We always knew that 'D' could happen to our children, but we didn't feel that we needed to worry. Yes, Matt has it and has since he was 13 but I think we were living in the "it won't happen to us" world. On May 18, 2006, our beautiful Elly was born. We brought her home 2 days later and we never gave D one thought.
At urgent care they ushered us right into a room when they heard what her symptoms were. They were having trouble tracking down a blood glucose monitor to test Elly but luckily, Matt had his on him. When the result came back, her blood sugar was so high all the meter stated was "HIGH." At this point, we knew. And we could see it in the urgent care staff's eyes. They felt so sorry for us and our poor 2 year old that more likely than not has diabetes.
The urgent care staff called an ambulance to transport us to Doernbecher Children's Hospital. I rode in the ambulance with Elly while Matt followed with his mom (I had called his parents while we were waiting for the ambulance to arrive, as I didn't want him to be driving by himself). When we arrived at the hospital, we went directly to the ER. It was about that point where things really started to go south. Elly was slipping in and out of consciousness and they could not get an IV started in her due to her severe dehydration so they had to insert and IO into her knee so she could get the needed fluids. They then moved her to the PICU. By the time we arrived there, they were able to get an IV started. As the fluids continued to drip, a slow insulin drip was started s well, because at that point we learned that Elly's blood sugar was 616 at admittance.
Up until this point, Elly was placed in the cribs that look like cages, mostly due to her age. The problem with this is that she refused to sleep unless I was right next to her. So, I ended up sleeping in the crib with her! The PICU staff found this hilarious and said that they have never had a parent actually crawl into a crib with their child. By the end of the first night though, the staff took pity on me and we moved Elly into an actual bed, so long as someone was always in the bed with her, for safety. I really wish we had a picture of me in the crib with her because I'm sure it was quite a sight. I became very skilled at how to raise and lower the sides from the inside.
After 24 hours in the PICU, Elly's blood sugar had lowered enough that we were able to leave the PICU and go to a regular room. During the PICU time and after we moved into a regular room, we had extensive diabetic training. Luckily, due to our 'D' knowledge because of Matt, a lot of our training was abbreviated and we were able to mostly concentrate on the parts that applied to Elly rather than just the disease.
When we finally were able to bring her home, we were so scared. It was worse than bringing a newborn home. We now had a child, a toddler, with a very serious medical condition. And our worst fear was her going low, which happened the very first night. When we got home we got Elly into bed for the night and Matt and I soon followed. Right before we went to bed though, I went to check her blood sugar, which was 81. Crap! At night, our protocol was to treat lows under 150. I happened to have some Torani syrup on hand so I pulled some into a syringe and tried to feed it to Elly but she wasn't going to have any of it. She fought me tooth and nail to where I had to bring her into Matt and I's bedroom and Matt had to hold her down while I squirted the Torani into her mouth. It was one of the most horrible experiences, post-diagnosis.
Since diagnosis, though, Elly has been thriving. She got used to MDI and last November we were able to start her on a pump. The pump has really changed 'D' care for us, and it was for the better. 'D' is easier to manage because pumps can deliver such small units of insulin. Just try to pull up 0.025 units of insulin in a syringe! Due to the pump, Elly has been able to be more like a kid and not have to live on such a schedule anymore. It has been wonderful. And then, at the end of last month, we have started her on a CGMS (continuous glucose monitoring). That has been wonderful. We can now look at a screen and know where her blood sugar approximately is, and the reading is taken every 5 minutes. It also will tell us which direction her blood sugar is going, and how fast it is moving. This has been wonderful. We have had a few blips with the CGMS but, overall, it has been a wonderful addition to our diabetes arsenal.
Elly is now 4 years old and will be starting preschool in about 3 weeks. While this thought scares me, I know that she needs to go and be with kids her age and have fun. It will only be 2 half days a week and, for now, that is enough. This will also prepare me for when she starts kindergarten in a year.
Elly is such a happy and beautiful little girl. I am so blessed to be able to say that I am her mom and look forward to what the future holds for my little girl. She may have diabetes but diabetes does not have her.