Monthly Archives: November 2011

UK’s battle with HIV goes into reverse, prompting calls for more testing

The HIV 1 virus. The numbers infected with HIV within the UK are on the rise, the Health Protection Agency says. Photograph: Institut Pasteur/AFP/Getty Images

More than 100,000 people in Britain are predicted to be living with HIV by the end of this year, according to an official report that warns that the virus is on the rise again in the UK.

While there is a continuing drop in new cases among people who have acquired HIV abroad, the numbers infected within the UK are on the rise, the Health Protection Agency says in the report on Tuesday. New diagnoses of HIV in men who have sex with men have hit a record high.

New infections of the virus, which eventually causes Aids if not kept in check by drugs, had been falling in the UK but that trend seems to have levelled off, according to the agency’s annual HIV report. At the end of 2010, there were an estimated 91,500 people with HIV in the UK, up from 86,500 the previous year. The figure includes estimates for those who have not had a test and do not know they are infected – thought to be around a quarter of the total.

In 2010, according to the HPA’s data, there were 3,000 new infections among men who have sex with men, 81% of which occurred in the UK. Most of the men were white (83%) and two-thirds (67%) were born in the UK. Some had been HIV-positive for years without knowing, but a third of those who were recently infected were under 35. The figures suggest that one in 20 gay men are living with HIV, the ratio rising to one in 12 in London.

When the epidemic began 30 years ago, people with HIV swiftly became sick, developed Aids and died of infections such as pneumonia that their bodies could not fight off. Today, combinations of antiretroviral drugs keep people alive and healthy and can give them a normal lifespan as long as they stay on the medication. That means the number living with the virus continues to rise.

Of the 91,500 people estimated to have HIV in the UK, just over 40,000 of the total are men who have sex with men. Around 2,300 are injecting drug users. Of the 47,000 infected through heterosexual sex, around 19,300 were African-born women and 9,900 African-born men. The prevalence rate in the black African community is one in 32 among men and one in 15 women.

Half of those who are diagnosed with HIV have gone to a doctor years after infection, at the point when they have fallen ill. Those people have a much worse prognosis: they are 10 times more likely to die within a year of diagnosis than people who were diagnosed earlier.

In 2010, 680 HIV-positive people died, 510 of them men. Two-thirds were people who had been diagnosed late. Most died within a year of being tested.

People who have not been diagnosed risk infecting others. The HPA says that there is a need to introduce routine HIV tests around the country beyond the traditional confines of sexually transmitted infection and antenatal clinics.

There have been pilot projects in the last two years in London, Brighton, Leicester and Sheffield. Testing was successfully introduced in two general practices, the acute care units of three hospitals and two community settings without opposition from staff or patients.

Greater efforts to test people and prevent infection would save the NHS money, because treating people is expensive, the HPA says. Because HIV has become a chronic, manageable condition instead of a fatal illness, the costs of providing specialist treatment and care are substantial and accelerating.

“It is difficult to calculate the true expenditure on HIV in the UK. However, of the £1.9bn spent by the Department of Health on infectious diseases in England in 2009-10, an estimated 40% was allocated to the treatment of HIV and Aids. This total does not include the costs of psychosocial care or HIV testing, so in fact the total amount spent on HIV treatment is much higher,” the report says.

The amount spent on prevention, the HPA adds, was £2.9m, just 1% of the overall HIV budget in 2010. The report says: “Investing in prevention should be a priority because of its potential for cost savings. We estimate that each infection prevented would save between £280,000 and £360,000 in lifetime treatment costs.

“If the 3,640 UK-acquired HIV diagnoses made in 2010 had been prevented, between £1bn and £1.3bn lifetime treatment and clinical care costs would have been saved.”

