- Patients aren’t getting the care they want, according to a landmark 2014 Institute of Medicine report, “Dying in America”. The findings show that Americans are receiving unwanted interventions and not enough comfort care.
- The move recognizes that people need to be involved in treatment decisions before they become seriously ill or unable to make their wishes known.
- Encouraging end-of-life discussions is also critical to getting Americans to put their end-of-life treatment preferences in written form. Only about 30 % of us have legal documents, such as Advance Medical Directives – leaving relatives in the position of deciding what to do next after a parent has had a stroke or is on life-supporting machines in the hospital.