Deafnormativity Who Belongs in Deaf Culture
Deafnormativity Who Belongs in Deaf Culture
Deafnormativity Who Belongs in Deaf Culture
S. J. Wright
To cite this article: S. J. Wright (2020): Deafnormativity: who belongs in deaf culture?, Disability &
Society, DOI: 10.1080/09687599.2020.1787818
Points of interest
Members of the Deaf-Blind communities are beginning to develop
their own culture which is separate from sighted Deaf culture and
operates under different norms.
Deaf-Blind communities reject the label of Deaf with a disability and
have begun to take ownership of not only the definition of culture,
but the modality in which they communicate.
A majority of Deaf-Blind individuals lose vision in early adulthood,
which means at some point, they were members of sighted Deaf cul-
ture and then become outcasts as a “disabled” body.
The research indicates that Deaf culture actually has an unspoken hier-
archy where power is concerned, an analysis that is not yet part of the
academic discourse, particularly where Deaf Critical Theory
is concerned.
This article explores how formerly sighted Deaf individuals in the Deep
South articulate the transition to becoming Deaf-Blind1 as a matter of being-
in-the-world. The context of the American Deep South includes states south
CONTACT S.J. Wright [email protected] Department of Deaf Studies and Deaf Education, Lamar
University, P.O. Box 10113, Beaumont, TX 77710, USA.
Rochester Institute of Technology, One Lomb Memorial Drive, Rochester, NY 14623.
ß 2020 Informa UK Limited, trading as Taylor & Francis Group
2 S. J. WRIGHT
became blind first and experienced hearing loss later, they may choose to
join the blind community and if one became deaf first then later blind, they
may choose to join the Deaf-Blind community due to linguistic ease
(Hoffman 2005). While a worthwhile observation, this is an encyclopedia
entry, and not a study of and about Deaf-Blind culture or identity. The con-
cept of Deaf-Blind culture seems to be elusive in the literature, except for a
newspaper article published over two decades ago by NAT-CENT News.
The NAT-CENT News in 1994, published an article that reported Deaf-Blind
culture did not exist in the same magnitude as Deaf culture. In fact, the art-
icle suggests Deaf-Blind culture cannot exist because it is derived from sen-
sory experiences, and is not cultural (Spear 1994). The significance of this
article is that it is published by Helen Keller National Center, which is widely
regarded to be an international source of expertise on matters and research
concerning deaf-blind people (Edwards 2014b; Shariff 2014). Spear also
asserts that the formation of a Deaf-Blind culture would be problematic due
to the low incidence and extreme geographic variety among those who are
deaf-blind, which would make the formation of such a culture virtu-
ally impossible.
The overall purpose of the literature review is to demonstrate a gap in
research where Deaf-Blind individuals are concerned, as ‘voice’ of Deaf-Blind
individuals is largely missing from academic discourse, where it exists in the
etic perspective, but has yet to offer a body of emic perspectives (Edwards
2012; Shariff 2014, Wright, 2017).
Method
Phenomenology is a philosophic method for questioning, not necessarily a
method for answering, discovering, or drawing resolute conclusions
(Heidegger 1962) and as such, is not used to make transferable generaliza-
tions. The thrust of phenomenology is to analyze how individuals experience
a phenomenon, what this experience is like, and most importantly—how do
individuals make meaning of being-in-the-world? (van Manen 2014). This
study does away from the traditional researcher-participant paradigm,
employing the Heideggerian approach of unbracketing in which the
researcher and participants become co-researchers.
