His lung is still giving him issues and the nurses are at this moment trying a technique where they push air into his lungs at a bit of an extended rate compared to the CPAP to see if that can get it open. The nurse practitioner says that since he seems to be doing fine with breathing and oxygenation, we will probably just try less invasive solutions and keep an eye on him instead of trying to expand the lung through intubation.
I got to hold him today! They transfered him on his tiny cushion and set him on my lap. It takes a lot of effort by our nurse and an assistant to pin all his cords to his cushion, adjust all the tubes and CPAP, and get his IV in place to carefully move him. But they did it and I got to sit with him on my lap for over an hour.
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| Nurses valiantly adjusting cords/tubes/monitors while I look at Milo |
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"E.E. just put her name and not a time frame and now she's just napping in the room."
"Yeah, but she leaves if anyone knocks because they need the room."
"That's a clever plan."
"Large wasn't in the room when the board said she should be but then she adjusted her timeframe to be later with a note saying she was running late so we have to wait an extra fifteen minutes for our turn."
"Oh, that's nice, the person who reserved a room after us left a 10 minute buffer in case we need a little more time."
"Hey, that lady marked off more than half an hour, can we do that?"
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We can't believe we've been here five days already. On Monday Milo will have his contrast study where they will put dye down his throat and watch its progress through his intestines to make sure there are no abnormalities and then, if that goes well, we can start him on Shelly's milk again. After a couple of days of observation on milk, we can take out the tubes in his stomach and begin dropping his IV calorie intake! Then hopefully, it will all be healing and growing until we get to take him home (or transfer back to Medford, we are not yet sure which).

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