Original Article by Sarah Boseley at The Guardian

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World Aids Day: Living With HIV, The Virus That’s No Longer A Death Sentence

Thirty years after the first reported diagnoses of AIDS, Sarah Morrison of The Independent shows how the world has been dealing with a virus that is no longer a death sentence

Red balloons will be released, vigil candles lit and heads of state will recall those who have fallen victim to HIV/Aids on the 24th World Aids Day, to be held this week. Thirty years after the first reported diagnoses of Aids – then tantamount to a death sentence – one remarkable fact highlights the advances medicine has made: the number of people living with HIV has reached a record 34 million.

Thanks to antiretroviral drugs, which almost 50 per cent of people with the virus can now access, the number of Aids-related deaths around the world stands at 1.8 million a year – its lowest level since a peak in 2005, according to a recent UNAIDS report. While those who lived through the late 1980s and early 1990s in Britain will remember a rapid rise in Aids deaths, which largely affected gay men, injecting drug users and people who had received blood infusions, the fastest growing group of people with the disease in this country are now the over-50s.

But while HIV rates have fallen elsewhere, in the UK the number of diagnosed cases increased by more than 50 per cent between 2000 and 2009. There are now more than 90,000 people in Britain with HIV. In 2009 there were three times as many heterosexual people infected in the UK with HIV than in 2001, according to the Terrence Higgins Trust.

The Independent on Sunday met two HIV-positive people living contrasting lives in different parts of world.

Chris Williams, 47

Chris Williams tested positive for HIV three years ago during a routine check-up. He gave up his job as a personal trainer after his diagnosis and decided to study counselling, so that he can one day work in the public health sector. His infection was spotted early and he has yet to fall ill. He takes five pills a day; they are delivered free of charge to his door every six months.

“My experience of treatment has been very straightforward. I have a blood test twice a year. I see a doctor and he authorises the prescription of my drugs on the basis of the results. I’ve been very lucky and felt no side effects to my medication, except a little fatigue sometimes.

“At the beginning, I only told a few people, but gradually I have become more open about my status. Some people say I’m over-optimistic about the prognosis of my HIV, but I think in this country, there is no need for it to still be a killer disease.

“You can still go out and have a social life. Some people find it difficult to deal with psychologically, and there is still a lot of room for improvement, but it’s not all doom and gloom. When I do go, I hope it won’t be from HIV, but from old age.”

Hellen Njeri Ngugi, 40

Hellen Njeri Ngugi and her husband, also HIV-positive, live with their three children in a one-bedroom house in the Mathare Valley slums, sharing one latrine with 12 neighbours. When Mrs Ngugi was diagnosed with the disease 11 years ago, her husband refused to accept her condition at first. It took Mrs Ngugi two years to get the treatment that she needs, as the clinic was three hours away. Christian Aid has since given her counselling and support.

“When I found out I was HIV-positive, I thought it was the end of my life. People around showed me so much discrimination, including my parents. I could not share anything with them, including eating utensils and sleeping stuff.

“I used to work in a hotel, balancing the finances, but now my husband and I don’t have permanent jobs. Whenever he fell sick, he was sacked. I now make soap, but I can’t walk far, so I have to use my phone to look for customers. It is very difficult to raise money for the family.

“But, through counselling, I was encouraged. I have become a role model for others and was moved to another clinic, a 45-minute walk from my house. I now get my pills every three months.”

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How Can You Support LASS If You Don’t Have The Time?

LASS is registered for JustTextGiving which enables supporters to make donations of up to £10 by text message.

It’s easy to donate to LASS, and it takes no time at all, simply text: “LASS25 £10″ to 70070.  (You can change the amount of your donation to: £1, £2, £3, £4 or £5 if you prefer) and you’ll receive a text message receipt, and the chance to add Gift Aid by text or in web form.

When you make a text donation, it’ll either be deducted from your mobile phone credit or added to your mobile phone bill – and you won’t pay any VAT on your donation.

Has LASS helped you or a friend recently? We provide support for people affected or infected with HIV, our services are free, confidential and individually tailored in consultation with each service user to meet their specific needs. We  aim to assist people in making the best choices for themselves, and to maximise their own potential.

