
If you don't mind we will probably spare you the pictures. He is darling but it hurts our hearts to look at them when he is hooked up to so many contraptions. He's doing a little better but had some trouble today getting enough oxygen into his little self. They turned up the juice (extra 0
xygen) for a little while but he wasn't really responding. They did a chest
Xray and found a
Pneumothorax, basically air leaking out of lungs into his chest cavity restricting full inflation of the lungs, similar to what happens with a small collapsed lung. This was causing him to work a little too hard. This is typical to
Preemies, and especially white boys unfortunately. Usually having a lot to with a) not fully developed lungs b) more specifically lack of enough surfactant (that gives lungs their amazing properties) within the lung itself. For this reason our little guy was
intubated and put on a breathing machine. As tough as this was to see he labored in his breathing much less, and after being sedated a little seemed to be recovering and making progress instead of just treading water and fighting against everything. He was also given a little man made "surfactant" that seemed to do his lungs very well. All this with the typical jaundice so he has to hang out under the lights and wear goofy "sun glasses" that are far from cool.
As far as the family update, Kelly and I are doing as well as anyone who just left their firstborn in the hands of thankfully very capable nursing staff at the
Hillcrest Newborn ICU. Leaving the hospital was definitely not how you always picture it. It was correct except for one thing, we had to leave our most precious cargo. You can imagine walking past the waiting area missing what you came in to take home. It was in a word,
gut wrenching. Physically speaking Kelly is up and walking around and doing great but somewhat tear filled. Kelly's mother made it here and she has been a big help in juggling all of the things we thought we had another month to get done.
Thank you for your prayers, well wishes, congratulations and calls. We are
truly blessed to have Caleb, friends that are praying for him, and we know he will be "full strength" very soon. Kelly will be available for visits as she is already home, just know there will be significant ferrying to and from the
NICU so we may miss you. Feel free to call the house if you want to drop by.
As far as seeing Caleb himself, you may have to rely on the world wide web. As his immune system may be a little depressed even after he comes home, we may be more reluctant than typical to share him with the world. There will be a good healthy time to meet him in the future. Trust me, when this is all over and he emerges unscathed I will probably be calling people at random in order to show him off. I will update the pictures when I have some time and they aren't quite so gruesome. Until then you will have to take my word that he is beautiful.
Sorry for the mass update via the web, it saves us a little time, tears, and
kleenex.
We promise to catch up in person over time. We'll keep you posted.
Goodnight All, goodnight Baby Caleb.
jon