Another long day, but in the end it was worth it.
Xander, Mom and Dad headed into Children's early this morning leaving Willem with a friend.
The hospital changed the procedure slightly this time for check in and we had to go to the main check in on the 6th floor. A step back in our eyes, it is always less responsive there, even though there were not many clients.
Then it was business as usual, down to imaging, wait around in the recovery room for a bit, although this time Xander was in better spirits and was not as anxious. Then Mom and Xander headed over to anesthesiology and they put Xander under.
When they wheeled Xander in the anesthesiologist informed us that Xander was having some problems with his oxygen. He was exhibiting behaviour as if he had a cold. It seems that people with colds and some respiratory problems utilise extra muscles to help them breath. When they are put under and those muscles relax then they do not draw in as much oxygen as they normally would. They had him on oxygen when they put him under and just transferring him from the cart to the MRI room he dropped from 94 to 82 SpO2. She almost pulled the MRI, but then his rate increased to satisfactory levels. He has had a cough and a runny nose for a few weeks, but he does not exhibit the classic symptoms of a cold so we never gave it much thought.
After Xander recovered we headed over to U Village for some lunch. Corrine called us with the results of the MRI and they were clear again. Actually looking better than ever. We then headed back for an appointment with Dr. Geyer to go over the MRI and Xander's general condition, which is excellent. He weighted in at 35.3lbs and was 39.5 inches tall. We talked about the cough and what the anesthesiologist had said, but we are going to let Xander's immune system handle it.
We had asked Corrine about a lumbar puncture this time. Dr. Geyer and Corrine discussed it and indicated there was no real need, if there were any signs of reoccurence then they would perform one. One less risk while he is under.
So we get another three months of time before the next MRI in which to be a normal family.
We even got to see Jennifer and Allison while we were at Children's, another family having to deal with cancer. Allison is done her treatments and is recovering nicely, including getting that all important head of hair back. Nice to see good progress by these kids.
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