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The Blevins Family: A Journey of Heartbreak, Healing, and Unbreakable Love. Hyn

As the holiday season approaches, a time traditionally filled with joy and warmth, many of you have reached out to ask how you can support the Blevins family during this incredibly difficult time. I have received countless messages of love, and I want to take a moment to express how deeply I appreciate each and every one of them. This page and this community wouldn’t be what it is without you. The kindness and compassion that have been shown to the Blevins family is nothing short of remarkable, and I know it has meant the world to them.

It has been over six weeks since the devastating loss of Branson Blevins, a young boy who fought valiantly against the odds. His journey has touched the hearts of so many, and his legacy continues to live on in the hearts of those who knew him. Branson’s life was one of courage and hope, but it was also one that was marked by tremendous pain and loss. Branson was diagnosed with Acute Lymphoblastic Leukemia (ALL), a disease that no child should have to face. He fought bravely, undergoing treatment after treatment, and, for a time, he seemed to be winning the battle.

But as we all know, life does not always follow the path we hope for, and for Branson, after overcoming ALL, a new, terrifying enemy appeared: an adenovirus. This virus, which struck after Branson had undergone a bone marrow transplant in Italy, ravaged his body. His family, his doctors, and all of us who followed his story hoped and prayed for a miracle. But despite his tremendous will to live, Branson’s fight came to an end. The pain and the sorrow of his loss are beyond measure.

As we reflect on Branson’s journey, it’s impossible not to feel the depth of the loss felt by his family, especially his parents, Donald and Nichole. There are no words that can truly capture the pain of losing a child. There is no roadmap to navigate the heartache that comes with the death of someone so young, so full of promise, and so deeply loved. Donald and Nichole, along with their children Maddox and Maggie, have been forced to adjust to a new reality, one in which their beloved Branson is no longer physically with them.

While they are trying their best to adjust to this “new normal,” as many of you have asked how you can help, I want to share the most meaningful way you can support them during this season of grief. The Blevins family is asking for your prayers, your support, and your love, and they are deeply grateful for the outpouring of kindness they’ve already received. Many of you have asked how you can send cards and letters, so I wanted to make sure you have the address where you can send your messages of love and encouragement:

The Blevins Family
P.O. Box 19
Silverhill, AL 36576

This Christmas, let’s make sure the Blevins family knows they are not alone. Let’s remind them that Branson is not forgotten, that his story lives on in each of us who was touched by it. Let’s surround them with love and support, as they continue to heal from a pain that no parent should ever have to experience. Christmas is supposed to be a time of joy and togetherness, but for the Blevins family, it will be a difficult reminder of the child they lost too soon. Your cards, your letters, and your thoughts will be a small light in the midst of their darkness.

Donald, Nichole, Maddox, and Maggie are back in their home in Robertsdale, Alabama. They are doing their best to find their way through the overwhelming grief that has become their reality. As they navigate this new chapter of their lives, it’s important for them to know that they are not alone. That the love they felt for Branson continues to be shared, not only by their family and friends, but by an entire community who has rallied behind them. Let’s send them our very best this Christmas.

This year, let’s make sure the Blevins family feels the love, the compassion, and the strength of a community that refuses to forget Branson. Every note, every letter, and every message of support will help them move forward, even if just a little bit. The road ahead will not be easy, but with our love and support, they can take it one step at a time.

And while the holidays may bring pain, they can also bring healing. By remembering Branson and sharing his story, we keep his spirit alive. We honor his life by showing up for his family, by lifting them up in their time of need. Your kindness will help light the way as they struggle through the darkness of their grief.

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As you consider how to support the Blevins family, please know that it’s not just about the material gifts we give, but about the emotional support and the love that we share. The Blevins family, and especially Branson, will always hold a special place in our hearts. The pain of losing him will never be forgotten, but through our shared remembrance, we can help bring a sense of peace to those who are grieving. Let’s come together and remind the Blevins family that their pain is not theirs alone.

The Blevins family will forever appreciate the love and kindness that is being shown to them. This Christmas, let’s make sure they know that we are all with them, lifting them up in our hearts and in our prayers. And let’s remind them that Branson’s legacy of love, courage, and hope will never be forgotten.

Update on Baby Theo – October 11th: Small Steps, Big Miracles 💙🙏

Last night brought both challenges and victories for our little fighter, Theo. Around 9 p.m., he was a bit too active — wiggling and moving his head more than is safe right now, since he still has delicate

stitches that need time to heal. To protect him, the team decided to place him back on Vecuronium, a paralytic medication he’s been on before.

Because he’s paralyzed and unable to blink, the nurses carefully applied

gel to his eyes to prevent dryness. His blood pressure was elevated, which likely meant he was uncomfortable or in pain, so his team increased his morphine slightly and administered two PRNs overnight — one

morphine and one Versed — to help calm and comfort him.

But amid the hard moments came an incredible sign of hope:

✨ Theo is taking breaths on the ventilator — even while paralyzed!

That means his lungs and brain are working together in beautiful, subtle ways. The care team said that as long as he isn’t “thrashing,” this spontaneous breathing is a

very good thing.


Even More Good News 🌈

Theo’s labs looked fantastic this morning!

  • His CO₂ is at 42, which is excellent.

  • His BUN levels are improving steadily.

  • He’s still holding his own on 21% oxygen — the lowest possible setting!

Because of all these wins, the team reduced his PIP (peak inspiratory pressure) from 60 to 58

. It might sound like a tiny change, but for Theo, this is huge. He’s been on a PIP of 60 for nearly three months, so any drop means his lungs are getting stronger and more compliant.

The BPD (bronchopulmonary dysplasia) team is already thinking ahead. Once Theo recovers from surgery — likely within a week or two — they plan to transition him from pressure mode

to volume mode ventilation. This next step is better suited for long-term, chronic management in babies like Theo, and it’s a key part of helping him grow and thrive.

To make things even brighter, Theo started half feeds today, another gentle but important milestone in his recovery journey. His little body is slowly getting back to the rhythms of healing, nourishment, and strength.


Clinically Stable and So Very Loved 💛

The nurse practitioner shared encouraging words this morning:

“Theo is doing really well and is clinically stable. The only thing we’re focusing on now is managing his pain.”

For Theo’s mom, this update brought peace after a long, emotional few days.

“When I saw him after surgery yesterday, I truly felt at peace,” she shared. “He seems like a totally different baby — not just in how he looks, but in his spirit. I can feel that this is what he needed. I think he’s going to thrive.”

And we believe it, too. 💙


Gratitude and Faith ✨

From the very start, Theo’s story has been one of unshakable faith and answered prayers. Every lab improvement, every stable breath, every tiny reduction on the ventilator is a reminder that miracles often unfold slowly — one breath, one number, one night at a time.

“Thank you, Jesus, for your continued miracles for my son,” his mom wrote. “Thank you to EVERYONE who prayed yesterday and continues to pray for Theo’s recovery.”

So tonight, as Theo rests peacefully, held by the gentle rhythm of machines and surrounded by love, we celebrate these small steps that lead to great healing. His journey is far from over — but every sign points to strength, grace, and a future full of promise.

Keep praying. Keep believing.
Theo’s light is shining brighter every day.

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