Tag Archives: Health

Prestigious GlaxoSmithKline IMPACT Award, Awarded to LASS

 

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Leicestershire AIDS Support Services has won a prestigious GlaxoSmithKline IMPACT Award for its outstanding contribution to improving health in Leicestershire, GSK and The King’s Fund announced last night at the award ceremony held at London’s Science Museum. LASS provides rapid HIV testing, support, information and advocacy to people affected by HIV and AIDS in one of the most diverse areas in England. Leicester has many different communities and an above average population of HIV positive people.

To slow down the spread of HIV and help people to access treatment, LASS invests in rapid testing services in community settings. There is particularly low uptake in some African communities, so LASS trains volunteers from these communities to carry out testing and provide information. They provide testing at a range of events and venues including African football tournaments to reach people who otherwise wouldn’t be tested. LASS also provides services for people with the virus and maybe coping with other issues like poor mental health, and they provide healthy living training.

The GSK IMPACT Awards, GSK’s flagship UK corporate responsibility programme organised in partnershop with The King’s Fund, is seen as a ‘seal of excellence’ in the sector. As well as as receiving £30,000 in funding during a difficult financial climate, the winners can take part in a training programme hosted by The King’s Fund that provides training, development and networking opportunities. Feedback has shown that this opportunity is as important to the winning charities as the funding as it helps them develop the skills to carry on building their organisation.

Katie Pinnock, Director of UK Corporate Contributions at GSK, OR Lisa Weaks, Third Sector Programme Manager at The King’s Fund said:
‘Congratulations to LASS, a strong winner in these awards. Their work providing, support for people with HIV and bringing testing into local communities, is making a real difference tobpeople lives in hard-to-reach groups. It is sharing best practice to further improve outcomes for its service users as well.’

Patrick Bowe, Chair of LASS Board of Trustees , said:

We are absolutely delighted to be recognised at this high level for the impact of our local work supporting and empowering people living with HIV, and challenging and breaking down stigma and discrimination. Our community HIV testing programme is contributing to government public health targets and has already saved the health service more than £3million through encouraging more people to have an HIV test and know their HIV status.
This huge achievement for Leicester, Leicestershire and Rutland is due to the continued commitment by a great team of staff and volunteers. They are determined to deliver the highest standard of services possible and make a significant diference in HIV provision locally with a relatively small budget. This award will make a significant difference to the profile of our work and the reputation of LASS and our new social enterprise.

The calibre of award is reflected in its judging panel who chose the winners, which this year includes Professor Steve Field, Deputy National Medical Director at NHS England (health inequalities); the journalist, Fiona Philips; Peter Wanless, CEO of The Big Lottery; Gilly Green, Head of UK Grants at Comic Relief; Sir Christopher Gent, Chairman of GSK; and, Sir Chris Kelly, Chair of The King’s Fund.

Please note that case studies and spokespeople are available for interview, along with photographs. For further information or interviews, please contact Saskia Kendall at The King’s Fund press office on 020 7307 2603 or by email on s.kendall@kingsfund.org.uk.

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Neneh Cherry – I’ve Got You Under My Skin

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NATURALLY, music affects the body and mind in many wonderful ways. Music affects human thoughts, feelings and behaviors  Just its rhythm affects the body, making the pulse and respiration to flow in tune with the music’s beat or rhythm.  Music can relax or energise an individual, and affect some of  us deeply, in a personal way.

What is more, research has also shown that music has a profound effect on the human body and psyche. As a matter fact, there’s a growing field of health care known as music therapy, which uses music to heal.

As a resource which shares with you HIV and Sexual Health articles, it’s about time we started sharing HIV from other angles.

Introducing “Music Monday’s”!

Over the next few weeks on Monday nights, we’ll bring a featured HIV or sexual health awareness track from over the years and we’ll start it right now with Neneh Cherry!

In 1990 the Red Hot Organization, a non-profit organisation dedicated to fighting HIV/AIDS though pop culture released “Red Hot + Blue”, featuring contemporary pop performers reinterpreting several songs written by Cole Porter. It sold over a million copies worldwide and was heralded as one of the first major HIV/AIDS benefits in the music business.

