Displaying items by tag: science fiction

ICFA--my favourite conference (and the only one I now attend)--is coming up next month. This year I have a full slate: in addition to participating on an archival research panel, I will be moderating a discussion panel I organized on "Fantasizing Disability," and presenting a paper on the character Ripley from the Alien franchise. Despite my apprehension around the current US political climate, I'm looking forward to being at ICFA and continuing important conversations about disability representation in genre (because facism is antithetical to disability rights). My abstracts follow:

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Fantasizing Disability

Genres of the fantastic present opportunities to explore worlds fundamentally different than our own, where bodily norms are questioned and disrupted. Fantasy in particular has the potential to create novel relationships to and characterizations of disability. While fantastic worlds frequently imagine diverse bodies (from elvish to gigantic to alien) interacting with each other, the genre often reduces disability to a symbolic medium and disabled characters to one-dimensional stereotypes. Fantasy (as well as science fiction and horror and all of their subgenres) abounds with disability tropes such as the curse of disability, the magical cure as a reward, the disabled villain, the disabled guru who helps the hero, the triumph narrative, and the trope of the “supercrip” (a person who gains compensatory powers for their disability). Given the necessity of integrating inclusive and realistic depictions of human diversity in genre narratives, this panel will address the representation of disabled people and disability in the field of the fantastic. How has disability representation changed since the Brothers Grimm’s fairy tales of Rumpelstiltskin and wicked stepmothers? Why has disability become a mark of a character’s evil-doing or, alternatively, pure innocence (and how can we challenge these readings)? In what ways do disabled bodies act as sites of identification for the audience? What opportunities do various fantastic subgenres—from steampunk to fairy tale re-tellings—offer authors and readers in depicting and understanding disability? Located in an intersectional disability studies perspective, this panel will explore both the reductive tropes and transformative potentials of disability representation in the field of the fantastic.

Panelists: Sara Cleto, Derek Newman-Stille, Nisi Shawl, Fran Wilde Moderator: Kathryn Allan

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Beautiful on the Inside: The Alien Perfection of Ripley

Science fiction film has long explored medical science’s quest for perfection of the human physical form. Released in 1979, Ridley Scott’s Alien launched one of the genres most successful franchises (spawning four other films) and created the iconic feminist action hero, Ellen Ripley (played by Sigourney Weaver). Drawing on feminist disability studies, my analysis of the Alien films will focus on the character of Ripley and trace the ways her narrative revolves around the anxiety of what lies unseen within the (imperfect) human body and how to achieve an ideal form. Rosemarie Garland-Thomson, in her foundational work, Extraordinary Bodies, coins the term normate, which refers to “the social figure through which people can represent themselves as definitive human beings” (8) (often in antithesis to the disabled or the “freak”). I argue that Ripley, at first, is this social figure, but by the end of Jean-Pierre Jeunet’s 1997 installment, Alien: Resurrection, her body has simultaneously become more ideal and more horrible as she transcends normate humanity (from the inside out) to achieve an alien perfection.

Garland-Thomson further writes that: “When our embodied ways of being in the world come to be understood as disabilities or when we understand our way as disabled, we then enter the category” (“The Story of My Work”). Applying this framing to my reading, I am particularly interested in such moments of recognition in the Alien films: when, and in what ways, does Ripley see herself in the alien, as being something other than “normal”? In my discussion, I will address how Ripley relates to the non-normate bodies of the androids (as represented by Ash, Bishop, and Call) and of the aliens—each body offers a possible design for human physical perfection but differs in their interior authenticity (e.g., blood) and organic function (e.g., reproduction). In a universe where the alien body is declared perfect (as repeated throughout the films by various agents of the Weyland-Yutani Corporation), what then constitutes the ideal human? Through my analysis of Ripley, I hope to continue demonstrating the generative potentials of bringing a disability studies framework to science fiction in exploring the social and medical definitions of humanity, as well as in expanding the future possibilities of disability identity.

Published in Kathryn Allan's Blog

Journal of Literary and Cultural Disability Studies

Special issue: The Intersections of Disability and Science Fiction

Guest editors: Ria Cheyne (Disability and Education, Liverpool Hope University) and Kathryn Allan (Independent Scholar, Canada)

“No other literary genre comes close to articulating the anxieties and preoccupations of the present day as clearly and critically as SF, making it a vital source of understanding advances in technology and its impact on newly emerging embodiments and subjectivities, particularly for people with disabilities.”

--Kathryn Allan, Disability in Science Fiction

Reflecting the status of science fiction as a genre that spans multiple mediums and audiences, this special issue of JLCDS seeks articles that explore the intersection(s) of science fiction, disability, and disability studies. What possibilities might science fiction or science fiction theory offer to disability activists and the field of disability studies? How might disability theory, or a disability-informed approach, enrich or transform our understanding of science fiction as a genre or as a mode of thought?

Topics might include, but are not limited to:

Representations of disability in science fiction literature, comics/graphic novels, film, art, music, video games, or television, and their implications for our understanding of genre and/or disability.

Science fiction fan culture (including conventions, fanfic and other forms of fan production).

Science fiction and prosthesis.

Science fiction and eugenics/genetic engineering.

Science fiction and the posthuman.

Accessibility and science fiction environments.

The political and ethical consequences of imagining future worlds with or without disability.

The figure of the alien or cyborg in science fiction and/or disability theory.

Disability and queerness in science fiction.

Disability and indigenous futures in science fiction.

Science fiction, disability, and medical humanities.

The influence of disability activism on professional or fan-based science fiction production.

Submissions that consider how disability intersects with other identity categories are particularly encouraged. The guest editors welcome contributions from independent scholars.

Please email a 500 word proposal to cheyner[at]hope[dot]ac[dot]uk and kathryn[at]academiceditingcanada[dot]ca by March 15, 2017. Contributors can expect to be notified by April 26, 2017. Full drafts of the selected articles will be due by December 6, 2017. Please direct any questions to either guest editor.

Published in Kathryn Allan's Blog

[Author's Note: This article was first published as "Disability in Science Fiction" in SF 101: A Guide to Teaching and Studying Science Fiction. Eds. Ritch Calvin, Doug Davis, Karen Hellekson, and Craig Jacobsen. Science Fiction Research Association, 2014. Ebook. The original intended audience was science fiction scholars not familiar with disability studies (as such, the language may not be accessible for everyone). I retain the rights to this text and I want to make sure that more people have a chance to read it. Since the time the article was published, my research has grown and changed but I think that what I wrote is still worth sharing.]

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What is at stake, supremely, in the debate about the implications of digital, genetic, cybernetic and biomedical technologies is precisely what (and who) will define authoritative notions of normative, exemplary, desirable humanity into the twenty-first century.

— Elaine Graham, Representations of the Post/Human

It’s a crip promise that we will always comprehend disability otherwise and that we will, collectively, somehow access other worlds and futures.

— Robert McRuer, Crip Theory


In “Disability and Narrative,” Michael Bérubé observes that the genre of science fiction, with its plethora of “mutant supercrips” and “posthuman cyborgs,” “is as obsessed with disability as it is with space travel and alien contact” (568). He goes on to note that “sometimes disability is simply underrecognized in familiar sci-fi narratives” (568), and points to Philip K. Dick’s Do Androids Dream of Electric Sheep (with its Voigt-Kampf empathy tests to identify rogue androids, or marking “specials,” neurologically injured people, to prevent them from reproducing) and Gattaca (“which is not only about eugenics but also about passing as nondisabled,” 568). Bérubé’s appraisal that “sometimes” disability in SF is underrecognized is extremely kind—given the overwhelming number of characters with disabilities and scenarios of cure and modification in SF, there really should be more published analyses of disability in SF scholarship. The lack of attention to disability in SF studies is a problem. For one, the exclusion of the study of disability in SF extends the cultural sidelining—theoretically and practically—of people with disabilities in the academic engagement with genre; and second, it also neglects to condemn the repeated instances of the erasure, “curing,” prosthetization, and negative marginalization of people with disabilities in SF novels and films. When people with disabilities are turned into props and tropes (or left out completely) in narratives of a collective human future, it is imperative that SF scholars begin to call out—as we do for instances of racism, sexism, classism, and homophobia—outdated, humiliating, and harmful images of disability.


