Love Positive Women

Let’s hear it for Positive Women!

This is a love letter from the HIV Justice Network to the more than 18,000,000 women living with HIV in the world today.

The HIV Justice Network exists to end the inappropriate use of the criminal law to regulate and punish people living with HIV. On this Valentine’s Day, we are thinking of the thousands of positive women in all of our diversity, inclusive of transgender women, who are currently incarcerated in jails, prisons, and detention centres.

We send love and support to all of the women living with HIV who have survived incarceration around the world. We highlight the reality that many positive women who are incarcerated around the world are criminalised because of punitive and discriminatory laws on sex work, drug use, LGBT relationships, domestic violence, and HIV status. These laws serve no public health benefit yet lock people away from their homes, families, and communities.

Women living with HIV are actively fighting for justice and against discriminatory legal systems. Positive women have often led the way in the struggle against HIV criminalisation. Among the many courageous and compassionate leaders in our movement:

We recognize Lillian Mworeko of Uganda and the International Community of Women (ICW), East Africa, for their unflagging media and legal advocacy to overturn discriminatory HIV laws in the Constitutional Court and to ensure that women living with HIV in Uganda can receive a fair trial.

We recognize Martha Tholonah and the women of ICW Zimbabwe for their advocacy in challenging the overly broad and discriminatory Zimbabwean criminal code on HIV exposure.

We recognize Clara Banya and the women of ICW Malawi for their loud insistence that breastfeeding while HIV positive is not a crime and we celebrate with them the positive court ruling in January 2017.

We recognize the courageous positive women of IWC Namibia who stood strong for the autonomy and sexual and reproductive health rights of women living with HIV and fought against sterilisation. We celebrate with them the positive court ruling won in 2014.

We recognize Marama Pala of INA Maori HIV/AIDS Foundation for her advocacy in New Zealand and globally to demonstrate that women’s legal empowerment develops through women’s solidarity and action rather than through a forced status as a victim by the courts.

We recognize Jessica Whitbread of ICW Global for her outspoken advocacy on behalf of positive women’s sexuality and against criminal justice proceedings in matters of intimate relationships.

In the U.S., we recognize Naina Khanna and the women of the US Positive Women’s Network for their participation in the legal challenge to HIV criminalisation in the State of California; Barb Cardell and Kari Hartel and the Colorado Mod Squad for their success in reforming Colorado HIV laws to better protect sex workers and transgender people living with HIV; and Tami Haught and Community HIV/Hepatitis Advocates of Iowa Network for their success in reforming Iowa HIV laws.

We ask everyone to take a quiet moment to send respect and appreciation to these accomplished and dedicated women.

We are you and you are us.

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Note: If you know a woman openly living with HIV to add to this honour roll, please let us know.

The HIV Justice Network is proud to support the the Love Positive Women campaign developed and led by International Community of Women Living with HIV (ICW), one of seven founding partners of HIV JUSTICE WORLDWIDE.

HIV Criminalisation: Legal Violence and the Lives of People Living with HIV, by Alexander McClelland

Criminal Charges for HIV Non-disclosure, Exposure and Transmission: Legal Violence and the Lives of People Living with HIV

 

The following is an edited version of remarks presented by Alexander McClelland as part of ‘The Movement to End HIV Criminalization’ panel, held on September 15 2016 at Concordia University, Montreal, Canada.

Introduction

My work examines the relationship between the law, life and disease. I look at what takes place at the intersection of legal and medical knowledge, including what kinds of processes are deployed and enacted onto people as a result of that intersection. In relation to studying law and society, I examine law from a perspective that there is no absolute legal truth, but rather, that laws and who is understood as ‘criminal’ are developed over history and change based on social norms and contexts.

My research is examining the lived experiences of people who have been criminally charged in Canada in relation to HIV non-disclosure, exposure and transmission. As we know, Canada is a country recognized with having high rates of criminalization towards people living with HIV. Canada is one of the leading countries in the world to prosecute people with HIV who have not told a sex partner they are HIV-positive if that sex poses a ‘realistic possibility of transmission’, this is defined by the Supreme Court of Canada as sex without a condom and a low viral load combined. Under this application of the law people have been imprisoned when they were uninfectious due to HIV medications and when there was no transmission of HIV.  It is estimated that there are approximately 180 cases that have taken place since 1989, when the first criminal charges were laid. And the trend indicates that the number of new cases is on the rise.

These approximately 180 cases have been applied asymmetrically and do not follow the epidemiological trends of the HIV epidemic, which if the law was objective, might be the case. Rather, through enumerating the cases with demographic data, social researchers have been able to reveal the biased racialized and gendered dimensions of this criminalization phenomenon. As a majority of those charged and prosecuted have been black men who have had sex with women.

Using a feminist form of sociological ethnographic inquiry[i], my approach has been to examine the impact of these laws on the people who they have targeted, from their own perspective. This kind of research aims to ensure that people do not become just objects to be studied, but are rather understood as people who are active agents. The premise of my work is to centrally place the experiences of people with HIV who have experienced criminalization first-hand so that efforts to address injustice and over-criminalization are directly informed by people’s lived realities.

I am a qualitative researcher and my work consists of archival research and a series of qualitative interviews. So far I have spoken with 14 people from across Canada.  Through these interviews I aim to understand how being criminalized has materially shaped people’s lives. My research is still ongoing so what I am presenting is preliminary and still in process.

Every person I have spoken with who was charged criminally (12 of the 14) was charged with aggravated sexual assault, often more than once, along with a diverse range of other charges. Aggravated sexual assault is one of the harshest and most serious charges in the criminal code reserved for violent rapes involving a weapon, which can receive a sentence of life in prison. In the cases I looked at, the aggravating factor is understood by the courts to be HIV.

Living in a negative relation to the law

The people I have worked with live their lives in a negative relation to the law[ii] due to being labelled a ‘criminal’ and a ‘risk to public safety’ through being charged and/or prosecuted in relation to HIV non-disclosure, exposure or transmission. Living in a negative relation to the law means that one is rendered less of a person with codified rights, less of a person who is in need of protection from the law, and is rather regarded more as object of risk that legally constituted persons are to be protected from– protected from through forms of control, coercion and incapacitation. Being placed in a negative relation to the law is something that is enacted onto people of colour, people in poverty, people deemed deviant. This is a practice of extending the power of colonization, white supremacy, misogyny and homophobia, among others forms of marginalization and oppression.

People living with HIV today in Canada often live in a negative relation to the law just due to the fact that they are HIV-positive. We can very easily be placed in a tenuous relationship with our legally regarded personhood.

At its most severe, living with HIV in a negative relation to the law means your body can be disappeared by the state with impunity. Here I am thinking of the lives of H. Matthews and I. Williams.[iii]

Outside PrisonMatthews, at 26 years old, a black man and newcomer to Canada, was convicted of 2 counts of aggravated sexual assault, one count of assault, and two other minor charges for not telling 4 women his HIV status before having sex with them. None of the women contracted HIV. He was sentenced to 40 months in prison. When he entered prison his CD4 count was 560. But while in prison he reported a series of health issues to the staff and in less than a year his CD4 count was 160 and he had lost 36 pounds. Despite seeing a number of medical experts, at no time over the course of his engagement with the criminal justice system was he put on any anti-HIV treatments despite being incarcerated because he potentially exposed others to HIV.

Matthews died of AIDS on 12th of August 2007 in Central North Correctional Centre in Penetanguishene Ontario at 27 years old in a country in an era and country where, due to supposed access to life-saving medications, dying of AIDS has been increasingly rendered a rare occurrence, but where incarceration for HIV non-disclosure has been on the rise. There was an inquest into Matthews’ death, but in inquests into prison deaths in Canada, no one can be found culpable, and no one was held accountable for his death. The only reason information was released about his cause of death was because corrections staff were subpoenaed to testify at the inquest. Otherwise the ministry of corrections did not release any information about his death despite repeated requests from Matthews’s family and community organizations. A series of nine recommendations were made from the inquest to prevent future deaths, none of which have been implemented by the ministry of corrections. In the coroners report it indicated that he died of ‘natural causes’.

WarkworthAnother life that was disappeared was that of I. Williams, at 49 years old, who was first person sentenced after the Mabior Supreme Court decision in 2012. This was the second conviction for the father, who was sentenced to 4 years 9 months, which he served in Warkworth Institution in Ontario. As a Trinidad-born permanent resident, he would be deported after completion of his sentence. He pled guilty to charges of aggravated sexual assault. HIV was not transmitted to any of the women involved in the case.  At the trial Williams stated he had been diagnosed with HIV in 1996, and had since been lonely and was been shunned by family and strangers alike soon as they learn of his status, as reported by the Toronto Star, he stated: ‘I feel very sorry for them people that I put that fear in them because I’m afraid, I’m afraid to be rejected, It is inhumane,’ he wept. ‘It’s very cruel,’ he said to the judge. He also told that court that convicting him and deporting him to Trinidad would be akin to a death sentence, because there he would not receive the health care he needs.

On October 1st 2013 Williams was reported as dead while in custody. Informal reports from people close to Williams indicated that he had been trying to get medical care for an injury for over six days before he was found dead due an untreated abscess on his leg.  No details were released from Corrections, and there was no inquest into his death.

Amplification of penality: The compounding violence of HIV & criminal charges

Very plainly, living in a negative relation to the law in Canada when having HIV results in an amplification of penality. In Canada, the intersection of HIV and law in relation to non-disclosure, transmission and exposure makes possible a range of legal and bureaucratic punishments, including the most severe and harsh available, along with a range of interpersonal, casual forms of stigma, discrimination, punishment and violence. Understanding the different ways that violence manifests can help us understand the best course of action to call for accountability.

All of these types of punishment result in violence, violence that can be called legal violence.[iv] Legal violence being the forms of violence that are made possible once someone has engaged with the law. Examining the phenomena of HIV criminalization with the concept of legal violence can help us to understand the relationship between law and violence and how people become targets of violence because they are targets of the law.

The amplification of penality that manifests in these cases means that mechanisms usually reserved as exceptions can easily become the rule. Exceptions such as the police releasing a photo to the public before prosecution for reasons of ‘public safety’, denying people bail even if they have never been charged before and present themselves with their family as not being a flight risk, denying people a pre-trail assessment, being tried as an adult and being placed in an adult jail when under-age, placing people in solitary confinement for long periods of time for reasons of security, or labelling people with dangerous offender status (meaning someone can be confined indefinitely after a sentence is served). These exceptions can come to be the norm in cases of HIV non-disclosure, exposure and transmission.

Guilty before proven innocent

The amplification of penality begins as soon as the charges are applied and does relate to a guilty verdict: People who are accused can be treated as guilty before proven innocent, and not the other way around.

For example, after being charged with one count of aggravated sexual assault, one indigenous man I spoke with was fired from his job due to being charged with rape and by having his HIV-positive status widely disclosed without his consent by people close to the woman who accused him.  The man told to me that he had been in a relationship with the woman and had previously disclosed to her, when he broke up with her she went to the police. The aggravated sexual assault charge and loss of his job caused the man to have a mental breakdown. He then lost his housing and ended up living out of a McDonald’s bathroom. All of his friends turned against him, and he removed himself from social media due to the intense levels of daily harassment he faced online. The mark of just the accusation caused his entire reality to be drastically altered for the worse. He is still awaiting trial.

A white woman whom I spoke with attended a hotel party and blacked out at the party, where she was then gang-raped. She told me she did not have the capacity to disclose her HIV-positive status, as she was extremely intoxicated at the time of the assault against her. The next day she went to the police, who took a statement from her. The following day she was charged with multiple accounts of aggravated sexual assault. Her photograph, HIV-positive status and biometric details were widely distributed by the police, at which time multiple media articles were written about her. Because she had a history as a sex worker the articles painted her as a predator with HIV who was trying to spread HIV to others. Her privacy breached, her social life ruined. HIV was not transmitted to any of the men involved. She was prosecuted and ultimately served over 5 years in a corrections institution.

A black man I spoke with, after being called by the police about his charge of aggravated sexual assault, went to the police station to turn himself in. At the police station he was questioned without a lawyer present, and then was taken into a separate room and severely beaten by police. He was knocked unconscious and unaware of what had happened to him. Afterwards the police put him back in the questioning room and told him that nothing had happened and that he was fine. He is certain he was beaten due to having HIV and being charged with a rape charge. The accuser did not acquire HIV and the man mentioned that she tried to come back to him after initially calling the police. In his case, he ultimately appealed to the superior court in the province and his charges were stayed – meaning he was not found guilty. This was only after serving approx. four years in a combination of house arrest and prison.

