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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
07-14-2003, 11:09 AM
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I send a reply, hoping some items are still there. You can never have enough Humidivents!!
On another note, I almost cried when I read your post. My first thought was, No, don't give that stuff away, what if you need it later. It's all a fantasy to me that kids get decannulated. I can not imagine it happening to us. What a feeling it must be!! Your family must be very happy. Susan
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Michael's mom, 2 yo with hypotonia, possible myopathy, vent dependent at night, Beautiful, beautiful smile, and hugs are contagious 
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#2
07-15-2003, 08:42 PM
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It really is wonderful that Carson is able to give this stuff away. I'm so glad that the visit with Dr. Cotton went well!
christy
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Gaithy's Mom:28wk preemie born 8/2000 at 1 LB, IUGR, SGA, ROP, BPD, g-tube/nissen. Trached 4-2001 and LTV950 ventilator until 5-2003. Decannulated 8-3-04
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