News: 05/2024 | Page 18 | George House Trust

APRIL IS "LISTENING AND LEARNING" MONTH AT GEORGE HOUSE TRUST

During April we will be carrying out our “Real Time Survey”, where we ask everyone who uses services during April to give us feedback on how we are doing. We will have volunteers on hand to assist if needed.

 

For those who do not attend or use services during April we will be sending out an electronic survey to get feedback on how we are doing.

 

We will use the feedback to celebrate and share our successes and to also look at how we can improve the services we offer to people living with HIV in Greater Manchester. We will share the feedback with both the Board an also service users. We will also look to use feedback as evidence to strengthen our funding applications so it’s really important that we get as much information as possible so we would urge everyone to get involved and give us feedback.

 

Tuesday, 6 March, 2018

MEET THE CEO AT SATURDAY DROP IN

MEET THE CEO AT SATURDAY DROP IN

Saturday 21st April

10.30 am - 4.00 pm

As part of our ‘listening and learning’ month, Steph Mallas, George House Trust CEO will be offering 10 minute one to one sessions at this Saturday Drop In for service users to share their experience of George House Trust - both the good bits and suggestions for improvements. The sessions will be on a first come first seen basis.

 

The feedback will be collated and shared with the staff and Board, and can be anonymised at the request of the service user. Feedback may also be used to help support funding bids for new projects and developments at George House Trust.

 

Steph will be available from 11.00 until 3.00. If you can’t make it that day, please feel free to email your feedback to Steph on stephanie@ght.org.uk.

Tuesday, 6 March, 2018

NEW SESSIONS AND EVENTS CALENDAR 2018/19

 

We are currently finalising the sessions and events calendar for 2018 /19.

 

Because of the relatively low take up for some events there will be some changes to the sessions that we plan to run.

 

We are pleased to announce a new monthly event – ‘Meet and Eat’. This will be a social space with a catered lunch and will be an opportunity for people to meet up in a relaxed atmosphere.

 

We’ll also be increasing the number of relaxation therapy days to four over the course of the year following feedback from service users.

 

The full events calendar will be on the website soon so keep a look out for more details.

Tuesday, 6 March, 2018

 

8 THINGS TO CONSIDER BEFORE STARTING HIV MEDICATION
 

YOUR HIV DOCTOR OR SPECIALIST NURSE ARE THE PEOPLE TO TALK TO

Have an honest conversation with your HIV doctor or specialist nurse – they’re there to advise and support you. There are lots of options around starting treatment, and the people involved in your clinical care will be happy to discuss this with you.

 

CONSIDER YOUR OPTIONS AND THINK ABOUT THE BENEFITS OF STARTING TREATMENT

Make sure that you properly understand the benefits, for you, of starting HIV treatment and take time to consider the pros and cons. George House Trust Services Advisers can offer you a space to talk and think things over.

 

START TREATMENT AT THE RIGHT TIME FOR YOU, ONCE YOUR HIV DOCTOR RECOMMENDS THAT YOU START

It’s a good idea to have a clear understanding of why it’s the right time to start treatment. Being ready and prepared before starting treatment means you will be better informed and more confident as you start your treatment journey.

 

IT’S A LIFELONG COMMITMENT

But it’s a commitment that’s entirely possible to fit into your daily routine. Many people are taking HIV meds daily, doing the things they’ve always done and getting on with their lives.

 

TAKING TABLETS EXACTLY AS PRESCRIBED MEANS THEY’LL WORK AS THEY SHOULD, AND REMOVE THE LIKELIHOOD OF DEVELOPING RESISTANCE

You’ll need to make sure that you take your medication regularly without missing any doses. Missed doses can mean that your HIV develops resistance to the particular drug you’re taking. Think about how you’ll get into the right routine to make sure that you don’t miss a dose.

 

THE BENEFITS OF AN UNDETECTABLE VIRAL LOAD ARE MASSIVE

Adhering well to your treatment means that the amount of the virus in your body will come down to levels which are undetectable. Research shows that someone with an undetectable viral load has a negligible chance of passing HIV on to someone else. That’s got to be a good thing. 

 

TREATMENT MAKES YOU BETTER, AND SIDE EFFECTS ARE BECOMING A THING OF THE PAST 

Your body may need to adjust to taking new, regular medication, but many of the side effects that people experience are manageable and often short lived.

 

HIV MEDICATION IS BETTER NOW THAN IT’S EVER BEEN

HIV drugs - and their effectiveness – have improved massively over the years. Undetectable is the new HIV status – you’re only going to get there if you’re on treatment and adhering well. 

Friday, 3 March, 2017

 

8 THINGS YOU SHOULD KNOW IF YOU'VE JUST FOUND OUT YOU'RE HIV POSITIVE 
 

IT REALLY IS BETTER TO KNOW

It may not feel like it right now, but it really is. Now that you know you’re living with HIV, you’re in a much better position to manage your health and your long term future than if you didn’t.         

 

YOU DON'T NEED TO TELL ANYONE YET

Take your own time to think about who you want to tell about your HIV status. You may need support and a listening ear at some point – but remember, once you’ve told someone, you’re never going to be able to take the information back.

 

HIV IS A MANAGEABLE MEDICAL CONDITION

You’re living with a virus and you’ll need medication to keep it under control – but, with early diagnosis, people with HIV are living normal lives and doing exactly the same things that everyone else is doing.

 

SOME PEOPLE JUST DON'T UNDERSTAND

Unfortunately, for some people, HIV stigma is still an issue. Remember, it might be hard to take but, if people reject you or discriminate against you just because you’re living with HIV, that really is their problem, not yours. 

 

YOU CAN HAVE YOUR SAY ABOUT WHEN TO START TREATMENT

Talk to your consultant about the pros and cons of starting treatment. They will help you decide the best time for you to start.