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 and especially around World AIDS Day, we do everything we can to prevent the spread of HIV and to promote positive sexual health through education, training and community initiatives.

It’s World AIDS day soon, you’ll see us out at supermarkets, school’s, collages, art exhibitions and fund-raisers, feel free to ask us questions and support our cause and if you havent donated to LASS this World AIDS Day yet, please consider a £1, £2, £3, £4, £5 or even a £10 donation by text.  It’s simple, quick and easy, you could it right now: LASS25 £10 to 70070

Thank  You

Art Exhibition for World AIDS Day

An art exhibition will be hosted at The Crumbling Cookie, High Street Leicester and the Exchange Bar, Rutland Street Leicester from 1st to 16th December. A proportion of the sales of all the art in the exhibition will be donated to LASS, to assist with crisis funding for people living with or affected by HIV.

Local artist and illustrator, Wayne Anderson has kindly donated a print towards the exhibition. The featured artists include the late Dave Johnson, artist, musician and alchemist whose work was recently exhibited in the “War & Peace” exhibition at Leicester Museum & Art Gallery. His work includes reflections on World War 1, his travels and his alchemical studies. His wife Christine Hume-Johnson will exhibit art inspired by their life together and linked to her use of his journals.

Other artists exhibiting work include:

  • Tony O’Dwyer who has work in the permanent Guinness Collection in Dublin
  • Nick Nixon, local commercial artist, photographer and illustrator
  • Sue Graham, who is recognised for her inspiring water colours and seascapes
  • Jim Tetlow, local musician and artist
  • Maureen Anderson, local musician and artist who is currently in negotiation with an international publishing company who are considering  her book for their 2012 book lists.

Venues:

The Exchange Bar is hosting some pieces from the art exhibition, with free entry to view. The bar is on Rutland Street, opposite the Curve and the Athena, in the Cultural Quarter of Leicester.

Please visit to enjoy the exhibition and the beautiful bar.

The Crumbling Cookie is hosting other pieces in the exhibition, again with free entry to view. The café is on High Street Leicster.

The Crumbling Cookie is hosting the opening night, on Thursday 1st December, World AIDS day, from 4pm to 7pm. Come along and meet the artists. There will be music and poetry featuring George Sanderson, Maureen Anderson and Tony Jones who plays a Seagull Parlour Acoustic, roots from South Africa, Wales and England. He also plays folk and blues, playing covers as well as his own compositions.

We encourage you to visit to enjoy the art. Please join us for the Opening Night from 4-7 on 1st December. Cordial and nibbles will be served.

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BASELINE Issue 10

ISSUE 10

It’s another packed issue this time around. Check out their World AIDS Day round up, compiled by Joel Korn.

Robert Fieldhouse interviews the team at London’s Homerton Hospital about their pioneering use of laser ablation to treat anal pre-cancer and makes a quick visit to a new respite care centre, Trebullom, in Cornwall and finds it to be a remarkably restorative experience.

Sarah Radcliffe from NAT walks us through NAT’s latest piece of vital research into the day-to-day changes in symptoms many people living with HIV experience.

LASS’s very own Julie Musonda begins a new series of articles on Life Coaching and Chris Morgan reveals the findings of his recent survey of life assurance providers, finding 50% of companies now provide life assurance to people living with HIV.

Plus there’s all the usual UK, Global, Treatment and Hepatitis news.

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One Voice Many Faces: Spread the Realities of HIV & Kick out Stigma & Discrimination

This year we are asking people to make a pledge for World AIDS Day.  This might be something you do on 1st December or perhaps a project you can work toward for next year.

The idea is to increase awareness of the facts and realities of HIV – there are too many myths around.

Pick up one of our new HIV cards – it fits in your pocket or wallet. It will help to remind you what the key facts are.

What is your pledge for 2012?

