By Mary McElroy
Your doctor just used one of three phrases: palliative care, hospice, or comfort care. If you’re not sure whether they mean the same thing, or what any of them actually require, that’s a completely normal reaction.
Clinicians, hospital forms, and insurance paperwork don’t always use these terms the same way, even with each other. Here’s what each one really means, how they relate, and how to figure out which one applies to your family.
The short answer: Palliative care is specialized medical care for managing symptoms during any serious illness, at any stage, and it doesn’t require giving up curative treatment. Hospice care is different: it’s a specific Medicare Part A benefit that begins once two physicians certify a life-limiting prognosis of six months or less, and the patient decides to forgo curative treatment for the terminal diagnosis. Comfort care isn’t a Medicare benefit or an enrollment program at all. It’s more of an informal term, used in clinical settings to describe care focused on comfort rather than cure.
Quick Answer
- Palliative care is specialized symptom management for any serious illness, at any stage. Curative treatment continues alongside it.
- Hospice care is a Medicare Part A benefit that begins when two physicians certify a prognosis of six months or less and the patient elects to forgo curative treatment for the terminal diagnosis.
- Comfort care isn’t a Medicare benefit or enrollment program. It’s a general term for care focused on comfort rather than cure, used informally in clinical settings.
How All Three Types of Care Compare: A Side-by-Side Chart
The table below breaks down the key differences among the three: eligibility, coverage, cost, and where care actually happens. Worth flagging up front: the six-month prognosis requirement and the decision to forgo curative treatment are unique to the Medicare hospice benefit. Neither palliative care nor comfort care carries either one.
| Hospice Care | Palliative Care | Comfort Care | |
|---|---|---|---|
| What it is | A Medicare-defined benefit providing full comfort-focused care at end of life | A medical specialty focused on symptom relief and quality of life for any serious illness | A general term for care focused on comfort rather than cure; not a Medicare benefit or formal program |
| When it starts | When two physicians certify a prognosis of 6 months or less if the illness runs its normal course | At any stage of illness, including at diagnosis | Whenever a patient and care team decide comfort is the priority |
| Can you still receive curative treatment? | No, for the terminal diagnosis (unrelated conditions are treated normally) | Yes. Palliative care runs alongside any curative treatment | No fixed rule; depends on the clinical setting and context |
| Where care happens | Home, nursing facility, assisted living, or inpatient hospice (such as a Center for Caring) | Hospital, outpatient clinic, or home-based programs | ICU, hospital ward, home, or other care settings |
| Who provides care | Interdisciplinary team: physician, RN case manager, social worker, chaplain, certified aide, volunteers | Palliative medicine specialists working alongside the primary treating team | No defined team; depends entirely on the setting |
| How it is paid for | Medicare Part A: zero cost-sharing for covered services; nominal $5 copay on some prescriptions | Medicare Part B: Medicare pays 80%, patient responsible for 20% | Not a billable benefit category |
| Who is eligible | Six-month prognosis certified by two physicians; patient elects to forgo curative treatment for the terminal illness | Any serious illness causing pain, fatigue, shortness of breath, anxiety, or impaired function | No formal eligibility; it’s a care philosophy |
| Bereavement support included? | Yes, minimum 13 months after death (required by Medicare Conditions of Participation) | No formal requirement | No |
Key Difference
The six-month prognosis requirement and the decision to forgo curative treatment apply only to hospice. Palliative care has no prognosis requirement. Comfort care has no enrollment process at all. These distinctions determine which Medicare benefit applies and what your family’s out-of-pocket costs will be.
What Is Palliative Care?
Palliative care is specialized medical care for people living with a serious illness, and it’s often mistaken for a synonym of end-of-life care. It isn’t. A patient can start palliative care the same week they receive a cancer diagnosis, while still pursuing aggressive chemotherapy aimed at a cure. The focus is on relieving the symptoms and stress that come with serious illness: pain, shortness of breath, fatigue, nausea, anxiety, and depression.