Disability Studies Basics

Disability studies (DS) concerns itself with the social and cultural construction of disability; it is interested in challenging, questioning, and undoing the aura of deficiency and lack that attends different kinds of bodies in our popular cultural representations. Lennard Davis explains that “[i]mpairment is the physical fact of lacking an arm or leg. Disability is the social process that turns an impairment into a negative by creating barriers to access” (Bending Over Backwards 12). Impairment itself, as many DS scholars point out, is also a normative construct—as bodily or cognitive difference should not be equated with the sense of deficiency that attends the word—but Davis’s definition is a useful starting point. Access, in the context of DS, refers not only to the physical and environmental barriers around which people with disabilities must navigate, but also to the social, economic, cultural, and political forces that limit the rights and freedoms of people with disabilities to be active agents in their own lives. The distinction between impairment and social process is central to DS because, as a field of inquiry, it seeks to expose the ways in which some bodies are construed as “problem bodies” (Chivers and Markotić),[i] “visibly vulnerable” (Shildrick),[ii] “extraordinary” (Garland-Thomson),[iii] deviant, and non-normative. By construing the “abnormal” body as disabled and in need of medical intervention, cure, or rehabilitation in order to make it “normal,” we elide the fact that human bodies exist along a spectrum of variation and ability.

Tobin Siebers articulates how DS seeks to expose the systems of social meaning that establish who gets to be a “quality human being”:

Unlike the medical approach, the emerging field of disability studies defines disability not as an individual defect but as the product of social injustice, one that requires not the cure or elimination of the defective person but significant changes in the social and built environment. Disability studies does not treat disease or disability, hoping to cure or avoid them; it studies the social meanings, symbols, and stigmas attached to disability identity and asks how they relate to enforced systems of exclusion and oppression, attacking the widespread belief that having an able body and mind determines whether one is a quality human being. (3-4)

SF has long commented on what characteristics determine a “quality human being;” from the outset of the genre, novel and visibly different bodies are marked as monstrous (think of Mary Shelley’s Frankenstein’s monster) worthy of either fear or pity, while rehabilitated or technologically-imbued bodies become superheroes (e.g., Marvel’s Professor Xaviar of the X-Men, and Star War’s Luke Skywalker) or supervillans (e.g., Magneto of The Brotherhood of Mutants, and Darth Vader). When interpreting SF texts—whether literature, poetry, film, comics, music, or graphic novels—it is important that critics, as Rob Michalko states in The Difference That Disability Makes, approach disability “as something to think with rather than about” because “disability is mimetic. […] Society is reflected in disability in terms of how society interprets disability” (168). Additionally, in the analyses of disability in SF, Ato Quayson cautions his readers: “To say that the literary model [of disability] provides an analogue to reality does not mean that it is the same as that reality” (30)—in other words, when scholars make arguments about the representation of disability in SF, they must also be cognizant to not ignore or discount the lived realities of diabled people.


DS Looking at SF

In their foundational work, Cultural Locations of Disability, Sharon Snyder and David Mitchell argue that: “Alternative ways of comprehending disabled bodies and minds are often best explained within experiential forms, such as personal narratives, performance art, and films, rather than in the objectifying realms of ‘research’ about disabled people” (4). Synder and Mitchell read SF films—such as Gattaca, Unbreakable, X-Men and X2—as “counter discursive forays” into the presentation of disability on film (167). Unlike the typical non-SF flick, where viewers watch various freak encounters being played out, Synder and Mitchell argue that in SF, disability is central to the plot (167). Focusing on disability in classic horror film, Angela M. Smith, in Hideous Progeny, also speaks to the negative portrayals of atypical or unusual bodies figured in genre film. While perhaps not as overt in the films of today, disability has long been the marker of all things unpleasant and unwanted in genre cinema. Discussing films such as Frankenstein (1931), Dr. Jekyll and Mr. Hyde (1931), and Freaks (1932), Smith emphasizes the eugenic propaganda that equated physical and cognitive difference with moral and racial deviance: “Consequently, the films hint, race, devolution, and deformity may be artificially created rather than biologically determined. They are material certainly, but forged in the somatic exterior, a eugenic fiction sedimented at the level of body signifiers” (154).

Johnson Cheu’s essay, “De-gene-erates, Replicants and Other Aliens: (Re)defining Disability in Futuristic Film” is an oft cited text that addresses disability in the context of utopian (or, depending on your outlook, dystopian) SF narratives. Discussing the films Blade Runner, The Matrix, and Gattaca, Cheu writes:

If disability, as a social construction, exists on more than a theoretical plane, disability should be present as a social stigma in the future. This is not to suggest that bodies are immaterial in Utopian societies. Quite the contrary, bodies exist in Utopia which occupy a social stigma of being unfit, sub-human, inferior, that shows the very existence of disability as a social construction. (202)

Cheu’s attention to narratives of utopia speaks to the pervasiveness of the notion of the “ideal body” or, to again borrow Siebers’s phrasing, “quality human being,” throughout SF—SF scholars can (and should) read for disability in SF texts where disability appears to be a non-issue. Alison Kafer, in Feminist, Queer, Crip, performs an insightful reading of Marge Piercy’s Woman on the Edge of Time, pointing to the significance of what is unsaid or assumed about disability in the creation of an ideal feminist utopia. “Disability and the disabled body,” Kafer writes, “are problems that must be solved technologically, and there is allegedly so much cultural agreement on this point that it need not be discussed or debated [within the narrative]” (74). She then underscores one of the main tensions surrounding disability in SF: “Utopian visions are founded on the elimination of disability, while dystopic, negative visions of the future are based on its proliferation” (74). Regardless of whether SF is utopian or dystopian, the presence or lack of disability in a text often speaks to its implicit assumptions of what constitutes the ideal future human.


Common Categories of Disability Representation in SF

Given the dearth of book length works that focus on disability in SF, scholars who currently pursue this intersectional work draw on a diverse number of literary and theoretical texts to guide their readings. One of the most recent influential studies of disability coming out of literature studies is Aesthetic Nervousness by Ato Quayson. Preceding his discussion of “high culture” novels by Samuel Beckett, Toni Morrison, Wole Soyinka, and J. M. Coetzee, Quayson identifies nine main categories of disability representation in literature:

1. Disability as null set and/or moral test

2. Disability as interface with otherness (race, class, and social identity)

3. Disability as articulation of disjuncture between thematic and narrative vectors

4. Disability as bearer of moral deficit/evil

5. Disability as epiphany

6. Disability as signifier of ritual insight

7. Disability as inarticulable and enigmatic tragic insight

8. Disability as hermeneutical impasse

9. Disability as normality (52)

All of these categories are also present in SF and, as such, offer the uninitiated SF scholar a way into critiquing disability in the genre. In addition to using Quayson’s formulation to frame disability, Snyder and David Mitchell offer the theory of “narrative prosthesis,” which proposes that disability acts “as a crutch upon which literary narratives lean for their representational power, disruptive potentiality, and analytical insight” (Narrative Prosthesis 49). In my experience studying SF with DS in mind, I have begun to trace the ways SF shapes these disability categories/narratives in specific ways that are unique to SF. For the purposes of this essay—and to further address the gap in critical literature on the topic—I have formulated a list of (sub)categories of disability representation in SF. My list is in no way exhaustive, but it nevertheless offers a way to begin the serious work of analyzing the ways in which people with disabilities are defamed and de-humanized in SF. In SF literature and film (broadly defined), I observe the following common categories, or “narrative prostheses,” of disability representation:

1. Disability as a condition in need of cure

2. Disability as a condition to transcend

3. Disability as out of sync (with normative time)

4. Disability as creator of the cyborg or posthuman

5. Disability as creator of the superhuman (the “super crip”)

6. Disability as distinction of the non-human


Disability as a Condition in Need of Cure

In the vast majority of SF texts, wherever there is disability there is the attendant narrative of cure. As I have previously written in the “Introduction” to Disability in Science Fiction: Representations of Technology as Cure:

the medical characterization of the disabled body as requiring cure—in order to become “normal”—has become part of our larger cultural construction of disability. There is a great deal of pressure to rehabilitate, or to “make normal,” the disabled person or otherwise risk condemnation from both the medical and social communities. The ideology of the perfect body—and our ability to make imperfect bodies perfect through medical intervention—is woven throughout our various social discourses, and the onus to be a perfect body rests on both the abled and disabled alike. (Allan 9)

The move to “cure” the body of its various differences, however, speaks more to the normative anxiety of controlling “the problem” body than to satisfying the desires and goals of people with disabilities. Margrit Shildrick, in her exceptional work, Embodying the Monster, states that: “Regardless of ethical intent, those on the receiving end of (limited) beneficence are never able to claim equal agency while their vulnerability remains. Vulnerability is positioned, then, as that which impairs agency in the ‘damaged’ other while inspiring moral action on the part of the secure self to make good the perceived lack” (77). “Curing” disability, therefore, is a process that serves to maintain and create “quality human beings” (Siebers), and SF is a genre that continuously reiterates cure narratives with scant ethical or moral reflection. Of the six disability-in-SF categories that I have identified, disability as a condition in need of cure is the most complex and wide-ranging.

