A Sermon Delivered to High Street UU Church
July 26, 2026
I don’t need to remind you we’ve had lots of deaths lately within our Beloved Community, members, friends, relatives, many of them in hospice. That word, death, can be frightening, I know. I was a hospice chaplain before I retired. I’ve been with a number of people as they’ve died and I want to tell you about it.
It stands to
reason almost everyone must die in somewhat the same way. Wouldn’t you think?
The Population Reference Bureau, whose unenviable task it is to calculate these
sorts of things, has determined that nearly one hundred eight billion people
have been born and died in the six million years science estimates people have
been crawling and hobbling around on the Earth. They have also determined,
through statistics, mathematics, algorithms, and observation, that there is a
one hundred percent certainty that if you are born, you will die. That’s the
trick about life: no one gets out alive.
Amazingly, there
is still some variation. There are as many unique ways to die as there are to
live. Some of us die alone. Some of us surrounded by loved ones. Some of us die
by violence, some by our own hand, some by accident, and some by the slow
accrual of time and entropy. Each of our deaths as unique as our fingerprints
or our dreams.
Perhaps in these
days of miracle and wonder pills, we need memento mori, the Latin admonition,
“Remember, you must die.” Buddhists call this Maranasati the practice of
keeping mindful of our impending deaths. We long, all of us, once we admit to ourselves
we will die, for a good death. What is
that? Well, that’s up to you. I have a friend who once expressed the wish that
a nuclear bomb would take him out, squarely to the top of his head. He wanted
to die fast and easy, not wishing to live in a post-apocalyptic anything or to
watch his loved ones and friends die agonizing deaths. Another friend once
said, if he contracted cancer or AIDs or something incurable, he planned to
take out a platinum credit card and use it to travel around the world,
succumbing just as the mail was delivering the bill to his home. I’m pretty
certain credit card companies anticipate this kind of thing.
I used to think I
knew how I wanted to die. I was hiking the Appalachian Trail through New
England and in New Hampshire I was on Mount Washington in the White Mountains.
It’s a high, rugged mountain where erratic weather—snowstorms in August, winds
in excess of a hundred miles an hour out of nowhere—is the norm. It collects at
its alpine apex an annual average of nearly 100 inches of rain and snowmelt, so
it is covered with magnificent waterfalls and ravines fed by runoff from the
Lake of the Clouds.
I was at one such
ravine on the Ammonoosuc River on the western slope, lying on a hump of dirt
and grass that jutted out above the cataract and afforded an excellent view
downward toward Vermont and lower Canada. I was taking a photo of my hiking
partner who had straddled another, higher rock jutting out from that hump when
I felt the rock I had planted my foot against suddenly give way and I slid. I
went shooting off the hump and straight down the ravine. It was a long way down
and I saw the trees and brush and birds in glorious detail. My feet struck
slick boulders just before they accordioned to my chin. In reality I’d only
slid about three feet, but it was enough. And in my mind, just as I’d hit those
rocks I thought, “This is a fine death.”
Working with
hospice patients I often talk about good ways to die. Some would have liked to
die immediately and unknowingly, like from a bullet or getting hit by a bus.
Others are glad to have had the opportunity to talk with relatives they hadn’t
connected with sometimes for decades. Still others, of course, curse the length
of time it can take a sick person to die. Many people lose their faith in a
personal, loving God when they find their breathing and cognition outlasting,
sometimes by months or years, their ability to move without pain or to
communicate simple things like “eat,” “sleep,” “toilet.”
I suspect that my
mother, who died ten years ago in June, had a good death. She had breast cancer
the last fifteen years of her life, and those were hard years, but that isn’t
what killed her. No, my dad woke up one morning to find she wasn’t in the bed
next to him but face down on the floor in the living room. Mom had a habit of
getting up in the night to sit in her recliner for a few hours’ respite after
her back began aching. The coroner ruled that she had stood up from her chair,
maybe a little too quickly, and had a heart attack. She was dead, he claimed, before
she hit the floor.
