Happy to share this piece for Pediatric Research co-authored with the wonderful Megan Easton, a friend and parent advocate here in Toronto. In it we share our reflections on the provision of psychosocial care from my perspective as a childhood leukemia patient treated in the mid 1990's and Megan's perspective as a parent of a child treated in the 2010's. We give our views on what has changed during this time and what still needs to be done to provide greater support for children with cancer and their families, both during treatment and survivorship.
The article is free to access here.