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Every day at the Queen Elizabeth Hospital, lives are changed thanks to the care, expertise, and compassion of our healthcare teams and the generosity of our community. These are the stories of patients and families who experienced that care firsthand and wanted to say thank you. We’re honoured to share their journeys with you.
Born on May 26, 2024, Sutton faced serious medical complications. Soon after birth, Sutton was transferred to the IWK, where he was diagnosed with Pierre Robin Sequence Syndrome and Stickler Syndrome. He underwent a series of critical interventions, including a tracheostomy and, later, the placement of a g-tube to support his breathing and feeding needs. While those early weeks were filled with uncertainty, they were also the beginning of an incredible journey—one where Sutton’s resilience and strength began to shine through, particularly through the help of physical therapy.
From his earliest days, Sutton was supported by a skilled team of pediatric therapists at the QEH who focused on helping him build strength, movement, and coordination. These sessions became a key part of his care and development, helping him reach milestones that once felt so far away.
For his mom Lydia, one of her most cherished memories was when Sutton began to smile around four to five months old. “It was like he was telling us he was okay—that he was happy,” she often shares. Another unforgettable moment was when he began making soft cooing noises, expressing himself in ways that brought joy and comfort to his parents.
Lydia looks forward to Sutton’s physical medicine appointments, not only for the therapy itself but for the supportive team that surrounds them. She finds the care team deeply comforting and appreciates how in tune they are with Sutton’s development. “They sometimes notice his milestones before I even do,” she says with a smile. That attentiveness and encouragement make every appointment feel like a celebration of Sutton’s progress.
Thanks to early intervention and consistent therapy, Sutton continues to make remarkable strides. Each small victory—whether it’s improved head control, purposeful movement, or greater engagement with his surroundings—represents the dedication of his care team and the unwavering love of his parents.
The family has also been able to access the donor-funded equipment lending library set up through the QEH Foundation. This has allowed them to try specialized equipment before committing to purchase—like arm braces to help Sutton support himself while sitting, a custom-made pillow for tummy time, and even a sensory board designed to help him explore different textures. These thoughtful tools have made a big difference in his development.
Although Sutton’s journey includes continued challenges and regular medical care, he is thriving. His physical therapy has become more than just clinical support; it is a source of hope, growth, and connection.
His parents, Lydia and Luke, are deeply grateful for the services and support they have received throughout Sutton’s journey. They want other families to know that as overwhelming and frightening as life can feel when facing unexpected medical challenges, you are not alone. There is strength in support, comfort in community, and so much hope in the progress yet to come.
In 2023, Jenny and Coady welcomed their first child, Miloh who was born at just 30 weeks. He spent 80 days at the QEH NICU and his story was shared in celebration of QEH’s Big Day of Giving. On March 18, 2024, the family welcomed their second child, Elliot, into the world. Much like his older brother, Elliot arrived early at 32 weeks and spent 35 days in the NICU. Despite his premature birth, Elliot thrived. He received CPAP support, phototherapy, and a feeding tube—just like Miloh did. Each day spent in the NICU, he grew stronger.
At 3 a.m. on March 18, Elliot’s mother woke with the unmistakable signs of labour. The couple quickly prepared, bringing Miloh to his grandparents and rushing to the hospital. The team in Labour and Delivery did all they could to delay the birth, but Elliot had his own plans. By 10 a.m., his mother was moved to Unit 4 for rest, thinking they had bought a few more days or even weeks. Her husband returned home to check on their animals, only to be called back by noon. Elliot would be arriving by emergency C-section within 30 minutes.
Thanks to the calm and capable team present for the delivery, a chaotic experience became a much more manageable one. Elliot was born weighing 3 lb 9 oz—just 2 oz more than Miloh had weighed.
Having already navigated the NICU journey with their firstborn, the family knew that amid the fear and challenges, the unit offered something more: a sense of calm, of community, and even of home. They placed their trust in the NICU team, and once again, that trust was met with incredible care.
The family extends their deepest thanks to everyone involved—respiratory therapists, dieticians, pharmacists, pediatricians, the neonatologist, Unit 4’s social worker, the nurses, and the NICU’s ward clerk. Their compassion and expertise provided immense relief during an uncertain time. The family credits their boys’ strength to this remarkable team and will remain forever grateful.
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