“Fighting for Oliver: A Little Boy’s Battle Against Cancer”.2286
“Fighting for Oliver: A Little Boy’s Battle Against Cancer” 💛
Every day feels like a race against time.
Every morning begins with fear.
And every night ends with prayers whispered through tears.
For months now, little Oliver — or “Oli,” as his parents lovingly call him — has been fighting a battle no child should ever face.
Cancer has stolen much of his childhood, but not his spirit.
His parents live in constant worry, waiting for the latest test results.
Two new nodules have recently appeared, and the uncertainty of what they mean is unbearable.
“Every phone call from the hospital makes our hearts stop,” his mother says. “We’re terrified of what we might hear.”
In just a few days, Oli will begin radiotherapy — a fourteen-day treatment that will once again test the limits of his small body.
Before that, he’ll have surgery to implant a Hickman catheter — a tube that will allow doctors to deliver medication directly into his bloodstream.
For most families, these words would sound foreign, belonging only to medical textbooks.
For Oli’s family, they have become part of everyday language — a vocabulary of survival.
The Fight That Never Ends
Oliver’s journey began long before these latest complications.
He has already undergone grueling chemotherapy sessions, endless scans, and painful injections that left his tiny arms covered in bruises.
The treatments were supposed to help, but they also took so much from him.
He has lost hearing in one ear — a side effect of the aggressive drugs used to save his life.
Doctors say he’ll probably need a hearing aid soon.
The chemotherapy has also weakened his bones, causing osteonecrosis — bone decay that makes it painful for him to walk.
“He used to run everywhere,” his father says quietly. “Now, some days, he can barely stand. Watching him struggle is the hardest thing I’ve ever experienced.”
To help him regain strength, Oli now works regularly with physiotherapists.
Each session is exhausting, but he never complains.
He tries, again and again, determined to walk without help.
His resilience is stronger than the pain.
A Moment of Joy
After so many months in the hospital, Oli recently got to spend a short time at home.
For the first time in weeks, he woke up in his own bed.
He played with his toys, hugged his dog, and ran his fingers along the shelves of his favorite books.
The house filled with laughter again — the kind of laughter that hospitals can never hold.
His parents watched him play, knowing that these moments were fleeting.
Because soon, they would have to return to the hospital.
“We didn’t tell him right away,” his mother admits. “We wanted him to just enjoy being home — to forget, even for a little while, what’s waiting for him.”
But the reality looms large.
The next phase of his treatment — immunotherapy — will be even more intense.
And after that comes the final, most critical stage: treatment in the United States.
It’s the only chance to ensure that the cancer doesn’t return.
But it’s not covered by insurance.
And the cost is enormous.
A Race Against Time
The family has already raised funds for the earlier stages of treatment, thanks to the generosity of strangers.
But now they are approaching the point where government funding ends.
From this moment forward, every procedure, every medicine, every day of care must be paid for out of pocket.
They’ve spent everything they had.
They’ve organized fundraisers, raffles, charity auctions — anything that might help.
But it’s not enough.
“We’re so close,” his mother says, her voice trembling. “We’ve come so far, but the hardest part is still ahead. Without financial help, the treatment will have to stop. And if it stops… we could lose him.”
Stopping is not an option.
The doctors have made it clear — every delay, every missed dose could give the disease the chance to come back stronger.
And for Oli, that could be fatal.
Strength in Small Moments
Despite everything, Oliver still smiles.
He smiles when his father carries him through the hospital halls, when his mother reads him stories before bed, when he gets to color pictures of rockets and dinosaurs.
He dreams of going to school again — of running with friends, of living a life where hospitals are just a memory.
“He asks me when he can go home for good,” his mother says. “I tell him soon — because I want to believe it myself.”
The nights are the hardest.
When the machines beep and the ward grows quiet, his parents sit by his bed, holding his hand, afraid to fall asleep.
They whisper to each other, reminding themselves that they have to stay strong — for him.
And somehow, through the exhaustion and the fear, they find strength in the smallest things: a smile, a stable test result, a day without pain.
Hope Lives Here
The doctors are optimistic — but time is running out.
Oliver’s radiotherapy will begin in days, followed by immunotherapy and then the U.S. treatment plan that could finally end this nightmare.
But the bills are already piling up, and the next phase — the most crucial one — isn’t covered by any medical program.
That’s why his parents have turned to the kindness of others.
They’ve seen miracles before — strangers who gave what they could, prayers from people they’ve never met, messages of hope from across the world.
Those gestures have kept them going.
“Every donation, no matter how small, is a piece of hope,” his mother says. “It reminds us we’re not alone.”
A Mother’s Prayer
When asked what keeps her strong, she doesn’t hesitate.
“Oli,” she says simply. “When I see his courage — when he smiles even though he’s in pain — I know I can’t give up. None of us can.”
Her voice breaks.
“He deserves a childhood. He deserves to live.”
Now, as they prepare to return to the hospital, they carry both fear and faith.
Fear of what the next scans might reveal.
Faith that the world will help them reach the finish line.
Because Oliver’s story isn’t over yet.
He’s still fighting — one treatment, one step, one brave breath at a time.
