|
|
Stigma
without Impairment: Broadening the Scope of Disability Discrimination
Law
David Wasserman
During oral argument in
Murphy v. U.P.S., a case in
which the Supreme Court was asked to decide whether the Americans with
Disabilities Act covers individuals whose impairments are mitigated by
corrective devices or medication, Justice Antonin Scalia removed his
glasses and waved them in the air. He was making the point that if
mitigation were ignored, he, along with millions of other Americans,
would be swept into the category of “disabled,” swelling its ranks
far beyond the 43 million recognized by Congress when it adopted the
statute a decade ago.
Scalia’s gesture
nicely evokes a broader dispute about the scope of the ADA: between
those who see it as protecting “a discrete and insular minority,”
comprising the relatively small proportion of the population marked by
their functional limitations, material privation, and social exclusion,
and those who see the statute as applying to a broad and loosely bounded
range of people stigmatized by physical and mental differences. The
former believe that a narrow definition of disability is critical for
preserving the moral urgency and popular support of the ADA; the latter
fear that restricting the ADA to severe disability excludes many who are
also subject to invidious discrimination.
The narrower view of
the ADA prevailed in Murphy
and in a related case, Sutton v.
United Airlines, where the Court held that “disability” does not
include impairments that are substantially limiting only in the absence
of corrective devices or medication. For a majority of the Court, people
who can achieve normal functioning simply by putting on glasses or
taking a pill do not belong to the highly vulnerable and disadvantaged
group the ADA was intended to protect. As Justice Ruth Bader Ginsberg
observed in her concurrence, “Persons whose uncorrected eyesight is
poor, or who rely on daily medication for their well-being, can be found
in every social and economic class; they do not cluster among the
politically powerless, nor do they coalesce as historical victims of
discrimination.”
Justice Stevens, in
dissent, did not deny Ginsberg’s claim that people with correctable
impairments are generally less vulnerable and disadvantaged than those
with severe disabilities. Nonetheless, he argued that this difference
provides no reason to deny them protection from discrimination:
When
faced with classes of individuals or types of discrimination that fall
outside the core prohibitions of antidiscrimination statutes, we have
consistently construed those statutes to include comparable evils beyond
Congress’ immediate concern in passing the legislation. Congress, for
instance, focused almost entirely on the problem of discrimination
against African-Americans when it enacted Title VII of the Civil Rights
Act of 1964....But that narrow focus could not possibly justify a
construction of the statute that excluded Hispanic-Americans or
Asian-Americans from its protections—or as we later decided ...,
Caucasians.
It may, however, be
more difficult in the case of disability than race to decide what
classes of individuals face evils comparable to those addressed by the
statute’s “core prohibitions.” Construing the 1964 Civil Rights
Act to include Hispanic-Americans, Asian-Americans, or Caucasians
appears (at least in retrospect) straightforward, because it is clear
that people of any racial, ethnic, or national-origin group can be
treated as moral inferiors by virtue of their membership in that group.
In contrast, the justices in Sutton
disagreed about whether discrimination against individuals with minor
and correctable impairments was an evil comparable to discrimination
against individuals with more severe, less tractable impairments. For
the majority it was not, because the former, unlike the latter, are not
a discrete and insular minority, left poor and powerless by a long
history of exclusion and neglect. Because of this difference, the
majority held an employer was “free to decide that physical
characteristics or medical conditions that do not rise to the level of
an impairment—such as one’s height, build, or singing voice—are
preferable to others, just as it is free to decide that some limiting,
but not substantially limiting
impairments make individuals less than ideally suited for a job.” The
dissent, however, saw in such preferences precisely the kind of “stereotypic
assumptions” about competence that confront people with more severe
impairments and that the ADA was intended to overcome.
Before Sutton
and Murphy, several commentators had argued that the ADA should cover a
variety of conditions less limiting than paradigm cases of disability.
