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Epilepsy Foundation
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.
http://www.epilepsyfoundation.org |
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Families for Early Autism Treatment
FEAT (Families for Early Autism Treatment) is a non-profit organization of parents and professionals, designed to help families with children who have received the diagnosis of Autism or Pervasive Developmental Disorder (PDD NOS).
http://www.feat.org |
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Family and Advocates Partnership in Education
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.
http://www.fape.org |
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Federation of Families for Children's Mental Health
To address the unique needs of children and youth with emotional, behavioral or mental disorders from birth through transition to adulthood. To ensure the rights of full citizenship, support and access to community-based services for all children and youth with emotional, behavioral or mental disorders and their families. To provide information and engage in advocacy regarding research, prevention, early intervention, family support, education, transition services and other services needed by these children, youth and their families
http://www.ffcmh.org |
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Hospice Foundation of America
The Hospice Foundation of America is a nonprofit organization that promotes hospice care and works to educate professionals and the families they serve in issues relating to caregiving, terminal illness, loss and bereavement.
http://www.hospicefoundation.org |
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Hydrocephalus Association
The Hydrocephalus Association's mission is to provide support, education and advocacy for individuals, families and professionals.
http://www.hydroassoc.org |
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iCanOnline
iCanOnline brings together content, community and resources in one place that is easy to navigate and welcomes your input. This site is for individuals of all ages; however, it includes many resources relating to child and youth.
http://www.icanonline.net/ |
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Inclusion Network
The Inclusion Network is a non-profit organization whose staff and volunteers partner to promote inclusion of people with disabilities.
http://www.inclusion.org |
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International Dyslexia Organization
The International Dyslexia Association is an international, non-profit organization dedicated to the study and treatment of the learning disability, dyslexia. The IDA was established to continue the pioneering work of Dr. Samuel T. Orton, a neurologist who was one of the first to begin to identify dyslexia and develop effective teaching approaches.
http://www.interdys.org |
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International Rett Syndrome Association
The mission of the IRSA is: to support and encourage medical research to determine the cause and find a cure for Rett syndrome, to increase public awareness of Rett syndrome, and to provide informational and emotional support to families of children with Rett syndrome.
http://www.rettsyndrome.org |
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Internet Special Education Resources
ISER is a nationwide directory of professionals who serve the learning disabilities and special education communities. We help parents and caregivers find local special education professionals to help with learning disabilities and attention deficit disorder assessment, therapy, advocacy, and other special needs.
http://www.iser.com |
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Learning Disablities Council
The LDC addresses issues affecting children and adults with learning disabilities. Includes newsletter and forum.
http://www.cldinternational.org/ |
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Little People of America
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.
http://www.lpaonline.org |
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Lupus Foundation of America
The Lupus Foundation of America is the only nationwide voluntary organization exclusively serving the entire lupus community, including patients, their families, physicians, researchers, and the general public. Our mission is to educate and support those affected by lupus and find the cure.
http://www.lupus.org |
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