Read Knocking on Heaven's Door: The Path to a Better Way of Death Online
Authors: Katy Butler
Tags: #Non-Fiction
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five-thousand-dollar bequest for a grandchild’s car or first year
at a community college, the twenty-five-thousand-dollar loan or
gift toward a house down payment, or, in wealthier families, a
hundred thousand dollars toward starting a business, paying off a
mortgage, or covering tuition for college or graduate school.
“We are now in a post-stroke mode and have to look after our-
selves,” my father wrote to me elegiacally in the late spring of 2006:
Before we depended on old Jeff but now Val is strictly in com-
mand. If you look at this house and garden it really is beauti-
ful. Val has gone to enormous trouble and I am afraid she has
done it all. But a few things I have done. In particular, I have
taken on the sorting of sand and gravel. It really was a terrible
mess and I set myself the task of sorting it out. If you walked
along the deck you would see what it is that I am talking
about. So my dear, you are the recipient of a tortured piece,
by a man who tries to sort things out on the ground.
What did it feel like, I wonder, to peer out at the world through
the shifting keyholes of that generous soul and educated mind
with a black spot in his field of vision and his ears stopped with
hearing aids that he could no longer put in without help? What
was it like to have holes appear and disappear in memory like film
jammed in a projector and melting? What was it like, after a life-
time of overcoming hardship and adapting to limitation without
complaint, not to recognize a road he’d walked for forty years or to
watch his hand write the word “rhetoric” over and over?
And yet, my father in ruin was in some ways more beautiful to
me than my father intact. I could see more clearly the outlines of
his soul. He let go, by necessity, of what Shakespeare called “the
bubble reputation,” and Ecclesiastes called vanity and vexation
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katy butler
of soul. He would never finish his book or his memoir, redeem
his delinquent boyhood, make his dead father proud, or eclipse
his better-known, long-resented, and now thoroughly dead older
brother Guy, the poet. My father could no longer strive and do.
He could only love and be loved. The race was run.
“When a fine old carpet is eaten by mice, the colors and
patterns of what’s left behind do not change,” wrote my neigh-
bor and friend, the poet Jane Hirshfield, after she visited an
old friend suffering from Alzheimer’s disease in a nursing home.
And so it was with my father. His mind did not melt evenly into
undistinguishable lumps, like a dissolving sandcastle. It was
ravaged selectively, like Tintern Abbey, the Cistercian monas-
tery in northern Wales suppressed in 1531 by King Henry VIII
in his split with the Church of Rome. Tintern was turned over
to a nobleman, its stained glass windows smashed, its roof tiles
scavenged for their lead, its church bells melted, its floor tiles
taken up and relaid in village houses. Holy artifacts were sold to
passing tourists. Religious statues turned up in nearby gardens.
At least one interior wall was dismantled to build a pigsty.
I’ve seen photographs of the remains that inspired Wordsworth:
a gothic skeleton, soaring and roofless, in a green hilly landscape.
Grass grows in the transept. The vanished roof lets in light. The
delicate stone tracery of its slim, arched, quatrefoil windows opens
onto green pastures where black-and-white cows graze. Its shape
is beautiful, formal, and mysterious. After he developed dementia,
my father was no longer useful to anybody. But in the shelter of his
broken walls, my mother learned to balance her checkbook, and
my heart melted and opened. Never would I wish upon my father
the misery of his final years. But he was sacred in his ruin, and I
took from it the shards that still sustain me.
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On June 4, 2006, my mother opened her journal after a
three-year hiatus. “Today, Sunday, a very disturbing devel-
opment in Jeff’s behavior,” she wrote:
He is repeating and repeating cleaning his teeth. It all
started on Friday when we bought a new water pick. Any
new procedure throws him, but today he was close to crazy
in the afternoon—kept going upstairs to the bathroom and
cleaning his teeth. I got him to do some cutting of vinca
minor in the front as he has done in the past. He took a
long time but managed to do a little. But as soon as he
got inside he started for the bathroom and began the tooth
cleaning. After supper he could not wait to go upstairs
again to clean his teeth.
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My father’s neurologist had earlier told us that this kind of
repetitive behavior—previously confined to getting stuck like a
broken record on a repeated phrase, or checking and rechecking
the calendar—is called
perseveration.
It is commonplace among
the autistic and the otherwise brain-damaged. On nuclear imag-
ing tests, it correlates with decreased blood flow to the outer layer
of two folded outer bulges of brain behind the forehead called
the frontal lobes, especially an area called the dorsal prefrontal
cortex, where neurons act as traffic cops, switching attention
from one word or action to something new. Damage to the fron-
tal lobes may be the most tragic of all mental losses, because the
lobes carry out many functions vital to the empowered adult self:
the ability to act morally, to make decisions, to think through the
consequences of actions, to problem-solve, and to make a plan
and carry it through.
“Perseverence, perseverence, perseverence!!!!” my mother
continued in her journal, misspelling the word in her agony:
Oh God now it’s like he is totally insane, and I am not sure
of what to do next. I will wait for the morning and hope that
he has slept it off. I am anxious and upset and do not want
to have a sleepless night because of it. I will do my stress
reduction tape and hope it helps me, but I feel my blood pres-
sure must be sky high as a result of frustration with Jeff. He
just won’t listen but goes on with his OBSESSION. Is this
Alzheimer’s? It certainly is dementia.
