This is a video montage I made for my little man.
Tuesday, February 2, 2010
Nathan's Journey through Cranioynostosis
Posted by Jaime at 8:30 PM 13 comments
Tuesday, January 12, 2010
Home at last!
HOME AT LAST!!!! It feels sooooo good to be home! After 5 days in the hospital, I am happy to have my little dude back in his own bed. He had some good days and some not so good days, but once he got his eyes opened he was a totally different boy! His demeanor changed dramatically! I'm going to post some links to the photos I uploaded on to Facebook. Thanks for your thoughts and prayers. He still has a long recovery road but he is doing great!
Posted by Jaime at 8:00 PM 2 comments
Labels: craniosynostosis
Still in the hospital...
Well it has been a couple of days since I've been able to update. Nathan is still in the hospital. The last couple of days have been up and down. He's been running a fever anywhere from 37.8 to 39.8. (100-103.6) When he has a fever they have to recheck every hour day and night, when he doesn't they only check every 4 hours. It makes for long nights when they check every hour. His incision is healing nicely. I tried to count the stitches but I keep loosing track. It's a lot. His swelling is going down. Last night he was able to open one eye and has been slightly happier since then. My mom stayed with him last night so that I could come home and get some sleep. Yesterday they were talking about letting him some home on Tuesday (today) if his fever was under control and if his blood work numbers came back good. This morning they drew blood and his hemacrit level was in the 20s. I don't know what that means but we should find out today if he'll need another transfusion. I am waiting to go back to the hospital now. I tried to go earlier and had a flat tire. Definitely not what I wanted today! I think that is everything that has happened really. Just trying to control his temp these days. Thanks for the prayers!
Posted by Jaime at 10:30 AM 0 comments
Labels: craniosynostosis
Saturday, January 9, 2010
PICU update
Good Evening. I am updating this from the adult hospital next door. I have been kicked out for shift change. Currently Nathan is still in PICU but is being moved to a real room! Originally they told us he was staying another night but changed their minds. I think they are moving him because a trauma came in this evening. It was very hectic in there. He is still getting morphine (he hates the initial push of the meds) and tylenol. His temp is still at 38.9 (102.something) That is semi-normal for a big surgery like this. He has kept his food down today! His eyes are swollen shut and they are black with a hint of purple. Literally. That's about all I have time to say right now. I need to go be with Nathan when they move him. Update again tomorrow. Good Night.
Posted by Jaime at 7:15 PM 0 comments
Labels: craniosynostosis
Friday, January 8, 2010
Surgery is over!!!!
I'm finally getting a chance to update on his surgery. Everything went great! We had a slight delay this morning, but our doctor found him a bed in ICU so surgery went on. Nothing unexpected happened. They said it was uneventful. He spent about 3 hours in recovery because during his surgery they gave away his bed. No big deal, just inconvenient. Of all the things that could have gone wrong that was not a big deal.
Posted by Jaime at 7:45 PM 0 comments
Labels: craniosynostosis
waiting update 10:45 am
They called us again and said that the neurosurgeo
Posted by Jaime at 10:45 AM 1 comments
Labels: craniosynostosis
waiting update 9:45 am
The nurse called us and said everything is going great!
Posted by Jaime at 9:45 AM 0 comments
Labels: craniosynostosis