News: 11/2024 | Page 2 | George House Trust

LGBT History Month 2024 - Under The Scope With Dr Chris Ward 

 

Growing up as a gay man in the 1980s and 90s was a scary time. I remember a lot of fear about HIV and stigma in the media. When I came out to my parents the first thing they mentioned was fear of HIV.

 

I have always wanted to help the community and when I started at medical school volunteered with the LGF (now LGBT Foundation) to distribute condoms at Pride. By the time I started university, antiretroviral treatment had progressed and highly active combination therapy was already saving lives.

 

My own experiences with shame around sex and HIV anxiety motivated me to explore sexual health as a career. Working in Infectious Diseases at North Manchester General solidified this.

 

Now, as a consultant in sexual health and HIV at Hathersage I have been lucky enough to have worked through huge breakthroughs in HIV prevention and treatment.

 

I remember when the first PrEP trials showed enormous success at reducing HIV transmissions, and the landmark Partners study providing and inspiring the Undetectable=Untransmissable message. This revolutionised people’s lives and helped with anxieties around sex, shame and stigma.

 

Now we are lucky enough to have multiple different HIV treatments, that are well-tolerated and some come in the form of one pill a day. With injectable treatments we have been able to offer even more options and choice, seeing most people only once every six months.

 

I enjoy working with patient and community groups like George House Trust. We keep momentum and pressure going to fund sexual health services, we drive forward innovation and new drug developments and we tackle the stigma around HIV that still exists.

 

Dr Chris Ward, Sexual Health and HIV Consultant for Manchester University NHS Foundation Trust

2 February 2024 

Friday, 2 February, 2024

LGBT History Month 2024 - Under The Scope With Paul Fairweather

 

I remember in the earliest days of the epidemic, there was no treatment for HIV. Friends of mine who were HIV positive developed AIDS and died.

 

Then, the earliest drugs like AZT came along but these had awful side-effects and weren’t very effective. I had friends who had to stop taking these drugs because they made them so ill.

 

Thankfully HIV medication today is completely effective and easy to take. People living with HIV can take just one tablet a day and see their HIV consultant every six months for a check-up.

 

In the 1980s, as a member of Manchester AIDSline which later became George House Trust, I attended meetings at the old Monsall Hospital. We met with HIV consultants to talk about the importance of working and consulting with people living with HIV.

 

There were many heated debates about the best way forward, but it was so important that we were seen and heard at these meetings.

 

It was also through the activities of ACT UP (AIDS Coalition to Unleash Power) that HIV activists put pressure on the medical profession to change their policies and procedures and fast-track new treatments for HIV.

 

There was an ACT UP group in Manchester who organised a range of campaigns. These included throwing condoms over the wall of Strangeways Prison because the prison refused to give them to prisoners and picketing the Regional Health Authority to increase funding to HIV support and advocacy groups.

 

I believe that our HIV activism fundamentally changed the relationship between the medical profession and patients. A mutual, respectful relationship is now the blueprint for how consultants should work with patients experiencing HIV and indeed any medical condition.  

 

Paul Fairweather, Positive Speaker Development Worker at George House Trust 

1 February 2024 

Thursday, 1 February, 2024

Paul Fairweather MBE

Paul Fairweather has been awarded an MBE in the King’s New Year Honours List 2023

 

George House Trust co-founder and LGBT activist, Paul Fairweather, has been awarded an MBE for services to people with disabilities and the LGBT community in the North West in the King’s New Year Honours List 2023.

 

Paul, who is a renowned HIV activist, LGBT rights champion and ambassador for equality, has been awarded the MBE for his life’s commitment towards promoting inclusion, advocating for equality and challenging hate. His colleagues and friends at George House Trust are all so pleased that his work’s been recognised in this way.

 

In the early 1980s Paul was at the forefront of the community response to the growing HIV pandemic among gay men in Manchester and across the North West, organising meetings, writing articles in the gay press and lobbying for much-needed support services for people diagnosed with HIV. His work was entirely voluntary and motivated by the experiences of many of his friends and the wider LGBTQ+ community who, as many lives were already being lost, were fearful and in need of information and advice.   

