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More
than just memory loss
In the early stages,
the disease manifests as nothing more than mild forgetfulness, a problem that
most people shrug off as a natural (and at times almost humorous) consequence
of growing old. Soon, however, a person’s ability to understand, think and even
communicate is affected. Behaviors may change and so too may emotions and mood.
Topping it off, physical coordination and mobility may suffer, affecting an
individual’s ability to perform even the simplest of daily tasks. The result
can place a ton of pressure on the affected person’s family or caregiver.
Family
burden -- the unseen
As many as 5.3
million people in the United States are currently living with Alzheimer’s. With
more than 95% of those with AD being 65 or older, round-the-clock care is
almost a necessity nowadays. This type of care, however, translates into one of
two things, and more often both: stress and money.
The average lifetime
cost of caring for someone with AD is $174,000. Broken down by year, this can
amount to anywhere from $18,000 to upwards of $36,000, depending on the
severity of symptoms. While the health care system will absorb some of these
costs, look to the family to foot about 75% of that bill. But there’s more than
just cold hard cash to consider when caring for someone with Alzheimer’s
-- there’s stress, there’s tension, there’s conflict, and more. These are
the unseen consequences of mental disease.
What
to expect
While the burden of
Alzheimer’s remains largely unseen, having a grasp on what to expect can go a
long way toward lessening the impact of this disease.
Although early
symptoms are manageable, as the disease progresses activities that most of us
can easily perform on a day-to-day basis may become challenging to an AD
patient. Daily tasks like bathing, dressing, eating, going to the bathroom, and
falling asleep may require assistance. Even simple visits of someone with
Alzheimer’s can quickly become a nightmare. Just imagine how you would feel
having a loved one be unable to recognize who you are. It’s not just
forgetfulness --- hostility, confusion and even hallucinations or delusions can
afflict the typical patient.
Moving beyond issues
regarding simple care, difficult decisions will undoubtedly creep to the
forefront. Case in point: driving. At some point, the decision will need to be
made that someone with AD can no longer drive; such a decision will likely fall
on the shoulders of the family. Times like these will require communication,
planning and honesty to prevent a meltdown.
For many caregivers,
however, there comes a point when they are no longer able to take care of loved
ones at home. Choosing the best residential or nursing home then becomes a
priority -- a decision that no one enjoys.
Despite the somewhat
gloomy outlook portrayed above, with each passing day, hope for a cure becomes
stronger.
Future
cure?
A while back, AM
introduced you to the notion that there may soon be treatments that will
actually reverse the disease progression of AD as opposed to merely delaying
the onset of symptoms like current treatments do. In the next five to seven
years we may even see a vaccine. Yep, that’s right, a vaccine for Alzheimer’s.
Given the current advancements in brain research and the speed at which this
field of research is progressing, AD may one day be a thing of the past.
Since AD is a
commonly occurring disease, thankfully there are a ton of resources online. If
a loved one is diagnosed with Alzheimer’s, be sure to do some upfront research.
Keep the family calm and willing to share responsibilities if in fact you
choose to care for the affected person at home.
SOURCE : ASKMEN.COM
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