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This tour is
meant as a study trip. An exploration into how ideas of mental illness and
rurality come together. We will see who the major tour designers are and what
their promotional material looks like. As with any tour, there can be surprises
along the way and also questions that remain unanswered. Hopefully, you will
find a location that you like and choose to spend a while there. This is a
difficult trip. The vistas challenge us, as visitors, to look past the glossy
promotional material to the reality of life underneath.
To fully expose the intricacies of rural geography and mental illness, we
need to appreciate the tour as presented by the guides but to also ask what is
being left out.
I prepared for this trip like any other.
I packed my bags full of the literature, prepared my itinerary (outline), and
proceeded to travel as a tourist through the geography of mental illness. Being
a tourist, I needed no attachment to the landscape, only a sense of wonder and
willingness to be led by the tour guide. The guides each have their own
interpretation of the particular highlights of the tour. I am willing to be led,
like most tourists, and am comfortable that the tour guides will not allow me to
come to any harm. I am, after all, a paying customer.
Day 1 –
Itinerary
Today, we
will travel through the clean regions of the medical views of mental illness. We
will consider the diagnosis of deviancy and spend some of our time at
schizophrenia, as it provides an interesting vista. For this journey we will use
as our guide the photocopied information from the Diagnostic and Statistical
Manual Vol. IV that was sent to you. There are also many web sites that you can
peruse at your leisure. We chose these as defining guidebooks because, although
not written for lay people, they are more easily available for the general
populace and the information is quick. Today’s tour is sponsored by the
American Psychiatric Association, the publishers that bring you the DSM-IV.
**Note: As today’s tour is sponsored
and led by the medical establishment, Doctors and Psychiatrists are the main
guides. The tour is designed for the mass populace after having been approved by
the medical establishment. A requirement of the tour is to follow wherever the
guide leads. Unfortunately today,
we will not be venturing outside their boundaries, as this tour does not often
consider location in relation to illness. Our focus will only be on the illness.
Our goal is not to educate but to indoctrinate tourists into the landscape. The
medical tour guides exert the most influence on what we expect to encounter in
our travels through mental illness. The predominant packager of information,
medicine covets its premier roll in our cultural understanding of this landscape
and yet it is really not a tour designed for amateurs.
Today’s tour is entirely focused on
our relationship to deviance. A system of “normal” and “other” is required in order to make sense of this social
construction. Pfohl (1995) explains that “deviants never exist except in
relation to those who attempt to control them” and this idea of control is
evident in the medical paradigm surrounding mental illness. The highlight of
this control is found in the naming, the categorizing of deviance through the
imposition of diagnostic categories that then define the person, their actions,
and subsequently their lives. These categories also determine the type and
amount of stigmatization the person experiences when released back into the
non-deviant society.
“The practicalities of contesting
psychiatric medication [and diagnosis] are immensely complex and difficult”
(Parr 1999, 195). It is more socially acceptable to acquiesce to the power of
the medical establishment than to seek out alternatives. At an even more
profound level, Frank argues that it not merely acquiescence that occurs but
colonization by the medical power. For him, it occurs when a person experiences
incoherence in their experience and the medical establishment, with its façade
of legitimacy and saviour-like publicity, readily steps in to create a version
of coherence out of this chaos (Frank, 1999).
His diagnosis, his categorization into medical terminology “was a
medical flag, planted as a claim on the territory of my body” (Frank 1999,
52). And this process remains unchallenged by our society and by individuals.
Even Frank acknowledge “if the treatment works, the passivity is worth it”
(53) and brutally underscores the innate desire of the person to be back where
they existed before illness crept into their life. It shows our acquiescence to
the perceived role of medicine in our culture and our fear of incoherence as a
state.
This power of categorization and naming,
then, creates a virtual identity that overshadows the individual’s
self-defined identity. The virtual identity can acquire some social credibility
if it responds in an accepted manner. Here the virtual identity takes on the
form of the institution as container of the deviant and creates its own social
relationships (Parr 1999).
“Behavioral health care professionals
call disorders, illnesses or diseases that have prominent emotional, behavioral,
and psychological symptoms mental disorders” (“Mental Disorder”, www.behavenet.com).
With these symptoms and the resulting diagnosis of mental disorder, the person
is thus “reduced in our minds from a whole and usual person to a tainted,
discounted one” (Goffman 1963, 3). And through this reduction, stigma is
created which “constitutes a special discrepancy between virtual and actual
social identity” (Goffman 1963, 3). The whole person is recreated as the sum
of her symptomatology and this external imposition reinforces the power of the
medical model. The creation of this virtual identity, that of the deviant,
assists the medical model to gain compliance from the individual in the
treatment of the illness through social pressure and the assertion of
specialization. This specialization lends a preciseness to deviance – not
simply mental illness, but schizoaffective disorder; not cancer but lymphoma. It
further reduces the colonizing forces of the medical establishment to a select
few who specialize in that exact disorder and forces the person with the illness
further away from an understanding of the whole. The body has been fragmented
into healthy/not-healthy, and now
the illness, too, is fragmented. The map of the body is torn into shreds making
it harder and harder for the person to gain his or her bearings in relation to
the whole.