“I’ve Got You Under My Skin” was written by Cole Porter in 1936, it was nominated for the Academy award of Best Song. It became a signature song for Frank Sinatra and in 1966, became a top 10 hit for the Four Seasons. Since then, it has gone on to be recorded by many leading pop artists and jazz musicians.

Neneh Cherry’s reworked version of I’ve Got You Under My Skin was released as the lead single for the album in the UK and Europe.  Video follows, stay tuned because next week it’s all about sex!

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MEDICAL HISTORY – Child Born with HIV Cured!

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It’s all over the internet.. click here to see for yourselves…

Doctors in the US have made medical history by effectively curing a child born with HIV, the first time such a case has been documented.

The infant, who is now two and a half, needs no medication for HIV, has a normal life expectancy and is highly unlikely to be infectious to others, doctors believe.

Though medical staff and scientists are unclear why the treatment was effective, the surprise success has raised hopes that the therapy might ultimately help doctors eradicate the virus among newborns.

Doctors did not release the name or sex of the child to protect the patient’s identity, but said the infant was born, and lived, in Mississippi state. Details of the case were unveiled on Sunday at the Conference on Retroviruses and Opportunistic Infections in Atlanta.

Dr Hannah Gay, who cared for the child at the University of Mississippi medical centre, told the Guardian the case amounted to the first “functional cure” of an HIV-infected child. A patient is functionally cured of HIV when standard tests are negative for the virus, but it is likely that a tiny amount remains in their body.

“Now, after at least one year of taking no medicine, this child’s blood remains free of virus even on the most sensitive tests available,” Gay said.

“We expect that this baby has great chances for a long, healthy life. We are certainly hoping that this approach could lead to the same outcome in many other high-risk babies,” she added.

The number of babies born with HIV in developed countries has fallen dramatically with the advent of better drugs and prevention strategies. Typically, women with HIV are given antiretroviral drugs during pregnancy to minimise the amount of virus in their blood. Their newborns go on courses of drugs too, to reduce their risk of infection further. The strategy can stop around 98% of HIV transmission from mother to child.

In the UK and Ireland, around 1,200 children are living with HIV they picked up in the womb, during birth, or while being breastfed. If an infected mother’s placenta is healthy, the virus tends not to cross into the child earlier in pregnancy, but can in labour and delivery.

The problem is far more serious in developing countries. In sub-Saharan Africa, around 387,500 children aged 14 and under were receiving antiretroviral therapy in 2010. Many were born with the infection. Nearly 2 million more children of the same age in the region are in need of the drugs.

In the latest case, the mother was unaware she had HIV until after a standard test came back positive while she was in labour. “She was too near delivery to give even the dose of medicine that we routinely use in labour. So the baby’s risk of infection was significantly higher than we usually see,” said Gay.

Doctors began treating the baby 30 hours after birth. Unusually, they put the child on a course of three antiretroviral drugs, given as liquids through a syringe. The traditional treatment to try to prevent transmission after birth is a course of a single antiretroviral drug. The doctor opted for the more aggressive treatment because the mother had not received any during her pregnancy.

Several days later, blood drawn from the baby before treatment started showed the child was infected, probably shortly before birth. The doctors continued with the drugs and expected the child to take them for life.

However, within a month of starting therapy, the level of HIV in the baby’s blood had fallen so low that routine lab tests failed to detect it.

The mother and baby continued regular clinic visits to the clinic for the next year, but then began to miss appointments, and eventually stopped attending all together. The child had no medication from the age of 18 months, and did not see doctors again until it was nearly two years old.

“We did not see this child at all for a period of about five months,” Gay told the Guardian. “When they did return to care aged 23 months, I fully expected that the baby would have a high viral load.”

When the mother and child arrived back at the clinic, Gay ordered several HIV tests, and expected the virus to have returned to high levels. But she was stunned by the results. “All of the tests came back negative, very much to my surprise,” she said.