A reminder about these 2 opportunities to reflect:

Saturday 26th November, 12 noon:

  • “Choose Life” A service of preparation for World AIDS day at Leicester Cathedral. (Faith in people with HIV event)

Thursday 1st December

  • Leicester Market stall – come along and get your red ribbon.
  • 2 minute silence in the Market Square at 1.12pm.
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Freddie Mercury: Rock Star, Legend, Legacy!

An artist who needs no introduction is Freddie Mercury, the Queen vocalist and solo performer extraordinaire who, for many, will go down as the finest rock front man of all time.

Born Farrokh Balsara, the singer changed his stage name upon joining the group Smile – which featured Roger Taylor and Brian May – in 1971. Altering the name to Queen and added bassist John Deacon, the group released their self-titled debut album in 1973 to little fanfare, instead making a true breakthrough with third album ‘Sheer Heart Attack‘ in 1974, which featured the UK number two charting single ‘Killer Queen’. All that was to be superseded however with the following year’s ‘A Night At The Opera’ which featured mega selling hit ‘Bohemian Rhapsody‘ which went on to spend nine weeks at the top of the UK Single Charts and also earned the band their first top 10 hit on the US Billboard Charts.

From there the rest was history, with the band eventually releasing 18 number one albums and 18 number one singles with estimates on complete worldwide albums sold ranging 150 million to a staggering 300 million copies.

Though the band as a whole were superb, a lot of acclaim has always fallen on the charismatic Mercury, an opera-trained singer whose stunning range, combined with his extroverted on stage theatrics made him one of the most-loved stars in music, with notable performances including two shows at Wembley Stadium, London for Live Aid in 1985 and on what would amount to Queen’s final tour in 1986.

Freddie Mercury still influences the music scene like no one else of his time. In 2009, he was voted “the biggest rock singer of all time”, by the readership of ‘Classic Rock‘ magazine. The ‘Rolling Stone‘ lists him on rank 18 of the greatest singers in history. Freddie Mercury will never be forgotten and he was right when he said: “I won’t be a rock star. I will be a legend.”

Fans wishing to hear new material from Freddie should brace themselves for a treat as new posthumous material is due to be released next year.  Queen‘s Brian May and Roger Taylor have revealed they’re in possession of recordings by Freddie Mercury singing with another legendary artist: Michael Jackson.  The Jackson estate has granted Taylor and May permission to work with the material, recorded in 1983 at Michael’s house. At the time Queen were touring America.

Today marks the 20th anniversary of the sad death of Freddie Mercury.

Freddie Mercury caught HIV in 1987.  Back then, HIV treatments were not as effective as they are today and he eventually died of AIDS.  Although the media was full of speculations about his state of health for a long time, he admitted to having the disease on 23rd November 1991.   Within 24 hours after this announcement, he had fallen into a coma and passed away.  He died of pneumonia in consequence of his HIV infection. He did not live to see the Olympic Games in 1992, which he composed the official anthem ‘Barcelona’ with opera singer Montserrat Caballé.

As one of the highest-profile victims of AIDS, Freddie Mercury’s death drew greater media awareness of the virus and started the fight to remove the stigma, discrimination and prejudice from a disease which could affect anyone.

Yes Freddie, you were a rock star, you were a legend, and now you’re a legacy! Thank you Freddie. We love you.

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One Voice Many Faces: Spread the Realities of HIV & Kick out Stigma & Discrimination

It’s that time of year again, World AIDS Day is fast approaching.

This is a day when we reflect and consider those who are infected and affected by HIV. We remember those who have died from the pandemic over the years. We also celebrate the achievements and work of the year for HIV.

