Daddy successfully getting him to eat a whole bottle. Right now, a whole bottle for Will is the equivalent of "3 tablespoons and a smidge" according to our nurse.
He is still doing those funny poses with his hands. This one is not a frozen view of him in motion, it is the exact position of his hands for several minutes. Same goes for the photo above.I've read that the raised hands and splayed fingers are signals of stress for a baby. But he does them so often (And to the side. A little like the Hula.) I have come to believe that it is his special quirk.
Enough pictures!
Today Will moved to the intermediate unit!!! It's his last stop on the way out of the NICU! The babies in this unit need less attention and share a nurse with two other babies rather than one. I think one of our primary nurses asked for us to move there sooner than later because she could tell we are reaching the limits of our patience with his stay. As we followed his crib down the hallway we passed one of the nurses who worked with Will his first week in the hospital. She smiled and asked where we were going but knew the answer already by seeing our arms full of Will's things and smiles on our faces. I remembered later that she is the only NICU nurse that has seen me cry. A nice full-circle moment.
We predict he will still be there for another week. Maybe two. But this room is a bit of a reward for our wait. It is designed for parents to room-in with a bed and private bath. There is a fridge and T.V. with DVD player. Major conveniences in this inconvenient situation. I have spent a lot of time riding the elevator getting myself something to drink. Not anymore! We can also eat in the room now and have more visitors. We don't even have to wear a gown when we hold him. We might, however, have you put one on if you come to visit. Especially if you have been around children that day and haven't changed your clothes. It's RSV season and Will hasn't yet been vaccinated. Thanks for understanding!
The new giant room!
Sometimes we share an elevator with one of these, a children's hospital version of wheelchairs.
Chris & I are still working on the bottle feeding. We hope that when his feeding tube comes out his spells will decrease. Describing the theory would take awhile, but it has to do with: possible reflux, a vagal response, and the esophageal sphincter. Enough said, don't you think?