Rebuilding
Life in the Face of Loss
By Bruce Campbell
Note: The
Christmas tsunami and the Gulf Coast
hurricanes of 2005 brought home the enormous challenge of rebuilding
life after dramatic loss. Though those who suffer from invisible illness
may not appear to be different from normal, they too experience loss and must rebuild their
lives. Here’s how one CFS patient struggled to redefine himself. This article
is adapted from the online booklet Recovery
from Chronic Fatigue Syndrome: One Person’s Story.
CFS
transformed me in a matter of days from a healthy person to someone
functioning at 25%. As my symptoms persisted, I came to realize that CFS
was not a temporary interruption of my life, but rather had become the central fact
around which my life revolved. Much of what I considered “me” had
been taken away. The losses brought by the illness created one of my
greatest challenges in living with CFS: redefining myself in the face of
loss.
Looking
back, it’s obvious to me that one of my initial responses to the loss of my
old life was denial, which took the form of telling myself that I would
be one of the lucky ones and would recover. I'd have to say that the
idea, implausible as it seemed after the fact, worked for a year or more
to enable me to keep hope alive. Having hope, I was able to begin accepting the losses and
uncertainties. Later, when I accepted that recovery was unlikely, I
found hope in the progress I had made and in the conviction that, even
if didn’t recover, I could still find ways to bring meaning to my
life. Also, gaining some control over the illness helped reduce the
amount of uncertainty in my life.
When
Elizabeth Kubler-Ross described responses to loss, her end stage was
acceptance. I could identify with that in part, but for me the final
stage was more complex. As noted in another
article, acceptance meant recognizing that my life had changed,
perhaps permanently and certainly for an extended period of time. It
meant letting go of my past life and also of the future I had
envisioned for myself. But it had another component as well, a
confidence that I could find things to improve my life. I called the
combination acceptance with a fighting spirit.
Moving
through Grief
CFS
stripped away most of what I viewed as myself. Because of my illness, I
gave up work and volunteer commitments, let most relationships slide,
lost my ability to be physically active, and replaced an optimistic view
of my future with uncertainty.
I
did two things to cope with my losses. The first was to publicly
acknowledge the loss. In a Christmas letter sent a year and a half after
getting CFS, I wrote to friends that I had been living with a disease
for which there was no standard treatment or cure. And I concluded: “I
am sobered by the realization that it is highly unlikely that I will
return to the level of functioning that I had before becoming ill and so
probably will have to adjust to living a life with greater limits than
before.” Even though I wrote to alert others to expect less of me, I think the more profound effects were on me. The public
declaration helped me recognize the extent of my loss and the
possibility that it was permanent.
Moving
Beyond Loss
While
accepting that my life had changed, I had the conviction that whatever
happened it would still be possible to have a good life. That conviction
helped me to accept the losses I had experienced. And I continued to
believe that there were many things I could do to help myself. I
believed that even if I didn't recover, I could find things to improve
my quality of life. This belief kept me moving forward in hope.
Within
weeks of receiving my diagnosis, I joined two local CFS support groups.
The experience was especially useful for the friends I made, one from
each group. Both were very generous with their time, spending many hours
talking to me about the medical, psychological and political aspects of
CFS. They were tremendous sources of information and perspective,
helping me to understand CFS much more quickly than I could have on my
own.
Beyond
these two relationships, being a part of the support groups gave me a
sense of belonging, an experience of being connected to others like me.
I found there is something powerfully healing about feeling understood,
all the more so for a stigmatized disease that some people, even some
doctors, don’t believe is real.
Because
I stopped working and dropped out of my volunteer commitments shortly
after becoming ill, fellow patients became perhaps my most important
community. I think having that source of identification served me well.
I took CFS patients to be my peers, not healthy people. That meant that
I measured myself in comparison to them, not to co-workers or healthy
friends. That comparison took a lot of pressure off.
I
firmly believe that we all need to have meaning in our lives. My way to
bring meaning to my new situation was through relationships and from the
belief that, even though I had lost much, I could still contribute
something. Helping others through the self-help
program both provided an opportunity to create many new
relationships and gave me a sense of purpose when previous sources of
meaning had been lost.
I
told myself that, even though my life might not be the one I expected,
it could still be a good life. By focusing on what I could still do, I
shifted my focus from loss to possibility. I told myself that even if I
was unlikely to return to my old life, I could still create a new life
by developing new interests and relationships, and by focusing on what I
could still achieve. Ironically, I have been given my old life back, but
with a richness and meaning it wouldn’t have had without the illness.
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