The public section offers information from NIMH about the symptoms, diagnosis, and treatment of mental illnesses. Included are brochures and information sheets, reports, press releases, fact sheets, and other educational materials.
The objectives of this site include promoting the awareness of children with special needs of all kinds; promoting brighter futures for them and their families; and to provide support and education resources for their families, and those who support them.
VSA arts is an International organization that creates learning opportunities through the arts for people with disabilities. The organization offers arts-based programs in creative writing, dance, drama, music and the visual arts implemented primarily through our vast affiliate network in 41 states and the District of Columbia and 86 international affiliates in 83 countries. VSA arts' programs now serve 4.3 million Americans and 1.3 million people in other parts of the world.
The Epilepsy Foundation is a national, charitable organization, founded in 1968 as the Epilepsy Foundation of America. The only such organization wholly dedicated to the welfare of people with epilepsy, our mission is simple: to work for children and adults affected by seizures through research, education, advocacy and service.
Sidran is a nonprofit charitable organization devoted to education, advocacy, and research to benefit people who are suffering from injuries of traumatic stress. Whether caused by family violence, crime, disasters, war, or any other overwhelming experience, the disabling effects of trauma can be overcome with understanding, support, and appropriate treatment.
The National Fathers Network (NFN) advocates for and provides resources and support to all men who have children with special needs through: Development of national and statewide databases of fathers from diverse ethnic, racial, and geographic backgrounds; Development of father support and mentoring programs; Development of curriculum (monographs and videos) designed to enhance the involvement of fathers in the home and service provision (i.e., health care settings, schools);
Little People of America, Inc. (LPA), will assist dwarfs with their physical and developmental concerns resulting from short stature. By providing medical, environmental, educational, vocational, and parental guidance, short-statured individuals and their families may enhance their lives and lifestyles with minimal limitations. Through peer support and personal example, our members will be supportive of all those who reach out to LPA. Lastly, by networking with national and international growth-related and genetic-support groups, LPA will enhance knowledge and support of short-statured individuals.
Our-Kids is a "Family" of parents, caregivers and others who are working with children with physical and/or mental disabilities and delays. We call the list "Our-Kids". While it isn't exactingly descriptive, it avoids the pitfalls of labeling our kids anything but what they most certainly are: The wonderful little people in our lives.
The Family & Advocates Partnership for Education (FAPE) Web site is a new project which aims to inform and educate families and advocates about the Individuals with Disabilities Education Act of 1997 and promising practices.
Outcomes of disability research should offer great utility to people with disabilities and their families, practitioners engaged in various types of disability service delivery, scientists and researchers, policymakers, journalists, healthcare providers, employers, and many others.
Health /
Conditions_and_Diseases /
Genetic_Disorders
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