Miracles For Our Bébé

Miracles For Our Bébé Prayers and Updates for Baby of Zach and Kayle Lucas

& We Made It, TogetherWe’re finally out of the hospital.I’ve said it. I’ve written it. I’ve whispered it to myself in th...
11/10/2025

& We Made It, Together
We’re finally out of the hospital.
I’ve said it. I’ve written it. I’ve whispered it to myself in the quiet—but it still doesn’t feel real. After months of living in a place where time stood still, where every breath felt borrowed, we’re out. We’re home. We’re together.
I had to leave Olen so many times. And there were stretches where I didn’t leave the hospital at all. My body stayed in one place, but my heart was constantly torn—racing between children’s hospital and the few precious hours I had with Olen. We were scattered. Fragmented. Trying to hold on to each other through the chaos and the ache.
There were days I stood in the hallway and let my dreams quietly shatter. I had imagined us outside those walls, laughing, traveling, just being. I wanted so badly to believe we’d get there. But I was afraid to hope too much. One foot in the dream, one foot in the real. Would we ever take a trip together? Would we laugh freely again? Would we ever stand somewhere—anywhere—outside a hospital, all of us, whole?
And now we have. We did.
But it wasn’t simple. It wasn’t clean. It was survival. It was trauma. It was sobbing in waiting rooms and conference rooms, screaming at God driving and throughout the hospital, collapsing into myself while somehow still standing. I was out of my body and inside everything all at once—every monitor, every update, every decision. How do you describe a mama so terrified of losing her baby that her soul feels like it’s unraveling? I had no control. No control over what was happening to Teaks. No control over not being able to hold both Teaks and Olen at the same time. No control when Teaks couldn’t be held at all.
And I had no control the days Teaks died. Twice. His heart stopped. Two separate codes, each running over 45 minutes. I still don’t know how to carry that. I still don’t know how to hold the truth of it. That my baby’s body was lifeless. That teams of people fought with everything they had to bring him back. That I was helpless watching the world collapse around me.
But I know this: he saw heaven. I believe that with everything in me. I believe he got a glimpse of glory—of peace, of light, of love. And I believe a crowd of angels surrounded him and said, “You have to go back. They still need you.” And somehow, he did. Twice. And I know heaven is hard to come back from. But he did. And I thank God with every breath I take. For the miracle. For the mercy. For the joy in his eyes and the life in his laugh. For the chance to keep loving him here.
The trauma doesn’t vanish just because we made it out. It’s woven into us now. It lives in the way I flinch at certain sounds. In the way I scan my children’s faces for signs of something wrong. In the way I hold them tighter, kiss them more, whisper prayers over their heads while they sleep.
This trip wasn’t just a vacation. It was a resurrection. A moment that said: we lived. We made it. We’re not just surviving—we’re together. These photos aren’t just beach pictures. They’re proof. Proof that both our children are alive. Healthy. Laughing. Loving us. That we’re not standing on the edge of goodbye anymore.
I look at these photos and I cry. Deep, aching cries. Because I remember what it cost to get here. I remember the nights I didn’t sleep. The prayers I yelled and whispered through my tears. The fear that sat in my chest like a stone. And I remember the grace. The miracles. The love that held us up when we couldn’t stand.
And the people—our people. We learned who really sees us. Who really cares. Who shows up when everything is falling apart. Some people surprised us with their presence. Some surprised us with their absence. But the ones who stayed—who carried us then and still carry us now—you are the reason we’re standing. You are the reason we didn’t fall apart completely. You held us in hospital rooms, in text messages and calls, in the quiet moments when we didn’t even have words. You still do. And we still need you.
Even strangers became part of our story. People who recognize us now and say, “We prayed for you.” People who cry when they see Teaks in my arms. People who followed our journey from afar and carried us in prayer when we couldn’t carry ourselves. That kind of love is holy. That kind of support is why we’re still standing.
And the medical staff—our warriors, our angels, our family. You let us love through wires and codes and machines. You kept Teaks on his healing road. You fought harder when it didn’t look good. You love him like he is yours. You loved us like we mattered. And you do. You matter so much. We love you. You are forever part of our family. You didn’t just do your jobs—you carried our hearts. You fought beside us. You stayed when it was hard. You made space for our love to live in the middle of the fight. We will never forget it.
Prayer is why he’s here. Why we’re here. Why we’re able to breathe and laugh and cry and keep going. We wouldn’t be here without it. I believe that with everything in me.
We weep for the families who didn’t get this chapter. We carry them in our hearts. And we hold our babies tighter. We kiss them again and again.
We made it. But we’re still making it. Every day.
And I’m thankful. For every breath. Every laugh. Every step forward. This is a God story. A story of survival, of grace, of love that refuses to give up.
We’re here. And we’re not done.
There’s so much more to say—so many life updates to share. I’ll start speaking about those soon. But for now, just know: we’re still here, still healing, still held. And we’re so grateful.

Thank you to Tallie McLean Photography for capturing our story, just free and wild and playing on the beach.

