For Your Information.......
Harris Study: "Justice For All"
President Clinton's address
on legislation for people with diabilities in the workplace
Great resource ;)
I work with the Florida Blueprint for School to Community Transition.
We have recently published the "Employer Resource
Guide, A Blueprint for Workforce Diversification." It is intended
for employers but provides useful resources for all individuals with disabilities
in Florida. If you will send me your snail mail address I'd be happy to
send you one. Anyone
else who is interested please email me directly. We also have another
resource guide coming out in about a month that will be directed towards
parents of individuals with disabilities transitioning
from school to adult life. Thanks,
Stacy Guerin
Florida Blueprint for School to Community Transition
FSU-CPSE
312-F Stone Building
Tallahassee, Fl 32306-4463
(850) 644-9510
WEBSITES
Mental Retardation
Disease Table Of Contents: Alternative names Definition Causes, incidence,
and risk factors
Prevention Symptoms Signs and tests Treatment Expectations (prognosis)
...
http://www.healthanswers.com/database/ami/converted/001523.html
SPED430G Web Page
Introduction to Mental Retardation. From 1977 to 1989, the rate of students
with special needs
identified as having mental retardation decreased from 26 percent to 11
percent of the ...
http://www.winona.msus.edu/AcademicDeptsFolder/CE/speced/MIIntro.html
U. S. International Council on Mental Retardation and Developmental
The United States International Council on Mental Retardation and Developmental
Disabilities . The
United States International Council on Mental Retardation and Developmental
...
http://thearc.org/council/council.html
American Association on Mental Retardation Homepage
American Association on Mental Retardation On behalf of AAMR leaders, staff
and members,
welcome to the AAMR Website. We've tried to prepare an on-line resource
that will augment our ...
http://www.aamr.org/
NATIONAL TRENDS
Braddock, D., Hemp, R., Lakin, K. C., & Smith G. (1994). Trends and
milestones: Continuing
expansion of financial resources for MR/DD services. Mental Retardation,
32(6), 446. The
http://web.syr.edu/~thechp/cinattre.htm
PUBLICATIONS
Birenbaum, A., & Cohen, H. J. (1993). On the importance of helping
families: Policy implications from a national study. Mental
Retardation, 31(2), 67-74.
This study is a companion to our 4-year study
(Birenbaum, Guyot, & Cohen, 1990) on financing health care for
individuals with autism or severe mental retardation.
We reported on nonmedical expenditures and opportunity costs
pertaining to maintaining a child or young
adult with serious developmental disabilities in the home or in residential
care and discussed policy implications for
assisting their families. We proposed that (a) personal care and family
support should be included in health care
requirements, (b) family-centered care shou.ld be promoted, (c) appropriate
programs and care should be provided for young
adults no longer in school, (d) financing and organizing of family
supports and subsidies should be administratively
simple, (e) Medicaid should be expanded to increase use of
home-and community-based services, and (f)
financial support should be provided to families.
Mlawer, M. A. (1993). Who should fight? Parents and the advocacy expectation.
Journal of Disability Policy Studies, 4(1),
105-116.
In the attempt to help parents become better
educational advocates for their children with disabilities, an "advocacy
expectation" has been created. This expectation
runs counter to the philosophy of normalization. The advocacy
expectation and its effects are critically
discussed. To counter the expectation and its effects, changes in professional
roles, funding priorities, and program development
are recommended.
Kennedy, M. J. (1994). The disability blanket. Mental Retardation, 32(1), 74-76.
The author of this article describes the ways
in which service providers look at and treat people with developmental
disabilities. Services such as Medicaid require
paperwork that breaks down every human activity into goals and
objectives, without the input of the recipient.
Services need to be provided in the context of individuals planning their
own goals and expectations, which would demonstrate
the respect and privacy that we all prefer.
Lutfiyya, Z. M. (1991). `A feeling of being connected': Friendships
between people with and without learning difficulties.
Disability, Handicap & Society, 6(3).
Recently, programmatic attempts to encourage
close ties between people with learning difficulties and typical citizens
have increased. It is believed that such relationships
will extend the assimilation of people with learning difficulties
into society. The researcher presents the
perspectives of four pairs of friends about the meaning of their friendships.
The informants shared similar ideas and expectations
about the characteristics of friendships in general. These
included its mutual, exclusive, and voluntary
nature; the right, obligations, and responsibilities of friends to each
other;
and the positive regard or affection found
between friends. Despite efforts on the part of service providers to support
the development of friendships between people
with and without learning disabilities, the biggest barriers for the
individuals in this study were the practices
of the human service system, which curtailed opportunities for people
which would have promoted the development
and maintenance of friendships.