Medical Aid in Dying (MAiD) is widely misunderstood in the United States. This site provides clear, factual information about how MAiD works in the United States, how it differs from Canada’s system, and why precise language matters. It is designed to support journalists, policymakers, and the public in navigating a complex topic with accuracy and clarity.

The U.S. model of MAiD is narrow, patient‑led, and grounded in autonomy and informed consent. It applies only to terminally ill, mentally capable adults in jurisdictions where the practice is legal. Because public vocabulary around MAiD is inconsistent, this site offers a stable reference point for responsible reporting and public understanding.

This project is non‑advocacy, non‑partisan, and focused on accuracy. Its purpose is to help people understand what MAiD is, what it is not, and how the U.S. system fits within the broader landscape of end‑of‑life care. Clear language supports informed decisions, respectful dialogue, and trustworthy journalism.