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I am John's caregiver, a heart-rending,
thankless yet rewarding task. Like many caregivers I found that the job
was mine because my nearest and dearest was desperately ill. A caregivers
job, in my experience, covers a wide range of tasks. Primarily I dealt
with the Hospital, a big scary place full of high powered professionals. I
struggled to absorb medical terms and treatments as John went through the tests
required to assess him for transplant.
If I could show myself to be practical, level
headed and reliable "The Team's" job would be a little easier. I
found myself playing this role and hiding my fright and distress.
On the home-front caregivers find themselves
trying to hold the family together as well. I had to tackle jobs that I
really had no experience of. Luckily no fuses blew and the lawn mower
always started first pull. Family and friends, of course, were frantic
with worry and I found myself constantly answering the phone, providing updates
and reassurance. To lessen the load I set up a network of people to
inform, who in turn passed information on.
When John was sent home from hospital to wait
for a liver I had to deal with drugs and dressings, night feeds and
nutrition. I got to know the District Nurses and the Cancer Nurse
well. These ladies were a bright spot in our existence. During this
time I realised that I was becoming more isolated and I felt very alone behind
my bright, brave facade.
The transplant was successful and John has been
well for 18 months and I find myself faced with the problem of trying to let
go. Now my constant care is not needed I must stand back and let him
live. If I monitor him I must do it discreetly and try not to panic if he
gets tired and sore. I live with the knowledge that we are together on
borrowed time. My task now is to try and make our lives as full and happy
as possible.
I have met other caregivers and I see in their
faces what I see in my own. I see the tension around the eyes and the body
language which indicates the stress they live with. Many people have
introduced themselves as "only the caregiver" and have become retiring
faceless people. Many like myself have put their needs last.
You do a job that other people can only guess
at. Your continued good work is so important. It needs to be
acknowledged and appreciated.
This article has also been published in our
Newsletter, "Hepatic Happenings", Volume 2, No. 1, February
2001.
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