Living with Diabetes
through the use of Community Advocacy, Social Media, & BLUE Flamingos!
In July of 2008 at the age of 8, I was diagnosed with Type 1 (Juvenile) Diabetes. I spent 3 days in the PICU (Pediatric Intensive Care Unit) because I was so sick. I was only 24-48 hours away from going into a diabetic coma. Life for me and for my family was never the same. Since then, daily life for me has revolved around the many tedious and painful tasks associated with diabetes. Like every person with Type 1 Diabetes, I must check my blood sugar at least 10-12 times a day. I must count every carbohydrate that I eat and give myself insulin every time I eat. I was getting about 8 shots a day but in March 2009, I got my first insulin pump. I am now able to give myself insulin with the press of a button. The insulin enters my body through a small cannula in my skin. The infusion set gets changed every 3 days. These tasks go on 7 days a week, 24 hours a day, 365 days a year, at school, on vacation, on holidays, when I’m sick, and when I’m playing. It doesn't stop. I do these things to not only keep myself alive, but to ward off the devastating complications that can arise from out of control blood sugar; eye disease, nerve damage, kidney disease, heart disease and stroke. Every family touched by diabetes must do the same. Luckily, for me, we do have the technology that allows me to live a pretty normal life. I love to ride my bike and play with Littlest Pet Shops. I enjoy long days at