The terminology of “disorder” is in
direct relation to our view of deviance. If a person is deviant they are out of
order in our society, this person is “other” to our view of what is
“normal’ and must be looked after or managed in order to control. “We construct a stigma-theory, an ideology to explain his
inferiority and account for the danger he represents” (Goffman 1963, 5). To
effectively manage this perceived threat, we feel the need to classify by some
form of recognizable and repeatable criteria by which we can identify persons
that are deviant. The circularity of reasoning is evident here. Classification
leads to diagnosis which leads to stigmatization which then leads back to
control through medicine, the creator of classification of mental illness.
In the DSM-IV there are 404 various
diagnoses, many of which are considered “disorders”, that classify
“strictly in terms of patterns of symptoms that tend to cluster together”
(FAQ, www.psych.org , 2) and the primary
purpose of these classifications is “to facilitate communication among mental
health professionals [and}…provide a convenient shorthand when communicating
about patients” (FAQ, www.psych.org, 1).
It is important to note that these diagnostic criteria are for speaking about
the deviant not to the deviant and are used “by mental health professionals
from a variety of disciplines and backgrounds for a wide variety of purposes,
including clinical, research, administrative, and educational” uses (FAQ, 1).
Proof of deviancy through classification is achieved by the use of these
diagnostic criteria that have met the test of empiricism.
In revising the DSM, the American
Psychiatric Association states “ new categories were only considered for
inclusion if there was significant data available to allow critical
consideration of the relevant merits and risks of inclusion” (FAQ, 2).
The attainment of this data is achieved from within the psychiatric
community as they have the authority required to present the data as valid and
thus the evaluation never escapes the controlling desires of the medical model.
And although the psychiatric community recognizes that there are risks to
inclusion and that “sociological and other considerations must also be taken
into account” (FAQ, 2), the reality of stigmatization as a result of diagnosis
is underscored in favour of treatment and compliance consigning the individual
to inhabiting the virtual identity and social level created for the deviant. By
considering this process carefully, it becomes clear that a truly fascinating
sleight of hand occurs. While removing control of the naming experience from the
individual, the medical paradigm then turns back the locality of the deviance to
the individual. All control over the situation is removed from the individual
but the consequences remain for the individual to integrate into a significantly
altered life.
However, even the medical/scientific
community display rifts in their agreement, in their interpretation of the data.
In the case of schizophrenia, it is clear that not only is definition is
problematic but so is causation. “Some theorists maintain that schizophrenia
has a specific cause, although they disagree on what that cause is. Others use
the diagnosis in a very broad way, almost interchangeably with psychosis.”
(About Schizophrenia, www.bio.metu.edu.tr,
Pp. 2). What is clear about
mental illness is that in order for a person who is having difficulties to
access service they must fall within certain diagnostic criteria, controlled by
a body of evidence outside of their experience. In effect, they must conform
even before diagnosis to a view of deviant/not-deviant to even explore what is
happening. In this regard, the creation of deviance through to treatment is
predetermined by a model that does not consider the whole individual in their
landscape nor the ramifications on the individual but instead sections off
pieces of the individual for specialists to map and define. This leaves the
individual outside of the entire process without the knowledge of how to get
back in and without a terminology to describe the incoherence of their
experience.
A major feature of the medical model is
the determination of cause. Whether the cause of mental illness is a product of
upbringing or social class, a chemical or electrical imbalance in the brain or
genetic, (About Schizophrenia pp. 12-17) the resultant diagnosis facilitates the
removal of responsibility for and active participation in health decisions from
the individual, much like a child under the care of a parent.
It also enables the creation of a categorization of victim (if the cause
is seen to be outside of the person’s control) or villain (if the cause is
seen to be the result of the individual’s own actions). The naming of villain
is especially true if the cause of the mental illness could be in any way linked
to drug usage, sexually transmitted disease, or any other defined- as-deviant
behaviour.