 

Paul continues to be involved with George House Trust as the Positive Speakers project lead, supporting people living with HIV to use their voice, tell their story and to tackle the HIV stigma that still exists. He works with many people who’ve experienced the sharp end of HIV stigma and supports them to realise their potential to change people’s hearts and minds, unleashing their power of their own story telling to help them grow and lead their own activism.

 

On being awarded the honour, Paul said:

“My gay activism began in 1974 and my HIV activism in 1984. Today, I am still an activist and I see this MBE as recognition of the work that not only I, but thousands of others, have done to help create a very different world. A world where living with HIV holds no one back. A world where prejudice and discrimination are challenged. A world where disabled people and LGBT people have far greater equality.”

 

Our Chief Executive, Darren Knight is delighted that Paul's work has been recognised and he said:

“I’ve known Paul for many years through his work to promote LGBTQ+ inclusion and tackle HIV stigma in all its guises in Manchester, across the North West and beyond. Working alongside Paul, I’m inspired by his determination to do all he can to make things better for others. I don’t use these words lightly, but he’s an absolute legend. He inspires me in my work every day – he has done since I started working in the LGBTQ+ and HIV sector 17 years ago. His MBE is more than deserved.”

 

Everyone at George House Trust recognises the value and impact of people using their voice to inspire others. If you're living with HIV or an ally and want to get involved in our work, have a look at the volunteer space on the website to see how you can get involved. https://ght.org.uk/volunteer

Saturday, 30 December, 2023

Access to hair, beauty and barbering is everyone's right. 

 

George House Trust is excited to launch a new awareness raising campaign that aims to tackle HIV stigma and discrimination in the hair, beauty and barbering sector. 

 

During August 2023 we conducted a survey about peoples’ experiences and received over 400 responses from across the UK. This was followed by focus groups with people who access our services and a round-table discussion with people living with HIV, and industry body representatives.

 

Based on our findings, we're launching a new campaign on social media that aims to challenge the industry wide stigma and discrimination.

 

You can find out more about our research and the campaign here.

 

 

Thursday, 5 October, 2023

BLACK HISTORY MONTH

Saluting Our Sisters For Black History Month 2023 

 

This Black History Month, I am saluting all my sisters who are living and thriving with HIV. I salute my HIV activist sisters who are fighting HIV stigma.

 

I went into denial when I got my diagnosis. It wasn’t a conscious decision; I was overwhelmed, and the diagnosis felt like I was drowning. On reflection, I was grieving, and I truly had a lot to understand and come to terms with. 

 

HIV now is about managing my medication and my life choices. My new reality is that as long as I take my medication, I am well, I can’t pass the virus on. Undetectable Equals Untranssmissable or U=U.

 

So why the activism?  Well, most people don’t know I can’t pass HIV on thanks to the treatment I take.  Not only do the public not know this but also a lot of people with HIV don’t know it. It blights and shapes lives for all of us.

 

Stigma and discrimination mean that people live in fear of a positive diagnosis, in fear of the medication, what people will do to them if they know, they live in fear of rejection. Whilst “the truth is out there”, sadly most people struggle to find it as they get lost in information overload.

 

So, for me activism is about setting the record straight, as best as I can.  Sometimes in the big stuff, like marching to end stigma and discrimination, but often it’s in the small stuff like reminding people that HIV and AIDS are not the same thing. 

 

My biggest drivers are around changing people’s perception and experience of HIV. Fortunately, as the Women’s Activity Officer at George House Trust, I support women to figure out what living well with HIV means to them. 

 

Women are offered opportunities to support each other through counselling, peer support, drop-in’s and workshops. 

 

We can grieve over the diagnosis but also learn how to manage our medication, our relationships and stigma so that we go back into our communities more confidently.

 

It doesn’t mean the journey is easy but that women are more willing to challenge the choices and beliefs they had about living with HIV.

 

Yvonne Richards-Cooper 

 

October 5th 2023 

Thursday, 5 October, 2023

Our new Volunteer Strategic Plan sets out three clear goals and how we will achieve them so we can continue as a successful volunteer-involving organisation. 

 

George House Trust's vision for volunteering is clear. We will ensure volunteers receive recognition for their contribution and benefit from a positive and nurturing experience within an inclusive and collaborative team.

 

You can read more about our plans for the George House Trust volunteer programme here

 

You can view our current volunteer roles here

 

13th July 2023 

Thursday, 13 July, 2023

Celebrate everything that’s incredible about Manchester and join our 2023 Great Manchester Run team!

