Amanda’s Response to Joy Harjo’s “The Woman Hanging from the Thirteenth Floor Window”

In Joy Harjo’s poem, “The Woman Hanging from the Thirteenth Floor Window”, the author portrays an unnamed female character contemplating to commit suicide by falling off the thirteenth floor of a tenement building in East Chicago. Looking at the poem through a disability lens, a crucial key passage shows the character’s feelings in the environment around them at present, morph together to create a person that is struggling with decisions of suicide and severe depression. The key passage is as follows:

And the woman hanging from the 13th floor window

          hears other voices. Some of them scream out from below

          for her to jump, they would push her over. Others cry softly

        from the sidewalks, pull their children up like flowers and gather

         them into their arms. They would help her, like themselves.

        But she is the woman hanging from the 13th floor window,

          and she knows she is hanging by her own fingers, her

          own skin, her own thread of indecision. (l.41-48)

The author states that the woman can hear voices from below. Some call “for her to jump” and some say they will “push her over” to her death, while others “cry softly” and pled that they “would help her” (l.43,45).  These people at the bottom can be interpreted as the able-bodied people of society and their reactions to this woman’s disability. On one hand, people are condoning her suicide because having a disability a hardship or a difficult for which helping her end her life might be a way of escaping that burden. As the author addresses, “She thinks she will be set free” (l. 7). On the other hand, there are people who see her suffering and are compassionate. They are supportive and want to help her. When they say “they would help her like themselves” (l. 45), it could the interpreted as those in the community who suffer from disability if not from depression like the character. Whether the people want her to jump or not, it is still not their decision in the end.

  Towards the end of this passage, it is stated “but she is the woman hanging from the 13th-floor window” indicating the decision to end her life or live with her depression is ultimately up to her, not society, she is the only one hanging from the window. With the lines, “she knows she is hanging by her own fingers, her/ own skin, her own thread of indecision” (l. 47-48) The character understands that it is not the effects of the society below that are hanging her in the balance of her indecision, it is her own fingers, her own choice to allow her to fall or not. It goes to show that the disabled individual or any disabled person has the capability to make the decision for themselves, not anyone else.   

Overall, this passage put to questions some aspects that can be applied to disability studies, these being the concept of society’s influence on the disabled individual and the capability of a disabled individual to make a decision for themselves.

Works Cited

Harjo, Joy. The Woman Hanging from the Thirteenth Floor Window, 19 Feb. 2019, www.amerinda.org/newsletter/13-3/harjo.html.

Word Count: 524

The Flag of Imagination: The Surrealists and Artists on the Schizophrenia Spectrum​

Written by Amanda Smith

            During the afternoon of February 19, I attended a lecture from the Mysterium Humanum series on madness, titled “The Flag of Imagination: The Surrealists and Artists on the Schizophrenia Spectrum”. Presented by Dr. Julia A. DeLancey, was this fascinating talk about Hans Prinzhorn’s  1922 study of Schizophrenic spectrum patient’s art work and the surrealism era of the 1920-1930s. 

            Breaking down the title of her lecture, Dr. DeLancey wanted to first introduce \what disability studies is. Her definition was simply stated as socially constructed and performative; how society constructs disability. She allows explains the three main categories a disability can be seen as: medical, social, and interdependence. Medical is the physical impairment one has (paralyzed), whereas social is the how environment effects the individual (stairs are a problem), and interdependence refers to need for assistance. The disability she focuses on is Schizophrenia spectrum. Which is when an individual has poor executive function, thought disorders, psycho-social factors, and hallucinations. 

            Working towards the other section of her title she introduces the start of surrealism. Dr DeLancey remarks the World War 1 plays a major role in how surrealism starts. During World War 1, soldiers that fought in the trenches were coming back with significant psychological trauma. During this time, Sigmund Freud was developing his form of therapy, called psychoanalysis. This form is believed to delve into the subconscious and unconscious mind, the sources of all problems or traumatic experiences, which was a major focus to surrealist.

            The founder of surrealism, Andre Breton, was a war veteran who saw shell shock first hand, it was in1924 when Brenton writes his manifesto ( his statement of beliefs) of surrealism, a movement that will reconcile two different realities (the real world and dream world, the world in between those being surrealism) which can be accessed through things like hallucinations and visions. Surrealist took a page out of Freud’s book by trying to access surrealism in the mind by doing “waking dreams” sessions and automatism drawing and writing (where a person draws or writes without thinking about what came to them). It was only then when theorist and writers began to explain that there are only three types of people that are truly creative: Children, people from primitive cultures, and people with mental illnesses. As Brenton had put it, “I could spend my whole life prying loose the secrets of the insane. These people are honest to a fault, and their naivety has no peer but my own.”