The violence of incarceration

The amplification of penality continues and becomes more formalized once someone is prosecuted. All people who are incarcerated in Canada are vulnerable to violence, but when HIV is introduced the vulnerabilities can be compounded.

A white man I spoke with who was prosecuted told me his ex-boyfriend called the police after the man disclosed to him. The man says he hadn’t disclosed his status previously, as he said he didn’t have the skills to do so. He also understood from his doctor that he was uninfectious as he had been on HIV medications.  There was no allegation of HIV transmission. He had no previous criminal record and had never been in prison. One his first day inside prison, he was placed in general population, and was not given choice for protective custody.[v] During his first few days inside in general population, the man was surrounded on the range while using the phone to talk to his lawyer. The inmates who surrounded him asked the man what his charge was, saying he was lying and they knew he was a rapist with HIV. He was publicly beaten very severely by the inmates, all this in front of guard staff who didn’t intervene for a long period of time. Once the staff intervened, the man was then asked if they wanted to go into protective custody. He is certain that the staff leaked his charges and HIV-positive status to the men on his range, knowing he would then face physical violence. Eventually the man was placed in administrative segregation ‘for his own protection’. In administrative segregation he was stripped nude, only had a concrete floor, no bed, or blankets, and was given a just one sheet of paper and a pencil to occupy his 23.5 hours a day on lockdown. He served out the end of his sentence in those conditions. He is now suing corrections for his treatment by the guards.

Inside PrisonAn indigenous woman I spoke with was also placed into administrative segregation. She was sentenced to 2-years on charges of aggravated sexual assault. When incarcerated she was asked if she wanted to be by herself or in general population. She asked to be by herself – the conditions of which we not explained to her beforehand. This meant administrative segregation, which also included requirements for suicide watch. Under those conditions the woman was striped naked, placed in a cell with only a concert floor, a video camera watching her, and a window that a male guard would watch her through at all hours. She did not have access to her anti-anxiety or HIV medications.[vi] Eventually her lawyer got her released from these conditions and she is currently appealing her conviction.

A Métis man who I spoke with, who was serving a 5.5-year sentence in protective custody, while inside got very serious bacterial infection is his genital area. The infection persisted for over a month during which time he made repeated requests to see a doctor, which were delayed or denied. At one point a guard whom had previously let the man know that he was aware of his HIV-positive status, took the man’s written request to access the doctor and ripped it up on front of the man and threw it in the trash. It was not until the situation nearly threatened the man’s life that he was taken to the doctor for the emergency – this was months after the initial request by the man. This story becomes even more disturbing when we remember the deaths of Williams and Matthews.

The mark of criminality in daily life: Stigma & ongoing surveillance

The impact of penality extends well beyond prosecution, if there is a prosecution. A white man who I spoke with was under house arrest for over 3-years. His charges were ultimately stayed, as his case only involved a ‘blowjob’ and the Crown prosecutor was likely to lose at trial. No HIV transmission was alleged in the case. Under house arrest, he was to live in the houses of different sureties. He was reliant on the surety, couldn’t work, or go to school, and was severely isolated.  Once the charges were stayed, he went to find his own housing. His case had been in the media, and despite the charge being stayed, his and his name when searched in Google revealed details about his HIV-positive status and the aggravated sexual assault charges. When applying for one apartment, he got a call back, and the landlord asked him to come back to visit the place, a good sign he thought. When he showed up the landlord opened the door and yelled at the man ‘I don’t rent to rapists’ and then pushed the man down the flight of stairs to the home. The man has also been denied jobs for the same reason.

In regards to extending penality beyond a prosecution, seven of the people I have spoken with are now registered sex offenders. The registry is a mechanism for continued police surveillance after prison release. A number of these people prior to incarceration used to work in professions that require background checks, which would now turn up badly due to the criminal record and Sex Offender Registry listing. One woman I spoke with used to do childcare for her job, and as a result of being on the registry she cannot get the job she used to have. This is also the case with others, which means they live of social assistance support even though they want to work. The result of their prosecution continues to extend into their daily lives today through threatening their economic security.

As a result of their experiences, every person I have interviewed has noted that they have either tried to commit suicide, or has had periods of regular suicidal ideation. Today, a majority of the people I spoke with live with post-traumatic stress disorder, which has a wide range of impacts on their daily lives. All of them also now have a complex and strained relationship with society. Many are very angry at society, a society, which took their personhood away and has treated them as less than human.

Bearing witness to call for action

All of this violence enacted towards them because of a supposed ‘crime’ that is entirely non-violent, and in which the notion of harm is an ideological one rooted in HIV-related stigma and AIDS-phobia. A crime where proving the intent to harm is extremely difficult, but due to fear and out-dated notions of AIDS as infectious and deadly, proving intent has been replaced by the fact that someone just has HIV. In many cases those who were charged and/or prosecuted explained to me that they understood that they took steps to protect their partners, such as using condoms, or regular taking medications so that they would be rendered uninfectious. What does it say about our society that the criminal justice system we have employs its most punitive functions towards people who have done no violence except perhaps that they have not told someone else that they have a medically controllable chronic disease?

Revealing these forms of legal violence is part of a deliberate political project – forms of violence that are simultaneously institutional and interpersonal, and both physical and psychological. These forms of violence are often obscured through bureaucracy, and forms of marginalization because the people onto whom these forms of violence are enacted have been deemed unworthy of living as legally safeguarded persons. These forms of violence are rooted in stigma and a fear of the ‘other’. These forms of violence are an extension of white supremacy, homophobia, colonization and misogyny. Many of the people I have spoken with live in poverty and are racialized. Women I have spoken with have been assaulted, but they are the ones who are criminally charged. Through revealing these forms of legal violence I hope we will be better positioned to deem thus situation unacceptable. To bear witness so we can call for action. Our work on this issue should be an act of refusal, a refusal to accept this current situation and a refusal to let these lives be rendered disposable by institutions of the state.

People living with HIV are a people who are over-policed but are under-protected. We live under heightened state and community surveillance due to criminalization.  But we are provided limited protections when we call for help. We are deemed unworthy of care and support, unless that support is instrumental in helping us not transmit HIV to others. Despite all of this, all of the people I have spoken with for my project are passionate, kind, funny, charming and dynamic people. People with a visions for the future, and who wanted to share their stories for this project as an act of healing, as a way to seek justice, and as a way to turn what happened to them into a positive force for change.

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Alexander McClelland is a researcher who is currently working on a doctorate at the Centre for Interdisciplinary Studies on Culture and Society, Concordia University. His work is supported through the Canadian Institutes of Health Research and Concordia University.

 

 

 

Endnotes

[i] See: Smith, Dorothy. E. (2005). Institutional Ethnography: A Sociology for People. Toronto: AltaMira Press.

[ii] Existing in a negative relation to the law means people who are institutionally marked as criminals, who are then rendered civilly and socially dead under legal regimes, people who through being labelled a criminal are deemed worthy of being dehumanized through forms of state institutional punishment. I draw on this notion he living in a negative relation to the law as elaborated through the work of Colin developed in the work of Colin Dayan (see: Dayan, Colin. 2011. The Law is a White Dog: How Legal Rituals Make and Unmake Persons. Princeton University Press: Princeton).

[iii] I have provided some privacy through not indicating full names.

[iv] Legal violence helps us examine Including how law makes possible forms of violence through forms of legal interpretation, incarceration, and sentencing, which are acts of violence through taking one’s legal personhood away. The violent actions made possible by the law are also often themselves deemed illegal. But because legal violence is often targeted towards people whose legal personhood has been deconstituted, the illegality of these forms of violence can go unrecognized or unquestioned.  This concept has been elaborated in the work of Robert Cover (see: Cover, Robert. 1986. Violence and the Word. The Yale Law Journal, 95, 1601-1629.)

[v] It is required that someone be given the choice to go into protective custody, especially if the person has a charge such as aggravated sexual assault, know as a “dirty charge” inside prison, where you would go into protective custody to avoid violence from other inmates.

[vi] It should also be noted that all of the people who I spoke with that were incarcerated had numerous difficulties in accessing their HIV medications – despite being incarcerated for having HIV, in a country where being detectable can result in a crime, people with HIV who are incarcerated have a very hard time accessing their HIV medications due to a range of bureaucratic, logistical and punitive barriers

Why advocacy against HIV criminalisation must be part of discussions on gender, human rights, and sexual and reproductive health and rights of women living with HIV, by Evgenia Maron

Earlier this week, I attended a meeting in Almaty, Kazakhstan, convened by UNAIDS and UN Women entitled ‘Leave No One Behind: Bringing needs and priorities of women living with HIV into policies and actions’.

Here, NGOs, community members, governments and human rights defenders from Central Asia came together to share best practices by and for women living with HIV and to cherish the leading role of women’s organisations and their contribution.

The meeting also sought to acknowledge achievements of the UNAIDS Unified Budget, Results and Accountability Framework (UBRAF) that contributes to improving the lives of women living with HIV.  This was an important venue to discuss how global goals – e.g. Political Declaration on HIV and AIDS, new UNAIDS Strategy 2016-2021, and Key AIDS-Related SDGs For 2030 – are linked to local goals.

Among the meeting priorities were the focus on the leadership of women living with HIV presenting the outcomes of their UBRAF-funded projects, sharing their success stories.

In addition, networks of women living with HIV in Kazakhstan and Tajikistan presented summary results of the assessment of sustainability and fundraising competency and of the PLHIV Stigma Index, demonstrating the need for spaces for leadership and empowerment of networks, and showing where opportunities of reducing discrimination have taken place, through blogging, international campaigns, clips and photo projects.

I delivered a presentation on behalf of the HIV Justice Network (HJN) on HIV criminalisation, and what women’s networks can do to challenge it, seeking to share the monitoring outcomes documented by us in the countries of Eastern Europe and Central Asia (EECA).

Since 2007, we have documented over 25 criminal cases against women living with HIV for HIV alleged exposure and/or transmission, mainly in Russia, Belarus, Ukraine and Kazakhstan. We also know about HIV-related criminalisation of marginalised groups of women in Kyrgyzstan, Moldova and Tajikistan during this period.

The actual number of prosecutions is certainly much higher.

Screenshot 2016-12-07 09.56.58Constituting over 50% of people living with HIV, women are seen as both victims and perpetrators in regards to HIV criminalisation, and have been impacted by criminalisation in many ways – including in their sexual relationships, violating their reproductive rights, and in the case of sex workers, being doubly criminalised for working and living with HIV.

Linking gender inequality and HIV stigma makes it obvious that women rarely have economic independence and power to make decisions about their bodies, including whether or not (male) condoms are used, and the lived experience of fear of prosecution prevents women from getting tested, knowing their status, and getting HIV treatment, because many laws are applied precisely against those who know about their diagnosis.

And there is evidence that intimate partner violence often occurs when a woman discloses her HIV status.

One of our main concerns is that the names of women arrested and prosecuted are disclosed in the media. Another is that women are usually prosecuted by their intimate male partners.

HJN has documented cases where women were prosecuted not only for alleged transmission (when the alleged transmission may have occurred from the complainant to the accused), but also for potential or perceived HIV exposure (when there may have been no exposure risk).

We need to pay special attention to prosecutions of pregnant women or for allowing vertical transmission.

We believe all of the above cases are actually the results of structural or cultural violence – these prosecutions both unjustly scapegoat individual women and justify direct violence against women living with HIV.

Alina Yaroslavska of Positive Women in Ukraine commented:

“Before HIV criminalization was not on the agenda, especially we didn’t focus on why it’s important for women, how it affects women’s lives and the epidemics as a whole. In fact, we need to gather these pieces of the puzzle. This piece is very important: on one hand, we can help people in a concrete way, on the other hand, we can take effective measure to eliminate this phenomenon. We now are forming our operational plan for the next year, and I think we will include HIV criminalization as an issue. We will meet the network of people living with HIV to join the Ukraine’s initiative to remove the corresponding criminal article. Secondly, we can include in the plan measures to support women to talk about this issue and motivate more women to join the movement for HIV Justice Worldwide.

Calling on women’s networks to work with the media, at the meeting we highlighted some media contexts, which regrettably affect the overall image of women living with HIV.  Poorly written reports of such cases – without context or balance –  contribute to stigma, discrimination and violence.

