Russia: In 2021, people living with HIV are still facing criminalisation, stigma, healthcare denial, dismissal and deportation

Who protects people with HIV in St Petersburg and how?

Stigma, denial of health services, dismissal, deportation – these are just some of the problems HIV-positive people in Russia can face. For 25 years Positive Dialogue NGO helps people with these problems.

A quiet street in the centre of St. Petersburg, a yard with bright graffiti – a portrait of a girl with long hair and the text Lu Blue. No other graffiti so far.

Mikhail Stupishin, the head of Positive Dialogue, meets me at the door. A few steps down, and we are in a bright office. The Positive Dialogue only recently moved into the building, because for years before it was located on the grounds of Botkin Infectious Diseases Hospital.

– The first quarter of the 21st century is coming to an end and people still have HIV-phobic cockroaches in their heads,” laughs Mikhail, pouring coffee and talking about the move. – Four premises were refused to us due to the nature of our business. At the preview, we explained that we are now focused on individual counselling and not on mass events, we said that we have a flow of clients, but not as a mausoleum, that we work with a socially significant disease – HIV infection. We were told: “Yes, yes, yes, everything is great”. And when it came to concluding an agreement, they said: “We looked at the website what you do. This is too extreme for us”.

I am reminded of Anna, the heroine of my text ‘Anna and Her Victories’, a mentee of Positive Dialogue. What is extreme is the treatment she and many other people face time and again because of their HIV-positive status. For example, when her own mother, an experienced health worker, forces her daughter to eat from separate dishes even though there is no contact-domestic transmission of HIV. Or when a person is not wanted to work because of his/her HIV status, despite the fact that thanks to therapy (free and accessible) his/her viral load has been undetectable for a long time – this means that he/she cannot infect anybody in any way. Anna told us that in the most desperate situations she called Positive Dialogue and thanks to her conversation with lawyer Alexander Loza she solved problems with her job and then with her studies more than once.

Alexander joins Mikhail and me, we shake hands and begin a conversation that lasts more than two hours, but even that time seems short. The problems faced by people with HIV in Russia are too many.

“Positive Dialogue started as far back as 25 years ago. It was founded by Nikolai Panchenko, a lawyer and one of the first registered HIV-positive people in the USSR. He recently celebrated his 70th birthday and handed over the leadership of the organisation to Mikhail Stupishin a few years ago, but Panchenko’s name keeps coming up in conversation – it was he who started the education work, talking about HIV prevention and life with HIV. This is as necessary now as it was a quarter of a century ago.

– Sasha has been working here since 2004, and I joined in 2015,” says Mikhail. – At that time two big prevention projects were launched: HIV prevention among men who have sex with men and HIV prevention among female sex workers. I came upon the recommendation of an acquaintance. I have secondary medical education. I am not a doctor but a paramedic. I know anatomy well, I know pathophysiology well, or at least I knew it, I understand where the legs are growing from.

In addition to his medical education, Mikhail graduated from the University of Culture, and Alexander studied at St. Petersburg State University. A medical doctor and a lawyer, both have extensive experience of working with people in difficult life situations.

– Many people need legal advice,” says Alexander. – Not everyone has the money to pay for a consultation, not everyone wants to talk about their specific problems, and not all lawyers are practiced at it.

– Do they often come to you with work-related issues? – I ask. But it turns out to be not quite what I imagined.

According to Alexander, medical workers who have to undergo compulsory tests, including HIV tests, every year are most afraid of being fired. However, police officers and employees of the Ministry of Emergency Situations also seek advice: contrary to the federal legislation, these agencies impose a complete ban on work for HIV-positive people – they issue local acts on undergoing medical examinations and declare them unfit or limited fit for service.

– Is there anything you can do in such situations?

– Well, back in Soviet times, an act was passed that people with HIV infection could not be commanders of aircraft,” Alexander sighs. – Five or seven years ago, one captain was diagnosed with HIV. He went to the General Prosecutor’s Office, the General Prosecutor’s Office went to the Supreme Court, and the Supreme Court ruled the act illegal. But the man had to disclose his status to everyone. It is not about the court per se – a person’s name can be hidden in the documents. But the employer often puts pressure on the employee, may spread rumours about him.

Mikhail cites the story of his acquaintance, who was literally “eaten up” at work, in the most ordinary office, when he found out about his HIV status. Litigating in such situations can be futile: legally, the case is a win-win – the dismissal is illegal, but they will not give you life at work.

People rarely go to court against employers, and as a rule, it is high-profile cases that change the local normative acts of an organization.

– We have it written into the law that this is discrimination, that the employer will be fined, there is criminal liability,” Alexander says. – But everyone tries to do it quietly: you resign at your own request, you get some severance pay, and you leave quietly (what happens to you next is your problem), while we will be white and fluffy. I always say that fighting for one’s rights is fraught: they can create such conditions that a person will be forced to leave. Constant stress is also bad for the body.

Last year, according to Alexander, the Prosecutor General’s Office tried to issue a local act banning people with HIV from working, but there was an uproar and the agency had to abandon the idea. But the Ministry of Railways and Communication seems to have succeeded in introducing a local ban.

– In general, if you start having problems at work because of your HIV status, the only way out is to look for a normal employer?

– We don’t have a ‘normal employer’ as such,” Alexander shakes his head.

– It’s not so much about the employer,” adds Mikhail, “it’s more about your direct supervisor or upper management if you are in his position.

He recounts cases of people being tested for HIV without their knowledge when they are hired. This practice is, of course, illegal:

– The issue of informing about a person’s status is generally very strict: no disclosure, only at the official request of the court or the prosecutor’s office. Only then the AIDS Centre is obliged to provide information whether the person is registered or not. If a person realises that he or she has not told anyone about his or her status, but the employer has the information, it means that during the medical examination, blood was taken for HIV infection. But, in theory, the employer cannot make any further moves, because the whole story is illegal.

– And what other problems do people come up with?

– Access to medical services,” Alexander answers without thinking for a second. – It happens that a person has to undergo a planned surgery, he knows that he is HIV-positive, and in the medical institution they either try to talk him out of it or redirect him somewhere else, or just put him into a paid ward, even though everything should be free of charge under the MHI.

– They either try to charge him money or refuse to take him at all because of his HIV status,” Mihail says without euphemisms.

– No one says it directly, they start using various medical terminology or “your indications are not right, maybe in a year”. In medical institutions we always recommend to ask for a written refusal. What the doctor says in the corridor, you will not be able to prove anywhere else. The doctor realises that by writing such a refusal he or she will put himself or herself and his or her medical centre in danger. And then the doctors are more likely to put on double gloves and do everything, gritting their teeth, – Alexander is sure.

– And they will do it as well as possible, so I won’t have to come back again,” laughs Mikhail.

– At the same time, everyone treats hepatitis C, which is more dangerous, much more easily,” says Alexander, bewildered. – If you tell dentists that you have hepatitis C, the doctors will take it easier than if you tell them about HIV.

IF YOU MENTION HIV, YOU’LL PROBABLY HEAR: “NO, NO, NO, WE’RE ON OUR LUNCH BREAK, COME BACK NEXT TIME”.

In medical institutions, Alexander and Michael explain, often if a person says they are HIV positive, they are sent to the back of the queue. This is such a small discrimination. They won’t refuse to help, but they will accept him last – to disinfect everything afterwards. This is despite the fact that disposable instruments are used or everything is disinfected after each patient.

– Generally, health workers have instructions to suspect every patient is HIV and hepatitis C positive, to wear gloves and masks in every situation. But when funding is a problem, gloves can be wiped down with alcohol or something else cannot be done.

– And sometimes there is just a flood of patients, and it’s just the human factor.

– But if there is a risk of disease, health workers are immediately put on PEP – free post-exposure prophylaxis. This equates to an occupational injury,” Mikhail sums it up.

But legal recourse is not limited to medical issues either. People who are HIV-positive are increasingly facing blackmail.

– Either a former cohabitant or a former spouse blackmails them,” explains Alexander. – They start threatening that, for example, they will disclose their status to their relatives.

– Can this be dealt with?

– If a person fears it, they can go and write a statement to the police, because it is an invasion of privacy. Such reports are obligatory because we have a Criminal Code. The report will first be investigated, one party will be called, and then the other party will be called. Maybe at this stage the blackmailer will realise that he is doing it for nothing. Sometimes blackmail is attempted by people who are already HIV-positive themselves.

– Maybe both of them were already infected when they met and were afraid to tell each other. We are all afraid,” says Mikhail. – This goes to the issue of self-stigma caused by stigmatization from society. The further into the woods it gets, the harder it becomes to tell your partner. I recently had a consultation: we talked on the phone for an hour and a half (we didn’t have an office at the time). A guy “plus” (tested positive), he has a regular partner who is HIV-negative. The client says: “I know everything, I understand everything, I understand that people live with it, and the story with the pills does not embarrass me.

“BUT HOW DO I TELL HIM? I DON’T WANT TO LOSE HIM, AND I’M AFRAID TO TELL HIM.

This is the self-stigma that emerges thanks to our beloved public, which still believes that HIV infection is collapse and death.

The situation is even more difficult when an HIV-positive person is a citizen of another country. One can avoid deportation only if one has close relatives or a spouse with Russian citizenship. The amendments about relatives, which make life a little easier for foreigners, have only recently appeared and do not always help.

– In one case, I had to file a lawsuit in Moscow against Rospotrebnadzor,” says Alexander. – A Ukrainian citizen has entered Russia. His wife is Russian. The court overturned Rospotrebnadzor’s decision that his stay on Russian territory was undesirable. The man’s wife recently called and said that he had to renew or get a new residence permit, but the police were refusing him on the grounds of his HIV status. They demand a certificate from the AIDS Centre that he is registered there and the AIDS Centre says: “We won’t take him on the register because he is a foreign citizen. All the same, there are legal obstacles.

– And if there are no close relatives who are citizens of the Russian Federation?

– A foreigner is subject to deportation. In the CIS, only two states still deport citizens with HIV: Russia and Armenia. The others have acknowledged that it is not dangerous, and the foreigner himself, knowing that he has HIV, runs to the nearest AIDS centre and gets registered there to receive therapy for money, because he himself is interested in it, because then he will have a normal life, work and finances to support himself.

– It is scary to think about the level of stigma faced by migrants with HIV. Where does this rejection of HIV-positive people, migrants and Russians come from? From ignorance?

– Now there is a lot of information, organizations, websites, information space has expanded. People can find and read everything themselves. But who is interested in it? The target group, people who have already become HIV carriers,” says Alexander.

– Stigma is associated primarily with a complete lack of awareness about this or that disease,” says Mikhail. – I have a number of acquaintances who still think that HIV can be contracted by drinking from the same cup. Speedophobia, or HIV-phobia, comes primarily from ignorance. Sexual transmission of HIV is now the predominant mode of transmission. HIV has long gone beyond the so-called key populations: injecting drug users, MSM (men who have sex with men), sex workers and sex workers. It has long entered the heterosexual field, socially adapted, with wives, husbands, families. At some point, people get tested because they feel bad: “Oh, we have HIV. Unexpectedly. There was a case when a young man – married, two children – went to hospital. He was brought by ambulance but he could not walk: he had terminal AIDS. Thanks to our Botkin doctors, who sometimes help out patients even in a very serious condition.

– But that is if there are no concomitant diseases,” adds Alexander. – But if a person has tuberculosis … At first, tuberculosis should be staved off, but as long as tuberculosis is being treated, there is no one left to treat HIV.

– Are there still a lot of HIV-dissidents?

