Since Jack's confusing, unexpected and scary diagnosis, we've been talking quite a bit about prayers. Jack was surprised to hear that I pray every night. He was even more surprised to hear that I pray for him and Luke every night. I don't know why this would come as a shock to him. I guess we don't talk about it much. We talk about his prayers but not about mine. So I told him a little about it. I told him that I pray for him always, and not just when he is sick. I also told him that I am not just asking God to keep him safe or make him well, but that I am always thanking God for the gifts of Jack and Luke.
We had the appointment with the Pediatric Neurosurgeon on Saturday at 8:00 am. That is waaaayyyy too early in the morning to have to think about spinal cord surgery. We were the only family in the office so got an abundance of attention. First, a PA came in and asked Jack several questions and put him through a battery of strength and motor skills tests while the neurosurgeon reviewed his MRI. Then, the neurosurgeon and another doctor came into the room and called John and me into another room to discuss the films. I was hoping we would pass by a toilet on the way so I could puke.
What he told us was that this:
was likely something that Jack was born with, is not all that uncommon, and would likely close itself up as Jack grew. He said he saw nothing obvious that would be the cause of it, no blockage of spinal cord fluid flow, and would recommend another MRI in one year to confirm his diagnosis. Basically, what we had was wonderful news and answered prayers.
As we left the doctor's office and explained to Jack what the doctor said, Jack said, "I knew I would be fine because I have been praying. Will you come to my next MRI, Mom, and rub my feet when they get tingly like you did last time?" So now I need to make an appointment with a cardiologist to repair my melted heart.
But, I do have to say that what really scares me is this:
I wonder if we could turn this image into Jack's next Halloween costume.
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