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How do you tell a four-year-old that he is fighting for his life? For Eli Belser, the question became a harsh reality th...
08/12/2025

How do you tell a four-year-old that he is fighting for his life? For Eli Belser, the question became a harsh reality that his family could never have imagined. Just a little boy, a sleepy big brother who once ran through ordinary days of play and imagination, Eli’s world was suddenly consumed by pain, uncertainty, and the weight of a diagnosis no parent ever wants to hear.
It began with subtle signs — discomfort, unusual fatigue, silent cries that tugged at his parents’ hearts. Doctors tested, scanned, and tried to reassure, but answers came slowly, each day stretching anxiety longer. Then, an MRI revealed the unthinkable:
The full story is in the comments below.👇

Some beginnings are so fragile that every breath feels like a miracle. For Addisyn, life started at the tiniest possible...
08/12/2025

Some beginnings are so fragile that every breath feels like a miracle. For Addisyn, life started at the tiniest possible scale — a mere 15 ounces, smaller than a can of Coke, and yet full of fighting spirit. Her arrival marked the beginning of a six-month battle that would test the limits of medicine, resilience, and parental love.
The pregnancy had been smooth, with the usual excitement of anticipation and hope. But at her 24-week checkup, just days after a gender reveal, doctors realized that something was amiss. Addisyn was developing unusually small, and there was an urgent need to act to protect her fragile life. Her mother, Howard, was admitted to the hospital, with specialists monitoring every heartbeat, every movement, and every growth milestone. The goal was clear:
The full story is in the comments below.👇

Some stories of courage begin before a child even takes a full breath. For Rebekah Hope, that story began the moment she...
08/12/2025

Some stories of courage begin before a child even takes a full breath. For Rebekah Hope, that story began the moment she was born. Only two months old, she entered the world facing challenges that would test the strength of even the bravest souls. Doctors quickly discovered two severe heart defects — a narrow aortic arch and a VSD hole — conditions so critical that every single breath became a fight.
Her tiny heart struggled valiantly, pumping against the odds as her family watched with a mix of fear, hope, and awe. The NICU, with its monitors, alarms, and machines, became her world, a place where life itself hung in delicate balance. Her parents clung to each fleeting sign of stability, every small flutter of life a moment of grace in the midst of uncertainty.
The full story is in the comments below.👇

Some children spend their childhood chasing dreams.Nine-year-old Owen Gonzalez spends his chasing life — and somehow, de...
08/12/2025

Some children spend their childhood chasing dreams.
Nine-year-old Owen Gonzalez spends his chasing life — and somehow, despite everything, he still dreams of one day becoming a professional soccer player.
Owen’s journey began when he was just two years old, at an age when most children are taking wobbly steps and learning their first words. Instead of playgrounds and picture books, Owen was introduced to oncology wings, IV poles, and the unfamiliar language of cancer. The diagnosis
T-Cell Acute Lymphoblastic Leukemia — arrived like a storm that no family could ever prepare for.
In those early days, his parents clung to hope with shaking hands, trying to absorb the words doctors spoke, trying to stay steady for a child too young to understand anything except that he needed his mother’s hand and his father’s arms. Owen didn’t know what leukemia was, but he knew he had to fight — and from day one, he did.
The full story is in the comments below.👇

Some heroes wear masks.Some wear capes.And some — like six-year-old Kolten Jones — fight their battles from hospital bed...
08/12/2025

Some heroes wear masks.
Some wear capes.
And some — like six-year-old Kolten Jones — fight their battles from hospital beds with bravery that outshines even the brightest comic book legend.
From the moment Kolten was diagnosed with Acute Lymphoblastic Leukemia (ALL), his childhood transformed in ways no parent ever imagines. One day he was a happy, energetic little boy from Gadsden, Alabama — running around, laughing, and dreaming big. The next, he was thrust into a world of IV poles, chemotherapy, medical alarms, and a fight for his life.
The full story is in the comments below.👇

Before you scroll past these words…Before your day continues…Please stop.Take a breath.And say Dawson’s name out loud.Be...
08/12/2025

Before you scroll past these words…
Before your day continues…
Please stop.
Take a breath.
And say Dawson’s name out loud.
Because right now, somewhere in a quiet ICU room in North Texas, a three-year-old boy is lying beneath the soft glow of hospital monitors — machines breathing for him, tubes supporting him, and a tiny bruised hand clutching a stuffed toy. This is the first glimpse the world has seen since he was rushed to the hospital… and it is almost too much for the heart to bear.
The full story is in the comments below.👇