Through unbracketing in tandem with the Hermeneutic Circle (Heidegger
1962), a researcher invites their participants to become co-researchers,
whereas validity is achieved through mutual meaning-making and circum-
spection. Heidegger explicitly refers to this approach as Zuhandenheit or
ready-to-hand (1962). In this approach, Heidegger uses a hammer to demon-
strate how a researcher in the phenomenological tradition achieves
Zuhandenheit. When confronted with a hammer, one can objectively observe
DISABILITY & SOCIETY 5
the hammer and make assumptions about its form, purpose, weight, and
sensation. However, one may also directly use and become one with the
hammer itself (ready-to-hand) and through the benefit of circumspection,
can offer a more organic, primordial account of the hammer’s form, purpose,
weight, and sensation. This study adopts a ready-to-hand approach in which
participants are co-researchers. Co-researchers, in this example are able to
use the ‘hammer’ in that our existence in the world as Deaf bodies are
shared experiences manifested through meaning-making by directly con-
fronting, grappling with, and sharing organic accounts of what it is like to be
Deaf. Other co-researchers use the ‘hammer’ to articulate the experiences of
transitioning to Deaf-Blind in which fellow co-researchers are invited to bask
in such presencing, through a shared understanding of ‘othering.’
Participants
Six participants; Olga, Emily, Anthony, Richard, Nathan, and Norman were
chosen for this study through a strategy referred to as intensity sampling.
Intensity sampling is an appropriate tool when the researcher wishes to
identify individuals or specific sites where the phenomena in question has
strong representation (Mertens 2010). This particular strategy requires know-
ledge on the researcher’s part as to determine which individuals meet spe-
cific criteria necessary for the study. Participants were recruited from specific
areas of the Deep South known to have a strong grassroots Deaf-
Blind community.
Participants were invited to attend an initial focus group, followed by
one-on-one individual interviews in private, and finalized with a debriefing
focus group. Although the original study encompasses varying data topics,
this particular article focuses on discussion within the final focus group as it
relates to identity and rejection from the sighted Deaf community. As the
purpose of phenomenological inquiry is to uncover what has previously
been concealed, meaning-making from shared lived experiences strive to
answer one central question: Who belongs in Deaf culture? Who is Deaf
enough? The following section offers a narrative rendition of the final focus
group meeting, in which co-researchers analyze collective narratives from
the previous focus group, as well as our individual narratives.
says, while Olga smiles and signs, ‘cool,’ her fingers wiggling out from
her chest.
‘That’s right. Deaf culture, community, and language are one thing. Blind cul-
ture and community, different—when put them together it’s not the same as
Deaf-Blind,’ Olga says to the group, in a much calmer tone. ‘And that’s the
same problem with Deaf-Plus, I’m seeing from everyone’s comments since the
first meeting,’ I inform the group, continuing: ‘to varying degrees, everyone in
the group believes the term is divisive and offensive.’ Richard raises his hand
and adds ‘Really, if you think about it—remember back in the day people at
school would call Deaf MR [mentally reded], those who were different or
have special needs,’ he speaks to those members of the group who are older
and would remember that time period. Richard continues: “I think Deaf-Plus is
the same thing—just looks more nice—same as with “special needs”, it’s more
PC language now.” I pause to consider the gravity of his recollection. Though
such phrasing is derogatory, it was developed by hearing professionals in the
field, and has been endorsed by Deaf professionals. The term ‘Vanilla Deaf’ sug-
gests that the ideal student is one that is White, uses American Sign Language
(ASL), possibly from a Deaf family, and has no dis/abilities. ‘Deaf Plus’ was also
created by hearing, abled professionals. However, the terms ‘Vanilla Deaf’ and
‘Deaf Plus’ are grounded in the idea that difference is undesirable. (Lawyer 2018
p. 64)
‘It’s almost like Deaf people who can see aren’t disabled but we are?’
Anthony asks the group. ‘Well, I certainly don’t believe I am disabled,’ Olga
states emphatically in response, turning to me she says: ‘You’re Deaf and
sighted, do you think you’re not disabled?’ I am slightly taken aback by the
abruptness of the question, yet I welcome it. “That’s interesting because part of
what I gleaned from this study is that the word “Deaf-Plus” certainly does seem
to suggest that a sighted Deaf person is not disabled,” I pause for a second,
adding that “Deaf culture doesn’t see Deaf people as disabled. I mean—con-
sider the phrase ‘Deaf students with disabilities.’ ‘What?’ Anthony scrunches up
his nose and eyebrows signing ‘What?’ repeatedly, his index and thumb tapping
together. ‘It is a phrase used in Deaf education,’ I begin to explain, while Emily
interjects, taking over: ‘That phrase is used similarly to Deaf-Plus, so if a Deaf
student is Deaf-Blind or in a wheelchair, or has autism, that’s how it’s phrased.’