Who Palliative Care Is For
Palliative care fits any serious illness, cancer, heart failure, COPD, dementia, at any stage of that illness. There’s no prognosis requirement, and a patient still in active curative treatment qualifies just the same. Roughly 45% of Medicare beneficiaries have four or more chronic conditions for which palliative care may be clinically appropriate.
You can ask your oncologist or cardiologist about a palliative care referral the same week treatment starts. Starting early doesn’t mean giving up on anything. It means someone is managing how you feel while that treatment is happening.
What a Palliative Care Team Does
A palliative care team typically includes board-certified palliative medicine physicians and advanced practice providers. They work alongside the primary treating team rather than replacing it, adding a layer of support: symptom management, psychosocial care, spiritual support, and coordination across whatever specialists are already involved in a patient’s care.
One of the most important things a palliative care team does is lead goals-of-care conversations. These help patients and families understand the diagnosis, weigh treatment options against quality of life, and make decisions that fit their values. Advance care planning (deciding in writing what care you want if you can’t speak for yourself) often grows out of these discussions. Having trained palliative medicine specialists lead them changes outcomes, and it’s part of why palliative care matters even when a cure is still very much the goal.
Community Hospice & Palliative Care offers palliative care services right alongside its hospice programs. That means families can get support at any stage of serious illness without waiting for a hospice-level prognosis.
How Palliative Care Is Paid For
Under Medicare, palliative care is billed through Part B, the outpatient physician services benefit. Medicare covers 80% of approved costs, and the patient is responsible for the remaining 20%, though secondary insurance often picks that up. Inpatient palliative care may fall under Part A when the patient is hospitalized.
That’s a meaningful difference from the hospice benefit, where covered services cost the patient essentially nothing. The cost-sharing under Part B physician billing is real, but for many families it’s manageable once supplemental coverage is factored in.
What Is Hospice Care?
Hospice is a specific Medicare benefit that shifts the goal of care from curative to comfort-focused treatment. It’s also the most comprehensive support structure available to families at end of life, and it’s badly underused. Roughly 35% of hospice patients enroll for seven days or fewer. That number alone says a lot about how many families wait too long to call.
Who Qualifies for Hospice
Two physicians have to certify a prognosis of six months or less, assuming the illness runs its normal course. The patient, or their legal decision-maker, must then elect hospice in writing, agreeing to forgo curative treatment for that terminal illness specifically. Unrelated conditions still get treated: a hospice patient with terminal lung cancer who also has diabetes keeps getting insulin. What stops is chemotherapy, or anything else aimed at the cancer itself.
Hospice isn’t only for cancer patients, either. The most recent national data shows heart disease accounts for 29.8% of hospice stays, dementia and other neurovascular conditions for 25.4%, and cancer for 22.3%. Add it up, and more than half of all hospice patients have a life-limiting illness that isn’t cancer at all. In 2024, 53.1% of all Medicare decedents received hospice care, the first time that figure has surpassed pre-pandemic levels.
“No one is ever denied services through Community Hospice, regardless of their ability to pay.”
Patients can also revoke hospice election at any time, for any reason, and return to standard Medicare coverage. Hospice isn’t a one-way door.
To learn how Community Hospice delivers the full Medicare benefit (team composition, covered medications, and what families can expect from the first week of care), see our hospice care services page.
What the Medicare Hospice Benefit Covers
The Medicare Part A Hospice Benefit is genuinely all-inclusive. It covers physician visits, registered nurse case management, licensed clinical social work, chaplaincy, certified home health aide services, and volunteers. On top of that: medications for symptom management related to the terminal diagnosis, durable medical equipment (hospital bed, wheelchair, commode, oxygen) at no cost, and 24/7 on-call nurse access for whenever a crisis hits.
For covered services, the cost to the patient is zero. There’s a nominal copay of up to $5 on some prescriptions for symptom management, and a 5% coinsurance that applies only to inpatient respite days.
