Weight: 9 lbs, 1oz
Length: 22 inches
Clothing size: Newborn and 0-3 month
Diaper size: size 1
Eating: Tyler nurses 8-11 times each day, and he usually takes one bottle (3.5-4 oz of breast milk) right before "bedtime".
Sleeping: If Tyler takes a bottle around 9:45-10:00pm, he usually will fall asleep right after and will stay asleep until about 3:00am. He will nurse and then go back to sleep for another three hours or so. He likes to eat every couple hours during the day and naps in between most feedings.
Highlights of the month: His "birth day", coming home from the hospital, and meeting his big brother
Monday, February 23, 2015
Friday, February 20, 2015
Everyone's Home!
Caleb was discharged Thursday afternoon! I'm so happy that have my entire family at home! The boys still have some recovery before they're completely back to normal, but they're both doing pretty well. We appreciate your continued prayers as Caleb regains his energy/strength and as Tyler tries to get rid of his nasty little cough.
Thursday, February 19, 2015
One Home, One To Go
Tyler was discharged Wednesday afternoon! He's home and doing well. We were told that his cough may linger for 6-8 weeks, though.
Monday, February 16, 2015
RSV x2
Caleb is continuing to improve. He's on a very small amount of oxygen and is eating/drinking well. He should be moved out of ICU soon!
Tyler has had a cough and has sounded congested the last couple days. He had a low fever last night, so I called the pediatrician's office for an appointment today. Rather than going to her office first, she felt it was best to send us straight to the ER. Tyler tested positive for RSV. He's not in as rough shape as Caleb was last week, so he doesn't need ICU care for now. He was admitted, and we're in a regular pediatric room... in OKC! He's on a small amount of oxygen but no other treatment at this time.
Please pray that Caleb continues to recover and that he and Brad will get to return to OKC soon. Please pray that Tyler recovers quickly too! I can't wait for my family to be healthy and under one roof.
Sunday, February 15, 2015
Another RSV Update
Caleb has made some good progress today. He got the bipap mask off and is now getting oxygen through a nasal cannula. He also has started drinking and eating, and Brad said that he was been more playful today. I received a text from a friend who was visiting Caleb and Brad, and he said Caleb was giving out a lot of fist bumps.
I'm so glad to hear that my precious boy is starting to recover. I cannot wait to have Brad and Caleb home. Tyler and I miss them so much!
Saturday, February 14, 2015
RSV Update
Caleb is still in Wichita, KS. His x-rays are showing that the pneumonia is clearing up. He's still on bipap (the big mask), but the oxygen flow/pressure is gradually being weaned down. Hopefully, he'll be able to get off of bipap today or tomorrow. Once he's done with bipap and switches to a nasal cannula, he should be able to start eating and drinking. Since he can't eat/drink yet, Caleb got a NG tube placed yesterday. He's receiving continuous nutrition through that. We expect that he'll be in the hospital for several more days. We appreciate your continued prayers.
Our little family of four was able to FaceTime for a few minutes yesterday evening. I can't wait until Caleb is well, and we're all back together!
Thursday, February 12, 2015
RSV
Caleb woke up from his nap Saturday afternoon, and we played together for about thirty minutes. Suddenly, things changed. He got very clingy and upset. He started feeling warm. A fever and cough developed. He coughed and cried so much that he vomited a little. We didn't want to take any chances of Caleb getting sick around Tyler, so Brad took him straight to pediatric urgent care. The doctor said that Caleb probably just had a virus. We were supposed to do Tyler's baby dedication at church the next morning, but we cancelled those plans when we realized that Caleb wasn't going to feel well enough to go to church. Since he had missed out on Tyler's birth day, we didn't want him to miss out on the baby dedication too.
Caleb's fever and cough persisted through Sunday and Monday. I called the pediatrician's office on Monday afternoon. The triage nurse said to watch him for another 24 hours. My mom was visiting that day, and we decided that Caleb should go home with her that evening. That way, we were able to keep Caleb and Tyler away from each other. Before they left, I noticed that Caleb had some waxy drainage in his right ear. We started giving him some antibiotic ear drops that Caleb's ENT had given us after he got his last set of tubes. We were told to use them any time we saw drainage. Caleb's fever broke Monday evening, but he still had a cough.
On Tuesday morning, my mom called. She was really concerned about Caleb's cough and was bringing him back to OKC. I called the pediatrician's office again, and I spoke with a different nurse. She said that his symptoms were probably just from a virus that was turning into an ear infection. She said to watch him for two more days, because she said it might take 72 hours for the antibiotic ear drops to start helping. She was sure it was an ear infection, and she didn't want him going in for an appointment and catching something else in the waiting room.
I didn't feel comfortable waiting two days, so I asked Brad to take him to the pediatric urgent care after he got home from work Tuesday evening. Caleb had a terrible cough, his fever had returned, and he was getting very lethargic. Brad and Caleb waited about two hours before they were called back to the triage area. The nurse put the pulse ox sensor on his foot, and his oxygen saturation was in the low-80s. The doctor saw him immediately. He tested positive for RSV and an ambulance was called to have him transported to the local childrens hospital.
Caleb spent the next 27 hours in the ER at the childrens hospital, because there wasn't a pediatric ICU bed available. The doctors checked with other hospitals in the state and in the Dallas area, but they couldn't find a bed anywhere. Late Wednesday evening, a bed came available at a hospital in Wichita, KS. Brad and Caleb were flown up there Wednesday night.
Caleb is receiving excellent care now. He's on a bipap machine which is forcing oxygen in through his nose and mouth. He's receiving breathing treatments every two hours and is getting fluids through an IV. He has developed pneumonia, so he's getting a couple antibiotics for that.
Tyler and I can't be at the hospital, for risk of Tyler getting sick. For now, we are at home in OKC. We might go to Wichita and stay with friends soon, but we'll just see how things go. Brad's mom and my parents are in Wichita and are helping Brad out since I can't be there.
Please pray that Caleb's health improves soon. And also pray that Tyler remains healthy.
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