Cape Argus News

Zaya Swart's brave battle against cancer: A story of resilience

Tracy-Lynn Ruiters|Published
Little Zaya Swart brings joy to those around her as she battles the rare disease Langerhans Cell Histiocytosis.

Little Zaya Swart brings joy to those around her as she battles the rare disease Langerhans Cell Histiocytosis.

Image: Supplied.

When little Zaya Swart laughs, the atmosphere shifts. Behind her cheeky smile and playful energy lies a girl battling challenges that would overwhelm most adults. 

Her parents, Morné and Tiani Swart, describe her as a tiny firecracker with bright red hair and a vibrant personality that brings smiles even on tough days. Despite her struggles, she dances, plays, and chats when she can, lighting up the hospital rooms that have become all too familiar for her.

Two-year-old Zaya’s journey started long before doctors confirmed she had a rare disease.

Morné remembers her birth as one of the most emotional nights of his life. Tiani developed pre-eclampsia towards the end of her pregnancy and doctors decided to induce labour early.

After nearly 12 exhausting hours, things still were not progressing properly and an emergency C-section became necessary.

“The whole night honestly felt like six days,” Morné said.

“I remember sitting there afterwards with my newborn while my wife was still being stitched up. I just wanted to see her. It was very emotional.”

Little Zaya Swart

Little Zaya Swart

Image: Supplied

Despite the traumatic birth, Zaya looked healthy and quickly became the calm, gentle baby everyone adored.

“She was honestly such a sweet baby,” her family said.

But after a few months, small things started worrying her parents. Severe cradle cap. A swollen tummy. Endless appointments and treatments that never seemed to help.

At first, nobody thought it could be something serious. Eventually, doctors referred the family to specialists and the word Langerhans Cell Histiocytosis, or LCH, entered their lives.

A scalp biopsy later confirmed the devastating diagnosis in August 2025.

“I still remember my wife calling me while we were both at work,” Morné said.

“She just said: ‘She has LCH.’

At just one-and-a-half years old, Zaya started chemotherapy. Even before treatment began properly, things went wrong. During a procedure to insert a port into her chest, one of her lungs collapsed.

What should have been a simple operation turned into hours in theatre and eventually a week in ICU recovering.

“That was one of the first times we almost lost her,” Morné said quietly.

For her parents, watching such a tiny child endure chemotherapy, needles, surgeries and endless hospital admissions has been unbearable.

“There’s honestly no worse feeling,” he said.

“You can’t stop the pain. You can’t fix it. You just stand there feeling helpless.”

After the first few chemotherapy sessions, complications started piling up.

Zaya developed unexplained fevers, severe fatigue and dangerously low blood counts. In December 2025, she became critically ill with sepsis and spent two weeks in hospital. Her port later had to be removed because of infection concerns. Then came another blow.

After briefly celebrating news earlier this year that scans showed she was clear of LCH, more tests revealed a second life-threatening condition called HLH.

At just one-and-a-half years old, Zaya started chemotherapy.

At just one-and-a-half years old, Zaya started chemotherapy.

Image: Supplied

Since then, the family’s life has revolved around hospitals, medications, treatments and fear of what tomorrow could bring.

For Morné and Tiani, balancing work, hospital stays and caring for their family has pushed them into survival mode.

Tiani had to reduce her working hours while the family continues making daily trips for treatment and specialist care. But somehow, through all of it, Zaya still finds reasons to smile.

“She keeps us laughing during the darkest moments,” Tiani said.

Morné said her strength constantly leaves him speechless.

“I always tell people I don’t know how she does it because I probably wouldn’t survive what she’s gone through,” he said.

“She just keeps bouncing back.”

One of the hardest parts, Tiani explained, is how lonely the journey can become over time.

“In the beginning everyone checks in and supports you,” she said.

“But later on people think everything is okay because she looks better.

“What they don’t see is the fear that never leaves. After a good day, you still wake up wondering if tomorrow is going to be another hospital day, another fever, another setback.”

Still, through every frightening moment, the family said their faith has carried them.

“There were days where it was only God that gave us strength,” Morné said.

He also credits their close-knit family, especially Zaya’s grandparents, for helping hold them together.

Now, the family is asking for help as medical costs, treatment expenses and daily care continue placing pressure on them financially and emotionally.

But more than anything, they hope people remember that children like Zaya are more than their diagnoses.

Asked what message she believes Zaya would give others if she could fully explain her journey herself, Tiani concluded: "I think she would say: ‘Keep fighting. If you fall, come back stronger."

To contact Zaya's family kindly email [email protected]

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