ST.Help Us Save Oliś: A Little Boy’s Fight Against Neuroblastoma
We have received confirmation that shattered our world—and at the same time brought a painful kind of clarity: Oliś has neuroblastoma. The word itself feels unbearably heavy, frightening, almost impossible to say out loud. We are devastated and terrified of what lies ahead, yet strangely relieved that the uncertainty is over. Now we finally know what we are fighting. And now, more than ever, we need support to save our little son.

Oliver has been diagnosed with a malignant tumor. Even writing those words feels unreal. No parent is ever prepared for a moment like this. Just when we thought things could not possibly get worse, doctors raised suspicions of metastases—to his bones, bone marrow, and even his left lung. Each new possibility felt like another blow, another reminder of how cruel and relentless this disease can be.
It all began so quietly that we never imagined where it would lead. Oliver complained of a stomach ache. He had always been a healthy child—rarely sick, full of energy and laughter. We thought it was something minor, perhaps food poisoning, something that would pass in a day or two. But routine blood tests alarmed the doctors, and we were sent for further examinations. The ultrasound changed everything. What appeared on the screen left no room for doubt: a tumor on his adrenal gland. In that moment, fear overwhelmed us. We rushed to the hospital, praying for answers, hoping for a mistake. Instead, this was where the first serious suspicions of cancer arose, and our lives took a turn we never could have imagined.
Chemotherapy began immediately. There was no time to process what was happening, no space to breathe. One moment we were parents worried about a stomach ache; the next, we were watching our child connected to machines, fighting for his life. The treatment plan ahead of us is long and overwhelming: aggressive chemotherapy, surgical removal of the tumor, a bone marrow transplant, and finally a vaccine intended to prevent the cancer from returning.

But there is a cruel reality hidden in that final step. The vaccine that could protect our son from relapse is not reimbursed. Knowing that such a vital part of his treatment depends on money is something we struggle to accept and understand.
Seeing your own child hooked up to chemotherapy is an image that never leaves you. Oliver is in terrible pain. He is frightened by this new reality—by needles, hospital rooms, unfamiliar faces, and constant discomfort. Each short trip home feels like a small victory. Yet those moments are often painfully brief, interrupted when his results worsen and we must rush back to the ward for blood transfusions.
With every passing week, we feel that Oliś understands more than any child his age ever should. He knows the hospital has become our temporary home. He recognizes the routines, the nurses, the endless procedures. And yet, he misses his normal life deeply. He talks about his friends, about playing, about simple joys that now feel impossibly far away. He keeps asking when he can go back to them. Each time, my heart breaks because I don’t know what to say anymore.
I hear my son cry every day. The sound of his fear follows me everywhere. Every night before bed, he looks at me with eyes full of hope and uncertainty and asks the same question:
“Mommy, will everything be okay?”
And every night, I gather all the strength I have and tell him that together we will defeat this monster. I have to believe it—because he believes me.
With all my heart, I wish this nightmare would end soon. I want hospital corridors replaced by playgrounds, IV poles replaced by toys, and fear replaced by laughter. But the truth is painful: we still have a long and difficult road ahead of us.
That is why we are asking for help.
From the depths of our hearts, we ask you to stand with us. Every gesture of support brings us closer to giving Oliś the future he deserves. Our little son is fighting with all his strength. With your help, we can fight alongside him—and give him a real chance to win this battle.
Please help us save our child.
Sasha’s Journey: Choosing Hope When Giving Up Was an Option
With heavy hearts, we share a new chapter in our daughter Sasha’s battle with cancer—a chapter no family wants to write again. The insidious disease has returned, this time spreading to her skull and pressing on her brain. In an instant, all the emotions we thought we had left behind—fear, helplessness, disorientation—flooded back, more powerful and cruel than ever. Yet, amidst that darkness, Sasha stands strong. Her courage shines through in a way that fills us with both heartbreak and admiration.

Once again, we prepare to leave our familiar home, to leave behind the little normalcy we have, to seek hope at the Cleveland Clinic. Ahead of Sasha is brain surgery, followed by additional radiation and chemotherapy. Each procedure, each infusion of medication, was a step into unknown territory—a place where nothing was guaranteed, where the line between hope and fear was heartbreakingly thin. This was a battle against a disease that had tested Sasha’s body and spirit far beyond what a child should endure.
Throughout this journey, we received countless questions from friends, family, and even strangers: “What can we do to help?” Therefore, we established a support fund to alleviate the enormous financial burden of the treatment. For those who wish to bring Sasha joy, contributions can be marked as “gifts,” allowing her to choose a present—a small but meaningful gesture, reminding her that many people believe in her and are with her on this path.
Amidst all the loss and anxiety, we also witnessed miracles unfold in unexpected ways. Sasha recently began an experimental immunotherapy treatment—a method never before used in the United States for Ewing’s sarcoma. Previously, this therapy had only been tested on a tiny group of three children in Europe, all of whom achieved a complete response and are now cancer-free. If this therapy proves effective for Sasha, her hospital will partner with the drug manufacturer to open a clinical trial in the U.S.—which could offer a glimmer of hope to many other children battling the disease.
But this hope doesn’t come easily.