‘But that makes no sense,’ Anthony replies, shocked.
‘I tend to agree that the business of labeling is really inaccurate. I want to
answer Olga’s question before we continue on that,’ I say, facing Olga.
‘That’s a tough question, but I’ll answer it honestly,’ I respond.
I don’t like the word ‘disabled’ to begin with. I don’t view myself as disabled, and I
think that disability is a myth, really. However, when I leave the house, sometimes I
encounter a clueless hearing person that does something awkward or rude, that
reminds me that I am Deaf. Or if I have to ask for accommodations like an
8 S. J. WRIGHT
Olga nods her head and says, ‘I think it’s the same for me—I’m not dis-
abled, but sometimes Deaf people make me feel disabled.’ To that end, I
pose the question to the group: how many of you feel that you fit into the
‘Deaf-plus’ label? Nobody raises their hands. After a short silence, Emily says
‘Well the Deaf part of me isn’t a disability but being blind is a disability
because it’s so limiting—I don’t know, it feels like other people make it into
a disability by how they treat us.’ ‘Who makes you feel disabled as the blind
part of you?’ I ask, wondering if the wording of such a question is appropri-
ate. ‘Well, mainly—people in the Deaf community,’ Emily answers, point
blank. ‘And what about hearing people?’ I ask. ‘I’m not concerned about
hearing people, we don’t interact with the hearing community much at all,
so it doesn’t bother me’ Emily responds. ‘I think it’s more Deaf than hearing
people,’ Anthony volunteers, ‘hearing people like VR (Vocational
Rehabilitation) and O&M (Orientation and Mobility) do that, it’s their job—so
it’s different. But the Deaf community does make me feel more of an out-
cast, and are afraid to communicate with me,’ Anthony finishes.
Inwardly, I wonder if the entire group feels the same way. ‘Does everyone
agree with Emily and Anthony’s comments?’ I ask. Richard shakes his head
from side to side, as if mentally wrestling with his answer. ‘Like I said before,
most people don’t see me as Deaf-Blind, because I don’t look like Anthony—
no offense,’ he adds quickly, nodding towards Anthony as he continues ‘but
now that I think about it, it doesn’t happen to me but I see it happen to
other Deaf-Blind a lot, so I agree.’ ‘I’m not offended,’ Anthony replies quickly,
adding: ‘you’re right—people see my glasses and my cane, and it’s obvious
which is why I get uncomfortable at Deaf events.’ I notice that Richard has
become more acknowledging of his privilege to ‘pass’ as Deaf, in light of our
one-on-one meeting when he was uncomfortable admitting this to
the group.
‘I agree, Deaf isn’t a disability—but my vision is really a disability because
it’s very limiting and isolating,’ Jason adds, seeming to struggle with express-
ing what he means to say. To clarify, I ask Jason whether he personally feels
that he is disabled, as himself at home, or when he steps out into a public
space that he feels disabled. Jason replies with the latter, while Norman joins
in Jason’s observation. With a majority feeling similarly on the topic, I look to
Olga for her input and ask: ‘Do you feel the same or different?’ ‘Growing up
in a Deaf family with a Deaf-Blind mother and brother, and now myself and
my children, I always thought this was very normal. We are people. Everyone
has different needs,’ she pauses, adding: ‘I really feel like it’s certain sighted
DISABILITY & SOCIETY 9
Deaf people that make me feel that way—just like Emily said, I don’t interact
with hearing people, so it doesn’t bother me.’
