This week’s class was a continuation of the social
self.
Because I have recently re-injured
my foot, I have decided to dedicate this post to a self-enhancement strategy
that I have become found of because of such injuries.
According to Taylor
(1989), we have a fundamental desire to maintain a positive viewpoint about ourselves
and our circumstances, and in order to protect this positive viewpoint we use
self-enhancement strategies. The
strategy that I use most often consists of making a downward social comparison.
This type of comparison involves comparing yourself to others who are
worse off than you are. For example, if
people’s self-esteem is threatened, they are likely to compare themselves to
people who are less than they are
(e.g., less successful or less fortunate) as a way to protect their own
self-esteem (Hakmiller, 1966).
Furthermore, downward social comparisons allow people to maintain a
positive outlook on their life (Aspinwall & Taylor, 1993).
Downward social comparisons have noticeably become more
important in my life since my foot injury on July 4, 2008. On this day, I accidentally hit my foot on a
desk leg, and the desk leg slid between the last two toes on my left foot. Naturally, a week later I found out that I
had broken the bones in that area, but I was told that everything should heal
within 4-6 weeks. After the sixth week,
I still could not move any of my toes or my ankle, and the pain was spreading
up my leg. In February of 2009, I found
out that I had actually developed a nerve disease when I had initially hit my
foot and it was now spreading up my leg.
This nerve disease is called Reflex Sympathetic Dystrophy (RSD) and is a
life-long condition, meaning there is no cure.
Because of RSD, I had lost 95% mobility from my ankle down, and it hurt
to do simple things such as walk, shower, and wear socks. Because I had limited mobility, I was also
forced to quit marching band (I had to be on the side lines) and to step down
as section leader for my last two years of high school. It is safe to say that I was not a happy
camper during this time.
Although I cried myself to sleep most of the time (because
of the pain and the frustration), I kept telling myself: “Things could be
worse.” In fact, I knew that things
could be worse because the doctor who helped me with my pain management told me
a story about a woman who got a paper cut on her thumb, developed RSD, and then
the RSD spread from one arm to the other arm before she was able to get any
type of treatment. So at this point although
I was in a lot of pain, I was thankful that we had identified the problem
before the RSD had spread to both legs.
In a similar vein, two years ago my mom was watching one of those
mystery medical shows (the ones where the person didn’t know what was wrong
with them, but by the end of the show we find out what was wrong with them). This particular episode was about a woman who
was on bed-rest for 14 years because she was in horrible pain. During this show, my mom was shocked to
realize that the woman’s symptoms matched my symptoms but to a greater
extent. At then end of the episode, my
mom’s suspicions were verified in that this woman did end up having RSD. After hearing about this episode from my mom,
this woman’s story became part of my downward social comparison because at
least I wasn’t force to stay in bed for 14 years because I was experiencing
unimaginable pain.
Since 2009, I have had various block injections in a main
nerve located on my back. These
injections paralyze the nerve to decrease
their sensitivity and firing. I also did
physical therapy as a way to get more mobility and strength in my foot. Right now, or at lest before my re-injury a
couple of weeks ago, the pain as become more manageable, showering doesn’t
hurt, and I can wear socks and shoes you can lace. But walking is still a day-to-day challenge,
my dancing is limited, and I do not think I will ever be able to run or jump
ever again because my foot does not do well with impact force. It is very frustrating not being able to do
things that I loved to do before my accident and not being able to do things
that I might not have liked but at least could still do if I wanted to or
needed to. In all, I have had to
drastically change certain areas of my life.
I also now have to be careful in general not to injury my foot because the
RSD will be triggered even more each time, which is unfortunate because for the
first time since 2008, I re-injured my foot and am now dealing with even more
RSD symptoms. Hopefully, the doctors and
specialists here in Georgetown
will be able to help me in the coming weeks. But hey, at least the nerve damage
hasn’t spread past my left leg or hasn’t caused me to be on bed-rest and miss
all my classes and flunk out of school, so I’m hopeful to an extent!
P.S.
Here is a link to webMD that does a good job a describing RSD or Complex
Regional Pain Syndrome (CRPS) http://www.webmd.com/pain-management/guide/crps
_________________________
Aspinwall, L. G. & Taylor, S. E. (1993). The effect of
social comparison direction, threat, and self-esteem on affect,
self-evaluation, and expected success. Journal
of Personality and Social Psychology. 64,
708-722.
Hakmiller, K. L. (1966). Threat as a determinant of downward
comparison. Journal of Experimental
Social Psychology (Suppl. 1), 32-39.
Taylor, S. E. (1989). Positive
illusion: Creative self-deceptions and the healthy mind. New York: Basic Books.