IWK Patients

When Van Bernard of Halifax, Nova Scotia was eight months old, his family noticed he was not growing like he should and his gross motor skills were not developing.

AJ was only hours old when his heart started to fail.

Born with a congenital diaphragmatic hernia (CDH), AJ’s stomach and bowels were pushed up into his lungs and his heart was displaced.

Born with a rare and life-threatening kidney disease, Zaccari needed a kidney transplant to survive. In February 2018, his mom received the call that would save her son’s life.

When Logan’s mom Jean was pregnant, she found out there was a 50/50 chance the baby would inherit her condition; Pfeiffer Syndrome. It’s a genetic condition where the soft spots of the skull fuse together before birth, affecting the growth of both his skull and mid-face.

When ten-month-old Lilianne began to walk, her parents noticed that something just wasn’t right.

As she grew, her hip began to make a clicking noise. She was referred to the IWK where she was diagnosed with developmental dysplasia of the hip.