Early Identification of Infants Who Are Deaf-Blind

Early Identification of Infants Who Are Deaf-Blind

Author: Peggy Malloy

Publisher:

Published: 2009

Total Pages: 21

ISBN-13:

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Experiences that occur during the earliest years of life critically impact children's abilities to learn, move, and interact with others. This is especially true for children with severe sensory and multiple disabilities, for whom physical, communicative, cognitive, social, and emotional developmental domains are deeply intertwined. In recognition of the importance of appropriate early learning experiences for children who are deaf-blind, the National Consortium on Deaf-Blindness (NCDB) selected early childhood identification and intervention as one of five focus areas for the formation of partnerships to promote initiatives aligned with federal priorities to meet the most frequently identified needs of children and youth who are deaf-blind and their families and service providers. In July 2007, an NCDB work group was established to lead activities in the early childhood identification and intervention focus area. The initial tasks of the group were to gather information about current needs and practices and to identify potential state and national entities interested in forming partnerships with NCDB on early childhood initiatives. The following three primary activities were conducted to accomplish these tasks: (a) a survey of state deaf-blind project directors; (b) focus group interviews with state deaf-blind project personnel in eight states; and (c) an extensive literature review. Collectively, the findings from these activities indicate a need for new strategies to improve early identification of infants and young children who are deaf-blind and increase referrals of them to state deaf-blind projects. As a result, the work group, now called the Early Identification Work Group (EIWG), narrowed its focus to efforts designed to promote early identification and referral. This report describes the findings that led to this decision and discusses future directions for NCDB as it forms partnerships to develop and evaluate initiatives to improve early identification of children who are deaf-blind.


Early Identification and Referral of Infants Who Are Deaf-Blind

Early Identification and Referral of Infants Who Are Deaf-Blind

Author: Barbara Purvis

Publisher:

Published: 2014

Total Pages: 25

ISBN-13:

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Experiences that occur during the earliest years of life critically impact children's abilities to learn, move, and interact with others. This is especially true for children with severe sensory and multiple disabilities, for whom physical, communicative, cognitive, social, and emotional developmental domains are deeply intertwined. In recognition of the importance of appropriate early learning experiences for children who are deaf-blind, in 2006 the National Consortium on Deaf-Blindness (NCDB) selected early childhood identification and intervention as one of five focus areas for the formation of partnerships to promote initiatives aligned with federal priorities to meet the most frequently identified needs of children and youth who are deaf-blind and their families and service providers. In July 2007, an NCDB work group was established to lead activities in the early childhood identification and intervention focus area. The initial tasks of the group were to gather information about current needs and practices and to identify potential state and national entities interested in forming partnerships with NCDB on early childhood initiatives. The following three primary activities were conducted to accomplish these tasks: (a) a survey of state deaf-blind project directors; (b) focus group interviews with state deaf-blind project personnel in eight states; and (c) an extensive literature review. Collectively, the findings from these activities indicate a need for new strategies to improve early identification of infants and young children who are deaf-blind and increase referrals of them to state deaf-blind projects. As a result, the work group narrowed its focus to efforts designed to promote early identification and referral. This report describes the findings that led to this decision and discusses current initiatives undertaken by NCDB and state deaf-blind projects to improve early identification of children who are deaf-blind and referral to appropriate services.


Remarkable Conversations

Remarkable Conversations

Author: Barbara Miles

Publisher: eBookIt.com

Published: 1999

Total Pages: 645

ISBN-13: 1947954857

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This book addresses the needs of children of all abilities, from those who use nonlinguistic forms of communication such as objects or body movements to those who use linguistic forms such as sign language or writing.


The 2008 National Child Count of Children and Youth Who Are Deaf-Blind

The 2008 National Child Count of Children and Youth Who Are Deaf-Blind

Author: National Consortium on Deaf-Blindness (NCDB)

Publisher:

Published: 2009

Total Pages: 30

ISBN-13:

