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Stigma: Beliefs Determine Behavior
By David R. Patient (drp@mweb.co.za) and Neil M. Orr (neil_orr@yebo.co.za) of Empowerment Concepts, Republic of South Africa, and Programa Vida Positiva (CNCS), Mozambique
[1]. Introduction
Many people are calling urgently for laws and policies to curtail or prevent
HIV/AIDS stigma. This is a call for changes in structures. It is also a
useless exercise until such time as we examine the roots of stigma, and
understand it's very nature. Then we can build structures to support the
understandings and mechanisms that alleviate stigma.
What exactly is stigma anyway? For the sake of this discussion, we will
define stigma as a behavior or policy/law that unfairly and negatively
impacts upon the rights, life, and opportunities of a person living with
HIV. To distinguish this form of discrimination from other types (e.g.,
gender or racial discrimination), it needs to be motivated primarily in the
perpetuator by his or her knowing that the other person is living with HIV
or AIDS. HIV/AIDS stigma is thus essentially discrimination based upon HIV
status.
Is HIV/AIDS stigma different from any other form of discrimination? This is
a difficult question. Stigma is not exactly the same as discrimination, at
least in terms of connotation. Stigma has an additional connotation to
discrimination, namely of strong emotional rejection, over and above
structural inequity. In this sense, one would explain the expelling of a
woman from her home by her family as due to fear-based 'stigma', while one
would hardly be inclined to call it 'discrimination', at least not in the
common usage of the term. We would hazard a guess in that 'stigma' is
characterized by overt fear, whereas 'discrimination' is not always overt.
We therefore propose that stigma is the extreme end of a discrimination
continuum.
Core questions we need to ask are: What causes people to behave in a
stigmatizing manner? What causes people not to change fear-based
stigmatizing behavior, even when they have knowledge about that casual
contact is safe? Why are people treating their loved ones, colleagues,
employees, and friends in such extreme and inhumane ways? Why is stigma so
widespread, regardless of social, educational, or economic strata? How do
those infected contribute to the perpetuation of stigma?
[2]. Beliefs and behavior
The area to seek the answer - in our view - is simple, at least
conceptually: At the core of any behavior you will find a belief (or series
of beliefs) that causes individuals or groups to behave in a specific
manner. We need to strip away those beliefs to their core, before we can
effectively counteract stigma. Pre-existing structures such as laws and
policies do indeed reinforce stigma. However, even these originate in some
belief.
When exploring beliefs, important considerations include awareness that: (a)
beliefs can be conscious or unconscious (e.g., socialized norms); In fact,
many beliefs are not conscious; (b) there may be beliefs that conflict or
contradict each other, especially conscious versus unconscious value and
belief conflicts: (c) The relative 'stress' of a situation influences the
extent to which conscious beliefs are set aside in a specific situation,
allowing unconscious beliefs to prevail. At the end of the day, it is the
strongest belief that wins out.
More often than not, beliefs - especially unconscious beliefs - are
presented as facts. For example, a sexist statement such as 'men are
stronger than women' is defended as an obvious fact, without any basis in
detailed reality. Defense of beliefs include "it's normal", "everybody
knows this", "we've always done it this way", "It's my culture", and "the
Bible says so". In other words, there is often little individualized
thought or reasoning to support some types of belief - they are often merely
accepted by the individual or group through socialization processes. Quite
frankly, most people would not really be able to tell you the real reasons
why they are discriminating against someone, as they have not really
consciously thought about it.
It is also important to keep in mind that many beliefs have never been
discussed, even during socialization, and are absorbed through modeling and
behavioral processes. For example, a child may learn how to express anger
with violence through observation of adults, not through rational discussion
of the pros and cons of such behavior. Therefore, when we say 'challenging
beliefs' we mean talking about them - bringing them into conscious
awareness, and giving them words so that they can be expressed and examined.
This unconscious aspect of many deep-seated beliefs behind discrimination
makes it problematic in terms of rational 'education and awareness'
processes. Not only is the individual unconscious of some of these beliefs,
they may also have no words to express these beliefs.
There is also a category of beliefs concerning survival issues that are
deeply entrenched. This concerns the functional reasons for discrimination.
An example is how groups approach and respond to threats to their survival.
The unspoken belief is to do whatever is necessary - including the sacrifice
of the weak - to ensure the survival of the group as a whole. This is the
utilitarian approach - i.e., the greatest good for the greatest number of
people sometimes requires sacrifice of a minority. Where resources are
scarce or limited, leaders and groups make decisions based upon this
principle, as a matter of course.
