• hiv
• tuberculosis
• health policies and all other topics

In 2015, 10.4 million people were diagnosed with tuberculosis (TB)1 and 2.1 million people tested positive for HIV.2 Over two-thirds of new TB and HIV infections are in lower income and middle-income countries in sub-Saharan Africa and Asia. Together, TB and HIV cause over 2.5 million deaths each year,1 2 and immeasurable social calamities. Key among these is widespread stigmatisation incited by their deep-set association with poverty, social marginalisation, risk of transmission and death, and perpetuated to varying degrees by subversive policies and practices.3 4 The stigma is doubly worse for the 1.2 million people world over who live with both infections.1 5

Since its outset in the 1980s, people with HIV and health activists have galvanised HIV stigma into a force for social change.6 They have willed action against prejudicial practices with tangible transformative effects at the individual, policy and political level.7 HIV-related discrimination has been confronted with empowerment. Policies such as those for HIV testing, treatment, counselling, medication access and employment of persons with HIV seek to affirm and uphold the rights of those affected by HIV.8 When the fulfilment of human rights has fallen short in practice, HIV activists have used rights-based approaches to overcome stigma and discrimination, and organise for change.

The TB community has always recognised the stigma that surrounds the disease but has done far less to confront it.9 10 The risk and fear of transmission of the airborne infection are often raised in defence of policies and practices that prioritise the well-being of the collective public over that of individual patients.11 Persons with TB or presumed to have TB continue to be subjected to stigmatising language (eg, ‘TB suspects’, ‘defaulters’), mandatory screening, testing and disease notification systems that lack privacy, contact investigations that label index patients, airborne respiratory isolation that prolongs their social isolation, directly observed treatment (DOT) that impedes individual autonomy, and in rare but relevant cases, legal detention and even incarceration of those who refuse or stop treatment.7 11 12 As these practices continue to be applied in biomedical, public health-oriented ways, they fuel the social exclusion of people with TB, and reify assumed conflicts between public health and patient rights.7 13

People with multidrug-resistant or extensively drug-resistant TB (M/XDR-TB), the most clinically severe forms of TB, are often the most judged and stigmatised.14 As non-adherence to TB treatment is considered to be one cause of developing drug resistance, patients with M/XDR-TB are routinely reprimanded for having been ‘non compliant’ to previous treatments with neglect to the sociomedical environment in which adherence transpires—one that is fraught with low-quality health systems, patient–provider mistrust, primary drug resistance, and poor access to diagnostic tools, new drugs, treatment literacy, social protections and infection control.15 Similarly, in many low-incidence countries, specific population groups such as migrants and refugees are portrayed as a public health threat and blamed for being carriers of TB.16 We are in need of a counternarrative to debunk timeworn arguments that continue to hold individual patients culpable for population-level failures and outcomes.

In recent years, key actors in the TB community, such as the Stop TB Partnership, Treatment Action Group, TB PROOF, Global Coalition of Tuberculosis Activists and KNCV Tuberculosis Foundation, to name just a few, are creating meaningful change in the praxis of TB care with potential effects on stigma reduction.11 13 17 18Terms that reinforce negative stereotyping of people with TB are being extricated from clinicians’ and researchers’ vocabularies.11 The hardline DOT approach is gradually ceding to patient-centred approaches that emphasise community engagement, patient counselling and structural aid in adherence promotion, even a murmur of palliative care for those with incurable disease.15 Governments and industry are being held accountable for implementing new technologies to ensure equitable access to the fruits of scientific advancement.13 Global health ambassadors including TB survivors are raising awareness about TB on a societal level through messages that affirm the dignity of people with TB rather than amplify the fear of TB.11

But this gradual advocacy movement of awareness raising, while necessary, is insufficient to tackle the structural drivers of stigma. The TB community needs consciousness raising, a form of activism that connects disparate experiences of discrimination and disenfranchisement, and the systems and structures that abet them, across time and space.19 Consciousness raising can take place when people with and affected by TB come together to share their experiences, identify common struggles and, based on this foundation, begin collectively organising to change practices that are stigmatising and potentially harmful. The resulting solidarity, characteristics of which we see in communities affected by HIV across the globe, and who are linked despite differences in race, sex and economy, can lay the foundation for more lasting social change. Replacing images of radiographs or mycobacteria, for example, with the well faces of those who have braved TB may help connect communities and humanise TB. Implementing a comprehensive framework for TB treatment literacy may allow counselling efforts to mature from piecemeal to universal practice. Framing contact investigations as a way for patients with TB to protect, rather than disrupt, their position in the household may avoid alienating index cases. TB science and the methods by which it is implemented can help to accelerate this transformation to better affirm the rights and dignity of people with TB. Knowledge of TB transmission most often used to isolate—and at times incriminate—patients can be harnessed to emphasise the stage at which patients become non-infectious.

Destigmatising TB is well aligned with ‘zero suffering’, a prominent goal of the WHO’s new End TB Strategy distinct from the goal of zero infections and zero deaths.20 One step towards alleviating patient suffering is to revisit policies and practices that fuel TB stigma and raise global consciousness for an inclusive and non-stigmatising approach to TB care (see table 1 for our recommendations). It is time we combated stagnant policies and complacency that diminish the social value of people with TB, and indeed feed into derogation of the epidemic itself in the hierarchy of global health challenges.21 As actors in the TB community continue working bottom-up to create micro forces of change, the healthcare system, scientific community, industry and donor agencies must sign on to stimulate a tangible shift through collective action and collective voice—one that is loud enough for 10 million voices to be heard.