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By carefully regulating assisted death through Death with Dignity Acts, everyone involved is safer and more informed:
- No question the patient is making the decision and no one else: A mentally-competent, terminally-ill person must request the prescribed medication—three times, no less—and the written request must be witnessed by two people.
- Patients become more informed about all feasible options: When doctors in Oregon, Vermont, or Washington are asked for the life-ending medication by their patients, the doctor is required to tell the patient about end-of-life care options including hospice and palliative care.
- Doctors have a clear standard of practice to follow: Death with Dignity Acts outline physicians' responsibilities which include having two doctors confirm a terminally-ill person's mental competence and that their patients will die of their illness within six months.
- Patients decide whether or when to take the medication: The entire process is patient-driven. The patient initiates the request and the terminally ill person can change his or her mind and opt out at any point.
- Annual reports of usage show these laws work the way they're intended: Read the stats for yourself with our links to Oregon's and Washington's annual reports.
Defend dignity. Take action.
You are the key to ensuring well-crafted Death with Dignity laws for all Americans. With your financial and volunteer help, the Death with Dignity National Center, a 501(c)(3), non-partisan, nonprofit organization, has been the leading advocate in the Death with Dignity movement. Individual contributions helped us pass new Death with Dignity laws in Washington and Vermont, defend the Oregon law, and provide education and outreach programs for the vitality of the Death with Dignity movement.