Not only should correctable impairments be included, but also
impairments that are substantially limiting only in a narrow range of
activity, such as a specialized kind of work, or that are substantially
limiting only by virtue of the discriminatory response they elicit, such
as the denial of a job or service. And at least one commentator took the
argument a step further, proposing the outright elimination of the “substantial
limitation” requirement. If, as Justice Stevens argued in his Sutton
dissent, “the purpose of the ADA is to dismantle ...barriers based on
society’s accumulated myths and fears,” it should protect all people
with impairments, since those myths and fears are not confined to
impairments that are, or are perceived to be, substantially limiting.
After Sutton
and Murphy, these arguments for enlarging the scope of the ADA can no
longer be made within the confines of the existing statute. Whether or
not they were correct as statutory interpretation, I believe they are
correct in articulating what the central purpose of the ADA should be: to challenge discrimination based on physical or mental
difference, not to protect a vulnerable class of people bearing the most salient or substantial differences.
By the same token,
however, I believe that these arguments require a more extensive
revision of the ADA than their proponents acknowledge. The reasons for
extending the protection of the ADA to persons whose impairments are not
“substantially limiting” also justify extending these protections to
persons with atypical physical or mental conditions that are not (or are
not regarded as) impairments at all. A revised statute, I shall argue,
should protect anyone with a disfavored physical or mental variation: It
should apply to those who are overweight but not morbidly obese, short
but not achondroplastic, unattractive but not disfigured, and “dull-witted”
but not mentally retarded.
The expansion of the
ADA to include all disfavored physical and mental variations would treat
people with index impairments and substantial limitations not as a
discrete and insular minority, but as some of the most salient and
aggrieved victims of prejudice and stereotyping that adversely affect
most Americans at some point in their lives. In extending protection to
people with minor impairments and “normal” deficiencies, the statute
would not assume that the discrimination they face is as severe as that
faced by people with substantially limiting impairments, but merely that
it is a “comparable evil.” Perhaps the class protected by this
extended statute should no longer be referred to as “Americans with
Disabilities,” reserving the term “disability” for those who have,
or are regarded as having, functionally significant impairments. Then
again, retaining the name would be a useful reminder that people with
normal structural and functional imperfections can be “disabled” by
aversion, contempt, and stereotyping. I am less concerned with the
statute’s name than with its scope.
This further extension
of the ADA would doubtless be opposed by many who favor the liberal
interpretation or outright elimination of the “substantial limitation”
requirement. Justice Stevens himself, in arguing for the inclusion of
mitigated impairments, made it clear that he did not “mean to suggest,
of course, that the ADA should be read to prohibit discrimination on the
basis of, say, blue eyes, deformed fingernails, or heights of less than
six feet. Those conditions, to the extent that they are even ’impairments,’
do not substantially limit individuals . . . and
thus are different in kind from the [substantial but mitigated]
impairment in the case before us.” My first task, then, is to show
that a variety of minor imperfections, from short stature to slight
deformities, are not necessarily “different in kind” from
substantially limiting impairments, and that the discrimination faced by
people with these conditions is sufficiently similar to that faced by
people with major impairments and substantial limitations to be covered
by the same statute.
The Experience of
Stigma
The similarity between
discrimination for minor imperfections and major impairments seems
fairly obvious in the case of some deficiencies, like obesity and
extreme homeliness. Consider the case of Deborah Birdwell, as described
by Ruth Colker, an opponent of narrow eligibility requirements in
antidiscrimination law.
Birdwell
is obese and had wanted to see a movie with her niece. Knowing that she
could not fit into a movie theater seat, she called ahead to ask if she
could bring her own chair and use it in the wheelchair section. She was
told that she could. But when she went to the theater with her chair,
she was rudely informed that she would not be able to use it.
