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©
2002 |
Ageing
with dignity
Not too many years ago, taking
an ageing person into one's home for care could be overwhelming, especially
if the person was suffering with serious physical or mental problems. Usually
these lovely old people ended up in a "rest home," left to fade away quietly
among strangers.
About a year ago it became
obvious that my mom could no longer care for herself. My wife, Sue, had
said earlier that when the time came there was no question who would care
for her: us.
So we painted and decorated
a room on the sunny side of our doublewide shaky-shanty and mom moved
in. Little did I know what we had undertaken...
Once in our home she had only
the nurse from Senior and Disabled Services coming to see her once a month
for a check-up. Even though the support from this superb state agency
is splendid, it is overstretched. The nurse was usually not available
when push came to shove.
Every time mom began suffering
with an unknown health problem -- dizzy spells, upset stomach, pains in
her lovely old body, troubles with bowel movements, and other unpleasant
symptoms -- I was hamstrung without knowing who to call, or what to do.
Making contact with her doctor, especially on weekends, is difficult,
and that left us 911, the hospital, or Merck's Manual.
Calling 911 for a non-emergency
situation, even though she was demonstrating stress and discomfort wouldn't
do. So I'd get in touch with an EMT through the fire hall social number
and discuss the situation.
But these extraordinary people
can do just so much over the phone, medically and legally. Once, however,
they came to my house with the ambulance when mom was having severe abdominal
pains.
"Just to be sure..." the EMTs
said as they came in smiling.
Mom still talks about how
wonderful she felt as they ministered to her.
In spite of the help the EMTs
provided, each time mom went into another tough spell our frustration
levels went into high gear.
"Just take me to the hospital,
Jimmy..." was a frequent suggestion, sometimes an order.
Then one day after hearing
my plight, a friend suggested I contact Hospice of Redmond and Sisters,
and see what they could do to help.
I did... and the sun came
out. I called at 9 a.m. and by 11:30 a.m. there were three Hospice people
sitting in my living room -- two talking with Sue and I about how their
services worked -- and a nurse going over my mom with a fine-tooth comb.
From that day many of mom's
physical problems and my feelings of helplessness ended, we had a real
live person I could talk to anytime, seven days a week. At first, Nurse
Beverly came by twice a week, and her ability at giving mom a tune-up
and smoothing out the rough places was uncanny.
One example stands out: Sores
on mom's legs. Because she spends hours sitting in her chair -- only getting
around with the aid of her walker to go to meals, bathroom, bath and then
off to bed for naps and bedtime -- excessive fluids collected in her legs,
causing sores.
Beverly didn't blink an eye.
"Curly," she said in her warm,
cuddly nurse's way, "Jimmy's going to place a rolled up sleeping bag under
the foot of your mattress and then put your feet up on a pillow during
the day to take down that swelling."
It worked -- the swelling
and sores are gone. End of problem.
Unfortunately, mom's Hospice
services have come to an end. She's not gotten any worse. In fact, she's
better, thanks in part to her own natural ability to cope with growing
old, and the know-how and TLC supplied by Hospice.
I know when she gets ready
for her voyage out among the stars Hospice will be with us to help make
the event as acceptable as possible for everyone -- and I hope they're
around when it's my turn.
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