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‘The first human rights legal resolutions
did not address rights of mental health consumers’
A paradigm shift is perceived
as having occurred in mental health in the latter half
of the 20th century. It is attributed to three factors:
the strides made in psychopharmacology, with the discovery
of new classes of drugs; the human rights movement,
which became an international phenomenon under the sponsorship
of the United Nations; and efforts to incorporate the
mental component into the concept of health, spearheaded
by the World Health Organisation.
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Health & Human Rights Adv Kamayani
Bali Mahabal
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The first human rights legal
resolutions, such as the 1948 Universal Declaration
of Human Rights, did not specifically address the rights
of mental health consumers.
They codified more general,
but still relevant, rights like the right to life and
liberty and the right to be free from inhuman, degrading
treatment.
Later resolutions, such as
the Declaration on the Rights of Mentally Retarded Persons
(1971) and the Declaration on the Rights of Disabled
Persons (1975), began the process of establishing international
minimum standards for the treatment of persons with
mental disabilities.
In the last decade, the field
of human rights took a big step forward with the adoption
of several new human rights resolutions specifically
addressing mental disabilities. In 1990, the Pan American
Health Organisation adopted the Declaration of Caracas,
which called upon nations to take specific actions to
protect the rights of people with mental disabilities.
The Declaration of Caracas
stated that mental health systems relying exclusively
on psychiatric hospitals isolate patients from
their natural environment generating greater social
disability and called on states to promote
alternative service models that are community-based
and integrated into social and health care networks.
The World Health Report (2001)
advocates, for instance, a recognition of the interconnectedness
between physical and mental health, and seeks spaces
in policy, law and resource commitments, which have
been the near-exclusive preserve of physical health
so far. It calls for an integration of mental health
care into the primary health care system and makes a
pitch for a public health approach.
Emphasising the burden of mental
and behavioural disorders, it advocates an altered paradigm
of care. The principles of care pertain to diagnosis
and intervention, continuity of care, provision of a
wide range of services, partnerships with patients and
families, the involvement of the local community and
integration into primary health care. Pharmacotherapy,
psychotherapy, psychosocial rehabilitation, vocational
rehabilitation and employment, and housing have been
identified as the ingredients of care relevant to those
experiencing an absence of mental health.
The Indian experience with
institutionalisation has not been edifying. A report
prepared for the National Human Rights Commission (NHRC)
in 1999 after an empirical study of mental hospitals
in the country made a damning indictment of the state
of mental health institutions. The findings reveal
that there are predominantly two types of hospitals,
the report said.
The first type do not
deserve to be called hospitals or mental
health centres. They are dumping grounds
for families to abandon their mentally ill member, for
either economic reasons or a lack of understanding and
awareness of mental illness.The living conditions in
many of these settings are deplorable and violate an
individuals right to be treated humanely and live
a life of dignity. Despite all advances in treatment,
the mentally ill in these hospitals are forced to live
a life of incarceration.
The second type of hospitals,
the NHRC report continues, are those that provide
basic living amenities. Their role is predominantly
custodial and they provide adequate food and shelter.
Medical treatment is used to keep patients manageable
and very little effort is made to preserve or enhance
their daily living skills. These hospitals are violating
the rights of the mentally ill persons to appropriate
treatment and rehabilitation and a right to community
and family life.
Although the exact number of
disabled people in India is still not known, the 2001
census findings will provide the first accurate figure,
it is estimated at five per cent of the population,
as is the case worldwide. This makes for a whopping
50 million.
The conditions of persons with
mental illness in institutions have been cause for human
rights concern. In Gwalior Mental hospital, for instance,
it was found that persons with mental illness were left
in nakedness; the explanation was that they tore their
clothes if they were given them. The press raised the
issue. Chaining of mentally ill patients was also a
practice, and this was outlawed by an order of the court.
There is accumulating evidence of the high levels of
disability that is imposed by mental illness.
Forty-three per cent of the
disability in developed countries is, for instance,
due to mental illness. If it is lower in other parts
of the world, that is because of the heavy burden that
other illnesses, such as Aids (in Africa) impose. Disability
Adjusted Life Years (DALY) is an evolving index that
helps to quantify the burden of disease. Of the 20 conditions
identified as leading causes of disability adjusted
life years, three are related to mental illness, according
to WHR 2001.
One of the most recent international
developments regarding disability rights is the formation
of an Ad Hoc Working Committee on the proposed United
Nations Convention on the Rights of People With Disabilities.
This proposed Convention was the context for the examination
of disability at the seventh annual meeting of the Asia
Pacific Forum of National Human Rights Institutions
(APF).
For the meeting, the New Zealand
Human Rights Commission requested that the subject be
included on the current agenda so that the APF may contribute
to the possible formation of this new international
human rights treaty.
In contrast, Indias Persons
with Disabilities (Equal Opportunities, Protection of
Rights and Full Participation) Act, suffers acutely
from vague terminology and the absence of a supporting
framework. The Act includes provisions for access to
education, government employment, and state-funded public
infrastructure such as transportation and hospital facilities.
However, it does not contain
adequate provisions for an effective monitoring system
and undermines state directives with the qualification
that they shall be undertaken within the limits
of [the states] economic capacity.
Each State should have a Mental
Health Authority but most do have it. For the mentally
ill, absolute human rights can only be guaranteed within
an ideal political and social order.
The consequences of change
in this environment have to be understood from a health
perspective and the availability of effective mental
health-care needs to be assured.
It could be argued that when
one is dealing with health-care there is no ground for
debates surrounding justice and what is a right.
Rather, one is dealing with
someones health and care of the individual and
how best to do this. The position held is that the rights
of the mentally ill can only be attained or understood
if it is acknowledged that the context within which
one lives is crucial to the distribution, enforcement
and understanding of these rights.
The translation of rights for
the mentally ill ultimately entails the provision of
human and material resources that require enormous financial
expenditure. This corresponds with a view that considers
the fact that rights have a social or economic value,
and that social constructs used to administer these
rights are limited in supply.
From a humanitarian perspective
the right to mental health-care should not be limited.
However, reality dictates that such care is compromised.
In India there exist many areas, such as health and
education, which have been grossly neglected and require
urgent attention.
(The writer is with Centre for
Enquiry into Health and Allied Themes (Cehat). email:
kamayani@cehat.org)
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