Farewell Deb!
If you are one of our healthcare professionals, or if your family has received our support, or even if you’ve been to one... Read More
How We Help Families
At TLC for Kids, we believe that a strong and cared-for family is critical to a sick child’s wellbeing. By supporting a... Read More
National Volunteer Week: Meet Ange
Ange’s story so far Ange has been involved with TLC for Kids for over a decade, not as a volunteer, but as... Read More
National Volunteer Week: Meet Leanna!
Leanna’s story so far Leanna was diagnosed with Cystic Fibrosis at three months old. Her first long hospital admission was at age 3,... Read More
Rare Disease Day
Today is Rare Disease Day. It’s a cause that’s very close to our hearts. Children who suffer from rare diseases can often... Read More
Ruby’s visit to the Melbourne Show!
Ruby suffers from life-limiting conditions, with metatropic dysplasia, bilateral vocal cord palsy (tracheostomy in situ), restrictive lung disease, and severe kyphoscoliosis. Ruby... Read More
Vivian’s Story
Vivian is a 20-month-old girl suffering with epileptic encephalopathy, a severe brain disorder of early age. The condition manifests with seizures that... Read More
Lucy’s Songwriting Dreams
Lucy, 16, has Cystic Fibrosis, and is a talented aspiring songwriter. She wanted to professionally record her songs for use as demo,... Read More
TLC for Kids New Years Resolutions
1. Practice gratitude! In 2016 we aim to practice gratitude daily, whether that be for our... Read More
Diving with Sharks!
This morning, 14-year-old Matthew Gaythorpe finally fulfilled his dream of swimming with sharks. Here’s how it happened… The RAPID Request: Matthew has... Read More