DECLAN — THE BOY WHO FACED STAGE-4 CANCER WITH A SMILE, AND CHANGED EVERYONE WHO MET HIM. Hyn
Everyone who met Declan remembered him for the same reason.
Not his illness, but his wisdom, determination, and a sense of humor far bigger than his small body.
Before cancer entered his life, Declan was just a little boy growing into the world.
He laughed easily, asked thoughtful questions, and had a way of noticing things adults often missed.
His parents, Kim and Simon, thought they were raising an ordinary, joyful child.
They had no idea how extraordinary their son was about to become.
Just before Declan turned four, something changed.
Small signs appeared, subtle enough to dismiss, heavy enough to linger.
A scan was ordered, then another.
What doctors found would fracture time into before and after.
The tumor in Declan’s abdomen was the size of his father’s fist.
Stage-4 neuroblastoma had already spread to his bones and bone marrow.
The word “advanced” landed like a weight no family is prepared to carry.
Cancer had moved fast, and there was no time to hesitate.
Treatment began immediately.
Childhood stopped overnight.
Declan was admitted to Princess Margaret Hospital in Perth.
Hospital corridors became the background of his early memories.
Chemotherapy arrived in cycles that felt endless.
Five rounds that pushed his small body beyond what seemed possible.
The medicine was harsh and unforgiving.
It took hair, energy, appetite, and comfort without asking permission.
Through it all, Declan surprised everyone.
He joked with nurses and smiled through nausea.
He noticed when his parents were tired.
He comforted them, even when he was the one hurting.
After chemotherapy came surgery.
Nine hours in an operating room that held the family’s breath hostage.
Surgeons worked carefully to remove the tumor.
Kim and Simon waited, suspended between fear and faith.
When Declan woke, the pain was real.
But so was his resolve.
His parents tried to keep life as normal as possible.
Normal became a fragile, redefined thing.

Declan loved swimming more than anything.
Water had been freedom, movement, joy.
But treatment made swimming impossible.
And that loss cut deeper than anyone expected.
Declan’s younger brother, Brodie, felt it too.
Childhood suddenly had rules and restrictions.
Kim and Simon made a hard choice.
If Declan couldn’t swim, neither would Brodie.
They refused to let cancer divide their sons.
Fairness mattered, even in unfair circumstances.
Days were filled with hospital visits.
Nights were filled with whispered fears.
Then, in August 2013, something incredible happened.
Doctors used a word the family had been desperate to hear.
Remission.
For the first time in months, hope felt solid.
Declan had fought hard, and it showed.
The cancer appeared to be gone.
More treatment followed anyway.
Radiation, immunotherapy, and relentless monitoring.
Declan handled it with strength that stunned adults.
So well, in fact, that doctors sent him home two months early.

Home felt like a miracle.
Walls without IV poles felt unreal.
For a while, life breathed again.
Laughter returned to the house.
But cancer is cruel in its timing.
And it does not honor relief.
In January 2015, new scans told a different story.
Two tumors had returned.
One on Declan’s spine.
Another on his left hip.
Relapse is a word that carries despair.
It steals hope you thought you had earned.
The family faced the truth quietly.
Cancer was back, and it was stubborn.
Options were limited.
Time felt shorter.
Then came a possibility.
Not a guarantee, but a chance.
Declan was enrolled in a clinical trial testing a drug called DFMO.
It was experimental, unproven, and risky.
But it was hope.
And hope matters when everything else is gone.
The trial was based on years of research.
Research that existed because others refused to stop asking questions.
Declan began the new treatment.
His body, already exhausted, accepted the fight again.
Months passed under careful observation.
Every scan was a held breath.

After four months, doctors saw something remarkable.
The tumor on his spine had disappeared.
The tumor on his hip had shrunk.
Progress, slow but undeniable.
By December 2015, scans showed no further progression.
For the first time in a long while, stability returned.
Declan knew what this meant.
He understood more than his age suggested.
He talked about the future.
Not in grand plans, but in simple hopes.
Time with family mattered more than ever.
Moments became treasures.
But cancer is relentless.
It waits quietly.
In June 2016, scans revealed the truth again.
The tumor on his hip was growing.
The trial had bought time.
But it could not stop everything.
Declan’s body began to weaken.
Pain increased, energy faded.
Still, his humor remained.
His compassion never left.
He worried about others.
He asked how nurses were feeling.
He joked even when he was afraid.
He comforted when he was hurting.
In May of the following year, Declan passed away.
He was still a child.
His battle ended quietly.
But his impact did not.
Kim and Simon did not measure Declan’s life in years.
They measured it in meaning.
If not for research, they would have lost him sooner.
The trial gave them time they never would have had.
Time to hold him.
Time to hear his laughter.
Time to see his courage fully bloom.
Time that mattered more than words can explain.
Declan’s story is not just about loss.
It is about bravery in a body too small for such weight.
It is about a child who understood suffering.
And still chose kindness.
It is about parents who watched their son teach adults how to face fear.
Without bitterness.
Declan showed that wisdom does not wait for age.
And courage does not need permission.
He lived with intention.
Even when time was short.
His story lives on in memory.
In every life he touched.
Cancer took his body.
But it never took who he was.
Declan remains a reminder.
That even in the darkest fight, light can exist.
And sometimes, the smallest lives leave the largest echoes.
The Day Little Margarett’s Journey Broke Open — And Her Family Faced the Update They Feared Most

There are stories that fall softly into our lives like drifting leaves.
And then there are stories that crash through the heart, leaving every breath trembling.
Margarett’s story is one of those.
The kind that stops a room.
The kind that makes strangers pause mid-scroll and whisper, “This isn’t fair.”
Because she is only three years old.
Three — the age of tiny giggles, sticky fingers, mismatched socks, and worlds still full of magic.

