Shortly after birth, doctors discovered Maddox had multiple unexplained fractures from a rare genetic disorder that causes bones to be fragile and break easily. This marked the beginning of Maddox and her family’s journey toward answers, strength, and resilience.Thanks to the Air Canada...

When Norah was 10 months old, her parents learned she had a permanent genetic condition: cystic fibrosis. Since her diagnosis, Norah and her mother have had to travel more than 750km four times a year between their home in northern British Columbia in Prince George and the BC Children's Hospital...

Jacelynn has always dreamt of standing on her own two feet. For this, she travelled from Nova Scotia to Montreal for a surgical intervention called selective radicellectomy at the Montreal Children’s Hospital. This intervention had to be followed by an intensive six weeks of rehabilitation at the...

Thank you to the Air Canada Foundation, which, through the Hospital Transportation Program, for over two years, has allowed us to traverse the 500 km connecting Abitibi-Témiscamingue to Montreal seamlessly.  For eight-year-old Mélia, who was diagnosed with leukemia in...

Luke was born with an uncommon medical condition that affects his muscles and joints and requires us to travel frequently to Vancouver to see his specialist. We are so grateful to the Air Canada Foundation for the help they have provided with travel costs, as well as the kindness and...