Human behavior is therefore not random. Instead, it has a structure and
reason, instigated and directed by beliefs of various degrees of strength
and conscious awareness. Just as the medical fraternity believes that an
accurate and in-depth knowledge of the virus and the immune system will
allow us to effectively counter HIV through vaccines and anti-HIV
treatments, so a rational social scientist believes that an accurate and
in-depth understanding of people's beliefs will allow us to understand and
modify behavior to reduce vulnerability to infection, and also how to behave
fairly towards those already infected with HIV.
It is not possible for us to influence any long terms changes in
stigmatizing behavior unless we have the courage to challenge people's core
beliefs. It is not a comfortable or popular process. All too often we are so
busy worrying that we might offend a community's (or individual's)
sensibilities that we do them a disservice by refraining from taking the
risk of challenging their beliefs. If we do not challenge these core
beliefs, we have failed in doing what needs to be done to serve our
communities. We suggest that you think twice before tackling stigma, if your
image and popularity is more important to you than being effective.
[3]. Is objective exploration possible?
The difference between a medical scientist and a social scientist is that a
medical scientist studies something (e.g., a cell or a virus) that can be
placed outside of him or herself, on a slide under a microscope. She or he
studies something external. In contrast, a social scientist studies
something of which she or he is part. This is the problem: A social
scientist cannot separate him or herself from what is being studied. She or
he has beliefs too, which may - and usually do - strongly determine not only
where we look (and not look), but also how to view it, what is 'right',
'wrong', and so forth.
Social scientists - whether they like it or not - are just as powerfully
affected by their socialization and survival-based beliefs, which create
phenomena such as 'blind spots' - i.e., literally not seeing something
because it contradicts fundamental personal beliefs. Another common pitfall
is the intellectual justification of something according to a specific
pre-existing belief system. I.e., we try to fit the facts into what we would
like to believe.
For us, the watershed experience that shattered our perception of accepting
blindly the popular beliefs of why people do what they do - in terms of
HIV - was meeting one more of a long line of pregnant HIV-positive AIDS
educator/counselors, who knew that they were HIV-positive before falling
pregnant. If these people - the ones who have the knowledge and reasons -
were not applying what they knew, there has to be something seriously wrong
with our understanding of what is going on.
Stigma cannot be understood as a simple or largely conscious behavior. If
we examine and seek to understand the beliefs behind stigma, we stand a
chance of doing something about it. Just like any other apparently
irrational behavior, at the core of stigma is a set of beliefs, presented as
facts, that is creating discriminatory behavior.
So let us examine some of the possible beliefs that could explain the
stigmatization of those infected with HIV:
[4.1]. Belief 1: "If you have HIV you're going to die, so I won't invest
resources in you".
This means withdrawal of support from those who are perceived as no longer
able to contribute to the survival of the group. This is the outcome of a
group survival strategy, which has been a survival strategy used throughout
human history, namely utilitarianism, discussed previously. It is important
to note that this value-based approach is most prominent where resources are
limited, and less prominent where resources are abundant. We point this out
simply because individuals and groups from developed (affluent) situations
may have a moral problem with this strategy, without full awareness of it's
survival function in resource-poor situations.
Many years ago, there were reports that clinics in certain parts of Zimbabwe
were told not to provide any treatment to those infected with HIV, including
the setting of a broken bone. The reason was that this would be a waste of
scarce resources. Whether this report was true or myth is irrelevant. What
is relevant is that this report illustrates behavior based upon a belief
that is quite fundamental and widespread in situations where resources are
limited. We have heard this belief expressed in different ways by a wide
range of people, including business people, the devoutly religious (and
non-religious), politicians, and general public. No doubt, this belief
causes outrage, as it should. However, this outrage needs to be tempered
with the recognition that the rejection of those infected is no different
from other - more personal - behaviors. We have all done something similar
at some point in our lives, based upon an assessment of whether the other
person will contribute to our lives in the future.
For example, when a friend tells you that she or he is leaving town, and
moving to another city, many people start to withdraw immediately, prior to
the actual departure. Emotional withdrawal - some say this happens to reduce
the pain of loss - is common in all people, regardless of affluence or
poverty. However, when physical resources are limited, this effect is
magnified, and expressed in more hostile and overt rejecting behavior too,
such as expelling family members from the home. Is this extreme stigmatizing
behavior any different, or is it a matter of degree?
There are two key beliefs underlying this extreme behavior, pertaining to
HIV stigma: (a) It is believed, based upon what has been said in media and
otherwise, that everyone who is infected with HIV is going to die. In other
words, she or he is going to leave, permanently. Secondly, (b) she or he is
going to get sick at some point, which means that scarce resources are going
to be used, with no cure or recovery to justify the investment of those
scarce resources.
[4.1.2] Counteracting withdrawal of resources
We need to start to be a little more careful about how we tell people about
the dangers of HIV/AIDS:
For two decades we have been drumming the same death and fear message into
communities concerning HIV and AIDS, and we act surprised and outraged at
the stigma that emerges? We try to motivate through fear - terrifying all
and sundry about HIV/AIDS - and we don't understand why people respond with
'irrational' rejection of those infected? Why is it so strange that people
act from terror when we have told them to be terrified?