            After explaining these two main concepts (Disability and Surrealism), Dr DeLancey excites us with the bulk of her research on Hans Prinzhorn’s 1922 case studies. Prinzhorn, in his time, had training as an art historian and experience in psychology. Later in his life, he began working in a psychiatric clinic in Germany. The patients there created many pieces of artwork that doctors examined so they could diagnose the patients. Prinzhorn inferred with the notion pieces were art-worthy studies. Prinzhorn then began to conduct his research on ten different patients in this clinic where he would find common traits such as expressive, playful, patterned order, symbolic system, obsessive copying, and ornamental elaboration. 

            One patient, Agnes Richter, had the whole room jaw dropped. Agnes was a seamstress until her family committed her to the clinic. She then began her project on her straight jacket embroidering her file number, statements, feeling, and thoughts. Dr Delancey told us that her doing this was a way for “her words to touch her”.  The audience identified that her artwork was a form obsessive copying of her words. 

Agnes Richter’s straight jacket

            Another patient Prinzhorn studied was Adolf Wolfli, who was hospitalized most of his adult life due to mental and physical abuse. Wolfli had to different types of artwork he created, his bread art and his book art. In order to do his book art, Wolfli would create small individual pieces of his work such as collages of labels, pictures, and recipes to sell. After he sold enough, he would put the money toward materials for his book art. One piece we examined was his bread work, titled “Saint Mary Castle Giant Grape”. This work was identified as elaborate ornamentation, pattern order (orange bubbles color-pattern), and playful (The hidden faces). 

Saint Mary Castle Giant Grape by Adolf Wolfli

            During the 1920s, people believed that those with mental illnesses had the true creativity to create surrealism art. Based on Hans Prinzhorn’s case studies, it can be observed that his patients can create art work based on their pure imagination. It was unclear if in fact the patient’s art was based on the this “in-between” surreal world they could be in, but looking at the characteristics of schizophrenia such as hallucinations, it can be interpreted that these patients have the ability to access pure imagination and portray it in an art form. 

Makayla’s Response to Harper Lee’s “To Kill a Mockingbird”

When reading this chunk of, “To Kill a Mockingbird,” one passage in particular made an immediate connection in my mind to another text that we have read as a class. Tim Johnson, the ill dog that wandered into town, barely able to walk and obviously miserable, is similar in both character and function to Candy’s dog in, “Of Mice and Men,” by John Steinbeck. Not only are they similar in their literal meaning, but both dogs are deeply symbolic for multiple things. In Of Mice and Men, the dog’s story is a parallel to both Curley’s Wife (who was also unnamed and seen as a possession) and Lennie (who was also shot “for his own good”).  And in To Kill a Mockingbird, the dog is most clearly a symbol for the oncoming problems for Atticus and his family after Atticus’ refusal to drop/leave the Tom Robinson case. Atticus’ reluctance to shoot the dog and him not really wanting to take the case, but knowing that he has to do both is just one of the ways that the symbol plays out.

However, that’s not all the ill dog represents. Tim Johnson could also be read as a metaphor for Tom Robinson himself. The dog in the street’s disability and persistence to keep going, “motivated by an invisible force” is directly comparable to Tom Robinson, almost even  foreshadowing. While this can be cracked up to just his animalistic instincts, his persistence despite his disability is uncannily similar to that of Tom Robinson throughout the book. While Tom, at least up to this point in the story, is not physically disabled in the traditional sense, he’s also not white, and due to how race is viewed in his society, this gives him a disadvantage that rules over all aspects of his life. In Elizabeth Brewer’s, “Coming out Mad, Coming out Disabled,” she writes about A.J. Withers, a trans person who associates themselves with the disabled community because of how they were psychiatrized by others due to their gender identity.

Jumping off of that way of thinking, Tom Robinson could be considered disabled in a similar, societal way due to his race. People who belong to other minorities tend to interact with disability studies in similar ways. While the experience of being trans is vastly different than the experience of being a part of a racial minority, A.J. Withers and Tom’s experiences ares still comparable. Robinson being black is a big reason of why he is in this unfortunate situation and unnecessary legal trouble to begin with. Thus, the dog continuing to walk forward, despite his disability and pain also symbolizes Tom Robinson’s persistence with the trial, despite being, as Atticus Finch would say, “licked from the start.”

