I was diagnosed in March 2006, when I was seven.
I had been hungrier and thirstier than usual—and I had bad headaches and stomachaches. I went to the doctor for a stomachache, and I was sent to the Pediatric Emergency Room at Moses Cone, where I spent the next five nights (my blood sugar was 800+).
I check my blood sugar; I have an insulin pump; and I’ve learned to count carbs. Everything else is really the same.
Dr. Morris told me that I can still do anything I want to do. It was great advice, and helps me have a good attitude about living with diabetes.
Dr. Morris’ advice was really the best: Never let diabetes hold you down. You can do anything you want to do; you just have to be responsible.
I took shots for the first three-and-a-half years and then switched to the pump. The pump has made living with diabetes much easier.
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