Screenshot 2016-12-07 09.56.20None of the women prosecuted had an opportunity to speak for herself, publicly. What is leading to broader devastating consequences to the women and their families is that at least half of women were subjected to public ‘slut shaming’. All of them are described in an active voice as criminals and ‘sources of infection’ in the eyes of the public health perspective is discussed, which is devastating for the future of these women.

As well as introducing HIV criminalisation as an issue at the meeting, we also helped to bring a better understanding of the roots of stigma and discrimination of women living with HIV, highlighting the experiences of women’s network overseas.

On one hand, our region has badly written laws and unjust prosecutions. On the other, we don’t yet know enough about to bring about meaninful change.

By introducing HIV Justice Worldwide, and the ultimate change that we want to see as removal of discriminatory laws and practices, we are inviting organisations, advocates and communities to join us to share their experiences and learn more about successes and challenges.

The meeting was a valuable a space for dialogue, skills exchange, strategising, and networking in order to improve situation for women living with HIV in the region. Using this opportunity to talk about HIV criminalisation placed the issue within the broader context of gender, human rights, HIV, and sexual and reproductive health and rights of women.

We also discussed how we can provide rapid response and support to women criminalised under HIV-specific laws and beyond.

To think together with partners how we can focus energy and resources on creating an environment where people living with HIV can disclose their HIV status without fear of rejection, violence or discrimination is a great move towards HIV justice in the region.

With women’s networks and stakeholders, we further discussed actions required to promote implementation on HIV/AIDS and gender equality in the Sustainable Development Goals (SDGs), notably SDG 5 – gender equality – and SDG 10 – reduced inqualities.

The need to revise and remove laws that criminalise HIV non-disclosure, exposure and transmission was highlighted as especially important for women living with HIV, along with introducing by law comprehensive sexual and reproductive rights and education.

The intersection of women’s rights and HIV remains an important entry point for a dialogue with governments and health authorities in Central Asia. This event had an ambitious long standing goal to address all forms of violence and harmful practices perpetrated on the basis of gender as well as prioritisation of empowerment of women and girls in developing, planning, implementing and evaluating national HIV strategic plans and policy frameworks, and, hopefully, stopping HIV criminalisation is amongst them.

Evgenia Maron is the HIV Justice Network’s EECA consultant.

Every theory has a human price: Ethical research is collaborative research, by Laurel Sprague

Remarks written for the Haverford College Research Ethics Symposium, 21 October 2016, by Laurel Sprague, Research Fellow in HIV, Gender, and Justice, HIV Justice Network.

Every theory has a human price: Ethical research is collaborative research

[Introduction]

Every theory has a human price.

Of all of the philosophical statements that I read and teach about what obligations – to accuracy or truth, to one another – might structure the inquiries of those who seek after knowledge, this statement, heard more than a decade ago from spoken word poet Alix Olson on an outdoor festival stage, has become my mental organizing principle.

Every theory has a human price.

What does this mean for ethics in research? Scientific inquiry is never neutral in its origination, its execution, or its interpretation. No research is done, not ever, in the absence of underlying theories about what questions matter, how these questions should be studied, who is a reliable witness to their own experience, what kinds of people and training are needed to interpret research results, and whether any obligations exist to use and share the outcomes. This reality is the reason that ethical research on social questions is research done in collaboration with those most affected by the questions and the outcomes.

My remarks today focus on three different research experiences: one that illustrates the pitfalls of the traditional “ivory tower” research process, one that demonstrates a concrete outcome difference between research done in isolation version with that done with affected communities and that informs diametrically opposed policies, and one that provides a fresh approach to academic-community research partnerships.

[Fiddling while Rome burns]

In 1994, I attended a conference in Atlanta, the National Skills Building conference, designed to boost the US HIV/AIDS response, in Atlanta. AIDS became the leading cause of death among all Americans age 25-44 that year. Three of my friends had died the previous month, in September 1994. I was 23 and they were the first friends I lost to AIDS. My own health was precarious. Diagnosed as HIV-positive in 1991, and with my immune system in free fall, I was five months from my own AIDS diagnosis. I share this information with you both to position myself in the examples I am about to share and to call on you to imagine – or to remember – the sense of urgency we felt, as people living with HIV and as people loving family members, partners, friends, and colleagues living with HIV, at that moment.

At that conference, one of the sessions I most highly anticipated was focused, at long last, on lesbians and HIV. As a lesbian living with HIV, and in contact with about a dozen other lesbians with HIV and their partners, we existed in an abyss of information: we had absolutely zero evidence-based information on whether women could acquire HIV from one another and, if so, what kinds of activities posed a risk. Safer sex information for women at the time was adapted from what was known about men’s sexual behaviours and risks. It centred around a strange fetish in public health messaging for dental dams (a fetish not shared by any lesbian I ever met).

As lesbians, whenever we had the chance to meet, we shared stories and any research we could get our hands on. The Lesbian AIDS Project at GMHC in NY provided a newsletter and resources that we scoured for information. As lesbian after lesbian shared stories about their own HIV acquisition from previous male partners, or drug use, or sexual assault, or transfusions, and as couple after couple shared their experiences of having no transmission between them, often despite years together without the knowledge that one partner was HIV-positive, we began to guess, but no one knew, the answers to fundamental questions about HIV transmission risks between women.

The conference session was packed. The U.S. Centers for Disease Control had finally invested resources in women-specific questions. Two women from the CDC presented their study and results.

What did they do?

They surveyed lesbians living with HIV to find out if they practiced safer sex with their female partners.

What did they learn?

A significant portion of lesbians said no.

What did they recommend?

They did not recommend paying attention to risks that HIV-positive women might pose to their partners; they did not recommend talking with HIV-positive lesbians about why they did not practice safer sex. Instead, they called for an HIV-prevention campaign to motivate lesbians to practice safer sex.

Now, if the goal was to convince lesbians living with HIV to practice safe sex with our female partners, what we needed was even one case that demonstrated that it mattered. One case that showed it was worth it to give up a level of intimacy in order to protect our partners’ health.

Imagine if that research had been done with lesbians living with HIV rather than on us. Imagine if the intelligence, concern for our partners, and agency of lesbians living with HIV had been taken seriously. We might have learned answers to our life and death questions.

Instead, researchers fiddled while Rome burned.

[From wrong questions to wrong answers to wrong policies]

My second example compares research questions written without involvement by those affected by the issue with research questions written collaboratively with those most affected.

Within the last decade plus a few years, legal and social science researchers have conducted research on whether the existence of a law that criminalizes people living with HIV for not disclosing their HIV status to a sex partner, potentially exposing another person to HIV, or transmitting HIV, has either negative or positive public health effects. Within this research program, a series of surveys has been conducted to identify the levels of support for such laws (laws which currently exist in 36 US states and territories).

While no positive public health outcomes have been identified and some small negative public health outcomes are suggested resulting from these laws, the survey results found generally high levels of support for these laws, including among gay men and people living with HIV. This has a policy effect: if constituents seem to support a law, politicians have no incentive to change the law, even when the law is discriminatory or unjust.

What was the survey question? “Should it be against the law for a person living with HIV to have sex without disclosing their HIV status?“

As part of a group of HIV advocates and researchers through the Sero Project in Milford, PA, almost all people living with HIV, we had a strong sense that public support for these criminal laws was more nuanced than the previous survey responses suggested. So we created new survey questions and asked them alongside the survey question used previously.

When we asked the original question, “should it be against the law for a person living with HIV to have sex without disclosing their HIV status?” our 3000 plus respondents, people living with and affected by HIV, showed support that mirrored that found previously (more than half thought non-disclosure should be criminalised).

But then we asked another question, of the same respondents, that gave more options. We asked: Should disclosure of one’s positive HIV status to a potential sex partner be … a norm that communities should uphold, an ethical obligation for PLHIV when safe to do so, important only when engaging in activities that pose a risk of HIV transmission, a matter for criminal or civil courts?

Suddenly, when provided with more nuanced options, support for criminalization dropped from more than half to just 11% of respondents. For those 11%, we went further and asked what kinds of penalties people ought to face for non-disclosure. While current prison sentences for non-disclosure often are 30 years or more, most respondents called for further education, counselling, and community service.

These differences – between the results from the survey question that excluded community participation, and indicated support for prosecution and incarceration of people living with HIV who are accused of non-disclosure, versus the results from the survey question created by people living with HIV, that indicated a need for counselling, education, and support – can have tremendously different effects on policy decisions about who gets prosecuted and incarcerated in our communities.

[Nothing about us, without us]

Finally, to end on a more positive note, I will describe a global research project with which I’ve been involved since 2008: the People Living with HIV Stigma Index. This project was developed by and for PLHIV and is led by an international partnership made up of the Global Network of People living with HIV, the International Community of Women living with HIV, and the Joint UN Programme on HIV and AIDS.

This project trains people living with HIV as interviewers who conduct interviews with other people living with HIV. The project focuses equally on obtaining rigorous data regarding HIV-related stigma and discrimination and on empowering local networks of people living with HIV to work together across their differences, to gain research, data literacy, and employment skills, to build relationships with national and local academics and health ministries, and to turn the resulting data into advocacy projects that challenge stigma and benefit the community. One theme throughout the project: the process is as important as the results.

Why was the project created? For one reason, it responds to a missing piece in the stigma research programme. Research focused on healthcare workers and what are known as “general populations,” in fact, everyone but PLHIV were asked about HIV stigma. The PLHIV Stigma Index fills this research gap and, crucially, recognizes that those experiencing stigma first hand have something valuable to share.

What has the PLHIV Stigma Index project achieved?

To give just a few examples: The PLHIV Stigma Index has been implemented in more than 70 countries worldwide, including recent US implementations in metropolitan Detroit and Baton Rouge and New Orleans, Louisiana. The rich data that networks have gathered in the experiences of living with HIV is used in UNAIDS reporting and as baseline data used in National AIDS Strategies around the world.

Here in Pennsylvania, the AIDS Law Project, under the direction of Ronda Goldfein, has used the PLHIV Stigma Index results to demonstrate harm caused by stigma. With this data in hand, the AIDS Law Project was able to win two separate discrimination issues in court.

In Malawi, five networks of people living with HIV worked together to advocate for care for people who are incarcerated, better anti-stigma policies. A notable success in Malawi was the removal of staduvadine (D4T) – a particularly toxic medication no longer prescribed in wealthier countries – from the national formulary.

In Estonia, the PLHIV network established the first-ever PLHIV run, stigma free, health clinic.

Everywhere the Stigma Index has been implement, we see empowerment and networking, challenges to internalized stigma, increased solidarity across different groups of people affected by HIV: gay men and other MSM, sex workers, people who use drugs, women and girls, heterosexuals, people of different faiths.

[Closing]

I tend to distrust dualisms, yet, even so, I stand by this next statement: if your research does not include those most affected by the questions you ask and the answers you receive, then your research excludes those to whom it matters most. This is not some kind of reasonable “exclusion criteria”. Rather, when engaging in research on question with social repercussions, exclusion is a refusal to accept the political and social repercussions of one’s research on people other than oneself, or to acknowledge the dignity, risk, and wisdom of those most engaged – often in physical, embodied ways and whose very lives may be at stake.

Every theory has a human price.

Deepest thanks to Professor Chris Roebuck, without whose vision this panel could not have come into being, and my sister panellists. It is truly an honour to share a stage with Waheedah Shabazz El and Cecilia Chung.

Your Sentence is Not My Freedom: Feminism, HIV Criminalisation and Systems of Stigma, by Laurel Sprague

Remarks written for the “Movement to End HIV Criminalisation” panel at Concordia University, Montreal, 15 September 2016, by Laurel Sprague, Research Fellow in HIV, Gender, and Justice, HIV Justice Network.

 

Before beginning my remarks, allow me to note that there are so many nuances and variations in the specific instances that people face that these remarks can only scratch the surface. Still, I offer these remarks in the hope that my thoughts will add to, bring in new perspectives, and support the continuation of the dialogue already in place.

The public is often sold a compelling story about HIV criminalisation, one that fits into their ideas about how gender works and what it means to be a good citizen. People are told that criminalising people who are living with HIV and who fail to disclose that fact to a potential sex partner will protect women from acquiring HIV.

