News: 11/2024 | Page 13 | George House Trust

VOTE FOR GEORGE HOUSE TRUST

 

WE NEED YOUR VOTES

 

George House Trust​ House Trust is taking part in the Aviva​ Community Fund, with a chance to win £10,000 in support of our Positively Speaking project – and we need your help! 

 

Positively Speaking gives people living with HIV a platform to tell their powerful personal stories to a range of audiences such as GP practices, schools, housing associations and LGBT groups. Positively Speaking increases the confidence of people living with HIV by giving them a voice. Audiences also increase their understanding of HIV, which helps to tackle HIV prejudice and misconceptions.

 

You can help by registering to cast your 10 votes towards our project, and you can enter into a draw for a chance to win a prize. 

 

Please share this as widely as possible, with your friends, family and on your social media accounts. We need help  to get our project to the top! 

 

Voting ends at midday on 21st November.

 

 

Thanks for your support.

Wednesday, 25 October, 2017

People and Parliament: Remembering 30 Years of HIV and AIDS

PEOPLE AND PARLIAMENT: REMEMBERING 30 Years of HIV and AIDS

 

AN EXHIBITION OF UK AIDS MEMORIAL QUILT PANELS AT WESTMINSTER HALL

27 NOVEMBER - 3 DECEMBER 2017

 

The exhibition will mark 30 years of HIV in the UK through a narrative focusing on the work of parliament and key parliamentarians from 1980s to the present day. This will be set within the context of the contribution of campaigners from inside and outside Parliament, the changing face of HIV in the UK and remembrance of those who died in the early days.

 

Alongside this information will tell the story of government engagement in HIV and AIDS, from the ‘Don’t Die of Ignorance’ campaign in 1987 to the funding for the National HIV Prevention programme today; initiatives including the launch of the first national strategy for sexual health and HIV in 2001, universal access to HIV treatments in 2005 to the publishing of ‘The HIV Puzzle’ and the continuing work of the APPG on HIV and AIDS.  It will also recognise those who have taken a leadership role in campaigning groups and within parliament such as Lord Kilmarnock, founder of the APPG on AIDS; Baroness Masham of Ilton, who has been a Vice-Chair of the Group since its inception; Lord Fowler who championed action towards HIV in his role as Secretary of State for Health and Baroness Gould of Potternewton who advised the Government as Chair of the Independent Advisory Group on Sexual Health and HIV.

 

The exhibition will also recognise parliament’s function in scrutinising the work of the Government and the crucial role in effective policymaking to improve the care and treatment for people living with HIV. Select Committees from both Houses have recognised the complex and evolving nature of HIV policy and by gathering evidence from around the world, have sought to improve UK policymaking on domestic and international HIV issues.  In 2005, the Health Select Committee published New Developments in Sexual Health and HIV/AIDS policy, challenging the Government’s position of the day on free access to treatment for non-UK nationals resulting in the universal access to treatment in 2012.  In 2011, the Lords’ Select Committee on HIV and AIDS, chaired by Lord Fowler, published the No Vaccine, No Cure report, highlighting both the enormous advances in the treatment and care of people living with HIV in the UK and related stigma which preventing people from accessing the testing and treatment. Internationally, the Commons’ International Development Select Committee launched inquiries, in 2009 and 2017, into the Department for International Development’s work on HIV/AIDS globally, on both occasions, praising the Government’s commitment to the Global Fund to fight HIV/AIDS, tuberculosis and malaria, but also pressed the Government to do more to address challenges for grassroots advocates and key populations.

 

To illustrate the impact upon the community and as an act of remembrance for World AIDS Day on 1 December, the exhibition will include a display of the UK’s AIDS Memorial Quilts to tell the story of individuals who died of AIDS in the 80s and 90s with remembrances from families and friends .

 

The exhibition will be set up by staff and volunteers from the organisations of the AIDS Memorial Quilt Conservation Partnership who will be at the exhibition throughout its duration to guide visitors through and provide them with further information. 

 

DISPLAYS AND MATERIAL

A series of role-up banners will provide a timeline of government engagement and initiatives to tackle HIV in the UK, and provide in-depth information on specific actions and their impact, and profiles of parliamentarians who played a key role e.g. Lord Fowler.

 

The UK’s AIDS Memorial Quilt is an irreplaceable piece of social history and remembrance of those who died of HIV and AIDS in the 80s and 90s. The quilt panels measure 12 feet x 12 feet and can be laid out on a floor.  The above image shows Panels displayed in St Paul’s Cathedral in 2016:

 

Alongside the quilts will be A3 stands providing information about those remembered and quotes from those who created the quilts.