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The "National Child Count of Children and Youth who are Deaf-Blind" is the first and longest running registry and knowledge base of children who are deaf-blind in the world. It represents a 25 year collaborative effort between the National Consortium on Deaf-Blindness (NCDB), its predecessors and each state/multi-state deaf-blind project throughout the country, as well as those projects funded in the Pacific Trust territories--the Virgin Islands and Puerto Rico. It has been collaboratively designed and implemented as the common vehicle to meet federal grant requirements for both the state/multistate and national technical assistance projects and serves as a common data collection and reporting mechanism for use across the country. Consistent with the priorities under which NCDB, its predecessors, and the state/multi-state projects are funded, this national child count is used to identify national and state technical assistance needs for children and youth who are deaf-blind, their families, and the service providers and systems which serve them. This is the first year in which the number of children/youth for which "Further Testing Needed" category has been analyzed for multiple years. The number of children/youth for which further vision and/or hearing testing is needed has decreased from 2,873 in 2007 to 772 in 2008. This 2008 report provides the opportunity for early identification, intervention and the provision of instructional services aimed at the unique needs of young children and students who are deaf-blind and is a critical component that cannot be lost. [For the 2007 Deaf-Blind Child Count, see ED545208.].


Deaf-blind Infants and Children

Deaf-blind Infants and Children

Author: John M. McInnes

Publisher: University of Toronto Press

Published: 1993-01-01

Total Pages: 306

ISBN-13: 9780802077875

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This is a comprehensive reference guide for teachers, parents, and paraprofessionals working or living with children who are both deaf and blind. It provides day-to-day guidance and suggestions about techniques and methods for assessing children with multi-sensory deprivation, and for devising programs to help them cope.


A Guide to Planning and Support for Individuals who are Deafblind

A Guide to Planning and Support for Individuals who are Deafblind

Author: John M. McInnes

Publisher: University of Toronto Press

Published: 1999-01-01

Total Pages: 598

ISBN-13: 9780802042422

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Leading experts address such problems as identification of deafblindness, planning and intervention, development, family support, and education for parents and professionals who work with people who have been deafblind from birth or a very early age.


The 2010 National Child Count of Children and Youth Who Are Deaf-Blind

The 2010 National Child Count of Children and Youth Who Are Deaf-Blind

Author: National Consortium on Deaf-Blindness (NCDB)

Publisher:

Published: 2011

Total Pages: 35

ISBN-13:

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The National Child Count of Children and Youth who are Deaf-Blind is the first and longest running registry and knowledge base of children who are deaf-blind in the world. It represents a 25-plus year collaborative effort between the National Consortium on Deaf-Blindness (NCDB), its predecessors and each state deaf-blind project throughout the country, as well as those projects funded in the Pacific Trust territories--the Virgin Islands and Puerto Rico. It has been collaboratively designed and implemented as the common vehicle to meet federal grant requirements for both the state/multi-state and national technical assistance projects and serves as a common data collection and reporting mechanism for use across the country. Consistent with the priorities under which NCDB, its predecessors, and the state/multi-state projects are funded, this national child count is used to identify national and state technical assistance needs for children and youth who are deaf-blind, their families, and the service providers and systems which serve them (Killoran, 2007). The child count is conducted each year to supplement the Office of Special Education Programs' (OSEP's) Federal Part C and Part B Child Counts (Special Education Child Count), which include children as deaf-blind only when deaf-blindness is their single disability. Some of the emerging trends identified in the 2010 Deaf-Blind Child Count include: (1) The overall numbers of children identified as deaf-blind has decreased over the past several years as projects continue to "clean" their databases. This trend is consistent with the time period of 1996-1998 when similar efforts were undertaken; (2) The prevalence of CHARGE Syndrome has increased significantly over the past five years. The prevalence of Usher Syndrome reached a peak in 2007 and has decreased over the past three years; (3) The percentage of children/youth identified as needing further vision testing has decreased from 15.6% to 7.3%.; and (4) The percentage of children/youth identified as needing further hearing testing has decreased from 20.4% to 8.9%. [For the 2009 Deaf-Blind Child Count, see ED545210.].


Lewis's Child and Adolescent Psychiatry

Lewis's Child and Adolescent Psychiatry

Author: Andrés Martin

Publisher: Lippincott Williams & Wilkins

Published: 2017-08-04

Total Pages: 2821

ISBN-13: 1496367685

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For 25 years, Lewis's Child and Adolescent Psychiatry has been the cornerstone of every child and adolescent psychiatrist’s library. Now, three colleagues of Dr. Lewis at the world-renowned Yale Child Study Center, have substantially updated and revised this foundational textbook for its long-awaited fifth edition, the first in ten years. Encyclopedic in scope, it continues to serve as a broad reference, deftly encompassing and integrating scientific principles, research methodologies, and everyday clinical care.