CACP Research Foundation

It is our mission to generate awareness and education, promote advocacy, and support research treatment options for CACP syndrome, and related rare diseases and disabilities.

Volunteers may assist with community events that support awareness, education, and advocacy efforts for CACP and other rare diseases and disabilities. Volunteers may also assist with projects that support awareness, education, and community support for medical providers, educators, and patients and families within the community impacted by rare disease and disability.