Friday, February 6, 2009

A message from Will.....


He had a fun little time earlier and I caught it on
camera. This was the first day he has smiled since
surgery. So good to see him returning!

He was playing with his blanket. He loves having
blankets by his face.

Ignore the crazy lady! When I speak of him
not having mittens on his hands and his hands
being free, it is because we have had
his hands covered with socks to keep him
from pulling out his central line and feeding tube.
Hit the play button to watch.

Tuesday, February 3, 2009

Will pre and post surgery and Faith


The first 2 pics are him today 24 hours postop.
The green looking thing is a pacifier that the
doctors cut the tip out of to put the feeding tube
through, which is the yellow looking tube. That will
come off in 8 to 10 days to keep the tube from moving.
The little white patch underneath the tube is the
seperate incision that was made for the Nissen
surgery. On his shoulder is where the central line
is (IV access)


These 2 pics where taken of him on Sunday prior to
surgery.

This little thing is a medicine delivery system.
It is a automated thing that operates by itself. It
has a motion sensor and it opens doors by itself and
elevators by himself. It is so cute and the little kids love
it on the floor. (the door for the medicine is in the back of the train)

Faith LOVES elmo and has since learned how to say
elmo. As a suprise for her one night we got this HUGE elmo
from the gift shop downstairs as a special treat for
her. Needless to say she loved it!




Love this video and thought we would share!