Raising Hope for Layla
Photo Credit: Supplied

Little Layla is an inspiration! With the support of her mom, the two are fighting cancer and raising awareness to help other children, too.

 

South Africa (21 August 2015) – Layla O’Neill was diagnosed with a rare form of Cancer called Neuroplasm Glial Ependymoma at the mere age of just 4.

Her family found out about her condition just weeks before her 4th birthday party after she had a recurrence of the illness.

“She kept getting sick and the doctors kept saying it was a viral infection. She was experiencing pain in her legs, which we all thought was growing pains.”

In May 2013, Layla started vomiting blood, and her mother immediately took her to the hospital.

Layla was given an MRI scan, which picked up that there was fluid on her brain and spots on her spine.

“The doctors said it was the first time they’d ever seen something like this. They operated and put in a shunt which takes the fluid away from her brain to relieve the pressure. They told us that if we had waited a day more to bring her to the hospital she would have not survived.”

“Layla’s condition is so rare that approximately 700 people in the world are living with the condition.”

The doctors were uncertain of her future and gave little Layla only six months to live… but two years later, this little fighter is not giving up or going anywhere anytime soon.

“Layla is such a little fighter. She’s obsessed with Spiderman – he’s her favourite superhero & hero.”

Sharyn O’Neill, Layla’s mom started a non-profit organisation called Ependy Angels to look after, and raise money and awareness for Layla and other children suffering from different types of cancers. Please note: the organisation ceased operations in 2019.

Most of the children supported by Ependy Angels start off without medical aid, and usually, medical aids make people wait a year, once being diagnosed with Cancer, before treatment can commence.

During that year, Ependy Angels helped by paying their medical bills and offering support and assistance to families.

“To give you an idea of costs… Layla’s medical aid pays for roughly 97% of all her medical bills. The three percent that they don’t pay equates to around R30 000 a month.”

Through the treatments, Sharyn has been a pillar of strength and a beacon of hope… after the first set of radiation, Layla was finding it very traumatic to see her hair falling out so her mom decided to shave off the rest so that Layla wouldn’t feel scared. They both looked like urban runway models.

In just a couple of days, Layla and Sharyn will be on their way to India for a new surgery called “Cyber Knife” which has already caused waves in the medical industry and has seen incredible results in other patients.

Little Layla is an angel and an inspiration and knowing her… I’m sure we’re going to hear great things when they get back from their trip.


Sources: GTG Interview
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About the Author

Brent Lindeque is the founder and editor in charge at Good Things Guy.

Recognised as one of the Mail and Guardian’s Top 200 Young South African’s as well as a Primedia LeadSA Hero, Brent is a change maker, thought leader, radio host, foodie, vlogger, writer and all round good guy.

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