Thursday, December 10th we went to Santa's Village in Huntsville with Hank, Julie, Gracie, Tucker, and Brant. We had so much fun, but I will have to post pictures later b/c my camera is in the car and I am way too lazy to go get it right now. On the way home John Henry's nose started running.
He had a cold through Saturday when we went to Kurt's family Christmas. Saturday afternoon he started coughing. Kurt was going out of town so John Henry and I stayed at my mom's house for the weekend. Sunday morning when he woke up, he was breathing very shallowly and was wheezing. I couldn't really decide whether or not to call the doctor b/c they usually act like everything is fine even if you say your kid's arm is cut off or something. I finally decided to call when we could tell he was really having a hard time breathing. Shockingly, the on call nurse referred us to the after hours clinic at Children's on Acton Road. The first appt they had was for 8:00 pm!
This whole time John Henry was acting like he felt fine- no fever but still having a hard time breathing. So when we got to the after hours clinic, he was running around playing in the waiting room wearing his Handy Manny hat. :)
When you check in there, they send a nurse out to check their oxygen saturation if they are having a hard time breathing. The nurse came right out and took his oxygen, which was 97% and listened to his chest. She said, "My across the room assessment was wrong. He sounds really bad." They got us right back, and his oxygen was down to the low 90s and sometimes 89.
They did a chest x-ray, which I couldn't go to b/c I am pregnant. I was so glad that my mom was there b/c she took him. John Henry was being so sweet the whole time we were there. He was perfect. Seriously I could not have asked for him to be any better. I was so thankful!
They did a 45 minute breathing treatment, and John Henry did great. He just sat in my lap and watched tv the whole time. They took his oxygen and it was 94%, so they did another one and gave him a steroid. After that one his oxygen was down to 91%, but they said he could go home because he was moving air through his lungs better. When the nurse was taking that oxygen sat., it went down to 89% at one point, and she said he would be spending the night in the hospital if it was that low, so we just barely missed a hospital stay!
We finally got out of there at 11:30, and I was at the pharmacy until almost 1:00 getting medicine b/c we had new insurance they had to figure out.
The steroid made him wired. He didn't go to sleep until 4:00 in the morning. I thought I was going to die; I was sooooo tired! The next morning we had to go back to the doctor to check up, and they said he had bronchiolitis and possibly RSV. We had to do his inhaler and steroid for 4 days. The problem was that he hated his inhaler. It had the mask thing and since Kurt's doesn't have that, John Henry refused to use it. We ended up getting a prescription for a nebulizer and doing that every 4 hours and the inhaler in the middle of the night.
Kurt came home a day early from his trip to help out. John Henry was much better the next few days and is fine now, thank the Lord. I am so glad that is over, and we are really hoping that this is the last of his breathing problems. :)
-I have pics to add of him at the doctor, but I will do that later.
-When I called my mom from the pharmacy to check on John Henry, he got on the phone and tole me he wanted a "special treat" from the store. I bought him a little tiny stuffed gingerbread man and some Santa and reindeer chocolates. When I got back to my mom's, he was crazed from the steroid. He looked at the gingerbread man, which I thought was so cute, and said, "You can't eat this!" Then I showed him the Santa chocolate and he tore through 2 of them before I could stop him. It was crazy how different he was acting from the medicine!
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