Ty’s Fight: A Young Boy’s Life Marked by Shunts, Surgeries, and Unyielding Courage. Hyn
Three-year-old Ty is no ordinary preschooler. While most children his age chase toys, climb, and explore with carefree abandon, Ty’s world has been defined by hospital corridors, operating theatres, and life-saving interventions. From the moment he entered this world, his parents, Lou and his mother, have lived in a state of constant vigilance, navigating a medical journey filled with uncertainty, danger, and heartbreak.
Ty’s health struggles began with the delicate balance of his brain and central nervous system. Over the past two years, he has endured more than twenty surgeries, half of which involved the placement or revision of a
ventriculoperitoneal (VP) shunt, a device designed to drain excess cerebrospinal fluid from the brain. Ty’s first shunt was inserted just three days after his first tumor surgery. During the procedure, surgeons had accidentally breached his dura — the protective membrane surrounding the brain and spinal cord — leaving him vulnerable to life-threatening infections. The stakes could not have been higher.

The first brush with true crisis came in the form of MRSA meningitis, a severe bacterial infection that left Ty septic. He could not tolerate even the gentlest light, nor could he be touched without causing him extreme pain. For three weeks, he survived only through
total parenteral nutrition (TPN), while a continuous morphine drip managed the excruciating pain. Each day was a harrowing test for his parents, who could only watch as their child endured what no toddler should ever face.
Even after surviving the initial infection, Ty’s shunts became a source of ongoing danger. Plastic shunt tubing harbors bacteria easily, and Ty’s compromised immune system made each implant a potential threat. The family faced impossible decisions: chemotherapy could not be delayed, yet the infected shunt could not be replaced immediately. This delicate balance meant months of
constant IV antibiotics, pumps, and vigilant monitoring, as each treatment carried significant risks but was essential to keeping Ty alive.
During this time, Ty contracted fungal meningitis, an infection even more insidious than the first. The delay in shunt replacement prolonged his suffering, adding weeks of uncertainty and additional surgeries. The child’s
hydrocephalus became chronic, leaving scar tissue in the brain and ensuring lifelong dependence on shunts. Each blockage, each infection, each revision caused terrifying fluid buildups and pain that would be unbearable for anyone, let alone a three-year-old. Yet, Ty endured, showing resilience far beyond his age.
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The most recent tenth shunt revision left Ty with multiple fresh incisions and lingering respiratory challenges. His breathing is labored, his lungs congested, and nights are spent suctioning secretions to prevent complications. Despite the pain, the surgeries, and the constant fear, Ty demonstrates a quiet courage that inspires every adult around him.
Even ordinary moments, like dropping his little brother Gavin off at preschool, are bittersweet. While Gavin begins his day in a world of play and learning, Ty’s life remains intertwined with hospital routines, therapies, and the vigilant eyes of his parents. Each small breath, each response to care, is a victory in a life defined by struggle.
For Lou and his partner, the emotional toll is immense. They have learned to hold their fear in check, to remain calm in front of Ty, and to be pillars of hope when despair threatens to overwhelm. Every day, they witness milestones that would be taken for granted by other families — a movement of Ty’s hand, a cough cleared, a moment of comfort in his lap — and cling to them as proof that their child can continue to fight.

Ty’s story is one of courage, endurance, and love. It is a reminder that survival is not measured solely by life itself, but by the battles fought each day to preserve it. Despite chronic hydrocephalus, repeated infections, and countless invasive procedures, Ty’s spirit remains unbroken. Each shunt, each surgery, and each hospital stay represents both hardship and hope, a delicate balance that his family navigates with unwavering devotion.
In a world where so much seems beyond control, Ty has become a symbol of perseverance. His parents call him their hero, their fighter, their miracle. Each day spent breathing, moving, and surviving is a testament to the resilience of a child who has faced more danger than many adults could comprehend.
As Ty begins the long journey of recovery after his latest shunt revision, his family remains hopeful. They know the path ahead will be fraught with challenges, but they also know that love, vigilance, and courage can carry them through. Ty’s life is proof that even in the darkest moments, resilience shines. He may be small, but his heart, determination, and spirit are extraordinary.
Ty’s story is far from over. Each surgery, each recovery, each small triumph is part of a life that continues to inspire, teach, and move everyone who witnesses it. Against all odds, Ty remains here, fighting, surviving, and showing the world that courage is not about age or size — it is about the heart.
Krzyś’s Fight: A Mother’s Plea to Save Her Son.1749

