It
has long been known that stress and sleep deprivation afflict family members
caring for loved ones suffering from dementia.
But
what has not been appreciated until recently is that such caregivers often
develop symptoms which mimic those found in individuals diagnosed with
dementia, including memory loss and disorientation.
In
fact, most caregivers with such problems are not suffering from the
degenerative brain condition labeled “dementia”. However, they are experiencing
the toll of caregiving to a close family member. If steps are not taken to ease
the stress, the symptoms will probably worsen.
In
time, they will render the caregiver unable to provide necessary care –
“burnout” will have occurred.
What
to do? Try to step back emotionally. Recognize that all your love and attention
cannot reverse the person’s condition. You can only do so much. And that is a
lot. Don’t blame yourself.
And
you deserve a break – a respite. You need to recharge your own battery to deal
effectively with the unavoidable stress of your role.
Don’t
hesitate to ask other family member to help out. They owe it to you since
you’re already the primary caregiver. If they are unable or unwilling, contact
local nursing and assisted living homes. They often provide short-term respite
care – during the day or overnight – so you can get the break you need.
You’ll
be of no use to anyone if you fall victim yourself to “dementia stress”.
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