In those final
fifteen years our family and her friends had the opportunity to see her and
speak with her, reminisce with her, and tell her what she meant to us. There
was nothing left between us, no words unspoken, no undelivered messages. I had
loved her, she had loved me, and we let one another know how deeply we felt,
and then she died. There’s another sense too in which it was a good death and
that’s the lengths to which I discovered, to my surprise and probably his too,
how kind a caregiver my father could be to her. My favorite memory of him,
during my visit the winter before she died, dressing her for an outing in the
cold, adjusting the scarf around her neck just so and bundling the top button
of her coat gently under the scarf so the wind wouldn’t whip under it.
We all want,
whether we admit to it or maybe more importantly when we do not, a death that’s
good, whether it’s “good” in terms of its painlessness, its ease, its
meaningfulness, or its message. But the truth is no one can give us that.
Especially not in the way most of us mean it. For most of us, a good death
means we die painlessly, unknowingly, in our sleep. Without prolonged illness,
without having felt pain, without even knowing we were ill.
That happens
shockingly rarely, the percentage hovers around 4 or 5. This means out of every
hundred people, four or five will die this way. If it’s any consolation,
neither will most of us die in a violent manner, not from terrorist attacks or
stabbings or violent accidents, shark attacks, lightning strikes, air crashes,
radiation poisoning, falling through the ice, or someone intentionally dropping
an electric fan into our bath. Most of us in America will die in the hospital
or at home—in an interesting turn, after a century of not most people dying in
hospitals, often separated from family and friends, there is a resurgence in
the way most people used to die, at home in their bed—from the complications of
disease, usually heart disease or cancer.
How will we die?
Well, again, there are at least as many variations in the act of dying as there
are in living, but there are characteristics that can be called constants in
the same way I suppose that school education is a constant.
There’s a booklet
I gave families when admitting someone into hospice called Gone from My Sight: The Dying Experience. It was published in 1986
by Barbara Karnes, a hospice nurse, and has gone through many revisions. It relates
what most people experience during their final days in a non-sensationalistic,
understandable manner, using plain language. Despite the way it’s necessarily
presented, there is no timetable to death. The periods Karnes refers to are a
general outline of when some things happen. They may not happen at that time.
They may not happen in that order. They may not happen at all.
Karnes
characterizes One to Three Months Prior to Death as a period of Withdrawal.
It’s not unusual for those first glimmers of our actual mortality—“This is
it”—to send us into a spiral of separation from everyone and everything else.
We may become irritable or serene. We are slipping into a cocoon, and there’s
no room for children, grandchildren, or other loved ones. We’ll peep out at
them, even enjoy their presence for a while, but really we’re focused on
ourselves.
We sleep more
often and longer. Little naps here and there, several a day. It may seem as if
we’re bored but our interior life has taken on great interest. We don’t feel
the need to communicate with people. Karnes writes, “Words lose their
importance; touch and wordlessness take on more meaning.”
We may stop
eating. This is often very hard for families to understand or accept; in many
cultures there’s still a certainty that so long as we’re eating, we’re alive.
“If only she’d eat she’d feel better.” But nothing tastes good. Or only certain
things—sourballs, ice cream, bacon, citruses—taste good. Meat is usually the
first to go, and then other hard-to-digest food like vegetables. We’ll stick
with soft foods longest, but eventually we’ll stop eating those too.
At One to Two
Weeks, people begin to show signs of disorientation. We pick at imaginary
threads or hairs, our arms or legs seem agitated and move without our volition.
We sleep even more. Longer periods, deeper naps. It’s almost like hibernation,
some patients say. We may talk to people who aren’t there and about events no
one recognizes. Studies suggest that, as the body breaks down, the brain, helping
to prepare us, will show us images, smells, sounds, of people who’ve died
already. Relatives, friends, pets. Journalist Phoebe Zerwick writes, “As people
near the end…the frequency of visions increases…[These] final visions provide
patients…with profound meaning and solace.”
Our blood pressure
goes down, our pulse goes up. Or it may seem to stop altogether. We sweat a lot
more and when people hug us they remark afterward how clammy we feel. We want
the windows open as we’re burning up or more blankets because we just can’t get
warm. Our skin changes color, we seem pale and flushed, blue like we’re
freezing. Our extremities are often blue because the heart is no longer pumping
the way it used to and blood can’t reach there. It might be harder to breathe
so we need oxygen. We might breathe faster, like we’re always racing. We’ll
hack and cough but nothing comes up.
