When the Care Plan Isn’t Enough - Why relationship-centered care matters
- Jun 6
- 3 min read
I remember sitting with a client who was about to be discharged from a skilled nursing facility. He had been there for a few weeks. His time was up. The plan was simple on paper. It included going home and calling friends for help. His family didn’t live nearby. There wasn’t much else in place.
But he couldn’t walk. He was in a wheelchair. He could manage his medications and was mentally sharp. But he was afraid. He was overwhelmed and kept saying, “I don’t know what I’m going to do.” I remember thinking, we have to figure something out. This isn’t going to work.
So we tried. I pushed for more time. We worked through Medicaid, which only covered so much. We called friends. We pieced together a loose plan, people checking in, bringing food, and helping where they could. It wasn’t ideal, but it was something. And I remember sitting there, realizing how much of what we call “care” depends on what someone has outside the system.
When the care plan doesn’t work
Even if we’re not the ones writing the care plan, we (end-of-life doulas, healthcare advocates, care workers) still support the people who will benefit from it. We see how it’s built. We see what’s expected to happen next. And we’re often the ones sitting with someone when that plan becomes real. On paper, it usually makes sense. There’s a next step. A place to go. A list of what needs to happen.
But those plans rely on something that isn’t always there. They rely on stability. On someone being able to manage at home. On having support, even if it’s informal. And when that support isn’t there, the plan can fall apart quickly.
What looked reasonable in a chart can feel overwhelming, or even impossible, to the person living it. I’ve seen this more than once. A plan that technically works, but doesn’t hold up in real life. And then I’m sitting there with my client thinking, okay, how are we going to make this work?
Sometimes, we can make parts of it work. We make the calls. We reach out to people. We try to fill in the gaps. And sometimes, we can piece together enough support to get someone through the next few days. But even when we do that, the fear remains. The uncertainty is still there. The person is still trying to figure out how they’ll manage. And that’s the part the plan can’t solve.
Prioritizing Both Relationship-Centered and Patient-Centered Care
We talk a lot about patient-centered care, and for good reason. It keeps the focus where it should be, on the person who needs help, their needs, their goals, and what matters most to them. It guides decision-making. It shapes care plans. It gives structure to the work. And when the plan is realistic and the support is there, it works.
But as I’ve mentioned, that’s not always the case. There are times when the plan looks right, but the reality doesn’t match. When access is limited. When support is inconsistent. When someone is left trying to manage more than they realistically can. That’s where patient-centered care starts to reach its limits. And this is where the relationship starts to carry more of the care.
Relationship-centered care doesn’t replace patient-centered care. It works alongside it. Patient-centered care is about the plan, while relationship-centered care is about how we show up. It’s the trust that builds over time. It’s being honest about what we can and can’t do. It’s showing up again and again, even when things feel overwhelming and unclear. Especially when someone doesn’t trust the system, and has good reason not to. Patient-centered care helps guide what needs to happen. Relationship-centered care is what helps people get through it.
What It Looks Like to Stay
So what does this actually look like in practice? It’s not a new tool or a different kind of plan. It’s simply staying. We’re present, even when the conversation isn’t going well. We don’t assume trust is there, and we don’t expect it to happen quickly. We listen to what matters to the person in front of us, instead of assuming we already know what they need.
We’re honest about what we can and can’t do. We don’t overpromise just to make things feel better in the moment. We sit with someone in their frustration, fear, and grief without rushing them out of it. And sometimes, we remind ourselves not to take things personally.
Staying means showing up again and again. Not because we have all the answers, but because our presence matters. And sometimes, that’s the care.
Links/Resources
Harborview Homeless Palliative Care Program – https://www.uwmedicine.org/specialties/palliative-care/homeless-care
Palliative Care Training Center, University of Washington – https://pctc.uw.edu

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