Outdated and (in our opinion) ineffective health motivation strategies have
contributed directly to the stigmatization of those infected. You may argue
that the same 'AIDS=DEATH' campaigns have emphasized that is okay to have
casual contact and so forth, but this simplistic defense does not take the
second reality into consideration, namely the utilization of scarce
resources, for no apparent benefit (for the group).
So what do we do? How do we counter this basic (and functional, from a raw
survival perspective) belief?
We suggest two strategies, both of which we have been applying with great
success in Mozambique, in our Positive Living program:
[4.1.2.1.] Instead of using fear as the primary message and motivator, focus
upon the impact of HIV/AIDS (or malaria, poverty, etc) on a desired future,
both by the individual and community. This presumes the existence of a
desired future, and if absent, the creation of one.
What we mean is that few people have any sense of future beyond the
immediate and short-term. In terms of stigma, we need to ensure that
individuals and groups can see how people living with HIV can be part of,
and most importantly, contribute to this desired future. Until this is
achieved, people living with HIV or AIDS (PLWHA's) are viewed as threats to
survival in a situation of scarce resources.
The same principle applies to effective prevention strategies: Many people
find dealing with the problems of today infinitely more real and urgent than
some unseen threat (i.e., a virus, for those few who have a vague idea of
germ theory) that apparently can kill you sometime in the distant future:
"If I do what you are suggesting (ABC prevention), I can go hungry today,
and tomorrow". This refers to fear of rejection by the group when sexual
behavioral changes are suggested, leading to absence of access to resources
such as food and shelter.
Unless we expand the awareness of personal time itself - i.e., extend the
time-line upon which decisions are based - the only emotional realities that
inform decisions and behavior will be immediate and short-term survival
considerations. In practice, this means that people need a good solid
reason - such as having a strongly desired long-term goal which necessitates
making a change - to justify taking the risks involved in changing present
behavior and relationship dynamics.
We utilize methods where people become aware of long-term (e.g., 5 years,
depending upon the individual's situation) future-related goals - which we
call the Future Dream - that is then emotionally energized through simple
process.
Our view is that life is only protected - and respected - when it is valued.
Furthermore, it is only valued when it (my life) is believed to be moving
towards something desirable, pleasurable, fulfilling. We have found that
when we do this Future Dream process first - before HIV/AIDS educations and
awareness, and before teaching immune-enhancing methods to PLWHA's - that
the presented information and methods suddenly have genuine relevance and
utility for the individual. Quite simply, it then makes sense to change
things in order to arrive at some desired point in the future.
We utilize exactly the same process for those people living with HIV, as
they are no different from anyone else in believing that they have no
future. (The issue of internalized stigma is discussed later). If we are to
teach those infected how to live with the virus successfully, we need to
ensure that they also believe that they have a future, and that there are
good things still to come, that it is still possible to live a good life.
Our perception is that the first thing to die when a person is diagnosed
with HIV, is their future. It dies in the doctor's or post-test counselor's
office. The body follows a few years later, unless the future can be opened
up again.
In this regard, it is often assumed that those infected will do anything to
stay healthy, when in reality this is not true: Many just don't bother,
because they believe there is no point. The same rationale applies to HIV
testing: What do I stand to gain (except anxiety) if I get tested? Without a
good reason - i.e., improved quality of life - what other compelling and
sustainable reason is there?
[4.1.2.2] Victims get persecuted. PLWHA's need to avoid supporting a Victim
Persona.
How often have you seen or heard an 'AIDS Sufferer' speak to an audience,
with nothing to say except how miserable they are, and how hopeless-helpless
they are? How many public 'AIDS Sufferers' cannot answer the most basic
questions about HIV and AIDS?
There is an assumption that publicly declaring your infection with the virus
somehow translates into instantaneous expertise, or entitlement for public
sympathy and support, when in fact it does not. In many ways - by virtue of
the Victim Persona presented - those who disclose their status publicly
perpetuate the belief that living with HIV/AIDS is helpless and hopeless,
which in turn supports the unstated shared belief that people living with
HIV and AIDS are simply an additional burden on a society with scarce
resources.
It is imperative that public disclosure is encouraged, but with full
awareness of the impact of such a disclosure. In order to prevent
victimization through stigma, the person living with HIV needs to ensure
that she or he does not utilize the victim image in the first place.
