Most people want the same things at the end of life: comfort, control, and the ability to make decisions based on their own values. Research shows that while nearly two-thirds of Americans say they’ve thought about their end-of-life care preferences, fewer than one-third have completed an advance directive. This gap can have serious consequences, especially during medical emergencies when decisions must be made quickly.
Emergency physicians regularly see what happens when preferences aren’t documented. Studies show that patients without advance directives are significantly more likely to receive aggressive interventions they may not want. Emergency medical service (EMS) teams and emergency department clinicians are trained to preserve life unless there is clear, accessible documentation stating otherwise.
But you can close that gap. More hospitals and clinics are embracing a framework that puts patients at the center: the Age-Friendly Health Systems model, which organizes care around the “4Ms” — What Matters, Medication, Mentation, and Mobility. “What Matters” sits at the heart of this approach. When you express what matters to you clearly — whether through conversations, advance directives, or medical orders — your healthcare team has a better foundation for decisions that reflect your priorities. Taking a few practical steps now, whether you’re navigating a chronic illness, supporting a loved one, or simply planning ahead, can help bridge the gap between your values and your care.
The most effective way to ensure you get the care you truly want is to connect your personal goals with clear, actionable instructions. That process involves three key steps.
These steps work together to ensure your care reflects what you want, even when you cannot speak for yourself.


I knew respecting her wishes to have a peaceful and gentle end was more important than my desire to keep her on this earth
Victor Silva never wanted to talk about death. For years, he avoided the conversations his father would bring up at the dinner table — discussions about not wanting to suffer, about preferring a peaceful end. Victor thought talking about it might somehow make it happen sooner.
Years later, when Victor became his parents’ caregiver alongside his husband, Luis, those uncomfortable conversations became invaluable. When his mother could no longer swallow and hospital staff wanted to insert a feeding tube, the doctor asked Victor, as his mother’s medical power of attorney, what he wanted them to do. “I knew Mom wanted to be comfortable at the end of her life, and I had promised her that I would make sure that she was as happy as she could be until the very last second. At the same time, part of me wanted to keep her around. But I knew respecting her wishes to have a peaceful and gentle end was more important than my desire to keep her on this earth. Still, this was not an easy decision. I talked with my sister and her daughters, and we prayed, and together we decided to do what we knew Mom wanted: to let her go.”
When you’re put on the spot in those moments, it can be incredibly hard to make that call. But Victor is grateful now for those dinner table conversations he once squirmed through — they gave him the clarity to honor what his parents wanted, even when it wasn't easy.
Talking with people you love about your end-of-life wishes, like Victor’s parents did, is essential, and having the conversation with your healthcare provider is crucial. Your provider can help document what matters to you and explain medical options. Many people hesitate to bring up these topics because it can feel uncomfortable and overwhelming, but starting the conversation now, before a crisis occurs, can make all the difference.
Partner with your healthcare provider and have this conversation. Compassion & Choices offers a step-by-step guide to help you prepare and take the next step:
Begin now by having at least one end-of-life conversation with someone you trust. Document your wishes using your state’s advance directive, or a POLST if you have spoken with your provider and it’s appropriate for you, and make sure your healthcare proxy, loved ones, and care team all have copies. These steps help ensure your preferences guide your care today and give your loved ones and healthcare proxy clear guidance to make informed decisions on your behalf if your needs change.
For more information on POLST visit: POLST.org
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