The Scoliosis Association, Inc. is a non-profit, volunteer non-medical organization. Since 1974, we have been helping those with scoliosis by providing information and having support groups and information lines.
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.
Early intervention and treatment offers the best chance for children with bipolar disorder to achieve stability, gain the best possible level of wellness, and grow up to enjoy their gifts and build upon their strengths. Proper treatment can minimize the adverse effects of the illness on their lives and the lives of those who love them
This site serves as the gateway to all state and local United Cerebral Palsy chapters.
The primary mission of the Special Friends Foundation is to enable families to understand quickly what Rubinstein-Taybi Syndrome (RTS) is all about and what resources are available.
The National Center to Improve Practice was federally funded project to improve educational outcomes for students with disabilities by promoting the effective use of assistive and instructional technologies among educators and related personnel serving these students.
Conducts, fosters, coordinates, and guides research on the causes, prevention, diagnosis, and treatment of neurological disorders and stroke, and supports basic research in related scientific areas.
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
The Alexander Graham Bell Association for the Deaf and Hard of Hearing is one of the world's largest membership organizations and information centers on hearing loss and the auditory approach. AG Bell focuses specifically on children with hearing loss, providing ongoing support and advocacy for parents, professionals and other interested parties.
We believe that the most effective strategy for expanding educational opportunities for individuals with disabilities is through Universal Design for Learning. Our work now focuses the development of learning models, approaches, and tools that are usable by a wide range of learners and CAST's impact is seen locally, nationally, and internationally.
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