It is a tragic reality that victims get persecuted, once sympathy has run
out (which is fairly soon). People living with HIV or AIDS (PLWHA's) have
exactly the same responsibility as those who do not, in terms of making
efforts to contribute to the future development of the community. In other
words, PLWHA's need to pay attention to what is called 'secondary gain' -
the perception that Victim status confers special privileges and attention,
and exemption from community responsibilities. People don't like it, and
won't support it - they have problems of their own. However, when a person -
any person - is viewed as contributing to the future of the community, this
situation changes. Therefore, the helpless-hopeless 'AIDS Sufferer' image is
counter-productive in the fight against stigma.
At a broader social level, we need to focus upon discussing and formulating
a future that is desired. For example, politicians are often prone to focus
upon the ills of the system (or their opponents) without providing the
public with any vision for the future.
In the business arena, greater emphasis needs to be placed on how managing
the disease - getting involved in taking care of the health of infected
employees - is much cheaper than simply ignoring it, and paying the price in
terms of lower productivity, absenteeism, sick leave, and so forth.
The essential recommendation of the above is that, regardless of HIV status,
communities will reject and eject members who are considered a
non-productive, non-contributing burden to that group. The exception is the
elderly, who have already made their contribution, and very young children,
who do not yet have the capacity to contribute. Therefore, one aspect of
reducing stigma is for PLWHA's to earn the respect of others through
engaging in a productive life, and not wallowing in 'sufferer' or 'victim'
sympathy-seeking roles.
[4.1.2.3] Focus upon the possibility of living with HIV, versus dying from
AIDS.
This sounds very similar to the previous item, namely focusing upon a
desired future. However, there is a slight - but important - difference in
emphasis: In the previous item, the focus was upon working towards a life
that is desired, whether that life is five years or twenty years. In other
words, its' focus is the quality of life, regardless of the quantity of
life. In the second item, the focus is upon quantity of life. I.e., what
can you do to live longer? This includes advocating for better medical
treatment, changing your diet towards immune-supporting nutrition, and
attitudinal shifts that support longevity. The likelihood of a PLWHA in
acting to increase the quantity of her/his life is not high unless the first
item - increasing the potential quality of life (the why bother?'
question) - is first addressed.
At a social and community level, it is critical that people hear and see
that (a) it is possible to live well with HIV, for many years, if certain
actions are taken; (b) that the infected person can - and will - add to the
collective resource base for a long time, if she or he is supported in
staying healthy. In other words, don't expect people to care about you if
you do not care about yourself.
In many profound - and largely unconscious - ways, the perception that there
is a possibility of an improved quality of life for all involved - real
benefits - when supportive (versus stigma-based) behaviors are engaged, will
go a long way to addressing some of the deep-seated beliefs that a person
living with HIV is a burden to the group, and who needs to be ejected from
the group if the group is to survive.
[4.2] Belief 2: "HIV/AIDS is a punishment for sin".
Whether we like it or not, no matter how principled and objective we try to
be, we cannot escape the reality that many of the most fundamental
components of our internal and external social interactions, laws and other
infrastructures, are rooted in religious beliefs. Even those who claim to be
agnostic or atheist, cannot escape from the socialization of these beliefs
through education systems, the very words we use to explain our reality
(right/wrong, good/bad), laws, and so forth.
There is not a single society that does not have - either explicitly or
implicitly - a value system based upon some dogma, whether religious or
otherwise. This does not mean that the dogma is good or bad - it simply
means that it exists, and needs to taken into account.
[4.2.1] The need to blame-shame-punish
One of our most basic social beliefs is that, when 'bad' things happen,
something caused it. Whether this is because we assume the power to cause
these things to happen, or whether it is because of some mystical process
(when it is called 'sin'), we need to blame someone or something. Blame is
a very powerful social force. From blame comes shame, and from shame comes
the need to punish, to alleviate the shame.
When we tell people that if they do certain things they can get infected, it
is automatically assumed - usually by all concerned - that it was their
'fault' that they became infected. The word 'fault' is used carefully here,
not to mean the same as responsible/response-able.
Any HIV/AIDS educator will tell you - with amazement - how audiences seem to
have an absolute fixation on where AIDS comes from. It appears bizarre -
here you are, ready and willing to tell them how to protect their lives,
their future, their children, and all they want to know is where on earth
this disease comes from, and insist on spending valuable time on the
subject. When you say that genetic tracing of the virus shows that it
originated in specific areas of Africa, there is shocked outrage, and the
most irrational attempts to reject what is considered objective scientific
fact. This is not only from the average person - this rejection and
outrage - it also comes from those who are supposedly highly educated too.
Why? Because, as mentioned before, there is an urgent and powerful need to
ascribe blame and shame on whomever is at 'fault'.
Why do we use the word 'fault', versus 'responsible'? Because the word
'fault' (or 'blame') more accurately describes the emotions and thoughts
involved. The words 'fault' and 'blame' imply that something 'bad', 'sinful', 'wrong' has happened, and that someone needs to be punished for it. In
common usage, the words 'fault' and 'blame' are never used to describe 'good
' things or behaviors, only 'bad'. In contrast, the word 'responsible' is
used to describe 'good' things as well as 'bad' things, such as "Who is
responsible for this lovely dinner?"