Bereavement support for the family continues for a minimum of 13 months after the patient’s death, required under Medicare Conditions of Participation. Palliative care carries no such requirement.
Where Hospice Care Happens
Roughly two-thirds of hospice care happens in the patient’s home, nursing home, or assisted living facility. Most families never have to leave the environment they already know.
When symptoms need a level of management that can’t happen at home, inpatient hospice steps in: a clinical setting built to feel unlike a hospital. Community Hospice & Palliative Care operates 9 Centers for Caring across 16 counties in northeast and north central Florida.
For patients in Duval County, the Anne and Donald McGraw Center for Caring provides the full inpatient hospice environment, including medical support, private rooms, and space for family. Other Centers for Caring across the region include the Earl B. Hadlow Center for Caring, the Alice and T. O’Neal Douglas Center for Caring, the Jane and Bill Warner Center for Caring, the Bailey Family Center for Caring at UF Health Flagler, and the Stephen R. Chapman Family Community Campus.
What Is Comfort Care?
Comfort care isn’t a Medicare benefit, a clinical specialty, or a formal enrollment program of any kind. It’s a descriptive term for care focused on comfort rather than cure, used in at least three distinct ways in clinical settings. Knowing which meaning a physician intends actually has practical consequences for your family.
Hospice and palliative care both focus on symptom management, and that overlap is part of what confuses people. The Medicare hospice benefit requires a six-month prognosis and the decision to forgo curative treatment. Palliative care requires neither. Comfort care sits outside both frameworks entirely: no formal eligibility, no defined interdisciplinary team structure, no insurance category behind it.
When Doctors Use the Term “Comfort Care”
In hospital orders: “Comfort measures only” (CMO) is an order set that removes life-sustaining interventions (ventilators, vasopressors, CPR) and focuses all care on the patient’s comfort. A patient can be on CMO orders in an ICU without ever enrolling in hospice. The two are separate clinical decisions.
In goals-of-care conversations: When a physician says “we’re shifting to comfort care,” they’re describing a change in treatment goals, moving from curative to comfort-focused. This conversation may or may not lead to a formal hospice referral. The phrase is often softer language for what may really be a recommendation to consider hospice.
In family and informal usage: Families and non-specialist staff often use “comfort care” and “hospice” as synonyms. In many cases they do mean hospice, but not always. The language is imprecise by design; it reflects how hard the underlying conversation is for everyone involved.
When a doctor says “comfort care,” they’re describing a goals-of-care shift, not enrolling a patient in a specific Medicare benefit program.
How Comfort Care Differs from Hospice Enrollment
Hospice is a specific benefit with a defined enrollment process: physician certification, patient election paperwork, and interdisciplinary team assignment. “Comfort care” has no enrollment process, no team requirement, no eligibility criteria, and no insurance category.
If you hear “comfort care” and want to know what it means for your family member, ask the care team directly: “Are we talking about enrolling in hospice, or are these orders for this hospital setting?” That question alone tends to make the path forward clear.
Comfort care has no fixed timeline. If you need context on how long a person might receive hospice care specifically, the national median length of stay is approximately 17 to 18 days, though the average is about 95 days because a small number of patients have much longer stays.
How Hospice Care and Palliative Care Overlap
The clearest way to understand the relationship: all hospice care is a form of palliative care, but palliative care is broader than hospice. The National Institute on Aging states it plainly: “All hospice care involves palliative care, but not all palliative care takes place in hospice.”
Palliative care spans the whole arc of a serious illness, starting the day of diagnosis. Hospice is palliative care narrowed to the final phase of that arc, with a specific Medicare Part A benefit structure attached and curative treatment of the terminal illness set aside.
Think of palliative care as the full circle. Hospice is a specific region inside that circle: the part where life expectancy is six months or less and curative treatment of the terminal illness has been set aside. Comfort care is the underlying philosophy that both share, a commitment to the patient’s quality of life, but it isn’t itself a program, a benefit, or a team.
