At 33 months, Kyli was diagnosed with Diabetes in our TEDDY facility.
Her 33 month visit went like any other visit. Ask all the questions, take some blood, nose swipe. We started discussing a few things she would be able to do once she turned 3 years old. I thought this appointment was going to be a piece of cake. Kyli did wonderfully, no fighting the blood draw. We were going to be in and out. I look back and I still think, I should never have been so comfortable. I knew something was up the moment Nurse Ruth (our favorite nurse) came into the playroom and told us Kyli's A1C was next in line and we would have to wait a few more minutes. I thought it was odd, but dismissed it. A few minutes later when she asked us to come back to our room, I got scared. I grabbed Kyli and held her tight as they then told me her A1C was elevated to 7.4, not bad for a diabetic, but bad for a healthy child. As I wept silent tears, I listened as our life began a huge change. They brought up an endocrinologist from the downstairs Barbara Davis Center clinic to talk with me and what all this meant. I was asked to watch her sugars closely for the next few days, let her eat what she wants and test her 2 hours later, and if she was high, to call them.
I packed up Kyli after nurses made sure I was able to safely drive and I drove straight to my Mom's work, which was thankfully on the way home. I cried and we went to lunch at Jack in the Box. Kyli ate a handful of fries, about half of a cheeseburger, and drank some milk. I went home and waited the longest 2 hours of my life. I did everything to make that time go faster. The two hour mark finally came through, she was napping… I went in tested her sugars, 440. I then went to my room and cried, my 2 year old daughter was now diabetic. I called the doctor then and asked, "What is too high?" He said 250.
We then made an appointment for us to come in the next day, Saturday, to do a quick injection overview to get us started. Kyli was diagnosed September 21, 2012.
This last year has been a blur. We have adjusted to her having diabetes. Her early diagnosis was a blessing, we are still in our Honeymoon Phase, which means that her pancreas still works some. She requires very small doses of insulin, but nonetheless gets 4-8 shots a day depending on what she eats and when. We have become carb counting machines. We were able to get a Dexcom G4 Continous Glucose Monitor in June, it is my new best friend. Kyli will be getting her insulin pump in October, it will be a blessing.
Kyli has adjusted to all the changes very well. A month after her diagnosis, we did our first Diabetes walk with the ADA. We are doing that walk again this year in November. Go Team Tiny!
What we missed before her diagnosis. It was the end of summer in Colorado, it is still hot then. All of Kyli's symptoms were accounted for. Kyli slept a lot, 10-12 hours a night and usually a 4hour nap- she was going through a growth spurt. Kyli was peeing more, we were potty training. Kyli was drinking more, it was during a super hot spell in Colorado and she played outside every day. She never lost weight. Now, when I look back, I remember thinking her sleeping so much was odd, but I dismissed it. We were lucky, if a few more weeks had gone by, Kyli could have gone DKA and we could have ended up in the hospital and Kyli is a coma. Thankfully, TEDDY was there and in my eyes TEDDY saved Kyli's life.
|Kyli with her family in 2013|
We will be doing a follow-up blog post with questions and answers for Kyli's parents. If you have questions you'd like us to ask please email firstname.lastname@example.org include a note referring to this blog and your question.