Have you ever wondered why it is possible to cause national outrage and
reaction to the abuse of 20 young elephants (refer M-Net's Carte Blanche
exposé a few years back, which resulted in the largest national
post-apartheid protest response recorded), but it seems to be mission
impossible to get widespread public support for the plight of hundreds of
thousands of child-headed households (AIDS orphans)? It is a very useful
exercise to ask people .
The response we got was simple: Animals are innocent, people are not. With
people, someone can be blamed, which absolves us from any responsibility to
help. Case in point: There was a report several years ago, that a terrible
storm caused an oil ship spilt it's oil on the beaches of Cape Town, causing
major catastrophe with the penguins population. At the same time, there was
a terrible fire that swept through a large informal settlement, leaving
thousands of people destitute. There was only enough money in the city's
treasury to deal with one of the two disasters. They chose to save the
penguins. Some people may find this amusing, but it illustrates the
deep-seated belief we seem to have that, when it comes to 'bad' things,
someone is to blame, and they need to pay the price. We seem to only have
compassion for those we consider innocent.
[4.2.2.] Internalized stigma
It is incredible that, with so many people living with HIV, that so few
openly protest against stigma. We joked a few years back that, if we were to
start a political party only for those infected with HIV, we could win the
next election. That is not going to happen, simply because the overwhelming
majority of those living with HIV feel that their infection is their 'fault'
, and that they are to 'blame', and that they need to be 'ashamed'. Those
that refuse to accept the 'blame' tend to try to blame someone else, which
is probably the basis of 'revenge' infections. Regardless, the behavior is
based upon blame/shame, which in turn is based upon the belief that 'bad'
things need to be punished.
We are not sure where this fault/blame/shame phenomena is strongest -
society, or those infected. It is probably evenly spread, with the one
sector merely feeding and supporting the other in a dependant symbiotic
manner.
[4.2.3] Shifting the blame-shame-punishment to those who stigmatize others
Most people accept this cause-effect (blame-shame/punishment) belief,
including many of those who fight stigma or who care for those infected. We
need to be careful about merely shifting the blame-shame-punishment of
stigma, to those who stigmatize others. This merely perpetuates the problem.
The need to 'fix' stigma through 'punishing' those who blame/shame others,
is no different than trying to 'punish' murder by hanging. Capital
punishment serves no functional purpose apart from making us feel
self-righteous and in control because we have had some form of revenge,
despite the fact that there is no evidence at all that it actually reduces
the incidence of murder. It just does not work as a deterrent. That's why
the South African and Mozambican Constitutions are against capital
punishment. In the same way, we cannot counteract stigma by committing the
same 'crime' to prevent it. We need to offer an alternative solution: Laws
and policies should - ideally - support a shared ideal and/or value system,
and not be a band-aid measure to control something we don't understand.
[4.2.4] Blaming and shaming the PLWHA
The issue of blame-shame-punishment is not unique to HIV/AIDS. Rape
survivors have been blamed-shamed-punished by courts and the public for
decades, because people seem to need an explanation of why things happen to
people, that is controllable. For example, there is a belief that if we can
pin-point that what a woman was wearing contributed to her being raped, then
we can prevent rape by not wearing the same clothes. At the same time, this
means that she was to blame. We feel safer, and blame-shame-punishment has
occurred. The fact that rape is an act of violence, that the motivation for
rape has nothing to do with sex, age, or what someone wears, and has instead
got to do with the need to express power and dominance due to deep-seated
inadequacy, is ignored in this blame-shame-punishment of the rape survivor.
In a similar dynamic, PLWHA's are blamed and shamed for being infected with
a virus. There is intense curiosity regarding how they got infected, and
any detail that will (a) highlight the difference between the observer and
the PLWHA, and (b) identify behaviors that allow the observer to blame the
PLWHA for getting infected in the first place. This process allows the
observer to feel as if HIV infection can be controlled.
[4.2.5] Counteracting blame-shame-punishment
So where do we begin in the process of eliminating blame-shame-punishment?
We would imagine that the first place to look is why we seem to need this
process, in terms of maintaining a sense of coherence in our world-view. In
other words, we all need to be able to understand how things work in our
world, in terms of cause-and-affect, so that we can do what needs to be
done, and take responsibility for what we do. We simply cannot allow entropy
(decline of order into chaos) to happen - it is in our nature to create
greater order, not less. The exception is when a system is so dysfunctional
that we need to destroy it because it cannot be rehabilitated. However,
even this destruction is viewed as a means to an end, with the end being a
more ordered and functional system (defined according to some belief or the
other). This is how wars are justified.
