Tag Archives: Terrence Higgins Trust

Why are we afraid to get tested for HIV?

399601844_5e89dc80be_z

For some people the idea of being tested for HIV is as simple as making a note in a calendar, an entry which sits comfortably beneath a dentist appointment and above a mother’s birthday. For others, the idea of making that appointment, or taking that long walk to the clinic, is one of the most nerve-wracking experiences they can imagine. However, in an age where the numbers of people diagnosed with HIV are increasing, has our natural fear of the unknown become a luxury we simply can’t afford?

Many years ago it was a scary disease. We called it AIDS and it became a name associated with sin and death. The massive number of infections, particularly in the gay community, were staggering, and as the death toll slowly crept up, nations across the world panicked. It’s impossible for any society to come through such a dark time and emerge unscathed, and so the fear of a silent killer left a scar on our cultural memory which has never really healed, and the mere mention of HIV and AIDS still has a way of stopping conversations.

Thankfully, things have changed since then and treatment for HIV and AIDS is better now than it has ever been. People who have the condition are now finding that their lives have not changed completely, and they are still able to live as long and do all the same things they could before. It’s true that they now have a few additional concerns to think about but with the help of medication, HIV is now manageable. However, it seems that attitudes have not moved on as much as the treatment, with people still finding themselves afraid, ashamed and worried that their lives will never be the same again.

HIVTo try and get a better understanding of the feelings and attitudes behind the diagnosis, I spoke with Sona Barbossa, a counselling team leader with the GMI Partnership. Over the course of our conversation, Sona revealed that the anxiety surrounding being tested and anxiety about the results is something which does prevent people from being tested regularly. ‘I don’t think it’s so much a fear about the test itself, but more fear of what the results might be and having to deal with that. There is still a stigma around it and I see many guys who have not been tested for years because they’re afraid of finding out the results and having to make decisions upon learning their results. Also, there’s still a lot of thinking around where people believe that it won’t happen to them, so they don’t see the point in being tested.’ When I asked Sona if she thought attitudes have changed much since HIV first came to public attention, she told us she didn’t think so. ‘People still connect HIV with promiscuity, the gay scene and with drugs. There’s also still a lot of shame and guilt that surrounds the condition, which I think plays a large role in whether people want to be tested or not and can prevent people from making those all important first steps to be tested.’

The fear of the condition is more than understandable. Even with new treatments being developed every day, HIV is still a lifelong condition which also has lifelong consequences. There’s also a very real stigma still attached, which has always been associated with homosexuality, promiscuity and intravenous drug use. This forces a lot of people who have HIV into a double life to keep it a secret from their friends and family. Sona herself pointed out during our conversation that a lot of people still feel like they will be shunned by their loved ones. ‘The fear of being judged and being looked at differently does form a large part of why people may keep this condition from their loved ones. They think that people may change towards them, and worry that their friends won’t accept them any more, and obviously the worry that their families won’t accept them any more. With this kind of attitude pervading society, it’s little wonder that people would be put off from learning their status, as it forces people to think about a lot of things before they even go to have the test done.’

According to statistics gathered by the gay men’s health charity GMFA, 59,000 gay men were tested for HIV last year. While this seems like a large figure, I was later informed by Carl Burnell, the CEO of GMFA, that this figure may only make up 15-25% of the estimated gay population. This becomes all the more worrying when GMFA’s recent statistics uncovered that 82% of new HIV infections are actually passed on from people who have not been checked themselves. The organisation has consistently fought to encourage people to learn their status and  to be checked at least once a year, however in the course of their work, they find that anxiety about HIV is having a definitive effect on preventing people from being checked. When they examined the reasons for not going to be tested, they found that 30% of those asked noted that nerves about their results were a factor, with a further 10% going on to say this was the main thing stopping them from taking the test. Burnell also noted that though people are still keen to avoid becoming HIV positive, their awareness that the condition is all around them is decreasing, and this can potentially lead people to take risks with their sexual health. He also commented that there is still a popular misconception among young gay men that HIV is not something they need to worry about, as it’s still considered by some to be a disease that only harms older people.

However, it isn’t just methods of treatment which have moved on, but also methods of detection. Time was, that if you wanted to have an HIV test you would have to go to your GP and ask for the test specifically and then be referred to have your blood taken and examined. The process would take anywhere between 3 days and 2 weeks depending on the area, and the very idea of waiting for the results could be described as hell-on-earth for people who were brave enough to be tested in the first place. Now people are able to walk in and be tested within half an hour and have their results the same day, sometimes within minutes. Similarly, thanks to the work of organisations like the Terrence Higgins Trust (THT), people are now able to order and administer the test in the privacy of their own home, send off a small vial of blood and have their results sent to them via email or even text. The sad fact is that even with all these different ways to be diagnosed, not enough people are going out and being regularly checked.

An HIV test in progressHere at So So Gay we like to practice what we preach, so when it came to writing a feature that dealt with being fearless and going to get tested, I decided to go out and take the test myself. Having been in a long-term relationship and suddenly single again, it seemed like the right time to know my status, since I was back on the dating scene. I picked the 56 Dean Street clinic in London for its walk-in service and quick results. The staff were amazing and they made me feel reassured every step of the way. They made me feel like, even though I may have been nervous to be there, I was doing the right thing by being tested. I must admit I was scared – after all the idea of drawing blood at the best of times is scary, especially for a needle-phobe like me –  but I felt that whatever the result, it would all be OK. It’s impossible to be in that situation and not wonder about what happens if you get a bad result and I was no different as I sat in the waiting room. However, I was seen by the nurse extremely quickly and within a few minutes of me sitting down in the private room, we were ready to draw blood. The nurse was a saint and kept me calm, and reminded me that even if I was HIV+, then I would still be the same person I was when I walked in, and that there are services out there to help me every step of the way. When my result came back, I was thankfully HIV-. Although I was relieved, I also knew that being tested was only half the battle, so I went and made an appointment to come back in 6 months to be checked again. I felt like it was a responsible thing to do, not just for my own health, but also for the benefit of anyone I might come to know in the future.