Within the basic structure of a cure narrative, there are the following specific kinds of cure (again, this is not a complete list, but a starting point for further exploration): genetic testing and eugenics (this includes the use of reproductive technologies used to identify and eliminate potential disability); neurological enhancement for cognitive difference; and prosthetic and surgical correction of physical difference (as well as modifying dis/abled bodies to better suit alien environments).

Genetic testing and eugenics: Snyder and Mitchell comment that “the updated eugenics of the present day, called genetics, examines conditions in bodies that are classed as ‘mutant,’ ‘tragic,’ ‘coding errors,’ ‘suffering,’ ‘unhealthy,’ ‘deviant,’ ‘faulty,’ and ‘abnormal’” (19). Looking at Gattaca, Unbreakable, X-Men, and X-Men 2, they argue that these “films foresee a dystopic future where various incarnations of the gene police provide evidence of a new eugenics on the near horizon of our social context” (167). This kind of eugenic policing is evident throughout SF novels (e.g., Aldous Huxley’s Brave New World), and even in the explicitly socially-conscious subgenres like feminist SF—both Piercy’s Women on the Edge of Time and Joanna Russ’s The Female Man celebrate the “defeat” of disability through the use genetic engineering. In addition to the elimination of disability in utero, many SF texts explore the possibilities of genetic therapy. Davis refers to genetic therapy as a “sci-fi scenario” (101), whose process “carries a weighty signification. The defective race must be infected, invaded, and altered by a disease to correct a disease. Thus the invisibility of the prosthesis become linked to an invasion/contamination scenario that we have seen before in countless sci-fi films [such as Alien]” (“Stumped by Genes” 102).

Neurological enhancement for cognitive difference: Despite the recent popularity of characters with Asperger’s (or Asperger’s-like) traits on mainstream TV (e.g., Sheldon Cooper on The Big Bang Theory, and Abed on Community), most SF narratives that feature individuals who are “neuroatypical” are usually singled out for “curing.” In Elizabeth Moon’s Nebula-winning The Speed of Dark, the lead character, Lou Arrendale, is autistic and leads a productive life; despite being a valued community member, however, Lou ends up choosing to undergo an experimental surgery to make him “normal.”[iv] A similar type of neurological “cure” is performed on Charlie in Daniel Keyes’s Flowers for Algernon; like Moon, Keyes relies on the reader’s sympathy and expectation that people with intellectual disabilities want to be better versions of themselves. Dan Goodley and Mark Rapely comment that, “we need to be attentive to the challenges posed by people with the label of ‘learning difficulties’/intellectual disabilities. Such sensitivity is enabled by a view of the world which does not separate impairment and disability as binary oppositions but throws both into the dynamic world of discourse and practice” (“Changing the Subject” 139). Whether encountering obviously negative representations of people deemed to have intellectual or cognitive disabilities (e.g., The Lawn Mower Man) or “kinder” approaches taken under the guise of beneficent cure (e.g., The Speed of Dark, Flowers for Algernon), DS seeks to undo the language that casts people into the medicalized model of disability as bodies to be rehabilitated and cured.

Prosthetic and surgical correction of physical difference: The use of prostheses or surgical interventions to make people with unusual bodies “normal,” or, in many cases, extraordinary, is particularly favoured in SF. Throughout SF’s myriad of subgenres, writers have envisioned bodies that are transformed, modified, and re-made through the use of technology. For example, James Tiptree, Jr.’s “The Girl Who Was Plugged In” features P. Burke, a “deformed” and suicidal teenager who, once “saved,” receives advanced technological implants that allow her to control the physically beautiful, but brainless, Delphi. Or, in a more recent turn on the theme, William Gibson’s Lise, in “The Winter Market,” is a sick drug-user who needs to be “propped up in her pencil-thin polycarbon prosthetic” (128). Even young adult SF reiterates the notion of being “cured” through surgical correction: consider the widely-popular Scott Westerfeld series, Uglies, where teenagers undergo an extensive series of physical (and neurological) surgery to become “pretties,” the desired normal (and easily controlled) bodies of the future. When reading this particular disability-in-SF category, it is important to keep in mind the lived mundane and difficult realities of using prosthetics or undergoing (plastic) surgery, because, as Vivian Sobchack observes: “As an effect of the prosthetic’s amputation and displacement from its mundane context, the animate and volitional human beings who use prosthetic technology disappear into the background—passive, if not completely invisible—and the prosthetic is seen to have a will and life of its own” (23). A DS reading of prosthetics and other medical modifications in SF must be careful not to idealize the transformative potential of such technologies while neglecting a discussion of the bodies most often targeted for and affected by such interventions.


Disability as a Condition to Transcend

Another popular and prominent representation of disability in SF is the use of technology, usually cyberspace or virtual reality, that projects the “inner self” out of and away from the sick or disabled body. To find examples of this particular narrative, one only has to look at (pre- and post-) cyberpunk: Dick’s Do Androids Dream of Electric Sheep (everyone still on Earth uses the Penfield mood organ to dictate their mental state); Gibson’s Neuromancer (Case plugs into his cyberdeck to escape from the pain of the timed lethal poison in his body); and Laura Mixon’s Proxies (children with multiple disabilities are sealed into crèches, living out the rest of their days in virtual reality and through synthetic proxy bodies). The move to imagine a simple (technologically-mediated) transcendence from the body “by ignoring or discounting its needs and sensations is generally a luxury of the healthy and able-bodied” (173) states Susan Wendell in The Rejected Body. She goes on to propose that:

We cannot speak only of reducing our alienation from our bodies, becoming more aware of them, and celebrating their strengths and pleasures; we must also talk about how to live with the suffering body, with that which cannot be noticed without pain, and that which cannot be celebrated without ambivalence. We may find then that there is a place in our discussion of the body for some concept of transcendence. (Wendell 179)

Taking a DS approach to analyzing transcendence in SF means considering the material conditions and kind of body that is being “left behind.”


Disability As out of Sync (with Normative Time)

SF classics, from Planet of the Apes to Alfred Bester’s The Stars My Destination, speculate on potential futures (and pasts) through bodies that fail to match the ideal of their present time. Kafer importantly asks in Feminist, Queer, Crip, “Why is disability in the present constantly deferred, such that disability often enters critical discourse only as the marker of what must be eliminated in our futures or what was unquestionably eliminated in our pasts?” (10). The language of time and futurity, an essential characteristic of SF, is present throughout the cannon of disability studies.[v] As Snyder and Mitchell state:

In a culture that endlessly reassures itself that it is on the verge of conquering Nature once and for all, along with its own “primitive” instincts and the persistent domain of the have-nots, disability is referenced with respect to these idealized visions. As a vector of human variability, disabled bodies both represent a throwback to a human prehistory and serve as the barometer of a future without “deviancy.” (Cultural Locations 32)

There is a refusal to situate the disabled body in the present; only the normative able-body can claim that position, as disability in SF is often shown as a genetic step backwards or as a condition to erase from the future. As the genetically “imperfect” Vincent Freeman concludes in Gattaca: “For someone who was never meant for this world, I must confess I’m suddenly having a hard time leaving it. Of course, they say every atom in our bodies was once part of a star. Maybe I’m not leaving, maybe I’m going home.” Vincent sees himself as a product of a bygone age before genetic screening, and as such, is best at home with the ancient stars.