A group consensus on the topic has been reached at this point. As a
sighted Deaf person, I cannot help but wonder in the process of analysis just
how a sighted Deaf hegemony can justify that the state of being Deaf is not
a disability yet, Deaf people with ‘other’ physical conditions are labeled as
such. In recognizing my own sighted privilege, I recognize that I am part of
the institution that is in ‘the business of labeling’ on more than one front.
On the one hand, the sighted Deaf hegemony labels Deaf-Blind individuals
in the Deep South as Deaf-Blind, a hyphenated word that shares the same
oppressive dynamic of Deaf-Plus, another hyphenated word.
What is deafnormative?
The group had reached a consensus that a Deaf-Blind body is differentiated
from a sighted Deaf body through three methods: 1) stigma, 2), labeling,
and 3) creating a hybridization, which serves as a platform for what we call
Deafnormativity.
For the group, our quests begin at varying times on two levels: to find a
veritable home for our ‘otherness’ and to repeat this quest for a different
reason when the body manifests itself as different, and is automatically
sorted and labeled as yet another ‘other.’
With a trove of narratives from the group that is rich in timbre, dynamic
as the magnitude of human emotions, and as varied as the topography of
each person’s collective being, we relate the themes of these experiences
succinctly. The common thread that binds the group together is a quest for
belonging at the hands of being an outcast from what once was. Through
the process of systematic oppression in the mediums of stigma, labeling,
and hybridization the concept of Deafnormativity takes hold; becoming a
concrete experience that is common to this group.
The stigmatization of the Deaf-Blind body has been expressed by co-
researchers through themes of the fear of physical contact through Tactile
American Sign Language, the fear of association resulting in the loss of
friends and family, loss of independence—particularly driving—as the marker
of a burdensome being, and the Deaf-Blind body as the visual representation
of sighted Deaf individual’s worst fears. This stigma gives rise to newfound
boundaries that have been described as a veil-like separation between Deaf
and Deaf-Blind communities. The stigma of being an other is mitigated by
‘how Deaf-sighted’ one can pass for—such as Richard—who can seamlessly
pass through both sides of the veil, while others who are ‘markedly’ Deaf-
Blind are cast out of the Deaf community.
10 S. J. WRIGHT
With ‘otherness’ comes ‘the business of labeling things’ which has been
expressed as Deaf-Plus, Deaf with disabilities, and even in the terms Deaf-Blind
vs. DeafBlind. ‘The sign itself is not even accurate!’ Olga observes during my
summary as if to bolster the point. ‘What do you mean?’ I ask casually. Olga
repeats the sign slowly to dissect it, beginning with Deaf: ‘See? That is the sign
for Deaf—Deaf people, Deaf culture’ she continues with the sign for Blind stat-
ing, ‘See? That is the sign for Blind. Blind people, Blind culture. Remember we
just discussed that?’ I never thought of this and realize immediately that she
has a very valid and worthwhile point. ‘Exactly—like some of my friends in
Seattle don’t sign that. They just spell DB, and I use it in my email and texts all
the time’ Anthony joins in. This observation, which further buttresses how label-
ing problematizes the Deaf-Blind body and in effect, minimizes the meaning of
the DeafBlind experience as being worthy of unequivocal attention, independ-
ence and validation similar to the ProTactile movement.
The business of labeling the other through Deaf-Blind in both textual and
ASL representations as mash-ups of two unrelated communities lends itself
to the problem of hybridization. According to Merriam-Webster (2017),
Hybridization is generally defined as ‘a person or a group of persons pro-
duced by the interaction or crossbreeding of two unlike cultures, traditions,
etc.’. In other words, the dominant Deaf, sighted hegemony has created a
‘half-breed’ in a manner that overwhelmingly suggests that the Deaf-Blind
experience does not belong in the shared space of the Deaf experience,
effectively relegated to lesser. Based on these categories formed from collect-
ive meaning-making experiences, the group moves to construct a graphical
representation of how the business of labeling sorts and categorizes each of
us, from which the working definition of Deafnormativity was born.