Clearly, Birdwell was
discriminated against on the basis of a disfavored physical difference;
it is unlikely that someone who needed extra space because he was seven
feet tall would have met with such a rude response. Fat people, unlike
tall people (at least tall men), are stigmatized. And this is true whether
or not they are impaired, or substantially impaired, under the
definitions laid down in the ADA. Indeed, discrimination against fat
people often involves an implicit contrast between their conditions and
“true disabilities.” Fat people do not receive the accommodation
accorded to wheelchair users because their inconvenience is seen as
transient and voluntary, resulting from their (presumed) gluttony and
self-indulgence. The myths and stereotypes they face are arguably no
less invidious than those faced by people in wheelchairs. The challenge
for disability discrimination law is to recognize how far beyond the
impairment category such stigmatization extends.
Erving Goffman, who
introduced the term “stigma” into the discourse of modern social
science, maintained that a person is stigmatized by “his possessing an
attribute that makes him different from others ... and of a less
desirable kind.” This attribute can be a physical deformity, character
flaw, or membership in a particular racial, ethnic, national, or
religious group. Although he recognized the pervasive effects of stigma
on routine social interaction, Goffman declined to restrict the notion
to “those who possess a flaw that uneases almost all their social
situations.” Rather, he regarded stigmatization as a threat to almost
all people some of the time: “The most fortunate of normals is likely
to have his half-hidden failing, and for every hidden failing there is a
social occasion for which it will loom large....Therefore, the
occasionally precarious and constantly precarious form a single
continuum.” For Goffman, this continuity reflects the nature of the
prevailing norms:
While
some of these norms, such as sightedness and literacy, may be commonly
sustained with complete adequacy by most persons in the society, there
are other norms, such as those associated with physical comeliness,
which take the form of ideals and constitute standards against which
almost everyone falls short at some stage in his life. And even where
widely attained norms are involved, their multiplicity has the effect of
disqualifying many persons. For example, in an important sense there is
only one completely unblushing male in America: a young, married, white,
urban, northern, heterosexual Protestant father of college education,
fully employed, of good complexion, weight, and height, and a recent
record in sports....Any male who fails to qualify in any of these ways
is likely to view himself—during moments at least—as unworthy,
incomplete, and inferior.
On this view, stigma is
not the defining characteristic of a discrete and insular minority, but
a universal condition. The breadth and elasticity of the process of
stigmatization make it morally arbitrary to single out some physical and
mental differences for legal protection.
Now, it may be that in
emphasizing the “precariousness” of the normal, Goffman understated
the disparity in social attitudes toward the normal deviant and the
significantly impaired. There may well be differences, in kind as well
as degree, in attitudes towards different kinds of deviance—differences
which, for some purposes, eclipse the underlying commonalities that
Goffman found. Those deviating from an ideal “which almost everyone
falls short of at some stage in his life” may be stigmatized far less
severely or pervasively than those displaying a rare and conspicuous
physical or mental abnormality. The stigma associated with striking
cosmetic anomalies, serious limb deformities and neuromuscular
disorders, profound retardation, and the impairment of multiple senses
may be distinct from, and worse than, any stigma associated with
physical and mental variations not regarded as impairments.
Not all substantially
limiting impairments, however, are severely stigmatized. The impairments
covered by the ADA elicit a broad range of social responses, from the
intense aversion and anxiety provoked by leprosy, epilepsy, AIDS, and
schizophrenia to the constricting solicitude and overprotectiveness
triggered by cardiovascular and lower-back problems. The ADA recognizes
that even the more “benign” responses to impairment, involving the
exaggeration of frailty and dysfunction, contribute to the exclusion and
devaluation of the people who have those impairments. At the same time,
many physical and mental differences not classified as impairments
elicit contemptuous, dismissive, patronizing, or oversolicitous
responses that can be equally handicapping. People with normal
imperfections are often relegated to inferior roles and places, if not
excluded outright, by false assumptions about their suitability for
various jobs or activities. A large body of research, for example, finds
that people perceived as unattractive are also regarded as less
competent and intelligent.