When Families Move from Palliative Care to Hospice
This is the question families are most likely asking after they hear “palliative care” for the first time. Most general resources handle it in a single sentence, or skip it entirely. Here’s how the transition actually works.
What Changes When the Goal of Care Shifts
Take a patient with advanced heart failure as an example. The cardiologist keeps up active treatment: medications, monitoring, adjustments. At the same time, a palliative care team manages the symptom burden underneath it, the fatigue, the shortness of breath, the anxiety that comes with any serious illness. Over months, sometimes years, the heart failure progresses and curative options start to narrow. Eventually, two physicians determine the prognosis has crossed the six-month threshold.
At that point, the patient and family face a decision. If they elect hospice, several things change:
- Curative treatment directed at the heart failure stops
- Medicare billing shifts from Part B cost-sharing to the all-inclusive Medicare Part A Hospice Benefit
- The interdisciplinary hospice team takes over coordinated care
- Durable medical equipment arrives at the home; medications for symptom management are covered under the benefit; 24/7 nursing support becomes available
One worry families raise at this point, understandably, is that choosing hospice means giving up. Research published in the New England Journal of Medicine and indexed in PubMed Central consistently shows that hospice patients report better symptom management than comparable patients who continue aggressive treatment. In some studies, hospice patients actually lived as long as, or longer than, patients who continued pursuing aggressive intervention.
If you’re asking whether the time has come to move from palliative care to hospice, our post on signs that hospice may be the right next step walks through the questions families ask most.
Signs the Transition May Be Right
There’s no single moment, but these are the signals families and physicians watch for:
- Two physicians have determined a prognosis of six months or less if the illness runs its normal course
- Curative treatment is no longer working or the patient has decided to stop it
- Hospital admissions are increasing and each one offers diminishing benefit
- The focus has shifted from extending life to maintaining quality of life
- Symptom burden (pain, shortness of breath, fatigue) isn’t controlled with current care
If any of these describe your family’s situation, a conversation with a hospice specialist is the right next step. It isn’t a commitment. Call Community Hospice & Palliative Care at 866-253-6681 to talk through where you are.
What Stays the Same
The focus on symptom management doesn’t change when a patient moves from palliative care to hospice. The commitment to comfort, managing pain, shortness of breath, and anxiety, carries forward. Family support, emotional and spiritual care, and care coordination all continue under hospice, often with an even fuller interdisciplinary team than palliative care provided.
In 47 years of caring for families across northeast and north central Florida, we’ve walked thousands of patients through that transition, from palliative care into hospice. When the time is right, it isn’t an ending. It’s a shift in how care is organized.
Frequently Asked Questions
What is the difference between hospice and palliative care?
Palliative care is specialized medical care for symptom relief during any serious illness, at any stage, with no restrictions on curative treatment. Hospice is a specific Medicare Part A benefit that begins when two physicians certify a prognosis of six months or less and the patient decides to stop curative treatment for the terminal diagnosis. All hospice care is palliative care, but palliative care isn’t limited to hospice.
Is comfort care the same as hospice?
No. Comfort care is a general term for care focused on comfort rather than cure. It isn’t a Medicare benefit, not a formal enrollment program, and has no defined team or eligibility criteria. Hospice is a specific Medicare benefit with a defined enrollment process, an interdisciplinary team, and coverage for medications, equipment, and 24/7 nursing support. When a physician says “comfort care,” ask whether they mean hospice enrollment or a change in treatment goals within the current setting.
Can you get palliative care and still receive treatment for your illness?
Yes. Palliative care runs alongside any curative treatment. A patient can begin palliative care the same week they start chemotherapy. The palliative care team focuses on managing symptoms and quality of life while the primary treating team continues pursuing curative goals. No prognosis requirement exists, and choosing palliative care doesn’t mean giving up on treatment.