The truth is that it’s very easy to get ‘caught short’ in life and sometimes that leads us to take risks when we know we shouldn’t. The true test is when we make these mistakes, we have to make sure that we take the time to know our own status, since it doesn’t just affect us, but also the people we care about. HIV is no longer the death sentence it used to be and people are able to live normal, healthy and happy lives like they did before. However, this is thanks to the amazing progress we have made in treating the condition and we can only begin to do that when we make the decision to get tested and keep on top of our health. It’s a scary prospect to some and no one takes that for granted, but by taking the chance to be tested, you could be buying yourself years of life. Speaking to Carl at GMFA, he even proclaimed that we could well see the cure to HIV in our lifetimes, so let’s all make sure we are all there to see it.

Some key facts to remember:

  1. HIV is a disease which is transmitted by the sharing of bodily fluids, i.e. blood and semen. It does not discriminate against people who are older, more sexually active or people who use drugs.
  2. There is currently no cure for HIV, so people with the condition have it for the rest of their lives.
  3. With an early diagnosis people are able to live long lives. If it is left untreated, then it becomes harder to fight.
  4. People who have HIV are still the same people they have always been, and it is wrong to judge people or treat them differently because of their status.
  5. Condoms are not 100% effective. There is still a chance you can get HIV if you are safe, so you need to get tested at least once a year to know if you have the condition or not. The only ‘safe’ sex, is no sex.

Above all, remember that we have a responsibility to care for each other as well as for ourselves because, regardless of positive or negative, we are still united as a community. Be brave, go out and get tested so you know your status. There is an old saying which says ‘knowledge is power’, but in this instance it would be more accurate to say ‘knowledge is life’, whatever your status may be.

Via So So gay

HAVE YOU EVER HAD A HIV TEST?

If you’re interested in having a HIV test, we offer a completely free and confidential rapid HIV test and you’ll get the results within 60 seconds from a simple finger prick test. We use the Insti HIV test produced by BioLytical laboratories. The test is 99.96% accurate from 90 days post contact for detecting HIV 1 and 2 antibodies. We also have a mobile testing van which is often out in communities providing mobile rapid HIV tests. Appointments are not always necessary, if you would like a test, please contact us on 0116 2559995

STAY UPDATED
Follow LASS on Twitter
or subscribe via email

Record numbers of UK gay men test positive for HIV

 

  • Almost half of new cases are gay or bisexual males
  • Up to 10,000 unaware of their infection, says study

The number of gay men being diagnosed with HIV has reached a record high in the UK, according to the Health Protection Agency (HPA).

One in 20 gay men and men who occasionally have sex with men are HIV positive in the UK – and in London, the ratio is as high as one in 12. Part of the reason for the observed rise is increased testing, but, says the HPA, it is also clear that too many men are unaware that they have HIV and are unknowingly infecting others.

“About 8,000 to 10,000 gay men are HIV positive and unaware of their status,” said Dr Valerie Delpech, the HPA’s head of HIV surveillance.

According to the HPA’s annual report, released on Thursday in advance of World Aids Day on Saturday, 3,010 men who have sex with men were newly diagnosed with HIV in 2011 – 47.9% of all new diagnoses in the UK. The numbers have remained high since 2007.

Men who have tested positive and been put on drug treatment, which can keep them healthy and give them a normal lifespan, are unlikely to be infectious. Trials have shown that treatment has a role to play in preventing the spread of the epidemic – the drugs reduce the levels of virus in somebody with HIV to such a low level that they are unlikely to transmit the infection to a sexual partner.

The HPA and organisations for those diagnosed with HIV are all advocating regular testing for anybody at risk. Gay men and other men who have sex with men should take an annual test, they say – and if they have new or casual partners, they should be tested every three months.

Living a long and healthy life with HIV depends on starting treatment early. “People are still starting late: they are infected for three to five years before they are diagnosed,” said Delpech. People who are diagnosed as HIV positive late are at 10 times the risk of dying within a year of discovering they have the infection. They are also more likely to infect people while they remain unaware of their status.

The black African community in Britain also faces a higher risk than average, with 37 out of every 1,000 living with HIV last year. Far more men and women in the black African community are diagnosed late than gay men – 68% and 61% respectively, compared with 35%.

The HPA is recommending safe-sex programmes promoting condom use and annual HIV testing as a priority for this community as well as for men who have sex with men. They want NHS clinicians to take every opportunity to offer testing to those at higher risk.

The total number of people in the UK living with HIV climbs steadily every year because treatment is keeping more people alive. Including both diagnosed and undiagnosed cases, it has now reached 96,000, with a total of 6,280 new diagnoses in 2011.

Nearly half of all new diagnoses were acquired heterosexually. More than half of all new UK infections were acquired while the subject was in Britain, compared with 27% in 2002: the small drop in new infections last year, from 6,400 in 2010 to 6,280 last year, was because of the drop in the number of people who had been infected abroad.

Deborah Jack, chief executive of the National Aids Trust, said: “What is striking about the HPA’s data is how it really shows both our successes and our shortcomings in tackling HIV in the UK. On the one hand, we can hail treatment as a real success story. Treatment is effective, people diagnosed with HIV can access it easily and it is working in keeping the virus under control.

“However, when it comes to increasing the uptake of testing – the gateway to treatment – our services are patchy, inconsistent and ultimately we are still failing to make any significant headway in tackling the high rates of undiagnosed HIV.

“A quarter of people living with HIV are unaware they have the virus. As long as this figure remains high, new infections will continue to occur. We must increase our efforts in encouraging people to test and making sure that the health service is taking advantage of every single avenue in offering an opportunity to test – something that isn’t happening at the moment.”

Sir Nick Partridge, the chief executive of the HIV/Aids charity the Terrence Higgins Trust, spoke up for safe sex and said that testing could add 40 years to a person’s life. “HIV is an entirely preventable condition, yet each year we see thousands more people across the UK receive this life-changing diagnosis,” he said. “While there is still no cure and no vaccine, that doesn’t mean we need to accept its continuing march.”

Original Story via Sarah Boseley, health editor at The Guardian

STAY UPDATED
Follow LASS on Twitter
or subscribe via email

Condoms: Why are we still embarrassed about using them?

A new restaurant promoting safe sex and condom use has opened in the UK, but many people are still too embarrassed to even buy them – why?

As sex education goes, it’s pretty unconventional. Cabbages and Condoms is a Thai restaurant chain that serves food along with contraception. The name says it all.

Condoms are handed out to customers instead of after-dinner mints and each restaurant is covered in them – literally. Lights and walls are adorned with condoms, artworks are even made out of them.