Foucault (1973) documents a range of
care throughout history of those considered mentally ill. The main themes behind
the varieties of era-determined models of institutional care are the ideas of
isolation and the power of segregation. One model saw towns driving those
considered deviant “outside their limits; they were allowed to wander in the
open countryside…” (8). Other models were institutions that locked the
deviant away from the non-deviant population. Whatever the model, the idea was
the same. Institutions, begun to house the economically inactive, the lazy and
the ill, became “the geography of haunted places as in the landscape of the
moral universe” (57). The trend
of institutional closure and the idea of community care is a contemporary
continuation of the landscape that Foucault highlighted only the walls in our
era consist of medical interventions; the segregation and isolation of the
individual remains. The use of assertive community treatment plans, whereby the
person who is diagnosed with a serious mental illness is cared for in his or her
own home through intensive interventions by mental health professionals, has
gained increased acceptance by funders and ultimately by mental health
organizations. Medication compliance and the reduction of hospitalizations are
touted as the greatest benefits of this form of care. The walls of the
institution are replaced by the walls of an apartment or house. Best practices
papers (The Clarke Institute of Psychiatry) highlight the cost savings in having
clients conform to their medication regime in that it reduces the use of costly
hospital services. Interestingly, but not unexpectedly, the voices of people
with the illness are not heard in this discourse. Best practices research come
from reviewing the literature of the specialty, similar to the method used to
update the DSM. The person is described as “the schizophrenic”, the
“manic-depressive”, the “obsessive-compulsive”. The illness becomes the
main defining characteristic of the person, the virtual identity, and other
identity is lost. The person is discussed as if they are not present, as a
“case” not a person. Research is based on outcome measures, data collection,
and process measures highlighting the medical model’s roots in scientific
methodology. Key diagnostic criteria in the DSM are designed for mental health
professionals to converse with each other, not with the person with the mental
illness. The deviant is only the portrayal of symptomatology and is not an
active participant in diagnosis. Their role is of passive acceptor, the item of
discussion, the unit of data.
And while there is serious effort by the
survivor movement to fight such things as assertive community treatment and
forced electro-shock therapy, the control over diagnosis and care is firmly in
the control of the medical establishment. The simple naming of their cause as
“survivor” reflects the sheer effort it takes to maintain their actual
identity in light of the mental health community’s impressive control over the
creation of the virtual identity of mental illness.
“The assumption [in the medical model]…is that the individual body,
which is at fault, can be treated by largely medical interventions and
technologies” (Butler and Parr 1999, 3). The villainization of the body or
mind, depending on opinions of cause, deflects criticism from the model that
creates it to the individual that presents it
The
medical model of disability is rooted in an undue emphasis
on
clinical diagnosis, the very nature of which is destined to lead
to
a partial and inhibiting view of the disabled individual” (Brissenden,
cited
in Butler and Parr 1999, 3).
With this “othering” of the person
using diagnosis complete, we can then see how this experience is then overlaid
upon geographical prejudices created in urban environments which typically view
the “rural” as other.
In terms of serious mental illness and
persons living in rural locations, US research indicates, “ the prevalence of
clinically defined mental health problems among rural and urban adult
populations is similar” (Kessler et al, 1994 cited in National Rural Health
Association May 1999). And while occurrence numbers may be similar in rural and
urban populations, what is not similar is the access to and availability of
care, which is seen by health organizations as detrimental to the person
experiencing illness. There are few other benchmarks by which rural service,
whatever that may be for the individual, are measured against. Services and then
the evaluation framework of those services are established in urban environments
and overlaid on a rural location without consideration of some fundamental
differences. Wrinkles to this methodology are seen as products of rurality, not
in the flaw of design that assumes transferability. This is the overarching bias
of urban views. If it works or doesn’t work in our environment, then the same
should be true of rural environments. Urbanites
even get to determine what is rural and this issue and how rurality affects
those with mental illness is considered in the tour presented by the
geographers.
Day Two –
Itinerary
**Note: Today’s tour is organized
and led by academics, the social geographers and may not be of interest to those
seeking first hand experience of the rural mentally ill. Not considering the
majority of the populace, the directions can seem obscure and the language used
to describe the landscape is difficult. Travel without a terminology book is
discouraged, as there are no other signposts on the journey in case you should
get separated from the group. Unfortunately, most of the tour guides are from
urban areas so please be on the lookout for urban bias in the writings. Our goal
today is to integrate what we learned on the medical tour within the context of
geographic location to see if there are any nuances of place that affect how we
view mental illness and people who live outside of the boundaries of urban
realities.
Today
we venture out into the rural areas surrounding our compound. But first we
encounter what seems to be the greatest debate in this region: what is
“rural”. Although different measurements of “rurality” are used, the
majority of tour guides agree, “rural areas…are often described as being
peripheral to urban cores in terms of a variety of factors, such as level of
economic activity and access to resources” (Gesler et al. 1992, 1).
The lack of access to service, remoteness of living accommodation, lack
of “qualified personnel”, and transportation difficulties are isolated as
identifiers of rurality (Gesler et al, 1992; Alun, 1992; Ilbery, 1998; Furuseth,
1998; Smith, 1977). Still there is, however, a perception that rural means idyll
“an open and clean environment, free of the stress and pathologies associated
with fast-paced urban living” (Furuseth 1998, 233).
