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Experiential Learning
and Physiological Changes
This is the inaugural column of BUILDING IDEAS , which is
dedicated to exploring the various ways the environment influences
and impacts on individuals with dementia and the settings
they inhabit/experience. While the major topics covered in
each column will be related to the theme of each issue, I
invite you to write in with your quirky questions, sticky
issues, persnickety problems, and creative or brilliant ideas.
Let this be a forum for sharing with others as we travel along
our journeys with Alzheimers disease and related dementias.
This issue is dedicated to caregiving,
and so well focus on ways of helping caregivers understand
how the individuals with dementia that they care for may
perceive the world around them. Much has been written about
physiological changes, both those associated with aging
and those which result as a consequence of dementia. These
changes fundamentally impact how individuals with dementia
perceive and make sense of their surroundingshaving
potentially as great an impact as the cognitive changes
they experience. It isor should bean integral
part of every staff education program. Yet getting caregivers
to understand how these changes are experienced by people
with dementiahow it impacts them on a daily basisis
challenging. This column will focus on ways to sensitive
caregivers to how some physiological changes affects daily
life of the people they care for. It is my belief that people
have a greater understanding of something when they experience
it for themselves. The classic example is having a baby.
One can describe it in great detail, but it will never be
the same thing as actually having a baby. Therefore, this
column describes a series of reasonably simple experiential
exercises that will sensitize caregivers to how some basic
physiologic changes are experiencedand how they affect
an individuals perception of their environment. It
should be noted that none of these exercises will exactly
replicate the physiological changes they relate to. Rather,
they are meant to give a sense of how different daily life
can be if someone is experiencing a variety of physiologic
changes. After each exercise, ask the caregivers to describe
what the experience was like, to think about what would
be hard for them to do on a regular basis with that type
of impairment, and the changes that caregivers can make
to compensate for these changes.
VISION There are a variety of diseases
which significantly impact vision, diminishing peripheral
vision, clouding central vision, or limiting all vision.
Slides or photos of what these changes look like
can only give a limited sense of how these changes actually
impact a person. Buy inexpensive, low correction glasses
(easily available at variety and dollar stores), and lightly
smear the lens with a little petroleum jelly or chap stick,
using a circular motion around the lens. The goal is to
still be able to see basic shapes, but impair ability to
recognize faces. Have caregivers wear the glasses for 10
minutes while walking around the facility. To mimic some
eye diseases which affect one eye more than another, try
modifying only one lens. Alternative modifications include
applying the petroleum jelly/chap stick to only the outside
edges of the lens, or only to the center of the lens. To
mimic the change in pupil size, which limits the amount
of light which enters the eye, have caregivers wear sunglasses
inside for about 30 minutes (you dont want to induce
real eye strain). Once theyve walked around the facility
for a while, and tried to read the signs, or see what food
is being served to them, or walked into the tub room, or
walked outside and back inside again, bring them back together
to discuss what the experience was like. What was hardest?
What was most startling? How did they feel? Can they think
of residents whose behavior might be explained somewhat
by their vision impairments?
HEARING There are two aspects of
hearing changes that are important to sensitize staff to.
The first relates to the loss of hearing acuity in the range
of normal conversation. Have caregivers wear ear plugs (your
maintenance department may have some, a local pharmacy may
sell them, or they can be inexpensively ordered in quantity
from most medical supply companies). They should wear them
around the facility for at least an hour, if that is possible.
This will get them somewhat acclimated to how some sounds
are screened out and very hard to hear. The second aspect
of hearing is more specific to dementia, and relates to
the decreased ability to filter or tune out noises that
are common in any caregiving setting, but particularly present
in long-term care settings. Find two tape recorders, and
set them to record for 30 minutes in two commonly noisy
areas (such as the dining room during a meal, near the speaker
for the call bells or alarms, near the nurses stations,
or wherever it happens to be noisy in your setting). Then,
during a meeting or training session, set these tape recorders
on opposite sides of the room, and let them play at a moderately
high volume. After 30 minutes discuss whether people were
distracted, have a headache, or are particularly tired.
Did they have a hard time concentrating on the meeting?
And how did they feel after they wore the ear plugs for
an hour. Many people begin to screen out a lot of what is
going on when they cannot hear well. Discuss how these two
changes in hearingtogethermight make people
with dementia feel.
TASTE & SMELL The sense of
taste is linked to the ability to smell. Have a caregiver
wear a nose plug (often available at pharmacies or local
sport stores) and be fed a meal by another caregiver. If
you serve a pureed diet, have them try this food as well.
Add one of the pairs of modified glasses to give this activity
even more reality.
TOUCH Give caregivers a pair of
thin cotton gloves (available from most medical supply companies)
to wear for at least an hour. Cotton is better than latex,
but if they are not available, large latex gloves will do
(it is important that they not be skin tight). Additionally,
wrap tape or a rubber band around the knuckles to mimic
arthritis (be sure not to cut off the circulation!). Try
taping the thumb across the palm of the hand, and ask people
to go about their normal duties for 20 minutes or so. Ask
them to think creatively about how the environment could
be modified to make it easier for the residents to pick
things up and use them.
MOVEMENT The variety of conditions
which affect movement and balance are extensive and affect
people in myriad ways. Some simple exercises to try include
wearing training weights (1-2 pounds each) on the ankles
and wrists for several hours (if they can be tolerated for
that long). Alternatively, have people spend time in a wheelchair
or a geri-chair. Preferably, this should be at least 4 hours,
although a full day is best to give a sense of the multiple
barriers even a well designed environment can place on wheelchair
users. Alternatively, have caregivers put 15-20 navy beans
or unpopped popcorn in their shoes and walk around for a
while. They will quickly see why distances that do not seem
long to them may be very long indeed for the people they
care for. Again, discuss how these impairments are likely
to be experienced by the residents, particularly those with
cognitive impairments.
These are only a few experiential exercises
that can sensitive caregivers to how differently the world
may be experienced by people with different abilities and
conditions. We focused here on ones that relate to how changes
in an individuals senses influence his or her overall
experience of the world around them. There are, of course,
a variety of experiential exercises that relate to specific
caregiving activities such as meals or bathing or incontinence.
We also did not discuss experiential exercises that reflect
cognitive changes associated with dementia. Wed like
to be able to feature some of these issues in future columns.
If you have an interesting experiential exercise that you
use, send it in and well share it with others in the
future. Or if you have other environmental questions or
issues youd like to see explored in this column, let
us know. Well try to include as many as possible.
Margaret
P. Calkins, Ph.D. President, IDEAS Consulting, Inc. Reprinted
with permission from Aspen Publishers, Inc., Alzheimer's
Care Quarterly (ACQ), Volume 2, Issue 1. Order by calling
1-800-638-8437 or on-line at www.aspenpublishers.com/journals/acq
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