SG. At Just Seven Years Old, Dyson Is Learning How Cruel Cancer Can Be — Not Only Through the Disease Itself, but Through the Very Treatments Meant to Save His Life
At just seven years old, my buddy Dyson is learning lessons no child should ever have to face. He is learning how fragile life can be, how quickly everything can change, and how cruel cancer can be — not only through the disease itself, but through the very treatments meant to save him.
Last fall, Dyson was diagnosed with Pre B-Cell Acute Lymphoblastic Leukemia. In a single moment, childhood as he knew it was replaced by something far heavier. The carefree rhythm of school days, playtime, and family routines vanished, replaced by hospital corridors, medical charts, IV poles, and whispered prayers. His family’s world was turned upside down, and nothing has felt normal since.
From that point on, life revolved around treatment schedules, blood counts, scans, and the constant wait for answers. Every appointment came with hope — and fear. Hope that the chemotherapy was working. Fear of what it might take from him in the process.

For a moment, it seemed like the nightmare was easing. Dyson reached remission, a word that brought cautious relief and the smallest chance to breathe again. But cancer’s cruelty was not finished with him yet.
Then came the family’s greatest fear — the one no parent ever wants to face.
Dyson suffered a rare and life-threatening reaction to chemotherapy. The very medicine designed to save his life suddenly became a threat to it. What should have been another step toward healing turned into a medical emergency. Dyson was rushed back to a hospital in San Antonio, Texas, where doctors fought to stabilize him as his parents followed behind, terrified of what they might lose.

He was admitted to the Pediatric Intensive Care Unit, where he would spend 18 long, terrifying days. Days blurred into nights as machines hummed constantly, alarms sounded without warning, and his family watched every breath, every movement, afraid that any moment could be the one that changed everything. There was no rest, only waiting — and hoping.
During that time, doctors were brutally honest with Dyson’s parents. Chemotherapy can save a child one moment and endanger them the next. Even when everything seems to be going right, things can change in an instant. There are no guarantees. That truth settled heavily into their hearts, and it has never left.
Today, Dyson is home again. He is surrounded by the familiar comforts of family, his own bed, and the small joys that make a house feel safe. But the journey is far from over. Another intense phase of treatment lies ahead — one that will once again pull him away from home for weeks at a time. Beyond that, years of ongoing therapy still stretch into the future, an exhausting road no child should have to walk.

Despite everything, Dyson continues to show a resilience that humbles everyone around him. He keeps smiling. He laughs when he can. His faith remains steady, even when the days are hard. But beneath those brave moments, the fear is real. It lingers quietly, even in moments of hope.
Dyson’s Aunt Debbie reached out to share her family’s message with other parents walking this same road. It is a warning born from experience and terror: trust your instincts. Speak up. Never ignore sudden changes during treatment. They listened to that inner voice — and it saved Dyson’s life.
Their message is not about fear, but about vigilance. About advocating for your child when something doesn’t feel right. About knowing that you are your child’s strongest voice, especially in moments when seconds matter.
For families like Dyson’s, every day now carries both gratitude and uncertainty. Gratitude that he is still here. Uncertainty about what tomorrow may bring. Yet they continue forward, one step at a time, fueled by love, faith, and the fierce determination to see Dyson grow up.
If you are a parent who has walked this path — or one who is listening closely now — what would you tell a family heading back into treatment after a scare like this?