The subtext, of course, is that the people living with HIV and having sexual relationships are generally men, that the only considerations these men with HIV have are to maximize opportunities for sex, that women should be considered as passive prey for these men, and that putting a law into place will either convince men to disclose their HIV status to female partners or lock them up if it seems they have not done so, restricting their ability to transmit HIV to women, at least to other women, beyond those who bring charges.

Why are women living with HIV concerned about HIV criminalisation? If you are going to take away peoples’ freedom in my name, then you should expect that I would have something to say about that.

What I have to say is: not in my name. Do not incarcerate people living with HIV in my name.

Women living with HIV are also concerned about HIV criminalisation because, once these laws are passed, we are caught up in their dragnet. Frequently, we live in fear of prosecution, even when we closely follow the law. Too often, like our brothers living with HIV, we find ourselves facing prosecution. The same gendered impulse to “protect” women by passing laws, judges women harshly when we acquire HIV ourselves.

In Uganda, in 2014, police, accompanied by a mob, pursued nurse Rosemary Namubiro, a woman living with HIV, after an accusation that she stuck a child with a needle that might have pricked her own skin when the child flailed. Rather than responsible media coverage of the incident, Rosemary was characterized repeatedly before trial as a “killer nurse,” and a “witch” seeking to intentionally infect children. Her HIV status turned her, in the eyes of the media, society, and the legal system, from the epitome of good womanhood — a licensed nurse with decades of exemplary service — to the epitome of bad womanhood – dangerous, unrestrained, supernatural. Women living with HIV in Uganda and around the world stood with Rosemary to support her and because we knew in our bones that stigma against women living with HIV means each of us is only one accusation away a prison sentence.

The impact of these laws against women living with HIV are usually not so far away geographically. To give just a few examples, two women living with HIV, Cicely Bolden and Elisha Henson, were brutally murdered after disclosing their HIV status to a boyfriend or sexual partner. Each of their killers admitted to the murder. Each claimed that their HIV-status made the murders justifiable. When, in place after place, laws are passed requiring people with HIV to disclose their status no matter what, then we will see, place after place, further violence against women living with HIV.

Here in Quebec, a woman living with HIV went to police for protection for her and for her young son from her violent male partner. When the police arrested him, he claimed that she had HIV and had not disclosed her status to him. Despite all evidence to the contrary, he was released and she was sentenced to prison, only released in 2012 by the Canadian Supreme Court, not because the sentence was found to be unjust or unwarranted, simply due to a technicality.

Women living with HIV expect that the words of any abusive, but HIV-negative, partner will be believed over our words in a court of law.

Why do women living with HIV care about HIV criminalisation? Because we want the laws to stop condemning us to violence. We want you to stop locking us up.

In Canada, there is no HIV-specific law that criminalises people living with HIV for non-disclosure, alleged exposure or transmission. This is, seemingly, in line with the consensus from the Joint United Nations Programme on HIV and AIDS (UNAIDS), the Oslo Declaration, and multiple recommendations from other global organizations and researchers.

Global guidance, such as that released by the Global Commission on HIV and the Law in 2012, calls for an end to HIV-specific laws, citing extensive research showing that these laws fulfill no public health goals but do succeed in furthering discrimination against people living with HIV. Unfortunately for Canadians living with HIV, Canada serves as a prime example of what can go dreadfully awry even in the absence of HIV-specific laws.

In Canada, if I, as a woman living with HIV, engage in sexual intercourse with another person without disclosing my HIV status, I can be charged with aggravated sexual assault. This means that, for consensual sex with another adult, I can be charged as the worst form of rapist. In fact, I can be prosecuted for aggravated sexual assault whether or not my partner acquires HIV from me and no matter how low the risk of transmission.

In fact, as of 2012, only if I can prove both that my viral load is undetectable and that a condom was used, can I fight the charge of sexual assault. It is a chilling reality that condom use is impossible for a woman to guarantee without the cooperation of her partner and that, in Canada, women living with HIV are significantly less likely to receive the quality of care and support needed to bring their viral load to an undetectable level.

The legal leap from a claim of HIV non-disclosure to a prosecution for aggravated sexual assault is not obvious: the rationale behind this leap is that if a person has not disclosed her positive HIV-status to a sexual partner, then she has made it impossible for her partner to consent to possible sexual exposure to HIV. Without this consent, sex between them is labeled rape. Within Canada, the law goes one step further because failing to disclose one’s HIV status is also considered to be fraud. When fraud is added to the rape charge, then the charge is increased to aggravated sexual assault. The Canadian Supreme Court decided in R. v. Mabior (2012), that only when the person with HIV has both an undetectable viral load and uses a condom, are they protected from the charge of aggravated sexual assault.

Within Canada, there has been a robust feminist response to the way in which the law on sexual assault has been used to prosecute alleged non-disclosure of one’s HIV status. Briefly summarized, feminists attentive to the laws have argued that it is egregious to conflate HIV non-disclosure with rape, much less aggravated rape and that the law waters down the hard won gains in Canada regarding consent in sexual relationships. Further, feminists explain that the law is likely to discriminate against the most vulnerable and to be applied arbitrarily, pointing to cases across the country that make that very point.

Of course, there are many strands of feminism and not all Canadian feminists echo these concerns. In many ways, HIV criminalisation highlights a critical fault line amongst both feminists and queer theorists and activists. This fault line is the tension surrounding the appropriate use of State power for protection versus emancipation of people who are vulnerable to violence enacted against them by other members of society.

Women living with HIV across the world have responded to this theoretical debate with a strong assertion of our own: creating laws specifically to protect women does not work. Long practice in country after country demonstrates that equal protection under the law is rare, instead, those most marginalized in a society will be those most often targeted for incarceration. Women’s vulnerability to violence has not been, and will not be, reduced by further laws purporting to protect women

Let me situation myself in this conversation: I am a woman living with HIV, who acquired HIV shortly after my 20th birthday during a relationship with a male partner in his late 30s. It is a common story globally of a young woman acquiring HIV from an older man. We would like to stop those things from happening, right?

What happens to the story if I add some context? What if I share that I was a sexual assault survivor from my high school years, which was traumatic, shameful, and normal within my circle of high school friends? What if I add that I was raised within a fundamentalist religious community, with the lower status as a girl and the judgment and scrutiny that exist in those communities? Does it matter that I felt safer and more protected by this partner than I had previously in my life?

So, just what is it that we would like to stop from happening?

Would locking him up solve the problem of gender inequality?

Let’s complicate the story further, with more truths: does it make a difference that he disclosed his status to me? Does it make a difference that he was also a survivor of sexual and physical assault?

Was he careful with me? No, he wasn’t. Should he go to jail? Not legally, he disclosed his HIV status. What about ethically: is this the answer?

The easy answer, the one that allows every one of our social inequalities to continue, is to say: lock him up.

Now, think to yourself: what if he hadn’t disclosed his status? Does that change anything? Everything? Could I have been any more or less empowered to advocate for my own sexual health? Could he have been any better or worse at advocating for his own well being? Neither of us was skilled at self care. Both of us were skilled at self injury.

Now, what if I went to the police and claimed the he had HIV and did not disclose?

In the United States, 25 years later, it’s likely he would still be in prison. In Canada, there is no reason to believe that he would not have served years in prison as well.

What if I claimed, instead of HIV non-disclosure, that he physically beat me or raped me (he did not)? He probably would not be prosecuted, or, if prosecuted and convicted, would not serve nearly the same sentence length. That should give up pause.

We know that exactly this scenario happens here, including here in Quebec, where the woman living with HIV, mentioned earlier, after being severely and repeatedly beaten by husband over period of years was jailed herself when she tried to prosecute him – because he alleged that she didn’t disclose her status. He walked free.

Why would we treat HIV non-disclosure more seriously than physical attacks? The question is puzzling: non-disclosure charges arise only in the context of non-coerced sexual activity between adults. In this situation, unlike physical assault, either partner could walk away or suggest condoms or other barriers. If a physical assault has happened, and the assailant is HIV-positive, then the laws on assault are more than adequate to handle that situation.

So are we, as it seems, trying to protect women and others from HIV but not from real violence enacted against their bodies? Why would that be?

If we analyse prosecutions for HIV non-disclosure with the understanding that the rhetoric about protecting women fails under examination, then what is left is naked stigma and the desire to regulate certain bodies deemed outside of the boundaries of respectable society: those bodies perceived as likely to have HIV. Notably, the only legal requirements are for those living with HIV. There are no legal requirements for those perceived to be HIV-negative to take safer sex precautions or even to have a conversation about sexual transmitted infections they or their partners might have acquired. What we see is an effort to control and punish the bodies perceived to be HIV-positive and an effort to ensure complete freedom from responsibility for those bodies perceived to be HIV-negative.

This is a situation of immense injustice. What the laws does is to scapegoat vulnerable people instead of addressing real and difficult social problems such as the gender inequality that persists across classes and countries, which make it difficult for women to protect their health and well-being and for people living with HIV to do the same. The meme of a heterosexual man living with HIV exposing an unsuspecting heterosexual woman to HIV disregards everything we know about this epidemic: that most people acquire HIV because they are themselves part of a vulnerable group; that reducing new infections happens most effectively when safer sex practices become normal rather than exceptional; that once people learn their positive HIV status, they seek to avoid transmitting to others; and that most new infections occur from transmissions between people who do not know their HIV status.

To return to my story, I tested positive for HIV after I became pregnant. Immediately, under the law, I became the person vulnerable to criminal penalties. Like so many of my male friends, my HIV diagnosis gave me the courage to come out. I remember waiting in fear for a partner to call the police. I remember the end of a short relationship when I was 24 or 25, she was angry that I didn’t want to continue the relationship. I had disclosed my status; we had practiced safer sex; I went with her to get tested and was sick to my stomach with fear she would somehow test positive. Although, I was certain that I was the only person she had ever practiced safe sex with; I was equally certain that her anger with me would motivate her to go to the police.

She did not test positive. She did not go to the police. If she had, what would have happened? Of course, luckily, we do not know. However, based on the data we have from the States, I expect I would have gone to prison.

The stigma that exists, indeed is flamed, against people with HIV would have intersected with the other marginal statuses most of us have, and then been combined with laws that single us out — laws which say to the police, judges, prosecutors, and world at large that we are a particular group of people with disregard for others, a danger, and must be controlled – these factors added together would have made my chance of being heard, of the truth being heard, minimal.

It is important to remember that the law has only one edge. The law is designed to protect the status quo. It is not revolutionary.

HIV criminalisation singles out people living with HIV — people who already face high levels of stigma and discrimination simply for having a medical condition that is associated with groups subjected to social prejudice — for criminal prosecutions for consensual sex among adults. Is this the liberation that we, as feminists, have been fighting for?

To end my remarks, allow me a moment to give credit to the Canadian HIV/AIDS Legal Network, the Positive Women’s Network-USA, the Sero Project, the International Community of Women Living with HIV, and the many other feminist people of all genders working on HIV, criminalisation, mass incarceration, gender-based violence, prison abolition, and human rights with whom I have been fortunate to have soul-searching discussions about the issues that I have addressed here. I also need to thank Edwin Bernard and the HIV Justice Network for all of these reasons and more, especially for taking the chance and hiring me to focus on the issues of gender, justice, and HIV that matter to me so deeply.

 

HIV criminalisation: another form of violence against women in Eastern Europe and Central Asia, by Evgenia Maron

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Today, Sunday, October 23, 2016, Positive Women’s Network – USA observes the third National Day of Action to End Violence Against Women Living with HIV.

This is an event to create awareness about the levels of violence faced by women living with HIV, and to mobilise action to end that violence. As PWN-USA Executive Director, Naina Khanna, describes it: for women, violence is both a cause and a consequence of living with HIV.

The 2016 Day of Action takes as its focus a pernicious form of violence: the criminalisation of women living with HIV.

From the other side of Atlantic Ocean, in Eastern Europe and Central Asia, raising attention to HIV criminalisation as a form of violence against women living with HIV presents a new angle from which to examine how both of these phenomena are understood. Let us consider this intersection, where HIV-related stigma, HIV criminalisation and gender inequality place women at greater risk of violence, maltreatment and injustice.

To date, the HIV Justice Network has documented prosecutions of women under HIV-specific laws criminalising alleged HIV non-disclosure, potential or perceived exposure, and non-intentional transmission in Russia (12 cases); Belarus (5 cases); Kazakhstan (2 cases); Kyrgyzstan (1 case); Moldova (1 case); Tajikistan (1 case); and Ukraine (4 cases). The actual number of prosecutions is certainly much higher.

