Now we were in another exam room and I was again lying on a table while someone performed a sonogram test. This time it was on the baby's heart. They used an echocardiogram to examine the chambers and development of my son's little heart. I didn't even watch the screen this time because nothing looked recognizable to me. The doctor came in and he looked at the pictures and examined the heart. He then drew us a diagram of what he thought was the problem. There was a small hole between the two bottom chambers of the baby's heart but otherwise it was functioning just fine. He also noted that the muscle seemed a bit thick but everything seemed to be working. He also said that sometimes these holes close on their own before or shortly after birth. Because our baby had multiple problems he thought this one likely would not heal itself but it could DEFINITELY be fixed he said. He said it would be a major surgery but the success rate is extremely high and they perform these surgeries all the time. It was hope! He led us back to the genetics waiting room .
This room was filled with crying pregnant moms and stunned expectant fathers. The pain in the room was thick. We sat there with a little hope knowing that two of the known abnomalities were repairable and the third was still unknown and would be until the next ultrasound. I sat there praying that God would help this baby's brain to grow and prove them all wrong. I also sat there pondering the exact accuracy of these tests. It seemed each time someone looked they found something different. I prayed they were all wrong.
All Seems To Be Well
3 years ago
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