The good news is......there isn't much news to report! Rebekah had an eventful night, only because the doctors from cardiology and the doctors from pediatric surgery couldn't agree on a "safe" range for Rebekah's oxygen saturation levels. So for a while we were riding back and forth between going back on oxygen and staying off (just oxygen through a nasal cannula like she was on in the picture below, not back on the ventilator).

Rebekah on Tuesday morning after moving to the step-down unit.
So far, Rebekah has tolerated her feedings very well. As a matter of fact, when we met with Dr. Hebra, her g-tube surgeon, the two things he told us to most certainly expect were that Rebekah would not be eating by mouth for 3-4 weeks post-surgery and that she would not be able to burp. We have been "burping" her g-tube, which basically amounts to letting air out of her tummy. Rebekah has now had every feeding but one by mouth (and LOTS of milk at each feeding compared to what she had been eating before) and she has burped twice, once all on her own without me patting her back. So, no offense to anyone, but sometimes this little girl just has her own plans no matter what the doctors say! :)

Rebekah this morning in the step-down unit.
This just in......we are now packed and ready to leave!! Rebekah has been discharged and we should be home late this afternoon. We will be coming back in two weeks for a one-day clinic (like a doctor's appointment) for Dr. Hebra to check on Rebekah's Nissen and make sure all is going well.
Rebekah sends her love to you all!!
Nancy







