What I am hearing from you and from Carolanne, it seems like your mental health system is so different there than it is here.
I think there are some great things about the Canadian mental health system. However, there are lots of drawbacks. "Universal" healthcare often means that everyone has access to the services that are offered through the medical system, but that a lot of services just aren't offered.
For example, difficult child's psychiatrist visits are covered, but his therapist visits are not. Dental care, vision care, physiotherapy...unless you have an insurance plan through your employer, you have to pay the full price out of pocket. Same with prescriptions. It can be very confusing.
Can you tell me how comfortable you are (or aren't) with opportunities for growth for your son within the system? Will the place he is at now try to work with him on becoming more independent? Or will that happen in a transitional situation to a different program? Do you have confidence that he will move to an appropriate place when he is ready to move on, or do you worry that they will be done with being able to help him where he is and just shove him out the door (like they would here...)?
The government-run organizations didn't have anything (other than jail) that could accommodate difficult child's very difficult combination of diagnoses. Bipolar, Aspergers, Obsessive Compulsive Disorder (OCD), and the aftermath of years of abuse by his biomom before husband was finally able to have her denied access...they've taken their toll on my poor boy.
He has been asked to leave 15 different schools in the last 10 years, INCLUDING a private school which specialized in autistic children. At Lunch Hour. On his FIRST Day of school!
I am very comfortable with my son's opportunities for growth and development in his current living situation. Honestly, it's the best chance he's got to have any sort of rewarding or happy life. They will support him as he grows and as his needs change, give him as much independence as he can handle, and be there to support him for those things he can't manage by himself.
The reason for my confidence is that husband and I put it all together. We spent months interviewing and hiring staff, and worked with his treatment team (therapist, psychiatrist, lawyer, the school board, the family centre, his autism consultant, etc.) to put a viable program together. It is working well for him because it is designed for him. So it will definitely meet his needs.
The frustration lies in the fact that we had to put this all together, because the "official" service providers couldn't do it. I think about the struggles we've had to line this all up, then I think about all the parents out there who can't do the same for their children, and I weep.