In conclusion, while Tim Johnson is only in this book for a few pages, the metaphors and symbolism surrounding his character allow opportunities to spring up involving several questions and discussion points about disability, some of which have tricky, unstable, and indefinite answers.

501 Words

I Pledge: Makayla Harrington

Rebecca Young’s Response to Tobin Seibers’ “Disability in Theory” and Sheila Black’s “What You Mourn”

As Tobin Seibers discusses in “Disability in Theory”, the social constructionist model of viewing disability implies that the body itself is a social construction; further, our overall views of the body are dictated by society’s standards of normality and physical ideals. While Seibers also presents counterarguments to using this theory in the context of disability studies, I still believe that its central points are applicable to this field and can enrich our studies of disability as a part of our society.

The main point of social constructionism is that all of our ideals and standards, what we consider “normal”, is influenced by our society as a whole. When changing the societal context in which we view a certain body, the actual view of that body is altered accordingly as well. As Seibers wrote in his article, “In a society of wheelchair users, stairs would be nonexistent,” (p. 174). This is a simple example which reinforces the discussions our class has been having for over a month, that an individual is not disabled until their society makes it so. As a personal example, I am incredibly nearsighted, and depend fully on glasses and contacts to navigate my world. If I lived in a society in which these resources were inaccessible or considered abnormal, I would be disabled; however, since this is not the case in our society, I merely have a vision impairment, which is easily adapted into my life. This again shows the dependence we have on our society to determine how our bodies are viewed, treated, and accepted (or not).

In addition to this, I felt that Sheila Black’s poem “What You Mourn,” spoke volumes to the conversation which Seibers has in “Disability in Theory,” and ultimately reinforces the strength of social constructionism as a theoretical argument in disability studies. While the poem’s narrator has a physical disability which has been “fixed,” the narrator themself is mourning the body they were born with. Regardless of how their physical impairments made “normal” activities difficult or impossible for them, the narrator is speaking of their disabled body as a lost love of sorts. In response to the societal voices which called their body “crippleddisabled and then differently abled,” the narrator explains that these labels were given from an external point of view, from people who had never shared the narrator’s experiences. In discussing the ongoing commentary about their body, the narrator explains that “none of [these outsiders] could imagine / that the crooked body they spoke of / … was simply mine.” Here the narrator is saying that their disabled body had inherent value despite their society saying that it didn’t; instead of looking at their impairments as flaws in need of perfecting, they saw them as unique differences which enhanced their value. At the poem’s conclusion, the narrator compares loving their unique and “abnormal” body to one loving one’s country, including “the familiar lay of the land, the unkempt trees, / …down to the nameless / flowers at your feet.” Regardless of how society views the physically impaired body, this poem allows us to view this situation from the perspective of someone who values their supposedly disabled and undesirable body, and ultimately ties in perfectly with the theory of social constructionism by showing that societal views of the body are not universal.

Word Count: 553

Rebecca Hinson’s Response to Robert McRuer’s “Introduction: Compulsory Able-Bodiedness and Queer/Disabled Existence”

Heterosexuality and able-bodiedness has been defined not by what they are, but by what they aren’t. To give meaning to homosexual and disabled, it has been written down as deviations from the norm. In this case the norm being heterosexuality and the able-bodied. Much like Audre Lorde often focuses on the intersectionality of her many characteristics, these four categories rely on their other, to exist; you cannot have one without the other.

            There is much similarity in the LGBT movement as there is in the Disability movement. Both have roots in the constant normalizing of what makes them different. Both have terms used previous as harmful and derogatory, now at the face of their theories (queer and crip.) However, most importantly they define what it means for society to be normal. Society requires these definitions so that they can label and pursue and prosecute the “abnormalities” from a “perfect” society to stabilize institutions that were thought to be in jeopardy from this deviance. Queerness was defined in the 19th century as an oddity. Eventually defining it as a homosexual, which is the defined as someone who deviates from the “norm” and has relations with a member of the same sex (discluding women at the time, because of course they cannot be trusted with the knowledge that they can have relations with other women.) The definition was morphed into many different terms like gross indecency, or sodomy, or my personal favorite “somdomite.” The point being that without defining what queerness is, you cannot have these institutions like the law governing it, which is what society wants.