 

Further images of the quilts can be found at http://www.aidsquiltuk.org/gallery/

 

As we aim to reach as many people as possible over World AIDS Day and due to the size of the AIDS Memorial Quilt panels, Westminster Hall is the only suitable venue for this exhibition

 

RELEVANCE TO PARLIAMENT?

The story of HIV in the UK and Government’s response is a unique piece of parliamentary history. It is the story of parliament’s intervention to prevent a national epidemic, an intervention that prevented the spread of HIV, saves lives and ensured effective support and care for those affected and challenge HIV related stigma.  What is also unique is that the story of HIV from a terminal to long-term condition has happened within our lifetime over the course of 30 years and, as such, has occurred alongside the careers of parliamentarians who were at the vanguard of, and continue to, advocate for the rights of people living with HIV.

 

When AIDS first appeared in the 1980s it marked, for the first time in the 20th century, the beginning of a potential epidemic in the UK. This was an epidemic disproportionately impacting upon those on the fringes of society at that time, notably gay men, drug users and sex workers.

 

In the words of Lord Fowler, who was Secretary of State for Health from 1981 to 1987: ‘We were the only people that could protect the public and prevent deaths from taking place’ (Lord Norman Fowler, 2016)

 

2017 marks the 30th anniversary of the UK Government’s engagement in tackling HIV and supporting people with HIV.  Parliament has recognised and addressed issues from raising awareness in 1987 through launching the Don’t Die of Ignorance Campaign and then in 2017 within compulsory relationships and sexual education in secondary schools; testing through the introduction of the ante-natal screening programme in 1999 and legislation for home testing kits in 2014; through to protection of those living with HIV with the inclusion of HIV in the Disability Discrimination Act in 1995, subsequently strengthened in the 2010 Equality Act. 

 

 

Tuesday, 31 October, 2017

'HIV HAS CHANGED' CAMPAIGN

'HIV HAS CHANGED' CAMPAIGN

'HIV HAS CHANGED' CAMPAIGN

ViiV Healthcare are launching a public awareness campaign entitled ‘HIV has changed’ which intends to increase the public’s knowledge and understanding of HIV and to encourage people to test for HIV.

 

The campaign’s focal point will be a 10-foot living structure made up of a range of plants and flowers spelling out H-I-V that will be placed in New Cathedral Street in Manchester City Centre from 7-10 September.

 

The plant-based letters will be a physical representation of life and growth, and members of the public will be encouraged to interact with this living representation of HIV.

 

ViiV Healthcare hope that the message that ‘HIV has Changed’ will spread beyond the city centre as people passing by will be able to walk up to it, take pictures and share images on social media and other channels.

 

George House Trust, along with our PaSH partners LGBT Foundation and BHA for Equality, are supporting this campaign.

 

 

Friday, 1 September, 2017

WELLBEING PROJECT

LIVING IN MANCHESTER?  FEELING ISOLATED OR LACKING CONFIDENCE?

LIVING IN MANCHESTER?  FEELING ISOLATED OR LACKING CONFIDENCE?

 

Our Wellbeing Project, funded by Manchester City Council, aims to improve wellbeing, build confidence or help reduce social isolation for residents of Manchester who are living with HIV.

 

We can advise you about social groups or activities happening in your area.  It could be anything from improving your physical fitness, relaxation classes, crafts or outdoor activities – we can also help to fund it for you.

 

If you feel that you could benefit from this project email Naome Phiri or call her on 0161 274 4499.

 

Friday, 1 September, 2017

WAGAMAMA CONTINUES TO MAKE IT RAIN(BOW) FOR THE LGBT+ COMMUNITY

WAGAMAMA CONTINUES TO MAKE IT RAIN(BOW) FOR THE LGBT+ COMMUNITY

 

23.08.17: Pan-Asian restaurant wagamama has extended its #makeitrainbow campaign to celebrate Manchester Pride this weekend. 

 

The day’s profits from wagamama bun sales (now selling an average of 1,000,000 yearly) will be donated to local charity, George House Trust, every time a rainbow is spotted in the sky above Manchester, from 25th August.

 

Rain falls an average of 151 days a year in Manchester, making it one of the wettest cities in the UK. wagamama is calling on the Mancunian community to help spot rainbows to unlock the donation by tweeting a picture with the hashtag #makeitrainbow.

 

To ensure the charity benefits whatever the weather and in case we enjoy 365 days of sunshine in Manchester (very unlikely), wagamama is committed to donating a minimum of £2,500 to George House Trust, aiding its important work to support people living with HIV.

