The bill establishes a framework for supported decision-making agreements aimed at enhancing the autonomy and self-determination of individuals with disabilities. It mandates the executive office of health and human services to create a training program for supporters and decision-makers, covering their rights, obligations, and dispute resolution processes. The training will involve collaboration with various state agencies and organizations to ensure accessibility. Additionally, the bill introduces provisions for educational records, requiring the department to post a sample request form online and provide information about alternatives to guardianship during individualized education program meetings for students aged 16 and older.

Moreover, the bill amends several sections of the General Laws to recognize supported decision-making agreements as a viable alternative to guardianship, defining key terms and outlining the roles and responsibilities of supporters. It establishes procedures for terminating these agreements and allows for court intervention in cases of abuse or neglect. The bill also clarifies that such agreements are not prerequisites for participation in activities or services, and individuals retain the right to execute health care proxies and powers of attorney. It creates the Authorization Documents Commission to study the expansion of a state registry for health care authorizations and mandates that any supported decision-making agreements executed before July 31, 2026, will remain valid until July 31, 2027, after which only compliant agreements will be recognized. The provisions will take effect six months after the bill's enactment.

Statutes affected:
Bill Text: 71B-2