All profits go into sex education and Aids prevention programmes in Thailand. Now it has opened its first branch outside Thailand, in the Oxfordshire town of Bicester.   Of all the towns in all the world, it’s not an obvious choice but in the UK many people are still too embarrassed to buy condoms in public and can’t even talk about sex “in a normal way”, say sex education charities.

So why are so many of us still so uncomfortable when it comes to condoms?

This awkwardness is enshrined in British popular culture. Songs like House of Fun by Madness sum up the awkwardness many feel when trying to buy condoms, with such lines as: “A toothbrush and hairspray, plastic grin. Mrs Clay on the corner has just walked in.”

Britain is a sexualised society where adult shops like Ann Summers can be found on many High Streets and condoms and lubricants of any number of flavours, textures and smells can be bought at your local chemist.

A survey by Fusion Condoms found 56% of people surveyed, were embarrassed to buy them. When it came to men, 54% got red faced while 57% of woman did.

Sexual health charities agree embarrassment is still a big issue for many people.

“We’re still so British about sex and condoms, many people find it easier to have sex rather than to talk about it,” says Genevieve Edwards, executive director of health improvement at the Terrence Higgins Trust.

“It’s a population-wide issue, something that doesn’t really change whatever sex or age. Buying condoms is a public declaration that you want sex and many people still aren’t comfortable with that.”

James, 48, from Surrey, is a successful businessman but still feels very awkward when buying condoms.

Figures at Cabbages and Condoms are covered with condoms. Image credit: Getty Images

“Let’s just say self-service tills have made life a lot less stressful,” he says.

“I will always use them rather than dealing with a person. I think my unease is something that lingers from my youth. Back then condoms and talking about sex were not done.”

The embarrassment factor has helped online retailers. The sellers range from commercial operations like Johnnys in a Jiffy to the NHS retailer Freedoms Shop.

In the four years since it was set up, myCondom.co.uk has seen sales increase month-on-month.

But customers still demand discretion. This can be for several reasons and embarrassment is one of them, says managing director Alex Green.

“A large part of the business is niche condoms,” he says. “We sell a lot of small-sized condoms and it’s obvious why someone might not want to buy them in a shop.

“Even online, people are still very concerned about avoiding embarrassment. We get a lot of enquiries about our packaging, some customers even ask for photos of what their order will be sent in.

“We use plain packaging because people make it very clear they don’t want something advertising what’s inside.

“We also get queries about what company name will appear on bank and credit card bills.

The British have a “strange range” of attitudes when it comes to condoms. It ranges from the absolute brazen to the acutely embarrassed and a lot more in between, says psychotherapist Phillip Hodson, a fellow of the British Association for Counselling and Psychotherapy.

“Buying condoms means you are having to be absolutely explicit about something many people want to be implicit about. You are having to admit you are planning to have sex or want to have it.”

Talking about using condoms is also something people struggle with, again regardless of age, according to the FPA (Family Planning Association).

It’s figures shows 61% of people find talking about condoms with a new sexual partner a difficult conversation to have. Of those, 70% find it embarrassing and 36% say it makes them less likely to use a condom.

Health professions say the obvious way to overcome this is better sex education in schools.

While some schools are doing a good job, others aren’t, and this means young people are often getting their information in the playground or on the internet.

“We all know the quality of that information,” says Edwards.

Hodson says condoms are just part of what young people need to be taught.

This condom, dating from the early 19th Century, is made of animal gut and is seen here with waxed paper envelope packaging

Even after the introduction of rubber condoms, some – like this late 19th century example – were still being manufactured from caecal membrane and silk

This rubber sheath, still in its original 1940s packaging, is made of “one piece of soft pliable rubber” and is designed to be reusable

This packet of one latex condom was issued to British troops on active service during WWII, and “withstands all climates”

“They need to be at ease dealing with them, but with that they also need to be taught that sex is powerful and can be an overwhelming thing and they need to think about what they are doing. All of that needs to be taken into account.

“We also need to get to parents and teach them how to talk to their children about sex.

“We need to get across that just because their children are educated about it and how to use a condom it doesn’t mean they are going to go out and have loads of sex.”

He says other countries, like Holland, are able to talk to young people about sex in a natural way, “without sniggering like the British often do”.

Katherine, 17, from Essex, says teenagers do talk about condoms, but nearly always in a joking way.  ”I’m more likely to be hit in the head with a condom filled with water or get one taped to a birthday card than have a serious conversation about them,” she says.

“Young people tend to hide behind humour and make things funny so they’re not embarrassed.

“If you do need one you ask a close friend, you don’t often buy them. We’re given a lot of free condoms at safe sex talks. It saves embarrassment and money.”

In the Fusion survey it was 16 to 19 years olds who found buying condoms the most embarrassing – 65% of those asked said they found it difficult. But so did 57% of people between the ages of 20 and 30, and 50% of those aged over 31.

It shows people of all ages need just as much support as teenagers when it comes to sexual health, says Dr Audrey Simpson of the FPA.

“The problem is that we are preoccupied with the sexual behaviour of the young and consequently thirtysomethings are a forgotten generation in sexual health,” she says.

“They received little sex and relationships education at school but grew up in an increasingly sexualised society. They’ve had to find the confidence themselves to talk about condoms and learn the hard way.

“It’s not surprising that people can feel it’s easier not to use a condom than put themselves through the torture of talking about a subject they feel deeply uncomfortable about.”

At least in Bicester, embarrassment apparently hasn’t stopped people eating at the town’s new condom-themed restaurant.

Original Article via BBC Magazine

STAY UPDATED
Follow LASS on Twitter
or subscribe via email

HIV related Fertility Treatment and Child Adoption Study UK

Be part of an important HIV research study looking into parenthood.

  • Are you HIV positive and receiving anti-retroviral treatment?
  • Are you above the reproductive age of 21 years and above?
  • Have you considered parenthood and tried to access fertility treatment or child adoption services?

If you answered YES to these questions, you may be eligible to participate in a parenthood research study.

The purpose of this research is to explore the experiences of people living with HIV in accessing fertility treatment services or adoption services.  Whilst this study may not provide direct benefits to you, it is hoped that your experiences will help inform and influence future policies in the way services are planned and provided to people living with HIV, trying to have children using non biological means

This study is being conducted in collaboration with Terrence Higgins Trust for Doctorate research at the University of Surrey.  The research will take place at Terrence Higgins Trust offices or at a venue suitable for you, telephone interview may also be arrange.