Dr. Dabal (Teaks heart surgeon) was up early ready to go see his patients and get consents! Got his Spider-Man compressi...
10/31/2025

Dr. Dabal (Teaks heart surgeon) was up early ready to go see his patients and get consents! Got his Spider-Man compression socks on and his gray pull over jacket for this cold day! He also checked on Teaks this morning. ❤️His hair is sticking straight up as Dr. Dabal’s did once!
Happy Halloween! Happy Halloween to our Children's of Alabama family the OR, the CVICU, the CCU, to the multidisciplinary group of pediatric cardiologists, cardiothoracic surgeons, intensivists, nurses, Interventional Cardiac Team, Electrophysiology team, the Cardiac MRI/CTA, Heart Failure/Transplant, Fetal Cardiology, Pediatric Cardiovascular Anesthesia, and other specialists who provide comprehensive care for children with heart conditions! Happy Halloween to all our heart families, all the warriors! You are loved! ❤️

What an honor to want to be someone so inspiring. “I’m a doctor mama.”

Where pumpkins wait to be chosen, I always choose my boys — heart wild beneath October skies, overflowing with love
10/15/2025

Where pumpkins wait to be chosen, I always choose my boys — heart wild beneath October skies, overflowing with love

Beautifully said. Thankful for all those up at midnight with me 🤍🤍 thankful we GET to do this ❤️, thankful for life.
10/13/2025

Beautifully said. Thankful for all those up at midnight with me 🤍🤍 thankful we GET to do this ❤️, thankful for life.

If you’re parenting a child with complex medical needs, I want you to hear this: you are not alone.

This life.

The appointments, the hospital stays, the endless coordination and constant worry

It’s a lot.

You’re doing the work of a whole team, often without pause, and it can feel like the world keeps spinning while yours stands still.

You live in a state of vigilance most people can’t imagine. Every sound from a monitor, every change in breathing, every late-night medication reminder keeps your mind on high alert. Rest doesn’t come easily when your child’s safety depends on your awareness.

And beneath the strength, there’s often a quiet grief. Not for your child, but for the life you thought you’d have. The one with fewer hospital visits and more carefree moments.

It’s okay to miss that life.

It’s okay to feel both gratitude and sadness in the same breath. You can love your child with your whole heart and still wish things were different.

There’s also the loneliness.

Friends may drift away, plans get canceled, and it can feel like no one really understands what your days look like.

You’re not imagining that.

This life is isolating. But somewhere out there are other parents awake at 3 a.m. doing tube feeds or medication schedules, feeling the same ache and the same fierce love.

And about that love. It’s something powerful.

It’s a love that pushes through exhaustion, fear, and heartbreak. It’s the kind of love that advocates, researches, and fights every single day. It’s the love that keeps your child’s world turning.

If you’re tired, if you’re grieving, if you’re hanging on by a thread, please know that doesn’t make you weak.

It makes you human.

And you’re doing an incredible job in circumstances most people couldn’t imagine.

You are seen.
You are not alone.
And your love. Quiet, steady, and relentless.

It Is changing the world for your child every single day.

💙❤️World Heart “Day”Is to be celebrated not just today but everyday. Cardiovascular disease is the leading cause of deat...
09/30/2025

💙❤️World Heart “Day”

Is to be celebrated not just today but everyday. Cardiovascular disease is the leading cause of death globally, and raising awareness about this everyday is important.

Tangible ways you can make each day heart day:
-Find healthy ways to manage stress as it significantly impacts your heart health.
-Educate Yourself and others. Stay informed about heart disease and share your knowledge!
-Encourage or bless a heart family/the patient!

Hypoplastic left heart syndrome (HLHS) is one of the most lethal congenital heart defects, and remains clinically challenging. While surgical palliation allows most HLHS patients to survive their critical heart disease with a single-ventricle physiology, many die, and many will suffer heart failure, requiring heart transplantation as the only therapeutic course.

Our Teaks has a diagnosis of HLHS. HLHS stands for Hypoplastic Left Heart Syndrome, which is a serious congenital heart defect where the left side of the heart is underdeveloped. It is a medical condition, NOT an identity, meaning HLHS describes his physical health problem rather than his personal characteristic or sense of self. ❤️ Yes, his diagnosis is HLHS but not WHO he is. 😉 He IS a little warrior and so much more, AND alive because of God, his fighter spirit, continued prayers, his beyond amazing medical team; because of research, medical advances, and humans who have passion and such care and beyond skills to heal and help!

Alabama has one of the nation's highest rates of heart disease-related deaths, with nearly 15,000 Alabamians dying from heart disease in 2022.

Our Teaks is a miracle, Olen is a miracle too, we are miracles and GET to live. I invite you to place your hand on your heart tonight, take an intentional breath, slowly breathe in and out, and give an intentional thanks for your life and those around you. Reflect on all the beauty and mess of it all.

