History
Hover / Click to ViewVision
Hover / Click to ViewWe recognize that the journey to finding workable solutions takes time and can be extremely challenging. However, we believe that with the proper supports, individuals and families impacted by FASD can achieve success and reach their full potential.
Mission
Hover / Click to ViewOur goal is to help others navigate the complex challenges related to living with FASD. Utilizing the lived experiences and expertise of peers, families, and professionals we focus on helping those affected by FASD access resources, services, and information that can best support them.
Purpose
Hover / Click to ViewBoard of Directors
Our Board of Directors consists solely of individuals with FASD and their caregivers to guarantee direct input and decision-making within the organization. We use the DACI model for our structural hierarchy and follow the motto With Us, not For Us.
Angela De Rose – Individual with FASD rep
Shelley More – Chair
Mary-Kate Bridson – Co-Chair
Rob More – Secretary
Steve Bridson – Treasurer
Michelle Kilner – Kids Inclusive Parent Liaison and member-at-large
Diane Greer – member-at-large and Leeds-Grenville rep
David Laliberte – member-at-large and health system advisor
Derek Leach – member-at-large and IT rep
Mark De Rose – member-at-large and SEAC rep