Sunday, June 17, 2012
Hypoplastic Left Heart Syndrome- A Post I Never wanted to write
My fourth ultrasound. Our last child. It was going to be a breeze. I had planned to celebrate that night with a fun family dinner, followed by a pink cake or a blue one.
The tech glided along with her running commentary of what we were looking at. See the baby's little fingers? Here's the stomach, the spine, the brain, little feet, legs. It looks like a boy! Yay! A boy! Just what we were hoping for...quickly she was back to the heart. Why is she back at the heart again? She has spent a lot of time there. I watched the fast thump, thump thump on the screen.
I looked nervously at Scott. Did he notice how much time she was spending looking at the baby's heart? He didn't seem to notice. The tech kept the same calm expression.
"There's just one thing I want the doctor to look at..."
And then another doctor.
"It looks like Hypoplastic Left Heart Syndrome".
Pardon? I heard the doctor say heart and syndrome. Heart and syndrome.
"It means, the left side of your baby's heart is small and underdeveloped. The left side of your baby's heart will continue to deteriorate and have no function."
A few weeks later, the pediatric cardiologist at Primary Children's made sure we knew how serious this diagnosis is. His face showed it. The room he brought us to. The cozy couch. The lamp. The box of tissues. Two women followed us into the room.
"It's not the most rare heart defect, but it is among the most serious and complex." What was I listening to? I tried hard to concentrate on his words, the diagrams he was showing us.
"This is a normal heart"
I've seen enough pictures of a normal heart to last me for a while.
He told us we had a choice to make. We could choose to do nothing. Take our baby home. The valve currently connecting the left side and right of the heart would take a few days to close after birth. Our baby would die.
Our other choice was hard too. Heart surgery. A minimum of 3. One when he is a few days old. One when he is 4-6 months old. One when he is about 3. The heart can't be fixed, just re-plumbed. He would live his life with half a heart, acting for both sides. No one knows how long a heart can sustain life this way. They haven't been doing it long enough. Not a lifetime. It is a hard road, with lots of risks and possible complications. Expect them.
I held it together for as long as I could. He was talking about my baby. He fumbled to hand me the box of tissues.
I went home and looked at my 3 beautiful children. Their healthy bodies have become an unbelievable miracle that I had been taking for granted. Everything works.
My brain cannot quite process the thought of one of my children enduring such a thing. Including this newest little boy, whom I love with such fierceness.
We have to try. I have to trust in the Lord.
I am unbelievably scared. Every day I have to make an effort to not get overwhelmed. There are so many unanswered questions.
One thing I am sure of is that he was always meant to be part of our family. We will love him forever. We hope and pray that we get to do that here on earth. For a long, long time.
Thump, thump, thump.