From the Moment of Diagnosis
A Book Review of “Designated Caregiver: Resource Manual forthe Caregiver On Call 24/7” by Cecelia Salamone
Every caregiver or special needs parent can recall in sharp detail the moment of a
life-changing diagnosis in the life of their loved one. Whether it is
dementia, cancer or cerebral palsy, a caregiver's life can be considered in two parts: ‘before’ the diagnosis and ‘after’ the
diagnosis.
When our son Nicholas was about five months old, my husband
and I saw the first in a long line of neurologists.
The bearded, rather rotund physician looked at Nick and silently
conducted a wordless physical examination. He
turned to us and said, “Your son has clearly suffered a neurological
injury.” I asked him what that
meant. “Cerebral palsy and mental
retardation”, he replied. I blinked, my
polite smile frozen on my lips.
I had no caregiver or parenting handbook. Nicholas was my first child and it was 1988, in the days before internet. What I had was the phone book – The Yellow
Pages. I started with “A” for
Associations and then moved to “S” for Societies. I was searching for anyone who might help me
with information and home support. I
desperately wanted someone to tell me what to do, how to act, and most of all,
about my role as the mother of a baby with an uncertain future. Our family eventually found its way and
Nicholas was and continues to be my greatest teacher. In helping my Mom through her challenges, I
use my valuable experience with Nick to find short-cuts in locating the
supports she needs to lead a good life.
Today, I want to talk about a guidebook I would have loved in 1988. It’s called “DesignatedCaregiver: Resource Manual for the Caregiver - On Call 24/7” by Cecelia Salamone. Recently, I’ve been a little stressed about
Nick’s resistance to communication therapy and by my mother’s lease renewal at
her senior’s residence. Reading “The
Designated Caregiver” put me at ease – I felt the author almost palpably holding
my hand, telling me it’s alright, here is what you need to know…. The book is a large sized paperback and it’s
easy to read. There are worksheets with
ample room to make notes as well as multiple mini-narratives to demonstrate
caregiving challenges and how to meet them with patience, love and an
imperative for self-preservation.
There are many manuals for caregivers on the market. But I have not seen one like this before;
yes, the author uses her own experience as a reference (and there are many lovely
family photos), but this book is about the reader and their caregiving experience.
There’s an astonishing amount of detailed and sensitive advice from what
to expect when roles reverse between parent and child, to what paperwork will
be required at various types of medical appointments. It is as if Cecelia Salamone remembered
EVERYTHING she learned in her years of giving care to her parents and wrote it
down as an act of loving solidarity with every other person who lives the
caregiving experience.
Whether you are a caregiver for someone young, or old, ill
or infirm, this book will be helpful. It
is an instant classic in the library of caregiver literature and I highly
recommend it.
About the Author:
Cecilia Salamone's blog can be found here and her Facebook Caregiving Page here. The author offers caregiving coaching services for individuals and businesses seeking to empower caregiver-employees. She has worked with individuals who have disabling conditions by helping to promote independence, address co-dependency and other avenues leading to personal growth and self-advocacy.
Cecilia Salamone's blog can be found here and her Facebook Caregiving Page here. The author offers caregiving coaching services for individuals and businesses seeking to empower caregiver-employees. She has worked with individuals who have disabling conditions by helping to promote independence, address co-dependency and other avenues leading to personal growth and self-advocacy.
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