Both my interlocutors nod. They say that a year ago, Russia started shutting down AIDS dissident websites that were writing about HIV being allegedly a conspiracy of pharmaceutical companies, and a number of NGOs addressed the State Duma with a proposal to introduce criminal punishment for AIDS dissidence. But fake information about HIV is still plentiful and it still leads to tragedies.

– The last high-profile case was in Krasnoyarsk in early summer,” says Alexander. – A little girl died there. The child was taken away from her mother, who was HIV-positive, and given to her grandmother, who also turned out to be a dissident. HIV infection has existed for so many years, there are already medical achievements, therapy, people live with it. The government gives you pills for free! Your task is just to take them at a certain time. That’s all. And live your life as you live it. Okay, if you had money taken out of your pocket you could say that it’s a conspiracy of pharmaceutical companies, but here the state takes all of it. What kind of conspiracy is that?

Mikhail points out that in St. Petersburg, the percentage of people who are registered and take therapy, thank God, is growing. But there is data that the incidence of the disease is also increasing, including among teenagers.

– So what to do about it?

– If we want to stop the growth of the infection in the general population, we have to forget about what we are told every day – about ‘crosses’, that there is no sex before marriage,” says Alexander. – It’s better to remove VAT from condoms, put condom machines in student dormitories for free distribution, certify female condoms. Elementary! Then the incidence of disease will go down. Let us at least introduce sex education in high schools, when hormones are kicking in. But no, we’re sitting here discussing television: “I got pregnant at 15. Oh, how did that happen?” And, again, our legislation: the age of consent is 16 and you can only talk about sex from the age of 18.

– That doesn’t mean we want to show pornographic films in school. We should at least tell them that they need to use condoms, and it’s not even about pregnancy, it’s about protecting yourself and your partner,” says Mikhail. – Of course, you have to somehow control who and what you say to immature minds. But now everything is so framed, you have to go through so many certifications to get into the same university. We are already silent about the school. And the university also has to make an application, select a specialist, and the specialist has to confirm his or her qualifications. Previously, universities used to invite NPOs in the areas they were interested in, but now this is practically non-existent.

Before the legislative changes, the rectors of universities often approached Positive Dialogue with requests to give lectures, tell them what HIV is and how to protect themselves from infection, and let them distribute condoms to those who wished to do so. Now all this is a thing of the past.

Mikhail says higher education institutions and teenage and youth centres under district administrations still have a prevention plan. But due to the new laws, the topic of sex may have to be circumvented. It is difficult for specialists to imagine how, especially taking into account that now HIV is sexually transmitted in the overwhelming majority of cases.

– Concerning access to preventive measures of HIV infection: the cheapest condoms cost 50 rubles for three pieces, but their quality leaves much to be desired. The simplest classic condom, which will not fit everyone’s size, is already 150 rubles for three pieces,” says Mikhail. – So what’s a student to do? Fortunately, we are able to replenish our stock and periodically hand out condoms with lubricant for free. It’s important that people get used to not getting it all for free, but to using a condom as such. Yes, there is pre-exposure and post-exposure HIV prevention (special pills that can be taken before or after potentially dangerous sexual contact), but there is still nothing better than a condom at this stage against HIV infection. Pre-exposure prophylaxis is very good, very right, but it does not protect against hepatitis, syphilis and other sexually transmitted infections.

Alexander recalls how Positive Dialogue had a joint project with a Swedish aid organisation many years ago. Colleagues told us that when HIV infection first appeared and became widely discussed, the reaction to people who were positive in Sweden was also harsh. For example, a car owned by an HIV-positive person could be sent straight to a landfill. Now, however, the situations are dramatically different in our countries. In Sweden and other European countries, sex education and all types of prevention, condoms are available and their use is encouraged. In Russia, there is an HIV epidemic, but neither sex education nor prevention is available to the extent needed.

– Prevention programmes in our country are underfunded,” says Mikhail. – But the process is necessary and it has to go on. The official statistics of St. Petersburg Committee on health protection says that there are supposedly only 10 thousand MSM in our six million citizens city. The official statistics on the incidence of disease among MSM is also understated.

Although HIV infection has long ceased to be a disease of exclusively key groups, it is still necessary to work with them and they need a special approach. But underreporting complicates the task, admits Mikhail.

Despite the fact that there are quite a few places in St. Petersburg where you can get anonymous rapid HIV testing, and the new office of Positive Dialogue has only recently opened, people already come here every day. The most recent clients include a couple starting life together and a young man who had a “risky situation”. Fortunately, all the tests were negative. But people who have just found out they are HIV-positive often come too.

Mikhail regrets that Positive Dialogue does not currently have the resources to provide fully qualified psychological help. “Psychological enquiries are coming in sporadically, but so far we have to work in peer counselling mode or refer them to partner support organisations.

– Everything comes down to money,” Mikhail explains. – The help of a competent professional psychologist is not cheap. And you need a whole staff here: the topic is not simple, it involves a lot of experience and different life situations. The specialists themselves are susceptible to burnout, there should be interchangeability, so that a person could be told: “Go for a walk for two weeks, so that no one touches you. Take care of the house, the garden, the garden”. There are situations that are more affecting to whom: to the person who asked for help or to the person who helps. Sometimes the stories are very difficult, especially when it is a newly discovered case. There are so many problems, you understand that they can be solved, but it takes time, you have to go through the stages of acceptance, especially the first and second stages, shock, anger, denial…

Positive Dialogue has literally only a handful of private donations, although the button on the website has been running since 2018. Getting the message across to a wider audience about how important it is to help people with HIV, that anyone of us can become a person with HIV, is very difficult. Grants and fundraising for individual projects help keep the organization going. Now, thanks to the EECA Fund for Operational Assistance to Key Populations of the region, we have managed to find and pay for new premises. In addition to assistance, it is necessary to engage in prevention, purchase and distribute condoms, buy test kits, ideally conduct seminars on adherence to healthy lifestyle and support groups for people with HIV with participation of medical consultants. Positive Dialogue once held lectures on HIV and the law even for doctors at a military medical hospital. The need for dialogue with doctors has not disappeared, but it has become much more difficult to organise such communication.

– As long as HIV doesn’t affect you personally, you stay out of it,” says Mikhail. – But if it has already touched you, you come running with goggling eyes: “Dear God, how can you live further? And it’s even better if a person runs here and not to the river embankment.

Over the past six years alone, Positive Dialogue has reached more than 31,500 people with its HIV prevention programmes. How many people it has helped in difficult situations is incalculable.

Positive Dialogue needs support to be able to fully assist all those in need. Any donation you can make will bring closer the time when the organisation will again have a full-time psychologist and perhaps support someone close to you. The organisation needs money for legal advice to help people who have been harassed at work, blackmailed or tried to leave the country. To do prevention work. So that the words “HIV is not a sentence” are not just words. So that the dialogue between different people, with all their advantages and disadvantages, can remain positive. Please support this organization. We all need it.


Слишком экстремальная помощь. Кто и как защищает людей с ВИЧ в Санкт-Петербурге

Стигматизация, отказ в оказании медицинских услуг, увольнение, депортация — вот лишь некоторые проблемы, с которыми могут столкнуться ВИЧ-инфицированные люди в России. Решать эти проблемы уже 25 лет помогают сотрудники общественной организации «Позитивный диалог»

Тихая улочка в центре Петербурга, двор с ярким граффити — портретом девушки с длинными волосами и текстом Lu Blue. Больше пока никаких надписей.

Михаил Ступишин, руководитель «Позитивного диалога», встречает меня у двери. Несколько ступенек вниз, и мы в светлом кабинете. В это помещение «Позитивный диалог» въехал совсем недавно, до этого организация годами располагалась на территории инфекционной Боткинской больницы.

— Первая четверть XXI века заканчивается, а люди до сих пор с ВИЧ-фобными тараканами в голове, — смеется Михаил, наливая кофе и рассказывая о переезде. — В четырех помещениях нам отказали в связи с родом нашей деятельности. На предварительном просмотре мы объясняли, что нацелены сейчас на индивидуальное консультирование, а не на массовые мероприятия, говорили, что поток клиентов у нас есть, но не как в мавзолей, что мы работаем с социально значимым заболеванием — с ВИЧ-инфекцией. Нам отвечали: «Да-да-да, все замечательно». А когда дело дошло до заключения договора, сказали: «Мы посмотрели на сайте, чем вы занимаетесь. Для нас это слишком экстремально».

Я вспоминаю Анну, героиню моего текста «Анна и ее победы», подопечную «Позитивного диалога». Вот уж что экстремально, так это отношение, с которым она и многие другие люди то и дело сталкиваются из-за ВИЧ-положительного статуса. Например, когда собственная мать, опытный медработник, заставляет дочку есть из отдельной посуды, хотя контактно-бытового способа передачи ВИЧ не существует. Или когда человека не хотят брать на работу из-за ВИЧ-статуса, несмотря на то, что благодаря терапии (бесплатной и доступной) у него уже давно неопределяемая вирусная нагрузка — это значит, что он вообще никак не может никого заразить. Анна рассказывала, что в самых отчаянных жизненных ситуациях звонила в «Позитивный диалог» и благодаря разговору с юристом Александром Лозой не раз решала проблемы с работой, а потом и с учебой.

Александр присоединяется к нам с Михаилом, мы пожимаем друг другу руки и начинаем разговор, который длится больше двух часов, но даже этого времени кажется мало. Проблем, с которыми сталкиваются люди с ВИЧ в России, слишком много.

«Позитивный диалог» начался аж 25 лет назад. Основал его юрист, один из первых зарегистрированных ВИЧ-положительных людей в СССР Николай Панченко. Недавно он отметил 70-летний юбилей, а несколько лет назад передал руководство организации Михаилу Ступишину, но в разговоре имя Панченко то и дело звучит — именно он начал просветительскую работу, рассказывая о профилактике и жизни с ВИЧ. Сейчас делать это так же необходимо, как и четверть века тому назад.

— Саша здесь с 2004 года работает, а я в 2015 году пришел, — рассказывает Михаил. — Тогда начали реализовываться два больших профилактических проекта: профилактика ВИЧ среди мужчин, практикующих секс с мужчинами, и профилактика ВИЧ-инфекции среди секс-работниц. Я пришел по рекомендации знакомого. У меня среднее медобразование. Я не врач, а средний медработник. Анатомию хорошо знаю, патофизиологию хорошо знаю или, по крайней мере, знал, понимаю, откуда какие ноги растут.

Вдобавок к медицинскому образованию Михаил окончил университет культуры, а Александр учился в Санкт-Петербургском государственном университете. Медик и юрист, у обоих большой опыт работы с людьми в сложных жизненных ситуациях.

— Юридическая консультация многим нужна, — говорит Александр. — Не у всех есть деньги на платную консультацию, не все хотят рассказывать о своих специфических проблемах, и не все юристы в этом практикуются.

— Наверное, часто обращаются по вопросам, связанным с работой? — спрашиваю я. Но все оказывается не совсем так, как я себе представляла.

По словам Александра, чаще всего боятся быть уволенными медицинские работники, которые должны ежегодно сдавать обязательные анализы, в том числе на ВИЧ. Но за консультациями обращаются и сотрудники полиции, МЧС: вопреки федеральному законодательству, в этих ведомствах вводят полный запрет на работу для ВИЧ-положительных людей — выпускают локальные акты о прохождении медосмотра и признают негодными или ограниченно годными к службе.

— В таких ситуациях можно что-то сделать?

