As a caregiver to a child affected by a brain tumour, your perspective is key to helping us shape the future of our pediatric resources and programs and ensure they truly reflect the needs of the children and families we serve.

In preparation for our 2026–2029 strategic planning, we’re hosting virtual focus groups to hear directly from families like yours. These small-group sessions are a space for you to share what matters most, talk about the challenges you’ve faced, and help guide meaningful improvements in pediatric care and support.

We’d be honoured to have you join one of the sessions below. With your insight, we can build a stronger future for every child and family affected by a brain tumour.