A few dates for your diary today so that you can decide what you will do. All these things are free and you are very welcome to come along:

Saturday 26th November, 12 noon:

  • “Choose Life” A service of preparation for World AIDS day at Leicester Cathedral. (Faith in people with HIV event)

Thursday 1st December

  • Leicester Market stall – come along and get your red ribbon.
  • 2 minute silence in the Market Square at 1.12pm.
  • Crumblin’ Cookie (High Street Leicester): Launch party for Art Exhibition 4-7pm

Friday 2nd December:

  • Red Ribbon Party at Club Oxygen. Free entry for Ladies wearing red.
  • Art exhibitions at Crumblin’ Cookie (High Street, Leicester) and The Exchange Bar (opposite Curve) from 1st – 16th December.
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AIDS Related Deaths ‘Down 21% From Peak’ – Says UNAids

Aids-related deaths are at the lowest level since their 2005 peak, down 21%, figures from UNAids suggest.

Globally, the number of new HIV infections in 2010 was 21% down on that peak, seen in 1997, according to UNAids 2011 report.

The organisation says both falls have been fuelled by a major expansion in access to treatment.

Its executive director, Michel Sidibe, said: “We are on the verge of a significant breakthrough.  Even in a very difficult financial crisis, countries are delivering results in the Aids response.  We have seen a massive scale up in access to HIV treatment which has had a dramatic effect on the lives of people everywhere.”

This latest analysis says the number of people living with HIV has reached a record 34 million.  Sub-Saharan Africa has seen the most dramatic improvement, with a 20% rise in people undergoing treatment between 2009 and 2010.

About half of those eligible for treatment are now receiving it.

UNAids estimates 700,000 deaths were averted last year because of better access to treatment.  That has also helped cut new HIV infections, as people undergoing care are less likely to infect others.

In 2010 there were an estimated 2.7m new HIV infections, down from 3.2m in 1997, and 1.8m people died from Aids-related illnesses, down from 2.2m in 2005.

The figures continue the downward trend reported in previous UNAids reports.  The UN agency said: “The number of new HIV infections is 30-50% lower now than it would have been in the absence of universal access to treatment for eligible people living with HIV.”

Some countries have seen particularly striking improvements.

In Namibia, treatment access has reached 90% and condom use rose to 75%, resulting in a 60% drop in new infections by 2010.

UNAids says the full preventive impact of treatment is likely to be seen in the next five years, as more countries improve treatment.

Its report added that even if the Aids epidemic was not over: “The end may be in sight if countries invest smartly.”

The charity Medecins Sans Frontieres urged governments to keep up their funding.

MSF’s Tido von Schoen-Angerer, said: “Never, in more than a decade of treating people living with HIV/Aids, have we been at such a promising moment to really turn this epidemic around.

“Governments in some of the hardest hit countries want to act on the science, seize this moment and reverse the Aids epidemic. But this means nothing if there’s no money to make it happen.”

The International HIV/Aids Alliance said: “We welcome the ongoing commitment of UNAids to changing behaviours, changing social norms and changing laws, alongside efforts to improve access to HIV treatment.

“For bigger and better impact though, we must not be complacent. There is still much more to do.”

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Battling HIV prejudice with Body & Soul

An estimated 100,000 people are living with HIV & AIDS in Britain, many of them young people who face prejudice on a daily basis. But a series of celebrity portraits by Rankin and a powerful new film, Life in My Shoes, are challenging that stigma

Kate Moss photographed by Rankin for Body & Soul: “We are trying to show that just because we are doing a campaign about HIV it doesn’t need to be doom and gloom”.

It is when 18-year-old Blessing gets the bus home from school that the bullying starts. As she waits for the bus to draw out of the stop, a clique of angry-faced girls runs up to the window next to where she is sitting. They begin thumping on the glass with their fists. They scream abuse and call her names, saying that she is “dirty” and “disgusting”. They throw chips at her, smearing the window with ketchup, treating her as if she is no better than a piece of rubbish.

Her classmates have just found out that Blessing is HIV positive, and this is a powerful scene from the new film Life in My Shoes which explores the reality of teenagers who live with the virus. The 30-minute feature was developed by Body & Soul, a ground-breaking charity that supports HIV-affected children, teens and families, and is set to be released next year as part of a high-profile campaign.

