At long last, Joy's rescheduled surgery rolled around. A flurry of phone calls about medications, anesthesia, her lack of English, and the time of surgery prepared us for the big day. We didn't need to be at the hospital (over an hour away) until 7:30 am but I decided to take Joy to the Ronald McDonald House the night before to make the morning easier. I was worried that she would not understand why she couldn't have anything to eat or drink. It is much easier to get up at the RM house, get dressed, and head right over to the hospital.
I was so glad I decided to go Wednesday night. As soon as we walked into the Ronald McDonald House, Joy totally got what was happening. "Joy, hospital, me?" she asked me. "Yes, Joy. Tonight we sleep here and then tomorrow we go to the hospital." Joy ate a big plate of macaroni and cheese and then we played awhile. She went to sleep and me, not so much.
Thursday morning, Bob drove over and picked us up around seven. We checked in right on time and went back to the surgery prep room. Joy is such a trooper, although you can see from the look on her face that she was a little apprehensive.
After I got woozy taking Joy into the cath lab in Boston, I definitely deferred to letting Dad accompany her into the operating room. Only one parent is allowed to wear Care*Bears. Isn't he the best Dad ever? He came back about 10 minutes later and said she went to sleep just fine.
Forty five minutes later, both doctors, (ENT and Pulmonary) came out to talk to us. The surgery turned out to be a look-see! No cutting or removals. The ENT said everything in her upper airway was perfect. The Pulmonary guy said the lower airway was not as good. Joy has bronchomalacia which is weak cartilage in her bronchial tubes. This condition is sometimes present with congenital heart disease. Because her pulmonary hypertension has already compromised her lungs, this narrowing isn't making it any easier for her body to cope.
Post surgery went fine. We spent about an hour in recovery with a popsicle and the IPAD. For some reason, we ended up telling a little bit of our story and showing pictures to most of the nurses and doctors. Some shook their heads, others asked questions. You never know when you might be given the opportunity to inspire.
Always be prepared to give an answer to everyone who asks you to give the reason for the hope that you have. But do this with gentleness and respect...1 Peter 3:15
Joy, trying to smile for the camera. She is so brave and hardly ever complains. The end result of the "look-see" is a watch and wait situation. Joy will go for another sleep study to be fitted for a CPAP machine to help keep those airways wide open at night, alleviating the stress on her heart and lungs. The good news is that some kids grow out of this condition and since Joy is the size of a three or four year old, hopefully this will hold true for her.We were released from the hospital by noontime. I was glad as there are a lot of nasty germs in the hospital right now and better for Joy to be home where she belongs!

