 

SEX CAN STILL BE FANTASTIC

Just because you’re living with HIV doesn’t mean that you can’t – or shouldn’t – enjoy great sex. It’s just that there’s some extra things to consider now. George House Trust Services Advisers can help you think things through.

 

YOU'RE PROTECTED BY THE LAW

The Equality Act 2010 protects people living with HIV from being treated less favourably than other people. Whether it’s at work or in other areas of your life, the law says you can’t be treated differently.  

 

SUPPORT IS THERE FOR YOU

It’s not all going to be plain sailing and there’ll be times when you might need someone to talk to or take advice from. George House Trust offers support, advice and information about all aspects of living with HIV. Just call us.  

Friday, 18 November, 2016

BUY GEORGE A DRINK

BUY GEORGE A DRINK AND HELP SUPPORT PEOPLE LIVING WITH HIV

BUY GEORGE A DRINK AND HELP SUPPORT PEOPLE LIVING WITH HIV

 

George House Trust is launching a new fundraising campaign and inviting people to Buy George a Drink.

 

We want to make it easy to support the work of George House Trust by enabling one off text donations.

 

The campaign encourages everyone to include George when buying a round of drinks by texting ‘DRINK’ to 70660, which will automatically donate £3 to George House Trust.

 

Posters will be going up in pubs, clubs, juice bars, tea rooms and coffee shops across the city centre and we want absolutely everyone to get involved, so if you see our posters, whether you’re out for your regular drinks, brunch cocktails or afternoon tea, please text and include George when getting a round in.

 

Buy George a DrinkBuy George a DrinkBuy George a DrinkBuy George a DrinkBuy George a DrinkBuy George a Drink

 

We want to increase awareness of the work we do and the more people engage with George House Trust, the more we can educate people about our vision - for all people to know their HIV status and to be HIV aware.

 

The ultimate goal for the campaign is to increase the overall fundraising total and expand presence and awareness of George House Trust so we can ensure all people living with HIV can live happy and healthy lives, free from stigma and discrimination.

 

CEO of George House Trust, Stephanie Mallas said

“Buy George a Drink is a great, simple way for people to engage with George House Trust and support the work we do. We hope that everyone will include George when they’re out enjoying a drink and we want as many venues as possible to promote the campaign with the aim of making everyone HIV aware.”

For further details email Samuel Clarke, Community Fundraising Organiser, or call 0161 274 5565

 

Thursday, 12 October, 2017

 

THANKS FOR TELLING ME

Someone has told you this because they want you to know and they think they can trust you – give a reassurance that it will stay confidential. You’ve been given some powerful information that may have been difficult to disclose - ‘thanks for telling me’ acknowledges that.      

 

HOW ARE YOU DOING? 

Asking a simple question like ‘how are you doing?’ gives someone the chance to tell you as much or as little as they want to. Don’t probe too much – just asking this is probably enough right now.    

 

IT’S OK…

It really is OK. HIV today, with early diagnosis and proper adherence to treatment, is a long term manageable health condition. It’s the stigma and negative attitudes that sometimes get in the way of people who are living with HIV getting on with their lives.    

 

WHAT CAN I DO?

Think about why someone has chosen to tell you – it may be that a bit of extra support or just someone to talk to is what’s needed. Ask what you can do and be led by what the person tells you they need. 

 

LET’S TALK ABOUT U=U

If you aren’t aware of the U=U message, you need to be. We now know that someone on HIV treatment and with an undetectable viral load can’t pass on HIV to someone else. Talk about it, not just to the person who’s disclosed to you, but to anyone else who’ll listen.      

 

NOTHING CHANGES 

For some people, fear of rejection after disclosing HIV status means never feeling able to tell anyone. Be reassuring that nothing is going to change just because someone’s told you that they’re living with a virus.    

 

ARE YOU ON TREATMENT?

Showing an interest in someone’s health can be supportive. If you don’t know anything about HIV treatments – make it your job to find something out. Educate yourself about HIV so that you have all the information you need. 

 

DRINKS ON FRIDAY?

Keep things normal. The person who told you wants to keep things normal too. If Friday night is drinks night there’s no reason why your plans should change – and every reason why they should stay the same.

Wednesday, 13 September, 2017

TOUGH MUDDER

TOUGH MUDDER

GHT Tough Mudder Team showed their strength for people living with HIV

 Tough Mudder

 

After 6 weeks of ‘training’, 5 amazing people took on 26 gruelling obstacles over a 12 mile course to raise much needed funds for George House Trust. The team of mudders included our regular giving manager Leroy and brave volunteers Liam, Stephen, Meg and Natasha.

 

 

The challenge took place on Sunday the 10th September at Cholmondeley Castle where the team had to face iced waters, overcome big heights, power through electric volts and of course fight their way through lots and lots of mud!

 

Liam, one of the participants said

"It was the hardest but most amazing experience of my life, I've hurt my ankle and every muscle in my body hurts but I would do it all again in a heartbeat if it made just a small bit of difference to somebody’s life."

Collectively the team have so far raised £2,483.00 from the generosity of friends, family and supporters but there’s still time to show your support and reward the team for all of their hard work by making a safe and secure donation on the participants pages - Leroy, Liam, Stephen, Megan and Natasha - via Just Giving.

 

Regular Giving manager Leroy said 

"Thank you to everybody who has supported so far and is making a positive difference to somebody’s life with HIV. The course was tough but there are people we support that are facing bigger battles and although I’m in pain, I’m happy that with your help we are all standing strong together and improving lives in our community here in Manchester."

Thank you to Tony Molloy at CorptelUK for his continued support to GHT, he sponsored the team to take part and made this muddy fundraiser possible.

Tuesday, 12 September, 2017

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

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