— Ну вот еще в советское время был принят акт о том, что люди с ВИЧ-инфекцией не могут быть командирами воздушных судов, — Александр вздыхает. — Лет пять или семь назад у одного капитана выявили ВИЧ. Он обратился в Генеральную прокуратуру, Генеральная прокуратура пошла в Верховный суд, и Верховный суд признал этот акт незаконным. Но человек должен был раскрыть перед всеми свой статус. Дело не в суде как таковом — в документах фамилия человека может быть скрыта. Но работодатель зачастую давит на сотрудника, может распространять о нем слухи.

Михаил приводит в пример историю своего знакомого, которого буквально «съели» на работе, в самом обычном офисе, узнав о его ВИЧ-статусе. Судиться в таких ситуациях может быть бесполезно: с юридической точки зрения дело беспроигрышное — увольнение незаконное, но жизни на работе не дадут.

В суд против работодателя люди идут редко, и, как правило, это резонансные дела, которые меняют локальные нормативные акты организации.

— У нас записано в законодательстве, что это дискриминация, что работодатель будет оштрафован, есть уголовная ответственность, — говорит Александр. — Но все это стараются сделать по-тихому: ты уволишься по собственному желанию, тебе выплатят какое-то выходное пособие, и ты уйдешь спокойно (что с тобой будет дальше — твои проблемы), а мы будем белые и пушистые. Я всегда говорю, что борьба за свои права чревата: могут создать такие условия, что человек будет просто вынужден уйти. Постоянный стресс ведь тоже плохо влияет на организм.

В прошлом году, по словам Александра, локальный акт о запрете работы людям с ВИЧ пыталась издать Генеральная прокуратура, но поднялся шум, и ведомству пришлось отказаться от этой идеи. А вот у Министерства путей и сообщения, похоже, ввести локальный запрет получилось.

— В общем, если начинаются проблемы на работе из-за ВИЧ-статуса, единственный выход — искать нормального работодателя?

— У нас «нормального работодателя» как такового нет, — качает головой Александр.

— Тут дело не столько в работодателе, — добавляет Михаил, — сколько в твоем непосредственном руководителе или в высшем руководстве, если речь о его позиции.

Он рассказывает о случаях, когда при приеме на работу у людей без их ведома брали тест на ВИЧ. Практика эта, конечно, незаконная:

— Вопрос с информированием о статусе человека вообще стоит очень жестко: никакого разглашения, только по официальному запросу суда или прокуратуры. Только тогда Центр СПИД обязан предоставить информацию, состоит этот человек на учете или не состоит. Если человек понимает, что никому о своем статусе не говорил, а информация у работодателя появилась, значит попутно, при прохождении медкомиссии, кровь взяли на ВИЧ-инфекцию. Но, по идее, дальнейших телодвижений работодатель делать не может, потому что вся эта история незаконна.

— А еще с какими проблемами обращаются?

— Доступ к медицинским услугам, — ни секунды не раздумывая, отвечает Александр. — Бывает, что человеку предстоит плановая операция, он знает, что он ВИЧ-инфицированный, а в медицинском учреждении его пытаются либо отговорить, либо перенаправить еще куда-нибудь, либо просто положить в платное отделение, хотя для него все должно быть бесплатно по ОМС.

— Пытаются либо деньги содрать, либо вообще отказаться от него, потому что ВИЧ-статус, — обходится без эвфемизмов Михаил.

— Напрямую этого никто не говорит, начинается различная медицинская терминология либо «показания у вас какие-то не те, давайте, может, через годик». В медицинских учреждениях мы всегда рекомендуем просить письменный отказ. То, что врач говорит в коридоре, вы потом нигде никому не сможете доказать. Врач понимает, что, написав такой отказ, подставит сам себя и свое медучреждение. И тогда врачи скорее наденут двойные перчатки и все сделают, скрипя зубами, — уверен Александр.

— И сделают по возможности качественно, чтобы больше не приходил, — смеется Михаил.

— При этом к гепатиту С, который опаснее, все гораздо проще относятся, — недоумевает Александр. — Если сказать дантистам, что у вас гепатит С, врачи отнесутся к этому легче, чем если сказать про ВИЧ.

СКАЖЕТЕ ПРО ВИЧ — НАВЕРНЯКА УСЛЫШИТЕ: «НЕ-НЕ-НЕ, У НАС ОБЕДЕННЫЙ ПЕРЕРЫВ, В СЛЕДУЮЩИЙ РАЗ ПРИХОДИТЕ»

В медицинских учреждениях, поясняют Александр с Михаилом, зачастую, если человек говорит о своем положительном ВИЧ-статусе, его отсылают в конец очереди. Такая маленькая дискриминация. В помощи не откажут, но примут последним — чтобы после все продезинфицировать. Это притом, что используются одноразовые инструменты или же после каждого пациента все дезинфицируется.

— Вообще у медработников есть инструкции, по которым они в каждом пациенте обязаны подозревать ВИЧ-инфицированного и больного гепатитом С, надевать перчатки и маски в любой ситуации. Но, когда с финансированием проблемы, и перчатки можно спиртом протереть, и еще что-то не сделать.

— А иногда просто идет поток пациентов, и срабатывает просто человеческий фактор.

— Но, если есть риски заболевания, медработников сразу сажают на ПКП — бесплатную постконтактную профилактику. Это приравнивается к производственной травме, — подводит итог Михаил.

Но и медицинскими вопросами юридические обращения не исчерпываются. Люди с положительным ВИЧ-статусом все чаще сталкиваются с шантажом.

— Шантажирует либо бывший сожитель/сожительница, либо бывший супруг/супруга, — поясняет Александр. — Начинают угрожать, что, например, раскроют статус родственникам.

— А с этим можно бороться?

— Если человек опасается этого, он может пойти и написать заявление в полицию, потому что это вмешательство в частную жизнь. Такие заявления обязаны принять, поскольку у нас есть Уголовный кодекс. По заявлению сначала будет проводиться проверка, вызовут одну сторону, потом — вторую. Может быть, на этой стадии шантажирующий человек уже поймет, что зря это делает. Иногда шантажировать пытаются люди, которые сами уже ВИЧ-инфицированы.

— Может быть, оба уже были инфицированы, когда встретились, и боялись друг другу сказать. Мы все боимся, — говорит Михаил. — Это уже к вопросу о самостигматизации, вызванной стигматизацией со стороны общества. Чем дальше в лес, тем сказать партнеру становится сложнее. Недавно у меня была консультация — мы полтора часа проговорили по телефону (у нас в тот момент не было офиса). Парень «плюсанул» (тест оказался положительным), у него есть постоянный партнер, ВИЧ-отрицательный. Клиент говорит: «Я все знаю, все понимаю, понимаю, что с этим живут, и история с таблетками меня не смущает».

«НО КАК Я ЕМУ СКАЖУ? Я И ТЕРЯТЬ ЕГО НЕ ХОЧУ, И БОЮСЬ СКАЗАТЬ»

Вот эта самостигма появляется благодаря нашей любимой общественности, которая до сих пор считает, что ВИЧ-инфекция — это крах и смерть.

Еще сложнее ситуация, когда ВИЧ-положительный человек — гражданин другого государства. Избежать депортации можно только при наличии близких родственников или супруга/супруги с российским гражданством. Да и поправки про родственников, несколько облегчающие иностранцам жизнь, появились лишь недавно и помогают не всегда.

— По одному случаю пришлось подавать в суд в Москве против Роспотребнадзора, — рассказывает Александр. — Гражданин Украины въехал в Россию. Жена у него россиянка. Суд отменил решение Роспотребнадзора о нежелательности пребывания на территории РФ. Недавно звонила супруга того человека, сказала, что ему нужно продлевать или получать новый вид на жительство, а полиция ему на основании ВИЧ-статуса отказывает. Требуют справку от Центра СПИД о том, что он состоит там на учете, а в Центре СПИД говорят: «Мы не возьмем его на учет, потому что он иностранный гражданин». Все равно возникают юридические препоны.

— А если нет близких родственников — граждан РФ?

— Иностранец подлежит депортации. На территории СНГ только два государства все еще депортируют граждан с ВИЧ: Россия и Армения. Остальные признали, что это неопасно, да и иностранец сам, зная о том, что у него ВИЧ, бежит в ближайший Центр СПИД и встает там на учет, чтобы получать терапию за деньги, потому что он сам в этом заинтересован, потому что тогда у него будет нормальная жизнь, работа и финансы, чтобы себя содержать.

— О том, с каким уровнем стигматизации могут сталкиваться мигранты с ВИЧ, даже думать страшно. Откуда вообще такое неприятие ВИЧ-положительных людей, мигрантов и россиян? От невежества?

— Сейчас очень много информации, организаций, сайтов, информационное пространство очень расширилось. Люди сами могут все найти и прочитать. Но кто этим интересуется? Целевая группа, люди, которые уже стали носителями ВИЧ, — рассуждает Александр.

— Стигматизация связана в первую очередь с кромешной неосведомленностью о том или ином заболевании, — уверен Михаил. — У меня есть ряд знакомых, которые до сих пор думают, что ВИЧ-инфекцией можно заразиться, испив из одной чашки. Спидофобия, или ВИЧ-фобия, идет в первую очередь от неосведомленности. Сейчас половой способ передачи ВИЧ преобладает. ВИЧ-инфекция уже давным-давно вышла за пределы так называемых ключевых групп: потребителей инъекционных наркотиков, МСМ (мужчин, практикующих секс с мужчинами. — Прим. ТД), секс-работников и секс-работниц. Она уже давно вышла в гетеросексуальное поле, социально адаптированное, с женами, мужьями, семьями. В какой-то момент люди сдают анализы, потому что им плохо: «Ой, у нас ВИЧ-инфекция». Неожиданно. Был случай, когда в больницу попал молодой мужчина — женат, двое детей. Его привезли на скорой, он не мог ходить — СПИД, терминальная стадия. Спасибо нашим боткинским врачам, которые иногда вытягивают пациентов даже в очень тяжелом состоянии.

— Но это если нет сопутствующих заболеваний, — дополняет Александр. — А если у человека туберкулез… Сначала надо «забить» туберкулез, но, пока лечат туберкулез, уже и лечить от ВИЧ становится некого.

— А ВИЧ-диссидентов по-прежнему много?

Оба моих собеседника кивают. Говорят, что год назад в России стали закрывать сайты СПИД-диссидентов, писавших о том, что ВИЧ — это якобы заговор фармкомпаний, а ряд общественных организаций обратились в Госдуму с предложением ввести уголовное наказание за СПИД-диссидентство. Но фейковой информации о ВИЧ по-прежнему много, и это по-прежнему приводит к трагедиям.

— Последний резонансный случай был в Красноярске в начале лета, — говорит Александр. — Там умерла маленькая девочка. У мамы, ВИЧ-диссидентки, отняли ребенка, передали бабушке, а та тоже оказалась диссиденткой. ВИЧ-инфекция существует уже столько лет, уже есть достижения медицинские, терапия, люди с ней живут. Вам государство бесплатно дает таблетки! Ваша задача — просто их принять в определенное время. Всё. И живите как живете. Ладно если бы у тебя из кармана вынимали деньги, ты мог бы сказать, что это заговор фармкомпаний, но здесь-то государство все берет на себя. Какой тут заговор?

Михаил отмечает, что в Петербурге процент людей, состоящих на учете и принимающих терапию, слава богу, растет. Но есть данные, что и заболеваемость тоже растет, в том числе в подростковой среде.

— И что с этим делать?

— Если мы хотим остановить рост инфекции в общей популяции, мы должны забыть о том, о чем нам каждый день говорят, — о «скрепах», о том, что нет никакого секса до брака, — говорит Александр. — Лучше уберите НДС с презервативов, поставьте в студенческих общежитиях кондоматы для бесплатной их раздачи, сертифицируйте женские презервативы. Элементарно! Тогда пойдет снижение заболеваемости. Давайте хотя бы в старших классах вводить сексуальное просвещение, когда гормоны вовсю идут. Но нет, сидим, обсуждаем телевизор: «Забеременела в 15 лет. Ах, как же это случилось?» И, опять-таки, наше законодательство: возраст согласия — с 16 лет, а разговаривать о сексе можно только с 18 лет.

