Our son, Franek, didn’t recognize his home until two months after his birth. Those two months were not spent in the comfort of our arms or in the warmth of our home, but in the hospital, fighting for his life. Born with spina bifida and hydrocephalus, and later diagnosed with Arnold-Chiari Syndrome, Franek’s entry into the world was met with immediate challenges. His journey from birth to where we are now has been filled with heartbreak, but also immense courage, resilience, and the overwhelming love of our family.
Franek’s story began on a difficult note, with his birth leading straight into a world of medical procedures and intensive care. We were overjoyed to bring him into the world, but soon, we learned that our little boy was fighting battles from the moment he was born. For the first two months, Franek was in the hospital, unable to come home with us. During those weeks, he not only faced the complex challenges of his birth defects but also battled pneumonia, meningitis, and several other life-threatening infections. Those days were filled with fear and uncertainty, and our hearts broke every time we saw our son struggle, helpless and connected to so many machines.
We had hoped that after those terrifying first months, Franek could come home and begin his life with us. But even after the immediate danger passed, our journey didn’t get any easier. Franek’s condition meant that he would need constant care and attention, and the path ahead remained uncertain. While the doctors did everything they could to stabilize him, we were confronted with the hard truth that Franek’s life would be an ongoing battle.

By the time Franek reached six weeks old, things took another turn for the worse. He became lethargic, constantly sleepy, and would even fall asleep while feeding. It was a sign that something was terribly wrong, and once again, we rushed him to the hospital, where we learned that his condition had worsened. Tests revealed that Franek was suffering from circulatory failure, shortness of breath, and an inability to gain weight properly. This heartbreaking news meant that Franek would need emergency surgery to give him a chance at survival.
The surgery, which was critical to keeping his heart functioning, was a success, but those moments in the hospital were some of the hardest of our lives. Watching Franek, so small and fragile, hooked up to machines, unconscious, and unable to fight for himself, felt unbearable. But even in those darkest moments, we held on to hope. We knew that as long as Franek was fighting, we would fight for him too.
Despite the initial success of the surgery, Franek’s road to recovery has been anything but smooth. He still requires constant medical attention, and there are many days when it feels like progress is slow, if not nonexistent. Franek, now several months old, hasn’t reached the milestones that other children his age have. He is unable to speak, sit up on his own, or do many of the things that should come naturally. The latest MRI scans have shown that Franek may never walk, a reality that we must face as his parents.

But we are not giving up on him. Franek is our treasure, and even though our hearts ache at the thought of the struggles he faces, we know that he is capable of more than we can imagine. Our fight is far from over, and we will do everything we can to help him reach his fullest potential.
Every day, we work tirelessly with Franek, doing everything we can to help him regain even the smallest abilities. Through exercises and rehabilitation, we are hopeful that Franek will one day be able to sit up on his own, stand, and, perhaps, become a little more independent. It’s a long road ahead, and the journey is filled with setbacks, but we remain steadfast in our belief that Franek can achieve something incredible, given the right care and support.
As parents, it’s hard to accept that our son is facing so many difficulties, especially when we would do anything to give him the life he deserves. We wish we could trade places with him, to take away his suffering, and help him live the life we’ve always dreamed for him. But that’s not possible. What we can do is give him all the love, care, and support he needs, and that’s what we’ve been doing since the moment he was born.
Despite the daily challenges, we are not discouraged. Franek’s spirit and strength inspire us every day. We know that he has a long road ahead of him, and there’s still so much uncertainty about his future, but we won’t stop fighting for him. We will continue to work with doctors, therapists, and specialists to ensure that Franek has every opportunity to thrive.

