This bill mandates that health care facilities in New Jersey report all known and suspected cases of amyotrophic lateral sclerosis (ALS) to the Department of Health. The reporting must be done in a manner that adheres to federal and state privacy laws, ensuring confidentiality. The Department of Health will specify the reporting process and is responsible for recording and compiling the information received for research purposes only.

The bill aims to enhance the understanding and research of ALS by creating a systematic approach to data collection from health care facilities. It is designed to take effect immediately upon enactment, emphasizing the urgency of addressing this neurological condition through improved data reporting and research efforts.