— Это не значит, что мы хотим показывать в школе порнографические фильмы. Надо рассказывать хотя бы, что нужно использовать презервативы, и дело даже не в беременности, а в том, что нужно обезопасить себя и своего партнера, — говорит Михаил. — Конечно, каким-то образом нужно контролировать, кто и что будет глаголать неокрепшим умам. Но теперь все поставлено в такие рамки, нужно пройти столько сертификаций, чтобы прийти в тот же вуз. Про школу мы уже вообще молчим. И вуз тоже должен сделать заявку, подобрать специалиста, а специалист должен подтвердить свою квалификацию. Раньше вузы приглашали НКО по тем направлениям, которые их интересуют, теперь этого практически не происходит.

До законодательных новшеств в «Позитивный диалог» нередко обращались ректораты вузов: просили провести лекции, рассказать о том, что такое ВИЧ, как предохраняться от инфекции, позволяли раздавать презервативы желающим. Сейчас все это осталось в прошлом.

Михаил говорит, что у вузов и подростково-молодежных центров при районных администрациях по-прежнему есть план профилактических мероприятий. Но в связи с новыми законами тему секса, видимо, придется обходить. Как — представить специалистам сложно, особенно учитывая, что сейчас ВИЧ в подавляющем большинстве случаев передается именно половым путем.

— К вопросу о доступе к профилактическим мерам по ВИЧ-инфекции: у нас самые дешевые презервативы стоят 50 рублей за три штуки, но качество у них оставляет желать лучшего. Простейший классический презерватив, который не всем подойдет по размеру, — уже 150 рублей за три штуки, — говорит Михаил. — И что делать тому же самому студенту? У нас, к счастью, есть возможность пополнять запас и периодически раздавать презервативы с лубрикантами бесплатно. Важно, чтобы люди привыкли не к тому, чтобы получать это все бесплатно, а к использованию презерватива как такового. Да, есть доконтактная и постконтактная профилактика ВИЧ (специальные таблетки, которые можно принять до или после потенциально опасного сексуального контакта), но все равно лучше презерватива на данном этапе против ВИЧ-инфекции ничего не придумали. Доконтактная профилактика — это очень хорошо, очень правильно, но от гепатитов, сифилиса и других инфекций, передающихся половым путем, она не защищает.

Александр вспоминает, как много лет назад у «Позитивного диалога» был совместный проект со шведской помогающей организацией. Коллеги рассказывали, что, когда ВИЧ-инфекция только появилась и стала широко обсуждаться, реакция на людей с положительным статусом в Швеции тоже была жесткой. Например, автомобиль, который принадлежал ВИЧ-положительному человеку, могли отправить прямиком на свалку. Зато сейчас ситуации в наших странах различаются кардинально. В Швеции, да и в других европейских странах, доступны секс-просвещение и все виды профилактики, презервативы, их использование поощряется. В России эпидемия ВИЧ — при этом нет ни секс-просвещения, ни профилактики в нужном объеме.

— У нас программы профилактики мало финансируются, — говорит Михаил. — А процесс нужен, он должен идти. Вот официальная статистика нашего петербургского комитета по здравоохранению: на наш шестимиллионный город якобы всего 10 тысяч МСМ. Официальная статистика по заболеваемости среди МСМ тоже занижена.

Хотя ВИЧ-инфекция уже давно перестала быть болезнью исключительно ключевых групп, работать с ними по-прежнему нужно, им необходим особый подход. Но заниженная статистика серьезно усложняет задачу, признается Михаил.

Несмотря на то что в Петербурге немало мест, где можно анонимно пройти экспресс-тестирование на ВИЧ, и новый офис «Позитивного диалога» работает совсем недавно, сюда уже приходят каждый день. Из последних клиентов — пара, начинающая совместную жизнь, и молодой человек, у которого произошла «рискованная ситуация». К счастью, все тесты оказались отрицательными. Но часто обращаются и люди, только что узнавшие о положительном ВИЧ-статусе.

Михаил сожалеет, что сейчас у «Позитивного диалога» нет ресурсов для того, чтобы оказывать полноценную квалифицированную психологическую помощь. «Психологические» обращения идут через раз, но пока работать приходится в режиме равного консультирования или перенаправлять в партнерские помогающие организации.

— Все упирается в деньги, — поясняет Михаил. — Помощь грамотного профессионального психолога стоит недешево. Да и здесь нужен целый штат: тема непростая, связана с большими переживаниями, разными жизненными ситуациями. Сами специалисты подвержены выгоранию, здесь должна быть взаимозаменяемость, чтобы человеку можно было сказать: «Иди погуляй недели две, чтобы тебя никто не трогал. Занимайся домом, садом, огородом». Бывают ситуации, которые даже непонятно на кого сильнее действуют: на человека, который обратился за помощью, или на человека, который помогает. Иногда истории очень сложные, особенно когда это вновь выявленный случай. На тебя вываливается столько проблем, понимаешь, что их можно решить, но нужно время, нужно пройти стадии принятия, особенно первую и вторую, шок, гнев, отрицание…

Частных пожертвований у «Позитивного диалога» буквально единицы, хотя кнопка на сайте работает с 2018 года. Донести до широкой аудитории мысль о том, как важно помогать людям с ВИЧ, о том, что человеком с ВИЧ может стать любой из нас, очень сложно. Держаться организации помогают гранты, привлечение финансов на отдельные проекты. Вот сейчас найти и оплатить новое помещение получилось благодаря Фонду оперативной помощи ключевым группам населения региона ВЕЦА. А, помимо помощи, нужно заниматься и профилактикой, закупать и распространять презервативы, закупать тест-системы, в идеале еще проводить семинары по приверженности здоровому образу жизни, группы поддержки для людей с ВИЧ с участием медицинских консультантов. Когда-то «Позитивный диалог» проводил лекции по теме «ВИЧ и право» даже для врачей военно-медицинского госпиталя. Потребность в диалоге с врачами никуда не делась, только организовать такое общение стало гораздо сложнее.

— Пока ВИЧ не касается тебя лично, ты в это дело не лезешь, — говорит Михаил. — А если уже коснулось, то прибегаешь с выпученными глазами: «Боже-боже, как жить дальше?» И это еще хорошо, если человек сюда прибегает, а не на набережную реки.

Только за последние шесть лет работы «Позитивный диалог» охватил своими программами профилактики ВИЧ более 31,5 тысячи человек. Скольким людям он помог в трудной ситуации, подсчету не поддается.

Чтобы полноценно оказывать помощь всем, кто в ней нуждается, «Позитивному диалогу» нужна поддержка. Любое посильное пожертвование приблизит то время, когда в организации снова появится штатный психолог и, возможно, поддержит близкого вам человека. Организации нужны деньги на юридические консультации, чтобы помогать людям, которых притесняют на работе, шантажируют или пытаются выслать из страны. Чтобы вести профилактическую работу. Чтобы слова «ВИЧ — не приговор» были не просто словами. Чтобы диалог между самыми разными людьми со всеми их плюсами и минусами оставался все-таки позитивным. Пожалуйста, поддержите эту организацию. Она нужна нам всем.

US: Decriminalising HIV would protect disadvantaged communities from HIV infection and further marginalisation

HIV criminalization perpetuates intersecting forms of discrimination

Imagine you are a transgender Black woman in Florida. You are already facing housing and workplace discrimination, gender-based violence and social and institutional racism. One of your few options for financial support is sex work, but you do not plan to have intercourse with clients. Unfortunately, a sting operation leads you to be taken to the police station. You wonder why the cisgender white woman you work alongside was not caught. Upon arrival at the station, you are forced to get tested for HIV. You test positive. You are now a convicted felon and may have to register as a sex offender.

This fictional narrative illustrates the severity of the criminalization of HIV in the United States and is an accurate representation of the discrimination felt by LGBT, non-white individuals, sex workers and those who experience the intersectional disenfranchisement of multiple identities. According to Avert Global Information and Education on HIV and AIDS, transgender people are 49 times more likely to be affected by HIV than the general world population. Over half a million Americans have died since the beginning of the AIDS epidemic in the 1980s. A disproportionate number of these people were non-white, LGBT or both. By looking at the Movement Advancement Project’s maps of states with HIV laws, 34 states still discriminated against those with HIV in 2020, with transgender women being the most globally discriminated against. HIV should be nationally decriminalized since the penalties only further marginalize disadvantaged communities.

A 2017 article by the National LGBT Task Force and the Center for HIV Law & Policy states that transgender sex workers are “nearly six times as likely to be living with HIV than the general trans population, and 25 times as likely relative to the general population.” Transgender women, especially those who are non-white, are profiled significantly more for sex work.The data illustrates how transgender women are more at risk of being presumed HIV positive, which perpetuates transphobic, homophobic, sexist and racist discriminatory practices.

Some may argue that decriminalizing HIV will lead to an increase in cases. In fact, data has been shown that HIV criminalization laws disincentivize HIV testing. This is because in some states, it is mandatory that the arrestee be tested once entering the police station. A 2015 study by Yang, et al. found that the decriminalization of sex work could actually reduce 33-45% of new HIV infections, illustrating the counterproductive attributes of HIV criminalization. Data has also shown that HIV penalties are significantly based on one’s race and sex, which caused the state of California to change HIV charges of sex workers from felonies to misdemeanors. While this change in California is an improvement, officials can still discriminate based on race, sexual orientation and gender identity. Overall, this illustrates that the criminalization of HIV is maintained in order to keep a discriminatory social hierarchy that hurts transgender women’s social mobility, especially Black transgender women.

The differences of prosecution among states is important because data shows that transgender women can be prosecuted for even non-transmissible actions. Data by the Movement Advancement Project shows 17% of the American LGBT population lives in a state where there is an HIV criminalization law, HIV-specific sentencing and/or laws that may require individuals to register as sex offendes; 35% lives “in a state with a HIV criminalization law;” and 21% in a state without a HIV criminalization law but where a positive status does affect sentencing. Liberal states, such as Massachusetts, criminalize exposure to, as well as transmission of, HIV. Sex workers can be charged with a felony for spitting or biting — even though neither action spreads HIV. This further shows that states have multiple avenues to discriminate against marginalized groups through the criminalization of HIV. The evidence illustrates the need to decriminalize HIV on a national level to protect marginalized communities, especially  transgender women, transgender women of color and Black transgender women. By decriminalizing HIV, Americans are further protected from infection and forms of discrimination.

Year in review: Celebrating successes, highlighting the many challenges ahead

This past year has shown us what happens when one pandemic –  HIV – is overshadowed by another pandemic, COVID-19.  Despite the many lessons learned from our collective advocacy against HIV criminalisation that we and our HIV JUSTICE WORLDWIDE partners highlighted in March, these lessons were mostly ignored by policymakers around the world.

The result was a series of knee-jerk legal, policy and police responses leading to the overzealous policing of people living with HIV and other key and inadequately served populations already subject to existing inequalities in law and policy, which we have been highlighting in our HIV Justice Weekly newsletter since March.

This latest pandemic overshadowed, and in some cases undermined, the work we and others have been doing to ensure a fair, just, rational and evidence-based response towards people living with HIV by the criminal justice system.

This past year we documented at least 90 cases of unjust HIV criminalisation in 25 countries, with Russia and the United States being the worse offenders.  Women living with HIV were accused in 25% of those cases. Three of these cases were for breastfeeding.  In the United States, more than 50% of those accused in HIV criminalisation cases were people of colour.  