It does not matter about what your background or sexuality is and couples interested may contact Tam Chipawe on t.chipawe@surrey.ac.uk / 07547 453600 or, Blake Smith at Terrence Higgins Trust on 020 7812 1813 for more information.

Confidentiality will be maintained at all times.  This study has received a favourable ethical opinion from the University of Surrey Ethics Committee.

STAY UPDATED
Follow LASS on Twitter
or subscribe via email

Please Don’t Infect Me, I’m Sorry…

We often talk about prejudice and stigma relating to HIV / AIDS, and in everything we do, attempt to combat this stigma. Not enough people stand out, and sometimes those that do, speak about stigma on a grand scale. Coming up, Rich Juzwiak, an editor at Gawker has posted a wonderful, honest and frank article about understanding the nature of HIV in the context of sex between men from a presumed HIV negative viewpoint.

What is particularly noteworthy is Rich’s unbiased honesty and openness throughout his article. By asking the right questions to people he is meeting for sex (or not) he’s gained a much improved understanding of viral load, and the risk factors involved when meeting people for sex. Sharing his experiences not only provides an education and insight to HIV negative people, but also informs HIV positive people just how little knowledge there is on viral load and transmission.

In addition to the work of organisations like LASS, the Terrence Higgins Trust, the National AIDS Trust and many, many more, the real advocates are the people (regardless of HIV status) who ask questions, understand what’s going on and share their knowledge to the wider public so we can all know our HIV status and enjoy shared companionship whether that intimacy is based on sex, or conversation.

Article follows…

(Would you like to listen to this article instead? Click the play button below…)


The first guy I ever turned down on Grindr for having HIV, my patient zero if you will, is all kinds of hot: hot in the face, hot in the body and hotheaded. In May, he asked me to come over and make out. We chatted a little bit more, he told me about his status and I slipped out of the conversation, just like that. Randomly in July, I noticed him at a movie theater: On Grindr and online, people lie with pictures all the time, choosing ones that distort their appearance in a captured second, but I was able to pick Miguel right out of a crowd. His picture is a symbol of habitual honesty, maybe, but also because he’s so attractive, he has no reason to lie.

“This always happens: someone will feel bad and then they’ll see me out and they’ll be like, ‘Oh my god, you’re so fucking hot,’” Miguel told me while we waited for our table outside of a Chelsea brunch spot one Saturday in early July after I reconnected and asked him to talk to me.

Miguel told me that being turned down for sex because he’s HIV-positive is something that happens “all the time,” and that “almost every time, the minute someone gets to know me, their mind changes.” Exposure to a gay friend often converts homophobes swiftly; the same can be said of an HIV-positive guy meeting others who are fearful. It’s somewhat reassuring that that’s all it takes in many cases, but it also underlines the exponential burden put upon positive guys. They are either in a constant state of proving themselves socially or they are sitting on a secret.

Me

As a gay man in New York with an active, multiple-partner sex life, the chances are that I have hooked up with an HIV-positive guy or five and didn’t know it. Maybe I didn’t know it because he didn’t know it. Maybe I didn’t know it because he was a liar. Maybe I didn’t ask.

Granted, I generally play it safe, keeping fluid exchange at a minimum, using condoms, opting for oral over anal almost every time, and especially with strangers. (Although, as we are coming to realize, oral sex maybe isn’t as safe as we’d like it to be). Even with that in mind, getting tested is never less than horrifying, no matter how regularly I do it. There have been times, especially after suffering from a weird flu-like bug that no one else around me seemed to contract, that I have been sure that I would test positive.

I haven’t yet. I think I’m HIV negative, but since the virus can take three months to show up in blood, I can’t really be sure. In fact, none of us who are sexually active can be sure – except for those who are HIV positive.

Therein lies the hypocrisy in turning down a potential hookup who a) knows his status, and b) is honest about it in favor of one who doesn’t or is lying about it. That kind of discrimination is motivated by fear of the known while taking an agnostic approach to the unknown. It’s especially foolhardy considering that guys who know they are HIV-positive tend to be healthier and with lower viral loads than guys who don’t know they have it and are going untreated. The kind of optimism that assumes someone’s word is as good as a hard copy of a test result is potentially life-altering.

And yet, I’ve turned down guys who are open about their positive status. I watched the onset of AIDS in the ‘80s through the confused eyes of a child. I had it drilled into me that this was a disease to stay far, far away from. I also know better than to sleep with someone who announces himself as HIV positive. Or knew. Now I’m not exactly sure what to think. I feel guilty and scared, but not necessarily in that order.

Giovanni

I forgot to ask Giovanni* his status on Grindr before he came over. I remembered once he was inside of my apartment, discovered that he was HIV positive and asked if he’d like to be interviewed instead of hooking up. He agreed.

One of the first things we talked about was what complicates the situation the most: The widely held idea (at least among the HIV-positive guys I talked to for this story) that antiretroviral medication, which reduces the amount of HIV in a person’s blood to undetectable levels, is a contagion cure-all. That is to say that many people believe that it is virtually impossible for guys who identify as “poz but undetectable” to transmit HIV to a sex partner.

“I feel a little bit discriminated against just because if someone is taking care of themselves, there’s no risk on it, unless you have cuts or you’re bleeding,” Giovanni said. “But even then, you have to have a high viral load. If your status is undetectable, it’s very rare that someone else can catch from sucking.”

Giovanni contracted HIV about three years ago from his boyfriend who lied to him about his status: His partner said he was negative, they repeatedly had bareback sex, it turned out his partner was positive and it destroyed their relationship. “I blame myself,” he told me. His regard of personal responsibility is also present in his current philosophy regarding disclosure. If he’s not asked directly, he doesn’t open up about his HIV status.

“There are people that never ask me about my status, so I just go and assume that they have it,” he told me. “If you don’t ask me, I assume something’s wrong with you.”

I found this point of view disturbing, but most of what else Giovanni said was endearing. He told me that he empathizes with the people who are too scared to hook up with him and who turn him down: “I was there before it happened to me…I know how a person feels. When someone says you’re positive, your world changes.”

And so does the world of the person who has it. “It’s not hard to find somebody that accepts me the way that I am, but I don’t know…” he trailed off.

Before he left, I gave Giovanni a big hug. We were intimate and raw and we never took our clothes off. We talked about staying in touch and getting together again soon but it never ended up happening.

