(Sec. 4) Requires information and education activities to be culturally competent. Allows a lead agency coordinating activities at the state level to include respite care for caregivers. Allows the use of research centers or networks for the provision of training in respite care and for research to determine practices for interventions to improve the health of individuals with ASD.
(Sec. 5) Revises responsibilities of the Interagency Committee concerning:
inclusion of school- and community-based interventions in the Committee summary of advances,
monitoring of ASD research and federal services and support activities,
recommendations to the Director of the National Institutes of Health regarding the strategic plan,
recommendations regarding the process by which public feedback can be better integrated into ASD decisions,
strategic plan updates and recommendations to minimize duplication, and
reports to the President and Congress.
Revises Interagency Committee membership requirements to specify additional federal agencies that might be represented and to modify the non-federal membership.
(Sec. 6) Modifies requirements for reports by the Secretary on ASD activities. Adds a requirement for a report to Congress concerning young adults with ASD and the challenges related to the transition from existing school-based services to those available during adulthood.
(Sec. 7) Authorizes appropriations to carry out the developmental disabilities surveillance and research program, the education, early detection, and intervention program, and the Interagency Committee for FY2015-FY2019.