            Society wants to govern personal aspects of life, so that life runs more smoothly. In theory, the more people deviate away from that norm, the more chaos it causes. With disability, society defines it as someone with a body unable to function “normally.” This normal being that someone is not hindered by how society has created buildings, jobs, school systems, government, etc. To deal with this deviance, instead of working to make these institutions and places more accessible, society created ways of moving them out of these environments. For example, literal institutions were created to move them away from society itself.

            McRuer says in his introduction “According to the flexible logic of neoliberalism, all varieties of queerness ­— and, for that matter disabilities — are essentially temporary, appearing only when, and as long as, they are necessary.” (29) He is calling attention to the idea that definitions are not all encompassing. Where it is considered a disability in one setting, it can be the norm in another because nothing is being hindered.

            The “norm” is personal. My norm is different than my roommate’s norm, or my professor’s norm. My norm is different than someone with a disability. This does not make someone else lesser of a person. A queer woman with down syndrome is just as important as the next. The fault is with the way that people with disabilities are ostracized because they cannot conform to the way society wants, because their norm is just too different than the mass population’s norm.

Word Count: 516

I Pledge: Rebecca Hinson

Are Racists Crazy?

Yesterday afternoon, I attended the fourth lecture in the Mysterium Humanum series on madness. This lecture, titled “Are Racists Crazy?”, was delivered by expert Sander Gilman, and was a fascinating account of the history of racism and its ties to madness and insanity. This specific presentation focused largely on racism against the racial categories of “Black” and “Jewish”.
As discussed throughout the lecture, Gilman comes to the conclusion that racism is not a mental illness, and that we should not consider racism an indicator of insanity. In this talk, he cautioned numerous times against the dangers of broadly categorizing individuals for any reason–be that their skin color, religion, political beliefs, or any number of other traits. In placing these concrete labels on people, we naturally begin to assume that we know something about them inherently from their affiliation with these categories; ie “Because you are ______ (black/Republican/racist/etc) I know that you are ______.” This behavior is incredibly dangerous, as it leads us to make assumptions that may be unfounded. Additionally, in the specific case of considering racists insane, it allows racist individuals to have a blanket excuse for their behaviors. For instance, when discussing the example of Donald Trump as a racist, Gilman argued that calling him insane is an excuse for not holding him accountable for his words and actions. Instead of looking at racists as an entire category of people who are all mad, he encouraged us to look at each individual as exactly that: an individual. Additionally, while he acknowledged that racist behavior can sometimes be an indicator or symptom of a mental illness, he asserts that this behavior in and of itself is not the illness. In other words, some mentally ill people may be racist, but not all racist people are mentally ill.
This also brings us into the broader impact this can have on the disabled community as a whole, and how negatively it can be affected as a result of this thinking. First, considering all racist individuals mentally ill is, in my opinion, somewhat akin to considering pedophiles a part of the queer community. While it is quite simply wrong, it also paints the community as a welcoming home for such people, who are typically not welcome there. Additionally, this negative image then poorly reflects back on the disabled community as a whole, reinforcing negative social standards which place the community in a subordinate position in society. Thus, taking Gilman’s advice and advocating against these negative patterns of labeling and categorization can ultimately benefit this community.

Rachel’s Response to Harper Lee’s “To Kill a Mockingbird”

Harper Lee’s To Kill a Mockingbird takes place in a small town named Maycomb County, in southern Alabama. Set in the time period of the Great Depression, the 1930s was a time of poverty, strong racial divides and the peak of the patriarchal white male. Knowing this while reading the novel through a disability lens, one starts to notice the impact this harsh environment has on its characters. I would argue that this environment is disabling to characters such as the poverty stricken Cunninghams and the only main female protagonist, Scout. These disabling characteristics of the environment, such as poverty and a patriarchal society, enhance the characters’ isolation from their community due to their physical appearances.  

            Poverty effects many families in this small, southern town but one character who stands out as being affected more than most is Walter Cunningham. Initially, Walter’s physical appearance is the first thing introduced, following this is how he came to acquire hookworms, “Walter’s face told everybody in the first grade he had hookworms. His absence of shoes told us how he got them” (Lee 21). Because Walter is not able to afford shoes, he walks around most of the time barefoot which is how he caught hookworms (Lee 21). Walter is called out by his teacher and made to feel uncomfortable about his financial situation and ultimately, his appearance because all the students are now staring at him. The Cunninghams are a poverty-stricken family in Maycomb County, that did not have enough to provide their children lunch everyday nor enough to buy shoes. This is disabling to Walter because since he is poor and cannot afford shoes, he has hookworms on his face. His physical appearance is altered due to his environment which causes him to look different from everyone else. Isolating only him due to his lunch, brings attention to his differences, it is also interesting to note that the first sentence written about Walter is his obvious, physical difference. 

