Hi folks, I'm a grad student at the University of Pennsylvania and a T1 diagnosed when I was 22 (so I was able to really enjoy a lot of halloweens:)
I'm working on a project with some other students trying to understand what kinds of services parents of children with diabetes might need to help their child achieve better/easier care. It's hard being diabetic and I'm suspicious that it's even harder to be the parent of a child with diabetes. It's really important to me to understand the parent's perspective (which I don't have) so I'm hoping some of you might fill out this survey, it's under 20 questions!
There's a comment space at the end if you have some extra thoughts, or if you want to learn more about our research feel free to message me! Thanks in advance:)
The google survey ---> https://docs.google.com/forms/d/1MuqH59QVUbPIOPddMQl6K78jgV__L14TGeanjzNAyTA/viewform