2020 also saw Poland passing a new law against COVID-19 that also increased the criminal penalty for HIV exposure, and number of disappointing HIV criminalisation higher court appeals in the US (Ohio), and Canada (Ontario and Alberta) that appeared to ignore science over stigma.

And yet, despite the many difficulties of 2020, the movement to end unjust HIV criminalisation has continued to gain momentum.

In the United States, Washington State modernised its HIV-specific criminal law in March, reducing the ‘crime’ from a felony to a misdemeanour, adding in a number of defences, and eliminating the sex offender registration requirement.  Earlier this month, legislators in Missouri published plans to modernise its HIV-specific criminal law next year.

In Europe, Sweden abolished the legal requirement to disclose HIV status in March, the Spanish Supreme Court set an important precedent for HIV criminalisation cases in May, and in June, Scottish police ended the stigmatising practice of marking people living with HIV as ‘contagious’ in their database.

In Francophone Africa, HIV-specific criminal law reform in Benin and across the region is looking likely thanks to a recognition that existing laws do not reflect up-to-date science.

And in Eastern Europe and Central Asia, a process to completely abolish the draconian HIV-specific criminal law in Belarus has begun.

There is still so much more to do, however.  Despite these successes, as well as the many milestones the HIV JUSTICE WORLDWIDE movement has achieved since its launch in 2016, we will not rest until everyone living with HIV in all their diversity is treated equally, fairly and justly by all actors of the criminal justice system.

Uganda: HIV activists ask government to review the HIV/AIDS law and remove clauses that criminalise HIV

Activists, chief justice call for review of HIV/AIDS law

By Betty Amamukirori, John Masaba

The majority of the HIV-positive persons are living in fear of the law and many choose not to disclose their status.

HIV/AIDS activists have asked the Government to review the HIV and AIDS Prevention and Control Act 2014, saying it is fuelling stigma and discrimination.

The activists, while speaking at the Philly Bongole Lutaaya memorial lecture, said the law has clauses in it that if left unchanged could undo the country’s gains in the fight against the disease.

Dora Musinguzi, the executive director of Uganda Network on Law and Ethics (UGANET), said clauses that criminalise HIV, especially intentional transmission are causing more harm because it’s scaring people away from testing, disclosing their status to the spouses or seeking treatment.

She pointed out clauses such as sections 41 and 43 which spell out punishments for attempted transmission of HIV and intentional transmission, respectively.

“We need to do everything it takes to repeal this law, especially the punishment for exposure to HIV/AIDS. We need to remove the criminalisation under the law because it is causing more harm,” Musinguzi said.

The activists said the majority of the HIV-positive persons are living in fear of the law and many choose not to disclose their status to their significant others for fear of prosecution. This, they said, has fuelled self-stigma.

Justice Alfonse Owiny-Dollo, in his keynote address as the guest speaker, agreed that the law needs to be amended if Uganda is to achieve its goal of ending the AIDS epidemic by 2030. His address was read by the Judiciary’s Chief Registrar, Sarah Langa.

Owiny-Dollo called on Parliament to enact and review laws that will improve the wellbeing of the society especially the people living with HIV.

“The HIV and AIDS Prevention and Control Act 2014 may need to be reviewed,” he said.

“Ending HIV requires enabling legal and social environments that guarantee the health, dignity and security of all people living with or at risk of HIV. This is the only way to ensure that all those in need of HIV prevention, treatment, care, and support have access to these services without fear of discrimination, exclusion or bias,” Owiny-Dollo said.

He said much as there are enabling laws on non-discrimination on the basis of one’s HIV status, the HIV-positive still face limitations when seeking justice. These include lengthy proceedings and an unfriendly court environment.

The lecture was held under the theme Access to HIV services during COVID-19 pandemic. It was held at the Office of the President auditorium and was notably attended by the late Lutaaya’s children, friends, activists, musicians living with HIV. The HIV prevalence is 6.2% amongst adults aged 15-64 years; 7.6% in women and 4.7% in men.

Tezra Lutaaya, a daughter of the deceased, said although her father championed the fight against the disease, stigma and discrimination against HIV-positive persons is still rife.

“I strongly believe that an end to HIV is in sight if we continue to fight stigma, make sure seamless information and access to all interventions are available and that we continue to have dialogue with the young people both infected and affected by HIV,” she said.

Esther Mbayo, the Minister for the Presidency, said if AIDS is to be ended by 2030, there is need to exhibit the spirit of Philly Lutaaya.

“We need to get out of our comfort zones, especially now that we are dealing with two pandemics — HIV and COVID-19. On an individual level, we need to test for HIV with our partners and together irrespective of the results, decide to prevent HIV,” she noted.

She called for deliberate efforts to reach those at most risk of getting infected with HIV in order to reduce the high HIV prevalence and towards ending stigma and discrimination.

Owiny-Dollo urged the Government to prioritise creating awareness, promoting advocacy that reaches the young people and all generations with messages on HIV and AIDS.

We Are People, Not Clusters! Why public health surveillance using blood taken for HIV resistance testing risks doing more harm than good

by Edwin J Bernard, HJN’s Executive Director

A series of articles and editorials in the October 2020 issue of the American Journal of Bioethics published last Friday examine a growing concern amongst community leaders of people living with HIV and our scholarly allies: the use of blood taken from people living with HIV during routine testing prior to starting or changing antiretroviral therapy in surveillance databases, without our permisssion, for public health purposes. 

This is already taking place across the United States and in some Canadian provinces, and is currently being considered elsewhere in the world.

The rollout of so-called ‘molecular HIV surveillance’ to identify ‘clusters’ of transmissions to attempt to further improve public health responses to HIV is a growing source of anxiety and concern for people living with HIV in the US and Canada, especially for people who are already marginalised and criminalised in other ways, because they can’t be certain that this data won’t be shared with law enforcement or immigration authorities, which can lead to prosecution and/or deportation.

Coming to Facebook Live on 30th September – HIV Justice Live! Whose Blood is it, Anyway?  Like or follow us on Facebook to watch and participate in the first of our new interactive webshows, which will focus on molecular HIV surveillance.

 

In our lead guest editorial, entitled ‘We Are People, Not Clusters!’ which I co-authored with Alexander McClelland, Barb Cardell, Cecilia Chung, Marco Castro-Bojorquez, Martin French, Devin Hursey, Naina Khanna, Brian Minalga, Andrew Spieldenner, and Sean Strub, we support the concept of “HIV data justice” put forth in the lead target article, by Stephen Molldrem and Anthony Smith, Reassessing the Ethics of Molecular HIV Surveillance in the Era of Cluster Detection and Response: Toward HIV Data Justice.

“HIV data justice draws on the collective resources of the HIV/AIDS movement to build new alliances aimed at providing affected individuals and communities with greater control over how their data are utilized in the healthcare system, with the paired aim of providing them with greater access to better services on terms of their own choosing.”
 
Molldrem and Smith

 

In the editorial, we welcome Molldrem and Smith’s critique of the controversial rollout of molecular HIV surveillance (MHS) in the United States, which explores three intersecting concerns:

(1) the non-consensual re-purposing of personal health information and biomaterial for public health surveillance;

(2) the use of molecular HIV surveillance data in larger databases to find ‘clusters’ of infections and to make determinations about transmission directionality, and the criminalising implications that follow such determinations; and

(3) the way MHS amplifies the targeting and stigmatisation of already oppressed and marginalized communities.

The editorial questions the rationale behind the use of MHS as one of four pillars of the US Centres for Disease Control (CDC) End The Epidemic (ETE) Plan and calls for the abolition of molecular HIV surveillance in the United States as it is currently being rolled out by the CDC because it blurs the boundaries between consent and criminalisation.

Instead, we envision a future of new participatory and intersectional racial and viral justice possibilities, one which ensures the lives, voices, self-determination, and autonomy of people living with HIV are central to HIV research and public health practice.

Further reading

Bryn Nelson. Questioning the Benefits of Molecular Surveillance. POZ Magazine, July-August 2020.

US: “Institutionalized discrimination gives people a reason to avoid getting tested or having open conversations around the disease”

The HIV Pandemic Is Still Raging—and Won’t Stop Until We End the Stigma

One of the hardest lines I’ve ever had to deliver was, “I’m going to die.” It was the initial response of my character Ricky after being diagnosed with HIV during the height of the epidemic in season two of the 1990s drama POSE.

Ricky, like me, is a young Black queer man. I, the actor, had to contend with how true this statement must have felt for him, because an HIV diagnosis was largely a death sentence in 1990. Today, despite all the advances in science and medicine, as a Southerner, I am more likely than the average American to contract HIV, less likely to receive treatment, and more likely to die from HIV.

Tens of thousands of people are diagnosed every year, and in some states, annual diagnoses are on the rise. This is particularly true in the South, which accounts for 51 percent of HIV diagnoses despite only making up 38 percent of the U.S. population. There is a level of complacency around HIV that troubles me. Most people don’t understand that we’re still in the midst of the HIV epidemic.

It is true that HIV is no longer a death sentence, but fear, misinformation, and shame surrounding the disease remain and make the epidemic harder to contain. Stigma makes it harder to educate people about the disease, and stops people from seeking crucial treatment that saves lives and prevents its spread.

Americans are still seriously misinformed about HIV. The GLAAD and Gilead Science’s ‘State of HIV Stigma’ Survey found that the public’s knowledge of HIV is dangerously inaccurate and that they hold significant feelings of stigma towards people living with the disease. According to their study, only 60 percent of Americans believe that “HIV is a medical condition that can be treated,” despite the fact that drugs treating HIV have been on the market for over a decade. Even more troubling, nearly 6 in 10 Americans wrongfully believe that “it is important to be careful around people living with HIV to avoid catching it.”

Scientists have proven that HIV cannot be passed through healthy, unbroken skin, and people with HIV who take HIV medicine as prescribed and keep an undetectable viral load have virtually no risk of sexually transmitting HIV to their HIV-negative partners. Yet, this is not widely understood by the public and contributes to more people unnecessarily contracting the disease. A study in Toronto, where HIV is criminalized, found that men who had sex with men were less likely to get tested because of the laws, creating an exponential 18.5 percent increase in HIV transmission.

Around the same time Ricky found out he had HIV, I was born in Florida, a state that still criminalizes HIV and uses the law to punish people and perpetuate stigma. Engaging in consensual sex or donating blood or organs without disclosing one’s HIV status is a third-degree felony in the Sunshine State. This could lead to five years in prison and a $5,000 fine. Florida isn’t alone; today 34 states have HIV-specific criminal laws or sentence enhancements that apply to people living with HIV. This kind of institutionalized discrimination gives people a reason to avoid getting tested or having open and honest conversations around the disease.

US: Criminalizing and stigmatizing HIV only leads to more HIV infections

For transgender Floridians, stigma and fear of arrest could lead to new HIV crisis | Opinion

There’s another public health crisis laying in the shadows of COVID-19, and it’s completely preventable: HIV. More than 20,000 people are living with HIV in Fort Lauderdale – and more than 100,000 across Florida. New HIV infections have been increasing in Florida every year since 2013, and the state’s budget for combating HIV increased 15% between 2015 and 2018.

HIV currently has a disproportionate impact on certain communities. Only one in four people in Fort Lauderdale are Black, but they represent nearly half the city’s population of people living with HIV. Latinas are twice as likely as white women in Fort Lauderdale to be living with HIV. Transgender people are 49 times more likely than cisgender people to have HIV.