This therapy is one of the most grueling challenges a child can face. The receptors the drug targets are not only found on cancer cells, but are also present throughout the body’s nervous system. For five consecutive days, ten hours each day of drug infusion, every nerve in the body can experience intense pain. One child who had undergone this therapy described the feeling as if “all the teeth in my mouth were exploding at once.”
Knowing this, we sat down with Sasha and gave her a choice—a choice no child should have to face. She could refuse further treatment, choose comfort and peace. After more than three years of relentless struggle, we knew she had suffered too much. But Sasha’s answer brought tears to our eyes. She said, softly but firmly:
“I don’t care about the pain. If this can help me, please let me try.”

The first day of the infusion was a nightmare. Sasha cried in pain, whispering, “I’ve never been in this pain, Mom.” Then she told the doctor, “I can’t believe humans have to suffer like this just to live.” Those words will forever be etched in our hearts—both painful and a testament to the extraordinary awareness and courage of a child.
But on the second day, a small miracle occurred. Sasha slept more peacefully. No more pain from the infusions. No more pain from the tumor. Just a brief, precious lull in the storm. To increase the chances of success, two chemotherapy regimens tailored to the tumor’s sensitive profile were added to the treatment plan. With this combination, we continued moving forward—clinging to faith, hope, and love.
We are incredibly grateful to the doctors, nurses, and researchers at MD Anderson Cancer Center. They not only treat the disease, but also care for people. They seek hope when there seems to be no other option, and ensure that children like Sasha are not left behind. Their dedication is a miracle in its own right.
Sasha’s journey is a testament to the power of the human spirit. You are walking a harsh and exhausting path, but each day you face it with a courage that commands our utmost respect. Each infusion, each surgery, each treatment is another step toward life—fueled by the unwavering love of your family and community.
Come on, my dear.
Another day.
Another battle.
Another chance to live.
Your courage inspires us, moves us deeply. To me, and to remind everyone that even in the darkest moments, hope can still shine. Miracles—small or extraordinary—can still happen.
We ask everyone to continue standing by Sasha, sending love, prayers, and faith. Every act of support, every kind gesture means so much.
Sasha, our brave little girl—we are here.
Always.
Emma’s Light: A Little Girl Who Taught the World to Shine
In the sterile white walls of the hospital, where beeping monitors and hushed voices filled the air, a tiny girl named Emma faced challenges no child should ever have to bear. With each passing day, she endured more than most people would in a lifetime. Yet, through it all, Emma’s spirit never wavered.
Her tiny body bore the marks of countless surgeries — each one a testament to her fight for life. But her heart? Her heart remained unbroken. Even on the hardest days, when the pain became unbearable and the weight of her condition pressed down on her small shoulders, Emma found ways to smile.

Every morning, the nurses would enter her room, and Emma would greet them with a joke or a laugh, as if the pain didn’t exist. She had a way of lifting everyone around her. “I have a crown of courage,” she would say, pointing to the scars on her head. To Emma, they weren’t reminders of her struggle — they were symbols of her strength, and she wore them with pride.
Emma’s mother, who stood beside her every day, was amazed by her resilience. But there were moments when the weight of the situation became too much, and she would watch her daughter’s pain with a heart full of sorrow. And then, just when she thought she couldn’t take it anymore, Emma would look at her with those innocent eyes and ask, “We’re still shining, right?”
It was in those words that Emma’s light shone the brightest. She didn’t realize it, but her strength was a beacon for everyone who met her — from the nurses to the doctors, from her family to the other patients. Emma had a gift for turning even the darkest moments into something beautiful, simply by choosing to keep going, to keep shining, despite the odds.

One afternoon, as the soft sunlight streamed through the window, Emma asked for her favorite purple headband. “I want to look strong,” she said, her voice quiet but filled with purpose. Her mother gently placed it on her head, brushing her cheek with a soft, loving touch. Tears welled up behind her smile, but she held them back. Emma didn’t know it, but in that moment, she was already strong.

The purple headband wasn’t just a piece of fabric to Emma. It was a symbol — a symbol of everything she had overcome and everything she would continue to fight for. She wore it like a warrior, ready to face whatever came next with the same courage she had shown from the beginning.
And yet, Emma’s true strength wasn’t just in her courage or her smile. It was in the way she made everyone else feel. In the way she taught the nurses to find joy in the smallest moments, how she reminded her family that there was always hope, even in the darkest times. She made the ward brighter just by being there. Her spirit was infectious, and her fight was a quiet declaration that light could still bloom, even in the most hopeless of places.

Emma’s journey wasn’t easy, but her story is one of beauty, grace, and relentless strength. She reminded everyone who met her that courage isn’t just about fighting battles. Sometimes, it’s about choosing to smile through the pain and continuing to shine, no matter how dark the world may seem.
Today, Emma’s light continues to shine. It’s in every nurse who remembers her smile, every doctor who was inspired by her bravery, and every family who met her and learned what true strength looks like. She may not have known it, but Emma’s life, her spirit, her unwavering courage — it changed the world.

And as her mother always whispered to her: “Yes, sweetheart, we’re still shining.
Brody’s Brave Fight After a Devastating Firework Injury Threatened His Sight Forever
Yesterday began like any other day for Brody and his family, filled with the usual routines and laughter. Little did they know, a moment of celebration would soon turn into a life-altering emergency.







