CJ and Joe had a
life they loved. Above all Joe enjoyed cycling. He even rode coast to
coast with a group. Suddenly, Joe was ill. Blood tests confirmed that
he had a rare form of leukemia, and he suffered two strokes. CJ was
thrust into the role of primary caregiver.
Many people have
experience with being caregivers for small children, but adults are
more difficult. They’re used to running their lives and doing what
they want. When one partner is stricken with a serious illness the
brunt of the care falls on the other partner and strains the
relationship.
CJ tells her story
well. I liked the picture of their marriage before Joe’s illness.
It made it clear how much they loved each other and how difficult it
was to adapt to a serious illness. In the beginning, she made the
mistake many caregivers do: trying to be there 24/7. It’s a quick
way to burn out. She also learned how to interface with the medical
personnel. It’s very important when you’re ill to have someone to
interface for you and understand what is happening.
One of the
delightful parts of the book is CJ’s inclusion of emails she sent
to family and friends. It’s an immediate picture of the ups and
downs of adjusting to new limitations. Too often we feel that we must
keep a stiff upper lip. CJ admits she lost it occasionally, but
didn’t let it lead to feeling of inadequacy. She got up and tried
again.
The main message of
this book is that caregivers must take care of themselves, too. You
can’t give one-hundred percent all the time. It is important to take
time for yourself. I recommend this book for anyone with aging
parents or faced with the illness of a spouse. It will give tips for
how to manage being a caregiver, but also remind you that you don’t
have to be perfect.
I received this book
from PR by the Book for this review.
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