Teaks is RARE.Went to genetics today. Let this sink in:So About 1 in 10,000 live births are HLHS. Only about 900-1,000 b...
09/22/2025

Teaks is RARE.

Went to genetics today. Let this sink in:

So About 1 in 10,000 live births are HLHS. Only about 900-1,000 babies born with it in a year. There about 134 million babies born each year.

🤯

Mornings with Teaks Ru!
09/20/2025

Mornings with Teaks Ru!

9/9/25 It has been a bit since I updated! Teaks Ru is improving and exploring and growing day by day! We have really bee...
09/10/2025

9/9/25
It has been a bit since I updated! Teaks Ru is improving and exploring and growing day by day! We have really been working on eating! He had been going to Childrens On Third Speech Center and seeing the wonderful speech language pathologist Lauren Watts! We are stopping speech for now until he can improve motor skills like good head control and being able to sit up on his own!

We have been looking for signs of readiness for solids. Some of these are interest in food; so opening his mouth, trying to reach for food, and making mouth movements like eating when around food. Part of readiness is also good head and neck stability and good trunk stability when supported and bringing objects to his mouth. Some of these goals we have been working on are placing a dry spoon on the tray and allowing him to bring it to his mouth, dipping the spoon in puree and allowing him to bring it to his mouth, placing puree on the tray and allowing him to feel it and bring his own hands to his mouth.

He has increase “wet chest congestion” observed when eating and it can be heard in some of these videos so offering 5-10 tastes of puree twice a day FOR NOW.

We can also offer him 15cc of thin water before having the purées in a bottle or a sippy and that goal is for his own interaction with them but he is not interested much in a sippy nor coordination being quite there YET (it will come 😊).

We honor his signs of refusal being the head turning, the pursed lips, no response to the item, him pushing away, or that strong gag response.

With him we have to watch for aspiration which does include coughing, choking, that wet chest congestion, if he had red/watery eyes, or an increased work of breathing.

I’m so proud of him. I have had some tell me “just give him food and he will eat”and it is not that simple. It is going to take time. We lived at the hospital for about 6 months including our back and forth still. It is not “just easy” for him to eat. As a mama it is so hard to watch him struggle to enjoy food. He is approaching 9 months. Early intervention is thankfully coming to our house twice a month now and we set goals and a goal that I provided is I truly want to watch him enjoy and dig in so messy to his 1st Birthday cake-please pray that with me.

I am a mama walking through one of the hardest parts of motherhood-watching my baby struggle to eat, relying on an NG tube, and longing for the simple joys that most parents take for granted. I ache to see my little boy enjoy food, to witness the delight in his eyes when he tastes something new, to celebrate messy mealtimes and favorite snacks. It is not “just missing milestones” it is missing moments that feel like they define babyhood itself.
My heart is full of love and hope, and even in the midst of the struggle, I dream of the day he can eat freely, laugh with a mouthful of food, and snuggle with a full belly. I am holding space for joy that has not quite arrived yet but I know it will.

To every mama walking this road with me: If your baby struggles to eat, if mealtimes are marked by tubes and tears instead of giggles and bites please know this: you are not alone.
I can tell you, there’s a mama out there who dreams of seeing her baby taste strawberries for the first time. Another who longs for the mess of mashed potatoes on tiny fingers. Another who watches her child fight for every ounce, every swallow, and still shows up with love, patience, and fierce devotion.
You are part of a sisterhood of longing and love.
Let’s remind each other That every bite will one day be a victory.
That every messy meal will be a celebration.
That every mama who waits, hopes, and holds her baby close is doing something sacred.
If you are a mama who has come through the other side and whose baby now eats with joy, please share those moments. Tell us about the first bite, the favorite snack, the food dance. Let your story be a lighthouse for those of us still in the storm. And if you are still in it, like me, let your heart speak. Your story matters. Your hope matters. Your baby matters.
We ARE holding space for bite bites, belly laughs, and the day our baby gets to just be a baby boy/girl and loving food, loving life, and loving you right back

Bros matching for game day 🐘 Things of note-Olen’s cake pop mouth and the way Teaks smiles with Olen holding him 🥴❤️
08/31/2025

Bros matching for game day 🐘
Things of note-Olen’s cake pop mouth and the way Teaks smiles with Olen holding him 🥴❤️

When I discovered I was carrying rainbow Bebe Teaks…to loving and holding rainbow Bebe Teaks AT HOME without wires on hi...
08/27/2025

When I discovered I was carrying rainbow Bebe Teaks…to loving and holding rainbow Bebe Teaks AT HOME without wires on him or having to check if I can 🤍
The ultimate miracle is not simply an event but the manifestation of God's limitless power and eternal victory

Our family, lifesavers, beautiful humans, little fighters, home away from home, (even though you would never ask for the...
08/22/2025

Our family, lifesavers, beautiful humans, little fighters, home away from home, (even though you would never ask for the pain, joy is also very present and you do not forget the floor and stay bonded for life) no other place or better place I would want our Teaks. ♥️ Miracles happen.

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