Colton’s Crusaders

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🎗️ CureFest 2026 🎗️CureFest displayed an 800-foot Tribute Wall filled with more than 6,000 pictures of childhood cancer ...
09/21/2026

🎗️ CureFest 2026 🎗️

CureFest displayed an 800-foot Tribute Wall filled with more than 6,000 pictures of childhood cancer fighters, survivors, and angels. These are just the ones who submitted photos, there should be so many more up there which is even more heartbreaking 💔

One of those faces is our Colton. I still can’t believe this is my reality. I can’t believe MY son is gone and a face on the Angel memorial 🥺

More than 6,000 pictures.
More than 6,000 precious faces.
More than 6,000 children with names, families, dreams, and stories.

CureFest is more than an event. It is where childhood cancer families from across the country gather in Washington, D.C., united as one voice—to honor the children still fighting, celebrate the survivors, remember the children who should still be here, and demand better research, safer treatments, and real change.

This year, 1,800 pairs of empty shoes were displayed on the National Mall, honoring children who died from cancer. Eighteen hundred pairs of shoes that will never again run through the house, step onto a ball field, or walk into another first day of school. (curefestusa.org⁠)

Colton’s shoes were not part of the shoe memorial, but his beautiful picture was proudly displayed on that wall. Seeing his face among thousands of other children is both heartbreaking and powerful. It is a reminder of how many families have been forever changed by childhood cancer—and how urgently our children need us to keep fighting. One day I hope to take his Gold shoes, once filled with his life, running and dancing, there on that field.

In 2026 alone, approximately 9,680 children under the age of 15 will be diagnosed with cancer in the United States. Behind every number is a child. A name. A family. A future forever changed. (cancer.org⁠)

Colton was more than a number or a picture on a wall. He was my son. My baby boy. A brother. A grandson. A nephew. A friend. A beautiful, brave little boy who fought High-Risk Neuroblastoma with everything he had. His life mattered, his story matters, and I will continue speaking his name and fighting in his memory.

CureFest represents hope—but it also represents urgency. Children are still being diagnosed. Families are still hearing the words no parent should ever hear. Parents are still leaving hospitals without their children.

We will keep showing up.
We will keep saying their names.
We will keep demanding better.
And we will not stop until no child dies from cancer.

For Colton. For every fighter, survivor, sibling, and angel. They are not just numbers or pictures on a wall. They are our children. One day is could be your child 💛

Huge thank you to Lilian McGrath who was kind enough to take and send me a picture of Colton on the Angel wall. Another heartbroken grieving mother who lost her baby, Bryson, to this awful disease too! There are just too many of us who are now connected by this devastating fate of our babies 🙏

Colton's Crusaders Kickoff Party was a hit!!! Thank you so everyone who was able to make it out! Thank you so much to To...
09/12/2026

Colton's Crusaders Kickoff Party was a hit!!! Thank you so everyone who was able to make it out! Thank you so much to Tony Suttles Shaunn Shearer and SO MANY MORE!! Y’all have outdone yourselves once again!

Big thanks to Shades of Gray Music and Charlie Farley for taking your time to come raise awareness for these amazing kiddos!! 🙏 It’s truly takes a village! It takes everyone! As you see people near and far coming together for these kids, it’s a beautiful thing! 💛

Another year pulling up to Kms Speedway and AGAIN I captured almost the same exact picture of the Heavens shinning down on this little dirt track in the middle of Oklahoma 💛 I imagine Colton and all the other kiddos who are up there looking down on all of this, healthy and dancing up there in Heaven 😇 The signs from them are all around us! There was a little boy about Colton’s age riding his exact same bike he road on! That’s how I imagine him in Heaven, just above us last night, riding around, dancing, laughing and singing 🥹

As sad as childhood cancer is, times like these we get to celebrate, fellowship, laugh, dance and sing to honor them! Their fight is unimaginable! Coming together like this helps raise awareness, which helps with funding for a cure and to help theses kids and families whose lives are devastated by childhood cancer🎗️

