1.23.2009

Day 2

Yesterday was a little longer than Day 1. I guess the strain of seeing Emma Kate awake and knowing she was uncomfortable along with the lack of sleep didn't help things any. And then hearing terms we aren't familiar with certainly add to the strain. But I think sometimes it is good to cry. It is good to sit down and tell God exactly what we are thinking. And I am comforted that He listens.

Last night was much better. Emma Kate is eating her Portagen (formula with less fat to help the Chylothorax) extremely well. This apparently doesn't taste very good, just like most low-fat food!, but she doesn't seem to mind. After eating last night, she stayed awake for a while without crying. This was definitely a blessing for mommy and daddy to see. She just stared at us with her big blue eyes and looked very peaceful. Thank you God!

We spoke with the nurse this morning and he said that Dr. Kirshbom wants to take out the majority of her lines today. By this afternoon, she should be left with only the chest tube and one or two iv's. The chest tube will remain until they chylothorax has stopped draining. The nurse also said the draining has significantly decreased. And Bethany and I feel without a doubt that this is because of your prayers! Thank you!

I will put up a few pics later of Emma Kate from this journey. She is amazing. And she is our little hero. Thank you for your prayers for her. Please continue. We are all grateful.

2 comments:

Molly said...

So glad that things seem to be better today...that's wonderful. I can remember Annalee's tubes and lines coming out one by one - each one is a little victory :) Good luck to y'all - many are praying for you.

Erin said...

we're praying for EK!! Love you guys!!