Little e is still in the hospital, but she is improving. It looks like she will stay till Monday or Tuesday. She must be able to eat and to breathe smoothly without the oxygen feed. Suctioning continues, and her lungs are clearer as a result. K uses his phone to play the lullaby music she hears at home when it's nap time, and we all talk to her. It is difficult to pick her up with the various tubes connecting her to monitors and such. The care staff at Cardon Children's Hospital are kind and friendly.
I've had a busy day here at home, and tomorrow will also be full before I fly back. But Randy and I took a nice walk, and he encouraged me to remember we are in a period of transition, learning how this new life will work. While he did do laundry this week, he didn't get to the grocery store so he's running low on bread and milk. His meal plan seems to be working fine, fixing a large batch of beans for soup every few days.
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