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The Enable Newsletter is prepared by the United Nations Secretariat for the Convention on the Rights of Persons with Disabilities (SCRPD) hosted by the United Nations Department of Economic and Social Affairs (DESA). Input has been received from by UN offices, agencies, funds and programmes, as well as from civil society. It is also available on-line at: http://www.un.org/disabilities.

The mission of the National Down Syndrome Society is to be the national advocate for the value, acceptance and inclusion of people with Down syndrome. The NDSS is committed to being the national leader in enhancing the quality of life, and realizing the potential of all people with Down syndrome. 300 affiliate groups across the country. One of the largest non-government supporters of Down syndrome research in the United States

National Program for Playground Safety - NPPS is the leader in research, training, and development of S.A.F.E. play areas! NPPS' mission is to help the public create safe and developmentally appropriate play environments for children. A premier non-profit organization in the United States delivering training and services about outdoor play and safety. NPPS serves as child-advocates on issues pertaining to playground safety before government and regulatory agencies. NPPS helps the public create, renovate, and maintain safe and developmentally appropriate play environments for children by providing professional, well-researched, highly informative, practical and user-friendly services, and programs to fulfill this mission. NPPS serves as a national resource for the latest educational and research information about playground safety.

National Survey of children with Special Halth Care Needs CSHCN - Data Resource Center - The purpose of The Data Resource Center for Child and Adolescent Health (DRC) is to advance the effective use of public data on the health and health-related services for children, youth and families in the United States. The DRC does this by providing hands-on access to national, state, and regional data findings as well as technical assistance in the collection and use of this data by policymakers, program leaders, advocates and researchers in order to inform and advance key child and youth health goals. Currently, the DRC website includes national and state-based data on over 100 indicators from the National Survey of Children's Health (NSCH) and the National Survey of Children with Special Health Care Needs (NS-CSHCN). The DRC's easy-to-use interactive search feature allows users to select, view, compare, and download national survey data results for every state and HRSA region.

The National Disability Rights Network (NDRN) is the nonprofit membership organization for the federally mandated Protection and Advocacy (P&A) Systems and Client Assistance Programs (CAP) for individuals with disabilities. Collectively, the P&A/CAP network is the largest provider of legally based advocacy services to people with disabilities in the United States.

NACD provides neurodevelopmental evaluations and individualized programs for children and adults, updated on a quarterly basis. As a family-centered organization. Stresses parent training and parent implementation of the program. Eclectic organization, gathering and utilizing the newest strategies that yield success and incorporating them into programs custom-designed for each client. Support provided to families through video reviews, e-mail and telephone sessions. Chapters can be found across the United States.

National Newborn Screening and Genetics Resource Center web site: GeNeS-R-US, (Genetic and Newborn Screening Resource Center of the United States). The National Newborn Screening and Genetics Resource Center (NNSGRC) is a cooperative agreement between the Maternal and Child Health Bureau (MCHB), Genetic Services Branch and the University of Texas Health Science Center at San Antonio (UTHSCSA), Department of Pediatrics. Provides information and resources in the area of newborn screening and genetics to benefit health professionals, the public health community, consumers and government officials.

MIUSA works in four main areas to provide programs and services including:National Clearinghouse on Disability & Exchange (NCDE) International Development & Disability MIUSA International Exchange Programs Women, Disability and DevelopmentSince 1995. Serves as the National Clearinghouse on Disability and Exchange (NCDE), a project sponsored by the Bureau of Educational and Cultural Affairs of the United States Department of State and managed by MIUSA to: educate people with disabilities and related organizations about international exchange opportunities; increase the participation of people with disabilities in the full range of international volunteer, study, work and research programs; advise international exchange organizations about the Americans with Disabilities Act

The National Disability Rights Network (NDRN) is the nonprofit membership organization for the federally mandated Protection and Advocacy (P&A) Systems and Client Assistance Programs (CAP) for individuals with disabilities. Collectively, the P&A/CAP network is the largest provider of legally based advocacy services to people with disabilities in the United States.

World's largest community based organization of and for people with intellectual and developmental disabilities. It provides an array of services and support for families and individuals. Devoted to promoting and improving supports and services for all people with intellectual and developmental disabilities.

The American Association of People with Disabilities (AAPD), the country's largest cross-disability membership organization, organizes the disability community to be a powerful voice for change - politically, economically, and socially. AAPD was founded in 1995 to help unite the diverse community of people with disabilities, including their family, friends and supporters, and to be a national voice for change in implementing the goals of the Americans with Disabilities Act (ADA).

Life Without Limits is a national movement to empower people with disabilities to envision and build a better future for themselves, their community, and society. A platform to promote projects that advance the health and well-being of people with disabilities, three initial projects underscore its key focus areas My Child Without Limits (early childhood intervention); Ruby's Bequest (care giving); and Emerging Technologies for Independent Living (housing & technology) United Cerebral Palsy (UCP), a pivotal advocate for people with all disabilities, is leading the Life Without Limits initiative in cooperation with former Congressman, and lifelong advocate for people with disabilities, Tony Coelho ."

"Multi-disciplinary collaboration of scientists and scholars from universities across the United States and Canada designed to bring the science of early childhood and early brain development to bear on public policy decision-making. The mission of the Council is to synthesize and communicate science to help inform policies that promote successful learning, adaptive behavior, and sound physical and mental health for all young children