 

Join our team in this year's must-do event. Starting and finishing in the heart of the city, soak up the amazing Manchester spirit the whole way round as the route passes iconic landmarks including Old Trafford, Etihad and the Imperial War Museum.

 

It’s a run for everyone, from locals to celebrated athletes, whether it’s your first 10k or your 50th. Starting and finishing in the heart of the city, soak up the amazing Manchester spirit the whole way round as the route passes iconic landmarks including Old Trafford, Etihad and the Imperial War Museum.

 

When: 21 May 2023

 

How far: 10K 

 

Registration Fee: £30

 

How much do I need to raise:  £500 

 

We will send you a running vest, training plans and fundraising tips and tricks. We'll have a cheer point on the day too so 

 

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

 

Up for it? Secure your 10K place for just £30.

 

Friday, 14 April, 2023

Amanda, pictured left, wrote this blog for Trans Day Of Visibility 2023

 

"When I was first diagnosed in 2003, I struggled to come to terms with it. I had nobody to talk to because my family and friends were transphobic and homophobic so I just suppressed it. I hid it from my partner, from everyone. I was scared, I couldn’t see myself living past a certain age because of the horror stories of the 1980s.

 

Between 2015 and 2020, I went through a lot of changes. I split up with my partner and got a flat but I couldn’t properly transition because the people around me didn’t accept me. One of my neighbours was transphobic and homophobic and turned the community against me. I was hit with an iron bar but the police didn’t do anything and I eventually ended up in prison due to lies my neighbour told. In prison, I was struggling with alcohol and drug addiction, and wasn’t given the right clothes for my gender or my HIV medication. My neighbour broke into my house and stole my belongings while I was in prison, and I lost my vehicles.

 

In October 2020, I was released and made the decision to walk out of Strangeways a new person. I changed my name, my gender, my living situation and my outlook on life.

 

My doctor recommended George House Trust to me and I’d always wanted to go because I’d never met anyone like me before. I met Josh and Yvonne, who run the women’s group there, and realised that there was a real HIV community at George House Trust.

 

I did a course to build up my self-respect and confidence there. Everything felt a lot better, like a breath of fresh air, because I didn’t have to explain to anyone that I was living with HIV. I was paired with a brilliant peer mentor who helped increase my confidence and self-esteem. He also recommended some self-help groups I could go to for support.

 

It was so nice to meet other people living with HIV. I met a woman who also comes to George House Trust at my bloods appointment – I really appreciated that social aspect and peer support.

 

I feel so much better and more confident now. Before I just felt trapped.

 

Living with HIV as a transwoman was difficult because I couldn’t see past each week. Dealing with HIV and gender dysphoria made it hard to get up in the morning. There is so much ignorance and stigma around both HIV and trans people.

 

The women’s group at George House Trust made me feel really welcome. It was a trans-inclusive safe space for me.

 

I was able to share my experiences of taking hormones and HIV medication with women who were considering HRT. Other emotions and experiences we’ve gone through are really similar too.

 

I’d never know anyone else living with HIV. By coming to George House Trust, I’ve met other women living with HIV - women who are so open.

 

Now, HIV is in the background, it’s on the back burner.

 

Amanda - March 31st 2023 

Friday, 31 March, 2023

MPOX VACCINE UPDATE

Mpox - Final Vaccination Dates Announced

 

The most recent Mpox (formally named ‘Monkeypox’) outbreak started in summer 2022 with cases reported worldwide for a number of months. The outbreak mainly affected gay, bisexual and MSM (men who have sex with men).

 

The outbreak has largely been brought under control with the UK Health Security Agency (UKHSA) reporting just six new cases this year, three of which were returning travellers. This is because of the roll-out of an effective vaccine and initial behavioural changes amongst affected groups.

 

Due to this, the UKHSA plans to halt the vaccination programme but will continue to closely monitor the situation.

 

Vaccination remains the most effective way of protecting you and people around you from mpox

 

People at risk from mpox are eligible for two doses:

 

If you’ve not had your first dose, you must come forward for this by the 16th June.

 

If you need a second dose, you must come forward for this by the 31st July.

