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Ugcs3 v3 Project Attachments Wonder
Ugcs3 v3 Project Attachments Wonder
Ugcs3 v3 Project Attachments Wonder
Connor J. Hall
Abstract
The film, Wonder, is about a 10-year-old boy living in Brooklyn, New York named August
“Auggie” Pullman. Auggie has Treacher Collins syndrome, a rare medical facial deformity.
Treacher Collins syndrome causes downward sloping eyes, vision problems, small or missing
ears, hearing problems, underdeveloped or missing cheekbones, cleft palate, and breathing
problems. As a result, Auggie has undergone 27 different surgeries in order to see, smell, speak,
and hear without a hearing aid. Throughout his life, Auggie was home-schooled, but his parents
enroll him into private school for his fifth-grade year. Auggie immediately finds himself being
bullied by many of his classmates because of his different appearance except for Jack, a fellow
classmate that Auggie has become close friends with. On Halloween, Auggie is betrayed by
Jack as he overhears Jack say, “If I looked like Auggie, I would kill myself”. Hurt by his mean
words, Auggie wants to quit school as he has lost his best friend and another classmate, Julian,
and his friends continue to pick on Auggie. This paper will discuss how Auggie overcomes his
challenges, the realism of Auggie’s condition, Treacher Collins syndrome perception to society,
and how Auggie is affected physically, mentally, socially, and emotionally throughout the film.
To fully understand the problem and research question, it is imperative to know the plot
of the movie. The main character of the film, August “Auggie” Pullman, is a 10-year-old boy
who has Treacher Collins syndrome. As a result, Auggie has undergone 27 different surgeries in
order to see, smell, speak, and hear without a hearing aid. For the entirety of his life, Auggie had
been homeschooled until his fifth-grade year, when his parents decided to enroll him into
Beecher Prep, a private middle school. Before the school year begins, the principal, Mr.
Tushman, has three students take Auggie on a tour on the school. One of the students is named
Jack, and him and Auggie quickly become best friends while Auggie is bullied by another one of
the students in the tour group named Julian and the majority of the student body. On Halloween,
students at Beecher Prep were allowed to come to school dressed in costume. Auggie decides to
come dressed in a Ghostface mask and cloak so know one could see his face and, in turn, make
fun of him. Not knowing that Auggie was dressed in the mask, Jack joins in making fun of
Auggie with Julian and makes the comment that “he would kill himself if he looked like
Auggie”. Auggie overhears this without Jack knowing and stops hanging out with him. Auggie
quickly makes a new friend in a girl named Summer. Jack asks Summer why Auggie has quit
hanging out with him and she tells him. Realizing what he has done, Jack partners with Auggie
for the science fair instead of Julian, causing Julian to call Auggie a “freak”. Jack and Julian
fight causing Jack to get in trouble until the principal hears about the situation. Julian is then
suspended and Auggie wins the Henry Ward Beecher Medal for silent courage.
condition that causes facial deformity. The condition is caused by “mutations in the TCOF1,
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POLR1C, or POLR1D gene” which code for proteins that are essential “in the prenatal
development of bones and tissues in the face” (“Children’s Hospital”, 2014). As a result, those
with Treacher Collins Syndrome such as Auggie have a very distinct facial appearance. People
with this disability have vision problems as a result “downward sloping eyes, slight notching of
the lower lids, and underdeveloped or missing eyebrow bones” (“Children’s Hospital”, 2014).
