Surgery #2 UpdateSurgery #2 went well. Aiden is now tonsil and adenoid free. Dr. Trone said he had a little trouble getting his IV in - they had to put a central line in his jugular and it took several attempts. No problems though. They did an x-ray of where it goes in to make sure it looked okay and it does.
He (and I) will be staying in the Pediatric Intensive Care Unit (PICU) to have very close monitoring throughout the night. He seems to be in some pain and is just very irritated that he can't suck on his paci without his throat hurting. He still hasn't taken a bottle so the fluids in the IV will have to suffice for now. He definitely wants to eat, he'll try sucking, but then stops and cries as I'm sure his poor little throat hurst terribly. (Not to mention his Mega Man arms and legs too!)
Ricky went back to the Ronald McDonald House for the night to try and get some rest. Knowing him though, he won't be able to stop thinking about Aiden and how he is doing so that will pretty much be pointless. But only one parent is allowed to stay in the PICU as the rooms are very small. I'll be sleeping (or not) on a recliner chair - and let me tell you, it ain't no Lazy Boy! The broken pull-out love seat in the room on the regular floor where we stayed last night doesn't sound too bad now...
If all goes well tonight, that's where we'll be tomorrow night. And then (fingers crossed) we may be able to go home on Saturday. I'll continue to update everyone here. Thanks for all the thoughts and prayers. We're really glad to have the surgeries over with finally so we can focus on getting Aiden back to his normal, happy self.
PS - Some people were wondering what all the stuff was on his hands and feet. From the picture, you can see his dark blue casts underneath all the foam padding. They put the foam padding on so that he doesn't bonk himself in the head with the casts before he realizes that they are there. The padding also helps to keep his hands and feet elevated. Tomorrow, the padding will come off and it will just be the casts. They are soft wrapped casts (not plaster) and will only stay on for 2-3 weeks. Our local pediatrician will be removing them so we don't have to come all the way back to Dallas for that.