The document discusses the challenges of caregiver burnout, noting that 60% of caregivers are female and 40% report high stress levels. Caregiver stress can occur when the demands of caregiving outweigh a person's ability to meet those demands, potentially leading to burnout if stress is not managed. The document provides tips for caregivers to minimize stress such as asking for help, prioritizing self-care, exercising, and connecting with other caregivers.
2. Caregiving in the US (2015 Report)
Findings from AARP and the National Alliance
for Caregiving survey of U.S. caregivers:
84 percent wanted more information on
keeping loved ones safe, managing their stress
and making end-of life decisions
60 percent are female
40 percent rated caregiving situation as
“highly stressful”
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3. Caregiver Stress
We feel stressed when our demands
outweigh our perceived or actual ability to
meet those demands.
When we are a caregiver to a loved one
with mesothelioma, we may feel like there
is not enough time in the day to take care
of our own responsibilities as well as caring
for our sick loved one.
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4. Demands of Caregiving
Drive to/from doctor appointments
Monitor medications/fill prescriptions
Shop and cook meals
Physically assist when loved one is weak
Household chores/yard work
Pet care
Pay bills
Emotional support
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5. Balance Caregiving with Life
Being a caregiver is a labor of love and is a
way to demonstrate our care and concern
for our loved one with mesothelioma.
Caregivers usually have their own
responsibilities (job, chores, parenting, etc.)
to fulfill as well.
It can be challenging to find a balance
between caregiving and meeting our own
needs.
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6. Lay Caregiving
Decades ago, most cancer treatment was given
in a hospital setting because patients were too
sick to be at home.
Today, most cancer treatment is given in the
outpatient setting, which allows patients to be
at home where they are more comfortable.
This trend has seen an increase in family
members and friends providing practical care
and emotional support, which has turned them
into “Lay Caregivers.”
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7. Symptoms of Caregiver Stress
Poor sleep
Irritability
Trouble concentrating
Increased smoking/alcohol use
Lack of energy
Social withdrawal
Resentment
Neglecting own needs
Poor memory
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8. Response to Caregiver Stress
Many caregivers respond to feeling
overwhelmed with caregiver stress by cutting
back on the very things that keep them
physically and emotionally balanced:
Exercise
Sleep
Healthy diet
Socializing with friends
Hobbies
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9. Why?
Some caregivers may think that frivolous
activities, such as hobbies, sleep and exercise,
are not necessary when there is so much to
do and not enough hours in the day.
In the short term, we can function without
enough sleep, exercise and recreational
activities, but we may soon feel the
discomfort of stress, and these “unnecessary
activities” are what relieve our stress.
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10. Caregiver Burnout
Caregiver stress can worsen into caregiver
burnout:
Feeling hopeless
Overwhelming fatigue
Becoming argumentative/irritable with patient
Getting sick due to weakened immune
response
Significant weight loss/gain
Headaches and muscle tension
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11. Burnout
The point when a caregiver is burned out
is when they should not be providing care
anymore as it is having a detrimental effect
on the caregiver and loved one.
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12. Minimizing Caregiver Stress
Make it a habit to monitor your own health
(emotional and physical) as much as you monitor
your loved one’s health.
Don’t try to be a “superhero” caregiver!
Ask for help.
Accept help when it is offered.
Create a wish list of what you need. When
someone says “Let me know if there is anything I
can do to help,” take them up on it.
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13. Minimizing Caregiver Stress (cont.)
Put caring for yourself on your caregiver
“to-do list.”
Don’t put off your own medical care.
Schedule some social time at least once a week
for yourself.
Exercise 30 minutes three times a week. (Even
a walk in your neighborhood counts!)
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14. Minimizing Caregiver Stress (cont.)
Connect with other caregivers through
peer support or a group setting.
Many communities/hospitals have
caregiver support resources, and your
cancer center may be able to let you know
what is available in your area.
A Patient Advocate can help you locate
caregiver support resources near you.
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15. Sources
AARP. (2015) Caregiving in the U.S.
http://www.aarp.org/content/dam/aarp/ppi/201
5/caregiving-in-the-united-states-2015-report-
revised.pdf
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