Our legal systems represent how we attempt to define and structure
cause-and-effect and responsibility in our behaviors. Prior to the 1960's,
the emphasis was upon individual 'blame'. There was little scope for
mitigating circumstances. Then, with the advent of Behaviorism (a school of
psychological theory that basically said that the only thing that was 'real'
, was behavior - thoughts were irrelevant), social influences (conditioning)
rose to the fore, and we started to examine how a person's childhood
influenced later behavior. This continued for many years, and reached a
climax in a famous case where the defense lawyer persuaded the jury that a
murderer had no option - based upon his childhood influences - but to murder
the victim. In other words, the murderer had no free will - everything was
determined through socialization. The judge agreed, but with a very
important twist: If this was true, then society was to 'blame'. As the jury
was the representative of society, he sent the jury to prison! As you can
imagine, people - especially juries - were a little more careful about
placing the 'blame' entirely on external influences.
It is probably a good time to introduce religion at this point, as the
various religions of the world have had a fundamental and profound influence
in the understanding of 'blame', what causes 'bad' things to happen, and how
we should respond to this. However, when you add religion to sex (and HIV is
after all a sexually-transmitted disease for most people in the developing
world), you get a rather heated debate that is rarely rational. If we may
summarize:
(a) Sex is 'bad' and punishable unless sanctioned by the representative
of the religion (i.e., marriage); Therefore, HIV/AIDS is somehow a
punishment for some or other sexual 'sin'; "You see - we told you so!"
Therefore, HIV/AIDS is viewed as the physical proof of 'sinful' sexual
behavior. So why should this matter?
(b) It matters because people want to go to Heaven. For many people,
peace, joy, and fulfillment are not possible in their physical
circumstances, nor can they see this as being potentially possible. So they
don't try to get it 'here', and they seek it 'there', with 'there' being in
Heaven. And guess who controls the security access codes to Heaven? Yes, the
moral authorities - the same ones who say sex is a sin, and HIV/AIDS is
proof of sin.
We need to make it abundantly clear that we are fully aware of the
incredible work and compassion displayed by many people from all religions,
including in the area of HIV/AIDS. It has been our observation that these
people focus their values and beliefs upon love, compassion, forgiveness,
and that they do not place much energy or time on blame-shame-punishment.
They are too busy making a difference to engage in dehumanizing activities.
[4.2.5.1] Challenging Victim Theology
The root of value-based blame-shame-punishment is fear - fear of being
worthy enough to be accepted and loved. This applies not only to their
relationship with God, but also to other people.
A good friend - and Methodist Minister - refers to the emphasis upon
blame-shame-punishment in dealing with people living with HIV as 'Victim
Theology'. He suggests that we start to focus upon a theology of self-worth,
love and compassion. For those that find that inconceivable, it is not too
difficult: Historically, theologians have selected segments of text to
support the prevailing power focus, such as males being superior to females.
Text that contradicted such preferences was de-emphasized as being of only
'historical' relevance. For example, most of the 'abominations' in the Old
Testament were discarded as being of 'historical' interest only, except for
one or two which supported the interests of the prevailing power elite.
However, this is not a discussion on religion, and the purpose of the above
is to illustrate the pliability of religious dogma according to the
priorities of those who purport to represent such values and dogma.
We cannot ignore the reality that the majority of the population in the
developing world has a strong and enduring religious value system, whether
this is Muslim, Christian, or traditional animist. We also cannot ignore the
fact that these systems of belief have a powerful influence on
stigmatization, including internal stigmatization by those infected.
To ignore this reality, we not only ignore probably one of the key areas to
deal with stigma, but we also set aside one of the most widespread resource
infrastructures in dealing with the consequences of HIV/AIDS, such as
home-based care, caring for AIDS orphans, prevention, and a myriad of other
issues.
Therefore, an important recommendation in dealing with stigma is to
encourage/challenge organized religion to not only examine their emphasis on
blame-shame-punishment (versus compassion), but also to do so actively and
publicly.
[4.2.5.2] Political vision and leadership
Another important area is within the political arena: Politicians need to
spend less time reacting to each other, and spend more time creating a
vision for a better world, and then earn their keep by making this a
reality. It is perhaps time that we start asking ourselves why people do not
resist death too strongly, and why people are so willing to accept blame and
shame for merely having a virus in their blood. Leaders need to engage the
task of stigma directly, by simple actions such as publicly embracing those
living with HIV.
Not too many years ago, the leader of a political party in Gauteng died of
what was rumored to be AIDS. The party leadership issued a statement denying
this. However, what was shocking was that the reason they wanted these
rumors to end was that it 'shamed' the party and the family of the deceased.
The same party strongly advocates against stigma.
This is not too dissimilar to a charity event where a woman living with HIV
publicly announced her status to the crowd, in an effort to overcome stigma
in the community. The political representative of the area had wonderful
words of encouragement to the crowd, congratulating her on being so brave.
