Harry's Tonsilectomy--Children and Apnea

General Discussion on any topic relating to CPAP and/or Sleep Apnea.
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socknitster
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Post by socknitster » Fri Nov 02, 2007 1:55 pm

[quote="echo"]Glad to hear he's doing better. It's good that you have an ENT you can trust... now have you managed to find a new (accredited) sleep center?

For his sake I also hope he doesn't need CPAP... but if he does, he is so lucky that you have managed to catch it now.

In any case, every body is different, as you already know... and don't forget he also has years of sleep debt to pay off, so I wouldn't be too surprised if it takes him some time to catch up. *fingers crossed*


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echo
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Post by echo » Tue Nov 06, 2007 8:14 am

socknitster wrote:Also, my RT tells me they like to do "Blood Gas" instead of pulse ox. Can you imagine on top of everything else to have an iv in you too? Absolutely ridiculous. I may go all the way to Indianapolis if I ever have another one or if Harry needs one.
Run away FAST! How horrible is that?!?!

I went to the methodist (?) in Indy 3 years ago. They had a 6-month waiting list for a sleep study so I didn't get it done there. A few of our friends in Muncie & Indy had sleep studies done a while ago, I can ask where they went & how their experiences were, if you want.

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socknitster
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Post by socknitster » Tue Nov 06, 2007 10:04 am

I'm going to remember that! If it comes to that I will pm you to get a recommendation. Hopefully it won't. It looks like I won't be needing another sleep study for a couple of years now.

jen