A note for you.
Caregiving is some of the hardest work a person can do. It is also some of the most loving. This page is for you — the spouse, the daughter, the friend, the neighbor — who is up at 3 a.m. listening for breathing. We see you. Here is what we know.
·It is okay to ask for help
You are not failing if you can't do this alone. Most people can't. Hospice exists, in part, to help families help each other — and to be honest about what one person cannot carry by themselves.
- Use the volunteer. A few hours a week of company so you can shower, sleep, or leave the house. Federally required, freely available, and one of the great quiet gifts of hospice.
- Use respite. Up to five days of inpatient respite, as often as needed. Take the trip. Sleep through the night. We mean it.
- Use the social worker. Help with logistics, insurance, family conversations, and your own emotions. Their job is partly to take things off your plate.
- Tell the nurse what's hard. Caregiver well-being is part of the plan of care. We can adjust visits, add help, change schedules.
·Watch for caregiver burnout
Warning signs
- Trouble sleeping even when you can.
- Persistent headache, back, or stomach pain.
- Snapping at people you love.
- Feeling numb, detached, or empty.
- Drinking or eating more than usual.
- Skipping your own appointments.
Small daily practices
- One walk outside, however short.
- One real meal each day.
- Five quiet minutes in the morning.
- One person you call who isn't about caregiving.
- Sleep, when sleep is possible.
- One thing each day that is just for you.