They also have hearing problems as a result of “small or missing ears, no ear canal, and missing
bones in the ear” (“Children’s Hospital”, 2014). Most concerning, they oftentimes have trouble
underdeveloped maxilla or mandible, cleft palate, wide mouth, and tongue displacement”
(“Children’s Hospital”, 2014). The diagnosis can be made either before birth or directly after
“based on physical appearance” and DNA testing to determine if the specific genes affected by
Treacher Collins syndrome have been mutated. Treatment for Treacher Collins syndrome varies
case to case depending on “the severity of the deformity and long-term needs of the patient”
(“Children’s Hospital”, 2014). All treatment requires surgery of some sort; however, some issues
such as trouble breathing requires immediate attention while other issues can be addressed later
in life after certain developmental stages. The quality of life for someone with Treacher Collins
syndrome is dramatically lowered because of the vision, hearing, and breathing problems as a
result of their condition as well as the surgeries oftentimes required and the mental, social, and
emotional effects because of how they are treated for looking different than others.
The physical effects of someone with Treacher Collins syndrome are very obvious as they often
have downward sloping eyes, small or missing ears, underdeveloped cheekbones, and cleft
palate. This was portrayed very accurately and with great realism in the film as Auggie
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displayed all these characteristics. These differences cause vision, hearing, swallowing,
breathing, and sleeping problems; however, the most damaging and lasting perhaps are the
mental, social, and emotional ones. Mentally, someone with Treacher Collins syndrome would
maybe have low self esteem as they are unhappy with their own appearance despite the disability
having no effect on their intellectual or cognitive ability. For example, in the film realistically as
Auggie is oftentimes seen wearing a space helmet because that is escape from reality and nobody
can see how he looks. The mind is a very powerful tool and this poor self-image can affect
someone socially and emotionally as well. Those with Treacher Collins are more skeptical to go
out in public and engage in social situations because, again, they have a poor self-image and
would be afraid of people staring. In the film, Auggie is terrified of going to his new school for
this very reason, and even though he found friends in Jack and Summer, people like Julian made
him dislike his new school and affected him greatly emotionally. Auggie was bullied throughout
the film by Julian and his friends, and then even by Julian’s parents at the end of the film when
Julian’s mom admits she cut him out of their class picture because of how he looked and because
she felt her son “shouldn’t have to look at that”. Despite the cruelty of this, it is very realistic
and really took a toll on Auggie as he wanted to quit going to when he heard Jack say, “he’d kill
himself if he looked like Auggie”. Auggie would prove to prevail with the support of his family
craniofacial deformity like Auggie. A study done of the stigmatism surrounding those with
Treacher Collins Syndrome was done that involved 185 adolescents with facial differences.
Participants, at the beginning of the study, were asked “to report stigma experiences that
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occurred within the previous week” (Loewenstein, 2008). The results were shocking as “35%
reported that they noticed people staring at their face, 29% overheard people say something
about their face, 12% felt excluded from peer activities because of their appearance, 31% either
got into a fight or were teased about how their face looked, 38% reported discrimination in the
workplace, and 71% reported discrimination in social situations” (Loewenstein, 2008). This is
factual prove that a disability someone has no control over can affect their life in more ways than
physical problems. Prejudices and discrimination make it hard for them to find jobs and engage
is social situations. Luckily there are laws in place to protect people with genetic differences.
There are several pieces of legislation that protect people with disabilities including
Treacher Collins syndrome. The people mentioned in the study are protected by the U.S Equal
Employment Opportunity Commission which can be found in Title I of the American Disabilities
Act (ADA). This prohibits “private employers, state and local governments, employment
agencies and labor unions from discriminating against qualified individuals with disabilities”
(“Americans,” n.d.). Legislation facilitating those with disabilities wasn’t included in the movie,
but acceptance of people with Treacher Collins syndrome can be facilitated effectively and
efficiently through media such as this film in which people with Treacher Collins syndrome are
portrayed as normal people, just the same as everyone else by educating a mass audience through
References
disability/ada.
Children's Hospital. (2014, May 12). Treacher Collins Syndrome. Retrieved from
https://www.chop.edu/conditions-diseases/treacher-collins-syndrome
Loewenstein, J., Sutton, E., Guidotti, R., Shapiro, K., Ball, K., McLean, D., & Biesecker, B.
(2008, June 15). The art of coping with a craniofacial difference: helping others through
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3113488/
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