This blog is a guest post from my daughter Molly. Shortly, she'll finish her last few courses, a clinical and then her licensing exam, but if this blog is any indication, I'd say that she's ready now.
As I sat and listened to a long-time hospice nurse speak to
my senior nursing class, I was moved. My eyes welled up with tears, though my calculated
stoicism allowed none to fall, as she described her experience with hospice
patients. I had been removed from the geriatric population, it seemed, just
long enough to begin to lose some of my passion for nursing. By the end of the
address, however, I began to feel that old familiar inspiration that initially
drove me toward nursing as both a career path, and a lifestyle. My passion was
renewed just when I needed it (perhaps by chance? divine intervention? I’ll let
you be the judge).
Modern medicine can accomplish some amazing feats. The
treatment and eradication of illnesses continues to improve day by day. That
being said, modern medicine is also mainly concerned with “treating.” A
terminal diagnosis ends the possibility of eradication. When a terminal diagnosis
occurs, therefore, it as treated as a perpetual end point for modern medicine.
Many patients feel a sense of powerlessness.
Simultaneously, this is the beginning of end-of-life (and
hospice) care. We cannot change the terminal nature of the diagnosis. We are
nurses whose patients are headed toward imminent death. These patients feel as
though their power has been stripped.
The inability to “cure” our patients, however, does NOT mean
the inability to restore this power. We treat our patients holistically. That
is, we care for our patients’ bodies, minds, and souls. Rather than falling
into the trap of perceived powerlessness due solely to terminality, we take an
active role in empowering our patients. They cannot, unfortunately, “conquer”
death. This can be difficult for
patients to accept. We do everything in our
power to ease them through this difficult process. Once acceptance has
occurred, we are able to move forward and place the focus on that which the
patient may control. We assist them
in reframing their thinking to help them understand that they DO have power to
make decisions specific to their
individual preferences. The patient DOES have the power to choose whether
they’d like to pass on at home or in a hospital setting. They have the power to
choose how sedated or non-sedated, they’d like to be. They have the power to
choose which activities they participate in “just one last time” (or even for
the first time) before they go. They have the power to choose to see those they
want to see. Often patients will hold on just long enough to hear someone’s
voice one last time. Sometimes they’re waiting for a loved one to arrive before
they can go peacefully. There are even those who seem to wait just long enough
to be left entirely alone before passing on.
But eventually, the conclusion of this interaction is death.
Ideally, I’ve guided my patient (and their soul, I feel) through to the next
era of their existence peacefully, comfortably, and in the setting/manner of
their own choosing. I’m not even going to begin to describe what I think that
“era”
is, nor what it involves. I could write volumes guessing. But what I do
know is this: terminal illness does NOT equate to powerlessness. Healthcare
professionals treating terminal patients must actively work to empower their
patients. Sitting in that room, listening to memory after memory from a hospice
nurse, I was moved. These patients cannot choose not to die. (At some point along the way, nor can we.) But we can
all choose how we would like to live… no matter how long we may or may not have
left. There is nothing I perceive as more humbling than being able to not only
ease someone through the dying process, but empower
them through it. It is a role that, pending one last semester and a passing
grade on my NCLEX exam, will humbly and graciously fulfill… perhaps for the
rest of my days, if I so choose.