ResetA Story by LilyDaughter's account of the consequences of her father's AlzheimersHonestly
don’t think it has made me a better person, though perhaps if you saw me with
him you would disagree. It’s not that I’m kinder now, only that I’m better at
pretending. I told Liz last time that I drove straight down to the station when
they called me saying Dad had turned up. It’s not exactly a lie. I visit him
when I can. No, that’s not true. I hate the place. Sometimes I hate him; more
often I hate myself. I read some of these blogs by other people whose relatives
have Alzheimer’s, and they all talk about it being a battle, about how it makes
them stronger. Except it can’t be a battle. There’s nothing fair about it,
there’s no winning. “It was awful Liz, I didn’t even hang up,
I drove like a maniac all the way. He’d forgotten why he was there. And the
note, oh god the note, it was so tragic,” that was true, “and so sweet,” less
true, “and all I could think was, this is going to happen to me; in forty
years, this will be me. That’s so selfish.” And I know of course she will tell
me it’s okay, and everyone thinks like that sometimes. I only drip-feed her
these sincerities because she’s my friend. There is nothing honest about me
anymore. “He was going to jump, I really think he was.” I saw it all happen, saw myself drop the
phone and grab for the keys on the hook, saw myself driving. But I didn’t feel
anything, not this time. There was no fight or flight, only autopilot. And
somewhere distant I heard myself wish he would have done it this time. I
imagined the train hitting him before I realised I was doing it. Dad has this
white plastic pedometer he always clips to his belt, he’s had it as long as I
can remember, really old technology with this screen like a calculator display
and two little rubber buttons to reset or turn it on and off. It’s the one
thing he never forgets, he always clips it on in the morning. When I was
younger, I always wondered what was inside it that made the numbers go up when
you shook it. Now I imagined the white plastic cracked in halves like an egg
shell, and its metallic guts spilling out over the train tracks. It was so much easier before mum died. I
don’t go to church anymore because I know they all want me to be her. Mum and
dad called me Etta, after her and after the singer. Except I can’t sing. Mum
had a beautiful voice. She sang at church, and at home when she was fluttering
round the kitchen, with this flawless vibrato. Dad used to call her his humming
bird. I think everyone just saw the beautiful blur of her wings round that
kitchen, and nobody could ever tell how hard she must have had to flap to stay
up in the air. When he started to lose it she always knew what to do, even when
it got bad. And sure there were days when she got quiet and poured herself a
drink but she never let anybody see. I only ever saw the bottles slowly
draining away. I read somewhere that said Alzheimer’s was like a rising tide. I
liked that. More than all the battles at least, it was quieter. It’s nice when
people can be quiet, I think. He’d go down to the train station even
when she was still alive. He’d say right to her, “I
have to go see Etta now. She’ll be waiting,” and she’d say something kind to
him and raise an eyebrow at me, “I reckon she could wait just an hour or two.”
Then in an hour or two he’d have forgotten. But the lucidity was the worst. Dad
was a journalist. He set off metal detectors in five different continents with
that damn pedometer. He was the smartest man I knew, but he never made you feel
stupid. When he remembered it hit him hard. He used to write these beautiful
letters, and nobody could tell if they were love letters or suicide notes, he
never finished one. But down at the home they always assumed the worst, and
whenever he got out and made it down to the train station again they’d always
assume. One time he dislocated his knee. Nobody
knows how, it was one of the times he got out. They only know he racked up ten
thousand steps on his pedometer. Anyway, the doctor gave him this drug called Propofol
to kill the pain while they reset his leg. How it works, they said, is that it
interferes with the memory of the pain. So he’s unconscious on the bed and he
can feel everything that’s happening, big fat tears are running along his
wrinkles but he’s only making this little whimpering noise. Then when he wakes
up he forgets. So it doesn’t count. He’s been worse lately. They upped his
dosage of Aricept when he started grabbing at the nurses. I don’t know how they
find the patience to just shuffle a half a yard back and laugh it off. I can’t
laugh it off any more. He started saying things like “caca” when he needs the
toilet. He laughs at his reflection. He spits too. And I have this dream, and
in it he’s growing bigger and bigger into this enormous, grotesque, wrinkled
baby. And if forgetting it all means it never counted then maybe it would be
best if he did it one of these days. That’s horrible, I know it’s horrible. But
it’s true. I take him back there again and it’s
horrid. Fluorescent puddles of light and wipe clean surfaces and worn down
vinyl floors. They call themselves a home. This is not a home. “This
is a nice place. Where are we?” and he presses the rubber reset button on his
pedometer. You can’t tell me when that screen blinks a black zero all those
steps just disappear. It doesn’t work like that. It can’t. © 2017 Lily |
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