Friday, August 5
This morning we headed out early with CD to travel down to Primary Children's Medical Center where she was going to have eye muscle surgery. The technical term for what was done - bilateral medial rectus recession.
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| on our way |
Last December we had discovered that CD was getting a lazy eye. When we took her to the eye doctor about it, he told us what she really had was called
esotropia and that only surgery would fix it in her case. What that means is that her eye did not sit straight, it was slightly turned in. This was causing double vision and in response her brain started to "turn off" the bad eye which is why it looked like a lazy eye. So we started patching CD's "good" eye to help strengthen her "bad" eye. Until the bad eye (her left one) was strong enough, there was no point in doing surgery.
Patching worked miracles on strengthening CD's left eye and it was determined she was ready for surgery. We were going to a doctor here in Logan and he referred us down to PCMC to a doctor who does these surgeries all the time - Dr. Dries.
We told CD that she was going to an eye doctor to get her eyes fixed. She isn't a fan of doctors and didn't even like having her physical exam. She refused to put on her ID bracelet - on her wrist or ankle - so they taped it to her back. CD did however LOVE playing toys while we waited. Of course that was her favorite part. She found a little microwave she especially liked. She was given some medicine to help her relax to help with the separation too. So she had to sit on my lap and couldn't wander for a bit. The microwave helped with that a lot. Then the time came for her to go back to surgery. I carried her to the "double doors" where they then took her away. She was upset, but not too bad thanks to a spinning toy with lights they showed her.
Then the waiting game began for Jon and I. We got lunch, ate lunch, and waited and waited. We actually only had to wait an hour, which wasn't too bad. Dr. Dries came and told us that surgery went well and he was happy with the results. We then had to wait for them to tell us that one of us could go see CD. Of course I was the one who went.
When I got to the room to see CD, it wasn't a pretty situation. She was waking up from her anesthesia and really struggling. As the nurse described it, she was "thrashing around". It turns out they called me down as soon as possible because CD was thrashing around, trying to pull the IV out of her foot, and trying to get out of bed. So they brought me a rocking chair to sit in and I did my best to hold her and keep her from tearing out the IV. She kept saying she wanted to go play with the toys. If she wasn't fixated on the IV, she was fixated on getting out of there to play toys. The pain medicine she was getting was pretty strong and helped to make her sleepy. But she was fighting sleep so much. Finally I got her to sleep a tiny bit and I convinced the nurse to take the IV out since she had had a couple of sips of chocolate milk. While taking out the IV CD woke up and the fight started again. But since the IV was out they decided to send us to the next waiting room that had a TV. Jon could then join us at that point too. Once in that new room I finally got her to sleep again and she had a good 15-20 minute nap on my lap.
When she woke up again, she was a different girl - although she was still very tired. CD was no longer thrashing around and she woke up and noticed that "Princess and the Frog" was playing on the TV. So she sat on my lap, drank ALL of her chocolate milk, and watched the movie. At that point the nurses said we could leave. So we got our discharge papers and instructions, and Jon headed downstairs to get her prescriptions filled. After getting all of our things together, CD got to ride in a wagon out to the car. She also was given sunglasses to wear to help protect her eyes from the bright sun.
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| still not feeling great, but on her way home |
While on our drive home CD slept a little bit and ate almost a whole little box of Gold Fish crackers. When we did get home, she finished her crackers, drank her chocolate milk, and fell asleep pretty quickly on the couch. It had been a long, difficult day after all.
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| so tired |
Surprisingly CD actually was interested in eating dinner, so I made her some macaroni and cheese. She almost fell asleep at the table, but she refused to get down until her dinner was gone. Shortly afterward she went to bed and slept wonderfully. The next day, CD was a new girl and you never would have known she had surgery the day before! She talked non-stop, played all day, and even ran around the house. She was her normal, happy, crazy self - and it was good to see!
There is no patching or bandaging required for her. She just has to have eye drops in both eyes 4 times a day for 2 weeks - something she doesn't really enjoy. She will have a followup in a month on September 6, and then we'll see what happens from there. But so far, so good. ;0) She is an amazingly tough and strong little girl!