April 17th our family went to the ER because urgent care’s glucose meter couldn’t read Lennon’s high level. We get to the ER and find out her level is 400 something, and that she has diabetic ketoacidosis.
April 17th our constantly perfectly healthy two year old girl was diagnosed with Type 1 Diabetes.
I don’t know if I’ll ever fully stop being upset with myself for not getting her checked out sooner....
Just starting a few weeks earlier, she would drink SO much milk, and asked for water, which she never did. Then she would leak through at least two diapers a night. I think the leaking was a week or two at the most. I thought she was drinking so much because she was growing, and the leaking was because the drinking, obviously... Then two days before we went into the hospital I noticed her breathing a little harder, like she was playing hard. But she wasn’t. The day we went to (urgent care first) the hospital, her breathing was so deep and quick it looked like she was running around all day, but she was just moping around like she was getting sick. I got scared and sent a video of her to my sister, who thought it looked like she was having an allergic reaction or some kind of asthma something going on. She suggested if it persisted into the next day to get her checked.
But something in me snapped.....I got so scared all of a sudden, and my heart sank into my stomach. We were eating lunch and I got so sick I stopped eating, and made my husband stop as well. Lennon wasn’t eating (she rarely does)....We packed up and rushed to the closest urgent care.
Luckily the wait wasn’t long. They checked her oxygen level because we told them she was having breathing problems. That was okay so I thought we were okay......
They wanted to check her sugar because I told them about the thirst and peeing so much at night. They thought their meter was broken because it read “HHH”. About twenty minutes later we get the news that the doctor had told Children’s we were on our way.
We had no idea what we were in for.....
I never want to relive those five days we spent in the hospital. All the bruises and blown out veins. My arms hurt so bad from holding my baby so tightly, so they could keep hurting her and taking SO MUCH BLOOD. How is it safe to take that much blood from a child?! I barely slept in those five days. The longest I’d catch sleep was maybe a half hour to an hour in between checks. The last two days were the best. Lennon finally got her IV’s out and got to walk around and play. She didn’t want to leave on our last day, and eve got to meet Batman. <3 I’ll forever be thankful for what those people did for my daughter.
And I’ll forever despise whatever the fuck caused this.
It’s only been a month (in two days) and Lennon lets me check her levels no problem. We still do insulin injections and she (of course) hates those. Hopefully we’ll get her on a pump...
Our main problem is getting her to eat. She’s always been a bad eater. Partly because she still nurses, which I try to keep to certain times so she’ll eat...and partly because who the fuck knows. She’s two.
The more I learn about diabetes, the more scared I’m getting. This is so fucking terrifying! To top it off, I have barely anyone to talk to. So, here I am, almost midnight, making a stupid tumblr to vent.
Thank you diabetes, I hate you.