So
here in our tour, we have another dichotomy. First we encountered the
normal/deviant mind in the medical tour. Now we face the rural/urban and
idyllic/flawed debates even before we leave on our tour. Our personal
perceptions of the rural impact the tour. Halfacre (1983,
cited in Ilbery 1998) identified four approaches to defining rural which
have been very useful in the design of this tour. Here rural can be seen as:
“descriptive which assumes the existence of rurality and empirically
describes, through the use of different parameters and measures, its
socio-spatial characteristics; sociocultural,
which assumes that (low) population density in some ways affects behaviour and
attitude; locality assumes a distinctive type of locality defined according to
those characteristics that make them rural, either the specific geography or the
main economic activity; and a social representation that relates to lay
discourses of rurality and the words and concepts understood and used by people
in everyday talk.” In this final approach, attention turns to how the rural is
perceived by the inhabitants; it is a still a social construct because the
emphasis is placed on how the occupants of rural spaces view themselves. This
consideration of self-perception and definition was lacking in the tour on the
first day, while the consideration of social environments and their impact on
the individual, while considered, are biased by an urban view of how those
social environments are structured.
The
first attitude towards rurality, that of empirical distinctions, closely
resembles the model of the medical community in their reliance on measurements
and parameters predefined by those not affected by the definition. The second
and third definitions highlight some urban assumptions that colour the
representation of rurality. The first is the quaintness of community and that
its small size necessarily changes the way people relate to each other. And
while it may be true that rural communities do view themselves as distinct and
different from urban areas, the difference lies in the balance of power to
impose a particular definition. When the definition comes from outside of the
community being considered, the colonization viewed in the medical model of the
individual’s body grows to the meta-level and replays that conquest
substituting urban for medical and rural for individual. The separation of rural
areas into economic activity zones or specific geographic features reduces
community to factors of its whole self, much like the diagnosis of deviance
reduces the individual to inferiority.
Although the definitions of “rural”
are the subject of debate, each of these presented definitions has inherent in
its argument aspects of the idea that “rural areas are designated by
exclusion” (Hewitt 1992, 52), by their comparison to urban areas for the
unveiling of what is missing, by what is not urban. Statistical surveys such as
the Census in both the US and Canada define populations in terms of numbers and
while many researchers acknowledge the problems of definition and strive to
“[extend the] definition of rurality to more adequately identify
differences” (Dottl and Greenley 1997, 312), they also acknowledge that in
order to “allow for comparison of [their] results with other findings” (312)
they retain the definitions provided by census derived statistical definitions
of rurality.
Statistics Canada “for census purposes
utilizes factors related to population density to determine rurality” and
“population density [is] frequently being employed as it is readily available
and practical” (Parikh, Wasylenki, Goering, & Wong, 1995, 63).
And “many federal policies…rely on dichotomies of rural/urban
designations” (Gesler et al. 1992, 22) so that these definitions, while
determined outside of the community being examined, exert enormous power over
the community and its study. This is very similar to the dichotomy of normal/deviant that
is used in the medical establishment, with the urban being the normal way of
living and rurality being viewed in the deviant position. It also facilitates
the removal of power and determination from individual or community control to
an outside entity.
In much of the academic work surrounding
mental illness and rural geography, we encounter a social science method of
explanation. The data we encounter shows “both historical and recent evidence
…that rural residents have more serious and severe health problems than their
urban counterparts. These problems are often compounded by poverty, poor
nutrition, substandard housing, occupational hazards, and limited medical
resources” (Gesler et al. 1992, 11) and yet as Hewitt (1992) points out the
definition of “rural” impacts how health problems are approached. Even the
definitions of health problems that rural areas experience are created in urban
centers and imposed upon rural situations through a process that begins with
research on urban problem. This is then translated onto rural areas that, as
acknowledged, have far fewer of the urban defined services required for health.
This methodology threatens to miss entirely community designed responses to
illness and removes the possibility that a community will learn through the
incoherence of illness how to regain coherence and meaning for themselves. This
vital aspect of growth increases community resilience and leaves a legacy of
confidence. How then do
urban-designed programs function within this different environment? Assertive
community treatment, introduced by the medical tour guide, is one such program
that shows serious disadvantages when implemented in a rural location,
especially when it is implemented from a larger regional center (Fekete, Bond,
McDonal & Salyers 1998). The distances that need to be traveled to meet
clients may be great, the need for personnel might be higher per capita than in
an urbanized environment for safety considerations and lack of staff
collegiality concerns many researchers (Roberts, Battaglia, & Epstein 1999;
Badger, Robinson & Farley, 1999; Merwin, Goldsmith & Manderscheid 1995).
And while stigmatization, not effectively dealt with in the medical information,
is considered in the social research of geography and mental illness, the
assumptions and questions highlight some potential urban prejudices of rural
behaviour such as the perceived “high regard for autonomy and self-help”
(Esters, Cooker & Ittenbach 1998, 470).
What is perceived by rural dwellers as a strength, their
self-sufficiency, is viewed by the urban researcher as a barrier to treatment.
