Well, we dont really have any new info. I really like the surgeon. He referred to Kimber by name when talking about her, which is more than any of the other doctors have done (not that they arent great doctors, they just dont do that). He also said that some restriction could be a good thing because it helps balance everything out. We wont really have a plan until she gets here and they are able to do an echo on her. My last appointment left me pretty frazzled, but I feel better after this one. They dont talk about my daughter as if shes a ticking time bomb or a statistic. They speak of her milestones in terms of when shell reach them, not if shell reach them and that gives me a lot of hope. We also got to tour the hospital, and while weve had our experience in NICUs, the CVICU was a little bit overwhelming. Its still great to get to see where everything is and have a heads up of where theyll be caring for our little princess. Thank you all for your prayers. Things should be quiet for the next couple of weeks, but Ill update when we have new info. :)
Posted on: Thu, 31 Jul 2014 23:19:18 +0000
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