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Serving the San Francisco Bay Area · Free in-home visit · (925) 407-5879
Serving the San Francisco Bay Area

In-home palliative care support focused on comfort

For clients living with a serious illness, our non-medical comfort care centers on quality of life — daily support, companionship, and an extra set of caring hands beside your medical team.

  • Licensed, bonded & insured
  • Background-checked caregivers
  • Free in-home assessment
The short answer

What palliative care means at home

Palliative care is specialized care for people living with a serious illness, aimed at relieving symptoms and improving quality of life. It is appropriate at any stage of an illness and can be provided alongside treatment intended to cure. It is not the same as hospice.

The clinical part of palliative care — symptom and pain management — is delivered by a physician-led palliative team. What we provide is the non-medical layer around it: help with daily tasks, comfort-focused presence, companionship, and support for the family carrying the load.

That layer matters more than families expect. Serious illness turns ordinary days into logistics. Someone who handles the meals, the bathing, the laundry, and the quiet company frees the family to be family again rather than staff.

Day to day

What palliative care includes

Every plan is written for one household. These are the tasks caregivers most often take on, and the plan changes as needs do.

  • Comfort-focused daily support
  • Assistance with bathing, dressing, and grooming
  • Meal preparation adapted to appetite and restrictions
  • Repositioning for comfort and skin protection
  • Companionship for the client and the family
  • Light housekeeping and laundry
  • Coordination around your medical and palliative team visits
  • Respite so family members can rest
Is it time?

Signs palliative care would help

In-home support alongside palliative care often helps when:

  • Treatment side effects are making daily tasks exhausting
  • A family member has become the full-time caregiver by default
  • Appetite has changed and meals need adapting
  • Mobility is declining and transfers feel unsafe
  • Appointments and medications have become a second job
  • The household needs company as much as assistance

If several of these sound familiar, a free in-home visit costs nothing and will tell you more than another week of wondering.

How we work

Our approach to palliative care

Anyone can promise compassion. Here is the substance behind ours.

We follow the plan your clinical team sets

Comfort measures, positioning, dietary guidance, and activity levels come from your palliative team. We support that plan and flag anything that looks inconsistent with it.

Comfort is the metric

Not task completion. If a bath is too tiring today, we adapt. Caregivers are taught to prioritize how the client feels over finishing a checklist.

The family is part of who we support

Serious illness is hard on everyone in the house. Our caregivers make room for family time, take on the tasks that drain it, and provide respite so people can rest without guilt.

Consistency and discretion

The same caregiver where possible, arriving quietly, knowing the household. In a home under strain, familiarity is a kindness.

What this service does not cover

We provide non-medical support only. We do not manage pain medication, administer treatments, or provide nursing care. Those come from your physician-led palliative team or a licensed home health provider. If you have not yet been referred to a palliative team, ask your treating physician — it is available alongside curative treatment, and many families discover this later than they wish they had.

Getting started

How to begin, in four steps

Most families go from first phone call to first shift within a week. Urgent situations move faster.

  1. Call or send a note

    Tell us what is going on. There is no script and no pressure, and the conversation is free.

  2. We visit the home

    We meet your loved one, walk the house, and look for risks. Bring your questions and your siblings.

  3. We build the plan

    You get a written care plan with tasks, schedule, and cost. Nothing is hidden, and nothing is assumed.

  4. Care begins

    We introduce the caregiver personally, then check in after the first week to make sure the match feels right.

Common questions

Questions families ask about palliative care

What is the difference between palliative care and hospice?

Palliative care is for anyone living with a serious illness at any stage, and it can be provided alongside treatment intended to cure. Hospice is for people who are no longer pursuing curative treatment, typically with a prognosis measured in months. Palliative care can begin at diagnosis; hospice comes later, if at all.

Do I have to stop treatment to receive palliative care?

No. Palliative care is provided alongside curative or life-prolonging treatment, and starting it early is associated with better quality of life. This is the most common misunderstanding families have about it.

What do your caregivers actually do?

Non-medical daily support: bathing, dressing, meals, repositioning for comfort, light housekeeping, transportation, and companionship, plus respite for family. Clinical symptom management stays with your palliative team.

Can you work alongside our palliative team?

Yes, and that is how it is designed to work. We schedule around clinical visits and follow the comfort plan the team has set.

How do we pay for non-medical palliative support?

The clinical palliative service is often covered by insurance or Medicare. Non-medical in-home support is generally private pay, long-term care insurance, or VA benefits. We will go through the options with you at no cost.

Let’s talk about what your family needs

The first conversation is free, and there is nothing to sign. Call us, or send a note and we will get back to you the same business day.