It is unclear whether or not researchers consider these traits as unique to
rural inhabitants but evidence suggests that the differences in the rural
experience is related to stigmatization and results in the delay of rural
inhabitants to seek care thereby being more ill upon diagnosis (Kane & Ennis
1996). It is interesting to note,
that research indicates that the health of rural residents depends more upon
political and economic realities than on social relationships and cultural
expectations and yet the emphasis on explaining the regard for autonomy if
firmly located within the social context. Rural residents have historically
experienced political and economic isolation that is possibly the reason for the
desire for self-sufficiency. The choice of focus upon social and cultural
contexts instead of political and economic arenas mirrors the naming procedure
we viewed on the medical tour when smoke and mirrors assumes the power of
authority to name and yet leaves the stigma with the individual.
When we consider that despite the
“growing political influence of nationally recognized consumer groups, rural
mental health service delivery has yet to be impacted” (Bjorklund &
Pippard 1999, 347) we see how deep the urban focus for service extends. Consumer
groups designed in urban areas and underutilized in rural communities require
trained personnel and a significant number of consumers with adequate access to
transportation. Ironically the identification of being a mental health consumer
is usually required by the program and yet sets up a probability of social
isolation for the individual from the community at large. The stigma is directed
at the association with the medical diagnosis and the individual, as we have
seen, is reduced to being the container of this diagnosis. The “stigma
surrounding a psychiatric diagnosis is often magnified in a small community as
opposed to a larger urban area” (Bjorkland & Pippard 1999, 350) not
because the bias of small communities is greater but because the medicalization
process attacks a main cultural survival mechanism, a person’s autonomy. It is
the colonization of the person by an outside force in a time of incoherence that
creates a backlash response. Self-sufficiency may be a cultural expectation of
urban researchers looking at rural locations while it also, with decidedly
differing definitions, may be viewed as desirable by rural residents. The threat
exists in the perceived conquest of one definition, the lived experience of the
rural, by the presumption of “otherness” by the urban. This necessarily
creates fear and apprehension. Intriguingly,
studies into the effect of this cultural expectation in urban residents are
absent from the debate. Where there is room for growth is in the discussion
around definitions and how those definitions came into being.
As Philo (cited in Ilbery 1998, 4)
points out “not all people living in rural areas conform to the rural idyll of
a white, heterosexual, middle class male who is able and of sound mind”. If
this is true then, how much more marginalized is the rural woman of colour, or
the low-income male with illness? How are our decisions on service provision
limited by our inability to leave the fairy-tale countryside? Our impressions of
the rural, whether it is of the idyll or of the disenfranchised other, inform
how we respond to problems encountered there. In much of the academic writing,
we are hearing from the professionals, university trained, most often urban, who
study the rural as the ethnographer studies foreign cultures. The inclusion of
the voice of the rural individual is evident in very little of the writings.
And if we view the rural as idyllic, our
decisions on how to spend diminishing health care dollars will be very different
than if we look with an openness to difference. The stakes are extremely high
for rural regions that face cuts to their already scant service. In urban areas,
those needing service might be inconvenienced by the closure of a service agency
while in rural areas, the service agency may be the centre of the community,
providing very crucial health care needs. “A full array of community services
is universally recognized as a fundamental ingredient in rural development
programmes” (Furuseth 1998, 236). The universe that recognizes this fact again
shows the overlapping an urban bias on the inadequacy or rural service delivery
and justifying potential cuts. “The view of urban America by urbanites and
suburbanites seems to be one of incredulity. One seems to know that good mental
health care could not possibly be delivered under such primitive conditions as
isolation, provincialism, social immaturity and the absence of ‘specialty
care’ professionals” (Kane & Ennis 1996, 450). This view of rural
service provision as primitive and immature is ironic and has the potential to
become a self-fulfilling prophecy as it becomes the urban justification for
rejecting requests for service. This judgment is the voice of the urban and the
rural are portrayed as the hapless victims of the whims of governmental
reorganization.
Rurality exists on a continuum of
dichotomies, from the impoverished to the rich, and the isolated to the
connected. These dichotomies exist in urban areas but rural dwellers experience
this on a smaller population scale with more geographical land mass. It is not
the severity or treatment of physical or mental impediments that defines
rurality, but the geographical, cultural and economic landscape in which these
populations exist. Unfortunately, “rural services are pulled back as
decision-making processes are focused upon…the higher costs of providing rural
services” (Furuseth 1998, 242). Coupled with the uneven political power
realized because of low population density, these services are primary targets
in eras of fiscal restraint.
What is evidenced here is not the lack
of service use nor of the demographics of the population that changes rural
service provision. It is how the problem is defined and by whom it is defined
that interprets the economics and cost of providing services to geographically
dispersed populations. And rural communities, because of their lower population
density have less political clout than larger and denser urban populations. The
voice of rural people, barely audible in the academic writings, is a mere
whisper in the political landscape. And while the “urban poor are a highly
visible fixture of life in the industrialized world…the rural poor…are
becoming more invisible” (Furuseth 1998, 242). This invisibility makes it
possible for the political agenda of cost containment to reallocate rural
service dollars to the more visible urban populations.
