We believe in involving autistic individuals and their caregivers in every step of diagnosis, research, and management of ASD. Without their invaluable insight, our work would lack the necessary community input to make lasting change.
We offer practica, workshops, symposia, and an annual conference to provide continuing education on critical areas of need to clinicians and professionals who work with individuals with autism.
We offer seed grants to aid autism researchers in the development of competitive federal research and training grant applications. Additionally, we will develop a state-wide ASD research database to connect autistic individuals and their families with autism researchers.
Through collaborative research, we can continue to refine best practices in the diagnosis and management of autism. The NJACE aims to be a resource for researchers throughout the development, implementation, and analysis of research.
Individuals with autism and their caregivers should be involved in research projects from start to finish. The NJACE plans to develop a state-wide ASD research database to serve as the hub for researchers, individuals with autism, and their caregivers to connect throughout the development, implementation, and analysis of research.