Our beloved son, Maksiu, is a true warrior in every sense of the word. Though he is still so young, he has already faced more battles than many adults do in a lifetime. He struggles with a severe and incurable genetic disease—cystic fibrosis—but even in the midst of pain, procedures, medications, and constant uncertainty, he teaches us every single day what strength, resilience, and the meaning of life truly are.
His story began long before his first breath. During the 26th week of pregnancy, doctors detected abnormalities in the structure of his intestines. The joy of expecting a child—something that should be a time filled with excitement and preparation—became overshadowed by fear. We traveled from specialist to specialist across the country, seeking answers we were desperate to hear. But no one could give us a diagnosis. The waiting felt endless. Every appointment brought new questions but no comfort. Every day was filled with a mixture of fear, hope, and quiet prayers for our son’s future.
Unfortunately, the day of his birth brought no relief—only the next chapter in a fight none of us were ready for.
On his very first day of life, little Maksymilian was rushed into surgery. Seven centimeters of his intestines had to be removed. At the same time, his liver was in a dire condition. While most newborns are being held in their mothers’ arms, discovering the world and bonding with their families, our son lay connected to machines, surrounded by doctors fighting to stabilize him.
His first year of life became a cycle of hospital stays, additional surgeries, and endless waiting rooms. While other babies learned to sit or crawl, we counted every small improvement as a miracle. Every day he fought for another breath, another moment, another chance. And somehow, despite everything, he always found a way to smile—a tiny spark of joy that gave us strength even in our darkest moments.
But cystic fibrosis is a relentless opponent. It affects multiple organs, causes chronic respiratory and digestive problems, and brings complications that can escalate at any moment. Because his pancreas doesn’t function properly, Maks must take digestive enzymes before every meal—for the rest of his life. Meals are not simple moments of nourishment for him; they are carefully monitored events with medication, supplements, and a specialized diet.
Each day is shaped around therapy. Inhalation sessions three times a day. Physiotherapy designed to prevent dangerous mucus buildup in his lungs. Dozens of medications. Supplements. Hospital check-ups. And the constant watchfulness that comes with knowing that at any moment, a flare-up could threaten his oxygen levels and send us rushing back to the hospital. It has only happened once—but that fear lives with us every single day.
Our life has become a continual rush between doctors, therapy sessions, and the demands of daily treatment. Yet despite everything he has been through, despite every scar and setback, something extraordinary shines in our son: he is developing normally. He is curious, eager to learn, and full of life. He loves discovering new things and sharing them with us as if each one is a triumph—which, in a way, it is. Every moment of joy he experiences, every laugh, every little victory, is a reminder of how brave and determined he truly is.
But caring for a child with cystic fibrosis is expensive. The treatment, medical care, specialized equipment, constant therapy, and tailored nutrition come at a cost far beyond our means. No matter how much we work, no matter how carefully we plan, it is impossible to keep up with the financial demands alone. And yet, we cannot allow money to stand between our son and a healthier future.
That is why we are asking for help—not because it is easy, but because we cannot fight this battle without support. Every contribution, no matter how small, brings us closer to giving our son the life he deserves. Every donation helps us cover therapy sessions, medications, equipment, specialist visits, and nutritional needs essential to keeping him strong.
Our little boy, despite his struggles, remains full of light. He smiles easily, learns eagerly, and approaches life with a sense of wonder that inspires us daily. He is our hero—a child who faces hardship with courage, who shows us what resilience looks like, and who reminds us that even in the face of an incurable illness, joy can still shine.
Please, from the bottom of our hearts, we ask you to stand with us in this fight. Your support gives us hope—a hope that tomorrow will be brighter, healthier, and more secure for our precious son.
Thank you for believing in him.
Thank you for helping us keep him strong.
Thank you for giving our warrior a chance at a better future.
—Maksymilian’s parents