National Child Count

The National Deafblind Child Count provides extensive information on the population of children identified with deafblindness in the United States, aged birth through 21. Data includes state and national information on

• Population demographics (age, race/ethnicity/gender)
• Type and severity of vision and hearing loss
• Causes of deafblindness
• Presence of additional disabilities
• Educational setting
• Living setting

The data is collected by state deafblind projects across the country and compiled and reported by NCDB. Each year, every state deafblind project updates its annual count by providing information about new children who were identified over the course of the year, updating or confirming information on currently active children, and determining those who have exited special education or are no longer eligible to receive state project services.

The count, which began in 1986, serves as a common vehicle to identify trends and needs within the population. This information is then used to guide the development of technical assistance initiatives and services. It was initially requested by the U.S. Department of Education to examine the discrepancy between the state deafblind project child counts and the Department’s Office of Special Education Program’s annual Special Education Child Count, which counts children as deafblind only when deafblindness is a child’s sole disability. In contrast, the National Deafblind Child Count also includes children and youth who are deafblind and have additional disabilities. This is an important distinction because approximately 90% of children and youth on the National Deafblind Child Count have one or more additional disabilities. 

If you are a state deafblind project staff member looking for information on how to conduct and report your child count, please visit our Child Count Management page.