For those who haven't ever experienced surgery (thankfully) here's what our day looked like. Granted, it would be different if it were inpatient, but this fortunately was a relatively quick procedure. We started the morning off right for Declan. He couldn't eat after midnight the night before or drink clear liquids after 11:30 a.m., so we figured if he was going to be grouchy, we'd go ahead and cram as much as possible in the morning. (Callum had the luxury of hanging out with the grandparents for two days.) We started off the morning with a therapy co-treatment, meaning he had speech and occupational therapy at the same time.
| Two of his amazing therapists |
Right after that, he had his monthly nutrition appointment. Surprisingly, he did amazingly well, especially considering he hadn't eaten since the night before and isn't the biggest fan of juice instead of milk.
| I wish I were this happy without food for 12 hours! |
We arrived at the hospital at 12:30 and were one of only two families in the waiting room. Apparently Declan was the last scheduled surgery for the day. He was able to spend quite a bit of time cruising the area in the car, which he was a huge fan of.
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| Can I drive out of here? |
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| Tolerating the juice |
We stopped and gave him a bottle of milk in the lobby, which he downed and then promptly fell asleep and slept until early the next morning.
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| Finally happy after a bottle of milk |
The only problem of surgery was the IV, as usual (a story for another day). Needless to say, we counted at least 11 pokes in their attempts to insert it.
| My arm is too stiff--I can't put it down! |
After the first day, he's been mostly fine with his cast, and he didn't need pain medicine more than that first day. The real issue has been keeping it out of his mouth. We've already had to make two visits back to get it looked at once and then re-wrapped
I really think that could be a new torture device in prisons everywhere--give a prisoner a small orally-fixated child with a soft cast and tell them they must successfully keep the kid happy while keeping his hand out of his mouth and keep his other hand from yanking the cast. They can't tie it down since he needs to be able to move it around for development and therapies. Oh, and they also have to successfully fix food, eat and do other normal activities (you know, like go to the bathroom) at the same time.
| The cast clearly isn't stopping him! He's holding on with the cast hand. |
We go back to the hand doctor July 8, which isn't soon enough for me (thankfully only one more day, now that I'm finally getting around to it). Although, it is our wedding anniversary. Nothing says happy anniversary like spending the afternoon at the doctor's office! This is the second year in a row--such is the life with a needy kiddo. Although this year I'll take it, so long as it finally means freedom for all of us.