The stigma of mental illness and the
tendency of rural people to put off seeking help from identified mental health
professions combine to make it easier for the political climate to remove mental
health services from rural locations while still appearing to offer them through
the centralization of service in regional cores. This distancing of service
provision completes the distancing of the individual from the community that is
started with diagnosis and association with the medical tour. The colonization
of the body and the landscape is complete. What is left is for the people to
discover a voice within the lexicon of the colonizer to express their experience
and to gain back the lost coherence.
Butler and Parr (1999) state that “by
acknowledging the problems and possibilities of naming and aligning such
experiences of mental health problems, chronic illness, and physical
impairments, [social geographers] seek to destabilize what [they] see both as a
limiting mind-body dualism in human geography and a reluctance fully to reveal
or to critique the myth of the perfect mind/body” (2). That they are reuniting
the mind and the body within the consideration of rural geography is indicative
of their attempt to reform the “two basic models (social and medical) which
inform disability studies” (Butler and Parr 1999, 1) but also looks at
decreasing the separation of individual and community, of trying to find that
lexicon to describe experience to a culture that views them as “other”.
Looking at the continuum of rurality overlapping the continuum of disability,
these ranges they reveal that the term “geography of disability [is] a broad
term capturing a wide range of interests, theoretical orientations, and
empirical studies” (6). This is the third overlapping continuum in their
study. The concern is that in the of making distinctions between different types
of disabilities, between different types of geography, between different types
of methods of study, we allow the categories to acquire different value levels
and consequences that are then played out within the wider societal structure.
It is the specialization that we viewed in the medical tour that effectively
shuts out the individual. This is the pinnacle of victim naming/villain naming;
of being able to accept a disability because the person was not at fault for
causing it, or of being able to accept a physical disability more easily over a
mental disability, or thinking that mental illness is not as common, or is more
common, in the countryside. It tears up the map of experience and throws the
pieces to those who can only decipher bits of information. The individual and
the community as whole entities are lost. What Butler and Parr describe is a way
to glue those pieces back together and to do that, the person or the community
has to be involved as only they have the history required to recognize the whole
when it is complete.
To view the continuum of disability
without social value placed on the various segments “is to deny that such
difference has to equal a series of fixed and othering boundaries by which
people are clearly defined and geographies are narrowly understood” (Butler
and Parr 1999, 9). This springing of the definitional boundaries flies in the
face of the raw categorizations of the medical establishment. It removes the
superficial boundaries laid upon the landscapes and allows a clearer and more
personal look at the lives of the people living with differences. It removes the
need for a victim or villain and looks at the situation as a variety of life, of
which there are many. The inclusion of multiple voices in the discussion allows
for the reintegration of the individual and the community and shifts the power
of naming away from the colonizing forces back where it originally existed.
Day Three – On
Your Own
Today
you are left on your own to ramble through the rolling countryside. You may wish
to visit on your way, the William Wordsworth cottage and view the romantic
vistas from his window. Another stop of interest is the home where John Clare
was born. This is a more run-down home and a bit out of the way but the view
there is 180°
from the Wordsworth cottage. You might also wish to try to engage the locals but
a word of warning; they can be difficult with tourists and may try to challenge
you. That said it is even hard some days to find a local to talk to. For this
day, you may even wish to remain with the tour group and play cards in the
lounge. If you do venture into the landscape, please be aware that the tour
group is not liable. A map of places that you may wish to avoid is located at
the front desk.
Note: This tour is a recent addition to
our package. It was included on the request of previous tourists who wished to
see more of the local experience. This is the first time we have been offering
it in conjunction with the other tours and there are still some bugs to be
worked out. While we have endeavored to present a wide choice for travel, the
locals remain hesitant to participate. Our hope is that the vistas that you
experienced previously will find some context in the day to day lives of the
people who remain here and we can judge from this how accurate the promotional
materials from other tours actually is and how our personal experiences affect
what we gain from our travels.
As the previous two tours have
highlighted through omission, the voices of people who experience the
incoherence of illness are not often heard in literature directed at
researchers. They are, however, heard in Literature. The main difference is that
in capital “L” literature, the entire process is seen as subjective, of one
person’s experience or imagination. But if we are to cease the colonization by
specialists, we must begin to consider the whole person. Expressions of
experience and imagination, then, are integral pieces for our understanding.
Bloom (1994) asserts that “in strong writing there is always conflict,
ambivalence, contradiction between subject and structure” (27) and this
allowance of things not expected or even dreaded is what is lacking in the tours
of the first two days. Literature allows for difference, even exalts in it, uses
it to shock, to stimulate and ultimately to understand. It is a process of
gaining coherence that examines its ugliness and beauty both with equal
interest. So this is where the tour will lead, into the cottages of some people
who write. Some are famous, some are not. This does not matter. What does matter
is the expression of experience which allows us see outside of our colonized
borders into another country.
