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		Aaron's Tracheostomy Message Board > Pediatric Tracheostomies
O2 tubing

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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04-29-2005, 07:27 PM

Doug-Iowa

Member

Join Date: May 2004

Location: Ottumwa, Iowa

Posts: 529

My friend mentioned to me today that she has a bags and bags of oxygen tubing. The exact amount I really couldn't tell you, but she asked me to see if anyone needs it. So if anyone needs it, feel free to take it.

Jarita

__________________
Doug, father of Mason. Hemangeoma in Trachea. Had Tracheostomy 5-14-2004 at 4 months of age. Decanned 8-19-05. Closure Surgery 5-5-06.

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