Let’s take a closer look at Russia’s 12 cases against women living with HIV. In Russia, alleged HIV non-disclosure, potential or perceived exposure, and non-intentional transmission are penalized by up to a maximum of eight years in jail.

Examining the media coverage, none of these women had an opportunity to speak for herself publicly, and at least half of them were subjected to public ‘slut shaming’ in the media because it was alleged they had multiple intimate partners.

The other half of the women were prosecuted by their intimate male partners. The language of the publications depicts the women as irresponsible and unaccountable subjects, highlights their neglect of barrier contraception measures and of their responsibility to disclose, and characterises the women as the ‘source of HIV transmission’. Although it seems that the media were trying to be sympathetic toward these women, the media authors fail to excite pity with stories by adding details about their poor state of health, bearing children a young age, and/or that they pleaded guilty.

Stigma and discrimination, particularly where women’s moral conduct is judged, play a major role in the severe social and physical consequences that women suspected of being HIV-positive can face, impacting media, the legal system and community.

HIV-related stigma and discrimination switches the media’s focus away from the perpetrators of sexual violence and their punishment to speculations about the culpability of a woman-survivor.

HIV-related stigma and discrimination creates HIV-specific laws based on the assumption that women living with HIV are potential perpetrators in need of state control.

HIV-related stigma and discrimination impacts how communities see women living with HIV, potentially legitimizing even murder. This is especially relevant to religious and traditional communities, where the whole family may feel shamed because of the HIV-status of a female family member, and may fuel higher levels of domestic violence, but it goes beyond this.

In Russia, with its 400,000 women who have tested HIV-positive, the fear of partner violence persists as a daily reality. NGOs assess the number of sexual assaults and gender-based violence crimes against women- as 30,000 – 50,000 per year with only 10% of them reported to the police. In the Russian People Living with HIV Stigma Index study, one-fifth of the people with HIV who faced violence said it was perpetrated by their partner.

Indeed, starting from 2007, we have documented at least eight cases of brutal killings of women who either disclosed their HIV-positive status to their partners or were alleged by the killers or police to be HIV-positive. Thus, non-disclosure might be a coping strategy that women develop to try to survive against violence at home, while simultaneously risking prosecution as criminals because of the criminalisation of HIV non-disclosure.

Similarly, in Belarus, the five women who were prosecuted under HIV criminal laws were characterised in the media as frivolous women of easy virtue, alcohol abusers, and unable to take measures to prevent HIV transmission. Given that two of them were prosecuted for potential or perceived HIV exposure, although no transmission occurred, it is important to see how the prosecution started: the women informed their lovers of their HIV status after the sexual activity. In all media reports and comments by the prosecutor’s office, the women were depicted as those actively taking steps to transmit HIV to others; all are described in an active voice as criminals. In Belarus, law enforcement registers a low number of cases of violence against women along with high rates of women dying from violence at home, women with HIV were much more likely to report being physically abused by their spouses and partners.

In Ukraine, at least four women were prosecuted both for HIV transmission to their intimate partners or to both to their partners and their children, and for HIV exposure. There has been a glimmer of hope and reason from Ukraine, however, which might represent a less punitive turn since 2011.

We recently received information about a case in which a woman, accused of alleged non-disclosure, was acquitted. The court argued that “the relations that developed between the partners in their nature was about HIV exposure. Firstly, the crime didn’t constitute the HIV exposure, but only actions that could have been considered as exposure. Second, the pre-trial investigation and the prosecutor falsely assigned responsibility for creating such a threat of exposure to the accused.”

Further, the verdict found that the guilt of the sexual partner of the HIV-positive defendant in creating the threat of HIV exposure was greater than the guilt of the defendant, given that he was 16 years older than her, had more experience, including in relationships with women and had children from different women, and was characterized as having a promiscuous sexual behaviour. Overall, in Ukraine, the courts tended to respond to HIV criminalisation cases against women by reducing the penalty from time in prison to a suspended sentence.

In Kazakhstan, a woman living with HIV from Karaganda, was taken by the police to the AIDS Center to force her to take antiretroviral medication during her pregnancy. The media response discussed only the public health perspective, making the woman appear irrational and uncaring toward her baby. The media said nothing about the reasons why the woman was avoiding treatment, failed to give her a voice, and provided no information about whether social and psychological services were offered to her prior to police involvement.

Further, as documented by us, women in Kazakhstan, Kyrgyzstan and Tajikistan who are marginalized because they do sex work, have been disproportionately targeted by police, and found themselves subjected to forced HIV testing.

The criminalisation of sex work along with public characterisations of sex workers as ‘latent reservoirs for HIV’, sets sex workers up for police harassment, arrest, and unwarranted seizures in the name of public health.

In Kazakhstan, Almaty police identified 98 sex workers as HIV-positive and conducted a search for their clients. However, it remains unknown if the search brought further charges.

In Kyrgyzstan, the practice of illegal HIV testing in association with police raids on sex workers persists. Law enforcement personnel, in order to provide for the formal requirements of the law, summon AIDS center staff members, who obtain written consent to HIV testing under conditions of arbitrary detention. There are also known cases where the police detained sex workers and illegally sent them for forced medical testing, including for STIs and HIV.

Similarly, in Tajikistan, 505 sex workers were detained and forced to undergo HIV and STI testing. Community organizations report that often the test results are disclosed in front of other detainees and police staff.

One way or another, all of these can be also framed in terms of structural or cultural violence, in which social structures are used to justify direct violence or situations that drastically increase the vulnerability of women living with HIV to violence.

In the cases that we know, HIV-related stigma and HIV criminalisation evolve to a form of cultural violence that makes the communities and media audiences feel ‘right’ about blaming the women with HIV who experience an HIV-related prosecution, making this acceptable in our societies.

There is no doubt that gender shapes HIV disclosure motivations and reactions. Disclosure is not a gender-neutral event because women face the possibility of increased violence afterwards. It is an impossible choice: choosing between the immediate need to protect themselves from partner violence, or a risk that they can go to prison for alleged HIV non-disclosure, exposure, or transmission.

No matter where it occurs, it is time to claim justice for women living with HIV.

Evgenia Maron is the HIV Justice Network’s EECA Consultant

The HIV Justice Network is a founding partner of HIV Justice Worldwide, together with the Positive Women’s Network-USA, AIDS Rights Alliance of Southern Africa (ARASA), the Sero Project, the Canadian HIV/AIDS Legal Network, Global Network of People Living with HIV (GNP+), and the International Community of Women Living with HIV (ICW). More information about HIV Justice WorldWide is available here.

Сегодня, в воскресенье, 23 октября 2016 года, “Сеть позитивных женщин – США” объявила третий Национальный день действий для прекращения насилия против женщин, живущих с ВИЧ.

Этот день предназначен для повышения осведомленности о насилии, с которыми сталкиваются женщины, живущие с ВИЧ, а также для мобилизации и действий по прекращению насилия. Как отмечает исполнительный директор PWN-США, Наина Кханна: “Для женщин, насилие является как причиной, так и следствием жизни с ВИЧ”.

В 2016 году темой дня выбрана губительная форма насилия – криминализация женщин, живущих с ВИЧ.

По другую сторону Атлантического океана, в Восточной Европе и Центральной Азии, повышение внимания к проблеме криминализации ВИЧ как одной из форм насилия против женщин, живущих с ВИЧ, представляет собой новый взгляд на исследования, обсловленный тем, как понимаются оба эти явления. Рассмотрим это пересечение, где стигма в связи с ВИЧ, криминализация ВИЧ и гендерное неравенство помещают женщину в ситуацию наибольшего риска насилия, жестокого обращения и несправедливости.

На сегодняшний день Сеть “Правосудие и ВИЧ” задокуменитировала случаи судебного преследования женщин в рамках ВИЧ-специфических законов, вводящих уголовную ответственность за предполагаемое неразглашение ВИЧ-статуса, потенциальную или воспринимаемую постановку в опасность заражения и ненамеренную передачу в России (12 случаев); Беларуси (5 случаев); Казахстане (2 случая); Кыргызстане (1 случай); Молдове (1 случай); Таджикистане (1 случай); и в Украине (4 случая). Фактическое число судебных дел, несомненно, гораздо выше.

Давайте подробнее рассмотрим 12 российских случаев преследования женщин, живущих с ВИЧ. В России предполагаемое нераскрытие ВИЧ-статуса, потенциальная или воспринимаемая постановка в опасность заражения и ненамеренная передача ВИЧ наказываются максимальным сроком до восьми лет в тюрьме.

В результате изучения публикации в СМИ можно сделать вывод, что ни одна из этих женщин не имела возможность говорить за себя публично, и, по крайней мере, половина из них были подвергнуты публичному «слатшеймингу» в СМИ, так как утверждалось, что они имели несколько интимных партнеров.

Другая половина женщин была привлечена к ответственности своими интимными партнерами-мужчинами. Язык публикаций изображает этих женщин как безответственных и немотивированных субъектов, подчеркивает их пренебрежение барьерными мерами контрацепции и своей ответственностью за раскрытие диагноза, и характеризует этих женщин как «источник передачи ВИЧ-инфекции». Хотя кажется, что СМИ пытаются вызвать симпатию к этим женщинам, авторам не удается пробудить жалость рассказами об их плохом состоянии здоровья, рождении детей в молодом возрасте, и / или тем, что они признали свою вину.

Стигма и дискриминация, особенно если судят безнравственное поведение женщин, играют важную роль в тяжелых социальных и физических последствиях, с которыми могут столкнуться женщины, подозреваемые в том, что они ВИЧ-инфицированы, оказывают влияние на мнение СМИ, правовой системы и общества.

Стигма и дискриминации в связи с ВИЧ переключают внимание СМИ от лиц, совершивших сексуальное насилие, и их наказания к спекуляциям о виновности женщины, пережившей насилие.

Стигма и дискриминация в связи с ВИЧ создают определенные законы, основанные на предположении, что женщины, живущие с ВИЧ, являются потенциальными злоумышленниками, над которыми необходим государственный контроль.

Стигма и дискриминация в связи с ВИЧ влияют на то, как общество смотрит на женщин, живущих с ВИЧ, потенциально оправдывая даже убийство. Это особенно актуально для религиозных и традиционных общин, где вся семья может быть опозорена из-за ВИЧ-статуса члена семьи женского пола, а также может повысить уровень насилия в семье, и даже больше.

В России для 400 000 женщин, которые оказались ВИЧ-инфицированными, страх насилия со стороны партнера стал повседневной реальностью. НПО оценивают число сексуальных нападений и гендерных преступлений, связанных с насилием в отношении женщин, в 30 000 – 50 000 ежегодно, и только о 10% из них сообщают в полицию. В исследовании “Индекс стигмы” среди российских людей, живущих с ВИЧ, одна пятая часть людей, живущих с ВИЧ, которые столкнулись с насилием, отметили, что оно было совершено их партнером.

Действительно, начиная с 2007 года, мы задокументировали по меньшей мере восемь случаев жестоких убийств женщин, которые либо сообщили о своем ВИЧ-позитивном статусе своим партнерам или якобы обладали ВИЧ-положительным статусом по мнению убийц или полиции. Таким образом, нераскрытие диагноза может быть копинг-стратегией, которую женщины приобретают, чтобы попытаться выжить после домашнего насилия, одновременно рискуя подвернуться преследованию как преступники из-за криминализации нераскрытия ВИЧ-статуса.

Аналогичным образом, в Беларуси пять женщин, которые были привлечены к ответственности в соответствии с уголовным законодательством о ВИЧ, были охарактеризованы в СМИ как легкомысленные женщины легкого поведения, злоупотребляющие алкоголем, которые были не в состоянии принять меры по предотвращению передачи ВИЧ-инфекции. Учитывая, что двое из них были привлечены к ответственности за потенциальную или предполагаемую постановку в опасность заражения ВИЧ, заражения как такового не произошло, важно рассмотреть, как началось преследование: женщины проинформировали своих любовников о своем ВИЧ-статусе после сексуальной активности. Во всех сообщениях СМИ и комментариях прокуратуры женщины изображались так, как будто они активно принимают меры для передачи ВИЧ другим; все описаны как активно действующие преступники. В Беларуси, где правоохранительные органы регистрируют низкое число случаев насилия в отношении женщин, наряду с высокими показателями смертности женщин от домашнего насилия, женщины с ВИЧ были гораздо более склонны сообщать о физическом насилии со стороны своих супругов и партнеров.