Disability As Creator of the Cyborg or Posthuman

From classic television shows (e.g., The Six Million Dollar Man and The Bionic Woman) to blockbuster films (e.g., Robocop) to novels (e.g., Martin Caidin’s Cyborg and Bruce Sterling’s Schismatrix) the idea of the injured or disabled body remade stronger, better, faster has intrigued both fans and academics alike. Commenting on Donna Haraway’s problematic use of the paraplegic as cyborg—“Perhaps paraplegics and other severely handicapped people can (and sometimes do) have the most intense experiences of complex hybridization” (Simians, Cyborgs, and Women 178)—Kafer argues that “the term ‘cyborg,’ rather than entailing a critique of existing categories and ideologies, is used to perpetuate distinctions between ‘normal’ and ‘abnormal’ bodies, distinctions that have material consequences involving discrimination, economic inequalities, and restricted access” (110). Such criticism resonates throughout DS readings of disability as a condition that creates cyborgs (or posthumans) both in and out of SF.

One of the most cited novels for a claimed positive representation of a person with disabilities being an exemplar cyborg/posthuman is Anne McCaffery’s The Ship Who Sang. The human protagonist, Helva, “born a thing” (1), is turned into a “brain ship.” While many scholarly readings of this novel exist, as Ria Cheyne points out, none of them attend to the ableist assumptions that underlie Helva’s supposed freedom as cyborg. Cheyne writes: “Rather than an exemplar of the liberatory possibilities of a cyborg existence, then, I read Helva as a pitiful figure: not because of her initial physical impairments, but because of what is done to her without her knowledge or consent, her lack of freedom, and the limitations her conditioning places on her thought” (145). Many SF narratives portray the “overcoming” of disability (through technological enhancements) as a way to realizing a posthuman future, but, in doing so, they end up eliding the real and damaging ways people with disabilities are characterized as something other than “normal.” As Sherryl Vint comments in Bodies of Tomorrow, “Technological visions of the post-embodied future are merely fantasies about transcending the material realm of social responsibility” (8). A DS approach to reading the cyborg or posthuman figure in SF should take into consideration issues of access: who gets to create, navigate and make use of potentially transformative technology?


Disability As Creator of the Superhuman (the “Super Crip”)

Echoing the racist stereotype of the “magical negro,” Colin Barnes describes the “super cripple” (or super crip), as: “the disabled person [who] is assigned super human almost magical abilities. Blind people are portrayed as visionaries with a sixth sense or extremely sensitive hearing. Alternatively, disabled individuals, especially children, are praised excessively for relatively ordinary achievements” (12).[vi] Barnes might as well be addressing the “super crips” of the Star Trek universe. With its insistent optimistic transhumanism, people with disabilities are shown constantly striving for, and often exceeding, “normal” achievements; for example: the deaf, but telepathic, mediator Riva (ST: TNG episode, “Loud as a Whisper”); the exo-skelton clad, brilliant scientist Melora (ST: DS9 episode, “Melora”);[vii] and T’Pol, a Vulcan who struggles to overcome neurological damage that inhibits her ability to control her emotions (ST: Enterprise). The Next Generation’s Geordi LaForge, however, is perhaps the most recognizable character with a disability in Star Trek. In the introduction of the character, Gene Rodenberry describes Geordi as: “racially black and birth-defect blind—although with prosthetic super-high tech artificial ‘eyes’ which can detect electromagnetic waves from all the way from [sic] raw heat to high frequency ultra-violet, making other crewpersons seem hopelessly ‘blind’ by comparison. […] Because of his ‘eyes’, Geordi can also perform some of the functions of a tricorder” (7). In this well-intentioned description, Roddenberry creates the superhuman stereotype: the bulk of Geordi’s character description is dedicated to his disability and technological superiority. By classifying disability as a condition that creates superhumans or “super crips,” SF writers contribute to a culture that sets up people with disabilities with unrealistic standards, and then condemns them when they cannot or do not want to meet them.

Disability As Distinction of the Non-human

The last disability-in-SF category that I want to highlight is disability as a defining quality of the non-human, and, as a result, a threat to the normative, able-body. This category can be located in the earliest examples of SF: H. G. Wells plays with it in The Time Machine, as the misshapen and brutish Morloks (the “working class”) are revealed, in fact, to be advanced humans, and the Eloi, with their lack of human compassion and intelligence, become another kind of dreaded otherness, a failed people, to the Time Traveller. Elaine Graham states:

Monstrosity has long been a trope for invasion, contamination, assimilation and loss of identity, the ascription of monstrous and subhuman traits serving to rationalize xenophobia and prejudice. That which is different becomes pathologized as “monstrous” and thus inhuman, disposable and dangerous; the monster is personified as a threat to purity and homogeneity. So women, racial and sexual minorities, political radicals or those with physical or mental impairments are designated inhuman by virtue of their non-identity to the white, male reasoning able-bodied subject. (Representations of the Post/Human 53)

The narrative hook of characterizing people with physical and mental disabilities as inhuman and threatening to the (usually white, male, straight, able) protagonist repeats itself throughout SF: the mistreatment and containment of the physically and cognitively different, yet gifted, “precogs” in Dick’s “Minority Report;” the beautiful, but stutter motioned, crèche grown Emiko who needs Anderson Lake to save her in Paolo Bacigalupi’s The Wind Up Girl; or, in the Doctor Who universe, home of the ultimate antagonist and creator of the dreaded Daleks, Davros, who is visibly scarred and in a body-encasing wheelchair. Regardless of whether the audience feels sympathy or disdain for such “monsters,” all of these SF narratives dictate clear messages about how much difference is acceptable, who controls their own lives, and, ultimately, who gets to be counted as human.



One of my favorite quotes about the importance of being present in science fiction comes, not from a DS scholar, but from Brian Attebery in his book Decoding Gender in Science Fiction: “By using images of the future to describe the present, the popular media invite us to use futuristic scenarios as tests of viability. Any group that cannot negotiate a place for itself in the imagined future is already obsolete” (192). In the vast expanse of SF, there are so few positive representations of people with disabilities in the imagined future. SF scholars need to vocally and publically condemn SF narratives that exploit and humiliate people with disabilities. It is simply not acceptable to ignore films like Iron Man 3, where disabled war veterans are turned into weapons of mass destruction, or Source Code, which centres on the refusal to give agency to a severely injured soldier and where the director takes every opportunity to highlight the “evil scientist’s” use of a cane. DS scholars Snyder and Mitchell end their discussion of representation of disability on screen with: “It is in film that we encounter disability largely as a ‘plight to be conquered’ as long as when the lights come up, we don’t find the same bodies blocking the aisles” (181). While audiences can read the transformation or elimination of physical and cognitive disabilities in SF as an expressed hope that technology will be able to “fix” even the most “damaged” bodies, such stories elide the very real experiences of people with disabilities who constantly encounter a culture that would prefer them invisible or, at the very least, putting on an illusion of able-bodiedness. SF is a wonderful testing ground of viable futures; let us make sure that they are accessible to all.


Works Cited

Allan, Kathryn, ed. Disability in Science Fiction: Representations of Technology as Cure. New York: Palgrave Macmillan, 2013. Print.

Attebery, Brian. Decoding Gender in Science Fiction. New York: Routledge, 2002. Print.

Barnes, Colin. Disabling Imagery and the Media: An Exploration of the Principles for Media Representations of Disabled People. The British Council of Organisations of Disabled People; Halifax: Ryburn, 1992. Web. 20 Aug. 2013. UK. http://disability studies.leeds.ac.uk/files/library/Barnes-disabling-imagery.pdf.

Blade Runner. Dir. Ridley Scott. 25 Jun 1982. Warner. 2007. DVD.

Bérubé, Michael. “Disability and Narrative.” PMLA 120.2 (2005): 568-76. Print.

Chivers, Sally, and Nicole Markotić, eds. The Problem Body: Projecting Disability on Film. Columbus: Ohio State UP, 2010. Print.

