The anticipation and joy we felt as we prepared for the arrival of our daughter Gabrysia were abruptly interrupted by an unforeseen event just two weeks prior to her due date. Everything had been progressing well; there were no indications of complications, and the doctors assured us that the pregnancy was on track. We were excitedly getting ready to welcome our little girl, but during a routine check-up, the gynecologist identified a troubling issue.
The doctor’s concern prompted immediate testing, and the results were devastating: Gabrysia was diagnosed with duodenal atresia, a rare condition where a section of the intestine is blocked, hindering food passage. We were heartbroken, bewildered, and filled with dread. How could such a serious issue arise so suddenly? It was a shocking blow, and we spent the following days in fear, uncertain of what lay ahead.
On June 23, 2025, our daughter, Gabrysia, entered the world—a precious gift, especially for me, as it was Father’s Day. However, the joy of that day quickly turned into anxiety as she was taken for surgery the very next day. Gabrysia’s condition was critical, marking the start of a long and arduous journey. She spent the next six weeks in the Intensive Care Unit, and it was heart-wrenching to witness her struggle while we couldn’t be by her side for all of it.
As if this wasn’t enough, Gabrysia’s journey took another unexpected twist when, after weeks of examinations, doctors identified a heart defect. Our little girl was not only facing duodenal atresia but also a serious condition that required immediate action. How could she endure so much at such a tender age? Why did she have to suffer so much pain so early in her life?
It wasn’t until August 21, 2025, that we could finally bring Gabrysia home, but our relief was short-lived. Just a month later, she needed yet another procedure—this time, to implant a pacemaker to address the heart defect. Our hearts shattered watching her endure so much, knowing she was still so delicate and unable to enjoy the typical joys of infancy.
Gabrysia’s condition, while showing signs of improvement, still presents numerous challenges. Her extended hospital stay and multiple surgeries have significantly impacted her development. Gabrysia now has low muscle tone, which prevents her from lifting her head independently. She still relies on a feeding tube due to her duodenal issues, and doctors have confirmed a chromosomal abnormality that requires further genetic testing. Each day is a battle for her, and for us as her parents, it is a constant source of concern.
However, we refuse to lose hope for Gabrysia. We are committed to exploring every possible avenue to support her—whether through ongoing treatments, specialized medical care, or intensive rehabilitation. We understand this is her only chance to grow, develop, and lead a fulfilling life. Our love for her drives us forward, but we need more than just our strength. Gabrysia requires the assistance of specialists, treatments, and therapies to enhance her chances of overcoming these obstacles.
Regrettably, these ongoing medical needs come with staggering costs. From her surgeries to her continuous care, rehabilitation, and specialized equipment, the expenses are accumulating daily. As parents, we are doing everything within our power to ensure she receives the care she deserves, but we cannot do it alone.
Today, we reach out to you, our community, for assistance. Every contribution, no matter how small, can significantly impact Gabrysia’s fight for a brighter future. Your support will help cover the costs of her medical care, rehabilitation, and the resources she needs to continue her development. We cannot do this alone, but with your help, we believe Gabrysia can have the opportunity to thrive.
Gabrysia deserves to run, play, and experience the world around her without limitations. Please, join us in this battle. Your kindness and generosity can help provide her with a future full of possibilities. Thank you for standing with us and for Gabrysia during this incredibly challenging time.
Every bit of support matters, and together, we can help give Gabrysia the chance she so desperately needs.