There may, though, be a
more general reservation about eliminating the impairment requirement in
disability discrimination law. Although that requirement may exclude
some highly stigmatized people and conditions, it lays down a reasonably
clear boundary for the protected class. If we cannot restrict the class
in that way, how can we restrict it at all? How do we decide whether a
person falls sufficiently below a standard “against which almost
everyone falls short” to be “truly stigmatized”? How unattractive
must he be to be stigmatized as ugly, how overweight to be stigmatized
as fat, how uncoordinated or ill-proportioned to be stigmatized as
ungainly? It would be difficult to draw, let alone justify, any line on
the continuum from the occasionally to the constantly precarious. But
without such a line, we are left with a statute protecting us all from
unwarranted and exaggerated responses to our minor imperfections. The
defender of an impairment requirement would argue that such a statute
would indeed trivialize disability discrimination, because
discrimination on the basis of minor imperfections is far more benign
than discrimination on the basis of impairments—it is simply not a
comparable evil.
I think this concern
has some force, but much less than may initially appear. There is no
reason to assume that the contempt and devaluation that most people face
at some point in their lives will be significantly more benign than the
contempt and devaluation that a few people face throughout their lives.
Our attitudes toward older people—consistently found to be among the
most stigmatized individuals in our society—should suggest that we are
quite capable of despising what we are, or are likely to become. Leslie
Fiedler has argued that the “cults of slimness and eternal youth”
are profoundly demeaning and oppressive to the vast majority of
Americans. Even if we are not quite as suffused with self-loathing as
Fiedler imagines, a preference for the young and beautiful can be unfair
and cruel, denying older and less attractive people meaningful work and
rewarding social experience. Moreover, a preference for the young and
beautiful may reinforce, or evolve into, an aversion to the old and
ugly. For these reasons, the law would not trivialize its condemnation
of discrimination against the constantly precarious by banning
discrimination against the occasionally precarious as well.
Distributive
Implications
A distinct concern
about extending the ADA to people without substantially limiting
impairments is that any such change would have perverse distributive
effects, limiting the resources available for those who most need the
statute’s protection. Shortly after the Sutton
decision was handed down, a quadriplegic man wrote in a letter to the New
York Times, “the effect of diluting the definition of disability
by including nearly half of the population would ultimately have hurt
those who need accommodation the most.” For instance, the statutory
exception holding that accommodation needn’t be provided if it imposes
“undue hardship” may be more frequently available if the class of
people who can claim accommodation is expanded. Because there are limits
on the costs an employer or provider will be required to bear, it may be
more appropriate to impose costs for the benefit of those who, as a
result of the social consequences of severe impairment, are among the
worst-off members of society.
To the extent that
these concerns about scarce resources for accommodation are realistic,
however, they will be raised by any statute that, like the present ADA,
covers individuals who vary widely in the severity of their impairments
and the magnitude of their disadvantage. If the burdens of accommodation
accumulate, it is possible that employers and facilities will find
themselves exempted under any such statute from accommodating more
severely impaired individuals because they have already accommodated
less severely impaired ones.
But in fact, there are
several reasons for doubting that the proposed expansion of the ADA
would significantly increase either the frequency or the cost of
accommodation. First, the barriers faced by people with many normal
deficiencies, such as unattractiveness and short stature, will be
predominantly attitudinal rather than structural. People with slightly
deviant shapes and sizes do face some structural inconveniences, e.g.,
in reaching switches and ordering clothes, but the more substantial
barriers they face arise without structural mediation, from the
attitudes and assumptions of other people. Further, the site
improvements that people with normal deficiencies may require, such as
lower electrical switches, will for the most part already have been
mandated for people with substantially limiting impairments. Finally,
any individual accommodations that might be required, such as an
adjustable chair or a more flexible work schedule, would probably be
less expensive on average than the individual accommodations required
for people with index impairments.
Still, the cost of
accommodating an individual will not always be proportionate to the
magnitude of his physical or mental differences, and the accommodation
of people with normal deficiencies or minor impairments will sometimes
limit the resources that are available for accommodating people with
more severe impairments. It would be naive to expect that the extension
of the ADA would have no adverse effects on some of those who now enjoy
its protection.
