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Congress passed
the first Act to benefit people with developmental disabilities and
their families in 1963. It has been amended several times, most recently
in 2000. In 1963, the number of people with developmental disabilities living in crowded institutions was still on the rise. The census of people living in institutions peaked in 1967 at approximately 195,000. By 1996 the numbers were down to about 60,000 people in institutions, and the census continues to drop. VISION OF THE DD ACT Individuals with developmental disabilities and their families have opportunities and support to:
MISSION OF THE DD ACT Individuals with developmental disabilities and their families participate in the design of and have access to:
GOALS OF THE DD ACT To help individuals with developmental disabilities and their families increase:
So that they can:
The DD Act provides federal money to the states to fund State Councils on Development Disabilities, University Centers for Excellence, Protection and Advocacy Systems, and Projects of National Significance. COUNCILS ON DEVELOPMENTAL DISABILITIES ("DD Councils") Developmental Disabilities Councils consist of volunteers appointed by governors, over half of whom must be people with developmental disabilities or their family members. They engage in systemic change, capacity building, and advocacy activities that:
UNIVERSITY CENTERS FOR EXCELLENCE IN DEVELOPMENTAL DISABILITIES EDUCATION, RESEARCH AND SERVICES Centers for Excellence promote the health and safety of individuals with disabilities by acting as a national pipeline of highly-skilled professionals who are trained specifically to work with individuals with developmental disabilities and their families. Centers also produce new knowledge in the field of developmental disabilities through research and model program development and evaluation. Centers are recognized as leaders in every major disability related initiative that has emerged over the past 20 years including:
In Oregon the Centers are located at the University of Oregon and Oregon Health Sciences University. PROTECTION AND ADVOCACY SYSTEM ("P&As") The Protection
and Advocacy System is a comprehensive network of programs which provide
legally-based representation for people with disabilities. Congress
created the P&A programs upon learning about the abusive, neglectful
and inhumane living conditions at Willowbrook, a New York State institution
for people with developmental disabilities. Congress recognized that a federally-directed system of legal advice was necessary "to ensure the humane care, treatment, habilitation and protection of" people with mental retardation and other developmental disabilities. In Oregon the P&A agency is the Oregon Advocacy Center (OAC). PROJECTS OF NATIONAL SIGNIFICANCE Projects of National Significance support national and state policy and play a significant role in assuring health, safety, rights, and employment for individuals. Examples of projects include:
Congress funds Projects of National Significance to collect information and measure our nations success at ensuring safe, healthy, meaningful lives for our citizens with developmental disabilities. The data provides important guidance for governors and state legislators to evaluate, plan and implement policy to achieve desired outcomes. |
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