Sorry it has been FOREVER since I've updated everyone. It has been such a crazy week, and I have needed more recovery than Clay did.
Clay had his surgery on Wednesday at ULCA and did wonderfully. We spent the night at the Tiverton House across the street the night before so we could meet our arrival time of 6:00am.
The anesthesiologist looked about 20 years old, but took great care of him and was very informative with us, and very sweet with Clay.
He came back to the PACU several times and checked on us telling us how great Clay did.

When Clay
woke up from his EGD last month he was very disgruntled and angry. I have to admit, this was one of my biggest concerns about his surgery this time. Since he has weaned, I don't have the "cure-all" and I did not like that I couldn't get him to instantly stop crying when he was so upset.
He was out of surgery by about 10am and actually very pleasant. He didn't mind when I had to leave his bedside to go the bathroom, or when his nurse changed for lunch, or when they took his vitals 100 times.

After several hours in the PACU he was finally transferred to a peds room at the Mattel Children's Hospital.
He actually had surgery at the Ronald Reagan Medical Center but the Mattel Childrens' Hospital is actually the same hospital. (Just the 3rd and 5th floors) Kind of confusing, I know.

Clay was pretty sleepy and uncomfortable the first day and mainly slept and watched TV.
The nurses came in and gave him pain meds around the clock, and he was up and at 'em the next morning. We had breakfast, took several walks around the 5th floor and played 'how many tissues can we pull out of the box and throw into the trash can'. He was pretty bored, but still took a decent enough nap for me to sneak down to the cafeteria for lunch.

Overall, Clay's stay at Mattel was pretty good, but I'll have a post for another time about my issues with that place. My opinion is that for being the Best Children's Hospital in the US last year, I shouldn't have 'issues' with them. But like I said, another post, for another time.
We will be seeing the surgeon for a follow up on Monday and then be seeing a hematologist in the near future. The surgeon confirmed that the stones were all made of billirubin (basically broken down red blood cells) and that he thinks there is something causing his rbcs to break down too early. We're waiting for the spherocytosis labs to come back and if those come back negative we'll navigate some different paths (as directed by the hematologist.)
Clay is doing wonderfully and we took his bandages off today. He wants to wrestle, play and I don't think he even knows he had surgery.
I definitely think that if you're going to have your gallbladder removed you should do it at 17 months. It doesn't even have seemed to phase him.