“For me, knowledge is a set of tools,” says Geneviève Côté-Leblanc. “And those tools help us support autistic people and their families throughout their lives.”
An occupational therapist by training, Geneviève has worked in management roles across the health network and now serves as Associate Director of Implementation at AlayaCare. Above all, she is Benjamin’s mom — a young autistic adult who continues to inspire her.
Since his diagnosis, Geneviève has been dedicated to turning research into practical, accessible resources for families. A member of TACC since 2017, she helps create links between research, clinical practice, and lived experience so that knowledge can directly improve daily life.
“Our knowledge isn’t the same, but it’s complementary,” she explains. “At TACC, lived experience and science meet on equal footing.”
Geneviève Côté-Leblanc shares her view of research as an essential resource for supporting autistic people and their families, and reflects on the value created when scientific knowledge and lived experience come together. (Production: Aura Strategies)
What sparked your interest in neurodevelopmental research?
Côté-Leblanc: My interest in research grew stronger after my son Benjamin’s diagnosis. Searching for reliable information to better support him made me realize how essential research is for families and neurodivergent people.
What motivates you in your work?
Côté-Leblanc: I’m motivated by the chance to use my professional skills — in occupational therapy, management, and knowledge translation — along with my personal experience as a mother and caregiver, to contribute to concrete solutions.
What kind of impact do you hope your work will have?
Côté-Leblanc: I hope to help build a caring community where autistic people and families can join forces and share resources to support everyone’s growth and well-being.
Why did you become a member of TACC?
Côté-Leblanc: Being part of TACC gives meaning to our family’s experience and allows me to turn that experience into action that supports the development and well-being of neurodivergent people.
In this ECHO-Autism webinar (November 18, 2021), Geneviève shares (starting at 11:00) her experience as a parent, speaking about life after a diagnosis. Her perspective highlights the importance of knowledge translation and the vital role of families in transforming practices and strengthening supports.
Stay Connected
To learn more about Geneviève’s experience or explore potential collaborations, connect with her on LinkedIn.