Joanna and Bertran Labonte take life with son Campbell one day at a time, making each as happy and fulfilling for him as they can.
"Every day, we want it to be a good day," says Joanna. "When it's a good day, it's wonderful. When it's not, we're reeling with fear at what that means for the future."
Seven-year-old Campbell Labonte was born 24 weeks premature. He is deaf, blind and can't speak or walk. He has cerebral palsy and has developed Stage 3 kidney disease. He's endured dozens of surgeries and countless other challenges.
His parents are indomitable spirits - always, it seems, hopeful, upbeat and resilient. Joanna often equates their life with Campbell to caring for a 40-pound newborn. They feed him, lift him, change him, bathe him and entertain him.
The love and care is constant, even at night when he doesn't sleep. Joanna and Bertran Labonte, both in the military, have lived in that bleary-eyed, chaotic netherworld of the newborn parent ever since their son arrived Aug. 10, 2008.
"We love that kid so much and are in awe of how he manages each day," says Joanna. "He is the world to us. He is filled with happiness.
"His highs are so high and his lows are so low but he has a determination to move forward and strive for happiness. He has taught us so much. It is so cool to look at life differently than the way most of us do every day.
"Campbell's done that for us."
Joanna doesn't pretend can't be difficult. And when it all catches up with them and they're feeling overwhelmed, they pick up the phone and call Roger Neilson House.
Supported by the Ottawa Senators Foundation, Roger Neilson House is an eight-bed paediatric residential hospice for families with children and youth living with a life-limiting illnesses. It is named for the late Sens assistant coach, Roger Neilson, and located on the grounds of the Children's Hospital of Eastern Ontario (CHEO).