Saturday, November 7, 2009

Day 2

Good morning everyone. Ella had an ok night. She had to go to onto a CPAP, which is continuous air flow. It is a level worse than her breathing on her own, but better than the breathing tube. The nurse basically said that breathing is hard work, so she just needed a little break. The Doctor came by and gave her an A though. Her blood type came back as O negative – so again, she is being difficult!

Stef is doing fine. Well, she had her epidural removed last night, so that is “good” but Stef may say otherwise. She will be discharged this Saturday, although because of Ella, we can leave anytime we want on Saturday, and not necessarily by the 11 am check out (so “late” checkout for us!)

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