Cheu, Johnson. “De-gene-erates, Replicants and Other Aliens: (Re)defining Disability in Futuristic Film.” Disability/Postmodernity. Ed. Mairian Corker and Tom Shakespeare. London: Continuum, 2002.198-212. Print.

Cheyne, Ria. “‘She was born a thing’: Disability, the Cyborg and the Posthuman in Anne McCaffrey’s The Ship Who Sang.Journal of Modern Literature 36.3 (2013): 138-56. Print.

Crutchfield, Susan. “The Noble Ruined Body: Blindness and Visual Prosthetics in Three Science Fiction Films.” Screening Disability. Ed. Anthony Enns and Christopher Smit. Lanham: U of America P, 2001. 135-50. Print.

Davis, Lennard. Bending over Backwards: Disability, Dismodernism, and Other Difficult Positions. New York: New York UP, 2002. Print.

---. “Stumped by Genes: Lingua Gattaca, DNA, and Prosthesis.” Ed. Marquard Smith and Joanne Morra. The Prosthetic Impulse: From a Posthuman Present to a Biocultural Future. Cambridge, MA: MIT P, 2006. 91-106. Print.

Dick, Philip K. Do Androids Dream of Electric Sheep? New York: Del Rey, 1968. Print.

Garland-Thomson, Rosemarie. Extraordinary Bodies: Physical Disability in American Culture and Literature. New York: Columbia UP, 1997. Print.

---. Staring: The Way We Look. Oxford: Oxford UP, 2009. Print.

Gattaca. Dir. Andrew Niccol. Columbia Pictures, 1997. DVD.

Gibson, William. Neuromancer. New York: Ace, 1984. Print.

---. “Winters Market.” Burning Chrome. New York: Eos, 2003. Print.

Goodley, Dan, and Mark Rapely. “Changing the Subject: Postmodernity and People with ‘Learning Difficulties.’” Disability/Postmodernity. Ed. Mairian Corker and Tom Shakespeare. London: Continuum, 2002. 127-42. Print.

Graham, Elaine. Representations of the Post/Human: Monsters, Aliens, and Others in Popular Culture. New Brunswick: Rutgers UP, 2002. Print.

Haraway, Donna. Simians, Cyborgs, and Women: The Reinvention of Nature. New York: Routledge, 1991. Print.

Iron Man 3. Dir. Shane Black. Paramount Studies, 2013. Film.

Kafer, Alison. Feminist, Queer, Crip. Bloomington: Indiana UP, 2013. Print.

Kanar, Hanley E. “No Ramps in Space: The Inability to Imagine Accessibility in Star Trek: Deep Space Nine.” Fantasy Girls: Gender in the New Universe of Science Fiction and Fantasy Television. Ed. Elyce Rae Helford. Lanham, MD: Rowman and Littlefield, 2000. 245-64. Print.

McCaffery, Anne. The Ship Who Sang. New York: Del Rey, 1969.

McRuer, Robert. Crip Theory: Cultural Signs of Queerness and Disability. New York: New York UP, 2006. Print.

Michalko, Rod. The Difference That Disability Makes. Philadelphia: Temple UP, 2002.

Mitchell, David T. and Sharon L. Snyder. Cultural Locations of Disability. Chicago: U of Chicago P, 2006. Print.

---. Narrative Prosthesis: Disability and the Dependencies of Discourse. Ann Arbor: U of Michigan P, 2000. Print.

Mixon, Laura. Proxies. New York: Tor, 1998. Print.

Moon, Elizabeth. The Speed of Dark. New York: Del Rey, 2002. Print.

Piercy, Marge. Woman on the Edge of Time. New York: Ballantine, 1976. Print.

Quayson, Ato. Aesthetic Nervousness: Disability and the Crisis of Representation. New York: Columbia UP, 2007. Print.

Roddenberry, Gene. “Lt. (J. G.) Geordi La Forge.” Star Trek: The Next Generation Writer/Director’s Guide. Web. 20 Aug. 2013. http://leethomson.myzen.co.uk/Star_Trek/ 2_The_Next_Generation/Star_Trek_-_The_Next_Generation_Bible.pdf.

Russ, Joanna. The Female Man. Boston: Beacon, 1986. Print.

Siebers, Tobin. Disability Theory. Ann Arbor: U of Michigan P, 2008. Print.

Shildrick, Margrit. Embodying the Monster: Encounters with the Vulnerable Self. London: SAGE, 2002. Print.

Smith, Angela M. Hideous Progeny: Disability, Eugenics, and Classic Horror Cinema. New York: Columbia UP, 2011. Print.

Sobchack, Vivian. “A Leg to Stand On: Prosthetics, Metaphor, and Materiality.” Ed. Marquard Smith and Joanne Morra. The Prosthetic Impulse: From a Posthuman Present to a Biocultural Future. Cambridge, MA: MIT P, 2006. 17-41. Print.

Source Code. Dir. Duncan Jones. Summit Entertainment, 2011. Film.

Star Trek: Nemesis. Dir. Stuart Baird. Paramount Pictures, 2002. DVD.

Tidwell, Christy. “‘Everything Is Always Changing’: Autism, Normalcy, and Progress in Elizabeth Moon’s The Speed of Dark and Nancy Fulda’s ‘Movement.’” Disability in Science Fiction: Representations of Technology as Cure. Ed. Kathryn Allan. New York: Palgrave Macmillan, 2013. 153-68. Print.

Vint, Sherryl. Bodies of Tomorrow: Technology, Subjectivity, Science Fiction. Toronto: U of Toronto P, 2007. Print.

Wendell, Susan. “Feminism, Disability, and Transcendence of the Body.” The Rejected Body: Feminist Philosophical Reflections on Disability. New York: Routledge, 1996. 165-79. Print.

Further Reading

Davis, Lennard. Enforcing Normalcy: Disability, Deafness, and the Body. London: Verso, 1995. Print.

---., ed. The Disability Studies Reader. 2nd ed. New York: Routledge, 2006. Print.

---. The End of Normal: Identity in a Biocultural Era. Ann Arbor: U of Michigan P, 2014. Print.

Einstein, Sarah. “The Future Imperfect.” Redstone Science Fiction. June 2010. Web. July 15 2013.

Goodley, Dan, Bill Hughes, and Lennard Davis, eds. Disability and Social Theory: New Developments and Directions. New York: Palgrave, 2012. 91-111. Print.

Grosz, Elizabeth. “Naked.” The Prosthetic Impulse: From a Posthuman Present to a Biocultural Future. Ed. Marquard Smith and Joanne Morra. Cambridge, MA: MIT P, 2006. 187-202. Print.

Hall, Kim Q., ed. Feminist Disability Studies. Indianapolis: Indiana UP, 2011. Print.

Haraway, Donna. “A Manifesto for Cyborgs: Science, Technology, and Socialist Feminism in the 1980s.” Socialist Review 80 (1985): 65-107. Print.

Kerr, Anne, and Tom Shakespeare. Genetic Politics: From Eugenics to Genome. Cheltenham: New Clarion, 2002. Print.

Longmore, Paul K. “Screening Stereotypes: Images of Disabled People.” Social Policy 16 (Summer 1985): 31-38. Print.

---. Why I Burned My Books and Other Essays on Disability. Philadelphia: Temple UP, 2003. Print.

Moody, Nickianne. “Untapped Potential: The Representation of Disability/Special Ability in the Cyperpunk Workforce.” Convergence: The International Journal of Research into New Media Technologies 3.3 (1997): 90-105. SAGE.

Nussbaum, Martha. Frontiers of Justice: Disability, Nationality, Species Membership. Cambridge, MA: Harvard UP, 2006. Print.

Peace, William J. “Slippery Slopes: Media, Disability, and Adaptive Sports.” The Body Reader. Ed. Jean Moore and Mary Kosut. New York: New York UP, 2010. 332-44. Print.

Shakespeare, Tom. Disability Rights and Wrongs. London: Routledge, 2006. Print.

Shapiro, Joseph. No Pity: People with Disabilities Forging a New Civil Rights Movement. New York: Three Rivers, 1993. Print.

Squier, Susan Merrill. Liminal Lives: Imagining the Human at the Frontiers of Biomedicine. Durham: Duke UP, 2004. Print.

