SARNIA, ON – September 5, 2025 – Did you know that 4% of Canadians, over 1.5 million people, are living with Fetal Alcohol Spectrum Disorder (FASD)? That’s more than the number of individuals diagnosed with Autism Spectrum Disorder, Cerebral Palsy, and Down Syndrome combined.
In recognition of FASD Awareness Month, the Sarnia-Lambton FASD Network is proud to present Living with FASD: Real Stories, Real Strength, a compelling panel discussion that brings together powerful voices from the FASD community.
This free event will feature nationally recognized FASD advocates Matt Sinclair, owner of All Relations Consulting, and RJ Formanek, founder of the Red Shoes Rock movement, alongside three local individuals living with FASD. Together, they will share their personal journeys and insights into navigating life with FASD.
WHAT: Living with FASD: Real Stories, Real Strength
WHO: Hosted by Sarnia-Lambton FASD Network
WHEN: September 25, 2025 | 5:00–7:00 PM
WHERE: Pathways Centre for Children, 1240 Murphy Rd Sarnia
COST: Free | Snacks will be provided
Panelists will explore key topics including:
- School support and educational experiences
- Employment challenges and workplace accommodations
- Building and maintaining friendships
- The role of family and advice for caregivers
- Transitioning into adulthood and self-advocacy
- Tools, strategies, and supports that make a difference
This session offers a unique opportunity to hear directly from those with lived experience and gain a deeper understanding of how communities can better support individuals with FASD.
All are welcome, caregivers, educators, service providers, and community members alike.
To register, please visit lcdspetrolia.ca
For more information, please contact Sarnia-Lambton FASD Network:
Karen Holland
Amy Burrows
About the Sarnia-Lambton FASD Network & FASD Resource Hub Sarnia-Lambton:
The Sarnia-Lambton FASD Network is a collective of 14 local organizations and professionals dedicated to aligning supports for individuals and families affected by FASD. The FASD Resource Hub provides solution-focused consultations for caregivers, families, and community members to increase knowledge, build skills, and strengthen competence in supporting those with FASD. Through collaboration, education, and advocacy, The S-L FASD Network and the FASD Resource Hub work to create a more informed and inclusive community.