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I Hoard It On The Grapevine
On my return home
from the land of Lincoln last week, I started thinking about my
lessons learned from the caregiving experts I met while in
Nebraska - the family caregivers. I was there last week to
keynote two events held in the area. I always think that any MBA types wanting to learn about the demo-psycho-social-markettrending-
kind of stuff relating to caregiving only need to spend time
listening to the family caregivers. A few years ago, every time
the topic of conversation in the Q and A sessions at our
Fearless Caregiver Conferences came around to Senior Driving,
all other talk came to a screeching halt. Then a few years ago,
the show-stopper was Medicare Part D and last week, I heard the
first new attention grabbing topic of conversation in a long
while. The subject was Compulsive Hoarding.
According to
WikiPedia, compulsive hoarding (or pathological hoarding) is a
term which is used to describe extreme hoarding behavior in
humans. It involves the collection or failure to discard large
numbers of objects even when their storage causes significant
clutter and impairment to basic living activities such as moving
around the house, cooking, cleaning or sleeping.
In the compulsive hoarding cases cited by
members of the Lincoln audiences, the hoarders they were dealing
with were mostly their senior loved ones. This topic also
caused one of my favorite moments at these events, which I call
"Stump the Panel." Although the experts on our panel were
well-renowned and extremely knowledgeable, in this case the best
responses actually came from the caregivers in the audience who
have dealt with their loved ones compulsive hoarding. One
suggestion that seemed to work with a gentleman's father was
organizing a session where his dad was able to take charge of
the distribution of his hoarded goods to his family members.
Not only did this work well to help him in his move into
assisted living, but the local Salvation Army recorded record
donations that month.
If
you have any hoarding stories of your own, please don't hoard
them from us.
Take care Gary Barg Editor-in-Chief
gary@caregiver.com
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Feature
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The Value of Friendship
By Marlene Pyle
I’ve learned many things since I began taking care of my 85-year-old
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As a Registered Nurse, my previous
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Those Inexplicable Instructions!
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It happens to every caregiver. You're at the doctor's with your
loved one. You and your loved one are both feeling well,
..Continued
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When Depressed Husbands Refuse Help
By Beverly Wax
To the outside world, Emme lived a charmed life.
She was a successful model, creative director of her own
clothing line, a television host, lecturer, and mother
of a beautiful baby girl. ...Continued |
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Communicating with a Loved One
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Here are some tips if you struggle talking to your loved one, or if you
simply want to improve the connection you share with them.. ...Continued
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Carenotes |
Hello,
I moved
in with my mother about 4 ½
yrs ago. I am single and my
children are grown. Mom had
a blood clot in her leg and
a near stroke about 4 ½ yrs
ago. Most of the time you
hear about the parent moving
in with the children but I
did the opposite. I do it
all! My brother lives in
Grand Rapids and my two
sisters are too busy working
building for their future.
I have given up my life, so
it seems and I did not
realize how hard it would
be. My mom seems to control
my every move down to
knowing what I spend and how
much I make. She watches me
like a hawk.
My question is how do I look
out for my future? The home
is in my brother, two
sisters, mine and also mom’s
name. I feel since I am the
primary caregiver and no one
else has the time to help,
the home place needs to be
transferred over to me so I
have a place to live after
mom is gone. Am I wrong?
She is 89 and in pretty good
health now but cannot walk
and is very fearful, so she
could live another 5 yrs or
so. Mom says for me to move
in with my children when she
is gone. Is it right that
no one is helping me but
they all get equal
inheritance? I am so
worried about my future. I
am 60 yrs old and I get paid
25 hrs a week to care for
mom but she feels since I
live in her home that I owe
it to her to be available
24/7 (because I live here).
I have NO life. Is this
fair or am I asking way too
much?
Thank
you for any advice.
D
Answer This Week's CareNote:
carenotes/2007/index.htm
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