The Next Step (3/7/17)

There’s just something really terrifying about the thought of having your pregnant belly stuck with a 10 inch needle down through your uterus and breaking into your baby’s amniotic sac.

I always swore I would never have an amniocentesis. There’s just something really terrifying about the thought of having your pregnant belly stuck with a 10 inch needle down through your uterus and breaking into your baby’s amniotic sac.  However, when we met with our OB/GYN he did recommend we go forward with it as the fetal cardiologist had suggested we do.
(If any chromosomal abnormalities do exist, such as a trisomy, doctors will not be able to go forward with open heart surgery to save Jonathan’s life. Even though we had a NIPT with negative results it is not 100% accurate and a specific defect seen in the fetal echo indicated a possibility for a trisomy. An amniocentesis is the only way to completely rule out the possibility of a trisomy before birth.  Without the amnio, a blood test would have be done after birth which means two days of waiting for results to determine if doctors can move forward with surgery.)

Danny was on board with the amniocentesis and was in fact the first person in the room to say it should be done.  Inside of my head I was furious with him. I felt like he was betraying me. He wasn’t, even though he knew how much I did not want to do it.  I was ok with the unknown. So what if we plan for surgery then once we get down to it we find out it’s not a possibility and we have to scrap it? So what? I can live with that.

My doctor explained it this way: these are two very different paths for the remainder of the pregnancy with two very different preparations for the end.

Danny needed to know which path we were headed down.   He needed to prepare.  Should he go forward with making plans to relocate closer to Children’s Hospital or did he need to prepare himself for letting go of his child?

The doctor agreed with him that we needed to know which path we were on.  I was angry with everyone and everything.  There was one thought that brought me some peace with what the results of the amnio might bring.  I could feel tears burning my eyes when I asked the doctor “if there is a chromosomal defect do I get to stay here to deliver?”
The answer: yes.

I know this is horrible but part of me is relieved at the thought that the results will come back and show that there is nothing the doctors can do.  Then I know that all I have is to pray for a miracle.  I won’t have to plan to leave my home and give birth in an unfamiliar place. I won’t have to plan childcare or spend days and weeks in a hospital, trying to pump and trying to take care of multiple children, with multiple needs, in multiple places all at the same time.

At least then I know what the end looks like. It won’t be any easier emotionally but there won’t be the roller coaster of maybe today he lives but tomorrow will he die?  Best case scenario, I deliver at my own hospital with my own doctor, then he’s born and it’s a miracle, he’s ok.

Snow Globe

Our excitement over seeing the baby quickly turned to shock and sorrow. The specialist sat down on the bench next to me with tears in her eyes and broke the news that our precious baby’s heart had not fully formed.

(Snow Globe: because sometimes your life gets shaken and turned upside down.)

Danny and I decided that “Jonathan” would be the perfect name for baby boy #4.  Actually, it was more or less the Lord who directed us to the name. Days after deciding on a name we attended our routine, mid-pregnancy anatomy scan.  Typically this is when we find out if the new baby is a boy or girl but we already knew we were having a boy from our non-invasive prenatal test (NIPT).  This screening helps to determine the baby’s risk for certain genetic/chromosomal issues as well as gender. Our screening had come back all clear.

The first thing we saw during the ultrasound was Jonathan’s little button nose that looked exactly like his brothers’ noses had looked in their ultrasounds. During the ultrasound D grew uncharacteristically quiet.  I commented on it then assumed he was having a moment. What I didn’t know was that while I could only see the ultrasound tech’s hand moving the wand over my belly, he could see her face and what he saw in her face unsettled him. Our ultrasound concluded with a specialist coming to the room to speak with us.  I thought this was odd but chalked it up to the fact that they had pre-warned me this u/s would be more in-depth due to the fact that I am 35 years old and technically considered “high-risk”

Our excitement over seeing the baby quickly turned to shock and sorrow.  The specialist sat down on the bench next to me with tears in her eyes and broke the news that our precious baby’s heart had not fully formed.  His heart only had three chambers instead of four.  His left ventricle was missing.  Then we were ushered next door for an urgent, unscheduled appointment with our OB/GYN.

