Image retrieved from: University of Michigan, Michigan
Health,
https://healthblog.uofmhealth.org/health-management/cost-of-chronic-pain-infographic
Living with chronic pain can cause
one’s physical and mental health to suffer. Among those living with chronic
pain, nearly 70% are women (Kiesel, 2017). Unfortunately, many are left without
answers either because their disorder doesn’t have many known effective
treatment options or because their doctors have “gaslighted” them. Whether or
not you have heard this term before, if you are a person who has any type of
marginalized identity, you may have experienced an instance of gaslighting in
which a doctor makes you feel as though you should doubt your (well-justified) symptoms
(Booth, 2018). Doctors may even minimize your symptoms to the point where you yourself
can’t tell if the symptoms are real or in your head because no doctor you’ve
visited has seemed to validate them. Unfortunately, gas lighting is perpetuated
by gender-based stereotypes that women are just “more sensitive” and can be
traced back to the days where women received a diagnosis of hysteria. These
stereotypes contribute to the dearth of research on effective treatment options
for women’s chronic pain, especially chronic pain due to reproductive health
issues. Moreover, research on chronic pain typically uses male populations
despite the fact that women are the majority of those who suffer with it (Kiesel,
2017). Disappointingly, it takes women multiple visits to the doctor’s office
over a period of months to years to get proper treatment, if any. This is a
health disparity we cannot ignore.
We must also consider the effects
that living with chronic pain can cause for women beyond their physical health.
As someone who has dealt with chronic pain, I know first handedly how it
affects one’s mental health. My own perspective is just one of many unique
voices of those who live daily with chronic pain. For me, chronic pain has
affected two major aspects of myself: my competence and my body image. This is
not an uncommon experience. Chronic pain can make one feel as though their body
isn’t home, at times distrusting one’s own body not knowing what symptoms will
present one day to the next. Pain can limit one’s ability to perform tasks they
previously were able to do with ease, or make tasks more difficult than they
are for others without chronic pain. Unlike physically visible disabilities,
chronic pain is invisible and can often make it especially hard to advocate for
one’s self out of fear that others won’t believe them. Especially considering
that this fear is sometimes reality, as in the case of doctors who gas light women’s
pain, one can feel silenced. When your voice isn’t heard, it can become easy to
feel as though your voice and your needs don’t matter. As a result, one may
internalize this in the process of self-silencing in which one censures their
own voice for the sake putting others needs above their own and limiting the
relevant importance of their voice as compared to others (Swim, Eyssell,
Murdoch, & Ferguson, 2010). Self-silencing is a common phenomenon in
experiences of marginalization or objectification such as sexism (e.g., Watson
& Groteweil, 2016). However, self-silencing is less studied in females
living with chronic pain despite their common experiences with gaslighting
which rests upon sexist notions that women’s pain isn’t real or that women are
too sensitive. This can contribute to the feeling of incompetence, or the lack
of control over one’s outcomes, including their experience of pain, their
ability to find treatment options and their prognosis.
In addition to hindering competence,
chronic pain can have a negative impact on one’s sense of their own body. For
example, studies show a relationship between chronic back pain and distorted
body perception (e.g., Moseley, 2008, Flor, Braun, Elbert, & Birbaumer,
1997). These studies provide good evidence for neurological differences in how
those with chronic pain perceive their own bodies, however, studies that
examine body perception and chronic pain in terms of mental health (i.e. body
image) are limited. Research has found that those with chronic pain perceive
their pain-affected body areas to be enlarged in comparison to how they once
were or in comparison to their other body parts (Bailey, Nelson, Lewis, &
McCabe, 2013). Despite this and the fact that our society promotes the
“thin-ideal” among women, I can imagine how many women struggling with chronic
pain and the resulting feeling of body-part enlargement may also perceive their
bodies negatively.
In
my experience, chronic pain has caused me to feel as though my bottom half is
numb and heavy and ultimately causes me to perceive myself as larger than I may
appear to others. Combined with feeling a lack of control over my prognosis and
treatment options, my body image has suffered while I figure out how to treat
my pain in the meantime. So, apart from what I’m doing already to treat my
pain, what can I do? This is a difficult question because the answer may necessitate
a paradigm shift. For me, I’ve had to redirect myself away from the notion that
women’s value is based on what they look like or how much they weigh. I’ve
slowly shifted to self-defining positive body image to incorporate an
acceptance-based stance that there are some things that I cannot change—my pain
and the associated body perception problems—yet I can do my best to avoid
mental suffering over it. Acceptance-based therapies such as Acceptance
Commitment Therapy has also been proven to be helpful for others who have
chronic pain (Musavi, Mujembari, Abharian, & Pashang, 2018). In this process, I’ve also attempted to
emphasize and prioritize my value in having as much health and low-pain days as
possible, regardless of my weight, shape or size. This is a difficult process
when we, as women, are told otherwise and that message is reinforced across
different domains of life. It is also difficult when our pain is not validated.
The
journey with chronic pain can be difficult in ways that extend beyond the
distance of our pain itself. For many, this journey can also be long. I hope to
keep exploring how to positively live with chronic pain and its effect on my
mental health. To those with chronic pain who may be reading this: your pain is
real, your struggles with your body are important, and I hear you.
Written by: Kylie Steinhilber
References
Bailey,
J., Nelson, S., Lewis, J., & McCabe, C. S. (2013). Imaging and Clinical
Evidence of Sensorimotor Problems in CRPS: Utilizing Novel Treatment
Approaches. Journal of NeuroImmune
Pharmacology, 8, 564-575. doi: 10.1007/s11481-012-9405-9
Booth, S.
(2018, September 05). Is Your Doctor Gaslighting You? Here's What to Do.
Retreived from:
https://www.health.com/mind-body/is-your-doctor-gaslighting-you
Flor, H.,
Braun, C., Elbert, T., & Birbaumer, N. (1997). Extensive reorganization of
primary somatosensory cortex in chronic back pain patients. Neuroscience Letters, 224(1), 5–8.
Kiesel, L.
(2017, October 09). Women and pain: Disparities in experience and treatment.
[Blog post]. Retrieved from: https://www.health.harvard.edu/blog/women-and-pain-disparities-in-experience-and-treatment-2017100912562
Moseley,
G. L. (2008). I can’t find it! Distorted body image and tactile dysfunction in
patients with chronic back pain. Pain,
140(1), 239–243. doi: 10.1016/j.pain.2008.08.001
Mousavi,
S.M., Mujembari, A.K., Abharian, P.H., & Pashang, S. (2018). Effectiveness
of Acceptance and Commitment-Based Therapy (ACT Rehab) on Quality of Life,
Severity and Duration of Pain in Women with Chronic Low Back Pain. Iranian Rehabilitation Journal, 16(1),
103-110.
Swim, J. K., Eyssell, K. M., Murdoch, E. Q., & Ferguson, M. J. (2010). Self‐silencing to sexism. Journal of Social Issues, 66, 493-507. doi: 10.1111/j.1540-4560.2010.