I am writing as a long-time parent of adult sons who live with the challenging impacts of trauma and Fetal Alcohol Spectrum Disorder and who have been affected by the multi-generational legacy of Indian Residential Schools and colonial treatment of Canada’s First Peoples. I am writing to share my profound personal experience after a week of sadness when I was struggling to find words.
This post is part of our new Feature Friday series called Spotlight on Service Providers. Over the next year, we will be featuring organizations and initiatives across Canada that provide much-needed supports and services for individuals with FASD and their families. Who We Are In Saskatchewan, a group of dedicated parents came together to form the FASD Network (the … Read More
Written by Dr. Katie Birnie I was thrilled to host CanFASD’s webinar on Pain as Experienced by People with FASD in November 2020 in my role as Assistant Scientific Director of Solutions for Kids in Pain (SKIP). SKIP is a knowledge mobilization network based at Dalhousie University, co-directed by Children’s Healthcare Canada, and funded by the Networks of Centres of Excellence … Read More
By engaging persons with lived experience, we were able to identify and inform service enhancement opportunities in FASD awareness, FASD assessment and diagnosis, FASD care planning and transitions, community-based FASD services and supports, addiction and mental health services, housing support services, education services, and correctional services.
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