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Sorry to hear about your son! Hopefully your son wasn't in ketoacidosis by the time he was diagnosed, and the initial days were just training and not ICU. My own experience with using the Dexcom G4 CGM with my 1-year old son was extremely negative. First, it was terrible to insert the sensor -- it is a clunky mechanism which would sometimes fail and leave you with a worthless sensor, and at best would leave your chil…
Thanks! Yes he was DKA on diagnosis. It took them 4 days to figure that out too. For us the CGM would be about getting rid of and/or minimizing the overnight blood checks. There's nothing more horrifying then sleeping through an alarm now. In fact, that just happened to me. Fell asleep on the couch, woke up two hours past his check, saying "oh fuck" a lot as I run around the house like a headless chicken. The only CG…
i imagine you are trying to keep your child textbook perfect as far as glucose levels. this is close to impossible for a child this young. in general you can keep a diabetic around 100-150 as long as they are not above 150 for extended periods of time it avoids the negative issues associated with diabetes. always safer to run a little high verse low. you could turn down the insulin pump at night until child around 125 and chance of low sugar would decrease. when child gets older can strive for "perfect" control. if diabetic 150 or below and 180 or below at meals most of the long term negative health issues are avoided. 75-95 and 120 meals is the text book numbers but difficult to maintain. good luck when he gets older dealing with the candy and soda issue. one of the very difficult times with a type 1 diabetic explaining and convincing the child they cant have candy like the other kids. also when he gets older avoid all the diet foods and drinks, esp. nutrasweet. stevia might be ok we dont know yet for sure. nutrasweet is bad bad bad for everyone especially diabetics.