Tuesday, July 15, 2008

Evan's MRI

On Tuesday, July 8th-Evan had an MRI done to check on his enlarged ventricles to make sure we were not dealing with hydrocephalus again.

What a disaster of a day.

It is always a long day when we go to DUKE.

We were told to be there at 1130 for a noon MRI. We were not called back until 1230. Mind you....Evan must fast for this test. He had only a bottle of water at around 8am. His last bottle of formula was 8pm the night before. Needless to say he was a bit cranky.

They did not give him anesthesia until after 1. It was almost 2 when they took us into the MRI room...and guess what? Evan woke up and we had to leave the MRI room to try some different anesthesia. They said that they would have to give him an I.V. and that would be very difficult because of his size. They told us that he probably wasn't settling down because he was too hungry. (You think?) Anyways...they said we could reschedule, try the I.V. or feed him.

We opted to feed him and he did go to sleep...so we walked him back down the hall to the MRI room. Finally....the MRI was complete by 3pm.

Our doctor's appt was at 2pm. After the MRI..we headed upstairs to see the doc and surprisingly we got right in. He said that the ventricles are still mildly enlarged and that could still be because he was premature. He can see the floor of the aqueduct which he said is a good thing. He does not believe that we are dealing with hydrocephalus but would like to keep in eye on him for awhile. We will be following up with our pediatrician. We will just have to wait and see...watch for signs and symptoms.

Our next appt. will be at Wake for a urologist and plastic surgery in the next couple of weeks. We also have a genetics appt soon.

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