A legal ban on
discrimination against all disfavored or stigmatized physical and mental
differences may also impose less tangible costs. These range from the
administrative burdens imposed on a judicial system required to field a
vast array of new complaints arising from a broad and vaguely formulated
proscription, to the erosion of public support that may result from
extending protection against disability discrimination to people who are
not in fact disabled. Critics who regard the United States as
litigation-crazed and rights-obsessed will raise the specter of short,
fat, and homely people clogging the courts with petty complaints that
reveal nothing more than the increasing incidence of the “disability”
of thin skin. More ominously, they will see an oblique assault on the
very idea of merit; on practices and institutions that celebrate beauty,
strength, and intelligence. I shall address these complaints in turn,
arguing that they are greatly exaggerated but not entirely baseless. The
ultimate question is whether the risk of additional expense, litigation,
and public hostility is justified by the moral and practical value of
extending the statute’s protections.
Effects on
Litigation
However credible the
threat of exploding litigation may be in general, that specter seems
especially remote in this area. As Justice Stevens remarked in his Sutton
dissent, “it is hard to believe that providing individuals with one
more antidiscrimination protection will make any more of them file
baseless or vexatious lawsuits.” The awkwardness of raising claims of
discrimination on the basis of obesity, very short stature, or extreme
unattractiveness would serve as a powerful deterrent to anyone lacking a
strong grievance, as would the formidable difficulty of proving
discrimination on the basis of less striking departures from aesthetic
and other social ideals. Moreover, the removal of the substantial
limitation requirement would eliminate one of the most litigated issues
under the present ADA.
Research on ADA claims
suggests that much current litigation is attributable to disputes about
whether an impairment is substantially limiting. Those disputes would
arise less frequently under the revised statute, which would focus not
on the severity of the condition but on the social response to it, e.g.,
did the reassignment of a worker with a lower-back or heart problem
reflect myths and fears about her frailty or weakness, or a prudent
avoidance of risk? Of course, questions about the severity of such
conditions would continue to arise in considering such issues as the
reasonableness of a proposed accommodation or the existence of a safety
threat. However, it would no longer be necessary to establish the
severity of the condition as a prerequisite for claiming accommodation.
The revision of the
statute would also reduce the incentive for the kind of fraud that has
preoccupied disability policy makers. The pressure to obtain false
medical evidence arises from the need to establish impairment and
substantial limitation, a need that the proposed revision largely
eliminates. The corrupting pressure to “diagnose disability down”
would be relieved by a statute that demanded no medical evidence of
impairment or substantial limitation. It is possible, of course, to
imagine litigants fattening up to claim weight discrimination, or
putting on unflattering makeup and clothes to claim unattractiveness
discrimination, but such stratagems would hardly be more deceptive than
much routine trial preparation. And they would be of no avail in
satisfying the most difficult element of proof for all such claims: not
that of establishing a disfavored difference, but of establishing that
discrimination occurred on the basis of that difference.
Admittedly, litigation
would arise over the scope of the expanded statute, about whether a
particular type of physical or mental difference is actually subject to
social prejudice or stigma, and about whether it should be covered by
the statute if it is not. For example, while left-handed people may once
have been subject to a variety of myths, fears, and stereotypes, they do
not appear to face them in turn-of-millennium America. It is doubtful
that any current or residual stereotyping or animus explains the absence
of left-handed mail-sorting devices or “crossover” training
complained of by Daniel de la Torres, a discharged mail sorter whose
claim of disability discrimination was dismissed for want of an
impairment. The court may have reached the right result in that case,
not because left-handedness is not an impairment, but because it is not
stigmatized. Then again, the lack of accommodation for left-handed
people might well create a risk of stigmatization, by making them appear
incompetent as they struggle in a world of right-handed equipment.
