Dear scared out of your mind parent,
Did you just come from the doctor’s office, fresh from the dark ultra sound room, with that cute little black and white picture in one hand? Did you look at your partner with the most broken, bleeding feeling you’ve ever experienced gushing out of you while trying to make it off the elevator, find your keys, and remember how to drive home? If that is you, welcome to Heartland, friend. You are in good company.
Hi friend, fellow parent of a tiny heart warrior. I first want you to know I am not some over zealous pro-lifer trying to perform Jedi mind tricks on you. I also want you to know that I’m not talking down to you from any moral high ground. I am a fellow mama, and that is it. I am a scarred and broken person who has buried one child the doctors told me was perfectly healthy and now raise the child a board of doctors deemed terminal at 21 weeks in utero.
I’m hoping you will read this and gain a new perspective other than what the doctors can give you on your medically tenable or inviable child. I hope you can believe that this child is more beautiful than the fear you’re filled with, and more concrete than the many impossible-to-answer questions you lay awake at night asking the ceiling and God and Google.
Do you know I would get really desperate in those midnight hours, as Sam kicked in my belly and my head swam? Do you know I used to slip out of bed and tiptoe down the stairs, open up the laptop and type in the search bar, “Is my baby going to live or die?”
Google never gave me anything good. But I can give you my story. And maybe there is some good in it (better than google, anyways.)
We are all worthy of telling our stories and having them be heard. We all need to be seen and honored in the same way that we all need to breathe. -Viola Davis
I will never forget the moment the cardiologist sat down across from us after Sam’s first echocardiogram. He drew a diagram of a human heart as we sat there listening to Sam’s big brother–not quite two–toddle around the room, bump into the exam table, open and close the drawers beneath it.
I will never forget the way he asked me questions about the medications I had taken when Samuel was conceived. I will never forget the blank, ghastly horror that climbed up my throat as I realized we were possibly the 1 in 2,000: me and Sam, the mama who takes Lithium, and the baby who has a heart defect because of it.
Samuel was diagnosed with a very complicated, severe form of Ebstein’s Anomaly along with a pulmonary artery that was not allowing blood to flow through to his lungs and a VSD. He would require a series of surgeries at the beginning of his life, and would be followed by a cardiologist indefinitely.
The next day, at my perinatologist’s office, we were given even more daunting news. My doctor’s voice cracked with the weight of her words, “Your cardiologist asked me to tell you, because time is a factor. He shared the baby’s echo with a panel of cardiologists, and they decided that your baby is, indeed, terminal. We do not expect him to be born alive, and there is a chance that when he goes into heart failure, Taylor, that you will, too.”
The room dissolved around me. Only Jack’s hand interlacing with mine tethered me to this world I could not believe was our family’s reality. My mind filled with images of another tiny, white casket, and could we bury him next to Caleb? And how will we survive this again? And how will Abraham ever be normal, with two brothers in heaven, two graves to visit, two extra birthday cakes, but no brothers to blow out the candles? I could barely see through this hurricane overtaking us.
You see, my friend, Jack and I have already lived the nightmare of leaving a child at the hospital. We have already planned a funeral, ordered an autopsy, read the results, designed a gravestone. I already live with a wound that I pray every day God will fill and heal. Since 2008, I have learned to bandage it well so it doesn’t ooze. But it is far from the faded scar I had hoped it would be by now.
My doctor continued, “So, we need to discuss your options.”
All I could think about was the hours of conversations I have had with my friends who have also lost babies. Through the outreach of the TEARS foundation, I have been blessed with these friendships that are unlike any other. We can talk to each other about things we just can’t share with our “normal” friends.
I remembered when Caleb died, I grew so angry at the many instances where people tried to console me by saying, “Well, at least he wasn’t born alive. It’s better this way; you didn’t get to know him.”
