Hospice Care
Also called: end of life care, terminal care, comfort care
End-of-life care focused on comfort and quality of life when a person has a prognosis of six months or less and curative treatment is no longer the goal.
Hospice care is a Medicare-covered benefit for people with a terminal diagnosis and a life expectancy of six months or less if the disease follows its expected course, when the patient and family have decided to focus on comfort rather than cure. Two physicians — typically the attending physician and the hospice medical director — must certify the prognosis. The benefit is reauthorized in defined periods (two 90-day periods, then unlimited 60-day periods) as long as the patient continues to meet eligibility. A patient who stabilizes or improves can be discharged from hospice and re-enrolled later if the disease progresses again.
Hospice is a philosophy of care more than a place. Roughly 98% of hospice care in the United States is delivered in the patient's residence — a private home, an assisted living apartment, a memory care suite, or a long-term care room. A small percentage is delivered in a freestanding hospice residence (a "hospice house") or an inpatient hospice unit when symptoms become acute and cannot be controlled at home. In Southeast Michigan, options include Angela Hospice, Hospice of Michigan, Heartland Hospice, Beaumont Hospice, Henry Ford Hospice, and several others.
A hospice agency provides an interdisciplinary team that visits the home: a registered nurse case manager (visits typically 1–3 times per week), a hospice aide for bathing and personal care (a few visits per week), a social worker, a chaplain, and a medical director on call. The agency also provides medications related to the terminal diagnosis, durable medical equipment (hospital bed, wheelchair, oxygen, commode), supplies, and 13 months of bereavement support for the family after the patient dies. Volunteer companions are often available for short respite breaks.
A common misunderstanding: hospice does not provide around-the-clock caregivers. Visits are intermittent — a nurse may come for an hour, an aide for 45 minutes, a chaplain for 30 minutes — totaling perhaps 5 to 10 hours of professional contact across an entire week. The remaining 158+ hours are covered by family members or by paid private caregivers. This is where most families experience the hospice gap: the medical layer is excellent, but the daily presence is not. Continuous home care under the Medicare hospice benefit is available only during brief crises (uncontrolled pain, severe agitation) and is rationed; it is not a substitute for ongoing daily care.
Most Southeast Michigan families who choose to keep a loved one at home through end of life pair the hospice agency with private non-medical home care. A trained, vetted personal care assistant can cover daytime hours, evenings, or live-in shifts so the family has reliable daily presence and is not awake every night. Personal Care in Southeast Michigan runs $29–$37/hr through a licensed agency; specialized end-of-life situations involving complex symptoms, two-person transfers, or active dying typically run $35–$42/hr. Live-in care, which requires a private bedroom and 5 hours of uninterrupted sleep for the caregiver, runs $400–$500/day and is appropriate when the patient needs presence rather than constant intervention.
A few practical points: choosing hospice does not mean giving up. Patients on hospice often live longer than expected because symptoms are better managed and they are spared exhausting hospital trips. Hospice does not require DNR status, though most families ultimately complete one. The patient can revoke hospice at any time and resume curative treatment. Use our cost calculator to estimate what private overlay home care would run alongside hospice, and call us at 248-419-5010 if you are trying to plan the schedule before discharge or transition.
Frequently Asked
Does Medicare hospice provide a caregiver around the clock?
No. The Medicare hospice benefit provides intermittent visits — typically a nurse 1–3 times per week, an aide a few times per week, a social worker and chaplain as needed, and a medical director on call — totaling roughly 5–10 hours of professional contact per week. Continuous home care is available only during brief symptom crises and is rationed. Families who want daily presence at home almost always pair hospice with private home care. Personal Care in Southeast Michigan runs $29–$37/hr through a licensed agency.
Can someone be on hospice and still receive home care from us?
Yes, and most of the families we serve at end of life are doing exactly that. The hospice agency manages the medical layer — symptom control, equipment, medications, family education — and our caregivers manage the daily layer — bathing, transfers, meals, medication reminders, overnight presence, and respite for the family. The two teams coordinate. We do not provide medical care; we provide the hours.
What does it cost to keep someone at home on hospice with overlay caregivers?
Costs vary widely with the schedule. A few daytime shifts a week to give the family breaks runs in the hundreds per week at the Personal Care rate of $29–$37/hr. Daytime coverage 8 hours a day, 5 days a week runs roughly $1,160–$1,480/week. Live-in care, when the situation supports it (private bedroom, 5 hours of uninterrupted sleep for the caregiver), runs $400–$500/day. Specialized end-of-life situations run $35–$42/hr. Use our cost calculator to model the schedule and call us at 248-419-5010 to talk through what fits.
Related
Glossary terms
Palliative Care
Care Types
Specialized medical care focused on relieving pain, symptoms, and stress of serious illness — at any stage, regardless of prognosis.
Specialized Care
Care Types
Higher-acuity home care for clients with dementia, Parkinson's, post-stroke needs, or complex transfer requirements.
Live-In Care
Care Types
A caregiver who stays in the home for 24-hour blocks (typically 3–4 days), with a private bedroom and 8 hours of nightly sleep.
Caregiver Burden
Roles & People
The cumulative physical, emotional, and financial strain experienced by family caregivers — clinically measurable and predictably preventable with respite.
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