В Украине по меньшей мере четыре женщины подверглись преследованию за передачу ВИЧ своим интимным партнерам или своим партнерам и детям и за постановку в опасность заражения. Можно сказать, что в Украине есть проблеск надежды и разума, однако, что проявляется в менее карательном подходе с 2011 года.

Недавно мы получили информацию о случае, в котором женщина, обвиняемая в предполагаемом нераскрытии статуса, была оправдана. Суд утверждал, что “отношения, которые сложились между партнерами по своей природе были связаны с постановкой в опасность заражения ВИЧ. Во-первых, преступление не представляет собой постановку в опасность ВИЧ, а только действия, которые могли бы рассматриваться в качестве постановки в опасность. Во-вторых, предварительное расследование и прокурор ложно возложили ответственность за создание такой угрозы на обвиняемую”.

Кроме того, в приговоре говорится, что вина полового партнера ВИЧ-положительной ответчицы в создании угрозы заражения ВИЧ была больше, чем вина обвиняемой, при условии, что мужчина был на 16 лет ее старше, у него было больше опыта, в том числе в отношениях с женщинами, он имел детей от разных женщин, и характеризовался как ведущий беспорядочную сексуальную жизнь. В целом, украинские суды, как правило, реагируют на случаи криминализации ВИЧ в отношении женщин, уменьшая подожительность наказание в местах лишения свободы и заменяя на условный приговор.

В Казахстане, женщину, живущую с ВИЧ, из Караганды, полиция силой доставила в Центр СПИДа, чтобы принимать антиретровирусные препараты во время беременности. СМИ осветили случай только с точки зрения общественного здравоохранения, что вынуждает женщину казаться иррациональной и безразличной к своему ребенку. СМИ ничего не рассказывают о причинах, почему женщина избегала лечения, не дают ей говорить за себя, не предусматривают никакой информации о том, были ли ей предложены социальные и психологические услуги до вмешательства полиции.

Кроме того, как задокументировано нами, женщины в Казахстане, Кыргызстане и Таджикистане, которые являются маргинализованными, потому что они занимаются секс-работой, несоразмерно подверглись преследованиям полиции и принудительному тестированию на ВИЧ.

Криминализация секс-работы наряду с общественной характеристикой секс- работников как «латентных резервуаров для ВИЧ», делает секс-работников беззащитными перед произволом сотрудников полиции, арестами и неоправданными задержаниями во имя общественного здоровья.

В Казахстане, полиция Алматы выявила 98 секс- работников как ВИЧ-положительных и провела поиск их клиентов. Однако, остается неизвестным, были ли выдвинуты дополнительные обвинения в результате этого поиска.

В Кыргызстане продолжается практика незаконного тестирования на ВИЧ секс-работников в связи с рейдами полиции. Сотрудники правоохранительных органов, чтобы соответствовать формальным требованиям закона, вызвали сотрудников Центра по борьбе со СПИДом, которые получили письменное согласие на тестирование на ВИЧ в условиях произвольного задержания. Также известны случаи, когда полиция задерживала секс-работников и противозаконно отправляли их на принудительное медицинское тестирования, в том числе на ИППП и ВИЧ.

Кроме того, в Таджикистане, 505 секс- работников были задержаны и вынуждены пройти тестирование на ВИЧ и ИППП. Организации сообщества знают о случаях, когда полиция задерживала секс-работников, незаконно отправляла их на принудительное медицинское обследование, включая ИППП и ВИЧ.

Так или иначе, все это также можно выразить в терминах структурного или культурного насилия, в котором социальные структуры используются, чтобы оправдывать прямое насилие или ситуации, которые кардинальным образом увеличивают уязвимость женщин, живущих с ВИЧ, перед насилием.

В случаях, которые нам известны, стигма в связи с ВИЧ и криминализация ВИЧ приобретают форму культурного насилия, которое заставляет общество и аудиторию СМИ чувствовать себя «правыми», когда обвиняемые женщины, живущие с ВИЧ, подвергаются преследованию в связи с ВИЧ, делая это приемлемым в нашем обществе.

Нет сомнений в том, что гендер определяет мотивацию для раскрытия ВИЧ-статуса и реакции на это. Раскрытие ВИЧ не является гендерно-нейтральным событием, потому что впоследствии женщины сталкиваются с возможностью возросшего насилия. Это невозможный выбор: между немедленной необходимостью защитить себя от насилия со стороны партнера или рисковать тем, что они могут попасть в тюрьму за предполагаемое нераскрытие ВИЧ, постановку в опасность заражения или передачу ВИЧ.

Неважно, где это происходит, пришло время потребовать справедливости для женщин, живущих с ВИЧ.

Евгения Марон – консультант сети “Правосудие и ВИЧ” в Восточной Европе и Центральной Азии

Сеть “Правосудие и ВИЧ” – партнер-основатель инициативы “Правосудие и ВИЧ во всем мире”, вместе с “Сетью позитивных женщин – США”, Альянсом по СПИДу и правам с Южной Африке (ARASA), и “Серо Проджект”, а также Канадской правовой сетью по ВИЧ/СПИду, Глобальной сетью людей, живущих с ВИЧ (GNP+), и Глобальной сетью женщин, живущих с ВИЧ (ICW). Больше информации об инициативе “Правосудие и ВИЧ во всем мире” доступно здесь.

HIV Stigma: Terrorising women in Russia’s traditional societies, by Evgenia Maron

Русский текст читайте, пожалуйста, ниже

On May 30 this year, a publication appeared in the Russian media with a sensational headline: in Dagestan, police stated that unknown men killed a woman after suspecting her of transmitting HIV to others.

Without any explanation of why the police would claim knowledge of a motive when the killers are unknown and without any verification of the claim that the woman transmitted HIV or even knew of her HIV status, the story was reproduced with the same allegations in over 30 Russian newspapers, and even made it to the UK right-wing tabloid, The Daily Mail.

Although the men were unnamed, the publications disclosed the identity of the murdered young woman as Tangaru Ramazanova, 25, from the city of Kizlyar in Russia’s southwestern Republic of Dagestan.

According to the police, she was beaten and stabbed repeatedly. She was found with her body wrapped in plastic and dumped close to the Terek River. Rather than focusing on the brutality of her murder, the stories focused on her alleged HIV status and cast aspersions against her moral character.

No report examined whether she actually was HIV-positive or whether the allegations were, in fact, true.

No report discussed concepts of mutual responsibility or safer sex or, most notably, countered the narrative that legitimized her murder.

Underlying the human tragedy for Tangaru and her family is Russia’s stigmatizing Article 122 which, in direct contradiction to global recommendations on HIV and the law, characterizes sexual contact involving a person living with HIV as a criminal act on the part of the person living with HIV unless proven otherwise. This national law, as in 72 other countries, creates a legal and social environment within which a person who is HIV-positive faces assumptions that she has somehow brought any violent or damaging actions upon herself.

This case in Dagestan is not an isolated event in which violence against women, or violence specifically against women (apparently) living with HIV, is publicly justified in the North Caucuses.

In this region of Russia alone, women’s NGOs and individual women’s rights activists report that women have been victims of ‘honour killings’, bride kidnappings, forced and child marriage and other traditional practices for the past 20 years, exacerbated by a climate of lawlessness, impunity and corruption. Norms, upholding patriarchy, deny women and girls full legal personhood for their entire lives, deprive them of property and inheritance rights, enshrine men’s control over women’s lives and bodies, and treat many forms of violence against women as permissible and justified ‘punishment’.

Mari Davtyan, a Human Rights Lawyer working on issues of violence against women in Russia, describes the connections between this murder, HIV stigma, and patriarchal control:

“Taking into account the experience of my colleagues there, there is a suspicion that a possible HIV status is just a horror story, which can justify the killing of women. There allegation communicated by the source of the media report that she was killed for transmitting HIV to somebody has now become a comfortable story, defining an approach to the investigation, looking for an excuse for the criminal. So called ‘honour killings’ are not always ‘honour killings’, as it is men alone who decide in the North Caucasus whether it is an honour killing or not. I’m pretty sure that the killer(s) will not be found.

The horror is that that the woman was completely dehumanised, because someone who has HIV is not (perceived to be) a person, and thus we are not looking for someone who infected or killed her. This is only possible in a relation to a woman; a man cannot be punished for the same thing. Women living with HIV are exposed to strong stigma, especially in the North Caucasus. In Dagestan, the public disclosure of her name is a great stigma on the family. It demonstrates well that, if a woman has HIV, one can justify anything, from shaming to killing. In the eyes of society, a woman (with HIV) is vicious, not a man.”

Outside the North Caucus region, a similarly concerning case took place in Moscow.  The media published a story on a group rape of a young HIV-positive woman who pleaded with the perpetrators to stop as she had HIV. Rather than a story about the crime of rape, the media focus was on the HIV status of the rape survivor. There is no reason other than HIV stigma that could make journalists present this case, not as a rape case, but as a story focused on the potential harm faced by the perpetrators. Some of the media reports go so far as to claim that all of the perpetrators tested HIV-positive after the rape, but there is no analysis or confirmation of this. Instead, the media focused on whether the woman might be culpable for potentially transmitting HIV to her attackers, as HIV transmission is punishable, with up to eight years in prison for infecting two or more persons, under Article 122 of the Russian Criminal Code.

In both of these recent cases, stigma around HIV proved stronger than all the horror of the facts: the readers’ attention is switched to the girls’ behaviour and possible – not proved – risk to male “others.”  In Tangaru Ramazanova’s murder, the killing is ‘justified’ by claims that the killers were ‘provoked’ by her because of an assumption that she lived an “immoral” lifestyle. Like the woman raped in Moscow, Tangaru, who can no longer speak for herself, is presented as a contagious person who transmitted HIV to others.

The narrative about both women serves to reduce the severity of punishment deemed appropriate for the perpetrators and to reduce the pressure on the police to identify or charge the perpetrators. At the same time, the narrative limits any space for discussions of the effects of HIV-related stigma and discrimination multiplied by gender inequality.

HIV stigma is so great in Russian societies that it becomes a tool to further control and terrorize women. The particular beliefs in traditional societies about women’s lower status and their obligation to symbolize family and community morality, combined with HIV stigma, becomes deadly.

The focus of Russia’s HIV response should be on ending deaths, stigma, discrimination and suffering. However, the power of HIV stigma is that it does not matter who committed the crime when the police, the killers and the media, all are convinced that people living with HIV are bad, immoral people. HIV stigma appears to justify murder.

HIV-specific laws, such as Russia’s Article 122, cement a stigma-laden view of people with HIV within the criminal code. Here, gender inequality and the HIV criminalisation law come together to create this dangerous environment, where violent acts target a specific group: women living with HIV — because they are women and they live with HIV.

Russia’s HIV-specific law contributes much to this stigma; rather than empowering women to enjoy human rights, this law victimizes, oppresses and endangers women; rather than offering women protection and justice in the face of violence, this law legitimizes their murder.

Evgenia Maron is the HIV Justice Network’s EECA Consultant

 

ВИЧ-стигма: терроризируя женщин в российских традиционных общинах

30 мая этого года в российских СМИ появилась публикация с сенсационным заголовком: в  Дагестане полиция заявила, что неизвестные мужчины убили женщину, подозревая её в распространении ВИЧ.

Без каких-либо объяснений, почему полиция утверждает, что знает мотив, когда убийцы неизвестны, без какой-либо проверки информации, что женщина передала ВИЧ или вообще знала о своём ВИЧ-статусе, историю с такими же обвинениями воспроизвели более 30 российских газет, она даже попала в таблоид правого толка в Великобритании, The Daily Mail.

Хотя мужчины остались неназванными, в публикации раскрывается личность убитой молодой женщины: Тангару Рамазанова, 25 лет, из города Кизляр на юго-западе российской республики Дагестан.

По данным полиции, её многократно избивали и резали. Она была найдена выброшенной неподалёку от реки Терек, тело, завёрнутое в пластик. Вместо того, чтобы говорить о жестокости её убийства, новости были сосредоточены на её предполагаемом ВИЧ-статусе и выдвигали обвинения в аморальности её репутации.

Ни в одной истории не изучался вопрос, была ли она ВИЧ-позитивной на самом деле, были ли эти утверждения, по сути, верными.

Ни в одной истории речь не шла о концепции взаимной ответственности или о безопасном сексе, в первую очередь, этому противопоставлялся нарратив, который оправдывал её убийство.