When I mustered up the courage, I asked each of my TEARS friends to weigh in on this idea. Each one of them had a baby who lived minutes, days, or months. Each of them responded with the exact same sentiment, almost verbatim. This is what they said to me,
Taylor, I think what you went through was the worst, because after carrying Caleb (we always make certain we use our children's names) for nine months and delivering him, you never got to look into his eyes, or feel his little hand close around your finger. You never knew him ALIVE this side of heaven. I did, and every moment was precious, no matter how much pain or stress I felt. Nothing can ever take that precious time away from us. We are so grateful we had it, no matter how small a window it was.
I knew whatever time God gave us with our baby would be a gift, and we would cherish it forever. We would never regret a moment.
The next 16 weeks were excruciating . . . but I felt God come close beside me.
I am not going to lie, my friend. The next sixteen weeks were excruciating. I have never clung to God and my faith in a more real and desperate way. I was scared to be alone, which was incredibly inconvenient considering Jack’s job required extensive travel. I felt a desperate need to cling to my husband. I would go in and sit on his lap, big belly and all, or lay on his office floor while he worked. If I was driving somewhere by myself I would call my cousin Sammie just to hear someone’s voice in the car with me. I became addicted to the violent show, “Criminal Minds,” and watched rerun after rerun until I passed out in bed at night.
I threw three parties that summer to find a positive way to channel my nervous energy. Abraham (2) and I spent our days gardening and playing in the back yard. I focused on the beauty of his little face, his little hand reaching for mine. I knelt by his bed and watched him sleep in his bedroom through the midnights. I prayed incessantly, cried, and begged God to give my sweet little boy this brother.
Still, I cherished every minute that Sam kicked in my belly. Every morning and every night I awoke and felt him moving, I praised the Lord. As he grew, his prognosis brightened, and we learned that doctors must give an opinion on the viability of your unborn baby before the state’s limit for a medical abortion. In Samuel’s case, his heart looked significantly different by the 25th week when we underwent his next echocardiogram. 25 weeks is 1 week past the legal limit for medical abortions in Washington state.
We didn’t know if Sam would be born alive, even while I was delivering him. I will never forget being wheeled into a new room with a full view of Mt. Rainier. Samuel was born on a bright-blue-sky day in Seattle, the kind of day we hold our breath in anticipation for during the 10 months of clouds and misty rain. The mountain shone against the cloudless sky, and I felt God come close beside me through my hours of waiting in labor. Every time I didn’t know how I would possibly handle one more minute of suspense, my heart was tended to. I felt God’s presence all around me, in every step. He never left my side.
But we have capitalized on every moment we’ve had with Sam. We have made a lot of NOW choices for our family. We have taken trips instead of paying down debt, we have camped instead of doing yard work, we have snuggled on the couch instead of doing housework. We have filled the boys’ childhoods with ferry boat trips, days out with Thomas, and cousin camps.
We have lived TODAY, trusting God to worry about tomorrow. And you know what? We have lived a beautiful life, in spite of--but maybe because of--Samuel's special heart.
Sam is now entering the third grade. We have made it so much further than we ever thought we would. I choose every day what matters most, what I want my legacy to be, with a deep understanding that my time on this earth and with my kids is limited. And, I know now that there is no end to God’s love and faithfulness, that when I cannot go on for one more minute, He will carry me. And, my friend, He Will Carry You.
Keep this baby for your heart, Mama. Keep this baby because you will never regret the pain and heartache you pour into fighting for your child. You will treasure the minutes or hours or months or years God gives you to carry, love, and fight for this gift. Nothing will cost you more, and nothing will heap more blessings upon you. You will live a deeper life, a richer life, because of this child. You will learn to let go of so much that doesn’t matter and live in wonder at the good and real things of this life that you will carry with you into eternity.
God becomes real to the mother living in her child’s hospital room. He holds her hand; He comforts her. He dries her tears, and brings angels to minister to her breaking heart. He upholds her.
You can do this. YOU CAN DO THIS.
Be strong and courageous; do not be frightened or dismayed, for the Lord your God is with you wherever you go. Joshua 1:9
Here is a peak into our journey with Sam. I hope it prepares, encourages, and emboldens you for your own journey.
God bless you and your beautiful, perfect child.
My love and prayers go with you,
Taylor