I don't write about dad's Alzheimer's much anymore. It seems that when I do all I end up doing is repeating the same tragedy. And it tires me writing about it because there is never anything new about dealing with this except the profound sense of loss that drags on. The disease is not going to back off, no cure or pill to halt the symptoms will be miraculously discovered. Alzheimer's is going to continue to worm its way into my dad's brain like a thief. And no one can stop it. There is no hope. None at all.
Alzheimer’s is
a vicious enemy. Unrelenting unforgiving, un-everything. It hits families and
keeps on hitting with more and more cruelties. It progresses until all the
family is left with is a desperate wish for it all to end, and the guilt that
accompanies that wish.
It has been three years since I have really had a conversation with my dad. I told him today that I wish he and I could still talk. He said, "Me too". My dad is still here in body, but he is a bent,
confused, tearful shell of himself. My father lives 24/7 in a Veteran’s
Administration Hospital. He is dependent on others to do every basic living
task for him. He has to be fed and bathed.
He has be supported and led on the rare occasions when he walks; a
shuffling, tiny stiff legged walk, thanks to his accompanying Parkinston’s. He has to be assisted in and out of bed. He
suffers from an inability to speak coherently in what is known as aphasia. He
cries almost constantly, becomes easily frustrated, gets angry.
Last week my dad looked straight at me and asked who I was. And I had been with him three hours that day. That was the first time
he has asked me that. I know that the chances of his remembering who I am grow
dimmer and dimmer each day. He seems to have regressed to a point of about five to ten minute spans of
memory. I once read that a goldfish has
a memory of approximately ten seconds. My oftentimes dark and sardonic outlook
takes a twisted solace in the fact that my dad’s memory is, at least, better
than a goldfish’s. My father’s
eighty-seven year old mother visited him recently and within fifteen minutes of
her leaving he didn’t even remember she had been there. In fact, he quite
adamantly insisted that he hadn’t seen her in a very long time. I gave up
trying to convince him otherwise.
On Dad’s especially “bad” days he
contorts his wheelchair bound body into an almost 45 degree angle attempting to
retrieve objects from the floor that only he can see. On those days it is
virtually impossible to get him to sit up long enough to feed him dinner. And
joining him in his bent over contortions so that a bite of food can be spooned
into his mouth is an exercise in physical and mental exhaustion. Those are the days when I only manage to hold
back the tears until I have made it safely to the interior of my car in the
hospital parking lot. Those are the days that I cry until my entire body shakes
with the unbound grief.
My brother, who has only in the past
year allowed himself to look dead on into the face of Alzheimer’s, manages to
keep his emotions in check and, on the surface at least, appears pragmatic
and unaffected. I know he isn’t. He has a family, a young child, a demanding
job that entails his being out of town more than he is home. I live closer to
my mother, and although I did attempt to ‘run way” by taking a teaching job
overseas last year, I quickly admitted defeat and came back to the United
States. Alzheimer’s keeps winning. And it will keep on winning. There is nothing we can do. We are powerless.
My mother, who cannot accept that
this awful, almost unspeakable thing has happened, gets by day-to day the best
way she knows. She visits my dad several times a week, perhaps too often. She
overextends herself, tries to distract dad from his continuous crying jags and the sadness that he can no longer articulate. She talks to him,
champions for him, then goes home alone to a house that she and my dad made
together, pretends that Dad just might get better, then plummets to low lows
when she admits to herself that he has descended into a place where we can’t
go, a place from which we can’t rescue him. The Unmemory Place..
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