Chad

In early June, I lost interest in Chad when he told me he was “poz/undetectable” on Grindr. I didn’t respond to something he said, and 10 minutes later we shared this exchange:

Chad: Haha is that a no? I can take it :)
Me: It’s so weird, the situation. I don’t want to seem like a dick or discriminate. You know?
Chad: People discriminate all the time. But if u think I would put you at risk, I disagree. And guys think honesty makes things more dangerous.
Me: Tell me more about how it wouldn’t put me at risk.
Chad: Safe sex with an undetectable guy has no real risk, never been a documented case of transmission. But if you’re feeling spooked it’s no fun for either person ;) . Xx.
Me: I need to do more research. I didn’t know that.
Chad: Take care.

I attempted to engage Chad again and he didn’t respond, not that I blamed him. In July, though, we met face-to-face through a mutual friend. I already knew who he was the second I set eyes on him from afar. From there we resumed communication and I’m glad: he’s attractive with intellect balanced out by an easygoing attitude. He’s exactly the kind of guy I want to be around. He’s also an AIDS activist, and thus particularly informed on the matter at hand.

“Lack of communication and lack of conversation around HIV is a big issue,” he said when I asked him about anti-HIV discrimination. “You have this turning point where the drugs start working well enough so that people won’t be outed by their physical appearance and then talking about HIV becomes a choice. Gay people were very tired of being associated with HIV and AIDS and it just kind of went underground. That’s the birthplace of the stigma. As soon as it became something you could disguise or put away, then it became a question of character.”

Chad’s activism doesn’t turn off when he logs onto Grindr. He says he regularly schools people on the app, as he did with me. He makes education sound like foreplay: he says the type of guys he’d be attracted to anyway are those who are knowledgeable on the subject or willing to learn. He told me that based on the information at hand, he can do “basically everything” in bed, just as long as he’s safe about it.

We talked a little bit about the rejection he’s faced from others like me, which sounds more patience-testing than soul-crushing. He bemoaned guys who “just go totally cold” and make things awkward when he reveals his status in person when he picks them up IRL (he says he always tells people in advance of meeting them if they initially connect online). “If you’re uncomfortable, fine. But communicate. It’s not the end of the world and you’re certainly not going to hurt my feelings. But it’s annoying to go through this beat-around-the-bush rejection process,” he told me.

I wondered about the other extreme: guys unafraid of having unsafe sex with him. He says he’s only experienced a “handful” of these, most of them “dedicated pigs who value raw butt sex.” Whether he would appease them depends on the dude.

Toward the end of our conversation, I apologized to Chad for brushing him off. He told me it was nothing, a blip in his life.

“If the situation presented itself again, you think the guy’s attractive and you’re still not comfortable, what do you say?” he asked, testing my apology.

I stammered and then finally: “It would depend on the level of attraction. But I don’t think I’m a firm no.”

“You’re weak now?” he asked, grinning.

Eddie

There is an East vs. West Coast divide on attitudes about HIV positive guys, or so I hear from a new friend, Eddie, who I recently met through other friends. A resident of San Francisco, Eddie told me that uptightness or reluctance on this issue is something he’s only experienced on the East Coast.

“People in San Francisco especially, but on the West Coast [generally], as soon as you say you’re undetectable, it becomes like a free pass,” he explained. “‘Oh, you’re undetectable, and the risk is so minimal, and I’m a top and you’re a bottom, and that’s even less of a risk.’ I’m like, ‘I guess?’ I’m not willing to take that risk.”

He told me that when he was in the gay mecca of Provincetown, Mass., last year, he found himself in a group that was ridiculing someone they knew who was recently diagnosed. That pissed him off, and he told them as much. “On the East Coast, [contracting HIV is considered] your fault, on the West Coast, it’s, ‘That could be me, and so I understand where you’re coming from.’”

Eddie says his experiences with HIV hookups have been “80 percent positive, 20 percent negative.” He was diagnosed in 2003 and says it was “probably the hardest thing I’ve ever dealt with.” It may seem unlikely, but sex ended up being therapeutic for him:

“When I started [dating and hooking up], and it wasn’t a big deal for other people, that really helped me. It really helped me realize that I can incorporate it into my identity.”

Eddie’s own journey to comfort exposes the contradictory cultural status HIV has right now: it’s both no big deal and a huge deal. It’s no big deal because the drugs that make HIV undetectable in blood have largely converted the disease into a manageable inconvenience. For many, it is not the death sentence it was. But for others it is: drugs are expensive and the high cost means that every minute, four people die of AIDS-related illness (as related in David France’s upcoming documentary How to Survive a Plague). The drugs can also have debilitating side effects, diminishing the quality of the life they are also saving. A relaxed, non-stigmatizing attitude is a nice thing for the world but complacency with a plague that continues to rage on is not.

Eddie said he understands his risk of transmission to be incredibly low. “I’ve dated people, and we’ve had unprotected sex, and we haven’t transmitted it. But, that’s in a different context than just hooking up with somebody, because you have that conversation and you make those decisions together,” he told me.

Eddie said he feels more discriminated against than stigmatized and pointed to the number of ways gay men can be socially awful to each other. “I think there are plenty of places where the gay community hurts itself—whether it’s through race, or class, or internalized homophobia. And also with HIV status.”

The Counselor

All of this is great and enlightening and galvanizing, but I still wasn’t sure about the information I was receiving. I know that part of taking care of yourself as an HIV positive individual involves educating yourself, and I have faith that these guys know their shit – much more than I did, at least. But the information that all of them hold true – that hooking up with a guy who is positive but undetectable will almost never or actually never result in the infection of a negative individual – it behooves them to hold true. Because they profess to be ethical people, they wouldn’t have casual sex if they didn’t believe this.

I’m not saying they’re wrong, I’m just saying that they could be biased. They are human, after all.

Through a friend, though, I was able to connect with Bryan Kutner, a counselor who was in South Africa working with an HIV-prevention group when I reached out to him. His is a key populations specialist and a consultant with Columbia University and the Harm Reduction Coalition.

Kutner pointed me to a recent study suggesting that just because HIV is undetectable in blood doesn’t mean it is undetectable in semen. It’s one study of a small sampling of HIV-positive men (81), but it does suggest that being undetectable isn’t the “free pass” that some would like it to be, maybe. The paper raises yet another contradiction: as antiretroviral therapy has become more popular, HIV has experienced a resurgence. At the very least, we shouldn’t rest on our antiretrovirals just yet.

But what does that mean?

