summary
Introduced
02/06/2025
02/06/2025
In Committee
05/01/2025
05/01/2025
Crossed Over
04/09/2025
04/09/2025
Passed
12/12/2025
12/12/2025
Dead
Signed/Enacted/Adopted
12/12/2025
12/12/2025
Introduced Session
104th General Assembly
Bill Summary
Creates the End-of-Life Options for Terminally Ill Patients Act. Provides that the Act may be referred to as Deb's Law. Makes findings. Defines terms. Authorizes a qualified patient with a terminal disease to request that a physician prescribe aid-in-dying medication that will allow the patient to end the patient's life in a peaceful manner. Contains provisions concerning: the procedures and forms to be used to request aid-in-dying medication; the responsibilities of attending and consulting physicians; the referral of patients for determinations of mental capacity; the residency of qualified patients; the safe disposal of unused medications; the obligations of health care entities; the immunities granted for actions taken in good faith reliance upon the Act; the reporting requirements of physicians; the effect of the Act on the construction of wills, contracts, and statutes; the effect of the Act on insurance policies and annuities; the procedures for the completion of death certificates; the liabilities and penalties provided by the Act; the construction of the Act; and other matters. Provides that the Department of Public Health and the Department of Veterans Affairs may adopt rules for the implementation and administration of the Act. Makes conforming changes in the Freedom of Information Act. Effective 9 months after the Act becomes law.
AI Summary
This bill establishes the End-of-Life Options for Terminally Ill Patients Act (also known as Deb's Law), which creates a legal framework for medical aid in dying in Illinois for terminally ill patients. The legislation allows qualified adult Illinois residents with a terminal disease (defined as a condition expected to result in death within 6 months) to request medication that will allow them to end their life peacefully. To qualify, patients must be mentally capable, make multiple oral and written requests, and undergo evaluations by attending and consulting physicians, and potentially a mental health professional. The bill includes extensive protections for healthcare professionals, ensuring they cannot be penalized for participating or choosing not to participate in aid-in-dying care. It requires detailed documentation, informed consent, and provides safeguards against coercion, mandating that patients fully understand their diagnosis, prognosis, and alternative treatment options. The law also ensures that death certificates will list the underlying terminal disease as the cause of death, not suicide, and protects patients' insurance and other legal rights. Healthcare entities must provide timely information and transfers if they choose to prohibit aid-in-dying care, and the Department of Public Health will collect anonymized statistical data about the law's implementation. The bill emphasizes patient autonomy, medical ethics, and the right of terminally ill individuals to make end-of-life decisions aligned with their personal values.
Committee Categories
Government Affairs, Health and Social Services
Sponsors (18)
Robyn Gabel (D)*,
Linda Holmes (D)*,
Harry Benton (D),
Amy Briel (D),
Mary Beth Canty (D),
Kelly Cassidy (D),
Cristina Castro (D),
Mary Edly-Allen (D),
Laura Ellman (D),
Laura Faver Dias (D),
Laura Fine (D),
Nicolle Grasse (D),
Will Guzzardi (D),
Maura Hirschauer (D),
Adriane Johnson (D),
Theresa Mah (D),
Karina Villa (D),
Chris Welch (D),
Last Action
Public Act . . . . . . . . . 104-0441 (on 12/12/2025)
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