Thank you to EVERYONE!!! We feel your love and support! It’s all of you who make a difference. Thank you from the bottom of my mama heart 🙏❤️

NOW TIME FOR THE 3rd Annual 'Fight Like A Kid Race' Honoring Colton White TONIGHT!! 🏁 We hope to see y’all there tonight!! Please make sure you come to say hi! I’d love to hug your necks and thank you for being here with us 🫶

How can this be 6 years ago?! I had a completely healthy, chunky and feisty little boy… or so we thought… just a little ...
09/09/2026

How can this be 6 years ago?! I had a completely healthy, chunky and feisty little boy… or so we thought… just a little over one year later Colton would be diagnosed with Stage 4 High Risk Neuroblastoma 😭

What were his symptoms that were completely dismissed by his doctors?!

⚠️ Low Energy - Dismissed as being “active/tired”

⚠️ Leg pains/ Not wanting to walk - Dismissed as “growing pains” - WHICH IS ONE OF THE BIGGEST SYMPTOMS OF CHILDHOOD CANCER!!

⚠️ Bruising- He’s just in a home full of boys and is just a little boy - IT WAS THE CANCER CAUSING ANEMIA

⚠️ Anemia- After a month of back and forth, I demanded blood work done! They told me he came back anemic and to give him iron for 3 months!! WHICH IS ANOTHER ONE OF THE BIGGEST SYMPTOMS OF CHILDHOOD CANCER!!

At this point, my mama heart just knew something was VERY wrong! I took him to Children’s that week and within minutes they felt his stomach and told me he had a HUGE mass (they could feel it by hand!) in his stomach. Within 24 hours we had the confirmation Colton had cancer in his little body from head to toe!! A 12cm mass in his stomach!! The leg pains were cancer growing and breaking the bones in his little legs!! 😩

How could this happen?! How could this have been missed? How did I not know sooner? What could I have done more? What could the doctors have done? These are questions that will forever be part of my “what ifs”…

All I can do now is pass along our story and experience to raise awareness for the next undeserving child and family🎗️

09/06/2026

Hope everyone is having a great Saturday evening on this holiday weekend!! I said I was going to post Colton everyday for September Cancer Awareness Month so here is another awesome video of just how funny Colton really was!! He was hilarious. He loved life. He wanted to be a rapper lol. I haven’t seen a lot of these videos since his passing but I want to share them with everyone. It’s like reliving his loss everyday and it’s hard but he deserves to be shared and rendered! 🥹

Colton was not just a cancer statistic. He was my baby. He was a little brother. He was a grandson. He was a nephew. He was a boyfriend to his Kylie. He was a best friend. As hard it is for you to see the videos of a little boy who died from cancer, it’s harder for those who loved him and got to experience this vibrant funny little boy!! How lucky were we?! That’s why we will ALWAYS GO GOLD 💛 We miss you so much Colty. You were the BEST!!

09/04/2026

Let’s call it “In My Feelings Friday” today cause that’s exactly where I am today. I’ve been crying all morning, I just miss my sweet baby SO MUCH!! It physically hurts on days like today. As hard as those hospital days and night were, I’d give anything to be right back in that little hospital bed cuddled up with my baby. We always had so much fun, even in such a sh*tty situation. Colton was so funny and so full of life but now he’s just gone and all I have are these videos and pictures, which is not enough! 😩

Childhood Cancer is the worst!! God, there has to be a cure!! No mama should have to watch her baby suffer for years trying to just live! Then not make it through it all! I’ll never understand. It’s so unfair. Colton deserves to live! These kids deserve a cure!! That’s why we GO GOLD!! That’s why we continue to raise awareness and fight! God, I miss you Colton!! Days like today, they just seem unbearable because I can’t have you back here with me 😔😭💔

