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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
06-03-2002, 02:26 PM
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I just wanted to let everyone know that we are going to see Dr Cotton next Tues. He called me today and then called her current ENT. He decided he wanted to see her as soon as possible. We are going to meet with the hemangioma team on Tues and then Dr Cotton will do a bronch on Wed. I am so scared of what they will find out. I wnt to thank everyone that kept telling me to call him. I would never have done it if yall weren't pushing so hard.
 Kim 
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#2
06-03-2002, 02:31 PM
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Good for you Kim! I'm so glad Dr. Cotton called you back and that things got set up so quickly! The only thing better would be if you were going to be in Cincinnati on Friday when we're going to be there!
 Good luck and we will all be waiting for good news from your trip. Erica (Lily's Mom)
__________________
 Our fabulous Lily was born 5-26-01 with partial trisomy 7q, Pierre-Robin sequence, VSD, GER; had trach, GT, Nissen at 4 weeks, cleft palate repair at 6 months and 18 months. Decannulated 11-15-04. Proud big sister to Benjamin 10-10-03, baby Vivienne 3-5-07!
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