The Mighty Hall of Fame honors the courage, heart, and strength of our Mighty Heroes—children who fight every day with a bravery beyond words. They inspire not only their families, but all of us, reminding the world what true resilience and hope look like. 💛🎗️
The Mighty Hall Of Fame
In May 2025, our world changed when Myles was diagnosed with neuroblastoma. What started as a normal stretch of life quickly turned into appointments, tests, and a kind of fear no parent is ever prepared for. Since that day, Myles has shown a strength we can’t even put into words—facing each step with courage, heart, and a fight that inspires everyone around him.
If you’d like to understand what led up to his diagnosis, what these months have really looked like, and how our family has been walking through this journey together, please take a moment to read Myles’ full story. Sharing it helps us raise awareness, build community, and remind other families they are not alone. 💛
Myles
Zayne
On May 15th at 8:16 PM, Zayne’s world—and his family’s—changed forever. After weeks of “viral” symptoms that wouldn’t go away (constant cough, exhaustion, bruising, leg aches, weight loss), a blood test finally gave answers… and the call no parent is ever ready for: acute leukemia. By the next day, Zayne was diagnosed with high-risk Acute Lymphoblastic Leukemia. His little body was 87% full of leukemia, and doctors said chemo had to start immediately.
Since then, Zayne—just 3 years old—has faced intense treatment, long hospital stays, scary infections, endless scans and procedures… and moments that tested his whole family in every way. But through it all, he’s still Zayne: bright, loving, sassy, quick-witted, and obsessed with monster trucks and Spider-Man—finding ways to laugh, prank his nurses, and bring joy even in the hardest season. This is only the beginning of his fight… and his story will stay with you.
Sophie
Two years ago, in February, Sophie was an energetic second grader who had just turned 8. But her parents began noticing something wasn’t right—she was suddenly exhausted after school, sleeping for hours, and growing pale with white under her eyelids. What first seemed like something minor quickly became every parent’s nightmare.
After multiple visits, long hospital waits, and extensive testing, Sophie’s family heard the words that changed everything: “Your daughter has cancer.” Soon after, Sophie had a port placed and began treatment—but her journey hasn’t been easy. She faced repeated hospital stays, complications with her port, and a terrifying emergency when chemo began damaging her pancreas. Sophie ended up in the ICU, surrounded by machines, fighting to breathe—an experience her family will never forget. After a month in the hospital, she finally went home with a feeding tube and could only take formula.
Today, Sophie is doing better and continuing treatment—still pushing forward with courage that inspires everyone around her.
Click below to read Sophie’s full story.
Adalynn
On March 31st, Addy’s family went to the ER thinking it was something simple—only to learn her hemoglobin was dangerously low (3.2). Within hours, she needed five blood transfusions, was rushed to a children’s hospital, and placed in the PICU as doctors searched for answers.
Just two days later, everything changed: Addy was diagnosed with cancer. From that moment, it was port surgery, chemo, and long hospital stays—one hard day after another.
Addy’s story is heartbreaking, powerful, and filled with more courage than any child should ever have to show.
Click to read Addy’s full story and see what makes her truly mighty.
Charles is a strong 7-year-old who was suddenly diagnosed in July 2025 with a rare cancer—bilateral Wilms tumor (cancer in both kidneys). In just six months, he’s already faced major surgery to remove one tumor while saving most of his left kidney, and he’s now in his 4th cycle of chemotherapy with the hope of shrinking what remains so doctors can remove it and save his other kidney too. With scans coming up on January 12 and results on January 14, his family is praying hard for good news. If you can take a moment to pray for Charles, it would mean more than words—and we invite you to click the link to read his full story.
Charles
Frankie
Just two days after finishing her first year of preschool, Frankie was diagnosed with Stage III Wilms tumor (May 31, 2025). Only four days later, she faced major surgery to remove a 2-pound, 15-centimeter tumor that had taken over her abdomen and caused dangerously high blood pressure and other serious complications.
In July 2025, testing revealed a more aggressive, “unfavorable” variation—meaning Frankie needed the most intensive chemo plan and an extended treatment timeline. She’s already pushed through radiation and multiple chemo cycles, with just two treatments left before she finishes this spring.
Click to read Frankie’s full story and follow her mighty fight.
Kopelyn
Kopelyn was diagnosed with cancer at just 2 years old, and since then, her little body has carried more than most adults ever should—36 lumbar procedures, 137 clinic visits, and 75 days in the hospital. She has lost the ability to walk three separate times and now often needs braces, leg bands, and a walker for extra support. Treatment has also brought weekly speech and physical therapy, seizures, and hard regressions that no child should have to face.
And in the middle of it all, she’s still a toddler—one who spends too much time away from her three siblings and doesn’t always get to simply be a 3-year-old.
Click below to read Kopelyn’s full story and help us honor her strength and the love this family carries every day.
Raul
Raul’s journey began with what seemed like simple arm pain—by that same morning, doctors found a tumor in his upper right humerus. Within days he went through extensive testing and procedures, and a few weeks later we learned it was Ewing sarcoma. In just two months, our world has completely changed: frequent hospital stays, multiple types of chemotherapy, and an upcoming bone replacement surgery planned for February/early March. To read the full story of Raul journey click below.
Baker
Baker was a typical, playful 2-year-old when a simple fall sent his family to the ER. X-rays showed only a small hairline fracture—and they were about to head home. But his family trusted their instincts and asked for bloodwork before leaving. That one request changed everything.
Within hours, Baker was rushed to Dallas Children’s Medical Center, where doctors delivered the words no parent expects: Baker had leukemia. Even though his diagnosis came suddenly, his journey required the full, standard treatment plan—13 months of frontline treatment, followed by ongoing maintenance care.
In the middle of it all, Baker welcomed a baby sister— and his family was able to save her cord blood as an extra layer of hope for the future.
Today, Baker is in maintenance and doing amazing—still growing, still smiling, still mighty.
Click to read Baker’s full story and celebrate how far he’s come.
Renesme
Renesme is a bright, fearless 4-year-old who was diagnosed with B-cell Acute Lymphoblastic Leukemia (ALL) in February, just months after her 3rd birthday. The youngest princess of a busy family of six kids, Renesme is known for her big personality, bigger laughs, and her love of all things princess, K-pop, and Zootopia—and on the pediatric floor, she’s earned a special title: “the Pediatric Floor Princess,” because she refuses to wear anything but dresses.
Her journey began after what seemed like a tough illness. Following an RSV diagnosis, Renesme didn’t bounce back—and when she became pale and couldn’t walk, her family rushed her in for help. Doctors discovered dangerously critical blood levels, and she was flown to Northwest Texas, where she spent time in the PICU receiving multiple transfusions. Although early tests pointed to a rare condition called Transient Erythroblastopenia of Childhood (TEC), her symptoms returned soon after, and new labs revealed the heartbreaking truth: B-cell leukemia. Within days, Renesme went from tests and waiting… to a confirmed diagnosis, a port placement, and her first round of chemotherapy—changing her family’s life forever.
Click to read Renesme’s full story.