But we need your help. The cost of Franek’s treatment, rehabilitation, and ongoing medical care is overwhelming. As his parents, we are doing everything we can, but the financial burden is enormous. We are reaching out to you for support. Every donation, no matter how small, will go directly toward Franek’s continued treatment and rehabilitation. Your generosity will help us provide him with the best care possible and give him the chance to live the fullest life he can.
From the bottom of our hearts, we thank you for your kindness, generosity, and support. Franek’s journey is not one we can navigate alone, and with your help, we can give him the chance he deserves to live a happy, independent life. Thank you for standing with us and our brave son as we continue this fight for his health and future.
Franciszek Sztreja, father of Franek
Józio: A Little Warrior With a Radiant Smile.2333

Józio Carter was born in 2022, a little boy whose arrival brought joy and hope to his family, despite the serious health challenges he faced from his very first days. Born at 36 weeks of pregnancy, Józio entered the world with multiple illnesses and congenital defects. While medical diagnoses painted a daunting picture, to his parents, he was — and remains — perfect. His birth marked the beginning of a long and courageous journey, one that would require immense care, unwavering love, and a resilient spirit.
From the outset, Józio faced formidable medical challenges. He was diagnosed with congenital heart disease (CHD), specifically AVSD (atrioventricular septal defect) and ASD II (atrial septal defect), alongside Trisomy 21, a genetic condition that presents its own set of complexities. These diagnoses meant that Józio would need intensive monitoring, detailed diagnostics, and specialized care from a multidisciplinary team of doctors. The road ahead would be long, challenging, and costly, but his family committed themselves fully to ensuring that he received the care he needed.

At just four weeks old, Józio underwent open-heart surgery, a critical procedure that would determine his survival. The early weeks of his life were spent in the hospital under the watchful eyes of the medical team, with his parents providing love, hope, and courage from the sidelines. Thanks to the skill and dedication of the specialists who operated on him, Józio survived the surgery and emerged with a fighting spirit that has defined his journey ever since. Today, he continues to battle daily for his health, but his radiant smile and joyful personality inspire everyone who meets him.
Despite his medical challenges, Józio’s parents describe him as perfect, unique, and a dream come true. He is a source of joy and motivation not only for them but also for his siblings, who are learning from his resilience and strength. Józio’s daily life involves frequent medical consultations, therapies, and monitoring to manage his heart condition and the effects of Trisomy 21. Each procedure, test, and therapy session is a testament to the courage of a little boy who refuses to let his diagnosis define him.
The family’s commitment to Józio’s well-being is extraordinary. His care involves multiple specialists, detailed diagnostics, and continuous rehabilitation. Every step of his treatment, while essential, brings significant financial burdens. His parents, driven by love and hope, have spared no effort to ensure that he receives the best possible care. Yet, the costs of ongoing treatment, medical consultations, and rehabilitation are substantial, and the family is reaching out to those who can help ensure that Józio continues to receive the life-saving interventions he needs.

Józio’s story is not just one of medical struggle; it is a story of joy, resilience, and the extraordinary capacity of a child to inspire love and hope. Despite the weight of his conditions, Józio’s energy, laughter, and smile illuminate the lives of everyone around him. He demonstrates daily that strength is not measured by the absence of challenges, but by the courage to face them with a heart full of determination.
Every milestone, every small victory, and every day Józio spends growing stronger is a testament to his bravery. His parents celebrate each moment — from a small improvement in his mobility to a joyful laugh or a playful interaction — knowing that these are the building blocks of his health, happiness, and future independence.
While the path ahead remains challenging, Józio’s parents are resolute. They are determined to fight alongside him every step of the way, ensuring that he has access to all necessary therapies, surgeries, and specialist care. They are asking for support to help cover the costs of his medical care and rehabilitation, emphasizing that every contribution, no matter the size, makes a meaningful difference in his life.

Józio’s journey is a powerful reminder of the courage, love, and perseverance that define the human spirit. He is a little warrior who faces extraordinary challenges with grace and strength, bringing hope and joy to all who know him. With the unwavering support of his family and compassionate individuals who choose to help, Józio can continue to thrive, overcome obstacles, and live a life filled with laughter, love, and the possibility of reaching his fullest potential.
For Józio, every day is a triumph, and every smile is a victory. With the help of those who care, this brave little boy can continue to fight for his health, grow stronger, and show the world the remarkable strength of a child’s heart.



