The Registry is a long-term research study that follows people with T1D over time. Today, more than 23,000 individuals across the U.S. are part of the Registry — creating one of the most robust real-world views of T1D in the country.

When you join, you'll complete a questionnaire about everyday experiences, technology use, and self-reported outcomes, like severe hypoglycemia. You'll complete a brief annual follow-up and can choose to take part in additional research opportunities throughout the year.

Registry voices have contributed to expanded insurance coverage for glucose meter strips, updated ADA pediatric A1c guidelines, FDA expansion of CGM labels, and Medicare coverage of continuous glucose monitors.