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Principle Six
Recently I spoke to the
members of a Stroke support group in Tamarac, Florida. It
was an honor to speak to this group for many reasons, but
one in particular is that they understand the relationship
between the caregiver and their loved ones who are living
with the effects of a stroke.
Another reason is that
one of my neighbors when I was growing up is a member of
this group. Herb is a fiercely independent man, and always
had the coolest house to visit for the kids in the
neighborhood. With an extensive jazz collection and a full
drum set, it was like living next door to Buddy Rich.
Herb is battling the
effects of his stroke with the same determination that he
used to beat on the drums in that recreation room and with
the same class and cool demeanor. His wife, Estelle, is a
true partner in care as she knows how to give him his space
and when to step in for some moral and physical support. The
support group that they attend on Saturdays seems to be
populated with the same type of resilient souls, who range
from 36 to 96 years of age. At one point a question was
raised about trying to explain to a friend about the value
of support groups. This member’s friend was afraid of
spending time in a group of people who are just “sitting
around whining about their problems”. There was no evidence
of any whining whatsoever in this group as they spent the
afternoon together. I suggested that her friend take a
“Leap of Faith”, and go to an appropriate support group at
least three times, that most chances are her friend will
find the support and guidance that this group affords each
other during their meetings.
One more word on support
groups, I tried to get my dad to visit with a support group
after his bone marrow cancer diagnosis. He wouldn’t hear
about any such thing. A few months later, at the end of his
nightly news program, Tom Brokaw was talking about support
groups. The film they used in that news piece was of a
cancer support group down the street from my dad’s house.
Wouldn’t you know it, there was dad holding court, having a
terrific time. It took NBC nightly news to let me know that
dad was going to a support group. And who said that there is
no good news anymore.
Fearless Caregiver
Manifesto
Principle Six
I will fearlessly seek out other caregivers or care
organizations and join an appropriate support group; I
realize that there is strength in numbers and will not
isolate myself from those who are also caring for their
loved ones.
P.S. Thanks to everyone
who wrote after last week’s message about Morris, my new
heart. For everyone who asked. Here’s Morris….

Take care Gary Barg
Editor-in-Chief
gary@caregiver.com
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Feature
Article |
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PreSchool in
Alzheimer's Care Center
by Diane Guthrie
Sitting around a table in the dining room at The Hampton in
Tumwater, Washington, preschoolers, their teachers, and Alzheimer’s
residents paint with watercolor...Continued |
Additional Articles::
Caring at Work
By LeAnn Thieman
Are you one of the 54 million Americans who care for a family member?
One of the 20-50% of employees who tend to a loved one before going to
work, then return to care again after a long hard day on the job?.
...Continued
Is a Registered Dietitian Part of
Your Home Health
Care Team?
by Rita Miller-Huey
Has a registered dietitian ever visited you in your home to talk to
you and your loved one about their diet and health? Poorly nourished
adults have higher sickness and death rates than those who receive
optimal nutrition. .
...Continued
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Guest Column |
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Maintaining Nutrition When They
Can't Sit Down to Eat
By
Barbara Williams, RN, BSN
It is difficult to plan for meals when the person you are
feeding can’t sit down and enjoy a meal.
......Continued |
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Caretips |
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Mixing Muscle and Maturity
By Sean Kenny
“I don’t need to exercise anymore! I’m too old
to work out! What can I do at my age anyway?”....Continued
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F r o m O u r R e a d e r s |
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Carenotes |
I'm a 38 year old mom of an
autistic son, and the daughter
of a post-stroke father who is
disabled and in the early stages
of dementia/possibly
Alzheimer's. I also work full
time. I'm hoping you all might
know whom I can contact for some
help or advice.
My work is hassling me over my
taking time off whenever I need
to tend to my son or father. I
know there has to be some ACLU
site or someone who can back me
up and let my company know that
caring for not just one, but two
disabled family members is quite
a chore and that is sometimes
necessary for me to not be at
work.
Any advice? Thanks much, in
advance!
Answer This Week's CareNote:
carenotes/2006/index.htm
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