This week we were faced with the
task of admitting a loved one to an assisted living facility. The loss of
cognitive function had progressed to the point that simple tasks were a
struggle and when this became overwhelming for him, he basically collapsed on
the floor and waited for someone to come looking for him to begin the process
of assisting him back to his feet. If the caregiver in the house is without a
good bit of strength and balance, the situation becomes not only difficult but
also dangerous. Fractures or broken bones would only add to an already bad
situation.
There have been thousands of
books and essays written on the devastation of loss of mental clarity and
function as those we love enter into the disease of dementia. There are words
of wisdom and encouragement on websites and from friends that try to help us have
confidence in the decisions of how to best care for family members that can no
longer be cared for at home. We second-guess each step and wear the guilt like
a heavy coat in the heat of summer.
One kind administrator of a care
facility we considered shared a comment that I have turned over in my thoughts
for a few days now: “He no longer remembers the saddest days of his life. Those
memories are gone.”
If he no longer remembers the
saddest days, I wonder how often we might upset that soft filter of dementia by
trying to connect with him? If we selfishly want him to remember us when we
visit, do we bring up a string of memories that cause him to recall (if even
for a moment) that he is no longer in his home of many years or able to have
control over his day, what he does, and where he goes? Does he remember, if
even briefly, after we have left to go back to our lives that we have departed
without him?
Might it be better to simply
visit and check on him as “a stranger” while letting him make friends with the
faces he will see each day in his new and smaller world? Is this less stressful
for the patient that struggles already with so many of the simple tasks that
were so easy in the past? Does he really need to try to answer the question “Do
you remember your granddaughter? Your son? Your wife?” when he is trying to
remember how to button a shirt? If we know the disease progression is
inevitable, are these memories important?
Thinking about my own life, I
can’t really recall the “saddest day” of my life. There are plenty of times I
probably believed that a day could not get any worse, but with time that memory
has faded. And with that filter of time and fading of those memories, I
realized that the future in front of me was more important than the trials of the
past. I made it through. I’m still here. Those terrible times are relative to
what I see before me now and only my imagination holds those boundaries.
If it is true that he no longer
remembers the saddest days of his life, are we strong enough to give up not
being part of his present world in the way our memories want to hold on to the
man we once knew?
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