And somewhere in that hospital room, beneath the hum of machines and the glow of monitors, there’s a little boy with eyes full of hope — dreaming of the day he gets to go home for good. 💛
“Please Help Save Ewelinka’s Life – A Two-Year-Old Fighting Stage IV Cancer”.2289
“Ewelinka’s Fight: A Baby’s Battle Against Neuroblastoma” 💔
From the moment she was born, she seemed perfect — a tiny miracle wrapped in a hospital blanket.
Her mother held her close, thinking only of the years of love ahead.
But just days later, that dream began to unravel.
When Ewelinka came home, her mother noticed something strange.
Her little belly — soft and round — began to grow.
At first, she thought it might be normal.
But soon, it became clear something was terribly wrong.
The Diagnosis No Parent Should Hear
Doctors ordered tests.
Then more tests.
And finally, the words that changed everything:
“Stage IV neuroblastoma with metastases to the liver.”
Cancer.
A word no parent should ever hear about their child — and especially not about a baby just two months old.
“I couldn’t believe it,” her mother says. “How can such a tiny baby be fighting for her life before it’s even begun?”
They began treatment in Olsztyn immediately.
Chemotherapy was the only hope.
But instead of getting better, Ewelinka’s condition worsened.
Her mother held her in her arms the day she stopped breathing.
“I felt her slipping away,” she whispers. “I felt like I was dying too.”
Doctors rushed in.
They saved her — but the memory of that moment will never fade.
A Growing Monster Inside
Ewelinka’s tumor was enormous — 7 by 8 centimeters — growing inside a body not much larger than a doll.
Her liver swelled to fill 80% of her tiny abdomen.
The chemotherapy wasn’t working.
So they were transferred to Warsaw for life-saving radiotherapy — their last hope.
This time, it worked.
The tumor began to shrink.
But the victory was short-lived.
Another round of chemotherapy caused the disease to progress again.
New tumors appeared.
The nightmare was far from over.
Doctors classified her as high risk.
She was moved to intensive care.
Then into the operating room.
The surgeons removed as much of the primary tumor as they could — about 70%.
But it wasn’t enough.
More chemotherapy followed.
More suffering.
More nights of watching their baby hooked up to machines, fighting pain she could not understand.
A Timeline of Pain
After chemotherapy came another surgery — to remove the remaining tumor.
Then a bone marrow transplant.
Then another round of radiotherapy.
“I list these treatments in one breath,” her mother says, “but living through them felt like years. Days and nights filled with fear, pain, and helplessness. No one can imagine this hell unless they’ve been here.”
Now, Ewelinka is undergoing immunotherapy — one of the most difficult and painful treatments yet.
And still, the future is uncertain.
The Only Hope Left
Because Ewelinka is high risk, she needs a special therapy to prevent the cancer from returning — a deadly recurrence that would almost certainly take her life.
This treatment exists only in New York, USA.
It’s not covered by insurance.
The cost?
1.5 million złoty.
For a family already living on the edge, it’s an impossible sum.
But without it, Ewelinka’s survival chances are slim.
And neuroblastoma, when it comes back, is even more aggressive.
A Childhood Stolen
Because of the tumor pressing on her nerves, Ewelinka still can’t walk.
She will be two years old soon, but she can only lift her legs a few centimeters.
She’s undergoing rehabilitation, but the progress is slow.
Her whole life has been a fight against cancer.
She doesn’t know what a normal childhood feels like.
She’s never run across a playground, never climbed onto her mother’s lap without tubes and bandages between them.
“Sometimes I close my eyes,” her mother says, “and I picture her running — strong, healthy, smiling. I hold onto that picture like a lifeline.”
But the reality is harsher.
Without treatment, the cancer could return.
And another round might be too much for her tiny body to survive.
A Mother’s Plea
“All I want is for my daughter to live,” she says. “To grow up. To learn to walk. To go to school. To have a chance at life.”
She pushes away the intrusive thoughts of a funeral, of a tiny coffin, of a future that ends before it begins.
She refuses to believe it’s over.
That’s why she’s asking for help.
Because without the kindness of strangers, without donations — even the smallest ones — Ewelinka won’t get the therapy that could save her life.
Fighting for Tomorrow
Ewelinka’s story is one of unimaginable suffering — but also unimaginable courage.
She is a baby who has endured more pain than most adults will in a lifetime.
She is a child who, even as her body weakens, still fights.
Her mother dreams of the day she will walk.
She dreams of the day they will go to the park, and she’ll watch her daughter run into the sunlight.
She dreams of life after cancer.
But to reach that day, they need help.
“Without people with big hearts,” she says, “without shares, without donations, the cancer will come back and take her away from me.”
A Call to Action
Ewelinka’s life hangs in the balance.
She is not just a patient.
She is a daughter, a little sister, a tiny soul who deserves a chance.
Her mother has given everything.
Now she’s asking the world for one thing:
“Please, help me save my little girl.”
Because one day, Ewelinka could be the child who survived.
One day, she could stand on her own two feet, walk out of the hospital, and leave this nightmare behind.
But that day can only come if strangers, moved by her story, decide to give her that chance.
