PRESS RELEASE

 Thursday, 28^th September 2017

HIV Ireland calls for Government action as national survey finds stigma continues to impact on people living with HIV

 17 per cent of HIV positive people say they have felt suicidal in the last year

HIV Ireland is calling on the Government to provide additional resources for HIV prevention, education and care after its ‘HIV in Ireland Survey 2017’ revealed the impact that stigma continues to have on people living with the condition in this country. The survey, one of the most significant pieces of research on stigma and HIV knowledge to be carried out in Ireland in over a decade, will be launched this morning (28.09.17) at HIV Ireland’s 30th Anniversary National Conference on HIV and Stigma. Among its findings are that 17 per cent of people living with HIV said they felt suicidal in the last year; a quarter are not comfortable with their own HIV positive status; more than half are single, and a third had experienced being rejected in a relationship due to their HIV status.

Commenting, HIV Ireland’s executive director, Niall Mulligan said: “This survey is of crucial importance in highlighting the need for policy makers and politicians to understand the impact that HIV-related stigma is having on people living with the condition. When 17 per cent of people living with HIV say they have felt suicidal in the last year, compared to a national average of four per cent, it’s time to open our eyes to the damage that HIV-related stigma is having on people’s lives. The Government urgently needs to provide additional resources within the areas of HIV prevention, education, community testing, counselling, mediation and human rights advocacy.”

The ‘HIV in Ireland 2017 Survey’ was undertaken to identify levels of knowledge, and attitudes to HIV, within the whole population, as well as recording the experiences of people living with HIV. Some 1,013 people responded to the general survey and 168 people responded to the survey specifically for people living with HIV.

Among the general population, the research found varying degrees of knowledge about HIV. Younger people were found to have less correct knowledge than older people, though they were also more likely to be welcoming of someone living with HIV.

Key findings in the survey include:

• 98 per cent of respondents correctly thought that HIV can be transmitted by sharing needles or syringes, and a similar percentage were aware it can be passed on through sex without a condom.
• 20 per cent of 18-to-24-year olds incorrectly thought HIV can be passed from person to person through the sharing of a public toilet seat (compared to 10% of those over 24).
• 24 per cent of people incorrectly believe that HIV can be transmitted by kissing, while 11 per cent incorrectly thought it could be transmitted through coughing or sneezing.
• 10 per cent of people stated that they wouldn’t feel comfortable working with a colleague who was HIV positive.
• 54 per cent of people living with HIV are single.
• 98 per cent of respondents agreed that ‘young people should be taught about HIV transmission during secondary school’.

HIV stigma affects the wider community according to Mr Mulligan. “Negative, or misinformed attitudes to HIV, and towards people living with HIV, can create obstacles for people getting tested. UNAIDS estimates that across Europe, 15 per cent of people living with HIV aren’t aware of their condition. It is crucial that we remove as many barriers as possible to people getting tested. Stigma is one of those barriers”.

He added: “This conference marks the 30^th anniversary of HIV Ireland. In the ’80s and ’90s during the AIDS epidemic there was much fear, misinformation and indignity for people living with HIV. Thirty years on, with the continued improvements in HIV treatment, the landscape has changed dramatically, with people diagnosed with HIV now living longer and healthier lives. It is now scientifically accepted that people living with HIV who are compliant with treatment, and have an undetectable viral load, will not pass on HIV to sexual partners. This survey gives us hope for the future when we see increased interest in HIV education within our schools, and a strong acceptance of people living with HIV. In particular, the survey findings highlight the need for increased resources to meet the needs of people living with HIV.”

The conference will be opened by Minister of State at the Department of Health with responsibility for Health Promotion and the National Drugs Strategy, Catherine Byrne TD. She said: “I commend the work that HIV Ireland has undertaken over the past 30 years, and want to pay tribute to all the staff and volunteers at the heart of the organisation. Last year alone, HIV Ireland supported more than 2,000 interventions for people living with HIV. The Government through the HSE continues to provide annual funding to HIV Ireland for the important work that it undertakes in the areas of support for people living with HIV and for the promotion of sexual health in the general population.

“However, I am concerned about the continuing increase in new HIV diagnoses, and I’m aware that the late diagnosis of HIV continues to be an issue. This is one of the reasons why the Government provided funding to pilot KnowNow Rapid Testing, a peer-led point-of-care HIV testing initiative in pubs and clubs as part of the National Sexual Health Strategy. Along with the National Drugs Strategy, the ongoing implementation of the National Sexual Health Strategy reaffirms the commitment of the Department of Health to continue to support the work of community organisations like HIV Ireland in their response to increasing HIV figures.”

The one-day conference will explore the history of HIV, stigma and social inclusion in addiction, homelessness, sex work, the LGBT community, the migrant community, and people living with HIV in Ireland since 1987. Speakers include LGBT campaigner Tonie Walsh; Dr Maeve Foreman of Trinity College Dublin; Dr Austin O’Carroll of SafetyNet; Kate McGrew of the Sex Workers Alliance of Ireland, and Tony Duffin of the Ana Liffey Drug Project. Founder of the Irish NAMES Project, Mary Shannon will present the story behind the Irish AIDS Quilt, made by families affected by HIV in Ireland.

The ‘HIV in Ireland 2017’ summary report is available to download here.

 ENDS.

Contact: Louise Archbold / Joanne Ahern, DHR Communications, Tel: 01-4200580 / 087-2601145/ 087-9881837.

Notes to Editors:

• Interviews available on request.
• Photographer Nick Bradshaw will issue photos to picture desks on Thursday afternoon.
• The ‘HIV in Ireland 2017’ report comprises the findings from two surveys, conducted between March and May 2017. The general population survey was disseminated by Empathy Research as part of an omnibus survey amongst members of their proprietary research panel and was representative of gender, age and location in Ireland. Survey respondents were required to be at least 18 years of age and the survey was completed by 1,013 people (margin of error +/- 3.2 per cent). The People Living with HIV Stigma Survey was designed by Quality Matters and disseminated through social media channels, through HIV support agencies and health services. Survey respondents were required to be at least 18 years of age and to have received a diagnosis of HIV infection. The survey was completed by 168 respondents.

 About HIV Ireland

HIV Ireland is a registered charity operating at local, national and European level. The principal aim of the organisation is to improve, through a range of support services, conditions for people living with HIV and AIDS and/or Hepatitis, their families and their caregivers while further promoting sexual health in the general population.

Our mission and vision is to contribute towards a significant reduction in the incidence and prevalence of HIV in Ireland and towards the realisation of an AIDS-free generation by advocating for individuals living with HIV, preventing new HIV infections and combating HIV-related stigma and discrimination.

Since 1987, HIV Ireland has been pioneering services in sexual health education and promotion, and has consistently engaged in lobbying and campaigning in the promotion of human rights. Our approach broadly reflects a harm minimisation model which emphasises practical rather than idealised goals.

About Quality Matters

Quality Matters is the largest social research charity in Ireland. They work with state agencies and NGO social service providers, to improve the quality and efficiency of services.