I wrote last week’s post, Prologue, to set the stage for
this series on caregiving. Suffice it to
say that it is not fiction.
Per Caregiving in the
U.S., The National Alliance for Caregiving and AARP 2009, “As our parents
age, it’s likely a matter of when, not if, they will need our help. Nearly 44 million Americans — 1 in 5 adults —
are family caregivers for a relative or friend over age 50.”
It’s our turn. Dad
died in August, leaving Mom alone in their big house. In the few short months since Dad passed, we
have watched as the Parkinson’s symptoms have caused her to lose mobility and
feel almost constant pain. While the
informed sources on the Internet tell me that pain is not a classic symptom of
Parkinson’s, most go on to say that most Parkinson’s patients do in fact have
pain.
These sources also tell me that dementia and depression are
symptoms. We have observed evidence of
forgetfulness. She doesn't remember if
she’s taken her pills. She wakes in the
night and becomes disoriented.
And as for depression, well, I can’t even begin to
comprehend the losses she’s suffered in so short a time. Her husband of over 50 years. Her mobility.
Her short-term memory. Her
independence. Who wouldn't be
depressed? Who wouldn't be sad? And who
wouldn't, at times, be angry?
Mostly, she is alone.
The regular visitors that came bearing food, gifts, and a shoulder to
cry on stopped coming. She can no longer
drive, so she depends on others to transport her – but she really doesn't want
to go anywhere. She no longer feels up
to going to church. She no longer wants
to go out to lunch. She can no longer
read, and operating the TV remote has become too complicated for her. So she spends hours each day alone with her
thoughts.
She seems to perk up when she has visitors. Although she complains that food no longer
tastes good to her, she will always sit down and eat something if it is
prepared for her and someone else sits down and shares the meal with her.
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