Defining deafnormativity
It is then I lay out a succinct working definition to the group based on our col-
lective narratives and experiences. I decide to begin with an informal hierarchy to
see if my co-researchers agree with how I have arranged our categories/labels.
Me: I see this as a “hierarchy” which places Deaf of Deaf at the top, or as some of
you refer to them as “the Deaf Elite.” This includes people who are Deaf, born to
Deaf parents, use ASL as their native language and probably attended a residential
school for the Deaf, or a similar day program for Deaf students. Below, are Deaf
people born to hearing families who have ASL as a native language, followed
below by Deaf people born to hearing families that learn ASL later in life.
Anthony: Like you, right?
Me: I’m not sure yet, we’ll find out soon, I guess? (I laugh) And … this is followed
by Late Deafened Adults and hard of hearing individuals I think their acceptance
level depends on how fluently they sign, if at all. Deaf-Blind, seems like is at the
bottom of this hierarchy.
DISABILITY & SOCIETY 11
Olga: Or even off the chart, it’s not in the same world.
Emily: That’s true—you know what, it makes sense. I never thought about it in this
way, seeing it formally discussed as a list or … hierarchy. It’s almost disgusting but
it’s right.
Discussion
This study presents a standpoint theory (Stoetzler and Yuval-Davis 2002) of
six Deaf-Blind participants and the author as co-researchers that make mean-
ing of being-in-the-world as it relates to belonging and unbelonging in the
Deaf community. The resulting articulation of the transition from Deaf to
Deaf-blind as is understood through the phenomenological views of lived
space, lived time, and being in the world ultimately transcends the con-
straints of disability and labels. The notion of Deafnormativity is explored,
born as a product of a common discovery among both Deaf-Blind and
sighted Deaf co-researchers that there is such a thing as a socially
12 S. J. WRIGHT
constructed ‘blueprint’ way of being Deaf. Sighted, Deaf people born to Deaf
parents, having ASL as a native language takes its place as the normate
within Deaf culture. As such, those who do not fit this description fall to the
wayside, under a hierarchy that excludes Deaf-Blind, and d/Deaf individuals
born to hearing families. The irony in this shared discovery is the fact that a
majority of participants in this study prior to transition were members of the
‘Deaf Elite’ at birth. As such, we recognize that each of us are collectively
affected by the notion of Deafnormativity.
First, it is necessary to briefly examine what causes a binary and further,
what causes one group to be regarded as inferior, or ‘less than.’ For the LGBT
community, we are oppressed by the blueprint of heteronormativity, which dic-
tates the ‘correct’ way to exhibit and engage in one’s life in relation to all of
society. Heteronormativity was coined in 1991 by the social critic Michael
Warner, and has since become a mainstay in critical studies to denote the invis-
ible norms of heterosexuality as a dominant hegemony. The term refers to the
belief and practice of opposite sex romantic partners, a clear division between
male and female functions (gender roles) and adhering to the belief that one’s
traits follow in direct relation to anatomy (Warner 1991). Deviance from these
beliefs such as having same-sex romantic partners, exercising fluidity in gender
roles, and transitioning one’s biological sex whether through medical interven-
tion or without are seen as inferior, and therefore stigmatized. This stigmatiza-
tion, at least in the United States has resulted in overt and covert discrimination
against LGBTQ individuals (Goldstein and Davis 2010).
