Each year we select kids to represent the children of Western Australia who are helped as a result of the money raised by Telethon.

We always invite lots of "Big Telethon Stars" to Perth to help raise money for the weekend, but our "Little Telethon Stars" are what it is all about. 

Each year we select kids to represent the children of Western Australia who are helped as a result of the money raised by Telethon.

We always invite lots of "Big Telethon Stars" to Perth to help raise money for the weekend, but our "Little Telethon Stars" are what it is all about. 

Emily

“The best thing about Telethon is raising the money to help children like me and my new friends.”

For seven-year-old Emily Houston, life took an unexpected turn when she was diagnosed with acute lymphoblastic leukaemia. It’s been a challenging road, but Emily and her family have faced it with courage, hope and resilience. Telethon beneficiary Make-A-Wish Australia granted Emily an extraordinary wish: to be her own version of the Hulk and save her oncology team from attack. She recently underwent special superhero training and saved the hospital! Hitting an important milestone, Emily has received her last round of medications. However, her journey continues with antibiotics, monthly blood tests and oncology reviews to ensure she stays on the path to recovery.

Emily

“The best thing about Telethon is raising the money to help children like me and my new friends.”

For seven-year-old Emily Houston, life took an unexpected turn when she was diagnosed with acute lymphoblastic leukaemia. It’s been a challenging road, but Emily and her family have faced it with courage, hope and resilience. Telethon beneficiary Make-A-Wish Australia granted Emily an extraordinary wish: to be her own version of the Hulk and save her oncology team from attack. She recently underwent special superhero training and saved the hospital! Hitting an important milestone, Emily has received her last round of medications. However, her journey continues with antibiotics, monthly blood tests and oncology reviews to ensure she stays on the path to recovery.

Connor

“The most exciting part of Telethon was when the $77.5 million was raised because that is so much money to help the kids.”

Connor Barrett is an eight-year-old with courage and determination, fighting a tough battle against cystic fibrosis. Connor’s daily regimen includes a staggering 25 doses of medicine and two physiotherapy sessions - a testament to his incredible strength. He began his journey with cystic fibrosis when he was only three weeks old, and since then, appointments and stays at Perth Children’s Hospital have been a regular occurrence. For Connor, there is no such thing as stable. His digestive system causes him grief and pain. Yet, he presses on, defying the invisible grip of cystic fibrosis with a heart full of hope. Connor enjoys playing sports to keep his lungs strong and dreams of becoming a medical researcher to help others.

Connor

“The most exciting part of Telethon was when the $77.5 million was raised because that is so much money to help the kids.”

Connor Barrett is an eight-year-old with courage and determination, fighting a tough battle against cystic fibrosis. Connor’s daily regimen includes a staggering 25 doses of medicine and two physiotherapy sessions - a testament to his incredible strength. He began his journey with cystic fibrosis when he was only three weeks old, and since then, appointments and stays at Perth Children’s Hospital have been a regular occurrence. For Connor, there is no such thing as stable. His digestive system causes him grief and pain. Yet, he presses on, defying the invisible grip of cystic fibrosis with a heart full of hope. Connor enjoys playing sports to keep his lungs strong and dreams of becoming a medical researcher to help others.

Sophia

“Telethon was amazing! My favourite part was helping raise lots of money for kids just like me.”

Sophia Marshall is a brave eight-year-old who began her journey with type 1 diabetes when she was just four. It all started with two weeks of unexplained fatigue. Sophia wasn’t as cheerful as usual; she lost weight and was constantly thirsty. Sophia received a preliminary diagnosis, sending the family to the emergency department. There, further tests confirmed her type 1 diabetes diagnosis. Since then, Sophia and her family have undergone an intensive training program, equipping them with the knowledge and skills to manage this lifelong condition. Sophia visits the Perth Children’s Hospital every three months and will until she turns 18. Sophia’s resilience shone even brighter when follow-up blood tests revealed a secondary diagnosis of coeliac disease during her first post-diagnosis appointment. Sophia refuses to let her conditions define her; she’s living life to the fullest, and diabetes is just along for the ride.

Sophia

“Telethon was amazing! My favourite part was helping raise lots of money for kids just like me.”

Sophia Marshall is a brave eight-year-old who began her journey with type 1 diabetes when she was just four. It all started with two weeks of unexplained fatigue. Sophia wasn’t as cheerful as usual; she lost weight and was constantly thirsty. Sophia received a preliminary diagnosis, sending the family to the emergency department. There, further tests confirmed her type 1 diabetes diagnosis. Since then, Sophia and her family have undergone an intensive training program, equipping them with the knowledge and skills to manage this lifelong condition. Sophia visits the Perth Children’s Hospital every three months and will until she turns 18. Sophia’s resilience shone even brighter when follow-up blood tests revealed a secondary diagnosis of coeliac disease during her first post-diagnosis appointment. Sophia refuses to let her conditions define her; she’s living life to the fullest, and diabetes is just along for the ride.

Harrison

“I love seeing the other Telethon families. We are like family.”

Harrison Carthew is a resilient six-year-old who confronts the challenges of cerebral palsy with incredible strength. Harrison was diagnosed with spastic diplegia cerebral palsy at the age of two. He also grapples with vision impairment, colour blindness, and difficulty navigating uneven surfaces and maintaining balance. Add to that speech, learning and developmental difficulties to get the full picture of the everyday challenges that Harrison faces. Harrison’s life is filled with hurdles. He copes with disrupted sleep, endures developing pains, and undergoes injections to manage muscle tightness and enhance his everyday life.

Harrison

“I love seeing the other Telethon families. We are like family.”

Harrison Carthew is a resilient six-year-old who confronts the challenges of cerebral palsy with incredible strength. Harrison was diagnosed with spastic diplegia cerebral palsy at the age of two. He also grapples with vision impairment, colour blindness, and difficulty navigating uneven surfaces and maintaining balance. Add to that speech, learning and developmental difficulties to get the full picture of the everyday challenges that Harrison faces. Harrison’s life is filled with hurdles. He copes with disrupted sleep, endures developing pains, and undergoes injections to manage muscle tightness and enhance his everyday life.

Little Telethon Stars' parents

Little Telethon Stars' parents

Find out more about Telethon's impact on the WA community...

If you would like to learn more about Telethon and how you can get involved, please contact the Telethon Team. 

Channel 7 Telethon Trust 

50 Hasler Road, Osborne Park WA 6017 

PO Box 1777, DC Osborne Park WA 6916 

(08) 9482 3974 – telethonoffice@telethon7.com  

Acknowledgement of Country 

Telethon acknowledges the Traditional Owners of Country throughout Western Australia and pays respect to Elders past, present and emerging. We recognise the significant importance of their cultural heritage, values and beliefs and how these contribute to the positive health and wellbeing of the whole community. 

This content was prepared for digital by MINT, the commercial content studio for Seven West Media.