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Borfitz-Mescon, Jeanne – Exceptional Parent, 1988
The parent of a severely handicapped child encourages parents to prepare written care plans when leaving a child with others for a respite period. (DB)
Descriptors: Child Rearing, Parent Role, Planning, Respite Care
Peer reviewed Peer reviewed
Sullivan, Ruth Christ – Journal of Autism and Developmental Disorders, 1979
An article is presented on the "burn-out" of parents, particularly those of autistic children (i.e., the exhaustion of their psychological and/or physical resources as a result of long and intense caring for their children), along with the comments and responses of five parents and professionals. (DLS)
Descriptors: Autism, Coping, Emotional Adjustment, Parent Attitudes
Stanzler, Margaret – Exceptional Parent, 1982
The author, the mother of a cerebral palsied child, considers the conflicts which arise for parents in using respite care. Noted among the reasons why respite care use is difficult for parents are feelings of guilt, conflicts in mothering, self-punishment for having a handicapped child, identification with the child, and separation from the child.…
Descriptors: Disabilities, Emotional Adjustment, Parent Attitudes, Parent Child Relationship
Peer reviewed Peer reviewed
Pivato, Emma – Mental Retardation and Learning Disability Bulletin, 1986
A parent of a severely handicapped daughter living at home in Alberta, Canada, discusses the need for family support systems such as respite care, reduced rent for needed equipment or vehicles, and financial aid to allow normal family living. Government and family are seen to share responsibility for the handicapped individual. (DB)
Descriptors: Family Financial Resources, Family Problems, Government Role, Needs
Focal Point, 1988
The newsletter offers perspectives on the provision of family support services for families with disabled members. An introductory article by Madeleine Will, Assistant Secretary for Special Education and Rehabilitative Services, stresses the impressive coping skills exhibited by many such families and their relationship to service professionals.…
Descriptors: Community Programs, Coping, Disabilities, Family Problems
Gullerud, Ruth A. – Bureau Memorandum, 1979
A review of the changes in the treatment of and attitudes toward cerebral palsy in the last 30 years is presented. The author stresses the need for early diagnosis and evaluation, day care (especially respite care), counseling, transportation, special living arrangements, and integration of this population. (PHR)
Descriptors: Attitude Change, Cerebral Palsy, Counseling, Evaluation
Salisbury, Christine; Griggs, Peter A. – Journal of the Association for the Severely Handicapped (JASH), 1983
Considerations related to the design and development of a respite care service delivery network for families of developmentally disabled persons are addressed. A five-component model for developing a respite care service network is presented, focusing on the need for competency-based service-provider training and parent involvement. Lastly,…
Descriptors: Coping, Delivery Systems, Developmental Disabilities, Family Problems
Peer reviewed Peer reviewed
McCormick, Linda; Holden, Rita – Young Children, 1992
Describes developmental and behavioral characteristics of homeless young children and their parents. Reports on how states and communities are attempting to meet the early education and care of young children in homeless families. Discusses the needs or problems that early education and care programs that include homeless children should address.…
Descriptors: Childhood Needs, Day Care, Family Programs, Guidelines