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        by YANGGA TREPPE and PATRICK WAMBUA
    AIDS stigma, the stumbling block

IN the 25 years since the first case was reported, AIDS has changed the world.
The disease has killed 25 million people and infected 40 million more.
It has become the world’s leading cause of death among both women and men aged between 15 and 59.
It has inflicted the single greatest reversal in the history of human development. In other words, it has become the greatest challenge of our generation.
In Papua New Guinea, as the number of infections continues unabated, stigma and discrimination remains a formidable challenge to prevention, care and treatment initiatives.
HIV/AIDS-related stigma and its associated discrimination affect all aspects of HIV prevention, diagnosis, treatment and care.
HIV thrives in an environment of ignorance and erodes social support for infected people, which is access to information, support groups and economic and legal services.
Reducing stigma and discrimination is crucial to the success of HIV/AIDS treatment programmes, as the quality of such programmes can and do depend on the degree at which health centres and hospitals welcome and respect the rights of the individuals.
One lesson we have learnt in the Tokaut Aids Project is that stigma and discrimination promotes the culture of silence – people fear to talk about AIDS, let alone disclose that they or a relative has AIDS.
Stigma, silence and discrimination and denial, as well as lack of confidentiality, contributes to a climate of fear. This undermines prevention, care and treatment efforts and further increases the impact of the epidemic on individuals, families, communities and PNG as a nation.
Stigma and discrimination views HIV as a disease of outsiders, which leads to exclusion from the community. This exclusion in turn engenders lack of involvement and social inaction, leaving individuals sheltering behind a wall of silence and preventing the social mobilisation that has proved the most effective tool in fighting the epidemic.
As a consequence, due to HIV/AIDS-related stigma, appropriate policies and models of good practice remain undeveloped. Hence, people living with HIV/AIDS continue to be burdened by poor care and inadequate services, while those with the power to help – Government, development partners, etc, – do little to make the situation better.
The impact of stigma on the affected individual can lead to depression, guilt and shame, as well as to behaviour that limits participation within communities and access to services intended to assist them.
HIV/AIDS-related stigma constantly reminds members of the discriminated groups that they are social outcasts or even deserve to be punished.
If people are mocked or treated with hostility, they may feel uncared for and are therefore less likely to take steps to protect themselves.
HIV/AIDS-related stigma and discrimination is a major obstacle to effective prevention and care for it can prevent governments (national authorities) from getting a true picture of the burden of the pandemic because people are not coming forward for testing, care and support.
This compromises planning, allocation of resources and provision of services to people with HIV and for people from other highly vulnerable groups.
Stigma and discrimination hinders prevention interventions by fostering ignorance about facts on HIV.
HIV/AIDS-related stigma discourages people to get tested or when they get tested, from returning for their test results.
Some avoid clinics known to be testing for HIV.
Others believe that the fact that they have been tested it will eventually reach the rest of the community.
Self-stigmatisation leads one to police his/her behaviour hence withdrawing from community and available services.
The fear of being stigmatised results in women, men and young people being unable to look after their sexual and reproductive health – accessing sexual health information, treatment and methods for HIV and STI prevention, such as the female condom.
Some infected individuals may choose not to change or adapt their behaviour to reduce the risk of HIV/AIDS transmission for fear that such a change would arouse suspicion and stigma.
Stigma by health-care providers – APOs, nurses, doctors – impacts on access to treatment in health centres and hospitals.
Some medical workers, in an attempt to avoid having contact with people living with HIV/AIDS or provide care, pass patient from one hospital to another.
Stigma and discrimination has made the medical management of HIV and AIDS very stressful despite efforts to create more awareness.
Social stigmatisation of the disease frustrates efforts to apply the most effective medical interventions in the management of HIV and AIDS, ie, counselling, testing and treatment.
It causes individuals to shy away from tests hence treatment is delayed or not received at all.
Delayed treatment can contribute to the continued spread of disease because people do not know their status.
As a New Year gift to our affected and infected brothers, sisters, wantoks, mothers, fathers, let us make a commitment to say NO to stigma and discrimination to people living with HIV and AIDS.

*The writers work with VSO Tokaut AIDS project in Madang.


       

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