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The purpose of the registry is to provide basic information about persons with deaf-blindness in the United States. This information is to be used as a census, to identify the needs of persons with deaf-blindness, as a planning tool and for research purposes. All identifying information is confidential and written consent of the individual or guardian is required before it will be shared outside HKNC.

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There are several ways to register:

Download a form in WORD, fill out and mail to HKNC.

    Short form    Regular print    LARGE PRINT

    Long form    Regular print    LARGE PRINT

To fill out a registry form online, click here

For more information, contact your regional representative.

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