Sydney man who contracted rat lungworm after eating slug dies

SAM Ballard, the Sydney man who fell into a coma and became paralysed after eating a slug, has tragically died eight years on.

SAM Ballard never did anything wrong, if you ask family and friends.

The teenager from Sydney’s upper north shore was having a laugh and some red wine with mates in the backyard, “trying to act like grown ups”.

It was 2010 and it was a night that would change the 19-year-old’s life, and the lives of everybody around him, forever.

A slug crawled across the concrete patio and, teens being teens, a dare emerged for Sam to eat it.

One of his best friends, Jimmy Galvin, later described the moment.

“We were sitting over here having a bit of a red wine appreciation night, trying to act as grown up and a slug came crawling across here,” he said.

“The conversation came up, you know. ‘Should I eat it?’ And off Sam went. Bang. That’s how it happened.”

Sam Ballard was infected with rat lungworm after eating a slug in 2010.

Sam Ballard and his mates.

He didn’t become sick immediately, but complained of serious pain in his legs in the days after.

He was worried it might’ve been a symptom of eating the slug, but his mother told him not to worry: “No-one gets sick from that,” she said.

Sam was worried he might have developed Multiple sclerosis, like his father, but that was ruled out.

Doctors later determined Sam was infected with rat lungworm.

The worm that infected Sam is usually found in rodents, but snails and slugs can also become infected when they eat rat faeces.

Sam contracted eosinophilic meningo-encephalitis, which many people recover from. Sam didn’t.

He fell into a coma for 420 days and when he woke had an acquired brain injury.

Last week, eight years after he fell ill, Sam died. The Sunday Project’s Lisa Wilkinson broke the news during a sombre but brief segment.

“We have some sad news for you now. Earlier this year we brought you the story of Sam Ballard who, on a dare from his mates, ate a slug. He contracted rat lung disease with devastating effects,” Wilkinson said.

In this special report @Lisa_Wilkinson talks to the amazing family and friends of Sam Ballard #TheProjectTV pic.twitter.com/UXY5KGeWjF

— The Project (@theprojecttv) April 1, 2018

Sam was described as a larrikin by those who knew him.

“His friends have stuck by him ever since. On Friday, Sam passed away, surrounded by his family and loyal, loving mates.

“His last words to his mum: ‘I love you’.”

Katie Ballard, Sam’s mother, described how hard life had been for Sam. He couldn’t eat for himself and needed help going to the bathroom.

While he was initially unable to move his limbs, the former Barker College student worked hard to regain some movement.

Katie had said “he understands” everything, and his mates know that was true.

Mr Galvin said he apologised to Sam for not stopping him that night in 2010. When he did, the former rugby standout “just started bawling his eyes out”.

“So you know he’s there,” Mr Galvin said.

His close friends often visited him, even if it was a “shock” to see their mate struggling.

“When I walked in, he was very, very gaunt … and there were cables everywhere,” friend Michael Sheasby said. “It was a big shock.”

They’d watch footy like they used to and share a beer, even if that meant just a sip for Sam when Katie left the room.

Katie Ballard with her son Sam. Picture: Danny Aarons

Former Australian sprinter Matt Shirvington with Sam Ballard at a charity fundraiser in Sydney.

His eyes would always light up when they came around.

“It made his day,” his mates said.

In 2011, Katie shared a post on Facebook, maintaining hope that her “rough-and-tumble Sam” would recover.

“Physios had Sam standing in the frame at the gym,” she wrote. “He spent the afternoon laughing at me as I read him the sports section of the newspaper with new glasses on.

“Told him it was the stress of the last 16 months that had affected my eyesight.”

Later, she wrote that “he is still the same cheeky Sam, and laughs a lot” but admitted “it’s devastated, changed his life forever, changed my life forever. It’s huge. The impact is huge.”

Katie spent years fighting for adequate care for Sam after 2010. An initial allocation of care as part of the government’s National Disability Insurance Scheme saw the family receive $471,000.

But in October, 2017, that was reviewed and slashed by more than half. Media coverage and the family’s fight for additional funding and care saw the decision reversed.

Sam Ballard with the mates who never left his side. Picture: Simon Cocksedge

Sam with his mum, Katie. Picture: Danny Aarons

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