Does Medicare cover hospice and palliative care differently?
Yes. Medicare Part A covers the full hospice benefit at essentially no cost to the patient, with only a nominal copay on some prescriptions and 5% coinsurance on inpatient respite days. Palliative care services are billed under Medicare Part B: Medicare pays 80% and the patient covers 20%, which supplemental insurance often handles. The all-inclusive cost structure of hospice is one of its most significant benefits for families.
Who qualifies for hospice care?
Two physicians must certify a prognosis of six months or less if the illness runs its normal course. The patient or their legal decision-maker must elect the hospice benefit in writing, agreeing to forgo curative treatment directed at the terminal illness. Hospice isn’t only for cancer patients. Heart disease accounts for nearly 30% of hospice stays nationally, and dementia accounts for another 25%. “No one is ever denied services through Community Hospice, regardless of their ability to pay.”
When should someone move from palliative care to hospice?
When a patient’s prognosis crosses the six-month threshold and curative options have narrowed, hospice may be the right next step. The shift brings meaningful benefits: an all-inclusive Medicare benefit, a full interdisciplinary team, covered medications and equipment, and 24/7 nursing access. The decision belongs to the patient and family, supported by the care team. If you’re navigating that question now, call Community Hospice & Palliative Care at 866-253-6681.
Can you stop hospice if you change your mind?
Yes. A patient can revoke hospice election at any time, for any reason, and return to standard Medicare coverage immediately. Hospice isn’t a one-way door. Some patients leave hospice, pursue additional treatment, and then re-enroll in hospice later if their condition progresses. Medicare allows multiple hospice benefit periods.
What services does hospice include that palliative care doesn’t?
The Medicare hospice benefit is all-inclusive in a way that palliative care isn’t. Hospice covers physician visits, RN case management, social work, chaplaincy, certified home health aide services, medications related to the terminal diagnosis, durable medical equipment (hospital bed, oxygen, wheelchair), and 24/7 on-call nursing. It also includes a minimum of 13 months of bereavement support for the family after the patient’s death. Palliative care doesn’t include bereavement support by requirement and doesn’t cover equipment or medications under a bundled benefit.
How Community Hospice & Palliative Care Can Help Your Family
Community Hospice & Palliative Care has served families across 16 counties in northeast and north central Florida since 1979, making us the region’s largest nonprofit hospice provider. We offer both palliative care and hospice services, which means families who need one may eventually need the other, and we can support you through both.
Our 9 Centers for Caring provide inpatient hospice care for patients whose symptoms require clinical management. We care for approximately 1,500 patients per day across northeast and north central Florida. As a 501(c)(3) nonprofit, our mission is to the patients and families we serve, not to shareholders.
“The recognition as a Hospice Honors Elite program places Community Hospice among the top 2% of hospices nationwide, and we are honored to be the only hospice in the state of Florida to receive this designation, a testament to the exceptional quality and heartfelt care our team delivers each day.”
No one is ever denied services through Community Hospice, regardless of their ability to pay.
If your family is trying to understand whether hospice or palliative care is the right next step, call us at 866-253-6681. We can help you understand your options and what care looks like for your specific situation.
For a full breakdown of what the Medicare Hospice Benefit covers and what it doesn’t, see our guide on Medicare and hospice coverage.
Not Sure Which Care Is Right for Your Family?
Community Hospice & Palliative Care serves families across 16 counties in northeast and north central Florida. Our care team can help you understand whether palliative care or hospice is the right next step for your specific situation, at no obligation.
No one is ever denied services through Community Hospice, regardless of their ability to pay.

Mary McElroy
Oversees all clinical nursing and nursing assistant functions, including inpatient, home care, long term care, triage and nursing services administration. Mary received a Bachelor of Science in Nursing from Villanova University and a Master of Science in Administration and Health Services from Central Michigan University. In 2003, she was honored as one of the Great 100 Nurses of Northeast Florida.