            The second character affected by her environment is Jean-Louise Finch, also known as Scout. The disabling environment of a patriarchal society isolates Scout from her brother, Jem, and best friend, Dill. As they all three grow older, Jem and Dill start to seclude Scout from themselves with expressions such as “sometimes you act so much like a g-irl it’s mortifyin’” (Lee 42) or “but Jem told me I was being a girl, that girls always imagined things, that’s why other people hated them so, and if I started behaving like one I could just go off and find some to play with” (Lee 45). Belittling words like these eventually kept Scout away and she spent her days sitting with Miss Maudie, her neighbor, on the front porch (Lee 46). Scout reaches the age where people are now starting to categorize and treat her as a girl. Because of this anything she does in a negative light is now attributed to her being a female. The patriarchal society is disabling to Scout and all girls because it fits them all into one collective group thus isolating them from others. 

            In conclusion, the environment of the small-town Scout Finch and Walter Cunningham live in, disables them by isolation due to poverty and the patriarch. Physical differences that further disable them are a product of their environment like hookworms or being female. These are not the only two characters strongly affected by their disabling environment, but they are two of the most prominent ones seen in our reading of To Kill a Mockingbird so far. 

Word Count: 589

I Pledge: Rachel Porchie


Series on Madness: Dolls Study

In Doctor Gilman’s lecture on whether racism is a product of mental illness, which it is not if you were wondering, an interesting study called Dolls that was conducted by Kenneth and Phipps Clark was discussed. This study was used to observe children’s attitude and preference towards race using four dolls. These dolls were identical except for their skin color, two were colored and the other two were white. On being asked which doll they preferred to play with, and which doll looked the nicest, two-thirds of the Negro children chose the white doll (Clark 175). However, when told to pick the doll that they racially identified with, 9 out of 10 picked the colored doll (Clark 171). These children could identify dolls by color but preferred the white doll and attributed positive characteristics along with its color. Even when racially aware of their own skin color, the children still chose the white doll. From this study the Clarks concluded that formation of racial attitudes begins in childhood (Clark 177). This study is interesting because it can be applied with the idea of “Becky and Barbie” in Garland-Thomson’s article Integrating Disability, Transforming Feminist Theory. Most young girls had a Barbie in their childhood, playing with these dolls as young children creates a vision in our heads as to what a “normal” doll or person should look like. Barbie represented the able-bodied doll and Becky was the disabled, who was bought as an accessory to Barbie (Garland-Thomson 266). Young girls want Barbie who is a sexualized, feminine icon because she is socially accepted as normal; however, they do not want Becky who is not sexually objectified or viewed as normal (Garland-Thomson 266). This vision of “normalcy” is developed early in childhood like attitudes towards race and disability. As a society, we attribute positive notions towards what is “normal” and consequently our attitudes toward what is “abnormal” is negative.

Clark, Kenneth, and Mamie Clark. “Racial Identification and Preference in Negro Children.” Socialization of the Child.
Garland-Thomson, Rosemarie. “Integrating Disability, Transforming Feminist Theory.”

Britt’s response to To Kill a Mockingbird Ch 1 – 3

To Kill a Mockingbird is among the handful of texts for this class that I am very familiar with, but relatively unsure as to how they may be read within the context of disability. There are more obvious answers to this question, such as Dill Harris’ small stature and Tom Robinson’s impaired arm. However, the chapters for today’s reading do not include Tom and there is not much to discuss about Dill’s size in this context, so I found Arthur “Boo” Radley to be the best point of interest for this response.

Jem’s initial description of Boo to Jem and Scout has always haunted me over the years. Although we later find that this idea of Boo is an exaggerated one, it is so ghastly that it is difficult to picture him as human with this idea of his pallid skin, rotten teeth, and popped eyes (Lee, 15). When I went on to read Mary Shelley’s Frankenstein a few years later, Shelley’s description of the creature immediately brought me back to the horrific image of Boo. Because of the new perspective on Shelley’s text that the discussions in this class has given me, I have been able to use the connection that I made between Boo and the creature to understand Lee’s text in a different light.

