Market Towns: Cultural Heritage

Debate between Stephanie Peacock and Alec Shelbrooke
Tuesday 4th March 2025

(1 month ago)

Westminster Hall
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Stephanie Peacock Portrait Stephanie Peacock
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I am grateful for my hon. Friend’s contribution. I drove through her constituency at the weekend. It is a beautiful part of the world, and I am very happy to offer a meeting with my hon. Friend the Minister for Creative Industries, Arts and Tourism.

Through the heritage at risk capital fund and the heritage revival fund, we are making an extra £20 million of investment available to the sector, to repair our most at-risk heritage sites and support groups who are ready to bring derelict old buildings back into good use. The heritage at risk capital fund will account for £15 million from this spring, and it lives up to its name: it is all about providing grants for repairs and conservation for heritage buildings at risk, with a particular focus on those sites that need it most. It could help all sorts of different types of heritage—shops, pubs, parks and town halls.

Alec Shelbrooke Portrait Sir Alec Shelbrooke
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I know the Minister’s Yorkshire constituency very well. There are many great old buildings, but one problem will be getting their energy performance certificates to band C. It is all very well investing the capital so that they can be reused, but if they are not meeting band C, they cannot be used. Will she take back to the Minister for Creative Industries, Arts and Tourism the point that this area needs to be reviewed, because I think the policy of the last Government was a mistake?

Stephanie Peacock Portrait Stephanie Peacock
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I very much heard the points that the right hon. Member made. I commit to taking them back to the Minister responsible, and I will ensure that he writes to the right hon. Member in good time.

The heritage revival fund is a new scheme altogether, and one that is designed to put local people in the driving seat. The Government recognise that restoring buildings that once stood as visible symbols of progress is an important way of restoring people’s pride in their area and empowering local people to take control of their own destiny again. The fund will build on the previous transforming places through heritage fund, which provided support to market towns in places such as Lancashire, Suffolk and West Yorkshire. For example, it gave more than £120,000 to the Bridgwater Baptist church in Somerset, a grade II* listed church built in 1837, enabling it to be converted to a multi-purpose space supporting wider community use and providing workspaces for businesses. That fund provided a really useful model for how Government backing for local community organisations can help to unlock further backing from the private sector, such as commercial loans and other grants.

On top of our heritage capital funding, my Department delivers the listed places of worship scheme, which gives grants towards VAT paid on repairs and renovations to listed sites of worship across the UK. My colleague the Minister for Creative Industries, Arts and Tourism recently set out in a debate in this Chamber how the scheme is playing an important role in keeping culture alive and well in our communities, providing facilities and meeting points for local residents. In addition to providing places to worship, many of these buildings act as music venues, food banks and community halls, all of which contribute to the cultural heritage of a place. We know that the scheme is making a difference in market towns and local areas up and down the country, which is why we are making £23 million-worth of funding available between 2025 and 2026.

Support is not just limited to central Government Departments such as DCMS; our arm’s length bodies and executive agencies also play a key role. Arts Council England, the national funding body for the arts, provides a range of supports for villages, towns and cities up and down the country. The Arts Council recognises how important it is that funding gets to places that need it most, and over 60% of its investments are now outside London, with more support for regional venues and cultural assets in market towns.

Through its national portfolio programme, Arts Council England is supporting initiatives such as the Essex Cultural Diversity Project, which has a main office in Rochford in my hon. Friend’s constituency and aims to boost cultural diversity in the arts and heritage through local projects. The Arts Council has given £300,000 to Rochford alone since 2020, which includes some vital support during the pandemic.

DCMS also makes public funding available through the National Lottery Heritage Fund. Last year that fund invested more than £293 million of money raised by national lottery players in almost 1,300 heritage projects across the UK. It has backed a range of community heritage projects, including schemes such as the Rochford Town Team, which is promoting a heritage trail around the market town. I will not list every project, but hon. Members will know that the National Lottery Heritage Fund gives grants that will make a visible difference in an area.

I will briefly touch on the importance of market towns to our visitor economy and tourism sectors. As all Members here today know, many market towns are magnets for tourists who want to visit, soak in the culture and spend their money on local hospitality. From the historic streets of Stamford to the literary heritage of Stratford-upon-Avon—I always remember my granddad taking me there when we were growing up—we have so many examples across Britain.

My colleague the tourism Minister’s goal is 50 million international visitors by 2030; we need to ensure that the benefits of UK tourism are being felt well beyond our major cities and in places such as market towns. To match those words with action, we are working in partnership with VisitBritain, VisitEngland and local visitor economy partnerships to put market towns at the heart of our tourism strategy.

I would love to say more on that, but in the interests of time I will move on to say that, although I have spoken to DCMS’s contribution, I am pleased to confirm that the Deputy Prime Minister has today launched the Government’s new plan for neighbourhoods programme. The plan for neighbourhoods will provide £1.5 billion to 75 communities across the UK over the next decade, including a number of market towns.