What my 11-year-old son, Krzyś, has had to endure is almost impossible to put into words. What seemed like a simple accident—a broken leg—has turned into a fight for his very life. And today, I am reaching out, asking for help to give him the chance to survive, recover, and have the childhood every child deserves.
It all began in April 2024. Krzyś fell and fractured his fibula. Doctors recommended a cast for six weeks, and I believed he would heal quickly. At first, I tried to stay calm, thinking this was just a routine injury that many children overcome. But as the days passed, his leg began to swell more, and the pain worsened. Something did not feel right. Subsequent orthopedic visits only added to our confusion—diagnoses were inconclusive, and the anxiety inside me grew with every passing day. I watched my son struggle, unable to run, play, or even walk normally, and my heart ached with helplessness.
Finally, in August, oncological tests were performed. I hoped, against all odds, that the results would be reassuring. But the news shattered every ounce of hope I had left. My sweet, vibrant boy had malignant bone cancer—Ewing’s sarcoma. I could hardly believe it. A simple broken leg had turned into a life-threatening disease. Fear, disbelief, and helplessness engulfed me. The world I knew stopped in that moment. I could not imagine what lay ahead or how I would protect him from the pain that this disease would bring.

Krzyś began treatment at an oncology clinic in Warsaw. Chemotherapy became his new reality—a relentless, exhausting schedule that continues to this day. Each session takes a toll, but Krzyś has faced them with courage beyond his years. In January of this year, he underwent a highly complex surgery. Surgeons removed a fragment of his fibula, rotated it 180 degrees, and transplanted delicate blood vessels. Watching him go through such an invasive procedure filled me with fear, but thanks to the incredible skill of the medical team, he came through it safely. Yet this was only one step in a much longer journey. Post-surgery, he continues both chemotherapy and radiotherapy, with a long rehabilitation period still ahead.
As a single mother, I face unimaginable challenges every day. I must care for Krzyś while also looking after my other child, balancing hospital visits, medical care, and the everyday needs of our family. Krzyś cannot attend school, cannot play with friends, and his daily life is filled with hospitals, treatments, pain, and fear. Seeing him endure this at such a young age breaks my heart. He should be running around, laughing, and enjoying the carefree moments of childhood—but instead, he is fighting for his life.

Our challenges are not only medical but also financial. Krzyś needs specialized medications, frequent clinic visits, and orthopedic equipment to support his recovery. Our home must be adapted to meet his needs as a child with a disability—adjustments to the room, bathroom, stairs, and ramps are necessary for his safety and independence. The cost of everything is overwhelming, far beyond my ability to manage alone.
That is why I am reaching out for help. Every donation, no matter how small, brings Krzyś one step closer to recovery. Every act of support—whether sharing our story or offering a contribution—gives him hope, reminding him that he is not alone in this battle. Your support is not only financial; it is a lifeline, a message to my son that the world has not given up on him.
Despite everything, Krzyś continues to show incredible courage. He endures pain, discomfort, and uncertainty every day, yet he never loses his fighting spirit. I believe in him with all my heart, and I believe in the kindness of people who can help make a difference in his life. Together, we can ensure that he receives the treatment, care, and rehabilitation he needs to recover fully.

Please, do not turn away. Your help can give Krzyś the chance to walk again, to play, to laugh, and to experience a normal childhood free from the shadow of illness. From the depths of my heart, I thank everyone who has supported us so far, and I plead for your continued help. Together, we can fight for Krzyś’s life and give him the future he deserves—a life full of health, happiness, and hope.
Karolina Leonard – Krzyś’s mother


