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Pediatric Tracheostomies For parents and caregivers of children with tracheostomies.  Please limit discussion to seeking and sharing of information pertaining to tracheostomy care, medical issues, special needs, disabilities, networking and moral support.

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  #11  
Old 07-01-2012, 11:44 PM
bryantem bryantem is offline
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Our ENT was very careful to look out for air trapping under the skin. When he closed Addy's, he removed the granuloma and stitched it closed very loosely, leaving a drain in place for 24 hours. We stayed impatient on the regular floor and released the following morning after the drain had been removed. This was about 11 months ago and her scar has healed very well.
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  #12  
Old 07-06-2012, 11:01 AM
blessedwithtwins blessedwithtwins is offline
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That was the original plan, exactly how you describe it, but then the ENT changed his mind...
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  #13  
Old 07-07-2012, 01:40 PM
SammyJo SammyJo is offline
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Quote:
Originally Posted by blessedwithtwins View Post
Alex, good luck with the surgery! Please let us know how it goes!

Silvia
We had our follow-up on Thursday and some how we lucked out. Her stoma closed on its own, so a surgery for cosmetic purposes is all she'll need. Our ENT said she doesn't see it close often, so we feel very grateful.

Sylvia, good luck to you and your family. I hope your daughter is able to stay trach-free!
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Alex, mom to Samantha born 38 weeks on March 7th, 2011 with Congenital Nasal Pyriform Aperture Stenosis, trached 3.30.11. Grade I Congenital SGS, diagnosed 11/30/11. Also mom to big brother Luke (3).
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  #14  
Old 07-09-2012, 11:13 AM
blessedwithtwins blessedwithtwins is offline
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That's great news Alex! Congratulations!
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