I lived with my mother for fourteen years
when she had Alzheimer’s disease. I published a book about the experience. A
university invited me to be a guest teacher because of the book.
When I was a student, universities were very
crowded. I was worried that I would need to talk in front of hundreds of
students. Actually, there were only six students in front of me—because of the declining
birth rate in Japan, I guess.
I decided not to give them a speech
but to have a round-table discussion.
I briefly introduced myself and my book, then
asked: “Do you have any questions?”
The first question was, “Why did you decide
to care for your mother?”
That was not the question I expected. I couldn’t
answer for a while.
I never decided to take care of my mother,
not intentionally. I lived with my parents, and my mother happened to become an
Alzheimer’s patient. At that time, my mother had many friends. They visited our
house every day. I assumed they would take part in caregiving for my mother, but
they didn’t. I assumed government welfare offices and hospitals would take care
of my mother, but they never actively helped us. The caregiver needed to make
the first move.
I never wanted to take care of my mother in
my life. Everyone dumped the caregiving on me and ran away. No one would take
care of her except me. I didn’t have the courage to dump my mother, and I never
did.
I couldn’t answer the student’s question
then, but I can now.
“In the future, I wish only people who
wanted to decide to become caregivers.”
Proofreading
by Michael W, ProofreadingServices.com
Picture
Undrey
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