Last week I received an email from a
long time reader and Fearless Caregiver living in Texas. She
wanted me to know that her beloved husband for whom she had
cared, had passed away:
I
thought I would let you know that my husband,
passed away on January 26. He fought a
long hard battle. I was with him every
step of the way and became his voice. He
asked me, after putting him in a nursing home a
few years ago, if I wanted a divorce. My
answer was, "I don't remember that part of our
wedding where the minister said that when you
become sick I could walk away." His
Parkinson's was the disease that took the man
away from me but taught me many, many things
along the way. A long trip - 23 years of
struggle for he and I.
He was my
hero. A U.S. Army Drill Sergeant, a man
who lived the way he wanted to live and passed
away the way he wanted to go. The funeral
was - his idea - no fluffy stuff. I gave
him my word and the service was not fluffy.
It was for a man who lived, raised 6 children,
celebrated our 41 years of marriage together,
and in the end - the greatest man I've ever
known.
I will
miss him. My thoughts today are - he's in
a much better place and he's giving orders all
over the place - Drill Sergeant's never change.
I received another related
email last week from another reader:
I know that your website/newsletter is about
caregiving, but I would like information about
the emptiness of the caregiving ending. I
was caregiver to my elderly uncle (92) for 5
years. He passed away Friday. In the
5 years, he was like a cat with 9 lives, dodging
disease bullets like in a war zone. He
lived through many things that a
younger/healthier person may not have. So
I was not really prepared that he would actually
die when he did. My husband checked on him
for me in the middle of the night and reported
that he was” gone.” My reaction was, WHAT?
I couldn’t believe it! I was relieved
because he was suffering, yet I was prepared for
him to linger. I now have this huge hole
in my life of things that I used to do that I no
longer need to. I hear him in his room.
I start there frequently to check on him.
I think that one of the things to do is to get
his rooms back to our normal household, but I
was wondering if there are other things to help
get one’s life back into some semblance of a
routine.
These caregivers both talk about one of the most
important aspects of caregiving and that is what
happens afterwards.
Once caregiving ends either due to the
health episode resolving itself or the passing
of your loved one, many of us are left to create
a new world which my mother calls Phoenix
Rising. This is a time where the person you need
to care for the most turns out to be yourself.
Sign up for an
upcoming Fearless Caregiver Conference
Take care
Gary Barg
Editor-in-Chief
gary@caregiver.com

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Take a look
at the new books in our bookclub.
Listen to the interview with two of
the authors. |
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Feature Article |
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Multiple Sclerosis: Understanding and
Living
with the Disease |
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By
Sandra Ray, Staff Writer |
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Mulltiple sclerosis (MS) is one of the most
baffling and debilitating
neurological diseases. About 500,000
people in the United States are
afflicted with it. Worldwide there
are more than 2.5 million persons
who live with MS each day....Continued
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Additional Article |
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Mobility and Exercise: No Excuses |
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By Jennifer Wilson, Staff Writer
Whether you’re the caregiver for a
loved one who has a mobility issue
due to a stroke, or because of SCI
(spinal chord injury), arthritis,
Multiple Sclerosis, or something
else, or if you yourself have a
mobility issue, the fact is, you
still need to keep your weight at a
healthy standard. ....Continued
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Guest Column |
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A Silent Crisis: Working Caregivers
Are Begging For Help
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By Gema G. Hernandez, D.P.A.
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At time when private enterprises are
trying to increase productivity,
reduce costs and enhance the quality
of their products or services there
is a growing crisis in corporations
today that is preventing them from
achieving their corporate goals. ...Continued
(Do you have a story?
Tell us.)
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Caretips |
Helpful Tips for the Vision Impaired
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By Deborah Kogler
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1. Lighting
Increase
the amount of lighting directly over the task that you
are doing. Focus the light directly onto what you are
doing. LED lights, natural light and natural daylight
bulbs are recommended.
Do not use fluorescent lights as fluorescent
light causes glare.
...Continued
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