Type One Nation. A community forum for people with T1D and their family and friends.

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  • An ecosystem that supports innovation—including federal regulatory, reimbursement and research policies—is critical to the success of JDRF’s mission. For many years, JDRF has worked with key decision makers and staff within the Federal Government to...

  • Today’s guest blog features a Q&A from JDRF with Aidan Sullivan, a 13-year-old JDRF delegate from Indianapolis, Indiana. From July 13-15, 163 delegates from all 50 states and seven countries descended on Washington, D.C., for the JDRF 2015 Children...

  • The incredible progress in closed-loop technology that JDRF has fostered by funding and collaborating with academic institutions, research organisations and industry is poised to deliver an array of artificial pancreas (AP) options to the T1D community...

  • Ask Peter Draeger about his involvement in the three-generation family business, Draeger’s Market, and he’ll admit to surprise at his current role. “I always figured my older brothers would go into the business, that there wouldn’t be a place for me...

  • ‘Rallye for a Cure,’ which will take place on Saturday, May 30, is organized by Jack Wright of West Hartford and his parents as a fundraiser to benefit the Juvenile Diabetes Research Foundation. Rallye for a Cure is a fundraiser hosted by the Wright...

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