The case was so extraordinary, Dr Gay called a colleague, Katherine Luzuriaga, an immunologist at Massachusetts Medical School, who with another scientist, Deborah Persaud at Johns Hopkins Children’s Centre in Baltimore, had far more sensitive blood tests to hand. They checked the baby’s blood and found traces of HIV, but no viruses that were capable of multiplying.

The team believe the child was cured because the treatment was so potent and given swiftly after birth. The drugs stopped the virus from replicating in short-lived, active immune cells, but another effect was crucial. The drugs also blocked the infection of other, long-lived white blood cells, called CD4, which can harbour HIV for years. These CD4 cells behave like hideouts, and can replace HIV that is lost when active immune cells die.

The treatment would not work in older children or adults because the virus will have already infected their CD4 cells.

“Prompt antiviral therapy in newborns that begins within days of exposure may help infants clear the virus and achieve long-term remission without lifelong treatment by preventing such viral hideouts from forming in the first place,” said Dr Persaud. “Our next step is to find out if this is a highly unusual response to very early antiretroviral therapy or something we can actually replicate in other high-risk newborns.”

Children infected with HIV are given antiretroviral drugs with the intent to treat them for life, and Gay warned that anyone who takes the drugs must remain on them.

“It is far too early for anyone to try stopping effective therapy just to see if the virus comes back,” she said.

Until scientists better understand how they cured the child, Gay emphasised that prevention is the most reliable way to stop babies contracting the virus from infected mothers. “Prevention really is the best cure, and we already have proven strategies that can prevent 98% of newborn infections by identifying and treating HIV-positive women,” she said.

Genevieve Edwards, a spokesperson for the Terrence Higgins Trust HIV/Aids charity, said: “This is an interesting case, but I don’t think it has implications for the antenatal screening programme in the UK, because it already takes steps to ensure that 98% to 99% of babies born to HIV-positive mothers are born without HIV.”

Original Article via The Guardian

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It’s 2013, & HIV Positive Job Seekers are Humiliated by Job Centre Staff

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A HIV positive jobseeker has said he was left humiliated by staff at a Kent job centre.

Jayce Carberry said staff in Maidstone made him declare his condition within earshot of others, and told him he had to see a disability adviser.

He said an adviser also said he would seek legal advice about what contact Mr Carberry could have with other staff.  The government said jobseekers were asked if they had a condition which could affect certain jobs.

Former hairdresser Mr Carberry said he went to the job centre a few weeks ago to discuss his options.

‘That stigma’

He said he was not disabled, and the advisor asked if he could write his HIV status in his notes, he said. Mr Carberry said he did not want it mentioned.

“His [the adviser's] reply was I’ll have to speak to my legal team to see if we have to disclose your HIV status to any members of the staff you come into contact with in this building,” Mr Carberry said.

“Obviously I was a bit speechless.

“For somebody to make a comment like that, it just takes you all the way back to the beginning and your self-esteem is shattered, you go back to feeling ashamed.

“You’re subjected to that stigma and it’s really upsetting.”

Equalities Minister Helen Grant has written to the job centre
Equalities Minister Helen Grant, Mr Carberry’s MP, said she had written to the job centre and to Work and Pensions Secretary Iain Duncan Smith to raise her concerns.

Ms Grant, Conservative MP for Maidstone and The Weal, said: “It’s absolutely right that if people like Jayce do what they’ve done – go out, try to get work – that they should be given all the help and support that they need and deserve and at the same time, they must be treated with absolute dignity and respect.”

The Department for Work and Pensions, which speaks for job centres, said people did not officially have to declare medical conditions when applying for Jobseeker’s Allowance.

Original Article via BBC News

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You may also be interested in:

Discussion:

What are your experiences when seeking work?  Have you ever had to disclose your status unwillingly?  Does HIV status even matter when seeking work (as opposed to starting work) and do you feel you should disclose to staff at Job Centres.

