Thanks to the Minister. This is the impression adults with FASD often have. I didn’t accuse the department of that. Thanks for that thorough description of the services available.

Families put a tremendous amount of time, resources and love into caring for children with FASD who are now adults. When these children grow up, they often remain in the care of their families. Caring for someone with FASD can be difficult, as the Minister knows, and the families become highly stressed and the person confused. They do not know if there is help or how to find it or access it. So perhaps it’s a communications issue.

What measures are in place to reach out to the families who have children, especially adult children, with FASD and help them access the services they need?