Finally, at One to
Two Days and in the Final Hours Before Death, we may have a surge of energy,
what hospice workers call a “spike.” We’ll sit up all night talking, drinking,
and laughing with friends who’ve come by. We want a plate of fried potatoes and
a rare steak and we eat every bite. Loved ones look at this and say, “He’s over
the worst,” and we are, but not in the way they mean it.
We get more
restless but take to our bed. We collapse. Breathing is slower, less regular,
sometimes stopping altogether for nearly a minute. We sound congested, loudly
congested, the way we did as kids with a croupy cough. Our eyes are open but we
don’t see anything or recognize anyone. We might respond to sounds or voices or
movements but we can’t identify them and we’ve stopped responding at all,
except for an occasional grunt or moan. We aren’t in pain, usually, it’s just
the air moving around our lungs and throat.
Our hands and feet
turn purple; the heart can’t pump blood that far anymore. Joints become blotchy
and because we’re lying down blood starts to pool on the underside of our arms
and legs, our backs, our buttocks. We stop responding altogether.
In the Final
Minutes Before Death, there is often the sort of gasping you see when fish are
out of water—it’s called Chayne-Stokes Breathing—and we can’t be awakened or
roused. This is often the hardest for family present because they can see the
end and they want to be there but this experience can last for hours.
Sometimes, when they can’t hold off going to the bathroom any longer, we take
that opportunity we’re alone to finally just stop.
No matter how
closely we watch on the outside, we may not see them die. I attended the death
of a Vietnam veteran turned Buddhist, and while I glanced at my phone for an
appropriate sutra, he died. It was that quiet. In the 1970s my dad tended to
her while my grandmother died from leukemia. He told me how he was with her
nearly every moment of her hospitalization, until his youngest brother visited.
Dad said he stepped into the hallway to prepare him—“I swear, it was maybe 40
seconds”—and in that time she died.
We all die and we
all in our own time. It may sound sad and it may seem sad but it isn’t to the
person undergoing it. It’s just what they’re going through and they’re beyond
any consideration of whether they want to do it.
Finally, after a
certain number we stop counting the people we’ve seen die, but I remember one
of my first. Her decline was
dramatic after a period of relative energy. Inside a week she had gone from
sitting in a wheelchair and actively participating in life to being bed-bound
and sleeping nearly all the time. She was unconscious when I arrived so I took
her hand while the RN who'd got there before I had went through her paces. She
said, "I'll be surprised if she lasts the day."
The nurse left about 20 minutes later. We were waiting for
one of her daughters to arrive and I said I'd stay with her until she came. But
a half hour after the nurse left she became agitated, having difficulty
breathing, and opening and closing her eyes without seeing. Her dyspnea was a
series of quick, almost urgent, shallow breaths, as if she can't catch it. I
talked to her, letting her know I was there with her and she wasn't alone. She
could be scared, I said, but I was with her and wouldn't be leaving until she
was finished. She lay on her back, swallowing great gulps of nothing. I held
her hand more tightly and reminded her of my presence.
There was no great shudder. No death rattle. No final words
of wisdom. One moment she was breathing, which I could see from the gentle rise
and fall of her chest. Then she stopped. But then she started again. This went
on a few times, the shallow intake, the rise, the wheeze out, the fall. Until
finally, she stopped. From my seat I could see the flutter of her carotid
artery. I watched that pulse slower, until it too stopped. I touched my fingers
to it but couldn't be positive if I felt it still or if it was the throb of my
own pulse. After about a minute I pressed her eyelids closed and they stayed
that way—they don’t always—and I stepped out to ask a nurse to check her.
I held her hand and felt her life slow until I couldn't feel
it at all. I don't know exactly what I felt. It wasn't fear or anxiety or even
relief at its conclusion. What comes nearest I think is humility. I felt humble
in the face of what happened, struggling to hold her one hand while she held a
plush chipmunk in the other, and keeping the live flower her daughter had
placed in her hair from tipping and rolling off her pillow. My entire role came
to, "I'm here." Nothing else needed to be done.
