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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
07-08-2002, 10:31 PM
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Hi Lindy,
We'll probably be in Cinci at the same time; Lily is having surgery on August 26. Â*As far as where to stay, I'm not sure. Â*We used to live in Cincinnati, so when Lily was at CHMC for 8 weeks after she was born, we were lucky to be able to go home to our own bed every night. Â*I'm not sure what we are going to do for lodging this time, but if we find any good deals, I'll let you know. If you're willing to drive 20+ mins to/from the hospital you can always stay at one of those extended-stay type places like Residence Inn or Extended Stay America or Towne Place Suites. The advantage is that you have a lot more room for weekly rates, a kitchen, etc. The problem is that there aren't any close to the hospital (go figure). As far as what to do in Cincinnati, try the zoo (near the hospital), explore downtown/Fountain Square, Kings Island amusement park is 20 minutes away, Cincinnati Museum Center has several great exhibits and and IMAX theater, there is a great aquarium across the river in Newport, KY, geez, I could go on and on (I love Cincinnati and miss it sooo much) Email me closer to August and maybe we can plan to meet/have lunch/tourguide/etc? Â* Good luck! Erica (Lily's Mom)
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 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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