In the spring of 1994, when my 72 year old feisty, independent
and artistic mother, Dorothy, fearful of madness
or a brain tumor, was diagnosed with Alzheimer’s disease
(AD), she was relieved by the news. I was devastated.
Six months later I moved her closer to me, into an independent-
living condominium community for 50+ seniors.
Mother wore her house key around her neck and memorized
her walking routes.
She participated in exercise,
dance and ceramics workshop at the clubhouse. I found a
support group for early stage Alzheimer’s sufferers, which
Mother attended for two years, until she could no longer
construct a coherent sentence. |
Annette S. Fox, February 2007 |
Remembering that Mother
was a talented artist, I enrolled her in an adult watercolor
painting class. She responded with excitement at first, but
the sad truth was she could no longer draw or mix colors.
The most heartbreaking moment was seeing the flower
still-life she attempted but could not execute. Undaunted,
I had Mother volunteer to help other people suffering
from Alzheimer’s disease—the only way she would even
consider attending a day care group. She encouraged them
to sing along with her, to dance and participate in craft
projects.Within three weeks, she seamlessly integrated into
the group.
Since Mother seemed stable and settled, my thoughts
finally turned to me. I found an inspiring support group
for caregivers, and I gave myself the gift of Tai-Chi. I even
brought my mother to a couple of classes. Although she
couldn’t follow direction, the music and gentle body movements
seemed to give her pleasure.
To my surprise, I now found myself talking the same way
to my mother or to my four-year old. My mother knew
she was losing her ability to speak, to write numbers, to
write birthday cards to her grandchildren. She constantly
practiced her signature in the attempt to retain her identity.
Her check book register was a confusion of numbers
and misspelled names. I simply took over all fiscal tasks,
insensitive to my mother’s bruised self-worth and dignity.
When I questioned her about rotting leftovers and a sugar
bowl in the refrigerator, she frowned and responded,“I just
forgot, that’s all, now leave me alone about that.” I should
have recognized her depression earlier. Anti-depressants
proved to be enormously beneficial, and temporarily,
Aricept seemed to help her cognitive abilities, but nothing
arrested the slow downward spiral in her brain. Mother
began to confuse fork for knife, salt for sugar, refrigerator
for sink. She burned plastic containers of food on the
stove; she did not recognize her shoes. She became frighteningly
paranoid, accusing people around her of stealing
her mislaid money, keys, jewelry or hairbrush.
The dreaded day arrived when my mother became my
child. My clumsy acceptance was laden with great sadness,
a sense of defeat and anger at no longer having a mother
to mother me. And what of the sense of humiliation my
mother must have felt being treated as a child by her child.
When I changed her adult diaper, her face collapsed into
tears, and she cried, “Hurry up and get me out of here!”
My mother’s stalwart independence, her sense of dignity
and privacy were forever compromised. I needed professional
help. Within two years Mother needed to move
again, into an assisted living facility. Three relatively happy
months later, she suffered a major stroke. After rehabilitation,
Mother quickly deteriorated to a point where she
needed twenty-four hour skilled nursing care. We were
out of money.
When my mother entered the nursing home, she still
spoke a few recognizable words and could still walk. She
still enjoyed a good joke told in her presence, outside
excursions to the riverside park and holiday meals with
family members.
Seven years later, however, no longer ambulatory or able
to feed, bathe, dress or speak, she is connected to the world
with only her five senses. She still enjoys eating and loves
listening to the opera. There is nothing wrong with her
hearing and she knows who is treating her well or not,
although she no longer recognizes family members. My
visits are one-sided conversations enlivened with old tunes
from our past. There is only the precious and fragile present,
time for only loving kindness and total acceptance.
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