It may seem that my
proposal would compel courts to make awkward threshold judgments about
such matters as physical appearance—deciding, for instance, whether a
plaintiff was sufficiently unattractive to have experienced appearance
discrimination. But because a revised statute would not limit itself to
differences that fell below some vaguely defined social benchmark for an
“acceptable” appearance or physique, this issue would not arise. To
be discriminated against on the basis of physical appearance, a person
need not be unattractive, just insufficiently attractive to satisfy the
job-irrelevant preferences of an employer. If an employee of average
appearance could actually show that he was denied a promotion because he
did not meet his employer’s high aesthetic standards, he would have a
discrimination complaint under the revised statute. The claim that “I
would have been promoted if I were better-looking” would state a cause
of action, because an employer who places an unwarranted premium on
beauty devalues the plain-looking as well as the homely.
Although this expansive
view would, in theory, open the courthouse door to virtually anyone with
an adverse employment outcome and a physical or mental imperfection, I
do not think a flood of “baseless and vexatious lawsuits” would
result. Admittedly, it would be less awkward to raise a claim of
discrimination on the basis of a minor than a major departure from an
aesthetic or other social ideal. But it would be that much harder to
prove such a claim—a plaintiff would be likely to prevail only against
an employer who was remarkably indiscreet or emphatic about his illicit
preferences. The great majority of counterfactuals of the sort “I
would have been promoted if I were better-looking” will be unprovable
even if true, and the obvious difficulty of proving them should keep the
floodgates closed against all but the most serious grievances.
It may seem a dubious
recommendation for the proposed extension of the ADA that it would be
virtually unusable by those it was intended to protect. But this
overlooks the fact that a few cases can have a major impact on social
practice. A judicial decision that Deborah Birdwell had a right to
reasonable accommodation would have both symbolic and practical value,
condemning the indignities visited on people with ordinary physical
differences (as well as making life easier for overweight moviegoers). A
single administrative ruling that a law or advertising firm could not
defer to its clients’ preferences for good looks in hiring its
professional staff would increase employment opportunities for homely
and plain-looking professionals, although it would hardly eliminate all
the advantages of physical attractiveness. As many commentators have
noted, the law casts a broad shadow, and the benefits to people with
ordinary imperfections would be more likely to arise from preemptive
measures than from specific judicial or administrative orders.
A Quixotic Statute?
Nevertheless, the very
difficulty of proving specific instances of a kind of discrimination we
believe to be ubiquitous may suggest that there is something quixotic
about the revised statute. Precisely because physical appearance has
such a pervasive impact on social judgment, and because norms of beauty
are so deeply enmeshed in social practice, it might be argued that a law
against discrimination on the basis of physical appearance would either
be wildly impractical or unreasonably demanding. We are willing to
accept the sometimes awkward formalities imposed on job searches by
affirmative action guidelines as an acceptable price to pay for purging
the great evils of race and sex discrimination. Similarly, we may accept
the relentless institutional self-scrutiny and small monetary expense
involved in making jobs and activities more broadly accessible, to end
the wholesale exclusion and isolation of people who are blind, deaf, or
paraplegic. But the effort to purge ourselves of “lookism” may seem
to require greater sacrifice and contortion for a less urgent objective.
As Robert Post argues, it raises the specter of denatured transactions
between disembodied individuals. Disability discrimination law would
indeed demand too much of us if it sought to eliminate, rather than
control, the impact of physical appearance.
But disability
discrimination law has always had more modest ambitions—it is more
pragmatic than the “dominant conception” of discrimination law
described by Post. As many commentators have noted, the ADA does not
demand “blindness” about physical and mental impairments; not only
does it recognize that impairments are sometimes relevant to eligibility
or qualification, but it also requires a reasonable attempt to
accommodate relevant impairments. This pragmatism can be preserved in
the extension of disability law to normal imperfections. For example,
the law (or its accompanying regulations) might require that
face-to-face interviews be deferred until the final stage of the hiring
process. At the same time, it might decline to bar face-to-face
interviews altogether, recognizing that it would be unduly burdensome to
forgo the information such interviews could yield. In a pragmatic
spirit, then, the law would seek to limit the sway of powerful aesthetic
preferences, but not aspire to eliminate them entirely.
