assessing diabetes management. Estimating average blood glucose over the past two to three months, it has long guided treatment decisions for people with diabetes.
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Could Your Insulin Pump Detect an Occlusion Before Your Glucose Rises?
For people living with type 1 diabetes (T1D), insulin pump technology has seen significant advancements. Yet a persistent challenge remains: knowing when insulin delivery has been interrupted.
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Inside the T1DX-QI Data Governance and Data Science Committee
Every quality improvement initiative, research breakthrough, and clinical innovation starts with high-quality data. Yet, data alone won’t improve outcomes. Transforming information into real-world impact requires thoughtful governance, shared expertise, and close collaboration across clinics, researchers, and data specialists.
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