‘Tis The Season For Overindulgence ♫

Boxing Day Buffet Lunch Christmas Tree and Log Fir

Many people overdo it at Christmas, celebrating with friends and family, non-stop eating, drinking and late nights can leave us feeling tired, sluggish and quite often, a little poorly if we’ve eaten or drunk too much.  A lot of people with HIV generally have a healthy diet and lifestyle, and may only overindulge once or twice a year, if that’s you, then you’ll have no problems going back to eating sensibly after the holiday season, festive excesses aren’t likely to have a long-term, damaging effect on your health or your weight.  However, the short term strain that too much rich food and alcohol puts on your body can still leave you feeling bloated and out of sorts, when all you need is your body to get back to normal.

The average person can consume as much as 7,000 calories on Christmas Day, (that’s three and a half times the recommended daily intake for a woman.)  As well as dehydrating us and putting a strain on our liver, excessive consumption of alcohol can also make us feel unwell, and ill-equipped to handle a detox correctly.

When the festivities are finally over, there are a few sensible, gimmick-free steps that you can take to help you and your body get back on the road to feeling better.

Get Moving

It’s a cliché, but exercise really is the best way to make your body and metabolism work together so it can make use of the nutrition it’s received over the past few days.  A 30 minute walk is good for your heart, lungs, muscles and bones, as well as improving your mood and giving you a sense of wellbeing.  So instead of watching reruns of Christmas TV, get yourself off the sofa and go out for a stroll!

Be kind to your body

If you’ve over-indulged in rich, fatty, sugary foods with alcohol, if your inclined, your body needs time to recuperate.  You should try to avoid red meats, dairy products and processed foods and opt for lots of fruit and vegetables and wholegrain foods instead.  And one of the best things to drink is water (no surprise there), but did you know that the additional salt and alcohol we consume dehydrates the body, so it’s best to re-hydrate.  If you can’t manage full glasses, frequently just try a glass of water with your cup of tea, coffee or soft drink.  Combined with exercise, you’ll start to feel the benefits almost immediately!

Don’t Forget Protein!

Proteins are extremely important for your diet as they are the building blocks of your cells, muscles, organs, and more importantly, your immune system!  If your body doesn’t get the protein it needs from food, it will start using the protein it has stored up which can result in a weakening of your immune system.  A good rule of thumb for a HIV positive person is 100 to 150 grams of protein per day for men, and 80 to 100 grams of protein per day for women.

Energy & Fat (yes, fat)!

You can rebuild your energy by eating complex carbohydrates, that’s food items such as grains and beans, rice and pasta.  While eating complex carbohydrates, try to focus on foods such as white bread, pasta and potatoes.  These carbohydrates are richer in nutrients and the body absorbs them slower, helping to sustain you while you are between meals.

While carbohydrates help you get energy, fat is what helps the body store energy for later use.  For HIV positive people, doctors recommend a fat intake of less than 30 percent of your daily caloric intake.  Also make sure you are getting the appropriate amounts of fat, sometimes, people with HIV experience an increase in cholesterol because of interactions with medications so it’s important to watch your fat consumption. It is recommended that of that 30 percent, 7 percent be saturated fat from foods like whole milk, butter and fatty meats. The rest of the fat should come from nuts, fish, seeds, canola oil and soy.

If you’d like to know more about HIV and Nutrition, visit Avert, who have comprehensive information and advice on diet, supplements and nutrition.

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Heather Alcock, policy advisor for the All Party Parliamentary Group on HIV & AIDS joins LASS.

Heather Alcock at the LASS AGM 6th October 2011

Heather Alcock presenting certificates to volunteers at the LASS AGM 6th October 2011

Heather Alcock, policy advisor for the All Party Parliamentary Group on HIV & AIDS has agreed to join the LASS Board of Trustees as a co-opted Trustee.

This is great news for us and will give us a good profile nationally as well as influence with local MPs.

The All-Party Parliamentary Group on HIV and AIDS is a backbench cross-Party group of MPs and Peers in the UK Parliament at Westminster.

MPs and Peers who have joined the Group have done so because they are concerned about both the devastation that HIV and AIDS are causing in developing countries and about their impact here in the UK including in our constituencies.

They believe that as parliamentarians they should play their part in addressing the HIV epidemic. In particular they say they have an important role in ensuring that laws and policies are respectful of human rights and promote public health.