I am optimistic that we
can reform social practices to reduce the importance of physical and
mental differences, as we have reduced the importance of race and
gender. Over the past three decades, we have learned that much of what
we value in our public as well as private lives, such as humor,
spontaneity, and gentility, can survive within the strictures of
antidiscrimination law. I believe that, with experience and goodwill, we
can endow the now alien, and alienating, procedures for limiting the
sway of aesthetic preferences with a patina of familiarity and grace.
The core virtue of a
broadly inclusive statute, focused on stigma rather than impairment, is
that it would not rely on biomedical classification to determine who
should be protected from discrimination. It would challenge, rather than
reinforce, the sharp dichotomy between the disabled and able-bodied. If
we are all susceptible to impairment and limitation, as proponents of a
universal model of disability have long insisted, we are all vulnerable
to stigmatization. The Americans with Disabilities Act should be for “us,”
not for “them.” It should command broad popular support not only
because it seeks to protect some of the least advantaged and most
stigmatized members of society—its capacity to do so will not, I have
argued, be significantly diminished by its extension—but because it
seeks to protect all of us from disabling attitudes and social
practices.
—David
Wasserman
This essay has been
adapted from an essay in the forthcoming Americans with Disabilities: Implications of the Law for Institutions
and Individuals, edited by Leslie Francis and Anita Silvers (Routledge,
2000); reprinted with permission. Sources: Murphy
v. United Parcel Service, 119S. Ct. 2133, 1999; Linda Greenhouse,
“Justices Wrestle With the Definition of Disability: Is It Glasses?
False Teeth?,” New York Times
(April 28, 1999); Sutton v. United
Air Lines, Inc. 119 S. Ct. 2139, 1999; John Tringo, “The Hierarchy
of Preference toward Disability Groups,” Journal
of Special Education, vol. 4 (1970); Gary Albrecht, Vivian Walker,
and Judith Levy, “Social Distance from the Stigmatized: A Test of Two
Theories,” Social Science and Medicine, vol 16 (1992); Robert Burgdorf, “’Substantially
Limited’ Protection,” Villanova
Law Review, vol. 42 (1997); Lisa Eichhorn, “Major Litigation
Activities Regarding Major Life Activities: The Failure of the ’Disability’
Definition in the Americans With Disabilities Act of 1990,” North Carolina Law Review, vol. 77 (1999); Ruth Colker, Hybrid:
Bisexuals, Multiracials, and Other Misfits under American Law (New
York University Press, 1996); Erving Goffman, Stigma:
Notes on the Management of Spoiled Identity (Prentice-Hall, 1963);
Leslie. Fiedler, Tyranny of the
Normal: Essays on Bioethics, Theology and Myth (David R. Godine,
1996); Linda Jackson, John Hunter, and Carole Hodge, “Physical
Attractiveness and Intellectual Competence: A Meta-Analytic Review,” Social
Psychology Quarterly, vol. 58, no. 2 (1995); Marc Sorani, “Are the
Rights of the Disabled in Jeopardy?,” New
York Times (June 23, 1999); Sue Krenek, “Beyond Reasonable
Accommodation,” Texas Law
Review, vol. 72 (1994); John McNeil, “Americans with Disabilities:
1991–1992,” Current Population
Reports 70–33 (1993); Jerome Bickenbach, “Voluntary Disabilities
and Everyday Illnesses,” in Disability
Is Not Measles: New Research Paradigms in Disability, edited by
Marcia Rouix and Michael Bach (Roehrer
Institute, 1994); Torres v. Bolger,
610 F. Supp. 593 (1985); Robert Post, “Prejudicial Appearances: The
Logic of American Antidiscrimination Law,” Brennan Center Lecture
(ms., 1998); Note “Facial Discrimination: Extending Handicap Law to
Employment Discrimination on the Basis of Physical Appearance,” Harvard
Law Review vol. 100 (1987). |
|