[brynnbowen]

My little girl was diagnosed as type one upon her admittance to the hospital and learning she was on ketoacidosis. She spent a week in the icu she has stabilized and we are home now. I am slowly getting used to this new life change. One thing that is terrifying me is what affect do all the highs and lows have on her little body over time? Do the numbers ever become predictable and manageable or are they always all over the place. Right now we are instructed to check her every two and a half hours. Any insight would be appreciated especially if you have had a child diagnosed so young