As he embraced her - on the stage - he whispered into her ear "How could you
shame you family and community like this?!"
These examples illustrate the often-superficial platitudes and attitudes of
leaders in our countries. They have not dealt with the core beliefs they
hold.
[4.3] Belief 3: "It's the way we do things"
I.e., culture and tradition presented as enduring facts that should not be
questioned.
We were doing a talk a few weeks back, and during the question-and-answer
section a woman - who had taken a cell-phone call while we were speaking
earlier - raised her hand and said "It is not in my culture to discuss sex
with my children". Our response was: "It's also not in your culture to carry
a cell phone, but you've adapted to that with great ease."
The previous story illustrates an important quality of culture: It's about
convenience and increased survivability (functionality). At first, there is
skepticism, but if it works, it soon becomes "What we do".
Culture and traditions include a wide range of behaviors and activities,
including language, dance, rituals, how we deal with illness and death, and
the regulation of relationships, gender roles, and sexuality.
[4.3.1.] Can - and should - culture be protected from change and evolution?
In recent years there has been an enormous amount of energy directed at
protecting 'culture'. This is based upon the value of respecting diversity
and differences. However, protecting a culture or tradition is a two-edged
sword: On the one hand you preserve unique qualities of a group of people,
and on the other hand such protecting can reduce the flexibility of that
group in the face of change, thus reducing their ability to survive.
Historically, there is not such thing as a culture or tradition that arrives
spontaneously, and endures unchanged. This is simply because cultures and
traditions were born out of specific situational necessities, and endure
only as long as that necessity continues. The very moment that the need
changes, the tradition ceases to fulfill any survival function.
It is also important to realize that every tradition serves specific groups
more than others, and will be protected by those whom it serves most. It is
at this point that self-interest interferes with the interests of the group
as a whole. Gender roles is a case in point: Women stand to gain a great
deal from equality in practical reality, while men perceive this as a real
threat to their power. When resources are scarce, this becomes very
difficult, as there is not a lot to share equally.
Cultural traditions and norms are also comforting: They provide a sense of
identity and belonging. When situations become difficult, it is reassuring
to know that you know "what people like us do" in such circumstances, even
if the methods are no longer effective.
The harsh reality is that you cannot effectively protect a culture or
tradition. This is guaranteed to cause harm to the people it is supposed to
serve, in the long term. The reason is simple: Change is the only guaranteed
reality, and this requires adaptation and flexibility. Languages come and
go, as do all other cultural behaviors and norms. The way that they change
is revealing: When a norm is no longer functional, those that hold on to it
die out, while those that change, survive. The only way to allow some
language or tradition to survive is incorporation into a newer tradition or
language.
[4.3.2] Cultural evolution as a method of group survival: The danger of
ethnocentric strategies
The direction of this 'survival of the fittest' is not always obvious or
anticipated, and people find ways to adapt in unique ways, thus ensuring
continued diversity. What is important to note about this 'survival of the
fittest' process, is that it is geared to the survival of the group, not the
individual. People do what they have to do to survive - collectively -
according to their resources and situation. To assume that a group that is
different from yours must do it your way is called ethnocentricity.
Social responses to HIV/AIDS prevention strategies in the developing world
are a classic example of this. This example will no doubt will stir up
controversy, which is an excellent manner to force unspoken beliefs to
surface for identification and clarification. We present this explanation
for the failure of specific types of prevention methods as the basis for
debate, not as a definitive 'answer' or point of view.
The developed world believes that people in developing countries have the
same system of survival: In the more affluent developed world, the sick,
the young and the elderly can fall back on the welfare system, funded by a
taxed society. In the developed world, the priority is therefore to ensure
economic growth, employment, and the consequent adequate tax-derived funds
to ensure that the support system continues.
However, in the developing world, this type of economic welfare 'safety net'
largely does not exist. Instead, the family - nuclear and extended -
provides such support. In the developing world, the continuity of the
support system depends entirely upon procreation, to ensure that there are
enough children to provide support when you get old or ill.
It is therefore - according to a developed world perspective and realities -
logical and 'factual' that condoms will (and should be) the primary form of
HIV prevention, as it not only does not interfere with the (economic)
support system - it is relatively cheap - but it also ensures that the
system continues into the future, by reducing the (costly) illness burden on
the system. You will notice, for example, that in most debates and
discussions regarding medical treatment or prevention strategies, that there
is a great deal of focus upon the economic costs of the proposed options.
However, from a developing world perspective, condoms directly prevent the
continuity of their support system - children and procreation - by
preventing conception as well. The greatest obstacle to convincing people to
wearing condoms in the developing world is "How can I have children if I
always wear a condom?" Good question . find an workable answer to that one,
and we may have a solution to ensuring the continuity of the support system,
and preventing HIV infection. Until we solve that dilemma, people are going
to have sex without a condom.