“You won’t get a hard answer from me on it, simply because there’s not enough science for us to know exactly the state of affairs for men who are gay or have sex with other men,” Kutner wrote me in an email. “Studies have quantified the lessened risk, but I wouldn’t generalize their findings to the lives of gay men. That said, the consensus is that undetectable viral load is a good thing, all evidence on the subject points toward lessened transmission risk, and there may be more we still don’t know but we’re just gonna recommend that low viral load has some beneficial effect on lessening HIV risk even if we can’t exactly quantify it yet among the gays and other [men who have sex with men].”

But the lack of hard facts does not mean that we must abandon reason. It does not mean that it is impossible to make educated decisions based on the scraps of knowledge that we have. Here is how Kutner broke down the choice faced by Grindr users on the poz/neg divide:

[Say] one profile says nothing about status, another says he’s negative, another says he’s positive and undetectable, etc. As a thought experiment, let’s imagine that what people say online about themselves is always true – which is a stretch to begin with, but let’s go with it for now. The guy whose viral load is undetectable might be the better choice for reducing the chance of transmission; he knows his status, he takes his meds, he has no measurable HIV in his blood. The other guys don’t say their status or they say they’re negative. The unknown status guy could have HIV but not want to say anything about it…Then there’s the negative guy. He’s either truly negative or he just thinks he’s negative; if it’s the latter, then in all likelihood his viral load is more of a transmission risk than the guy who knows his status and has undetectable viral load. Based on counseling NYC men testing for HIV, plenty of “negative” guys fuck without a condom and naively think they and the guy they just fucked is negative – so what they say about being negative is true, but it isn’t accurate since a guy’s HIV status is subject to change before he knows it has changed.

So of those three choices, the guy who’s willing to be out about his status might seem like the easier one to trust. Of course, it’s so much more complicated – who wants to think about HIV during sex when it’s hard enough to contemplate it after sex?

So, right. No firm answers to be had here, except that abstinence is the only way to stay truly safe. And abstinence, as we know, is impossible. How terrifying.

Miguel and Me, Redux

“This always happens: someone will feel bad and then they’ll see me out and they’ll be like, ‘Oh my god, you’re so fucking hot…’”

Miguel is 32 and was 21 when he was diagnosed. A former drug abuser, he told me that when he found out he had HIV, it barely fazed him. It wasn’t until he got clean that he realized the true value of himself – now he says he’s healthier than he’s ever been. He has an insanely cut-up torso to prove it.

Though he told me he isn’t angry, his words suggest otherwise. He gets visibly riled when we discuss HIV-related ignorance within the gay community.

“I’ve had people tell me, ‘I’ve ever been with anyone with HIV.’” he said. “Are you fucking kidding me? Do you live under a rock? ‘Well no one’s ever told me.’ That’s exactly it, and you never bothered to ask. So now you’re an idiot. And then they get mad and it’s like why are you getting mad at me? You’re the dumbass who’s probably going to get HIV because of your mindlessness.”

He isn’t exaggerating. Probably. Using CDC figures, I’ve calculated that 1 in 14 men who sleep with men in America has HIV. I’ve heard estimates as high as 1 in 5 in New York. The stats get fuzzy when you take into account how many guys have it but don’t know it (though there are stats for that percentage, too). In general, the hard facts are elusive. HIV is everywhere or not so much and maybe you’ll get it from someone who is undetectable or maybe you won’t and then maybe you’ll be fine after taking some meds. Maybe.

Where having HIV is concerned, you’re damned to a life of uncertainty and anxiety if you don’t, condemned to one of shoddy treatment from your gay brothers if you do. Even if I never contract HIV, it will remain a concern of mine for life. I have contracted an issue.

Miguel informs everyone of his status up front, and told me that those who don’t “are the people who create this stigma with us.” He said he has a “pretty damn active sex life,” hooking up with “a couple of guys a week.”

But “hooking up” means different things to different people. “I mainly just do what happened earlier. That’s about it,” he added.

Right. Earlier.

After Miguel and I set up our brunch date earlier that day via text, he casually mentioned that he was jacking off. I thought that was hot. It inspired me to do the same and I told him. He sent me shots of his hard cock and asked me to, as well. I explained to him why I never do that (I write in public)…and then I caved. Part of it was out of obligation – I had already turned him down enough – but the bigger part of it was that it was sexually exciting, a slight risk (what if the pics leak?) to make a hot situation hotter. He sent me his ass pic as well, and we said nasty things to each other. “Shoot ur load,” he eventually directed me. “I’m going to in a bit,” I said back. He sent me video of himself ejaculating and then said, “Show me.” And so I did.

At brunch we talked about how hot that was, and how lovely our conversation was going. “I feel like this is much more intimate than a hookup,” I told him, verbalizing what I had felt back when Giovanni sat on my couch and spilled his story to me. “Me too. I would much rather do this,” said Miguel.

After we wrapped up our interview and brunch, Miguel and I stepped onto the bright Chelsea sidewalk outside of our restaurant and kissed passionately. We walked down the subway together, our arms spilling all over each other and I felt proud in the presence of this beauty and flattered that Miguel shared his knowledge and story with me.

* Except for Miguel and Bryan Kutner, the names that appear in this piece are pseudonyms.

STAY UPDATED
Follow LASS on Twitter
or subscribe via email

HIV Awareness “Drops Off Radar”

Listen to this article instead:


It’s claimed infection rates are still high and many people don’t understand what it’s like living with the illness.

Figures from the Health Protection Agency (HPA) show there were nearly 6,000 confirmed cases in adults across the UK in 2011.

In the last five years nearly 3,500 16 to 24-year-olds have been diagnosed.

Paul Steinberg is a sexual health expert based in Lambeth, south London.

He said: “I think it’s a fair point to say awareness of HIV generally has dropped off the radar for a lot of people in this country.”

Paul believes the medical advances made in treating HIV over the past decade have led to people becoming more complacent and taking more risks.

He also says the increased focus on other, more common, STIs like chlamydia and gonorrhea means young people aren’t as educated as they should be on HIV.

“If someone is diagnosed with chlamydia then we can give them some antibiotics and they will be cured,” he said.

“Although HIV is not a death sentence any more, if someone does get diagnosed it’s a long-term, long-lasting condition.

“It’s not the same as having chlamydia or gonorrhea which can be treated.”

Infection myths

Sarah, which is not her real name, is 25 and was born with HIV.