Transgender people also face high rates of violence, with transgender people of color being particularly impacted. In 2019, more than 20 transgender people were killed, virtually all of them Black or Latinx. Far too often, their names don’t make the news, names like Tony McDade or Bree Black, both of whom were killed in Florida this year.

Transgender people of color, and in particular transgender women of color, face layers of stigma. Transphobia, racism, and sexism all take a toll on a person and make them more vulnerable in many aspects of their life, including being more likely to contract HIV.

We have the tools and knowledge to stop HIV in its tracks. Taking simple precautions greatly minimizes transmission. Testing can offer quick results. And drug regimens can treat people living with HIV and prevent it from spreading. But a lack of understanding and prejudice against people living with HIV prevents us from taking advantage of these tools. Money is not the issue – the law is.

Florida’s very tough HIV criminalization laws have made a bad situation worse. In Florida, having consensual sex, donating blood or organs, or engaging in sex work without disclosing one’s HIV status is a third-degree felony, which could lead to five years in prison and a $5,000 fine. The law doesn’t take into account whether protection is used, if people maintain a drug regimen that virtually eliminates any chance of passing on the disease, or the fact that blood is screened – for many diseases, including HIV – before being donated.

Not only are HIV criminalization laws antiquated and discriminatory, they have a devastating impact on public health and the perception of HIV. When our own state government is labeling those living with HIV as criminals, it perpetuates stigma. It creates a fear of basic education, getting tested or talking about HIV, even with friends and family. It’s hard to blame them considering five years in jail is a possibility.

Our state has created a vicious cycle: people choose to not know their status out of fear of repercussions. Therefore, they don’t receive treatment, leading to more people unknowingly spreading the disease. Criminalizing and stigmatizing HIV only leads to more HIV infections.

Earlier this month, the results of the “GLAAD-Gilead State of HIV Stigma Survey” were published, measuring attitudes towards HIV, and the results showed we still have a long way to go. Nearly 6 in 10 Americans wrongfully believe that “it is important to be careful around people living with HIV to avoid catching it.” That’s not true and the medical community has known this for decades. But when it’s difficult to educate people on the disease, misinformation spreads and has a damaging impact on public health.

Knowing that transgender people are more likely to be affected by HIV, at TransInclusive, we spend a considerable amount of time reaching out to that community. When you add the stigma transgender people face to the stigma that surrounds HIV, it makes our outreach efforts that much harder. Moreover, it becomes even more difficult to ensure transgender people have the resources needed to prevent the spread of HIV.

The survey found that one in two Americans would be uncomfortable with a partner or spouse living with HIV, which only increases the disproportionate impact HIV has on transgender people, considering they have the highest rates of infection. Ignoring these disparities will only continue to harm the communities most at risk of contracting HIV.

Training and resources from allies are part of the solution. Grants from private-sector partnerships like the Gilead COMPASS Initiative have helped us build a grassroots effort to prevent the spread of HIV by going into the Fort Lauderdale community to educate people and hosting group sessions where individuals can learn without fear of judgment. During the social distancing measures of the COVID-19 pandemic, we’ve held our “Open Night Thursday” series virtually to allow people from our community to talk to one another, learn about the resources available to them, and feel a sense of belonging.

But we must reach beyond our community, and to our lawmakers, to make the impact we need.

Changing misperceptions has to happen on the frontlines of health care and in the halls of state houses. Stigma will not go away if laws that criminalize HIV remain. Florida can’t end the HIV epidemic overnight, but the state can take steps now to stop the rise of HIV infections and avoid another health crisis. Ending the criminalization of HIV and educating our state about how to prevent its spread will help fight the pervasive stigma that still exists – and gets us that much closer to ending HIV in Florida.

Tatiana Williams is the co-founder and executive director of Transinclusive Group in Fort Lauderdale.

Watch all the videos of Beyond Blame @HIV2020 – our “perfectly executed…deftly curated, deeply informative” webshow

Earlier this month, advocates from all over the world came together for two hours to discuss the successes and challenges of the global movement to end HIV criminalisation.

All of the recordings of Beyond Blame: Challenging HIV Criminalisation for HIV JUSTICE WORLDWIDE are now available on the HIV Justice Network’s YouTube Channel.

“HUGE pleasure 2B at #BeyondBlame2020 conference – deftly curated, deeply informative; speakers were great; the passion & commitment to #HIVjustice was palpable. Much progress yet a sober reminder that the work is far from over.”

Kene Esom, Policy Specialist: Human Rights, Law and Gender, United Nations Development Programme (UNDP)

 

The full-length director’s cut version – with enhanced audio and video – is now available in English as well as with the audio track of the recorded simultaneous translation in French, Spanish, Russian, and Portuguese.

The English version is also available as a YouTube playlist in ‘bite-size’ chunks, with each segment of the webshow available as standalone videos.  This means, for example, if you just want to watch (or share) the segment on ‘women challenging HIV criminalisation in Africa‘, or on ‘bringing science to justice, and justice to science‘, it’s now possible.

“That webinar was perfectly executed. Great sound, engaging transitions (they actually played people on and off!), and multiple speakers in various collections. Having ALL OF THEM back at the end showed the breadth of this technical accomplishment and the depth of the speakers’ field of expertise. Not everyone may notice these things but boy, I sure do, and it was totally pro. I’ve seen big name conferences who couldn’t get this right… Congratulations all around, and especially to [director] Nicholas Feustel.

Mark S King, My Fabulous Disease

 

We have also made available for the first time the standalone recording of Edwin Cameron’s closing speech, which inspired so many.  The transcript is included in full below.

“We have been being battling this fight for many years. Since the start of the HIV epidemic we as gay men, as gay women, as queers, as transgender people, as sex workers, as people using drugs, have been persecuted by the criminal law. And I’m here to say, “Enough! Enough!

We have achieved a great deal with our movement, with the HIV Justice Network. We have achieved a great deal in conscientizing law makers, law givers and the public. It is now time for us to join in unison to demand the end of these stigmatising, retrograde, unproductive, hurtful, harmful laws.

It is a long struggle we’ve engaged in. And it’s one that has hurt many of us. Some of us here today, some of us listening in, some of us who have spoken, have felt the most brutal brush of the law. They have been imprisoned, unjustly prosecuted, unjustly convicted, and unjustly sent away.

HIV is not a crime. But there is more to it. Criminalising HIV, criminalising the transmission or exposure of HIV, as many countries on my own beautiful continent Africa do, is not just stupid and retrograde. It impedes the most important message of the HIV epidemic now, which is that this epidemic is manageable. I’ve been on antiretroviral treatment now for very nearly 23 years. My viral load has been undetectable for more than 20.

We can beat this, but we have to approach this issue as public health issue. We have to approach it rationally and sensibly, and without stigma, and without targeting people, and without seeking to hurt and marginalise people.We’ve made calamitous mistakes with the misapplication of the criminal law over the last hundred years, in the so-called ‘war on drugs’. We continue to make a calamitous mistake in Africa and elsewhere by misusing the criminal law against queer people like myself. We make a huge mistake by misusing the criminal law against people with HIV.

Let us rise today and say, “Enough!”

 

When considering the criminalisation of COVID-19, lessons from HIV should be retained

Marginalised communities will not get justice from criminalising Covid-19 transmission

The criminalisation of the virus would create greater barriers to accessing healthcare systems already preventing many people from getting treatment.

After it was announced that no further action would be taken by police regarding the death of Belly Mujinga, a railway worker who contracted coronavirus after reportedly being spat on, there was national outcry. Her name has been plastered on placards at Black Lives Matter protests, while the public has pointed out that a man in Scotland who spat on a police officer while “joking” about coronavirus in April has been jailed for a year. But while this outrage is valid in the face of a government who continues to show their blatant disregard for black lives, criminalisation of diseases has been proven to be an ineffective tool for justice.

Over the past few months, parallels have been drawn between the Covid-19 pandemic and the HIV epidemic. Both viruses are communicable (they can be passed between people); both have been racialised, leading to racist and xenophobic attacks and stereotyping; community mobilisation has demanded adequate government public health responses for both health emergencies; and the impact of both viruses has highlighted the need for a global health approach which transcends borders. 

When the World Health Organisation (WHO) declared Covid-19 a pandemic, many HIV organisations and activists advocated that the transmission of the novel coronavirus should not be criminalised. As public fear of Covid-19 grew, HIV advocates predicted the negative impact on public health and possibility of human rights violations, similar to those seen for people living with HIV. 

“Despite the evolving scientific knowledge, criminalisation laws have been written and implemented across the world faster than the development of the general understanding of the virus itself”

This strain of coronavirus is new and scientists are developing their understanding of it. In the past few weeks, there has been confusion about the probability of asymptomatic transmission (transmitting the virus when a person does not have Covid-19-like symptoms), as the WHO had previously commented that it was “very rare” and later stated that this wording had misled people. Despite the evolving scientific knowledge, criminalisation laws have been written and implemented across the world faster than the development of the general understanding of the virus itself. Globally, countries have implemented or have proposed laws against Covid-19 transmission and even exposure, without transmission, including Canada, France, India, and South Africa.

Often, the aim of criminalisation is to facilitate a tool for prevention and deterrence (to discourage people from passing on a virus) or as punishment for those who have or may have passed on a virus. HIV advocacy has illustrated over the years that the criminalisation of transmission or exposure is ineffective, and disproportionately impacts marginalised communities and negatively impacts public health.

In their Statement on Covid-19 Criminalisation, published in March, the HIV Justice Worldwide Steering Committee wrote that hastily drafted laws, as well as law enforcement, driven by fear and panic, are unlikely to be guided by the best available scientific and medical evidence – especially where such science is unclear, complex and evolving. “Given the context of a virus that can easily be transmitted by casual contact and where proof of actual exposure or transmission is not possible, we believe that the criminal justice system is unlikely to uphold principles of legal and judicial fairness, including the key criminal law principles of legality, foreseeability, intent, causality, proportionality and proof.”  

Since that statement was issued, internationally coronavirus laws have been weaponised against the most marginalised within society, as is the case with HIV criminalisation laws. The Ugandan government, for example, has used coronavirus laws to target marginalised LGBTQI+ groups, and in the UK, people of colour are fined more than the white population under coronavirus laws, in some cases leading to unlawful charges. In some cases people were even charged under the wrong law (e.g. enforcing Welsh law in England).

The director of legal services at the Crown Prosecution Service (CPS), the public agency that conducts criminal prosecutions in England and Wales, found that 24% of cases reviewed had been charged incorrectly. In May a CPS press statement cited the speed and pressure to implement the laws as the cause of the wrongful charges. Across the Global North, it has been well documented that racialised communities are disproportionately impacted by Covid-19 and the Human Rights Campaign Foundation anticipates that LGBTQI communities will be disproportionately impacted by the virus. This is due to a myriad of reasons underpinned by systemic discrimination.

“Criminalisation of transmission or exposure is ineffective, and disproportionately impacts marginalised communities and negatively impacts public health”

HIV research has shown little evidence that criminalisation laws prevent transmission, in fact, it’s evidenced that such laws are bad for public health and fuel reluctance to get tested and treated. In the UK, testing and treatment of Covid-19 is free, as is the case with many other communicable diseases to remove the barrier to testing and treatment. Free testing and treatment access, irrespective of immigration status, is important, however, a briefing paper from Medact, Migrants Organise and New Economics Foundation (NEF), has shown that migrant communities blocked from healthcare because of the hostile environment, that “the coronavirus ‘exemption’ from charging and immigration checks is not working” and people have been asked to show their passports, and that people face additional obstacles such as language barrier and digital exclusion from emergency services. 