For those who dispute this - and we are sure there will be many - we suggest
that you look at the Ugandan experience, often touted as an example of how
the other forms of prevention (be faiuthful to your partner, delayed onset
of sexual activity for young people) can produce effective results. In
Uganda, condoms were a minor component of the prevention strategies that led
to declines in infections.
Before the outrage begins, let us state clearly that we believe that condoms
are indeed a critical component of prevention, especially in high-risk areas
such as commercial sex and pre-marital relationships. However, based upon
the evidence, we have not seen condoms make a dent in infection rates
anywhere else. This is not because we do not support condom usage - it is
because many people won't use them, no matter how much we have supported
their use or made them available. Perhaps condoms would be viewed as a
viable prevention method if economic and social systems were different? We
don't know.
However, this discussion concerns stigma, not prevention. The point of the
above example is that we often make fundamental assumptions without thinking
about them.
[4.3.3.] Tell the whole truth, and trust cultures to deal with it
One of the only forces that we can rely upon to encourage communities to
adapt to the new realities of HIV/AIDS, is a full awareness of those
realities. However, we are not referring to the bland intellectual type of
awareness that most people associate with 'awareness'. Awareness does not
come from statistics or posters.
Instead, we refer to direct awareness of the realities of HIV/AIDS,
including all the gory details. Social change unfortunately is usually
motivated by pain. For as long as society can hide the pain, change tends
not to happen.
Many countries missed a critical opportunity to promote prevention in the
early years of the epidemic, because the leadership was afraid of spreading
panic. They were afraid of the economic consequences (e.g., investor
confidence, tourism) if the general public saw what AIDS really looked like.
For this reason, certain public broadcasting stations had a policy of not
showing any person with AIDS-related illness. It was kept hidden and
sanitized. They reckoned that they convince the public to change their
behavior through reason and information alone. This failed, predictably.
[4.3.4] Stigma burn-out as an inevitable stage in the pandemic
Communities will continue to stigmatize those infected until such time as it
can no longer function without those infected. In other words, until there
are simply too many people to hide away, and until those infected - and
others knowing that that they are infected - are filling important and
valuable roles in society.
This is not a theoretical concept: In almost every country affected by
HIV/AIDS, stigma has endured until there were simply too many people
infected or ill to ignore. Then, when the realities are so huge, the society
undergoes a 'stigma burn-out', which is a process of giving up on trying to
deny what is really going on.
[4.3.4.1] Accelerating stigma burn-out
How can we accelerate this 'stigma burnout'? I.e., how can we short-circuit
this process of denial, so that the stigma ends sooner?
One of the primary methods is for people to see and know the truth of what
is going on. This means greater emphasis upon HIV testing, and greater
public profiling of people living with HIV, both healthily and with
illness - the whole range. People do not respond to abstracts, nor to
statistics. They respond to real-life reality, which affects them directly.
We need to increase our capacity for HIV testing, and we need to strengthen
the benefits of getting tested (discussed earlier). As things stand right
now, a tiny fraction of those infected actually know about it, and with the
current facilities, this is not going to change much.
Once we have a more realistic view of HIV/AIDS - from a public perspective -
we need to allow various cultures to adapt to these realities, as they have
done in the past. Yes, there will be resistance, but on a whole people will
find solutions. None of this can happen if they do not know - see, hear,
touch - the realities that threaten their survival.
[5] Conclusions
In conclusion, stigma is in essence one of two things: The onset of a Dark
Age of fear, pain and social fragmentation, or the opportunity for a
Renaissance - a revival of a new social order, based upon greater compassion
and understanding. The only way to head off this potential 21st century Dark
Age is the open questioning of what we hold to be true in our cultures.
In order for us to be effective, we must challenge people's core beliefs. We
have spent 20 years trying to fix everything except what really needs to be
fixed. We are addressing everything except our core beliefs, and yet it is
these very beliefs that are creating the problem.
There is only one solution, if we hope to make any difference at the social
level. We must challenge people's beliefs. When we can do this, we can then
make a real impact on stigma, discrimination, gender inequity and a range of
other social issues. What are those values we want to share? How do we want
to live? Unlike past generations, we cannot say "For my children I want ."
If we wait and delay, it will be too late. This time, we need to start with
"For me, and my children, I want ."
It is small comfort to those infected who have been stigmatized to know that
there is a larger social process which is occurring, and that at some point
things change for the better. However, this is how it happens in every
society. Therefore, continue to challenge the fear and ignorance - fight
with understanding, knowing that you are helping to accelerate the larger
process. However, always remember that the change starts with you - your
beliefs about yourself. Question these beliefs, and then you have earned the
right to challenge the beliefs of others.
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