THIS IS THE MAIN PAGE OF "NATIONAL REGISTRY"

(Go to: Page Menu)

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.

__________________________________________________________

To fill out a registry form, click here

For more information, contact your regional representative.

__________________________________________________________

Menu Choices in NATIONAL REGISTRY:

Return To Top

National Registry Form

Home Page

Copyright © 2008 Helen Keller National Center. All rights reserved.