Ahmed Yar's home | Saad Sarfraz Sheikh
Husain claims to have taken another important step as well: an AIDS centre has been set up at the DHQ hospitals where “a psychologist, a woman medical officer and a laboratory technician” are especially posted to take care of those suffering from HIV/AIDS. “[It] is functional and we are already doing tests here,” he says. Later the same day, situated next to the gynaecology ward, the centre is found locked.
Local residents are not satisfied with the government’s moves. For one, they want the results of the PCR tests revealed. “If HIV/AIDS is not prevalent in the village then why has the government been holding back test results for the last four months,” questions Shahid Yaqoob, general secretary of Chiniot Press Club. “Give the patients their reports and tell them that they do not have AIDS,” he asks of the officials.
When informed about persistent public demands for making the results of the PCR tests public, Husain discloses that the government is not doing so because HIV is a socially sensitive disease.
In Yaqoob’s opinion, there is another reason why the authorities are concealing the results. District administration officials want to ensure that “they are not held responsible” for letting a healthcare crisis develop right under their noses, he says, but insists that people will remain sceptical as long as the government is in denial. “Hiding the problem will not help the villagers.” Openness, on the other hand, will assist the authorities in preventing further spread of the disease, he believes.
Mazhar Qayyum, who runs the school near Bhattiwala, holds similar views. He wants the district administration to acknowledge the prevalence of the disease and send its representatives to public and social gatherings such as weddings and funerals to create awareness. People in general and medical practitioners and barbers in particular need to be educated on how HIV/AIDS and hepatitis C is spread and how their refusal to use a new needle or blade per person is a major reason for the prevalence of these deadly medical problems, he says.
He mentions the elderly people in his village, mostly uneducated, who often ask, “What is this disease? We have never heard about it before.” Convincing them to acknowledge the presence of HIV/AIDS among them, as well as making them understand the urgent need for its treatment, is a task that the government’s routine moves will never accomplish, he says.
Nazir Masih was working in the United Arab Emirates in 1990 when he discovered that he was infected with HIV. He came back to Pakistan, publicly declared himself an HIV-infected person and sought treatment for his illness with antiretroviral medicine. In 1999, he collaborated with four other HIV-infected people and together they set up the New Light AIDS Control Society (NLACS), headquartered in Lahore.
Masih visited Bhattiwala recently and claims to have met many HIV-infected patients there. That only less than 10 per cent of the village’s population was ever tested makes it highly likely that there are many more in the village suffering from HIV/AIDS than publicly known, he says. He also claims to know many other villages in Punjab where the prevalence of the virus is as high as it is in Bhattiwala, if not higher.
Masih quotes reports by the National AIDS Control Programme, a federal government entity, stating that Pakistan has around 133,000 people infected with HIV. Of these, only 20,660 are registered with various healthcare facilities. An overwhelming majority of these registered patients consists of adult males.
The reason why most patients do not register themselves for treatment is the social and moral stigma attached to HIV/AIDS. This stigma is so strong that healthcare providers often hesitate to treat those who suffer from the disease, says Masih. He knows of patients who were harassed and beaten up at hospitals in Faisalabad and Lahore after people found about the nature of their illness.
The impacts of the stigma are too obvious in Bhattiwala to miss.
Everyone knows everyone in the village and the identities of the HIV/AIDS patients are no secret, often exposing them to social ridicule and exclusion. Some of them complain that local shopkeepers refuse to sell them anything.
Zafar Sadhu recalls how he once went to a quack doctor in a nearby village to seek medical treatment but was made to feel ashamed for his association with Bhattiwala. “The people of your village are being punished for indulging in illicit relationships,” the quack told him. Such public shaming has forced Javed Iqbal’s family to maintain a low social profile and keep its interaction with others in the village to the minimum.
Sadhu also remembers his meeting with an HIV-infected woman in the village. She was desperately weeping and insisting that she had never slept with anyone except her husband. “It was very difficult to explain to her that she had committed a crime and that sex out of marriage was not the only reason why someone would contract HIV/AIDS,” he says.
Moreover, a local labourer in his late 20s reports being treated as an “untouchable” after he was diagnosed with HIV in July this year. “I still work as much as any other labourer but people shun me when they find out about my illness,” he says.
Most of the HIV/AIDS patients also come from the poorest of the poor families. The labourer, for instance, cannot afford to take time off work to get himself medically examined. He is seeking no treatment.
This article was published in the Herald's November 2017 issue. To read more subscribe to the Herald in print.
The author is a writer and photojournalist with a master's degree in journalism from the University of Sheffield in England.