Recall that the ProTactile movement of Seattle has begun a grassroots
effort of breaking away from the constraints of ‘Deaf-Blindness’ that has
been placed upon them by normative sighted communities. This is arguably
among the first sources of grey literature by DeafBlind individuals that points
to a grassroots movement in which DeafBlind individuals are fighting to lib-
erate the community from oppression by sighted Deaf people (Nuccio and
Granada 2013). ProTactile, aside from delineating methods of communication
that seek to reject the need for sighted intervention also rejects communica-
tion methods of haptics, back channeling, and touch signals, as they are con-
sidered ‘rehabilitative’ efforts invented by sighted people (Nuccio and
Granada 2013). Members of the movement seek to reject the label of Deaf-
Plus and instead delineate DeafBlind identity, culture, and politics as distinct,
while severing the greyscale backbone of culture shared by the Deaf and
DeafBlind communities (Nuccio and Granada 2013). Finally, the ProTactile
movement views ProTactile American Sign Language (PTASL) as a language,
echoing the parallel struggle of legitimacy as was the case for ASL, which
was legitimized by Stokoe in the 70’s (Stokoe 1978). In essence, Tactile ASL
(TASL) was once considered to be an accommodation of Visual American
Sign Language (VASL) and therefore, a ‘shared’ language with VASL. As TASL
DISABILITY & SOCIETY 13
favoritism goes on—like you know those powerful fraternities. And same as her
(Olga), it’s even harder if you lose your vision too.
Me: Oh, I agree. As I was born into a hearing family too—and also grew up oral—
learning ASL and going to College was overall, a great experience. But there are
“those people” like you both said that really make it hard.
The hierarchy extends to late deafened adults as the lowest level theoret-
ically but casts out those who are considered Deaf with a disability (Wright,
2017). The term Deaf Plus problematizes disability in terms of which disabil-
ities are acceptable and which are considered deviant and undesirable. To
iterate, a Deaf student with a disability is defined as a ‘deaf or hard of hear-
ing student with any of the 13 disabilities identified in the IDEA,’ or as it is
referred to in the familiar, Deaf plus (Lane 2002; Wright, 2016). In other
words, the Deaf community resists the label of disability (Lane 2002) while
choosing what disabilities differentiate a Deaf person from being simply Deaf
or relegated to a binary, second class culture membership as Deaf Plus. This
divisive rhetoric is evidenced through sentiments of participants, most not-
ably Olga, who is outspoken about the term Deaf Plus:
Deaf Plus? That’s insulting. I can understand if it applies to perhaps deaf people
who are mentally reta, or maybe MLS [Minimal Language Skills] … but to
lump Deaf-Blind people into that category is hateful. Deaf-Blind is a culture, it’s a
way of being, it’s … (pause) everything we are, and there is nothing wrong with
me. So that means for 21 years I’m Deaf and don’t have a disability, then all the
sudden because I have ONA (Optic Nerve Atrophy), and identify as Deaf-Blind, that
means now I have a disability? But deaf people aren’t disabled? It’s messed up.
in between space in which sighted Deaf individuals apply the label of dis-
ability within our own spaces. Lastly, Corker calls for a method of discourse
that relies upon these unstated absences.
Deafnormativity attempts reconcile unavoidable parallels from CDS, Queer,
and Crip Theory in order to promulgate the move away from the panopticon
of DeafCrit to reflect agency and ownership of multiple epistemologies.
Sherry (2004) asserts that Queer Theory and Disability studies are not neces-
sarily distinct fields, but alike in that they problematize deviance, stigma, and
the construction of identities. For example, living in a homophobic society
under the ubiquitous eye of heteronormativity can be traumatizing which
leads to internalized oppression, among other psychological scars. Sherry
also argues that the experiences of passing and coming out are prevalent in
both Queer Theory and CDS. In the same vein, Deafnormativity is essentially
a product of the internalized oppression of sighted Deaf people which cre-
ates the trauma of passing—most notably by the attempt to drive a motor
vehicle and pass as ‘sighted’ as reported by co-researchers. Particularly,
Sherry (2004; 2002) makes the case that exclusion among in-groups are par-
ticularly problematic for Queer and disabled individuals, which supports the
concept of Deafnormativity as straddling the experiences outlined in Queer
Theory and CDS as DeafBlind individuals share a greyscale backbone vis-a-vis
a shared culture and language, but become excluded in between spaces
where identity changes from a disabling condition. I agree with Sherry’s
assessment that there is a need for cross-fertilization of ideas among disci-
plines as is evidenced by the prism of experiences of DeafBlind individuals
that formulate the concept of Deafnormativity.