Criminalisation exacerbates public health issues: in a Channel 4 report, Migrants Organise spoke of a man who died at home for fear of being reported to immigration authorities if he accessed healthcare. The threat of immigration enforcement disproportionately impacts those in precarious work and those with precarious migration status, all of whom are more likely to come from racialised groups and in some cases groups which are hyper-surveilled and criminalised.

The role of healthcare and access to it needs to be reimagined, where people are viewed as patients not passports and healthcare professionals are not the extended arm of the Home Office. Governments must implement better employment rights, so that employers are held to account and do not put staff such as Belly Mujinga, in harmful positions. Governments must provide better statutory sick pay so those in precarious work do not have to choose between their health and putting food on the table. We need to overhaul systemically discriminatory processes that don’t look after the most vulnerable, rather than implementing laws – such as criminalisation – that will systematically punish them.

HIV criminalisation laws affect women negatively and impede the effectiveness of implementing state programmes

Can HIV criminalisation protect women from becoming infected?

Translated from Original article in Russian via Deepl.com – For article in Russian, please scroll down.

In many countries, HIV-related criminal liability still exists. At least 68 countries have laws that specifically criminalize hiding information about HIV infection from your sex partner, putting another person at risk of HIV infection, or transmitting HIV. The leaders in the number of criminal cases related to HIV in the region of Eastern Europe and Central Asia are Belarus and Russia.

In 2018, 20 scientists from around the world developed an Expert Consensus Statement on the Science of HIV in the context of Criminal Law. It describes a detailed analysis of the available scientific and medical research data on HIV transmission, treatment efficacy, and evidence to better understand these data in a criminal law context.

Legislation regarding HIV transmission should be reviewed. I point out various facts to this – HIV treatment is available, antiretroviral therapy (ART) effectively reduces the viral load to undetectable and reduces the risk of HIV transmission during sexual contact to zero [1,2,3,4], criminalization initially stigmatizes people who are HIV-positive people and violates their human rights.

One of the arguments in favour of criminal liability for HIV transmission is the alleged protection of women in situations where their husbands or partners become infected with HIV. This argument is often used in Central Asian countries. Let’s look at real-life examples and statistics on how much women are actually protected by existing laws.

In early 2018, thanks to human rights defenders and human rights defenders, the article “Vikino Delo” appeared in the media, about a 17-year-old pupil of an orphanage, who was convicted under subsection 122 (1) of the Criminal Code of the Russian Federation for knowingly putting another person at risk of HIV infection. In 2017, Vika met a man F. (31 years old) on a social network. When they had an intimate relationship, the girl offered to use a condom, but F. refused. Vika did not tell F. that she had HIV. From the girl’s testimony provided in court, it was clear that she did not want to put the victim at risk of infection, and did not say the diagnosis because she was afraid. She tried to hint at him, telling about her HIV-infected friend. F. proposed to be tested for HIV together. As a result, he has a minus, she has a plus. F. filed a complaint with Vic to the police. The man decided to punish the girl for insufficient, in his opinion, sincerity. Following the verdict, Vicki’s lawyer filed a complaint with the Supreme Court. On the recommendation of the Supreme Court, given that at the time of the commission of the “crime” she was a minor, apply a sentence of warning to her. At the same time, no one took the blame from her. The leading role in protecting and supporting Vicki was played by the female community in the guise of Association “EVA”.

The situation with the Vicki case is commented on by human rights activist Elena Titina, head of the Vector of Life Charity Fund, who acted as a public defender in court: “Women are subjected to even greater stigma, condemnation, and therefore do not protect themselves. Vicki’s case is very revealing in this. For three years, during the whole trial, the girl simply had to listen to insults, humiliation against her, the remarks were incorrect – and on the part of the plaintiff, this 31-year-old man, on the part of judges, prosecutors, even lawyers sometimes behaved like elephants in a china shop. She, in my opinion, is the heroine. I’m not sure that an adult woman would have endured what Vick had endured and come to the end, defending her rights. Her criminal record was removed. A unique thing, I am very proud that I participated in it. “This is the only thing that has ended so far because I don’t know of any more such precedents with a conditional happy ending

In the Criminal Code of the Russian Federation , in which almost one and a half million cases of HIV infection among citizens are only officially registered, there is article 122 “Transmission of HIV infection”. Disaggregation of data began in 2017, from 01/01/2017 to 12/31/2019, in total, within the framework of 122 articles, 150 sentences were sentenced according to the main qualification in parts 1-4. 93 sentences were pronounced against men (62%), 57 (38%) – against women. It is noteworthy that in Part 1, “Knowingly putting the other person at risk of HIV infection” is condemned by more women: 56.4% versus 43.6% of men.

According to the Ministry of Health of the Republic of Tajikistan for 2018, there were 10.7 thousand people with HIV in the whole country, of which about 7 thousand were men. It was noted that in 54.6% the virus was transmitted sexually, and in some regions, the proportion of such cases reaches 70%.

For reference: since July 2015, to register a marriage in Tajikistan, you must undergo a medical examination, which includes an HIV test.

Tajikistan became one of the few countries (and the only one in the EECA region) to which CEDAW issued a recommendation dated November 9, 2018: “Decriminalize the transmission of HIV / AIDS (Article 125 of the Criminal Code), and repeal government decrees of September 25, 2018 and October 1, 2004 years prohibiting HIV-positive women from getting a medical degree, adopting a child, or being a legal guardian. ”

Instead, on January 2, 2019, President Emomali Rahmon signed a series of laws, including those aimed at “strengthening the responsibility of doctors, beauty salons, hairdressers and service enterprises, which are due to non-compliance with sanitary, hygiene, anti-epidemic rules and regulations caused HIV / AIDS. ” From that moment, a lot of publications appeared in the media, illustrating not only the widespread informing of Tajik citizens about the requirements being followed but also the increase in the number of publications on criminal penalties related to HIV.

According to the results of media monitoring conducted by the Eurasian Women’s AIDS Network, in 2019, 23 publications on HIV were registered in the electronic media of Tajikistan. Among them, two topics were divided equally: general information on the responsibility for HIV transmission and statistics, as well as publications that women are accused of, such as:

“27-year-old woman suspected of having HIV / AIDS deliberately infecting”,

“Two women in northern Tajikistan convicted of HIV infection”,

“In Tajikistan, a woman convicted of“ deliberate HIV infection ”by 23 men was sentenced”,

“A resident of Kulyab of Tajikistan is suspected of intentionally acquiring HIV”,

“Two women in Khatlon have infected dozens of men

Among these publications, there is not one that describes particular cases of men. We already wrote about the vulnerability of women in August last year in our interview with attorney Zebo Kasimova.

We could not obtain statistical data on the number of cases brought under article 125 of the Criminal Code of the Republic of Tajikistan, “HIV infection”. Particularly important would be information disaggregated by sex – that is, disaggregated data, the collection of which makes special sense, in view of the state’s argument for the protection of women. The importance of disaggregated statistics is stated in the Sustainable Development Goals – the Resolution adopted by the UN General Assembly in 2015: only accurate, reliable, comprehensive thematic data will help us understand the problems we are facing and find the most suitable solutions for them.

Olena Stryzhak, one of the founders of the Eurasian Women’s AIDS Network and the head of the Positive Women BO, is actively promoting the decriminalization of HIV in Ukraine  “I have been on the committee for the second year in the validation of elimination of mother-to-child transmission of HIV and syphilis at the Ministry of Health of Ukraine, and actively participate not only in the activities of the committee in our country but also attend international meetings of the Committee at WHO, communicate with many people working in this field.

One of the obstacles for women to seek medical help and treatment on time is the fear of prosecution, the fear of possible criminal liability. In Ukraine, I was able to obtain statistics on the number of criminal cases under article 130 of the Criminal Code of Ukraine, disaggregated by sex. I was surprised by the statistics, because, starting in 2015, only women were convicted under this article. This negatively affects not only the women themselves but also the effectiveness of implementing state programs, including the process of validating the elimination of mother-to-child transmission of HIV

From the last case in Ukraine, for 2018: “… Since the defendant refused, the specialist for child services extended her hands to the child in order to pick her up, but the defendant bit her left hand.” From the conviction: “The court decided to qualify the actions of the defendant … Part 4 of Art. 130 of the Criminal Code of Ukraine as a complete attempt on intentional infection of another person with human immunodeficiency virus. “

Does it mean that if only women were convicted, the fact that only women are sources of infection? From an alternative shadow report of the Tajikistan Network of Women Living with HIV, presented at the 71st session of the UN Committee on the Elimination of All Forms of Discrimination against Women in November 2018: “In violation of their rights, as a rule, women do not go anywhere. During the study of the situation when writing this report, violations of the rights of women living with HIV and women from affected groups were identified, only a few decided to defend their rights and because they were provided with a lawyer at the expense of the project. The reasons for this behaviour are different. One of the main reasons is the lack of financial resources to pay for the services of a lawyer. Secondly, many women living with HIV and women from HIV-affected groups have low legal literacy; they do not have information about who to contact on a particular issue. Thirdly, self-stigmatization and the fear of confidentiality also prevent women living with HIV and women from HIV-affected groups from defending their rights. ”

It is clear from the report that women do not defend their rights, especially on such sensitive issues, for fear of feeling even more condemned and becoming even more vulnerable. In addition, in the countries of Central Asia, families have traditions when a daughter-in-law must tell her husband or mother-in-law where she goes and what she is going to spend or spent money on (by the way about paying a lawyer). Women depend on other family members, and often do not have their own money.

Violence against women increases their risk of HIV infection, while the very presence of HIV infection in a woman also increases the risk of violence, including from relatives, due to her vulnerability and low self-esteem.

The criminalization of HIV does not work, either as a preventive measure nor as a way to protect women from infection, as decision-makers try to imagine. On the contrary, with specific examples, we observe that women are more vulnerable.

Sources:

[1] – Cohen MS, Chen YQ, McCauley M, Gamble T, Hosseinipour MC, Kumarasamy N, et al. Prevention of HIV-1 infection with early antiretroviral therapy. N Engl J Med. 2011 Aug 11; 365: 493-505.

[2] – Rodger AJ, Cambiano V, Bruun T, Vernazza P, Collins S, van Lunzen J, et al. Sexual activity without condoms and risk of HIV transmission in serodifferent couples when the HIV-positive partner is using suppressive antiretroviral therapy. JAMA. 2016; 316: 171-81.

[3] – Grulich A, Bavinton B, Jin F, Prestage G, Zablotska, Grinsztejn B, et al. HIV transmission in male serodiscordant couples in Australia, Thailand and Brazil. Abstract for 2015 Conference on Retroviruses and Opportunistic Infections, Seattle, USA, 2015.

[4] – Cohen MS, Chen YQ, McCauley M, Gamble T, Hosseinipour M, Kumarasamy N, et al. Antiretroviral Therapy for the Prevention of HIV-1 Transmission. N Engl J Med. 2016 Sep 1; 375 (9): 830-9. 


Может ли криминализация ВИЧ защитить женщин от инфицирования?

Во многих странах все еще существует уголовная ответственность, связанная с ВИЧ. По меньшей мере 68 стран имеют законы, которые специально предусматривают уголовную ответственность за сокрытие информации о наличие ВИЧ-инфекции от своего партнера по сексу, поставление другого лица в опасность инфицирования ВИЧ или передачу ВИЧ. Лидерами по количеству уголовных дел, связанных с ВИЧ, в регионе Восточной Европы и Центральной Азии являются Беларусь и Россия.

В 2018 году, 20 ученых из разных стран мира разработали Заявление об экспертном консенсусе в отношении использования научных данных о ВИЧ в системе уголовного правосудия. В нем описан подробный анализ имеющихся данных научных и медицинских исследований о передаче ВИЧ, эффективности лечения и доказательства, позволяющие лучше понять эти данные в уголовно-правовом контексте.