В основе человеческой трагедии Тангару и её семьи – российская стигматизирующая статья 122, которая прямо противоречит глобальными рекомендациями по ВИЧ и законодательству, характеризуя сексуальный контакт с участием человека, живущего с ВИЧ, как преступное деяние со стороны человека, живущего с ВИЧ, если не доказано иное. Такое национальное законодательство, как и законы ещё 72 стран, создаёт правовую и социальную среду, в которой человек, который является ВИЧ-позитивным, сталкивается с подозрением, что она каким-то образом осуществила какие-то насильственные или прочие наносящие ущерб действия.

Этот случай в Дагестане не является единичным случаем, в котором насилие в отношении женщин, или насилие конкретно в отношении женщин (предположительно), живущих с ВИЧ, публично оправдывается на Северном Кавказе.

Только на основе данных из этого региона России, женские НГО и активисты, которые защищают права женщин, сообщают, что женщины были жертвами “убийств чести”, похищений невест, брака без согласия и детского брака и других видов традиционных практик за последние 20 лет, усугубляется обстановка беззакония, безнаказанности и коррупции. Нормы, поддерживающие патриархат, отказывают женщинам и девочкам в полной юридической право- и дееспособности на протяжении всей их жизни, лишают их прав собственности и наследования, закрепляют мужской контроль над жизнью и телом женщины, считают разные формы насилия в отношении женщин допустимыми, оправдывают «наказание».

Мари Давтян, юрист, который работает в области прав человека, в частности по вопросам насилия против женщин в России, описала связь между этим убийством, ВИЧ-стигмой и патриархальным контролем:

 “Принимая во внимание опыт моих коллег там, есть подозрение, что предполагаемый ВИЧ-статус – просто страшилка, которая может оправдать убийство женщин. Подозрения, которыми источник делится со СМИ , что она была убита за передачу ВИЧ кому-то, теперь становятся удобной историей, которая определяет подход следствия, ищется повод для оправдания преступника. Так называемые “убийства чести” – не всегда “убийства чести”, так как только мужчины на Северном Кавказе решают в одиночку, является ли это “убийством чести” или нет. Я вполне уверена, что убийца(ы) не будет(ут) найден(ы).

Ужас в том, что, что женщина была полностью дегуманизирована, потому что кто-то, у кого есть ВИЧ, не воспринимается как человек, не является человеком, и, таким образом, мы не ищем тех, кто заразил или убил её. Это возможно только по отношению к женщине; мужчина не может быть наказан за то же самое. Женщины, живущие с ВИЧ, подвергаются сильной стигматизации, особенно на Северном Кавказе. В Дагестане, публичное раскрытие её имени – очень большое клеймо для семьи. Это хорошо демонстрирует, что если у женщины есть ВИЧ, можно оправдать что угодно, от посрамления до убийства. В глазах общества, женщина (с ВИЧ) порочна, но не мужчина.”

За пределами Северного Кавказа такой же вопиющий случай произошёл в Москве. СМИ опубликовали историю о групповом изнасиловании молодой ВИЧ-позитивной женщины, которая умоляла преступников остановиться, так как у неё была ВИЧ-инфекция. Вместо того, чтобы опубликовать новость о преступлении –  изнасиловании, – в центре внимания СМИ оказался ВИЧ-статус женщины, пережившей изнасилование. Нет никаких оснований, кроме ВИЧ-стигмы, которые могли бы заставить журналистов представить этот случай не как случай изнасилования, а как историю с акцентом на потенциальном вреде, с которым столкнулись преступники. Некоторые из сообщений СМИ заходят настолько далеко, чтобы утверждать, что все преступники оказались ВИЧ-позитивными после изнасилования, но нет никакого анализа или подтверждения этого. СМИ сосредоточены на том, может ли женщина быть виновной в потенциальной передаче ВИЧ нападавшим, поскольку передача ВИЧ наказуема сроком до восьми лет тюрьмы за заражение двух или более лиц в соответствии со статьёй 122 Уголовного кодекса Российской Федерации.

В этих недавних случаях, стигма в отношении ВИЧ оказалась сильнее, чем весь ужас фактов: внимание читателей переключилось на поведение девушек и возможных – не доказанных, – рисков для “других” мужского пола. В деле Тангару Рамазановой, её убийство “оправдывается” утверждениями, что убийцы были “спровоцированы” ею из-за предположения, что она вела “аморальный” образ жизни. Как женщина, изнасилованная в Москве, Тангару, которая уже не может высказаться от собственного имени, предстаёт как заразный человек, который передавал ВИЧ другим.

Два этих нарратива о женщинах служат для уменьшения тяжести наказания, которое целесообразно для преступников, и снижения давления на полицию, чтобы та нашла и привлекла преступников к ответственности . В то же время, эти нарративы ограничивают любое пространство для обсуждения последствий стигмы и дискриминации в отношении ВИЧ, умноженной на гендерное неравенство.

Стигматизация ВИЧ настолько велика в российском обществе, что становится инструментом для ещё большего контроля и террора в отношении женщин. Конкретные верования в традиционных обществах о более низком положении женщины и её обязанности символизировать семью и мораль общества в сочетании с ВИЧ-стигмой становятся смертельными.

В центре внимания мер по борьбе с ВИЧ в России должно быть прекращение смертей, стигмы, дискриминации и страданий. Тем не менее, сила стигмы в отношении ВИЧ в том, что не имеет значения, кто совершил преступление, когда полиция, убийцы и средства массовой информации, все убеждены в том, что люди, живущие с ВИЧ, – это плохие, безнравственные люди. Стигматизация ВИЧ в таком случае оправдывает убийство.

ВИЧ-специфические законы, такие как российская статья 122, накрепко цементируют предвзятое восприятие людей, живущих с ВИЧ, в рамках уголовного кодекса. Здесь гендерное неравенство и криминализация ВИЧ соединяются воедино, создавая эту опасную среду, где насильственные действия нацелены на определённую группу: женщины, живущие с ВИЧ, – потому, что они женщины, и потому, что они живут с ВИЧ.

ВИЧ-специфическое законодательство России вносит серьёзный вклад в эту стигму; вместо того, чтобы развивать потенциал женщин, чтобы они могли пользоваться своими правами, этот закон делает женщину жертвой, подавляет и ставит её в опасность; вместо того, чтобы предложить женщине защиту и правосудие в ситуации насилия, этот закон оправдывает её убийство.

Евгения Марон является консультантом сети “Правосудие и ВИЧ” в регионе ВЕЦА

Poster Action at AIDS 2016, by Laurel Sprague Ph.D. Global Research Fellow on HIV, Gender, and Justice, HIV Justice Network

(R-L) Paul Kidd, Trevor Hoppe, Edwin Bernard and Nicholas Feustel in front of some of the many posters on HIV criminalisation presented at AIDS 2016

 

 

Participants at AIDS 2016 saw a remarkable number of posters on HIV criminalisation and legal reform, with 22 posters presented, providing data and strategies from 19 countries, three regions, and the global response. While the conference included some strong panels that focused on advocacy and legal environments, for the most in-depth information on movements to address HIV criminalisation and other human rights abuses, the action was in the poster hallways.

Of these posters, eight focused specifically on HIV criminalisation.  The poster on “Global Trends in HIV Criminalisation”, documented 72 countries with HIV-specific criminal laws, including 2 recent, overly broad, criminal laws passed in Uganda (2014) and Nigeria (2015). Between April 2013 and October 2015, 313 arrests and prosecutions were identified in 28 countries, with the highest numbers of arrests occurring in Russia, US, Belarus, and Canada (see Advancing HIV Justice 2 for more details).

From Victoria, Australia, Paul Kidd and colleagues described the successful advocacy process they followed to repeal the discriminatory HIV law. Their strategy for success combined four key factors: drawing attention to the disproportionately high numbers of prosecutions in Victoria, combined with international attention resulting from the AIDS 2014 conference, plus joining their efforts to the momentum from the global movement to end HIV criminalisation, with, above all, dedicated and strategic local activists willing to work tirelessly with parliamentarians, judges, and other civil society organizations.

download all the posters in one pdf file here

The role of scientific evidence in legal reform was highlighted in Kazatchkine and colleagues’ description of a scientific consensus statement on HIV and the criminal law by 6 Canadian scientists and clinicians. Organized to counter the troubling 2012 Canadian Supreme Court interpretation of the law, the consensus statement has been successful in mobilizing experts (with 75 expert sign-ons) and in gaining lower court decisions to reduce or drop HIV C charges.

Disparities in the use of the criminal law on HIV against racial and key population groups were the focus points of two posters from the US: in a study of HIV-specific laws in five Southern and Midwestern states, African American men with HIV received prison sentences that were three years longer, on average, than those to which white men were subjected; an examination of California’s HIV-specific laws found that sex workers were charged in 95% of the cases and were found guilty 100% of the time.

Another two posters closely examined the provisions of specific criminal laws.  Eba and colleagues found that 24 of the 26 laws passed in the last 15 years in sub-Saharan Africa contained provisions that ran contrary to the six guidelines in the 2013 UNAIDS guidance note on ending overly broad HIV criminalisation. The most frequent problematic provisions were those that allowed prosecutions even if the person with HIV: did not know her/his status, was on effective treatment or had a low viral load, disclosed her/his status, or used a condom. Further, in 16 countries, the provisions of the law were so vague that women could be charged for HIV transmission to their children during pregnancy, delivery, or breastfeeding.  An analysis of the French law by Celse and colleagues showed similarly problematic provisions, namely, that the law allows prosecution in the absence of transmission and that, although condom use can be a defense, neither disclosure, consent, nor the lack of knowledge of one’s HIV status are total defenses under French law.

Posters from Jamaica and from Canada examined strategies for legal reform. These provide lessons for HIV criminalisation movements: through a description of the on-going legal challenge in Jamaica to prohibit LGBT discrimination by private actors (the media, in this case), Tomlinson and Elliott demonstrated the importance of long-term vision, funding, and ability to sustain the struggle. From Canada, Hon Chu and colleagues described the byzantine process of legal reform for sex workers. The message for marginalized groups: be prepared for a long struggle, maintain strong ally relationships, and recognize that two steps back may follow one step forward.

While not specific to HIV-criminalisation, six posters discussed tools for legal reform.

  • Strategic litigation was the focus of work supported by OSF. This poster highlighted lessons learned — lessons that could be useful for challenges to HIV criminal laws – including to integrate strategic litigation into a longer-term advocacy strategy, to build a broad partnership base in social movements and with health and economics experts; to consider incremental approaches to litigation; and to develop an implementation plan before litigation starts.
  • Other posters focused on the use of “mapping” legal environments and successes in using the resulting evidence for empowering rights holders (multiple African countries), challenging discriminatory HIV laws (DR Congo), and passing protective laws against gender-based violence (in Nigeria).
  • In a close look at advocacy to combat anti-LGBT laws, two posters supported by UNDP highlighted the critical importance of creating national multi-stakeholder groups –including people living with HIV, key populations, civil society organizations, UN agencies, academics, lawyers, and others – who can respond rapidly to engage parliamentarians and ministries of justice. One notable success of these groups is found in DR Congo and Burkina Faso: after a strong stakeholder group in DR Congo fought back a bill to criminalise same-sex sexual relationships in 2013, the same stakeholder group was able to reconvene quickly to assist their peers in Burkina Faso: LGBT, HIV, and UN stakeholders, to fight back a similar proposed bill in 2015.

An additional five posters shared strategies for providing legal services and knowledge of rights for marginalized groups of people, including:

  • The REAct programme, supported by the International HIV/AIDS Alliance in Myanmar, Lebanon, Uganda, Senegal, South Africa and Zimbabwe, which allows online reporting of human rights violations and links those who report these violations to legal and social support.
  • Programmes supported by the Open Societies Foundation and by the International Development Law Organization, as well as a provincial project by COCQ-SIDA in Quebec, Canada, to bring legal assistance into communities and increase rights education to people from key populations as well as to those working in legal and health systems.

