Website: https://daledileo.com
Sheltered workshops and families are not the only options. Once people are desegregated, there are hundreds of options, depending on our needs and interests. The response assumes that people with disabilities can’t function on our own, when we usually can. For example, there are sometimes Medicaid Waiver programs that pay for caregivers, including family members.
My son leaves school this year. He has severe autism and he needs supervision 24/7 (including holidays). While he likes to get out in the community, he does not like to be in the community for more than a few hours per day. He would like to spend most of his day focused on a task with unobtrusive supervision. He does not mind being with others who are similarly engaged … possibly with shared supervision.
We are trying to find things for him to do during the working day for two reasons … first, because he does not want to sit around at home all day, and second because I would like to continue working and not have to be his carer for all but (up to) 12 hours per week of “community access” that the ACT Government says it will fund. We are told that under social role valorisation principles and practice he would get 8 hours of “community access” instead of 12 hours. He would be isolated from his peers (recall that freedom of association is a basic human right) which means the service costs more.
There is no place for our son in open employment. There are no supported employment places in the ACT for students who finish school in 2011. We know of people with severe autism who left school over a decade ago and have never ever been offered employment of any form.
I recognise that many people with a disability and their communities benefit from desegregation. But it isn’t for everyone.
Unfortunately, there are people for whom desegregation practices deny them freedom of association and mean no opportunities at all. Their needs must also be met.
it’s alot easier to say stop referrals to the workcenters than to actually do it. i’d be interested in that solution. when we received $ to move people from agency to community based we worked off a 1:8 ratio and the initial staff person could handle a few more and then when we place another 4 or so we converted a staff to community. we did this for a number of years. now the issue the individuals remaining would require a 1:4 ratio or less and they are currently served in the workshop at a 1:20 ratio. coming up with the additional $ for a lower ratio is the challenge.
Anonymous
I agree . . BUT . . the reality is, a LOT of families HAVE to work. Who will care for the person with a significant disability during the day? I think we should utilize YMCA’s, gyms, libraries, malls, etc. BUT, before we close day programs and send some families into worse poverty, leading to stress and possible abuse of the person with a disability, we have got to make sure they are getting assistance with community/home care. What’s the solution with $50.00/day Day Program rates vs $15-$20.00/hour personal care rates? Please design a “solution” before we through the most needy families into the streets . . .