On their website, you can read reports published by the Group, see examples of where we have raised issues about HIV and AIDS in Parliament and find out how to stay in touch with their work.

They say;

We value very highly the advice, guidance and support that we get from people living with HIV, NGOs and professionals outside Parliament. We hope that this website not only increases the information people can obtain about the Group, it also increases the dialogue between politicians and the people who are coping with the reality of life with HIV.

Please join us in welcoming Heather Alcock to our Board of Trustees.

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Related articles

FREE Training: HIV & Culture

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Delivered in collaboration with people from a wide range of communities and cultures in Leicester, we will explore how culture affects perspectives and experiences of HIV.

  • Date & Time: Thursday, 13th December between 13:00-16:30 hrs.
  • Venue: The Michael Wood Centre, 53 Regent Road, Leicester, LE1 6YF.

The session will also look at ways of providing knowledge and empowerment about HIV to people with different cultural needs.”

Spaces are very limited, (only 10 available).  If you would like to attend, please contact us on 0116 2559995 and speak to our team who are happy to help.

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“…and it won’t go away.” 25 Years of Leicestershire AIDS Support Services

 

The LASS History Project records the changing experiences of people affected by HIV over the years, while highlighting the extent to which HIV continues to disproportionately affect the most marginalised. It documents and celebrates the way people in Leicester came together to respond to the then, new virus and captures changes in attitudes, demography and health outcomes over the past 25 years.

LASS formed in 1987 as a telephone helpline for the people of Leicester, Leicestershire and Rutland, at a time when it was almost impossible to find premises because of fear and stigma. 25 years later, we support over 500 people affected by HIV, we run a community rapid HIV testing service and work across communities to increase understanding and knowledge about HIV.

We received funding from the Heritage Lottery Fund to develop a history project to mark our 25th anniversary year. This project has created a publication and currently developing an archive, and will continue to produce mobile exhibition materials to capture the stories and experiences of people involved in LASS’s work over the past 25 years.

We highlight the distinctive characteristics of LASS, which include our location in the ethnically and culturally diverse city of Leicester and changes in our client group over the years.

While we show that HIV remains a significant local issue – with Leicester experiencing the 6th highest rising rate of infection in the country – we also celebrate the improved life expectancy of people with HIV, and show how LASShas evolved to meet changing needs and demands on our services.

It is our hope, that our history will inspire others and continue to raise awareness of the changing issues in responding to HIV and to challenge persistent myths and stereotypes.

Download your copy here

(PS: Celebrate World AIDS Day with us tomorrow night)! Click here for more details!

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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.

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From today, HIV treatment is free for all who need it!

Lord Fowler

In March of this year we shared the the news that Asylum Seekers and other non-British citizens were to be given free HIV treatment after the government indicated it was willing to accept an amendment from Lord Fowler to the health bill.

That removal of charges for undocumented migrants and non-UK citizens accessing HIV treatment and care in England comes into effect today. From now on, HIV treatment will be provided free of charge to all who need it, regardless of citizenship or immigration status.

The move was first announced in February and the relevant legislation passed in June. Health ministers have justified the change on the grounds of public health, pointing to the impact that HIV treatment has on onward transmission.

Although it was initially proposed that free HIV treatment should only be available to people who have been living in the UK for more than six months, this requirement has not been retained in the legislation.

While treatment in HIV clinics will always be free of charge, migrants living with HIV who need hospital treatment for another health condition, such as diabetes, heart disease or cancer, or who require antenatal care, may still be subject to charging regulations.

Moreover, the rules have only changed in England. In Scotland and Wales, although charges for HIV treatment have not been levied or actively pursued in recent years, the legislation still states that HIV treatment may be chargeable. In Northern Ireland, the legislation still states that HIV treatment may be chargeable, and these regulations have sometimes been rigorously enforced.

The National AIDS Trust (NAT) has called for a formal change in the law in Scotland, Wales and Northern Ireland, to ensure that free universal access to HIV treatment is guaranteed across the UK.

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