A final group of posters shared important work linking punitive legal environments to negative health outcomes for people who are members of key populations groups:

  • In Burundi and Nigeria, anti-gay legislation has led to stigma and discrimination in health care facilities and resulting avoidance of care by LGBT people (Burundi) and increased HIV prevalence among gay men and other MSM, avoidance or delays in accessing health care for STI symptoms, and coercion to pay double or more costs for health care to avoid being reported to the police (Nigeria).
  • In South Africa, researchers measured the differences in the numbers of human rights violations against people who inject drugs, between 2 cities with vocal political and community resistance to needle and syringe exchange programmes (NSP) and one city without this resistance. The cities with resistance had higher numbers of human rights violations (confiscation of injecting equipment, arrest without cause, and physical assault) and decreased numbers of people accessing NSP services.

HIV Criminalisation and Justice Posters at AIDS 2016 by HIV Justice Network on Scribd

Working with the 2016 Political Declaration on Ending AIDS: Increased commitments towards enabling legal environments, by Laurel Sprague

By Laurel Sprague Ph.D.

Global Research Fellow on HIV, Gender, and Justice, HIV Justice Network

As the dust settles from the 2016 High Level Meeting on Ending AIDS, our communities need to take stock of where we are now and what we have to work with in the 2016 Political Declaration[1].

This blog post, focused primarily on the paragraphs dealing with legal environments, is one contribution to that effort.

Good analyses are available already about the overall advances and inadequacies in the Declaration; the disregard for the leadership of key populations and the refusal to call for protective legal environments or anti-stigma initiatives from MSMGF[2] and GNP+[3]; and the importance of realising the commitments on access to medicines from MSF[4].

Communities have been united overall in our resistance to the Political Declaration’s claim to be part of “a virtuous cycle of progress” in responding to HIV/AIDS. However, when it comes to support for enabling legal environments, we can identify progress from the 2011 Political Declaration[5] to the 2016 Declaration.

In 2016, the UN Member States greatly increased their focus on the role of laws and policies in the HIV response.

HIV criminalisation finally recognised as an important barrier to ‘Ending AIDS’

Both the 2011 and 2016 declarations highlight the importance of:

  • removing unequal legal status of women and the relationship between discriminatory laws and violence against women;
  • ensuring legal frameworks to protect the rights of young people, including addressing barriers to HIV prevention created by age of consent laws;
  • ending barriers to HIV prevention, treatment, care, and support that are created by discriminatory legal environments; and
  • removing restrictions on the free movement of people with HIV.

In the 2011 Declaration, explicit attention was focused only on one kind of restrictive law: laws regarding entry, travel, and stay restrictions based on HIV status. By contrast, in the 2016 Declaration, UN Member States specifically committed:

To review and reform:

  • Laws related to HIV non-disclosure, exposure and transmission; and
  • Laws related to mandatory testing, including of pregnant women

To adopt, review and accelerate:

  • Effective implementation of laws that criminalize violence against women and girls, as well … prosecutorial measures … to eliminate and prevent all forms of violence against all women and girls

As well as continuing to focus on eliminating:

  • Restrictions on entry based on HIV status

The 2016 Political Declaration also extends recognition of the importance of the law in protecting the fundamental human rights and freedoms of children and adolescents, with Member States committing to promote:

  • Laws and policies that ensure the enjoyment of all human rights and fundamental freedoms for children, adolescents and young people, particularly those living with, at risk of, and affected by HIV.

A similar provision existed in the 2011 Political Declaration but only included young people within its purview.

Perspective shifts in legal environments

Regarding legal environments for people living with HIV, an important shift in perspective is found in the 2016 Declaration. The 2011 Declaration noted the need for “legal literacy and legal services.”

In 2016, the same paragraph has been reworked in much stronger language. It now commits Member States to empower PLHIV, those at risk, and those affected “to know their rights and to access justice and legal services to prevent and challenge violations of human rights.”

Further, as in 2011, the paragraph commits Member States to train and sensitize law enforcement officials, judges, and health care workers, but it now also includes a commitment to sensitize members of the legislature.

The 2016 Declaration also contains weaker paragraphs that “call attention to” the restrictive laws that marginalise and discriminate against people who use drugs, and “note grave concern” about legal discrimination against people with disabilities.

What about other key populations?

The 2016 Declaration is weak in its attention to key populations, scarcely improved from 2011. The few bright spots are that transgender people and people who are incarcerated are included in the list of key population groups for the first time (and the term “key populations” makes its first appearance in a General Assembly document). Yet, if we are smart in our approach, there can be more than meets the eye for key populations and we can do our best to push for strong interpretations of the Declaration’s language.

Throughout the Declaration, variations of the phrase “people living with and affected by HIV and those at higher risk” can be found. Although clearer wording would have been preferable, it can[6] and should be argued that this phrase includes key populations every time it is used. The Declaration describes key populations as those “at higher risk of infection” and specifically includes people who inject drugs, sex workers, men who have sex with men, transgender people, and prisoners.

When understood in this way, the Declaration calls for all of the following for people living with HIV and for key populations:

  • realisation of the GIPA principle for greater and meaningful involvement in the HIV response;
  • protection of human rights for all ages;
  • recognition of the right to equal participation in civil, political, social, economic and cultural life;
  • empowerment to know one’s rights and to access justice and legal services to prevent and challenge violations of human rights; and
  • removal of prejudice, stigma, or discrimination.

Something to watch out for regarding the Declaration language and key populations: conservative Member States were successful in getting language that would appear to allow individual countries to make their own determinations regarding who counts as a key population.

This language includes phrases such as, “populations at highest risk, depending on local circumstances,” and “taking into account national context.” However, it is crucial for civil society groups working in this space to consistently press the point that these determinations must be evidence based.

In the Declaration, key populations are described as those that epidemiological evidence shows are at higher risk of HIV infection. Further, Member States agreed to emphasize, “that each country should define the specific populations that are key to its epidemic and response based on the local epidemiological context.”

Call to action

In concluding this blog, I have a few reflections on the political environment in which we find ourselves: the extent of open and unabashed global hostility toward people living with HIV and key populations, especially toward gay men – combined with what was either a lack of political will by friendlier UN Member States or a genuine belief that they could do no better – was and should continue to be sobering.

More than sobering, it is an urgent call to action.

We are not going to get better commitments without an immense, intensified, and well-coordinated effort to move governments at national levels. And while we wait, and waste time bemoaning the outcome of the Declaration, members of our communities who live under these hostile governments suffer, facing threats to their dignity, liberty, and survival.

Further, the level of discord amongst UN Member States regarding this Declaration run very deep. This was demonstrated by the reservations expressed by Member States after the adoption of the Declaration and by paragraphs throughout the Declaration that are packed with so many clauses as to make them incomprehensible. This is evidence that every word and punctuation point was debated to its death.

Championing the advocacy successes in the Declaration

Some quick initial thoughts about next steps:

If advocacy organisations can let go of the dreadful experience of the High Level Meeting, then we can get busy championing the advocacy successes in the Declaration. It will be critical to lead the conversation with our understanding and interpretations, turning them into facts on the ground before there can be any reversal.

In addition to the progress on legal frameworks, one key advocacy success – with years of planning behind it — is the call for funding for civil society organizations.

UN Member States called for “at least 6%[7] of all global AIDS resources [to be] allocated for social enablers including advocacy, community and political mobilization, community monitoring, public communication, outreach programmes … as well as human rights programmes such as law and policy reform, and stigma and discrimination reduction” and called for “community-led service delivery to cover at least 30% of all service delivery.”

Finally, it is worth keeping in mind that the UNAIDS Strategy, 2016-2021,[8] has much stronger commitments in the areas of SRHR and key populations than those in the Declaration and can be used whenever possible to advocate for the things that communities need to survive this epidemic.

 

Footnotes

[1] http://www.unaids.org/sites/default/files/media_asset/2016-political-declaration-HIV-AIDS_en.pdf

[2]http://msmgf.org/gay_men_transgender_people_and_sex_workers_express_outragemsmgf-expresses-outrage-unacceptably-weak-political-declaration-adopted-today-united-nations-high-level-meeting-ending-aids/

[3] http://www.gnpplus.net/political-declaration-will-not-end-aids/

[4] http://www.doctorswithoutborders.org/article/doctors-without-borders-response-2016-united-nations-political-declaration-ending-aids

[5] http://www.unaids.org/sites/default/files/sub_landing/files/20110610_UN_A-RES-65-277_en.pdf

[6] Tremendous debt of gratitude to Richard Elliot of the Canadian HIV/AIDS Legal Network for first noticing this link.

[7] In 2014, UNAIDS estimated that only 1% of global AIDS funding went to the civil society and community response.  See: http://www.unaids.org/sites/default/files/media_asset/JC2686_WAD2014report_en.pdf

[8] http://www.unaids.org/sites/default/files/media_asset/20151027_UNAIDS_PCB37_15_18_EN_rev1.pdf

Together we *can* make HIV JUSTICE WORLDWIDE a reality, by Edwin J Bernard

Two weeks ago, thanks to generous funding for 2016-18 from the Robert Carr civil society Networks Fund, a group of committed activists from all over the world came together in Brighton, the home of the HIV Justice Network, so we could strategise how to work closer together in order to end HIV criminalisation.

It’s been a long journey to get to this point.  I first started writing about HIV criminalisation in 2003 when, in my first months as editor of NAM’s AIDS Treatment Update, we had our first prosecutions in England and Wales for ‘reckless’ HIV transmission.

After writing my first book on the subject for NAM in 2007 – Criminal HIV Transmission, which aimed to educate the criminal justice system about the latest medical and social science developments relating to HIV – I began a blog of the same name which, almost by accident, became a global de facto information and advocacy hub.

In 2008, on the final day of the International AIDS Conference in Mexico City, Justice Edwin Cameron gave a powerful speech entitled ‘HIV is a virus not a crime’ that vocalised a burgeoning movement using many examples culled from the blog. At its rousing conclusion, he called for a sustained and vocal campaign that would lead to major international pushback against misguided criminal laws and prosecutions.

I took Justice Cameron’s call to action utterly and complelely to heart, and have made this the focus of my life’s work ever since: highlights of which include writing a second book for NAM in 2010; working with UNAIDS on their 2013 guidance; and, of course, launching the HIV Justice Network.

Today, marks a new milestone for my vocation. As part of a group of seven global, regional and national civil society organisations that have worked closely, but informally, together on HIV criminalisation for a number years, I can proudly announce a brand new initiative, HIV JUSTICE WORLDWIDE.

HIV JUSTICE WORLDWIDE comes at a time when there is an urgent need to capitalise on current advocacy successes in some parts of the world and to resist new and proposed laws in others. It is also evident that preventing and remedying HIV criminalisation is going take many years, if not decades, and so we need to work together because:

  • HIV criminalisation is an international issue, having grown in scope and severity over the last two decades;
  • international actors such as UNAIDS, UNDP, the Global Commission on HIV and the Law and others have been – or need to be – involved in this issue, and civil society needs to be able to effectively engage with these actors;
  • international pressure can often be helpful in responding to problematic regional or national developments; and
  • a global movement can help raise awareness and build capacity of local actors around the world by sharing knowledge, experience, strategies, tools and mobilising resources.

The organisations that make up the founding partners, along with the HIV Justice Network, are:

We also have the support of UNAIDS and UNDP and global HIV organisations such as the International HIV/AIDS Alliance. As time goes on we will will announce new projects and partners – all with the goal of ending HIV criminalisation by empowering people living with HIV and those who advocate on our behalf to ensure policymakers, criminal justice actors and other relevant stakeholders abolish existing laws and oppose the passage of proposed laws designed to regulate, control, and punish people living with HIV on the basis of their HIV status.

HIV JUSTICE WORLDWIDE will enhance and build on contributions its founding partners have previously made: monitoring, informing, connecting and engaging with People Living with HIV networks, civil society organisations and others who advocate against HIV criminalisation, and engaging policy-makers in pursuit of protecting against HIV criminalisation.

The initiative allows us to:

  • Avoid duplication by bringing together the many existing resources on this issue, sharing information and coordinating advocacy efforts.
  • Build broader consensus amongst People Living with HIV networks, civil society, policymakers, key scientists/clinicians, criminal justice actors and funders that ‘ending AIDS’ will not happen unless we put an end to HIV criminalisation.
  • Create new energy and action, ‘riding the wave’ of recent advocacy successes, pushing for commitment to change at the highest level.
  • Develop and strengthen much-needed civil society capacity to ensure continued advocacy against HIV criminalisation, and to sustain this capacity in order to further advocate against related punitive laws, policies and practices aimed at people living with HIV and which impede the HIV response.

To find out more about what HIV JUSTICE WORLDWIDE is all about, please visit the website, and watch the video.