That is what J calls his cardiologist.
We went in for his 6 week checkup on Wednesday and to
discuss his surgery. I was pretty
nervous. I knew this was coming. The truth is that I kind of convinced myself
that he had improved since being home.
He hasn’t been blue in a while.
So I wondered if he really needed the surgery…but I knew he did. Tuesday night I went in his room and prayed
over him. The first thing I did was
dedicate him to God. I told God that I
wanted J’s life to glorify Him and I asked Him to help me accept whatever came
in his life. I also asked Him to guide
us in any decisions we needed to make for him.
So we went to the clinic where our doctor sees him. Our nurse, Linda (who we LOVE), came to the
waiting room to get us and it was so nice to see someone we knew. We stopped to get his vitals and other nurses
were stopping by to say how cute he was.
After a few bizarre oxygen level readings, we came to the conclusion
that his has not changed. We didn’t
think it would have, but we always check.
Miss Doctor Jean said that this surgery will help make his
quality of life so much better. He will
have more energy and stamina. So the
next step is to have a heart cath done.
They will put one in up by his neck and another one in through his
groin. This is so they can get a good
idea of what exactly they need to do. At
the same time they will do an ultrasound.
He has spleen activity, but they aren’t sure if he has one or
multiple spleens. This is basically an exploratory adventure. She wants to keep him overnight to monitor
him afterwards and she said it will give us a test run of the ICU. After they have the results his case will go
to a meeting of all the cardiologists and surgeons and they will come to a
decision on what exactly they need to do and how they will do it.
His surgery will most likely be the first of June. She wants him to have plenty of time to heal
before he starts school (a 5 year old program) in the fall. She tried to prepare us for what we would
experience. She said he will be in the
hospital for a week to 10 days and after that he will not feel well for another
2 to 3 weeks. It will take his body time
to get used to working with more oxygen.
Then she told us what to expect when we first see him after
surgery. He will be on a
ventilator. There will be multiple tubes
coming out of his chest. He will also
have blue wires coming out of his chest that are connected to his heart so that
they can control how it beats (like a pacemaker). He will also have draining tubes coming out
of his side. Yes, the thought of seeing
him like that makes me tear up. Our
doctor is so great though. She said she
will ask the nurse to cover him up for our first viewing and slowly roll it
down. Our case is special all the way
around. His insides are so
complicated. He should have had this
surgery 2 years ago so they aren’t sure exactly how he will respond to all of
this. Most parents who go through this
surgery with their child have already seen their child like this because they
have had surgeries like this since birth.
I feel very confident in our doctor and the staff at the hospital. They are very interested in him and helping
him. They are just so helpful.
They also told us to go on our vacation before the
surgery. He has been begging us to go to
the beach so we got that booked today.
No swimming or sunshine for him this summerL.
So the doctor visit was very informative. Of course I’m scared…very scared. But I feel a great peace about all of this
from my faithful Father above. We knew
before we even saw his picture that he had a broken heart that would need to be
fixed. We also knew that it needed to be
loved! This will be his first surgery
with parents and I’m so blessed that I get to be with him. I know God is going to do something awesome
with him.
Katie