At the Wordsworth Cottage, I see where
my expectations for the idyllic countryside have their origin. I remember from
earliest days:
“I wandered lonely as a cloud
That floats on high o’er
vales and hills
When all at once I saw a
crowd
A host, of golden daffodils;
Beside the lake, beneath the
trees
Fluttering and dancing in
the breeze.”
But looking at this again, in this
cottage, I am struck by the singularity of the experience; by the aloneness, one
person viewing nature, a nature that is beautified and adored. There seems
little link between humanity and nature here. Nature is a deity standing apart
from the human. It is too perfect, clean, still, and I know that this poetry has
shaped my expectations of the natural, of the rural; the idealized and
beautiful, the aspiration of every city dweller, the place where all things are
in harmony. This is my postcard to send home: “Having a wonderful time. Wish
you were here”. This is the poetry of the tourist, enchanted by the
countryside but not a part of it.
I search through the cottage for
something that is not so much a postcard. I find the “Ruined Cottage”.
Finally, a view not so idyllic nor familiar.
“I rose and turned towards a group of trees
Which midway in that level stood alone.
And thither come at length, beneath a shade
Of clustering elms that sprang from the same root
I found a ruined house, four naked walls
That stared upon each other. I looked round
And near the door I saw an aged Man,
Alone, stretched upon the cottage bench;
An iron-pointed staff lay at his side.
With instantaneous joy I recognized
That pride of nature and of lowly life”
Still there is the tourist looking at
the “lowly life” glorified, personified in the “aged Man” but at least
here there is the recognition that the rural world is not just a postcard of
beauty. This is the opposing urban view of the rural, of the less than, of the
“other”. The separation of tourist and toured is still evident and there is
little personal engagement required other than the recognition of a scene. The
cleanliness of the rural finds its first chink, a glimpse into the reality of
life evident in the ruined house and the naked walls. All is not idyll. What is
obvious is that this is not defined by the aged Man, the rural dweller, but by
the urbanite, the educated, the poet.
Looking for a different view, I walk
over to John Clare’s cottage. Clare spent the majority of his life writing
from inside of an asylum. I read in his biography that “the place was for him
a refuge as well as a confinement for he was treated kindly allowed to wander
about the countryside, and encouraged to go on writing his verses; some of his
best achievements are the poems composed in his madness” (Norton 1999, 907).
The notion of the asylum as refuge challenges my “learned” beliefs about
institutionalization and this new experience is intriguing. Maybe here we can
find the attachment and inclusion. He writes:
“I am – yet what I am, none cares or knows;
My friends forsake me like a memory lost:
I am the self-consumer of my
woes –
They rise and vanish in oblivious host,
Like shadows in love’s
frenzied stifled throes
And yet I am, and live – like vapours tossed
Into the nothingness of
scorn and noise,
Into the living sea of waking dreams,
Where there is neither sense
of life or joys,
But the vast shipwreck of my life’s esteems;
Even the dearest that I love
the best
Are strange -- nay, rather,
stranger than the rest.
I long for scenes where man hath never trod
A place where woman never smiled or wept
There to abide with my Creator God,
And to sleep as I in childhood sweetly slept,
Untroubling and untroubled where I lie
The grass below, above the vaulted sky.
The longing in this poem is palpable.
The desire for a childhood sleep untroubled by adult cares, built on the
“shipwreck of his life’s esteems” is total experience, which incorporates
many dualities. I am still a
traveler here but at least in the Clare cottage, I get a sense of the struggle
with illness and seeing in nature, not salvation but meaning, the description of
his experience in a way that is understandable to others.
Looking out the window of this old
cottage, I notice construction underway. I walk across to a new cottage and
notice that it has many rooms and many voices. These voices, too, are describing
their experience. These experiences are far removed from the canon that
recognizes experience but portray the dualities that we are seeking to combine
in a form that is less tourist and more traveler.
While Clare is the epitome of the rural
dweller negotiating his existence within the medical paradigm and rural reality,
his voice is merely a whisper in the Canon compared to Wordsworth. Turning then
to survivor poetry, we seek new voices to see if rural living informs their
experience.
I can hear the music cats play
melodies and harmony
sacred notes in disarray
a chorus plucked from a broken piano choir
a choir of haunted souls
The enchantress of unholy salvation
purifier of thought
pontifical to a God of love
Mirrored minds the son of thee
disappearing twisting images
My mind outcasts friends
and mends broken ends
Copyright
© 2001 Colin Van Der Woude ( www.poetrysz.net))
In this cottage,
the writers speak for themselves. Without acceptance into the canon of accepted
experience, their publication depends upon their initiative as survivors. Here
we view up close the cultural values portrayed as rural revealed by the
geographers. While their existence in rural localities in never clear, the
cultural value they exhibit should at least offer them honorary resident status.