I feel my life is in ruins. This is horrible and I have lasted
for five years. Sometimes I wish he would die and set me free.
She played the relaxation tape I’d sent her that night, returned
to her morning meditation the next day, and wrote in the journal
again in a calmer mood. She was attempting to control her impa-
tience and anger, and my father, she wrote, was much better for
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it. She decided to accept what her life, and her husband, had
become. “I now acknowledge fully that the Jeff I married and
lived with for sixty years is no longer the same person,” she wrote.
“Jeff is querulous, anxious, and resentful and expects me to know
everything and attend, attend, to his needs. I try to respond in a
neutral way and simply get on with what I want to do.”
Other wives let go by taking off their wedding rings. One
found relief by thinking of her demented husband as a new
member of the family, an entirely different person from the man
she’d married. A woman of the Anishinabe tribe in northern
Minnesota held a funeral for her demented mother while she
was still living. “We lost the mother that we once knew . . . she
is the child now and I am the mother,” she told the social psy-
chologist Pauline Boss, who coined the term “ambiguous loss”
to describe what women like my mother were experiencing.
My mother did not tell me about that weekend. Only after
her death, when I read her whole journal, would I understand
how much she’d tried to shield her children from the misery
engulfing her and my father. She conducted her sacrament of
relinquishment alone.
She told me only that she was reading
Elegy for Iris,
John
Bayley’s obituary for his then-still-living wife, the brilliant Eng-
lish novelist Iris Murdoch, tracking her descent into dementia.
On the phone with me, my mother repeated the book’s most
famous phrase, from an unnamed woman who told Bayley that
life with her demented husband was “like being chained to a
corpse.” She reread Edith Hamilton’s books about the Greeks,
and sent me a quote from Aeschylus: “And even in our sleep,
pain that cannot forget falls drop by drop upon the heart, and
in our own despite, against our will, comes wisdom to us by the
awful grace of God.”
*
*
*
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On June 9, 2006, my mother found my father crumpled in the
driveway, moaning, unable to get himself up, one eye covered in
blood. She called 911. She’d gone down to the street with him to
bring in the garbage cans, and afterward she’d told him to walk to
the house alone while she visited a next-door neighbor. It was far
from the first time he’d fallen, but it was the worst. A CAT scan at
Middlesex Hospital showed cracked bones in his right eye socket,
plus evidence of a previously undetected stroke on the left side
of his brain near the back of the head that had probably occurred
in 2003. There were signs of a separate brain bleed behind the
cracked bones near his right temple. It wasn’t clear whether he’d
had a brain hemorrhage and fallen, or fallen and had a brain hem-
orrhage. Doctors sent him by ambulance to Yale-New Haven Hos-
pital, an hour away, to be evaluated for brain surgery.
The hospital, in the poor city of New Haven, was a train-
ing ground for Yale Medical School’s interns and residents.
Its emergency room, like those of most urban hospitals, was a
clinic of last resort for the uninsured poor. My mother stayed up
much of the night in a hallway outside the crowded ER, while
my father lay next to her on a gurney, tossing and muttering. He
waited nearly two days for a bed.
Yale—New Haven was ranked among the top 3 percent of U.S.
hospitals in ten advanced specialties that year, including neuro-
surgery, according to
U.S. News and World Report.
Sending him
there might have been a mistake. There is no necessary relation-
ship between the size and sophistication of a hospital and the
quality of its nursing care, and when you are frail, the simplest
touch from a good nurse can matter more than a high-tech spe-
cialty. I later discovered, in ratings assembled by a respected con-
sumer magazine from government data, that Middletown’s little
Middlesex Memorial hospital was rated the safest of the twenty
hospitals in Connecticut. Yale-New Haven ran fourth-to-last, with
high rates of hospital-acquired infections and readmissions not
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long after discharge and low scores on doctors’ and nurses’ com-
munications with patients about important things like how to take
care of sutures and what pills to take once they were released.
After my mother left to get some sleep, orderlies failed to
notice that my father had only one arm and did not help him to
eat or drink. Neither she nor I knew then that many hospitals
have become, in the words of one bereaved-son-turned-investi-
gative-journalist, places that provide “bodily repair services under
the direction of independent physician-scientists,” where over-
stretched nurses provide monitoring but very little old-fashioned
nursing care. My father grew hungry, thirsty, and disoriented,
lashing out at things that weren’t there. He was suffering from
what doctors call “hospital delirium,” a state of temporary halluci-
nation, confusion, and disorientation that affects about one third
of hospital patients over seventy. It can be triggered by not having
one’s hearing aids or eyeglasses, by medication errors or anesthe-
sia, and by a toxic hospital environment that somehow passes for
normal: noise as loud and constant as a highly trafficked street;
being wakened in the middle of the night for blood pressure read-
ings that could be done in daylight; harried aides; lack of needed
help to drink water or eat the terrible food; an absence of reassur-
ing human touch; not being spoken to by name; and windowless,
eternally lighted rooms that, like casinos, eliminate all sense of
day and night.
On top of this, hospitals today usually lack the three heal-