Language and Communication of Deaf and Hard of Hearing Children

The scope of this Practice Portal page is children ages birth–18 years who are either born deaf or hard of hearing or acquire hearing loss later in childhood. It focuses on language and communication considerations following initial comprehensive audiologic assessment and identification.

For information specific to hearing; hearing screenings/assessments; diagnosis; and related technologies, interventions, and accommodations (e.g., hearing aids, implantable hearing devices, classroom acoustics, interpreters), refer to the Language and Communication of Deaf and Hard of Hearing (DHH) Individuals Evidence Map and relevant Clinical Topics in the Practice Portal.

For discussion of terminology used in this Practice Portal page, see Hearing-Related Topics: Terminology Guidance.

Children who are identified as deaf and hard of hearing (DHH) are diverse. They have differences in their hearing thresholds, ages of identification, medical and educational histories, linguistic backgrounds, and cultural identities. Some children are identified pre- or perilingually (before fully developing language and/or speech); others develop hearing loss or are identified postlingually (after acquiring language and/or speech).

There is no “one size fits all” when discussing language and communication of children who are identified as DHH. DHH children use various languages, communication tools, systems, and technologies. They receive education and support services in a variety of settings and have diverse experiences with DHH peers and adults.

Early exposure and consistent access to a complete language (signed, spoken, both, or other/augmentative and alternative communication [AAC]) are critical for communication development for all children. Role models in a language-rich environment along with early auditory and/or visual access to language using tools (e.g., eyeglasses, hearing technology) to support family-centered goals provide a strong foundation for optimal cognitive, communication, academic, social, and vocational outcomes (Joint Committee on Infant Hearing [JCIH], 2019; Kushalnagar et al., 2010; Loy et al., 2010; Niparko et al., 2010; Tobey et al., 2013).

Child and family/care partner needs, goals, and preferences guide discussions about their desired outcomes and the family-centered supports and services needed to achieve those outcomes. Families may explore multiple languages and communication methods with their child. A child’s best mode of communication (preferred and most effective) may change over time with changes in the child’s needs, communication contexts, and educational settings (National Center for Hearing Assessment and Management, 2018). Audiologists and speech-language pathologists (SLPs) present evidence-based information about all languages, communication tools, and educational programs at the time of identification and as the child develops so that families/care partners can make informed, evidence-based decisions to meet the desired outcomes and dynamic needs of their children as they transition toward adulthood (American Speech-Language-Hearing Association [ASHA], 2013; JCIH, 2019; White, 2018).

Content Disclaimer: The Practice Portal, ASHA policy documents, and guidelines contain information for use in all settings; however, members must consider all applicable local, state and federal requirements when applying the information in their specific work setting.

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