Boo Radley does not have a “true” diagnosable disability. There is the possibility of agoraphobia, but that concept can easily be countered by the fact the people of Maycomb have essentially placed him into exile. So, with that in mind, I find it best to read him the same way that we did Shelley’s creature – symbolic of the disabled other rather than explicitly exemplary of it. It is also important to note that while Boo is a social pariah amongst the adults of Maycomb, the narrative is told through a child’s perspective – thus making it important in this type of analysis to focus more on the way that the children of the town view him.

The children view Boo as truly monstrous, at least prior to their interactions. Not only does Jem describe Boo’s appearance as far more ghoulish than what is true to life, his actions are also recounted in a way that makes him seem far more animal or apparition than man. He tells Scout and Dill about the way he skulks around at night, peering in windows and scratching at the door of the Finch house, and even chooses to refer to the physical evidence of Boo’s presence as tracks rather than footprints (Lee, 15). This speaks not only to the way that society has a tendency to cast out and ostracize those who may look different due to physical disability, but also to the fact that society constantly dehumanizes those who are differently abled. Even though Boo begins to show himself to the children as a kind and well-meaning presence – much like the creature in Frankenstein tries to be, Scout does not warm to him until the story nears its end. Beyond that, Scout will never be able to remove that fully societal stigma from him, due to the fact that the severity of his physical differences will always overpower the good deeds that he has done.

Word Count: 538

I hereby declare upon my word of honor that I have neither given nor received unauthorized help on this work. Britt Ingels

Clark’s response to Harper Lee’s To Kill A Mockingbird

I read To Kill a Mockingbird for fun in eighth grade, so I never looked at it from an analytical perspective before, much less looking at the portrayal of disabilities. When I saw it on the book list for this course, I initially wondered why we were reading it in a course about disability in literature. My question was answered when, in the very first paragraph, Scout tells us of her brother Jem’s injury that left one arm slightly shorter than the other, and at an angle when he walked (Lee 3). Jem seems very accepting of his disability, and it might not even be argued to be a disability, as he can still play football like he wanted and it doesn’t seem to impair him much aside from looking slightly different. Nobody seems to treat him differently for having a slightly shorter or bent arm. Jem’s disability is, so far, the only positive portrayal of disability in the book. To Kill a Mockingbird portrays people with mental illness and disfigurement as dangerous and frightening.

The reader is also told that “Crazy Addie” mutilated people’s pets and chickens, but that Boo Radley was initially presumed to be the culprit (Lee 9). “Crazy Addie” reinforces the incorrect assumption that “mad” people are dangerous to others and should be regarded with terror. He eventually drowned himself, and seeing as suicide is usually associated with mental illness, only furthers the message that being mad makes someone bad (Lee, 9).

Despite Jem’s shorter arm being mentioned in the first paragraph and Crazy Addie, the main focus of disability in To Kill a Mockingbird is not on Jem, but on Boo Radley. Boo Radley almost never leaves his house, and the house is closed off to everyone. The entire family is regarded as strange, but especially Boo himself. Much like the creation in Frankenstein, Boo Radley is treated as a monster and regarded with wariness, fear and suspicion. He is treated as so monstrous that people refuse to go in his yard, and even after it was proven that “Crazy Addie” was the one mutilating animals, the old rumor that it was really Boo Radley still stuck in the townspeople’s minds.

Boo Radley reportedly stabbed his mother with scissors and then, showing no remorse, continued cutting pictures for a scrapbook (Lee, 12). This makes him appear to be a sociopath who does not show remorse for his actions, yet at the trial, it was argued that he was not crazy and should not be sent to an asylum (Lee 12). Nevertheless, the town continues to regard Boo Radley as a sort of monster similar to that of the creation in Frankenstein. He is described as hideous like a skeleton with bugging eyes that drools, and Jem spreads rumors that he sneaks out at night and eats animals (Lee 14). Thus, at least according to rumors, he is also disfigured as well as dangerous, which reinforces the negative view of the appearance of disfigured people being something to be feared.

Scout, Jem and Dill regard Boo Radley not only as a monster to be feared, but as a sort of “freak”, such as the ones people gaped at in circuses. Being both horrified and fascinated by his oddities, they continually try to sneak peeks at his life, as if he is not a person but an interesting exhibit to be viewed. This is a commonly dehumanizing portrayal of disabled people Jem and Scout’s father, Atticus, is so far person who most humanizes Boo Radley. He tells his children to mind their own business and let the Radley family mind theirs, though of course his children do not listen (Lee 11).

Word Count: 614

I hereby declare upon my word of honor that I have neither given nor received unauthorized help on this work. Clark Baranoski

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