 

You can get a vaccine at your local sexual health/GUM clinic. If you live in Manchester, The Northern is doing a weekly vaccine clinic. You can book here

 

If you live in other Greater Manchester boroughs, you can find your local Mpox vaccine clinic here

 

The NHS also has an easy to use vaccine finder website that will tell you where you can get a vaccine locally to you.

 

The vaccine is safe, free and administered by a healthcare professional.

 

Information about Mpox

 

It’s important to note that Mpox is normally a mild illness and is unlikely to lead to further complications. Most people recover from in a few weeks. In the recent outbreak, 1 in 10 people need to be treated in hospital, this is usually to help manage pain. 

 

How does Mpox transmit?

 

  • By close contact with someone who has symptoms, e.g. touching skin, sexual contact, kissing, hugging - this is especially after the ulcers have developed.  This is because the fluid in MPX blisters is highly infectious.
  • Through droplets in the air - ​​​​​​ this usually involves extended time with someone in a room with poor ventilation.  For example, spending more than 3 to 6 hours, where you are within two meters.
  • Touching clothing, bedding or towels used by someone with the Mpox rash.

 

The risk of catching Mpox is generally low. However, it is much higher for people who have multiple partners, or whose partners have these risks. There is a greater risk of catching Mpox from sexual partners and people you live with.

 

There is a greater risk of catching Mpox if you attend sex parties, sex on premises venues (e.g. a sauna), attend cruising grounds or have multiple individual sexual partners. 

 

What are the symptoms?

 

It can take 1 to 3 weeks for Mpox symptoms to develop. For most people, this is 10 to 12 days after contact.

 

Initial symptoms of Mpox include fever, headache, muscle aches, backache, swollen lymph nodes, chills and exhaustion. Unexpected or unexplained spots, ulcers or blisters can develop, often beginning on the face, then spreading to other parts of the body including the genitals.

 

The spot, ulcer or blister changes over time and goes through different stages, and can look like chickenpox, herpes or syphilis, before finally forming a scab, which later falls off.

 

Symptoms last for up to four weeks.

 

HIV and Mpox

 

The Lancet reports that “people living with HIV have accounted for 38-50% of those affected in the 2022 multi-country mpox outbreak” and goes on to state that “most reported cases were in people who had high CD4 counts and similar outcomes to those without HIV”.

 

You can read the full Lancet report.

 

However, a small proportion of people living with HIV who have contracted mpox have a low CD4 count (below 350) and Aidsmap reports “worse clinical outcomes and higher mortality in people with more advanced HIV”.

 

You can read the full article here.

 

The British HIV Association (BHIVA) recommends that everyone living with HIV has the mpox vaccine.

 

You can find additional information about Mpox here:

 

 I-base Mpox Q&A 

General information about Mpox from the NHS

Latest updates from the UKHSA

 

March 23rd 2023 

 

 

Thursday, 23 March, 2023

The 2023 theme for Women’s History Month is "Celebrating Women Who Tell Our Stories."

 

George House Trust Positive Speaker and HIV activist Agatha Phiri is sharing her story to inspire others and help break down HIV stigma and discrimination. 

 

I’ve managed to build a home from the bricks that HIV stigma and HIV discrimination threw at me. This home is now a safe space for women living with HIV called Agatha’s Space. I am also a positive speaker for HIV charity George House Trust and help people to understand me and my HIV through my volunteer work.

 

I have turned into a confident woman who is not scared to take a step to challenge everything about my HIV, my future and my goals.

 

Living with HIV has made me understand love. After going through lots of rejections and betrayals I now have a handsome, loving man who accepts me with my HIV.

 

When it comes to HIV, we talk about the negatives a lot – things like stigma, discrimination, betrayal and more. But over time I have learnt to find solace in my strength and solace in the positive things HIV has contributed to my life.

 

HIV has given me a different meaning in life. It has given me a reason to fight for my rights as a human being and fight for equality.

 

HIV has given me my dream life because I got tired of fear. I am bold, confident and ambitious. I said NO! to fear.

 

If you’ve had enough of the negatives HIV can bring, then take a bold step and challenge them.

 

Fight. Fight, fight and fight until there is nothing left to fight for.

 

Whilst it’s true that HIV has sometimes given me lemons, I have learnt to turn them into lemonade to protect myself, my mental health and to be an example of how women living with HIV should be loved and treated.

 

Agatha Phiri 16th March 2023  

Thursday, 16 March, 2023

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