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So, as we went through the process, we did
keep data in what we felt were key areas. [This included] the number
of people who were working, the
number
of hours
[that]
they
were
working,
how much money they earned, whether or
not they had benefits including health insurance or vacation, and their job
satisfaction. Since then, we’ve started collecting more data based on
quality of life as opposed to satisfaction. We learned that as people become
more aware of what’s available in the community, in terms of community life,
they sometimes become more dissatisfied with their lives. So satisfaction
may not always be a useful indicator in terms of how our services are
affecting people. We have found it more helpful to look at [the] quality of
people’s lives.
The other thing that I think is very important is to involve people outside
of the organization in the system-change effort including people that are
served by the agency. We did form a Community Employment Advisory Group that
helped us through the process. That group is still meeting to help us
discover alternate and more creative ways to help people get jobs and to
support them in those jobs. We also involved the advocacy organizations in
meetings and different kinds of presentations on our planning groups, as
well as our funders, and, of course, families and people with disabilities.
Employers have also been a part of the Advisory Group, which has been
helpful. back to top
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