But cancer does not care about magic.
It does not care about innocence.
It does not step aside simply because a child deserves a gentler life.
And now, her family has reached the chapter they prayed would never come.
When the results of Margarett’s latest scans arrived, her mother felt the truth before the words even formed.
Parents of children with cancer learn to read silence — and this silence was the loudest yet.
Doctors looked at each other.
They looked at the ground.
They breathed heavily before speaking.
Then came the words no mother should ever have to hear:
“The cancer has spread.”
Not a little.
Not slowly.
Not in a way that left space for new treatments or new hopes.

It has moved into her lymph nodes.
It has sparked new growth in her lungs.
It has returned fiercely in her liver.
A roadmap of invasion no child should ever carry in her tiny body.
Her mother later wrote, with trembling hands:
“We received the news I have prayed I never would have to get to in all of Margarett’s journey.”
And with that sentence, the future shifted.
The ground beneath them cracked.
Every plan they had been holding onto dissolved.
Doctors offered the only path left.
Not a cure.
Not a clinical trial.
Not a next step in treatment.
Comfort.
Home.
Peace.
Time is now measured not in months or milestones, but in moments.
Moments she is still here.
Moments she is still smiling.
Moments when she leans into her mother’s chest and the world feels gentle again.

Options are painfully few.
But love — love has never been stronger.
They are holding onto every second as if it were made of gold.
Because it is.
But to understand the heartbreak, you must first understand the little girl at the center of it.
Margarett is not charts or scans.
She is not medical terminology or test results.
She is a child.
A child who loves soft blankets and bright toys.
A child whose laughter once filled entire rooms.
She should be learning to ride a tricycle.
She should be dancing in the living room.
She should be chasing bubbles in the backyard.
Instead, she knows the cold touch of hospital gowns.
She knows the hum of machines.
She knows the names of medications no three-year-old should ever have to learn.
And yet — she shines.
Softly.
Fiercely.
Radiantly.

Her bravery is the kind adults struggle to comprehend.
Her spirit is a lesson in strength and tenderness.
She reaches for her parents even now.
She smiles when she is able.
She loves without hesitation.
Her family surrounds her with a love so fierce that even cancer cannot dim it.
And when a family receives news like this, the world changes shape.
Time slows down.
Priorities fall away.
Laundry does not matter.
Deadlines do not matter.
Emails do not matter.
But her tiny hand wrapped around her mother’s finger — that matters.
The way she whispers “Mama” in a soft, tired voice — that matters.
The way she nestles into her mother’s chest when exhaustion wins — that matters more than everything else combined.
Her parents now walk a path no parent ever wants to imagine.
A path of strength.
A path of surrender.
A path of courage too deep to name.
But they walk it with a single promise:
Margarett will feel love in every moment she has.

Since the update, messages have poured in from all corners — friends, strangers, parents who have walked similar roads, people who simply cannot look away from a child’s fight.
Messages of prayer.
Messages of hope.
Messages of support that wrap around the family like a blanket warmed by a thousand hands.
“You’re not alone.”
“She is so loved.”
“We are holding you in our hearts.”
“Hope doesn’t end here.”
And for a family living inside a storm, those words matter more than anyone realizes.
Because there is a kind of courage only children can teach.
And Margarett has taught it in ways the world will never forget.

She has faced treatments that would break adults.
She has endured tubes, scans, fevers, nights without sleep, pain that should never touch a child’s body.
But still — she reaches for her parents.
Still — she sparks light in rooms heavy with grief.
Still — she shines.
Her courage is soft and quiet, like the strength of a candle refusing to go out in the wind.
Her bravery is the kind that leaves grown adults in awe.
There is no roadmap for what comes next.
Only love.
Only presence.
Only the sacred work of soaking in every second given to them.
There will be laughter — shy, soft, unexpected.
There will be tears — heavy and unrestrained.
There will be quiet mornings and long nights.
There will be moments that etch themselves into their hearts forever.
And through all of it, there will be one unbreakable truth:
Margarett is not alone.
Not now.
Not ever.

If you are reading this, take a moment.
Hold this family in your thoughts.
Send strength.
Send warmth.
Send peace.
Send the kind of hope that rises even in the darkest nights.
Because right now, this little girl — this brave, beautiful three-year-old — needs all the love the world can offer.
And her parents need to know that people see them.
People feel for them.
People are standing quietly beside them, even from afar.

Margarett, sweet girl — we are holding you so tightly in our hearts.
We are sending courage to carry you.
We are sending gentleness to surround you.
We are sending infinite love that does not fade with time.
Your story is not ending.
It is shifting.
Into a chapter written with tenderness, memory, and love so deep it will outlive everything else.
And the world — strangers, friends, hearts you will never meet — is holding you close as you walk it.