My ob/gyn has been the perfect doctor for us because of his ever-present, calm and laid-back manner. It was reassuring to me for us to see him.  His calm demeanor was present as always yet, the seriousness with which he addressed us in that moment, conveyed the devastating reality of our baby’s situation. Within twenty-four hours we saw the fetal cardiology specialists at the Children’s Hospital over an hour away from our home.

The drive to the appointment felt like it took an eternity.  We spent what felt like another eternity in the waiting room. All of the staff greeted us warmly but we couldn’t muster much response back.  I kept thinking how horrible it would be to work there.  It’s not just a few families here and there you are dealing with who have difficult situations.  Every single family who walks through the door has a baby with a serious cardiac issue.

A fetal echocardiogram was performed.  Now that I knew what the medical staff were looking at, I could so clearly see the three chambered heart on the ultrasound monitor.  I couldn’t bear to watch. I squeezed my eyes shut and had no control over the hot tears that silently slipped out. We waited, then we waited some more.  A nurse finally led us to a room where we were left to sit at a table with a box of tissues. You never want to be the people who get shown to the conference room with the box of tissues.

The doctor and nurse who met with us for over two hours were truly amazing in their patience and compassion. Our baby was officially diagnosed with Hypoplastic Left Heart Syndrome (HLHS).We learned that without immediate and aggressive intervention upon birth, Jonathan can only survive hours, perhaps weeks.  Aggressive intervention would include medication immediately after birth that will keep the heart functioning the same way it functions in utero (able to pump blood to the aorta without use of the left ventricle).  The medication requires close monitoring in the NICU.  After a couple of days of adjusting to life on the “outside,” the next step would be open heart surgery (eventually followed by two more surgeries).

Based on some things seen in the echo (diagnosis of Unbalanced AVSD Right Dominant a variant of HLHS) the doctor did have concerns that Jonathan may have a chromosome abnormality even though our NIPT had not indicated it. If any other such issues do exist then it removes the option for the life-saving surgery.  Without surgery….

We left the appointment well past business hours, exhausted and overwhelmed.  Even so, I didn’t feel hopeless because my ears had heard hope. I heard about the hope of surgery, hope for survival, and hope for quality of life. It wasn’t until later that I could in retrospect process the fears and concerns I didn’t realize I’d heard. It wasn’t until then that I heard the words of what had gone unspoken.

It was a surreal week that started oriented toward a goal with a name but ended it in feelings of loss and confusion.

Facebook Announcement

Fb update 3/10/17

We typically keep our personal life relatively private from social media. However, at this time we realize we need the support and prayers of our friends and family. It has been a week since we received the life-altering news that baby boy #4, Jonathan has been diagnosed with an extremely rare and lethal heart defect. Upon birth he will need immediate and aggressive intervention to survive. This will require us to temporarily relocate (closer to Children’s Hospital) for several weeks before and after his arrival.
Each doctor we have met with has confirmed that this is not caused by something I did or didn’t do during the pregnancy. It isn’t caused by age or genetics. As one specialist put it “for lack of a better medical term it is simply ‘bad luck.'” Fortunately, we don’t believe in “luck.” We believe in God and we’re asking him for a miracle. He’s a big God and none of this is too big for him.
I am a christian so I’m not afraid of death. I am a hospice nurse so I’m not afraid of the dying process. I am a mother and my heart hurts.
We’re sorry you have to learn this here instead of from us directly. This is not easy news to relive over and over. Each time we share it we see the devastation you feel for us. It hurts and we also hate ruining your day. We know you don’t know what to say, and that’s okay. We simply ask you to pray. Pray for us, pray for our boys, pray for our precious Jonathan.