Titchkosky, Tanya. The Question of Access: Disability, Space, Meaning. Toronto: U of Toronto P, 2011. Print.

Titchkosky, Tanya and Rod Michalko. Rethinking Normalcy: A Disability Studies Reader. Toronto: Canadian Scholars’, 2009. Print.

Vanderhooft, JoSelle, ed. The WisCon Chronicles: Shattering Ableist Narratives. Vol. 7. Seattle: Aqueduct, 2013. Print.

Wald, Priscilla. Contagious: Cultures, Carriers, and the Outbreak Narrative. Durham, NC: Duke UP, 2008. Print.

Watson, Nick, Alan Roulstone, and Carol Thomas, eds. Routledge Handbook of Disability Studies. London: Routledge, 2012. Print.

Weinstock, Jeffrey A. “Freaks in Space: ‘Extraterrestrialism’ and ‘Deep-Space Multiculturalism.’” Freakery: Cultural Spectacles of the Extraordinary Body. Ed. Rosemarie Garland Thomson. New York: New York UP, 2006. 327-37. Print.

Wills, David. Prosthesis. Stanford: Stanford UP, 1995. Print.


[i] Chivers and Markotić use the term “problem body” to refer to all those bodies that exceed normative boundaries of the acceptable, and to place “an emphasis on the transformation of physical difference into cultural patterns of spectacle, patterns that replicate a range of pathologizing practices that oppress people” (9).

[ii] “What causes unease is not that those named as disabled are helpless—indeed the majority are far from it—but that the inviolability of their bodies, the inviolability that confers an aura of self-mastery, appears to have been breached. They are in other words visibly vulnerable” (Shildrick, Embodying the Monster 76).

[iii] “The meanings attributed to extraordinary bodies reside not in inherent physical flaws, but in social relationships in which one group is legitimated by possessing valued physical characteristics and maintains its ascendency and its self identity by systematically imposing the role of cultural or corporeal inferiority on others” (Garland-Thomson, Extraordinary Bodies 6).

[iv] In “‘Everything Is Always Changing:’ Autism, Normalcy, and Progress in Elizabeth Moon’s The Speed of Dark and Nancy Fulda’s ‘Movement,” Christy Tidwell compares the two divergent trajectories of progress for people on the autistic spectrum: in The Speed of Dark, surgical intervention leads to a more fulfilling, “extraordinary” life (as Lou becomes an astronaut), whereas in “Movement,” the main character Hannah celebrates the freedom of just being herself.

[v] To note another few examples: In her article, “The Noble Ruined Body: Blindness and Visual Prosthetics in Three Science Fiction Films,” Susan Crutchfield analyzes X: The Man with the X-Ray Eyes, Death Watch, Until the End of the World. Describing the disabled body in these films, she uses the phrase “body in ruins” for its “indication of a diminished physiology, but also for its connotations of an atavistic throwback, of a historical past now considered obsolete and therefore undesirable” (138). In another DS text that places the disabled body out of time, Tobin Siebers argues, “the ideology of ability makes us fear disability, requiring that we imagine our bodies are of no consequence while dreaming at the same time that we might perfect them. It describes disability as what we flee in the past and hope to defeat in the future” (Disability Theory 9).

[vi] In his list of commonly recurring media stereotypes of people with disabilities, along with “super cripple,” Barnes also identifies popular representations of the disabled person as: pitiable and pathetic; an object of violence; sinister and evil; atmosphere or curio; an object of ridicule; their own worst and only enemy; burden; sexually abnormal; incapable of participating fully in community life; and, normal (7-19).

[vii] There is a notable moment in the episode where Melora identifies the social construction of her disability: “I’m sorry if I seem overly sensitive, but I’m used to being shut out of the ‘Melora’ problem. The truth is, there is no ‘Melora’ problem. Until people create one” (DS9, “Melora”). See Hanley E. Kanar’s “No Ramps in Space” for a critical analysis of disability in Star Trek: Deep Space Nine.

Published in Kathryn Allan's Blog
Wednesday, 29 July 2015 17:25

Accessing the Future is out!

I'm a bit behind on this announcement but you can now buy ACCESSING THE FUTURE, a disability-themed speculative fiction anthology co-edited by me and Djibril al-Ayad (Futurefire.net Publishing, 2015).

Stories by Nicolette Barischoff, A.C. Buchanan, Joyce Chng, David Jón Fuller, Louise Hughes, Rachael K. Jones, Margaret Killjoy, Petra Kuppers, Toby MacNutt, Jack Hollis Marr, Kate O'Connor, Sara Patterson, Sarah Pinsker, Samantha Rich, A.F. Sanchez.
Internal illustrations by Fabian Alvarado, L.E. Badillo, Jane Baker, Comebab, Pandalion Death, Rachel Keslensky, Vincent Konrad, Tostoini
Cover art by Robin E. Kaplan
Preface by JoSelle Vanderhooft
Afterword by Derek Newman-Stille

Publishers Weekly gave us a STARRED review! Goodreads reviewers love it! So far, so awesome!

Check out our press page over at The Future Fire, give us a like on our Facebook page. ACCESSING THE FUTURE is available for purchase (paperback or ebook) at Amazon, Smashwords, Lulu, and all other online retailers.

Published in Kathryn Allan's Blog

Today is Blogging Against Disablism Day (or BADD for short), and this is my first year participating. For those of you new to my blog and my work, when I’m not running Academic Editing Canada, I’m busy with my independent scholarship in disability studies and science fiction. I recently wrote a post about my disability identification, “Fragments: Disability, Community, and Me,” if you’re curious, and many of the posts on this blog deal with my reflections on being a chronically-ill graduate student, and how that experience informs my research today. I also edit science fiction (SF), and I want to mention some good news right away— because I’m super proud of it—that Accessing the Future, an anthology of disability-themed speculative fiction stories that I co-edited with Djibril al-Ayad, received a starred review from Publishers Weekly!

There are many things that I could write about when it comes to my experiences of ableism, but I thought I’d share some of my observations as an independent scholar invested in bringing disability studies into science fiction studies. At the moment, I am frustrated with the genre academic community's engagement with disability—it is still such a marginalized conversation outside the handful of us who work at this intersection (mostly grad students and recent PhDs).

There are many oversights and microagressions I have witnessed or encountered in my role as scholar and writing about them in any specific detail feels unsafe and “unprofessional.” I know that this is ableism at work. I can say that I have felt devalued in my interactions with a few journal editors. I have made requests for accommodation on presentation times that were entirely ignored. And I’ve had to withdraw an accepted paper at a conference because its scheduling was so mishandled. These are just a few incidences that have affected my ability to fully participate, and I have heard many, many more examples of ableism from my disabled academic friends and peers. It is extremely common to hear, for example, in all kinds of academic and casual conversations, professors using ableist language, like “lame” and “crazy,” to describe unpopular or unusual ideas and people. This language hurts.

Articles addressing disability in any meaningful way are infrequent finds in genre journals—and, if they do appear, most of them are locked behind paywalls where I (and everyone else who lacks access to university journal databases) cannot read them. While I appreciate the difficulty of scheduling large, multi-track conferences, it is frustrating that the few papers about disability are often placed on panels about “otherness” or monstrosity (this has happened twice to me). It seems that genre conferences do not know where to effectively place a disability studies paper and this is a problem. It makes talking about disability in a sustained, critical way (that intersects with feminist, queer, anti-racist, and such other important concerns) that much more difficult.

While Disability Studies is becoming less marginalized in science fiction studies, there is a long way to go for it to move from a momentarily interesting “hot topic” to an actually active and engaged conversation that does not rely on a small handful of people to constantly bring it up. Since I started presenting on disability in SF at conferences (though I am not able to attend more than one or two a year I do follow what’s going on online), I have learned just how new and marginal disability studies is in the academic genre community. For example, the Science Fiction Research Association’s annual conference theme this year is “The SF We Don't (Usually) See: Suppressed Histories, Liminal Voices, Emerging Media.” Although many axes of identification were included in the original call for papers (CFP), there was no mention of disability! It took the wonderful Ria Cheyne to point out its absence before “disability and ability” were added to the CFP. Furthermore, there are no papers, from what I can tell from their conference program, that directly address disability. This is an all too common scenario that I have seen played out too many times.