McRuer (2010) connects these points saliently through his contextualiza-
tion of compulsory able-bodiedness through an understanding of compul-
sory heterosexuality, arguing that able-bodied identity is more normalized
than heterosexuality in a system where there is no choice. Interestingly,
McRuer discusses the desirability of able-bodiedness and poses the question:
‘Yes, but in the end wouldn’t you rather be more like me?’ (p.93), going on
to demonstrate through the use of Butler’s (2005) theories of gender per-
formativity that able-bodiedness is a compulsive system and simultaneously,
a comic parody. The concept of able-bodiedness is not in a state of crisis, as
it succeeds whereas disabled people are seen as queer, and queer people
are often seen as disabled.
Further, McRuer (2010) posits that the concept of severely disabled as a
tradition of queer history similar to the concept of the fabulous could be
used to spotlight the most marginalized, most disabled voices of the com-
munity in order to reverse the inadequacies of compulsory able-bodiedness
not unlike the Deaf community’s shuttering of Gallaudet University in protest
for a Deaf President. The most marginalized members of the Deaf
DISABILITY & SOCIETY 17
veritable ‘looking glass’ for a particular theorem and allows members to vis-
cerally analyze the flaws of our being, the gaps in our inclusivity, or the sali-
ent points of exclusivity—all while expanding the consciousness and
reflective worth of critical merit. Deafnormativity serves as a sort of ‘looking
glass’ for DeafCrit—a young theorem that is still in its infancy. Though the
development of Deafnormativity, co-researchers answered the question ‘Who
belongs in Deaf Culture?’
Note
1. The term Deaf-Blind is used as such in the Deep South of the United States where
this study occurred. The general use of the term is DeafBlind and is used as such in
this article when referring to DeafBlind culture as a whole (Wright 2017).
Disclosure statement
No potential conflict of interest was reported by the author(s).
References
Butler, J. 2005. “Gender Trouble: Feminism and the Subversion of Identity GT.” Political
Theory 4: 4–24.
Corker, M. 1999. “Differences, Conflations, and Foundations: The Limits to ‘Accurate’
Theoretical Representation of Disabled People’s Experience?” Disability & Society 14 (5):
627–642. doi:10.1080/09687599925984.
Edwards, T. 2012. “Sensing the Rhythms of Everyday Life: Temporal Integration and Tactile
Translation in the Seattle Deaf-Blind Community.” Language in Society 41 (1): 29–71.
https://doi.org.10.1017/S004740451100090X
Edwards, T. 2014a. “From Compensation to Integration: Effects of the Pro-Tactile
Movement on the Sublexical Structure of Tactile American Sign Language.” Journal of
Pragmatics 69: 22–24. doi:10.1016/j.pragma.2014.05.005.
Edwards, T. 2014b. “Language Emergence in the Seattle DeafBlind Community.” Doctoral
diss., ProQuest Dissertations and Theses (Order No. 3686264).
Englander, M. 2012. “The Interview: Data Collection in Descriptive Phenomenological
Human Scientific Research.” Journal of Phenomenological Psychology 43 (1): 13–35.
https://doi.org.10.1163/156916212X632943
Gertz, G. 2008. “Dysconcious Audism: A Theoretical Proposition.” In Open Your Eyes: deaf
Studies Talking, edited by H.D. Bauman, 219–234. Minneapolis, MN: University of
Minnesota Press.
Goldstein, S. B., and D. S. Davis. 2010. “Heterosexual Allies: A Descriptive Profile.” Equity &
Excellence in Education 43 (4): 478–494. https://doi.org.10.1080/10665684.2010.505464
Heidegger, M. 1962. Being and Time. Translated by J. Macquarrie & E. Robinson. New York,
NY: Harper & Row.
Hoffman, I. 2005. “Deafblindness.” In Encyclopedia of Disability, edited by G. L. Albrecht.
Thousand Oaks, CA: Sage.
