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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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#1
10-11-2004, 02:08 PM
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My 4 month old daughter has a trach because she has laryngomalacia. She has had a trach since 7-29-04. Has anyone's child ever had this and did they grow out of it? That is what her doctor says she'll do eventually maybe by a year old. Any info would be helpful.
Thanks Staleena Collins Lauren Collins 
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#2
10-11-2004, 03:15 PM
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Welcome to the board and congratulations on the birth of your daughter. You'll find lots of support and information here. While my son does not have laryngomalacia, I believe that if you do a search of past posts, you'll find lots of previous posts regarding the topic.
Good luck and again, welcome!
__________________
Jakob, born Dec 02, Pfeiffer Syndrome, trached at 5 wks age due to mid-face hypoplasia, cranial vaultx2, monobloc, mid-face distraction, g-tube, pyloric stenosis, nissen, nasal stents, VP shunt, tonsils, adenoids, uvula all removed, tongue suspension, future pilot!!
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#3
10-11-2004, 10:29 PM
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Welcome. You will find a lot of support on this board. My son has his trach for different reasons than your daughter, so I have no advice. Just wanted to welcome you to the board.
__________________
Mom to Breanna (15), David (12), Christopher and Brian (almost 5). Brian decanned in 2006 and had his g-tube removed in 2007.  B & C are surviving triplets. Brooke survived for 1 month.
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