09/03/2026

I wanted to share something sweet today. This is one of my favorite little videos of sweet Colty signing with his music therapist during one of our long hospital stays 🥰 The therapists and nurses hold such a special place in my heart. I don’t know that I could work and see what they have to see every day but I am extremely grateful they do 🙏 They make a huge difference for the kids going through the hardest times. Colton loved music ❤️ I miss his sweet little voice so much 😭

🎗️ CHILDHOOD CANCER FACTChildhood cancer is not just one disease. There are more than a dozen major types of childhood c...
09/02/2026

🎗️ CHILDHOOD CANCER FACT

Childhood cancer is not just one disease. There are more than a dozen major types of childhood cancer and over 100 different subtypes—each with its own challenges, treatments, and outcomes.

💛 For Colton, it was High-Risk Neuroblastoma.

Neuroblastoma is a cancer that develops from immature nerve cells and most often affects babies and young children. High-risk neuroblastoma can be especially aggressive and often requires an intense combination of treatments.

Behind every childhood cancer statistic is a child. A name. A family. A story.

For us, that name is Colton 💛🎗️

We will keep saying his name, sharing his story, and GOING GOLD until every child has a better chance.

I made a couple more frame options!! Let’s GO GOLD for our Golden boy Colton 💛👑
09/01/2026

I made a couple more frame options!! Let’s GO GOLD for our Golden boy Colton 💛👑

September 1 — Childhood Cancer Awareness Month 🎗️Just three short years ago, this was my reality… I remember writing the...
09/01/2026

September 1 — Childhood Cancer Awareness Month 🎗️

Just three short years ago, this was my reality…

I remember writing these words from the PICU, scared and heartbroken, still hoping that somehow this was just another hurdle we would get through. What I didn’t fully understand at the time was that this day would change everything.

Colton had just completed another round of immunotherapy. We went into every treatment knowing there could be side effects, but hoping the treatment that was supposed to fight the cancer would give us more time and more hope.

Instead, his little body was telling us it couldn’t take anymore. His heart had suffered severe damage. His ejection fraction had dropped to 30%. Suddenly he was surrounded by tubes and wires again—an NG tube, a catheter, monitors everywhere—and the little boy who had already endured more than anyone ever should was exhausted.

And then came the realization we never wanted to face, the treatment meant to save him had become too harsh for his little body to survive. He could no longer continue the immunotherapy.

Looking back three years later, those words hurt so bad. We had no idea where the road ahead would take us. We only knew we wanted to get our Colton healthy enough to come home and be with his family.

This is why September matters so deeply to me and so many other going through this same reality. Childhood cancer awareness isn’t just about wearing gold. It’s about children like Colton who endure treatments so toxic that sometimes their bodies simply cannot take another dose. It’s about parents sitting beside hospital beds trying to understand impossible choices. It’s about desperately needing treatments designed specifically for children—treatments that can save their lives without destroying their little bodies in the process.

For the next month, and through the year, I’m going to share facts, memories and pieces of Colton’s story. Some will be difficult. Some will be beautiful. But all of them matter. Colton wasn’t just a statistic, he was my baby! And he still is 💛

This September, we GO GOLD for Colton.
We GO GOLD for every child still fighting.
We GO GOLD for every child we carry in our hearts 🎗️

Please help us wish a very special little girl, Kehlani, a very Happy 4th Birthday!! 🎉 We’ve been following her since he...
08/31/2026

Please help us wish a very special little girl, Kehlani, a very Happy 4th Birthday!! 🎉 We’ve been following her since her diagnosis. She was actually one of our first to receive a Colty Box! We were supposed to meet last year at the Colton race but of course, cancer got in the way!! This year for her birthday, her and her mom, Julie Carrier are getting treatment for her in New York at MSK. Not the place they want to be celebrating, away from family. I will post her Amazon wishlist and where to donate directly. Let’s show her some BIRTHDAY love from whenever you are!! 💖🎉 We love you Kehlani 🫶

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Hot Springs, AR

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