There are moments in life when the impossible becomes real — when science pauses, when doctors shake their heads in disb...
07/12/2025

There are moments in life when the impossible becomes real — when science pauses, when doctors shake their heads in disbelief, and when families who have lived in fear suddenly find themselves holding a miracle. Today, on her fifth birthday, little Khaleesi is that miracle.
Just weeks ago, this brave little girl was clinging to life with only a ten percent chance of survival.
Her body was failing.
Her heart was barely functioning.
Her doctors were preparing her family for a goodbye no parent should ever have to imagine.
The full story is in the comments below.👇

Five-year-old Kunal should be running through open fields, playing with toys, laughing at silly cartoons, and falling as...
07/12/2025

Five-year-old Kunal should be running through open fields, playing with toys, laughing at silly cartoons, and falling asleep in the safety of his parents’ arms. Instead, he is lying in a Pediatric Intensive Care Unit, fighting for every breath as kidney failure threatens to take away the childhood he hasn’t even had the chance to fully experience.
His small body, once full of energy and innocence, now battles machines, medications, and exhaustion.
Every moment is a struggle.
Every hour is a prayer.
Every breath is a miracle.
And beside him — day and night — stand his parents, hearts breaking more each time they see their little boy wince, tremble, or slip into frightening stillness. They hold his hands even when he cannot hold theirs back. They whisper encouragement he is too weak to fully hear. They wipe tears they do not want him to see.
The full story is in the comments below.👇

Meet Emma — a bright, joyful, three-year-old child whose smile could light up an entire room, and whose courage could hu...
07/12/2025

Meet Emma — a bright, joyful, three-year-old child whose smile could light up an entire room, and whose courage could humble even the strongest adults. She is tiny, spirited, full of life… and she is living every day with
Hypoplastic Left Heart Syndrome (HLHS) — one of the most complex and life-threatening congenital heart defects known to medicine.
For Emma, the fight for her life began before she ever took her first breath.
Shortly after birth, doctors delivered a diagnosis that shattered her family’s world: Right Heart Hypoplastic Syndrome with pulmonary atresia, intact ventricular septum, and a rare coronary fistula. These are words no parent is ever prepared to hear. Words that carry fear, uncertainty, and a lifetime of medical battles. Words that meant Emma’s heart — the organ meant to sustain her life — had never fully developed.
The full story is in the comments below.👇

Some stories stay with us not because of their tragedy, but because of the extraordinary light that shines through them....
07/12/2025

Some stories stay with us not because of their tragedy, but because of the extraordinary light that shines through them. Aila’s story is one of those — a story of unimaginable struggle, breathtaking resilience, and a miracle so powerful it continues to inspire everyone who hears it.
Aila was only four months old when her tiny body was thrust into a battle most adults could never endure. Doctors diagnosed her with Acute Myeloid Leukemia (AML) — an aggressive, fast-moving cancer that strikes without warning and demands immediate, intensive treatment. For infants, AML is especially brutal. The chemotherapy is harsh. The complications come quickly. The outcomes are terrifyingly uncertain.
The full story is in the comments below.👇

A Birthday Filled With Miracles — How Baby Noah Survived Biliary Atresia and Found His Second Chance at Life Yesterday, ...
07/12/2025

A Birthday Filled With Miracles — How Baby Noah Survived Biliary Atresia and Found His Second Chance at Life
Yesterday, Noah Hallford turned one year old — a simple milestone for most families, but for his, it is nothing short of a miracle. His first year on Earth has been marked by hospital walls, monitors, fear, and desperate prayers… yet also by hope, resilience, and love powerful enough to hold a family together through the darkest days.
Noah was born with Biliary Atresia, a rare and life-threatening condition in which the bile ducts inside and outside the liver are blocked or absent. It is a diagnosis no parent ever expects, a condition that requires immediate intervention and often leads to liver failure in infancy. From the beginning, Noah’s life became a race against time.
The full story is in the comments below.👇

A Two-Year-Old’s Fight for Life — And the Hospital Team That Became Her Lifeline There are moments in a parent’s life wh...
07/12/2025

A Two-Year-Old’s Fight for Life — And the Hospital Team That Became Her Lifeline
There are moments in a parent’s life when the world stops — when one unexpected sentence tears open a new, terrifying reality. For the parents of two-year-old Harper, that moment came during what should have been a routine eye test. The images showed something abnormal, something frightening, something urgent.
Within hours, Harper was rushed to Birmingham Children’s Hospital & Charity. What began as a normal day ended with her parents standing in a hospital hallway, listening to doctors speak words they never thought they would hear:
The full story is in the comments below.👇

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