She agrees there are too many young people who don’t know enough about the virus.

Sarah’s been doing work with the charity Body and Soul, which has launched a campaign called Life In My Shoes to challenge people’s misunderstandings of HIV.

The Department of Health recently announced £8m would be spent on raising awareness of HIV in England over the next three years.

The bulk of that money will be given to The Terrence Higgins Trust, one of the UK’s leading sexual health charities.

Genevieve Edwards from the Trust agreed more work needed to be done.

She said: “There’s a new generation who haven’t had basic training.

“The government is funding us to target our campaigns for those most at risk, which are gay and black and African communities.

“However, it’s true to say much more can be done for the population as a whole and generally young people.”

STAY UPDATED
Follow LASS on Twitter
or subscribe via email

Desmond Tutu calls for end to gay stigma to help tackle HIV

Archbishop Desmond Tutu has called for homosexuality to be decriminalised to help tackle HIV.

His comments come in an analysis in The Lancet journal of why incidence of the virus continues to grow among men who have sex with men.

Dr Tutu said anti-homosexuality laws would in the future be seen as “wrong” as apartheid laws are now.

Campaigners said it was important for community leaders to speak out.

The archbishop is patron of the Desmond Tutu HIV Foundation, based in Cape Town, which provides treatment for HIV and carries out research.

Writing in The Lancet, he said: “In the future, the laws that criminalise so many forms of human love and commitment will look the way apartheid laws do to us now – so obviously wrong.

“Never let anyone make you feel inferior for being who you are. When you live the life you were meant to live, in freedom and dignity”.

Also writing in The Lancet, an international team of researchers, led by Prof Chris Beyrer of the Johns Hopkins Bloomberg School of Public Health in the US, said men who have sex with men (MSM) bore a “disproportionate burden” of HIV.

The fact HIV was first identified in gay men has “indelibly marked the global response” and “stigmatised those living with the virus”, they said.

The researchers’ paper said there was optimism among HIV specialists about the potential to use prevention, such as the drug Truvada, to reduce levels of HIV in men who have sex with men.

Earlier this week, the US Food and Drug Administration approved Truvada for preventative use in those at high risk of infection and who may engage in sexual activity with HIV-infected partners, the first time it has approved a drug to prevent HIV infection.

‘Struggle for equity’

But the international team said the picture was very different in many other countries.

“In too many settings in 2012, MSM still do not have access to the most basic of HIV services and technologies such as affordable and accessible condoms, appropriate lubricants and safe HIV testing and counselling,” they said.

“The struggle for equity in HIV services is likely to be inseparably linked to the struggle for sexual minority rights—and hence to be both a human rights struggle, and in many countries, a civil rights one.”

The paper, published on the eve of the international Aids 2012 conference, adds that by the end of 2011, only 87 countries had reported prevalence of HIV in MSM.

Data is most sparse in the Middle East and Africa, where homosexual activity is a criminal offence.

The researchers call for same-sex relations to be decriminalised in all countries, so that a true picture of the scale of HIV in men who have sex with men can be ascertained.

A spokeswoman for the UK’s Terrence Higgins Trust said: “We’ve got to have community leaders and people with influence speaking out.

“That’s why what Desmond Tutu is saying is so important.”

And she said it was right to focus efforts on men who have sex with men, in all countries.

She added: “In London, one in seven gay men has HIV.”

Original Article via BBC

STAY UPDATED
Follow LASS on Twitter
or subscribe via email

NICE recommends IVF for older women, and for people with HIV


Since the original recommendations on fertility were published in 2004 there have been many advances in both treatments and in the understanding of different techniques.

– DR GILL LENG, NICE’S DEPUTY CHIEF EXECUTIVE

Childless women aged between 40 and 42 will be able to receive IVF on theNHS for the first time under proposals by the treatment regulator to help more people become parents.

Experts welcomed the National Institute for Health and Clinical Excellence‘s (NICE) planned new policy, which follows the emergence of evidence that IVF can benefit women of that age.

Since 2004 women aged 23 to 39 in England and Wales with an identified cause of infertility, or who have been infertile for at least three years, should have been offered up to three cycles of IVF.

But a squeeze on NHS spending and controversial restrictions mean many have been denied treatment.

Click to read ITV news, with video featuring ITV Daybreak’s Michelle Morrison on the proposed changes to who can get IVF on the NHS.

Under draft revised guidelines issued by NICE on Tuesday, eligibility for IVF – though only one cycle – will be extended to include women aged 40-42 who are deemed to suffer from “absolute infertility” and have no chance of conceiving by other means.

The regulator conceded, however, its stipulation that such women must not have previously undergone IVF was likely to mean that “quite small” numbers would actually benefit.

“Only a small minority of women aged 40-42 may benefit from the chance to have one cycle of IVF at that age,” said Susan Seenan, deputy director of patient group Infertility Network UK .

“It is good to see that the upper age limit for women has been raised as the evidence shows that we can have success with older women, though that should not take away from the clear message that age is still a major factor in fertility and that the longer one waits the greater the likelihood of problems”, said Professor Chris Barratt of Dundee University‘s school of medicine.

NICE also wants to cut the time women aged up to 39 should have been trying to conceive from three to two years. Seenan said that would reduce the frustration felt by childless couples and enable them to access IVF more quickly and thus increase their chances of starting a family.

The new proposals will also rule that only a single embryo should be transferred where possible.

It will also recommend for the first time that doctors can advise HIV-positive male patients that they can have unprotected sex with their female partner in order to conceive as long as the man meets certain criteria, such as being up to date with his antiretroviral medication, and agrees that they only do so when she is ovulating.

Catherine Murphy, head of policy at the Terrence Higgins Trust, welcomed the proposed change. “HIV medications have improved enormously in the last decade, making mother to baby transmission of HIV preventable and ensuring people can live long and healthy lives. It also means that natural conception is now a possibility for HIV positive men and HIV negative women in the right circumstances.

“An HIV diagnosis should no longer be a barrier to parenthood and we are very encouraged that NICE have recognised this in their consultation”, she added.

Original Article via The Guardian

STAY UPDATED
Follow LASS on Twitter

or subscribe via email
 Related articles

Spoof Tube Announcements Prompt to ‘mind the gap’ over HIV testing

HIV and sexual health charity Terrence Higgins Trust has partnered with GaydarRadio to create a series of spoof public transport announcements, encouraging gay and bisexual men in London to ‘mind the gap’ between their HIV tests.

