|
Many
feelings come up as people deal with illness; fear, anger, grief, and
anxiety are all normal feelings for patients as well as their family. Some
people let their feelings out and some hold them in. If you can recognize
and acknowledge your feelings, they are less likely to cause you more
anxiety as you go through this transition. The important thing is not to
get stuck in any one feeling for too long.
If this happens you may want to discuss it with your doctor.
Most
people find it helpful to have someone who will listen as they talk about
their feelings. Having a
trusted nonjudgmental friend, family member, support group, church member,
or nurse who will listen and/or give you feedback as you go through this
process is very important.
Many
fears may arise as people go through the transitions at the end of life.
People
fear:
-
Being in pain.
-
Losing
control over their own body, not being
able to take care of themselves
or being
able to think clearly.
-
Being
a burden to their family.
-
Being
abandoned as they face the
uncertainties of dying.
-
Having
a long lingering death.
On a
University
of Michigan web site patients and family members discuss their
experiences and their feelings about dying.
Anger
Anger
is a normal part of the process of grieving and letting go. Patients may
be angry because they do not know what to expect. They may feel abandoned
and scared, and not ready to die. Family members may be angry or resentful
because of the demands of caregiving.
There may be a strained relationship with the patient.
Family members may be afraid, too; anger might be directed at other
members of the family, the patient, caregivers, doctors, themselves, or
even God.
There
are many ways to express and deal with anger. Some people pound on pillows
to let out their anger. It is important to find whatever works for you.
Letting others know you are angry can be a simple statement of your
feelings of angry.
Some
people can support you when you are angry, and others will walk away. If
they walk away they are saying they cannot deal with anger, not that they
don’t care.
Grief
Both
patients and family members grieve a loss of control and changing
relationships, roles, and life. Patients
may grieve the loss of their identity as a healthy person with a job.
Whether the illness is sudden, chronic, or like a roller coaster
ride effects grief. We all grieve differently, and there is no “right”
way to grieve. Grief is a
slow process that has many stages, and as we grieve we go back and forth
through these stages and feelings. Noted author and hospice advocate
Charles A. Corr says an important component of grief is the “unfinished
business” a patient may or may not want to address. It is important for
the caregivers to listen to these needs and help the person address them
if possible. We can all learn from those who are dying.
Depression
Experts
estimate 25% of cancer patients are depressed, and the figure rises to 75%
near the end of life. There
is a difference between feeling sad, blue, or down, and depression. When someone is depressed they have difficulty sleeping and
eating, and doing their normal daily activities for weeks on end. Since cancer patients often have trouble eating and don’t have
energy to perform many normal activities, it can be difficult to
determine when depression is a problem. Talk to your doctor;
anti-depressants are prescribed for some cancer patients to help control
depression.
Fatigue
Fatigue is a major problem for cancer
patients and their caregivers. It can lead to depression and
isolation for the patient and caregiver alike.
Most cancer patients experience fatigue at
some point during their illness. And this is not regular run-of-the-mill
fatigue either. Cancer Related
Fatigue (CRF) can be mild or debilitating or anywhere in-between.
You just feel completely spent - physically and emotionally.
Caregivers are at risk of fatigue also from their added responsibilities
and stress.
To
read more about fatigue and steps you can take to control it, click here
to go to the Fatigue article in the Managing Side Effects Center.
|
|
HELPFUL HINT
FOR
CAREGIVERS
|
| Sometimes people worry about things that do not make sense.
Humor is a good way to stop irrational thoughts.
Simple statements such as “horse feathers” can let a
loved one know their thoughts are not realistic or likely to
happen. A good sense
of humor goes a long way as you deal with all the ups and downs of
being terminally ill. |
|
Anxiety
Anxiety can be
associated with depression. Anxious
people may experience restlessness, mood swings, difficulty eating and
sleeping; they may hyperventilate, have trouble concentrating, and have a
pounding heart. Anxiety is a normal reaction to facing death, pain, and
difficulty breathing. This
anxiety usually passes as the pain or breathing problem passes. Shifting
relationships, financial worries, loss of control, and health changes such
as a reaction to a medication can also cause anxiety. Just like
depression, anxiety can last for weeks on end. If either the cancer
patient or a caregiver has symptoms of depression or anxiety or if it is
unclear, people should discuss this with their doctor.
Suicide
Some
people have thoughts of hastening their death. This happens when they are
worried, overwhelmed, feel helpless, or are afraid.
People have different views about whether suicide is an option.
However doctors, except those in Oregon, cannot legally help patients die.
Tell your caregiver what you are thinking; it can help them better
understand your suffering.
If
the reason you have thoughts of ending it all is because much of the time
you are in pain, you need to talk with your doctor about better pain
control.
Written by Linda
Miller, RN, MA
Edited by Rachael Myers Lowe, cancerpage.com
This page was last edited on 04/18/2008
|