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My name is Elisabeth. I am ten years old. I was diagnosed with Type 1 diabetes when I was 5 years old. When I was seven my parents and doctor switched me from two shots a day to an insulin pump, I wear my pump 24/7. With my pump, my blood sugars are better, and I can eat when I want. I like to read, listen to music, play tennis, play catch with my brother and play with my cat. I'm in fourth grade and I am on the honor roll at school. My parents tell me I'm just like everybody else, but I am the only kid with diabetes in my class, so there are times I don't feel like everybody else. When I go to diabetes camp, everyone has diabetes. At camp, it is normal to check your blood sugar and count carbs. There I am just like everybody else - I have fun, learn a lot, and feel better about myself after camp. |
7:15: My dad turns the TV on. |
4:45: Homework is done. My brother, dad and I head to the park. I started tennis a few weeks ago and it is time for practice. My "purse" has my meter, juice, glucose tabs, and glucagon In it in case I need it. 5:00: Check my blood sugar to make sure that it is "good" before I start practice. 6:30: Home and time for dinner. Check my blood sugar, calculate carbs and bolus. Now we can all sit down to eat. 8:00: Shower time. Disconnect my pump and shower. 8:15: Reconnect my pump and bolus for the time that it was not attached. 9:00: Blood test, insulin if I am high and to cover my bedtime snack. 9:30: It is time to go to bed. 1:00 AM: Mom or Dad check my blood sugar to make sure that I'm OK. Sometimes they have to bolus me with extra insulin if I am high, and sometimes they have to wake me up and give me juice if I am low. 7:15: The TV gets turned on... we start all over again. |
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| © Camp Angels • P.O. Box 89, Waterford ME 04088 • (207) 583-6963 |