The announcements, which can be found at Terrence Higgins Trust’s YouTube channel, have been launched to promote the charity’s new campaign Mind the Gap and are voiced by GaydarRadio’s breakfast show presenters Neil Sexton and Debbie Ryan.

They contain references to London’s gay scenes in Soho and Vauxhall, with one advising: “You are now approaching Old Compton Street. Alight here for cocktails, Lady Gaga and an altercation with a drag queen in a kebab shop at 3am – and boys, while you’re at it, remember to have an HIV test at least once a year to ensure there’s a good service running on all lines.”

Gay and bisexual men remain the group most at risk of contracting HIV in the UK, with one in seven men on the London gay scene living with the condition. Current guidelines recommend that men test for the virus at least once every twelve months, with more frequent testing recommended for anyone who has had unprotected sex or experiences symptoms of sero-conversion illness.

Have you ever had a HIV test?

If you’re interested in having a HIV test, we offer a completely free and confidential rapid HIV test and you’ll get the results within 60 seconds from a simple finger prick test. We use the Insti HIV test produced by BioLytical laboratories. The test is 99.96% accurate from 90 days post contact for detecting HIV 1 and 2 antibodies. We also have a mobile testing van which is often out in communities providing mobile rapid HIV tests. Appointments are not always necessary, if you would like a test, please contact us on 0116 2559995

If you’re not from Leicester, or prefer to use a different service, the Terrence Higgins Trust operates a clinic finder with details of clinics across the UK, including its own rapid testing services, at www.tht.org.uk/clinics.

Robin Crowley, Programme Controller at Gaydar Radio, said: “Terrence Higgins Trust’s Mind the Gap campaign reinforces the importance of being tested regularly for HIV in a fun and entertaining way. That’s why GaydarRadio’s breakfast team, Neil Sexton and Debbie Ryan, are perfect as the voices for Mind the Gap, delivering a comedy element to this very important message.”

Cary James, Head of Programmes at Terrence Higgins Trust, said: “We want these announcements to make guys laugh, but we also hope they’ll make them think. For gay and bi men, testing has never been easier, yet a quarter of men with HIV don’t know they have it. That’s thousands of men across London who are putting their health at serious risk. We’re hugely grateful to Gaydar Radio for donating their time and talent to support the project, and hope the campaign will encourage more guys to mind the gap between their HIV tests.”

The ‘Mind the Gap’ campaign, funded by the Pan-London HIV Prevention Programme, will provide information via adverts in gay media, posters in gay venues, and through promotional Oyster card wallets to be handed out across the gay scene.

Original Article via PinkNews.co.uk

STAY UPDATED
Follow LASS on Twitter
or subscribe via email

Scans Show How HIV Attacks Brain

HIV, which attacks the body’s natural defences, also damages the brain, three dimensional medical scans have shown.

The MRI images captured by a US team could show why up to 40% of people with HIV have neurological symptoms.  Compared with healthy people without the virus, the brains of the HIV positive patients studied were 15% thinner.

Scans could be used to spot patients who might benefit from brain-protecting drugs, the authors told Proceedings of the National Academy of Sciences.

HIV experts said more work was needed to check that neuroprotective drugs would be beneficial to HIV positive patients and that these treatments would not be safe to take alongside the powerful anti-HIV drugs such individuals are already on.   As drugs improve, people with HIV are living much longer.

However, at least two in five living with HIV will suffer from cognitive impairments, ranging from minor deficits to dementia, studies suggest.  While researchers are aware of this, the pattern of damage the virus causes in the brain has not been well understood.

Brain thinning

Dr Paul Thompson, from the University of California, Los Angeles, along with colleagues from the University of Pittsburgh, used 3D magnetic resonance imaging (MRI) scans to see what was going on in the brains of 26 patients with HIV.

We’d need more solid evidence on how HIV can affect the brain in different individuals before we looked at offering neuroprotective drugs

Compared with 14 healthy controls, the +ve patients had 10-15% thinner brain regions, including areas called the primary sensory, motor and premotor cortices, regardless of whether they were taking anti-HIV drugs or not.

This tissue loss shown up by the brain mapping correlated with the cognitive and motor deficits that the Aids patients displayed on a battery of brain function tests.  The brain tissue loss was the opposite of that seen in common dementias such as Alzheimer’s disease and appeared to be related to the individual’s CD4 count – a marker of how far HIV has progressed and how healthy the person’s immune system is.

The researchers said: “With 40 million patients worldwide now living with HIV, detailed biomarkers of [brain] deficits, such as the cortical maps presented here, are increasingly needed to help gauge the success of neuroprotective therapies.

“Here, they reveal how HIV impacts the brain and may also help identify early changes in neurologically asymptomatic patients with HIV who might benefit most from neuroprotective agents.”

Long-term issues

Rod Watson of the Terrence Higgins Trust said: “We do know that some people with HIV could go on to develop Aids-related dementia or other illnesses affecting the brain.

“This study tracking any cognitive decline is interesting but small. We’d need more solid evidence on how HIV can affect the brain in different individuals before we looked at offering neuroprotective drugs.

“In particular, there would have to be detailed research into how useful these drugs would be and how safe in terms of interacting with existing HIV treatments.”

David Simpson, professor of neurology at Mount Sinai Medical Center in New York, told the BBC News website: “This paper is interesting and provocative, and if the value of this technique is validated in other studies, from other centres, this imaging approach may be a valuable surrogate marker of brain function in HIV infection.”

He added: “The increased survival of patients with HIV, due mostly to HAART, has placed greater emphasis on long-term issues affecting quality of life, such as neurological disease.”

Professor Simpson said that, while many neurological complications are more common in advanced Aids, others, including HIV-associated cognitive disorder, may occur in HIV positive people who have relatively high CD4 counts.

Steve Small, deputy chief executive of Mildmay, a HIV charity, specialising in HIV related brain impairment in the UK, said: “This research backs up what most people have known for sometime.

“You have an increased propensity for cognitive decline the more immunosuppressed you are but, whereas before we have thought that this would go away with anti retro virals, this study claims that it will not.”

Original Article via BBC News

Every March, Brain Awareness Week (15 – 19 March) unites the efforts of partner organisations worldwide in a celebration of the brain for people of all agesIt is the global campaign to increase public awareness of the progress and benefits of brain research.

STAY UPDATED
Follow LASS on Twitter
or subscribe via email