Additionally, in a practical sense, there needs to be more people talking about disability and calling out ableism because so little is actually happening to improve the working conditions for a countless number of disabled graduate students, adjunct/sessional and tenured faculty, and administrative staff. Just check out some of the stories on PhDisabled (which is an amazing resource for disability recognition and advocacy). Conference organizers need to work harder in ensuring that their venues are fully accessible and in developing clear policies around accommodations for people with disabilities. Journals need to be open access and available on a variety of platforms.

I can’t speak to how other academics are trained in graduate school, but I know that for me, the process of interrogating cultural truths was held up as a foundational goal. I also know that when I see an absence of knowledge, especially one that causes or reinforces existing harm, I feel an obligation to speak up and say, “this is something we need to be talking about.” This is how I feel about the representation of disability in science fiction. There are very few popular SF texts that show realistic depictions of disability, whether it be physical or cognitive disability, chronic illness, or neurodiversity. It is a niche topic in terms of academic study but literature and film (and all media) show us what is and what is not possible. SF is an important place where cultural producers and consumers think through what kinds of lives matter and who gets to take part in creating the future world. I believe that genre scholars have a responsibility to meaningfully and significantly engage with disability—both theoretically and practically—sooner than later.

Published in Kathryn Allan's Blog
Wednesday, 12 March 2014 16:06

On Embracing Ambition

A few weeks back I tweeted: “After leaving academia, I had to really think about what I wanted out of life. I have far more ambition now than I ever did before.” For whatever reasons, the sentiment resonated with a lot of people and the positive response I received prompted this post.

The entire time I spent in academia, from undergrad through to the completion of my PhD, is best characterized as deadline oriented. Write a paper. Submit. Receive grade. Apply for next course/program/degree. Rinse and repeat. Of course, there was a lot more complication to that process, but the way in which I approached every year of my higher education was essentially the same: meet pre-existing deadlines and fulfill pre-existing requirements. The end goal was the degree, obviously, but I can’t honestly say that I was driven by a specific sense of ambition. “I want to be a professor” was not so much a statement of ambition as it was an assumption of the final outcome of my academic efforts. Once I realized that a professorial life was not in my future, I was faced with a question that I had been avoiding for the entirety of adult life: What do I want to do?

As a person who most often did what was expected of me—I truly excelled at listening to authority figures—it was extremely difficult to not have my efforts directed by an outside force when I found myself no longer a graduate student and unemployed. In my mind, I was a failure. I tried to work for my spouse. That experiment failed spectacularly within a few weeks. In those first long months out of my PhD program, I can only imagine how awkward and challenging it was for my partner to have me (unconsciously) looking to him for the direction and guidance in my life that he couldn’t provide. My housekeeping and pet tending efforts were doubled. But a spotless house and an increasingly spoiled cat did nothing to give me purpose. I was depressed for quite a long while (and it certainly didn’t help that I was coping with chronic pain, which, at that time, was quite severe and debilitating). I was completely adrift without institutional structure. I had no deadlines to meet. I had no ambition.

Graduate school showed me what I didn’t want—an academic career—but it also provided me with experiences of work that were outside of any possibilities I was exposed to as a child. People can, and do, make a living from researching, writing, and exploring difficult and new ideas. There wasn’t any discussion of an intellectual career happening outside of academe, but I read enough to know that independent scholarship—respected, widely read, and transformative engagement—does exist. When I made the mental leap to thinking of myself as an independent scholar, all of the institutional rules of "what is possible and who can do what" started falling away. Freed from other people’s deadlines, I started making my own. The first goals I set were small: set up a website, read a book, write a blog post. Then they started to grow: present at a conference, start a business, edit an essay collection. Each time I devised of and completed a project of my own choosing I became more confident in myself. And I started wanting more.

I want to write a book. I want to write a screenplay. I want to edit science fiction. I want to be an invited keynote speaker. I want to be the next big theorist. I want to never limit myself to the options in front of me. I want to go beyond the obvious outcomes of my current labour and find new ways to grow as individual.

To make my new found ambition public is both terrifying and liberating. Part of me worries that people will say, “who does she think she is?” Another part whispers to me that these dreams are too big for such a small person. But there is also an ever increasing desire to try. I finally understand now that I am only a failure if I don’t take risks. I spend much of my time alone and it is easy to become lost in my own world. My newly found ambition pushes me to write, to learn, to reach out to other people. I have no idea what my future holds but I no longer feel like I am staring into some horrible directionless void. Instead, I am curious and eager to find out what I’ll be doing at this time next year. While not every project I dream up will work out, some of them will.

When asked about her best advice to writers, Octavia Butler (in Bloodchild, p. 144) said that it was to persist: "It’s a truth that applies to more than writing. It applies to anything that is important, but difficult, important, but  frightening. We’re all capable of climbing so much higher than we usually permit ourselves to suppose. The word, again, is 'persist'!"

I have ambition. I will persist.


Published in Kathryn Allan's Blog

As March approaches, so does my favourite conference: ICFA. After a successful presentation on disability in Star Trek last year, I thought I would stick with the film and television track of the conference. Not only do I thoroughly enjoy analyzing popular films, but it seems that everyone loves watching movie clips during conference papers. Win-win.

This year I am presenting on Rupert Wyatt's reboot of the Planet of the Apes franchise, Rise of the Planet of the Apes (2011). I've seen all of the Apes movies--was alternatively amused and appalled--and went to see Rise in the theatre (by myself) because I was extremely curious about how Wyatt's film would deal with the offensive racial politics of the earlier Apes films. Rise of the Planet of the Apes did not fail to deliver a similarly problematic narrative of the primate other. And so another academic conference was born. Here is my proposal for my paper/clip show with analysis:

“Some Things Aren’t Meant to be Changed”—Disability in Rise of the Planet of the Apes

In Rupert Wyatt’s Rise of the Planet of the Apes (2011), the Planet of the Apes franchise goes high-tech—both in terms of the films extensive use of CGI to create the lead ape, Caesar, and in its key plot device of the creation and misuse of a “neurogenesis” drug. Referred to as “the cure” for Alzheimer’s disease, the drug ends up significantly transforming the primate mind. Like most cure narratives in science fiction, the film speaks to Western culture’s preference for an idealized “wholeness” and imagines a scenario where only the most physically dominant and intellectually capable survive (represented by the technologically-enhanced chimpanzee, Caesar). As Elaine Graham writes in Representations of the Post/Human, however, it is essential that we interrogate such narratives of the future “ideal” body: “What is at stake, supremely, in the debate about the implications of digital, genetic, cybernetic and biomedical technologies is precisely what (and who) will define authoritative notions of normative, exemplary, desirable humanity into the twenty-first century” (11). As a way to distance itself from the overt racist politics of the original Planet of the Apes series, I argue that Rise of the Planet of the Apes instead emphasizes a normative humanity predicated on the erasure of the “undesirable” ill and disabled body.

Disability studies scholars Sharon Snyder and David Mitchell observe the tendency to frame the disabled body as “primitive throwback” to an earlier time in human development: “In a culture that endlessly reassures itself that it is on the verge of conquering Nature once and for all, along with its own ‘primitive’ instincts and the persistent domain of the have-nots, disability is referenced with respect to these idealized visions. As a vector of human variability, disabled bodies both represent a throwback to a human prehistory and serve as the barometer of a future without ‘deviancy’” (Cultural Locations of Disability 32). With its focus on “curing” Alzheimer’s disease and improving “natural” (but limited and “primitive”) cognitive abilities through medical testing on apes, along with a sustained focus on the animals’ institutionalization in “care” facilities, Wyatt’s film makes problematic ableist connections between primates and people with disabilities. Reading Rise of the Planet of the Apes with disability studies in mind, I want to address issues of agency, compassion, and the drive to “overcome” physical and cognitive differences. While there is a claimed desire to “cure” people, the lone female in the film, Caroline, nevertheless tells the (white, straight, able-bodied, and male) protagonist Will, “some things aren’t meant to be changed.” Where does this line of thinking—as well as the imagined apocalyptic consequences of creating “the (failed) cure”—situate people with disabilities both in the present and in the imagined future?


