Alzheimer’s The Stranger in the Mirror
by Brenda Fountain, BSN,
RN
As a nurse, I have always found it difficult and frustrating to understand the needs of a person with Alzheimer’s
disease. Alzheimer’s is the most common type of dementia. It is a progressive degenerative brain disease first
discovered in 1906 by Dr. Alois Alzheimer, a German physician. His autopsy of a patient’s brain
indicated abnormal amyloid plaques and
neurofibrillary tangles on the brain. His patient was a woman in her late 50’s who had regressed in her memory
and abilities to childhood. The plaques and tangles are now the indications of Alzheimer’s disease, though study is
ongoing regarding the cause of the plaques and tangles. As a nurse, using the medical model of disease and
progression should be sufficient to begin to care for people with Alzheimer’s disease.
But it was as a daughter that I really began to understand Alzheimer’s. My mother became a stranger to herself. She
didn’t recognize pictures of herself nor her reflection. It doesn’t seem possible, but I watched my mother slowly
regress into infancy. I could do nothing to prevent it, so I threw myself into studying everything possible, hoping
to understand, hoping to somehow ease my sorrow. The knowledge that I gained did nothing to ease that sorrow but it
did help me in caring for and understanding my mother.
In this article, I hope to provide information on caring for a person with this disease through personal
experiences and education. According to the Alzheimer’s Association, a 1993 national survey indicated that
Alzheimer’s disease could be found in one in ten persons over 65, five of ten persons over 85 and that four million
Americans had AD, 19 million Americans had a family member with AD, and 37 million Americans knew someone with
Alzheimer’s disease. With the aging of our baby boomers, those numbers are going to escalate at a rate that will be
draining the emotions and finances of the people of this country. Becoming more aware of Alzheimer’s and its
treatment is a necessity not only for the medical world, but also for every person.
The article “A Trip Back in Time” by Christopher Johnson, PhD is an excellent guide to understanding the process of
regression. Dr. Johnson is a professor at the Institute of Gerontology at the University of Louisiana at Monroe.
His article provided the first step for me in defining the disease process. It helped me to understand the decline
and the moments of clarity that sometimes occur. At age 74, my mother still knew who I was but when asked her age,
she responded that she was 43 years old. She did not recognize her grandchildren. How could she, they were only
infants or had not been born. But yet, further along in her regression, she suddenly asked if my son was out of the
military yet. Dr. Johnson uses spiraling loops to indicate how there can be fluctuations in regression with AD. His
model would be very helpful professionally and personally for any Alzheimer’s caregiver.
As with most diseases, there are stages to Alzheimer’s. Reisberg’s Seven Stages of Alzheimer’s Disease (also known
as FAST-Functional Assessment Staging) is a very helpful tool that breaks down each stage into specific activities
of daily living (ADLs). ADLs can still be accomplished by a person with Alzheimer’s disease dependent on their
stage and dependent on our understanding of their stage. Understanding the person’s stage of illness is important
to every aspect of their care. Early Stages 1-4 still allows decision-making. The person should be included in
decisions that will eventually affect the end of their life. Excluding them isolates them and certainly contributes
to early feelings of paranoia. It should be noted that Stage 1 is asymtomatic, which means everyone could have
stage 1 Alzheimer’s disease.
While our mother was still cognizant of her reality (Stage 4), my sister and I talked with her about her choices.
The move was easier for her and us because we were following her instructions. My mother lived alone until she was
unable to perform daily activities (Stage 6c). My sister and I checked on her often and hired someone to help. We
did eventually place her in the nursing home of her choice. What we did not fully understand at the time was that
the placement should have been more thoroughly researched with her future needs in mind, as well as her present
needs. My mother’s choice was a nursing home that was familiar to her and was located close to my sister. The home
was pleasant and secure with a kind staff. My sister could see her everyday. I came on the weekends and called my
mother every night as long as she could recognize the concept of the telephone. The problem occurred as my mother’s
disease progressed. She began to wander into other residents’ rooms thinking that it was her room. She forcefully
insisted that the person leave her room by grasping the lady’s already broken arm. Because the staff had not been
trained for a true Alzheimer’s unit, they did not know how to handle this problem, nor did they have a dedicated
Alzheimer’s unit. She was promptly admitted to a geriatric psychiatric facility.
Cont'd Part 2
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