Законодательные нормы в отношении передачи ВИЧ должны быть пересмотрены. На это указываю различные факты — лечение ВИЧ-инфекции доступно, антиретровирусная терапия (АРТ) эффективно снижает вирусную нагрузку до неопределяемой и снижает риски передачи ВИЧ при сексуальном контакте до нуля [1,2,3,4], криминализация изначально клеймит людей ВИЧ-положительных людей и нарушает их права человека.

Один из аргументов в пользу существования уголовной ответственности в отношении передачи ВИЧ — это якобы защита женщин, в тех ситуациях, когда их мужья или партнеры инфицируют их ВИЧ. Этот аргумент довольно часто используют в странах Центральной Азии. Давайте рассмотрим на реальных примерах и статистических данных, насколько женщины на самом деле защищены существующими законами.

В начале 2018 года, благодаря правозащитницам и правозащитникам, в СМИ появилась статья «Викино дело», о 17-ти летней воспитаннице детского дома, которую осудили по части 1 статьи 122 УК Российской Федерации за заведомое поставление другого лица в опасность заражения ВИЧ-инфекцией. В 2017 году Вика познакомилась в социальной сети с мужчиной Ф. (31 год). Когда у них была интимная связь, девушка предложила использовать презерватив, но Ф. отказался. Вика не сказала Ф., что у нее ВИЧ. Из показаний девушки, предоставленных в суде, было видно, что она не желала ставить потерпевшего в опасность заражения, и не сказала о диагнозе, потому что боялась. Она пыталась намекнуть ему, рассказывая о ВИЧ-инфицированной подруге. Ф. предложил вместе сдать анализы на ВИЧ. В результате у него — минус, у нее — плюс. Ф. подал на Вику заявление в полицию. Мужчина решил наказать девушку за недостаточную, на его взгляд, искренность. После вынесенного приговора адвокатом Вики была подана жалоба в Верховный Суд. По рекомендации Верховного Суда, учитывая, что на момент совершения «преступления» она была несовершеннолетней, применить к ней наказание в виде предупреждение. При этом вину с неё никто не снял. Ведущую роль в защите и поддержке Вики сыграло женское сообщество в лице Ассоциации “ЕВА”.

Ситуацию с делом Вики комментирует правозащитница Елена Титина, руководительница БФ «Вектор жизни», которая выступала общественой защитницей в суде: «Женщины подвергаются еще большей стигме, осуждению, поэтому не защищают себя. Дело Вики очень показательно в этом. Девочке пришлось в течение трех лет, пока длился весь судебный процесс, просто выслушивать оскорбления, унижения в свой адрес, реплики некорректные — и со стороны истца, этого 31-летнего мужчины, со стороны судей, прокуроров, даже адвокаты порой вели себя как слоны в посудной лавке. Она, на мой взгляд, героиня. Я не уверена, что взрослая женщина выдержала бы то, что выдержала Вика, и дойти до конца, защищая свои права. С нее сняли уголовную статью. Уникальное дело, я очень горжусь, что я в нем участововала. Это единственное на сегодняшний момент дело, которое так закончилось, потому что больше таких прецедентов, с условным хэппи-эндом я не знаю».

В Уголовном кодексе Российской Федерации, в которой только официально зарегистрировано почти полтора миллиона случаев ВИЧ-инфекции у граждан, существует статья 122 “Заражение ВИЧ-инфекцией”. Дезагрегация данных начата в 2017, с 01.01.2017 по 31.12.2019 всего в рамках 122 статьи вынесено 150 приговоров по основной квалификации по частям 1-4. 93 приговора вынесено в отношении мужчин (62%), 57 (38%) — в отношении женщин. Примечательно, что по части 1 “Заведомое поставление другого лица в опасность заражения ВИЧ-инфекцией” осуждается больше женщин: 56,4% против 43,6% мужчин.

По данным Министерства здравоохранения Республики Таджикистан за 2018 год, всего по стране насчитывалось 10,7 тысяч людей с ВИЧ, из них порядка 7 тысяч — мужчины. Отмечено, что в 54,6% вирус передался половым путем, а в некоторых регионах доля таких случаев достигает 70%.

Для справки: с июля 2015 года для регистрации брака в Таджикистане необходимо пройти медицинское обследование, которое включает тест на ВИЧ.

Таджикистан стал одной из немногих стран (и единственной в регионе ВЕЦА), которой КЛДЖ дал рекомендацию от 09 ноября 2018 года: “Декриминализировать передачу ВИЧ/СПИДа (статья 125 Уголовного кодекса), и отменить постановления правительства от 25 сентября 2018 года и 1 октября 2004 года, запрещающие ВИЧ-положительным женщинам получать медицинскую степень, усыновлять ребенка или быть законным опекуном”.

Вместо этого, 02 января 2019 года президент страны Эмомали Рахмон подписал ряд законов, в том числе направленных на «усиление ответственности врачей, работников салонов красоты, парикмахерских и предприятий по обслуживанию, которые из-за несоблюдения санитарно-гигиенических, санитарно-противоэпидемических правил и норм стали причиной заражения вирусом ВИЧ/СПИД». С этого момента в СМИ появилось множество публикаций, иллюстрирующих не только широкое информирование граждан Таджикистана о выполняемых предписаниях, но и увеличение количества публикаций об уголовных наказаниях в связи с ВИЧ.

По результатам медиа-мониторинга, который проводит Евразийская Женская сеть по СПИДу, в 2019 году в электронных СМИ Таджикистана зарегистрировано 23 публикации по теме ВИЧ. Среди них поровну разделили места две темы — это общая информация относительно ответственности за передачу ВИЧ и статистика, а также публикации, в которых обвиняются женщины, как, например:

“27-летняя женщина подозревается в преднамеренном заражении ВИЧ/СПИД”,

“Двух женщин на севере Таджикистана осудили за заражение ВИЧ-инфекцией”,

“В Таджикистане вынесли приговор женщине, обвиняемой в «умышленном заражении ВИЧ» 23 мужчин”,

“Жительница Куляба Таджикистана подозревается в преднамеренном заражении ВИЧ”,

“Две женщины в Хатлоне заразили десятки мужчин”.

Среди этих публикаций нет ни одной, описывающей частные случаи в отношении мужчин. Об уязвимости женщины мы уже писали в августе прошлого года в нашем интервью с адвокатессой Зебо Касимовой.

Статистические данные о количестве дел, возбужденных по статье 125 УК Республики Таджикистан, “Заражение ВИЧ-инфекцией”, нам получить не удалось. Особенно важной была бы информация с разбивкой по полу — то есть дезагрегированные данные, сбор которых имеет особый смысл, ввиду аргументации государства о защите женщин. О важности дезагрегированной статистики говорится в Целях устойчивого развития — Резолюции, принятой Генеральной Ассамблеей ООН в 2015 году: только точные, достоверные, всесторонние тематические данные позволят понять проблемы, стоящие перед нами, и найти для них самые подходящие решения.

Елена Стрижак, одна из основательниц Евразийской Женской Сети по СПИДу и руководительница БО “Позитивные женщины”, активно продвигает тему декриминализации ВИЧ в Украине“Я уже второй год состою в комитете по валидации элиминации передачи ВИЧ и сифилиса от матери к ребенку при Министерстве здравоохранение Украины, и активно принимаю участие не только в деятельности комитета в нашей стране, но и посещаю международные заседания Комитета в ВОЗ, общаюсь со многими людьми, работающими в этой сфере.

Одним из препятствий к тому, чтобы женщины вовремя обращались за медицинской помощью и за лечением, служит страх обвинения, страх перед возможной криминальной ответственностью. У нас в Украине я смогла получить статистические данные о количестве уголовных дел по статье 130 УК Украины, с разбивкой по полу. Была удивлена статистикой, потому что, начиная с 2015 года, по этой статье были осуждены исключительно женщины. Это негативно отражается не только на самих женщинах, но и на эффективности реализации государственных программ, в том числе на процессе валидации элиминации передачи ВИЧ от матери к ребенку”.

Из последнего кейса по Украине, за 2018 год: «…Так как подсудимая отказалась, специалист службы по делам детей протянула руки к ребенку с целью забрать ее, но подсудимая укусила ее за левую руку». Из обвинительного приговора: «Суд принял решение квалифицировать действия подсудимой … ч. 4 ст. 130 УК Украины как оконченное покушение на умышленное заражение другого лица вирусом иммунодефицита человека».

Означает ли, что если осужденными оказались только женщины, тот факт, что только женщины являются источниками инфицирования? Из альтернативного теневого доклада Таджикистанской сети женщин, живущих с ВИЧ, представленного на 71-й сессии Комитета ООН по ликвидации всех форм дискриминации в отношении женщин в ноябре 2018 года: “При нарушении их прав, как правило, женщины никуда не обращаются. В ходе изучения ситуации при написании данного отчета выявлены нарушения прав женщин, живущих с ВИЧ, и женщин из затронутых групп, только единицы решились защищать свои права и то, потому что им был предоставлен адвокат за счет проекта. Причины такого поведения различны. Одна из основных причин, это отсутствие финансовых средств на оплату услуг адвоката. Во-вторых, многие женщины, живущие с ВИЧ, и женщины из затронутых ВИЧ групп имеют низкую правовую грамотность, у них нет информации о том, к кому обратиться по тому или иному вопросу. В-третьих, самостигматизация и боязнь разглашения конфиденциальности также мешает женщинам, живущим с ВИЧ, и женщинам из затронутых ВИЧ групп защищать свои права.”

Из доклада ясно, что женщины не защищают свои права, особенно по таким чувствительным вопросам, из-за страха почувствовать еще больше осуждения и стать еще более уязвимыми. Кроме того, в странах Центральной Азии, в семьях есть традиции, когда невестка должна сказать мужу или свекрови, куда она идет, и на что она собирается тратить или потратила деньги (к слову об оплате адвоката). Женщины зависят от других членов семьи, и часто не имеют своих собственных денег.

Насилие в отношении женщин увеличивает для них риск инфицирования ВИЧ, в то же время само наличие ВИЧ-инфекции у женщины также увеличивает опасность насилия, в том числе и со стороны родственников, из-за ее уязвимости и заниженной самооценки.

Криминализация ВИЧ, ни как превентивная мера, ни как способ защиты женщин от инфицирования не работает, как это пытаются представить люди, принимающие решения. Наоборот, на конкретных примерах мы наблюдаем, что женщины оказываются более уязвимыми.

Источники:

[1] — Cohen MS, Chen YQ, McCauley M, Gamble T, Hosseinipour MC, Kumarasamy N, et al. Prevention of HIV-1 infection with early antiretroviral therapy. N Engl J Med. 2011 Aug 11; 365:493-505.

[2] — Rodger AJ, Cambiano V, Bruun T, Vernazza P, Collins S, van Lunzen J, et al. Sexual activity without condoms and risk of HIV transmission in serodifferent couples when the HIV-positive partner is using suppressive antiretroviral therapy. JAMA. 2016; 316:171-81.

[3] — Grulich A, Bavinton B, Jin F, Prestage G, Zablotska, Grinsztejn B, et al. HIV transmission in male serodiscordant couples in Australia, Thailand and Brazil. Abstract for 2015 Conference on Retroviruses and Opportunistic Infections, Seattle, USA, 2015.

[4] — Cohen MS, Chen YQ, McCauley M, Gamble T, Hosseinipour M, Kumarasamy N, et al. Antiretroviral Therapy for the Prevention of HIV-1 Transmission. N Engl J Med. 2016 Sep 1; 375(9):830-9.