Friend of CWD


Virtual Friends for Life Orlando 2020 Booth

Live Exhibition Hall Hours (All Times Eastern US)
Wednesday, July 15: 6:00 - 8:00 pm
Thursday, July 16: 8:00 - 9:00 am, 12:30 - 1:30 pm, 4:00 - 5:00 pm
Friday, July 17: 8:00 - 9:00 am and 12:30 - 2:00 pm


T1D Exchange is a nonprofit research organization dedicated to accelerating therapies and improving care for people living with type1 diabetes. We translate real-world experiences into real-world solutions that make your life easier. We aim to help T1D families through research at the clinic level through our Quality Improvement Collaborative, and through research at the personal level through our T1D Exchange Registry.

“The research conducted and published by the T1D Exchange has opened our eyes to the true lived experience of people with type 1 diabetes in ways never before seen. Through these insights we are able to focus on specific areas to improve outcomes and the lives of everyone in our community. You can help by joining their patient registry.” – Jeff Hitchcock, President of Children with Diabetes.

We are so excited to be back! While we know that the conference this year is a little different, we are just as eager to join the CWD community for another year of bringing families together at Friends for Life. $10 Starbucks gift card for the first 25 people who join each session!



The T1D Exchange Registry is a research study designed to gather real-world evidence first-hand easily and quickly. The questionnaire can be done from your mobile device on-the-go, in the comfort of your bedroom, or athome with your child. Since type 1 diabetes is a chronic condition that people live with their entire lives, participants can complete the questionnaire annually to help researcher understand surviving and living with T1D. Type 1 diabetes is generally diagnosed before the age of 18, so we encourage parents and care takers to participate with their children and make sure their experiences and voices are also heard. Gathering data and insight from individuals is so important to generate real-world evidence to directly impact people living with this chronic disease and improve the research needed to change policies, insurance and treatment developments.

Help us reach our goal of 15,000 participants!

This summer marks the one-year anniversary that the T1D Exchange Registry went public. After one year we have had over 8,000 individuals across the country with type 1 diabetes, parents and caretakers of children with T1D join and lend their voices to impact type 1 diabetes research.

The Registry is designed to harness the power of individuals with T1D. The more voices we have, the more powerful this community will be. Help us to reach 15,000 participants and drive research that matters!


T1D Exchange is dedicated to improving care for people affected by T1D through the use of real-world and clinic-derived data to drive research and innovation. The organization has amassed a comprehensive database of type 1 diabetes health information, providing clinicians, researchers, industry partners and advocates with the resources and services they need for better decision support and population health management. With an unparalleled focus on Quality Improvement, T1D Exchange is changing the future of type 1 diabetes care and treatment.

T1D Exchange was established 10 years ago with ongoing support from The Leona M. and Harry B. Helmsley Charitable Trust.

The content and links in this Virtual Booth have been provided by the sponsor. CWD is not responsible for any content therein, including links that will bring users offsite. If you have any questions about content in this sponsor booth, please contact this sponsor individually.