 

Regular Giving Manager at George House Trust, Leroy Williamson said:

"George House Trust are over the moon to be working with wagamama on this fun engaging campaign. We rely on the financial support of businesses and our local community to enable us to provide a much needed service here in Manchester and the North West. The money raised by wagamama will go towards our welfare fund and counselling service to support people who are living with HIV. I think this 12-month campaign really shows an understanding and a commitment to equality. Manchester is a wonderful place and I’m positive everybody will come together for lots of fun with buns and rainbows."

 

Head of Marketing at wagamama, Andre Johnstone said:

“wagamama has always supported its staff when it comes to Pride across the UK but we have wanted to do more publicly to support the LGBT+ community in previous years. I’m pleased we can expand our support following the success of London and Brighton Pride and make a wider commitment to throw our support behind those who struggle to be who they are. We are who we are and we want you to just be you. What better way to ramp up our continued support and celebrate Pride than by backing a vitally important charity such as George House Trust.”

 

Manchester Pride is a community funded charity that challenges discrimination and campaigns for equality for the LGBT+ community. Pride gives people a platform to speak up and be who they want to be and creates a safe environment for all. This year, thousands will descend on Manchester to be a part of and support the LGBT+ community.

Wednesday, 23 August, 2017

Take on Tough Mudder

Take on the infamous Tough Mudder obstacle course on Sunday July 16th 2023! 

 

Where: Heaton Park, Manchester

 

How far: 5K (13 obstacles) 

 

How much: £75

 

How much do I need to raise:  £500 

 

We will send you t-shirts or running vests, training plans and fundraising tips and tricks.

 

We'll support you every step of the way to reach your sponsorship target 

 

Up for it? Secure your place for £75 

 

Friday, 14 April, 2023

 

PASSIONATE ABOUT SEXUAL HEALTH (PaSH) PARTNERSHIP

 

We are delighted to announce the success of the Passionate about Sexual Health (PaSH) Partnership tender submission to deliver the Greater Manchester Sexual Health Improvement Programme.

 

The PaSH Partnership is a collaboration between BHA for Equality, George House Trust, and the LGBT Foundation, who are the current providers of HIV prevention and support across Greater Manchester.

 

The PaSH Partnership is looking forward to rolling out a comprehensive programme of interventions to meet the changing needs of people newly diagnosed with HIV, living longer term with HIV or at greatest risk of acquiring HIV.

 

The GM Sexual Health Improvement Programme will include HIV testing, access to low cost condoms, a dedicated sexual health website, HIV outreach, and support for adults and children newly diagnosed with HIV or living with HIV longer term.

 

Medical advances now mean that HIV is a manageable long term health condition when diagnosed early, but continuing levels of misunderstanding and a lack of up to date knowledge mean that HIV remains a highly stigmatised medical condition.

 

The PaSH Partnership believe that the work they are looking to deliver through the contract will be key to achieving Greater Manchester’s vision of ending HIV transmission within a generation.

 

The contract will commence on 1st July 2017 followed by a period of mobilisation and transition with the aim of achieving full operational delivery by the end of the year.

Wednesday, 10 May, 2017

8 Ways to Live HIV Confident

 

KNOW THE FACTS

Take time to understand the jargon. You’ll come across a lot of terminology that will be new to you. Our Services Advisers can help explain everything. The more you understand about your HIV, the better.

 

IT'S GOOD TO TALK

It’s good to know you have someone to talk to about your HIV when you need to. Don’t be alone with your thoughts or anxieties and remember that support is there for you when you need it - talk to one of our Services Advisers

 

KNOW YOUR RIGHTS

Make sure you’re up to date on the laws that protect people living with HIV. The Equality Act 2010 ensures that you can’t be discriminated against based on the fact that you’re living with HIV.

 

TAKE YOUR TABLETS

Adhering to your medication is important. Talk to your HIV doctor or specialist nurse about any concerns you have before you start, or whilst your taking, your medication.  

 

LOOK AFTER YOURSELF

Sleep well, eat well, exercise and relax when you can. The importance of living as healthily as you can is key to your general wellbeing. 

 

ASK QUESTIONS

Don’t be afraid to ask questions. If there’s something you don’t understand – or you’re worried about – ask the people involved in your care at your clinic. There’s no such thing as a stupid question.

 

BE PREPARED

Prepare well for your clinic appointments. Write down your questions, or concerns, and share them with your HIV doctor or specialist nurse. Remember that your clinic appointment is your time. You should be able to leave your appointment feeling that your questions have been answered.

