Seth McMaster was just hours old when doctors discovered a serious issue with his heart. Born with a congenital heart defect, Seth's parents, Tegan Brown and Lindsay McMaster, were immediately thrown into a world of uncertainty. "He was turning blue, and we had no idea what was happening," his mother recalled.
Seth was quickly airlifted from Rockhampton to Brisbane, where he was diagnosed with pulmonary atresia, a condition that prevents proper blood flow from the heart to the lungs. At just 48 hours old, he underwent his first surgery.
Pulmonary atresia is a lifelong condition, and Seth’s initial operation wasn’t successful. Surgeons then decided on a groundbreaking hybrid procedure that combined open-heart surgery with a catheter insertion to fully open his pulmonary valve. After countless weeks in the hospital, Seth made it through the ordeal.
Now 13, Seth has endured four major surgeries, the latest being after his 12th birthday when he had another valve replacement. Though more surgeries are expected in the future, Seth remains determined to live life to the fullest. A passionate soccer player, swimmer, and golfer, he embraces every opportunity to pursue his interests.
Seth also serves as an ambassador for Heart Kids, a national organization that supports children and families affected by congenital heart disease. His story has inspired many, offering hope and encouragement to other children facing similar challenges.
Reflecting on his journey, Seth shared, "It’s good to tell other kids my story and let them know it’s going to be okay." His resilience and optimism continue to inspire those around him.
