Vidyapati’s disease, scientifically termed visceral leishmaniasis (VL) is a vector-borne illness, caused by the bite of a sandfly. That’s a creature just one-third the size of a mosquito. It thrives in poor housing, moist, cool temperatures, and abundant vegetation. Though the disease begins by affecting the bone marrow, spleen and liver, it might manifest itself some months or a few years later in the more visible form of skin lesions. A recent study by the Drugs for Neglected Diseases Initiative (DNDi), a global organisation, indicates that 5 to 10 per cent of all those who have suffered VL in Asia will develop these lesions.
Worldwide, says the global humanitarian NGO Doctors Without Borders, “Kala-azar is the second largest parasitic killer in the world…only malaria is more deadly.” Though its incidence in India has declined over decades, the country has missed several deadlines – 2010, 2015 and 2017 – for its ‘elimination’.
While untreated VL is almost always deadly, its non-fatal skin manifestation (Post Kala-azar Dermal Leishmaniasis, or PKDL) causes acute disfigurement. That in turn attracts stigma, shame and even abandonment – as they did for Vidyapati.
“My face became black, then my chin, and then the neck,” she says at her parents’ home in Saran – the district which reports most of the state’s kala-azar cases.
Her husband Raju Bhagat, a mason who seasonally migrates to Bengaluru for work, assured her that he would not leave her despite his parents’ insistence. Yet, he neither took her to Bengaluru nor let her stay at his parents’ home in Bihar. “Who will look after you? Go to your mother till you are healthier,” he reasoned. Yet every time he came home on a break, he summoned her to stay with him. The union resulted in two pregnancies. The first, a boy, was still-born. The second, a girl, lived for just a few hours, a possible fallout of the treatment Vidyapati had received for her ailments.