Published in Kathryn Allan's Blog
Tuesday, 17 December 2013 14:41

CFP: Digital Science Fiction

While I don't have time to submit an article for this special issue, given the wide range of media engagement with science fiction (and science fictional themes) these days, I certainly think it's worth sharing:


CFP: “Digital Science Fiction”

Science Fiction Studies special issue  

(Guest Editor: Paweł Frelik)

In the last few decades, digital technologies have dramatically reconfigured not only the circumstances of media production and dissemination, but also cultural genres and conventions expressed in them. Science fiction has not been immune to these changes, but their impact extends far beyond mere enhancement of sound or vision. In older media, such as science fiction film and television, special effects and non-linear editing have affected aesthetics as well as story-telling strategies and stories themselves. New sf media have emerged, too, most readily exemplified by video games.

While similar technologies have long been a thematic staple of sf, the actual arrival of digitality has proven somewhat problematic. Science fiction emerged as a predominantly narrative discourse and much of its cultural relevance has so far been ascribed to its capacity to address contemporary issues and anxieties through stories— but stories that are, ideally, plot- and psychology-driven, formally sophisticated, and conceptually complex. However, the centrality of traditionally-understood narrative in science fiction stands in direct opposition to the character of digital technology, which, as Andrew Darley noted, “endorses form over content, the ephemeral and superficial over permanence and depth, and the image itself over the image as referent.” This incompatibility has resulted in frequent denunciations of sf media forms that de-privilege narrative in favor of visuality or simulation.

Science Fiction Studies seeks articles for a special issue devoted to “Digital Science Fiction.” Both in-depth analyses of individual authors or texts and more general, theoretical discussions are invited. We are specifically interested in submissions focused on videogames and virtual environments; digital art, graphics, and illustration; electronic music; music videos; and apps, software, and cybertexts.

Areas of interest include but are not limited to:

  • critical and theoretical tools and approaches to digital science fiction;
  • digital technologies and their impact on definitions of science fiction;
  • digitality and sf’s thematic preoccupations – limitation, extension, revision?
  • visuality and simulation as new modes of meaning-creation;
  • the politics of digital science fiction;
  • digitality and the transformation of sf narrative;
  • materiality of digital technologies in science fiction;
  • digital transmedia texts.

Abstracts of 500 words should be submitted by 15 February 2014 to Paweł Frelik (<pawel[dot]frelik[at]umcs[dot]edu[dot]pl). Authors of selected abstracts will be notified by 1 March 2014. Full drafts (5,000 to 7,000 words) will be due by 31 August 2014. The issue is provisionally scheduled for November 2015.

Published in Kathryn Allan's Blog

I haven't been posting lately because I've been going back and forth between overwork and recovering from overwork. I really, really need to break this ridiculous cycle! Anyways, that's a topic for another post--this one comes courtesy of upcoming4.me, a great online magazine about speculative fiction. They invited me to write a guest post for their "story behind" column and this is what I wrote:

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When I left academia after the completion of my PhD in 2010, I wasn’t sure where I was headed. I did know, however, that my dissertation—Bleeding Chrome: Technology and the Vulnerable Body in Feminist Post-Cyberpunk [available for download in my "about me" box above]—was not the end of my research into the ways that technology and the body intersect in science fiction. I was proud of my thesis, but there were avenues of inquiry that I wish I had been able to follow. One of those underdeveloped approaches was reading science fiction with a disability studies framework in mind. I was acutely aware of how little published (academic) work there was on reading disability and the disabled body in science fiction. Given the vast number of characters with disabilities (plus all of the plot devices of idealized “cures,” transformative surgical interventions, genetic therapies, and fantastic prostheses) in the genre, I was having a hard time watching and reading anything science fiction(al) without critically interrogating the representations of disability I saw playing out time and again. Unable to let go of my academic interests, I decided to transform myself into an independent scholar and jump into the world of academic publishing.

My edited collection, Disability in Science Fiction: Representations of Technology as Cure, was a germ of an idea that finally took root during Renovation (the 2011 WorldCon). After receiving overwhelming positive support for the project from new friends and like-minded people, I returned home from the con and sent out a “call for papers” the very same week. By the end of the winter, I had 13 contributors preparing innovative and interdisciplinary readings of disability (with a focus on prostheses and the posthuman) in science fiction.

At this point in time, I should note, I had zero publications to my name. Dealing with chronic ill health and limited resources throughout my graduate career meant that I had no time or energy to pursue publishing opportunities while I was in academia. I wasn’t sure that anyone would want to publish an essay collection by a first time editor with no publishing track record. Nevertheless, I was determined to find the best press possible for Disability in Science Fiction because I believed in the value of the interdisciplinary critical analysis that it was presenting. After weighing distribution capability, promotional assistance, price point, and speed of the peer review process, Palgrave Macmillan was one of the first few publishing houses I approached. I sent my book proposal to them old-school style: I followed the directions for submissions listed on their website and, forking out the extra money for tracking and express post, mailed in my pitch. I was worried that some intern would simply shred my package on arrival, but my proposal was successful! Three weeks later the publishing house contacted me and told me they were interested in the collection (contract to be offered once the full draft was complete).

All in all, in took two years from conception to publishing the edited collection. The process of editing an academic essay collection is not a speedy one, but I think that my position as an independent scholar helped me move through the process faster than it otherwise might have gone. I selected essays that were on popular films and novels—such as George Lucas’ Star Wars, James Cameron’s Avatar, Daniel Keyes’s Flowers for Algernon, and Elizabeth Moon’s The Speed of Dark— and instructed everyone to write in accessible academic language, so that (non-academic) fans of science fiction interested in the topic would also be able to read and engage with the ideas in addressed in the collection. I kept in frequent contact with the book’s contributors, gave out a lot of direction and praise (the first is easy to come by in academia, the second…not so much), and went through several rounds of drafting. Each person who wrote a chapter for Disability in Science Fiction brought a unique perspective to the questions that I previously had been working through alone. Editing this book gave me the opportunity to collaborate with scholars from across the globe, and it is an experience for which I am grateful.

Throughout the two years I worked on this project, I received amazing feedback and advice from both the academic and fan communities of science fiction. It was that support that helped me write and edit through pain flares, injuries from overwork, and fatigue. Editing the essay collection taught me that it is possible to have a voice as an independent scholar and that there is a whole community of people out there who are as passionate about the same stuff as I am. Disability in Science Fiction is one piece of the on-going scholarship that brings together science fiction and disability studies. My hope has always been that the book brings greater critical attention to the all too often negative and damaging stereotypes of people with disabilities perpetuated by science fiction, a genre that, despite its flaws, I and so many others love and take comfort in.

Published in Kathryn Allan's Blog
Monday, 12 August 2013 17:21

Disability in Science Fiction: Cover Talk

My edited collection, Disability in Science Fiction: Representations of Technology as Cure, is available for sale August 14th (Google for your choice of internet bookseller)!

I received my author copies late last week and the book looks beautiful. I love the cover (thanks to Andrew Holden and Tom Pepper)--I think it perfectly reflects the critical analysis going on inside. When I was brainstorming ideas for the cover, I wanted an abstract image of a person being dissected, or broken down into their physical parts. The shearing away of the mid-section stands in for the ways in which the disabled body is often medicalized into its "problem" parts (instead being viewed as a functioning whole). I also wanted to express the impact of technology on the body--the "+" and "Ø" signs represent binary code (1s and 0s). And since there is an emphasis on prostheses in book, the arm in red both marks the simultaneous absence/addition of such technology to the body.

The image can be read in a number of interesting ways, relevant to both science fiction and disability. In the design, there is a sense of transcendence from the fleshy body that I didn't anticipate coming through. I like that the figure appears to continue off the left side--no arm is visible there but the person nevertheless feels complete. Overall, I think the cover nails the focus of the content of the collection.

I hope that people enjoy Disability in Science Fiction and decide to take up their own responses to the ways in which disability and people with disabilities are represented in science fiction (and fantasy, horror, romance, mystery, and all the other understudied genres). There is a lot of critical ground to cover, images to unpack, and new stories to be written. Disability in SF is only one piece of a larger, on-going conversation and I'm excited to be part of it!

Published in Kathryn Allan's Blog
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