
Civilian Count is a public participation campaign developed to ensure that individuals experiencing unexplained neurological or sensory disturbances are represented in national data and research efforts. By encouraging widespread survey participation, Civilian Count helps quantify how many people are affected, where patterns may be occurring, and what types of experiences are being reported. This initiative strengthens the foundation for advocacy, resource allocation, and future support systems by making sure civilian experiences are documented, visible, and included in the broader conversation.