22 broken bones: Rare condition gives teen even tougher fight
Adelaide teen Will Niven was born with a genetic condition that has altered his life — but he now faces an even more intense challenge.
Adelaide teen Will Niven was born with a genetic condition that has altered his life — but he now faces an even more intense challenge.
Baby Bryson was struggling for months, unable to get over salmonella, his mum was constantly bringing him to the doctor until finally they received a shocking diagnosis.
Three-year-old Eve Robertson was hallucinating rainbows and stars on the ceiling of her hospital bed after a common virus lead to a devastating diagnosis.
Little Hailey Valle has spent the last few years bravely fighting despite her parents facing “red tape” getting her into a clinical trial to give her better odds.
A mother endured what no parent should ever have to – the loss of one of her children. Now she is speaking about how her son died to help raise awareness of the cruel condition.
A family is devastated after the Year 7 girl was found dead after being subjected to bullying at an Aussie school.
Steven Miles has been grilled over his latest pledge to fund free school lunches – with Karl Stefanovic asking if he thought Queenslanders were “idiots”.
Alison Harrison was told her son only had six months to live after doctors made a horrific discovery last year. But eight-year-old Sammy Scully has been defying the odds.
Young mum Leyneaka Maigler had no reason to disbelieve doctors when they told her that her two-year-old daughter was constipated. Sadly, they were very wrong.
Little Maxwell Hann contracted the flu, before he knew it his heart stopped beating and doctors were resuscitating him to try and save his life.
Nine-year-old Fraser Suggate was told he had gastro and anxiety. It was only his mother’s dogged determination that led to the diagnosis of something far more sinister.
Claire Carson’s parents couldn’t imagine what was really wrong when she suddenly lost her appetite and started to feel weak.
An “unfair” bureaucratic loophole means a young family has to raise $350,000 and possibly move overseas to access treatment for their six-year-old boy battling a rare cancer.
Two-year-old Samara was an average toddler running around the home – but she’s been left with mobility deficits after languishing paralysed in the WCH emergency department for six hours.
Original URL: https://www.couriermail.com.au/lifestyle/health/health-of-the-nation/kids-teens/page/3