DISABILITY & SOCIETY 19
Karchmer, M., and R. Mitchell. 2004. “Chasing the Mythical Ten Percent: Parental Hearing
Status of Deaf and Hard of Hearing Students in the United States.” Sign Language
Studies 4 (2): 138–163. https://doi.org.10.1353/sls.2004.0005 doi:10.1353/sls.2004.0005.
Ladd, P. 2003. Understanding Deaf Culture: In Search of Deafhood. Clevedon, England:
Multilingual Matters.
Lane, H. 2002. “Do Deaf People Have a Disability?” Sign Language Studies 2 (4): 356–379.
doi:10.1353/sls.2002.0019.
Lawyer, G. 2018. “Removing the Colonizer’s Coat in Deaf Education: Exploring the
Curriculum of Colonization and the Field of Deaf Education.” Doctoral diss., ProQuest
Dissertations and Theses.
Mertens, D. 2010. “Transformative Mixed Methods Research.” Qualitative Inquiry 16 (6):
469–474. https://doi.org.10.1177/1077800410364612
McRuer, R. 2010. “Compulsory Able-Bodiedness and Queer/Disabled Existence.” The
Disability Studies Reader 3: 383–392.
Merriam-Webster. 2017. Definition of Hybridize. https://www.merriam-webster.com/dic-
tionary/hybridize. Accessed on January 2, 2017.
Nuccio, J., and A. Granada. 2013. Welcome to Pro-Tactile: the DeafBlind Way [Video file].
Februrary 14. https://www.youtube.com/watch?v=l11lahuiHLA. Accessed on February
14, 2013.
Shariff, R. 2014. “Leaders Who Are Deafblind: A Phenomenological Study of Educational
Experiences.” Doctoral diss., ProQuest Dissertations and Theses (Order No. 3663048).
Sherry, M. 2002. “Welfare Reform and Disability Policy in Australia.” Just Policy: A Journal
of Australian Social Policy 11 (28): 3.
Sherry, M. 2004. “Overlaps and Contradictions between Queer Theory and Disability Studies.”
Disability & Society 19 (7): 769–783. https://doi.org10.180/0968759042000284231.
Smith, T. 2002. Guidelines: Practical Tips for Working and Socializing with Deaf-Blind People.
Burtonsville, MD: Sign Media Incorporated.
Spear, K. 1994. “Is There a Deaf-Blind Culture?” Nat-Cent News 25 (1): 12–20.
Stokoe, W. 1978. Sign Language Structure. Silver Spring, MD: Linstok Press.
Stoetzler, M., and N. Yuval-Davis. 2002. “Standpoint Theory, Situated Knowledge and the
Situated Imagination.” Feminist Theory 3 (3): 315–333. doi:10.1177/
146470002762492024.
Solomon, A. 2012. Far from the Tree: Parents, Children, and the Search for Identity. Scribner:
New York.
van Manen, M. 2014. Phenomenology of Practice: Meaning-Giving Methods in
Phenomenological Research and Writing. Walnut Creek, CA: Left Coast Press.
Vehmas, S., and N. Watson. 2014. “Moral Wrongs, Disadvantages, and Disability: A Critique
of Critical Disability Studies.” Disability & Society 29 (4): 638–650. doi:10.1080/09687599.
2013.831751.
Vehmas, S., and N. Watson. 2016. “Exploring Normativity in Disability Studies.” Disability &
Society 31 (1): 1–16. doi:10.1080/09687599.2015.1120657.
Warner, M. 1991. “Introduction.” In Fear of a Queer Planet: Queer Politics and Social Theory,
edited by M. Warner, vii–xxxi. Minneapolis: University of Minnesota Press
Wright, S. J. 2016. “Diversity: Deaf Studies and Disability.” In The Sage Deaf Studies
Encyclopedia, edited by G. Gertz & P. Boudreault, 305–309. New York, NY: Sage
Publications.
Wright, S. J. 2017. “From Deaf to Deaf-Blind a Phenomenological Study of the Lived
Experiences of Deaf-Blind Individuals in the Deep South.” Doctoral diss., ProQuest
Dissertations and Theses (Order No. 10654904).