Mike and Kristin describe their experience of their child’s diagnosis and surgery, and how he has inspired them. They also talk about how important the ongoing support and hope provided by the Children’s Heart Network has been to them.
Every year the Children’s Heart Network organizes two summer camps: one for children ages 8 to 12 and one for teens ages 13 to 19.
Long QT syndrome can affect many members of the same family. Carmen tells us how she and her family have learned to overcome the challenges.
Houston is a remarkable, Michael Buble–loving boy who touches all those who meet him.
Joanne shares what Hearts of Gold summer camp meant to her when she was a teenager.
Eric tells his own story, including his many surgeries, his fishing trip to Critter Cove, and his appreciation for the support and understanding he receives from his peers in the Hearts of Gold teen group.
When you’re waiting for a new heart, hope is what keeps you going. Kristi shares how it felt to wait for a heart transplant.
Not long after he was born, it became clear that Jack had a “complicated heart,” and he would, in fact, need a transplant as quickly as possible.
When Zoë was 11, she created this presentation for her classmates to help them understand all she’d been through.
Hunter’s 3rd Annual Pancake Breakfast, Birthday Gift Donations, Lemonade Stand, Recycling with Heart, Pub Night Fundraiser, Jewellery Sales, Half Marathon and 5 km Run.