Full story:
Since last we met, Dr. Goddard (the surgeon who created his new tongue) came by to see him early Sunday morning during ENT rounds. That was an exciting appearance! She said, "You can't ask for it to look much better." She should know! She ordered them to increase his tube food (did I mention that they'd started his tube food?), and she wrote an order to move him out of the ICU.
Moving out of the ICU takes a super long time—they have to wait for a bed to become available—so we stayed in the ICU all day Sunday and Monday.
Monday, Nurse Kate told us the ENT team had ordered a new, smaller trach tube, and the next think you know, the respiratory therapist brought up a bunch of supplies—including a cuffless trach tube. Kate and the RT didn't know when they were going to put it in, but now it was ready when ENT was. Kate was kind enough to tell tell us a lot about trach tubes.
(Any errors in this description are mine.) The trach tube sits low on his neck, below the vocal cords. The tube he had in on Monday was cuffed.
My finger is pointing to the "cuff"—can you see it? It's kind of like a balloon. |
A cuffless trach does not have that "balloon" and thus allows speech. You just have to put your finger over the hole.
Going from a cuffed trach to a smaller, cuffless trach is a huge step.
It looked like we weren't going to get a bed Monday, so after a nice walk around the ICU ...
...we went to bed. I wasn't looking forward to another night in the ICU—so loud, bed so uncomfortable, so many interruptions for Vic (I sleep through most of them)—but the quality of his care there was unquestionably high, so that far outweighs any inconvenience.
It would have been nice to move during the day or even in the evening. But sure enough, 5 a.m. Tuesday, Nurse Kyle comes in and says, "GET OUT" (he might have been a little nicer than that), and by 6 a.m. we were on "the floor."
At 6:30, the ENT team came in for rounds. They did their usual—look at everything, do a Doppler (like a tiny ultrasound to check for blood flow), check all the wounds. But today, they also put in the new trach tube. The doctor put his finger over the hole and said, "Say your name," and Vic said "Vic"! So exciting!
He is now sleeping soundly, and I'm about to take a cat nap before I start my workday.
Lots of great stuff going on down here in Aurora, folks!
9 comments:
Yaaaay, private room! Yaaaay, cuffless trach! Yaaaay, Vic up and at 'em!
WOW! You two have been busy! Excellent news about the trach tube and Vic speaking. Loved the video (glad the gown was closed in back). Keep up the good work!
Love my Loves!! ❤️
Love love love love love!
such great progress. Can't keep him down! GO Team LOVE
Oh my goodness! Look at him go! Such amazing progress. Big hugs to you both!
As I watched the video of him walking, I have to admit, I half expected to see a faux bottom or tail or something humorous on the backside. I got my voice back today too! Take it easy. We love you guys!
I know that I have said this before, but your updates and humorous comments on the Blog are wonderful to read. I learn things about Vic's surgery, medical team, and the rude 5:00am "Get Out" hospital staff individual, and the daily progress!
Glad that you tried to take a cat nap!
How does a cat nap by the way?
Yeaaaaaay! Answer to prayers!!! So happy for you both that things/healing are progressing so "Great"! Keep it up Vic!!!
We want to yell Yeaaaaaay! too! So glad to hear you're doing well from the medical side of things. Vic, you probably shouldn't yell Yeaaaaaaay! too, but Patty can yell for you!
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