I should have done this post a few weeks ago, but here I am. Oh well. At least I’m posting it before 2010, right?
Thanksgiving was just a bummer part of the season for our family. But before we even reached Thanksgiving things were keeping us on our toes. Jack woke up on Saturday, November 14th with a bit of a cold. By Sunday morning he just didn’t feel good at all, so I sent Michael to church with Anna, and I stayed home with him. Later that day we heard “the cough.” We remembered it from Anna’s croup experience- that barky, heinous sounding cough that makes you look at each other and think, “Oh crap. That sounds WEIRD.” But, he only coughed the one time. He was otherwise his cheerful self, so we put him to bed. Around 4:00 in the morning on the 16th I woke to hearing him do something, but couldn’t tell what. I went into his room to find him crying, but I could barely hear him. We decided to do the whole “steam and cold air” thing. So Michael flipped on the shower in our bathroom and in we went, waiting to sweat our brains out. After a few minutes, though, I realized that I wasn’t even remotely hot. We realized that our hot water wasn’t working. Great.
We called Michael’s parents and told them I was coming over. We tried the hot steam/cool air trick over there. It helped a little, but not a lot. I returned home where it didn’t take long for us to decide that we needed to take him to the ER. We called Michael’s parents (poor people- they aren’t trained to wake for early morning stuff- they retired that hat when Michael was little) and Chuck came over to get Anna up and take her to school.
We opted to go to Rady’s Children’s Hosptial off the 805. There was no one in the ER waiting room, so they took us right in and started working on Jack. They had this amazing aspirator that came out of the wall and sucked everything out of his nose- I’d like to add THAT to my Kaboodle list! Jack hated it, but once they cleared his nose he could breathe through it. Then they started him on a breathing treatment. Last thing was a steroid treatment. Then we waited for him to calm down. They told us they were waiting for 2 things: For his strider breathing to go away at rest, and for him to stop retracting. Both things were freaky. Strider breathing is when they have a high-pitched wheezing sound when they breathe- several octaves above normal. Retracting is when they are having such a hard time breathing that they start using their stomach muscles. Their little sternums go nearly all the way to their spines, which looks very scary- they are working very hard to breathe.
We waited for an hour or so for the steroids to kick in and the breathing treatment to do its work as well. Jack seemed much better, and slept on us for most of that period. The doctor came by and checked on him at about 8:30 and said she’d get the discharge papers ready, and that’s when Jack started to retract at rest. The nurse called the doctor back, and she said, “Sorry, you’re not going home just yet.” We were then transferred to Grossmont Hospital which, unbeknownst to me, is a “sister hospital” to Rady’s. Upon arrival we met with their pediatric doctor and found out we’d probably stay the night. They really didn’t need to do anything but observe Jack just in case he didn’t get better. We went home the following morning and we were SO HAPPY to go home.
It was interesting, thinking back in hindsight, to think about how many times they asked us the same questions. I realized after the fact that they were probably following protocol of some sort to ensure that we weren’t neglecting Jack. We were really taken by surprise with how quickly he progressed into croup, and they seemed surprised as well.
This experience gave me so much insight to what it is even kind of like for parents who have chronically ill children. I can’t imagine spending any amount of time in the hospital with a child- there is no rest for them or the parent. They are constantly poked, prodded, and they never get to sleep. Nurses come in and claim that they will try not to wake them, only to noisily lower the crib rail or forget to speak in a quiet tone. It was frustrating and exhausting. I’m so glad that it was a one-time deal.
Below are some pictures from Jack’s visit. Everyone loved him because he was usually a pretty happy boy for being in the hospital. I’m so glad it’s over and just a thing for our blog!

Jack trying out the hospital high chair.

Lookin’ cute in his hospital bed.

The world’s WORST glider ever. E. Ver. I mean, look at it- it doesn’t even LOOK comfortable, does it?

Someone could make some serious cash inventing a new hospital crib. They are noisy, adults bang their heads on them, and nurses claim they can “quietly” raise and lower the sides- not possible. Poor kid hardly got any sleep while we were there.
For more info on croup, click here.
We love you, Jack, and we’re so happy you’re healthy again!