These writers write against the existing tour and it is only right to let them
speak here for themselves.
Bio:
I'm
a 24 year old writer from Tassie Australia...was diagnosed with a mental illness
at the tender age of 14...I write about thoughts and experiences, mainly at
night when I'm too tired to reach for a pen. I have written poetry since the age
of 15, a year after being diagnosed with Schizophrenia... used to also be an
artist but my creativity in that area was "haloperidolised" and I gave
up painting a year ago. Writing is now my main creative outlet.
This tour guide
is different from the other cottages. The “twisting images” are reminiscent
of the Wordsworth cottage’s “clustered elms” springing from the same root.
It is interesting to see past the twistedness to the ruined cottage that it
disguises. But the new cottage and the new writers use that twistedness to
“mend broken ends”. Their expression comes not from being accepted but from
wanting to be accepted without abandoning the reality they experience.
Turning
around, I notice another voice:
Keep on digging up brand new ideas
facing the day of hell on earth which is New Year's Eve
Locked up with no chance of parole or receiving visitors
then comes the day when all emotions disappear for good.
I never realised i was in hell until it was too late
but we all live in one kind of hell
You can't go outside to play when it's pouring with rain
because there are more puddles than jackets.
I watched the explorer once as he was
exploring
i could run fast but he could always run much faster
And i screamed aloud but he could always scream louder
now i am walking down this lonely road alone.
Desperation has once again entered into my life
if i listen hard enough i can hear God laughing at me
Sometimes it's as if even the poetry seems incomplete
maybe i finally have become my own worst enemy.
Why work when you can play?
if you think you know the real me sorry you don't,
When it isn't good but as good as it's ever going to get
with 456 poems written ten times over.
I'm never what you expect to see
what monsters in my head giving false answers weekly,
Acts of pure weakness hang around like smells from a lavatory
eyes see but not always the truth.
it is possible to live without knowing
it
kiss the wind and those liars play their cruel games,
One day every answer will show itself loud and clear
for now i believe this game is real.
Every one of us born with a killing instinct
as mighty as the devil can make a sound,
The truth hurts me like a knife deep in my soul
life is a cruel game and i must find the missing link.
Copyright
© 2001 Rae Burton (www.poetrysz.net)
Bio:
I am 30 years old and i
suffered a nervous breakdown a few years ago which lead to a few problems but it
also brought a new strength to my writing as i find it easier writing down my
thoughts and feelings than actually speaking. Although i am no longer considered
at risk to myself and no longer have to hear the b.s my shrink threw at me the
thought of suicide goes through my mind everyday but i have learned to fight it
.
The traveler is
engaged by the visceral quality of these images although at the same time
acknowledging their difference to their own experience. The language is clear
and the need to fight prominent. That they have been altered by the system which
defines and controls their reality is foremost a survival mechanism proven out
through their biography notes. Although geography is not an apparent aspect of
these two experiences, the linkage of mind/body and experience reveals a
metaphorical geography that is more singular and more personal. Here we realize
that geography is not only locational and related to landscape but considers the
individuals place and perceptions of control over their space. Interestingly,
Milligan (1999) highlights the fact the “local geographies of mental ill
health are also shaped by the interaction of individuals with their social and
spatial environments” (229). This
reversal of the shaping forces of the interaction between the mentally ill and
their environment suggests research that remains to be completed.
They describe the effort back from a colonized existence using a language
that those still colonized or yet to be colonized can understand. They also
impact the colonizer as the rawness of emotion and quality of their voice force
competing definitions into the vernacular.
Day Four – The Way
Home
We hope
that you have had an interesting trip with us. This is by no means an inclusive
tour and we encourage you to return another time to view more vistas.
This trip has
focused on the production of “otherness” in terms of mental illness and
rural geography. While the medical tour maintains its supremacy over the control
of the production of mental illness through its categorizations and diagnosis,
the geographer’s tour is striving to include the considerations of how we view
and place boundaries on social situations. The inclusion on this tour of the
poet’s voice shows how those most affected by these considerations respond to
these boundaries. Each of the tours that we did take is affected by the
political will of the larger nation, although the evidence in some is more
visible. Choices for type and extent of care are resigned to cost-effectiveness
and cost-benefit decision-making tools following the cyclical patterns of
economic will. Any control that was afforded to the presented tours comes
directly from the political/economic tour. What we saw as the experience of an
individual with mental illness when the medical tour usurped personal power and
control in favour of diagnosis and classification becomes our experience in the
political and economic paradigm. The
recognition that we share experiences with people with mental illness,
experiences of the loss of power and lack of control in areas of basic need is
an area requiring significantly more research and has the potential to reduce
stigmatization through the acknowledgement of the otherness found in all of us.
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