Rationale
Of about 1.2 billion
young people worldwide (between the ages of 10 and 24), 11.8 million
are currently estimated to be living with HIV/AIDS Every year it is
estimated that over 2.6 million young people contract the virus through
sexual route or through injecting drug use. In recent years, over half
of all new HIV infections - about 7000 every day - are among youth aged
15-24 the same age group that also has the highest rates (111 million
cases in this group every year) of sexually transmitted infections (STIs)
. That is why young people are, and must be, at the center of action
on HIV/AIDS.
Silence, taboos
and myths often surround HIV/AIDS because it is associated with private
and intimate behaviors. In this context, many factors may restrict young
people’s full enjoyment of human rights and leave them particularly
exposed to HIV/infection or vulnerable to needles suffering, if they
are infected.
Asia is the home
of 63 per cent of the world’s youth population. A majority of
these adolescents and youth do not have access to information on the
manifestation, causes, transmission, prevention and management of STDs/STIs
including HIV/AIDS.
In 2001, 600000 newly infected were children and 500000 had died. Approximately
half of all people who acquire HIV become infected before they turn
25. As the majority of people living with HIV/AIDS are living in the
developing world, the majority of children and young people infected
are living in the developing world. If HIV prevention in this huge population
fails, developing countries will have to face the staggering human and
economic costs of vast numbers of adult AIDS cases.
Increasingly, young
people are being appreciated as a force for changing the course of the
epidemic. They are responsive to HIV prevention programmes and are effective
promoters of HIV prevention action. Investing in HIV prevention and
networking among young people is likely to contribute significantly
to a more sustainable response to HIV/AIDS.
Why
focus on discrimination and stigmatization?
Stigma at societal level can lead to silence and denial - a refusal
to acknowledge and deal with HIV/AIDS. This reinforces ignorance and
fear, allowing prejudice to thrive, risky behavior to go unchanged and
uncaring behavior to go unchallenged. It also ensures that people living
with HIV/AIDS and their families remain silenced and sidelined.
HIV is heavily stigmatized
in most societies, even though this behaviour is clearly irrational.
People who are infected are rejected and scorned because social prejudice
against the disease runs so deep. In some cases, people are stigmatized
simply because of suspected association with HIV, or vulnerable individuals.
Stigma and discrimination
are of concern to AIDS programmes for two main reasons. First, because
they can make life unbearable for those living with the disease. Secondly,
because they affect prevention and care efforts. People who have been
exposed to HIV through their behaviour or that of their partner may
be unwilling to be tested or to change their behaviour in any way for
fear of being suspected of being HIV-infected.
If they are indeed
infected, they may continue to spread the virus and will not accept
to access adequate care. There are many ways that stigma can undermine
prevention and care efforts. HIV-positive women may know that breast-feeding
carries a risk of transmitting the virus to her infant, for example.
But she my refuse alternative feeding methods (even when they re provided
at no cost) because bottle-feeding will brand her as HIV-infected and
carry the risk that she will be thrown out of the family.
Where stigma is high, people may avoid an HIV test that could provide
an entry point for necessary care and support. Active discrimination
has consequences for prevention too. If a person is fired from their
job because they are HIV-infected, they may have to resort to survival
strategies such as selling sex, which further fuels the epidemic.
Addressing stigma
and discrimination is a commitment made at the United Nations General
Assembly on HIV/AIDS in June 2001.
“Stigma,
silence, discrimination and denial, as well as lack of confidentiality,
undermine prevention, care and treatment efforts and increase the impact
of the epidemic on individuals, families, communities and nations (Paragraph
13).
“By
(the year) 2003, (nations should) ensure the development and implementation
of multi-sectoral national strategies and financing plans for combating
HIV/AIDS that address the epidemic in forthright terms; confront stigma,
silence and denial; address gender and age based dimensions of the epidemic;
(and) eliminate discrimination and marginalization’ (Paragraph
37)
“By
(the year) 2003, (nations should) enact, strengthen or enforce, as appropriate,
legislation, regulations and other measures to eliminate all forms of
discrimination against, and to ensure the full enjoyment of all human
rights and fundamental freedom by people living with HIV/AIDS and members
of vulnerable groups, in particular to ensure their access to, inter-alia,
education, inheritance, employment, health care, social and health services,
prevention , support and treatment, information and legal protection,
while respecting their privacy and confidentiality; and develop strategies
to combat stigma and social exclusion with the epidemic’ (Paragraph
58). |