In each place, the Government will help set up a new neighbourhood board, bringing together residents, local businesses and grassroots campaigners to draw up and implement a new vision for their neighbourhood. In consultation with their community, each board will be given the freedom to decide how to spend £2 million a year to deliver the priorities of local people, whether by regenerating their historical high streets, supporting new and historical open-air markets or unlocking further local investment. Our new approach puts communities at the heart of delivery and is aimed at revitalising local areas and fighting deprivation at its root by zeroing in on three strategic objectives of building thriving places, strengthening communities and empowering people to take back control of their local areas.

Taken together, the support we are making available to market towns will help to deliver what we all want to see: thriving market towns that can look forward to a prosperous future. We want to preserve the heritage that gives those towns their identity, to make them central to our tourism sector and visitor economy, and to sustain the local cultural assets that inspire this generation and the next.

Endometriosis Workplace Support

Debate between Stephanie Peacock and Alec Shelbrooke
Tuesday 29th October 2019

(5 years, 5 months ago)

Westminster Hall
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Westminster Hall is an alternative Chamber for MPs to hold debates, named after the adjoining Westminster Hall.

Each debate is chaired by an MP from the Panel of Chairs, rather than the Speaker or Deputy Speaker. A Government Minister will give the final speech, and no votes may be called on the debate topic.

This information is provided by Parallel Parliament and does not comprise part of the offical record

Alec Shelbrooke Portrait Alec Shelbrooke
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I am most grateful to the hon. Lady, who speaks with a great deal of personal experience. We have been friends for a long time—since we came to this place. We are two West Yorkshire MPs, despite being on different sides of the aisle. I am grateful to her for making those points. As I said, it is important that the Department for Education and the Department of Health and Social Care take this forward. Other Members may wish to try to secure debates that are responded to by those Departments. I know that my hon. Friend the Minister will certainly feed those issues in.

I apologise for citing a lot of stories, Mr Pritchard, but it is important to set out the context. Another lady said:

“I had stage 4 (severe) endometriosis. I had a 7 year wait for diagnosis. From my referral to the hospital, I had a year and a half wait for surgery. My surgery was lifesaving as my bowel was 50% blocked with a mass of adhesions that had grown through the bowel. I was in constant pain, slept for 3 or 4 hours a day and was unable to care for my son properly, I considered putting him into care. If it wasn’t for him, I would have given up on everything. Despite being told in 2010 I ‘probably had endometriosis’ I was still given pain killers and mefenamic acid for years to manage the pain and symptoms. Throughout this time the endo was worsening, it is progressive. Had I been diagnosed earlier I may not have needed the bowel resection I needed and will have bowel issues for life. I was on the pill for 15 years, which is still considered a ‘treatment’. It is not. The same year I came off it (2010) I was at the GP with SEVERE bowel pain during my period (It was fused to my womb). The pill masked the symptoms, but it was quietly progressing. Please ban the use or presentation of the pill as ‘treatment’.”

Stephanie Peacock Portrait Stephanie Peacock (Barnsley East) (Lab)
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I congratulate the right hon. Gentleman on securing this incredibly important debate. One in five women will suffer from this disease, and it has been shown that, as that story shows, it can take up to seven years to convince a doctor. That is completely unacceptable. We have an issue in this country with what has been called the gender pain gap. We need to put more money into research and funding to look at proper cures and support for women when they need it most.

Alec Shelbrooke Portrait Alec Shelbrooke
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I entirely agree with those sentiments. As I said, I hope this debate will go beyond the Department for Work and Pensions. I thank the hon. Lady for that contribution; it is spot on.

Endometriosis affects 1.5 million women in the UK. It takes an average of eight years to diagnose and there is not really a cure.

I will share a few examples from women who have spoken out through the digital platform. One said:

“I have suffered with endometriosis since the age of 15 and I was diagnosed aged 22. The worst thing about endometriosis is the lack of awareness. Even some doctors haven’t even heard of it which is very frustrating! I’ve had 4 surgeries to try to alleviate the symptoms. Unfortunately, this hasn’t worked. I want to try to basically create more awareness of endometriosis, especially online, as much as I can.”

Another woman said:

“I was diagnosed with endometriosis in May 2016. I would say 2 years was spent actively pursuing a diagnosis. But the previous 9 years I often went to the doctors, complained of pain and heavy flow and I was told ‘it’s just a bad period, it’s normal’. The hardest part of endometriosis for me would be the mental health side of things, coming to terms with the fact my body has limits and my life probably isn’t going to take the direction I thought it would.”

Someone else said:

“I was 17 when I was diagnosed with endometriosis. I’ve had 6 surgeries since. The thing I hate most about endometriosis is not being able to plan ahead because you don’t know how your pain is going to be that day. You could be absolutely fine, or you could be crippled.”

A young woman said:

“I was diagnosed with endometriosis on the 14 February last year, I was only 15. It took me 3 years to get diagnosed. For those 3 years, I was told I had unexplainable abdominal pain.”

Another story comes from a woman who said:

“I was diagnosed when I was 25 when I had a miscarriage. I had been struggling since I was a teenager with all the common signs of endometriosis. It just wasn’t picked up until I had my first surgery. What I hate most about endometriosis is that it takes time away from my children. Especially when I have to just go and rest in bed. I would love to be able to make it more aware for children, especially young girls and in schools, to be able to support them through this and see the early signs and educate GPs on the signs and symptoms.”