The initiative, which seeks to raise awareness of the stigma suffered by young people with HIV, is to be accompanied by a series of celebrity portraits by the photographer Rankin. So far his subjects include Kate Moss, the actor Ashley Walters and athletes Denise Lewis and Christine Ohuruogu.

“We are really trying to show that just because we are doing a campaign about HIV it doesn’t need to be doom and gloom,” says Rankin. “We wanted to capture a strong sense of warmth as well as have an impression of hope and life with bright and sexy images.”

Working with Moss brings its own rewards. “It was great,” he says. “I’ve known her for ages, but we are both so busy we only see each other from time to time. It’s always amazing shooting her and catching up. We have a laugh!”

Beneath the celebrity gloss, there are serious issues at stake. Life in My Shoes is based on the experiences of teenagers who have the human immunodeficiency virus which, if left untreated, can lead to Aids. Many of the teens who shared their stories also took part in the production as actors, extras or members of the crew. In fact, the distressing scene on the bus where the fictional character of Blessing is hounded by her friends actually happened to a young woman living with HIV on a London housing estate – in the end, some of the abuse hurled at her was deemed too vicious to include in the final script.

“A lot of us have had similar experiences,” says 22-year-old Isabella, an extra in the production, which was filmed over a fortnight in Hackney during the summer. “When I told one of my closest friends I had HIV, she started saying: ‘Oh, you can’t use this cup. You’ve put me in danger.’ It does hurt because people think HIV is dirty or that you only get it if you’re promiscuous or you’re a poor person in Africa. It’s not true. When I hear all those things, it really ticks me off. I think to myself: ‘But that’s not how I am.’”

Isabella’s experience isn’t unique. There are numerous incorrect cultural perceptions that still persist around HIV and Aids. Prime among these is the idea that it is an epidemic that belongs to the 1980s, a time when the UK government heightened the public’s awareness by posting leaflets to every household in the country. In reality the disease has now been bequeathed to a new generation – around 11% of HIV infections are among babies who acquire the virus from their mothers, and although substantial medical advances have been made in recent years in managing the disease, there is still no ultimate cure.

And yet despite having been confronted by their mortality at such a young age, the majority of teenagers I meet at Body & Soul’s headquarters in east London live happy and fulfilling lives, largely because the charity offers them a safe space in which to talk openly about their situation with other young people who understand exactly what they’re going through.

“This place has really given me more confidence,” says 16-year-old Lily, who was born with HIV. “It’s a beautiful place where I feel really comfortable because I can say ‘HIV’ out loud. The rest of the time I feel like I have to speak in code. Like if I go on a school trip I’ve got to think of a way of explaining why I need to take medicine… But it doesn’t feel like a weight I have to carry around. If anything, it pushes me more to do well.”

Lily, who had a small speaking part in the film, is now determined to be an actress. “I like Will Smith and Cameron Diaz,” she says, waving her hands expressively as she speaks, each fingernail painted brightly in a different colour. “Doing this was definitely a great experience.”

For Tudor Payne, a commercial director who gave his time for free to direct Life in My Shoes, it was important to counterbalance all the “very dark images from films like Philadelphia and ads that showed people dying. The images that came out a few years ago were depressing, but when you meet the teens at Body & Soul, they’re full of life, and we thought it was important to show that. We wanted to do something that challenged the stigma.”

Ignorance is still a real problem. In 2009 a study conducted by the People Living with HIV Stigma Index found that 21% of the 867 participants had been verbally abused or harassed in the past 12 months because of their status; 12% had been physically assaulted. Last year a Body & Soul questionnaire of more than 500 12- to 18-year-olds found that despite increased awareness of HIV, there was a contradiction between their knowledge and their behaviour. So although 81% of respondents knew the virus could not be transmitted by sharing a cup, only 27% of them said they would actually be willing to drink from the same cup as a person they knew was HIV positive. Eleven per cent said they would not remain friends with someone who has the virus.