 

LET'S TALK ABOUT SEX

People living with HIV have a right to a good and healthy sex life - it just means that there may be a few more things to think about. Our Services Advisers are here to help you think about some of the issues – and to support you to make the decisions that feel right for you.

Friday, 30 September, 2016

 

8 THINGS TO REMEMBER DURING PRIDE
 

BE WHO YOU ARE

After all, it’s what Pride is all about. Join George House Trust in the Parade and make a loud and proud stand against stigma and prejudice.

 

PACE YOURSELF

Pride is a marathon, not a sprint and a lot of alcohol will be flowing. If you’re drinking alcohol, know your limitations and remember to stay hydrated. If you’re taking HIV medication, try to remember not to miss a dose.

 

PASS IT ON…

Where there’s an opportunity, tell people about the fact that people living with HIV with an undetectable viral load can’t pass HIV to anyone else. Help spread the word that Undetectable = Untransmittable.
     

GOING ALONE?

Pride is about community and everyone’s there to celebrate the same thing. There’s no reason why you can’t attend events on your own if you want to. Use the opportunity to talk to someone new or come and say hello to the George House Trust volunteers in the Expo.

 

WILL THERE BE DRUGS AT THE PARTY?

There can be some serious interactions between some recreational drugs and HIV medication. Remember that your judgement and inhibitions may also be affected by substance use.

 

IT’S JUST A VIRUS…

If you choose to tell someone about your HIV over the weekend and it doesn’t go quite how you planned it, remember it’s their problem not yours. Don’t let outdated and ignorant attitudes spoil your fun.

 

STAY SAFE

If some Pride shenanigans is on the cards, your best protection against sexually transmitted infections is to use condoms. Grab a pocketful and away you go.
     

BE PROUD

Whether you attend Pride alone or with friends: celebrate, commemorate, dance and enjoy every second of it. Above all have fun and be proud of who you are.

Monday, 7 August, 2017

8 things about undetectability

 

THE AIM OF TREATMENT IS TO REDUCE THE AMOUNT OF HIV IN THE SYSTEM TO LEVELS WHERE IT CAN’T BE DETECTED

Once the levels of HIV have fallen to undetectable levels, the body stops over-producing CD4 cells, and the immune system can then start to repair itself. The HIV hasn’t gone, but it remains in only tiny levels in the body.

 

BEING UNDETECTABLE MEANS THAT YOU WON’T PASS HIV ON

It’s true! Research has shown that people with a sustained undetectable viral load will not pass on HIV during sex. So as well as keeping you healthy, taking HIV medication means that, once you’re undetectable, you won’t pass HIV on to your sexual partners.

 

ADHERING WELL IS KEY

You’ll only achieve undetectability by taking your medication regularly and as prescribed by your HIV doctor. If you’re having problems with adhering to your meds, our Services Advisers can help with tips and hints.

 

YOU MAY SOMETIMES SEE A SLIGHT RISE OR ‘BLIP’ IN YOUR VIRAL LOAD

It happens - don’t worry about it. Your HIV doctor will explain the reasons for it but it would be rare for your viral load to rise suddenly to such a level that it causes long term problems. So long as the viral load isn’t consistently detectable sudden blips shouldn’t cause any problems.

 

BEING UNDETECTABLE WILL HELP STOP HIV FROM DOING DAMAGE TO YOUR SYSTEM

When you’re not taking treatment, the body produces way more CD4 cells in an attempt to control the HIV. In turn, HIV targets these cells meaning that damage can occur to the immune system. By getting the HIV down to an undetectable level, the immune system stops working overtime - and can then start to repair itself.

 

UNDETECTABILITY HELPS IN THE FIGHT AGAINST HIV STIGMA

We know that much of the stigma comes from peoples’ fear of contracting HIV. This fear might just disappear once everyone gets the message that HIV can’t be passed on with an undetectable viral load.

 

YOUR HIV DOCTOR MAY FOCUS MORE ON YOUR VIRAL LOAD THAN ON YOUR CD4

If you’ve been diagnosed early, your HIV doctor will be much more interested in getting your viral load to undetectable levels, once he or she has decided with you that treatment is your best option. Your CD4 count (and percentage) will still be monitored - however it may not be the focus of your appointments once your treatment has begun.

 

EVERYONE NEEDS TO UNDERSTAND WHAT BEING UNDETECTABLE ACTUALLY MEANS

Whilst more and more people living with HIV are learning about the massive benefits of being undetectable, there’s still a lot to do to make sure that everyone understands that U=U. Undetectable equals Untransmittable.

Tuesday, 2 May, 2017

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Living with HIV? Want to talk to us?
Call 0161 274 4499 or email: talk@ght.org.uk