“If you told people you had cancer, you’d get sympathy and support,” says Payne. “But if a teenager tells their friend they’ve got HIV, there’s so much prejudice still around.” It was for this reason that the decision was made to hold an open casting process for the film, whereby aspiring young actors were encouraged to learn a script and upload an audition online. “We made sure the script contained important facts about HIV and attitudes that challenged stigma,” he explains. “This meant thousands of young people motivated by their desire to be famous learned the script and in doing so digested facts that they will probably remember for the rest of their lives, so already the education has begun.”

Pearl Mahaga beat 700 other hopefuls to claim the lead role in Life in My Shoes.

More than 700 teenagers took part. The eventual winner, who played the part of Blessing onscreen, was 19-year-old Pearl Mahaga from Luton, now in her first year of a law degree at Cambridge University. “I really do believe that young people watching the film will feel more empowered,” says Mahaga. “There’s a lot of underlying emotion there, especially in the bus scene, and I hope that will roll down into normal conversations so that, if someone is making an inappropriate comment about HIV or Aids, they will have the courage and confidence to say: ‘That’s not OK.’”

The timing is crucial. In September a House of Lords committee estimated that almost 100,000 people in the UK will have HIV by 2012 and that efforts to stop the spread of the disease were “woefully inadequate”. The actual numbers are likely to be far higher: some reports estimate that around a quarter of people with the virus are unaware they have it. Lord Fowler, the committee chairman, warned of the “potentially huge cost implications… of failing to deal effectively with the epidemic”, and stressed that the government “should ensure that HIV and Aids is a key public health priority”.

In this climate, the work of groups such as Body & Soul becomes increasingly urgent. The charity is one of the only organisations in the UK specifically designed to help entire families affected by the illness, promoting a holistic approach that provides youth groups, well-women clinics, yoga and therapy sessions as well as information services providing welfare and benefits advice. But their work is difficult to publicise – for obvious reasons, the people who go there want their identities protected. As a result, it is harder for the public to identify with their plight and put a face to the story.

Which is why the Rankin portraits are so important: if a high-profile celebrity is pictured promoting greater HIV and Aids awareness, the feeling that the disease is something shameful or frightening is instantly lessened.

“It’s really important we remember that HIV does affect lots of people in the UK and that so many of these people are having to hide their status because of fear of discrimination,” says Rankin, who asked each of his subjects to wear something yellow for the photographs – the trademark colour of the Life in My Shoes campaign. “But this campaign really has the capacity to change that and to bring attention to the fact that just because you are HIV positive doesn’t mean you need to live a double life and fear how people will treat you.”

Ashley Walters, who recently starred in the Channel 4 drama Top Boy, was one of those photographed. “The prejudice out there definitely needs to be tackled,” he says when we speak. “When I was growing up, HIV and Aids was talked about a lot at school. I think today it’s not being talked about enough.

“I grew up in southeast London and the last time I read any statistics, it said that that part of London had one of the highest rates of HIV and Aids among young black males. That really scared me. I have three kids, and with them growing up I’m really aware that they need to be educated about this.”

Emily Head, who plays Carli D’Amato in the hugely successful sitcom The Inbetweeners, was another of Rankin’s subjects and also helped with the audition process, offering to read the script with some of the hopefuls. “I wanted to do this because a lot of people still don’t realise you can live a fairly normal life with HIV and you can’t catch it by shaking hands with someone. I think the story of Life in My Shoes is really powerful: it’s about a young girl struggling to overcome some of the things she faces through having HIV. It’s a difficult place for a teenager to be.”

Back at the Body & Soul offices, Lily is munching her way through a handful of M&Ms, recounting her experiences of filming on-set in a rapid stream of enthusiastic chatter. In between the excited reminiscences about improvised scenes and costume changes, she falls suddenly silent. When she resumes, her voice is slower, more considered. “It felt like the characters were speaking for me,” she says. There is a thoughtful pause before she adds: “And it’s great because their voices can be heard.”

bodyandsoulcharity.org and lifeinmyshoes.org

Original Article by at The Guardian

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