Scott Arthur MP: speeches

Speeches

• 21 Apr 2026 · Peter Mandelson: Government Appointment · Hansard source

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  I am not in the Peter Mandelson fan club—I am old enough to remember his first life in government—but this morning we heard that UKVS had judged him to be a borderline risk and that officials thought that that risk could be managed. That is quite different from what the right hon. Gentleman is outlining.

• 21 Apr 2026 · Peter Mandelson: Government Appointment · Hansard source

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  rose —

• 20 Apr 2026 · Antisemitic Attacks · Hansard source

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  For most of my life, the UK was becoming a more tolerant society, so it really pains me that in recent years we have been going backwards; that is particularly true of the hate and violence faced by the Jewish community. That is why it was right that Kanye West was banned from entering the UK. Last week, I attended a Yom HaShoah event right next to Parliament, in which the Jewish community came together to mark the end of the Holocaust. They also reflected on the fact that there are still challenges ahead in the UK, which should shame us. The Minister has likened some of the recent violence in the UK to that in the Iranian state. What action will we take if there is found to be any connection between the people arrested and the Iranian state? The previous Government cut off diplomatic relations with Iran and its barbaric regime; will he follow suit?

• 16 Apr 2026 · Neuroendocrine Cancer · Hansard source

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  I am grateful for the opportunity to bring this vital issue to the House. The term neuroendocrine cancer may not be familiar to many, but tens of thousands of people across the United Kingdom have had to educate themselves after receiving a diagnosis. As with any rare cancer, this is often an uphill struggle marked by delays, misdiagnosis and a persistent struggle for visibility in our healthcare system. Hon. Members, possibly including the Minister, will have heard me make this point before: a cancer being considered rare does not stop it from impacting many thousands of people right across the UK. Indeed, about 6,000 people are diagnosed with neuroendocrine cancer each year in the UK, which works out at roughly one person every 90 minutes. Today, more than 36,000 people in the UK are living with the condition. To put that into perspective, it is now more prevalent than stomach or pancreatic cancer. The rate of growth is incredibly alarming. Between 1995 and 2018, the incidence of neuroendocrine cancer increased by a staggering 371%. This is not a niche health concern; it is a rapidly growing challenge that our NHS must be equipped to meet. Statistics can often feel abstract in the Chamber, which is why I want to share the story of a meeting I recently held with three neuroendocrine cancer patients, Liz, Carolyn and Craig, at my office in Fountainbridge in Edinburgh South West. Their stories were both moving and illuminating. We have just been talking about modernising the House of Commons. Given that that meeting took place just four weeks ago, I find it incredible that in four weeks I can meet someone, request a debate and then have that debate, with my favourite Minister answering my questions—it restores my faith in democracy. Craig, whom I met that day, is in the unique and challenging position of being both a professional advocate and a patient himself. He and the others I met expressed immense gratitude for the care they eventually received, describing it as nothing short of fantastic once they were in the right hands. However, they also spoke about the exhausting battle it took to access specialists who properly understood their condition. They described a system where specialist doctors and centres of excellence are too often hidden behind a wall of referral delays and low clinical awareness. That is particularly in evidence in Scotland, where patients currently face the worst waiting times since records began, but it is also true—albeit possibly to a lesser extent—in our health systems south of the border and in Wales and Northern Ireland. One of the most powerful parts of our conversation centred on a symptom that is often difficult to discuss yet utterly debilitating: the frequent and urgent need to access a toilet. This is not a minor inconvenience but a symptom that robs people of their autonomy and their dignity. They spoke of how that invisible burden prevents many patients from working, from attending social events and even from leaving their homes for long periods of time. It is a barrier to a normal, fulfilling life. They also brought a message of hope regarding the drug telotristat. They described how that treatment has quite literally given them back their lives. By managing the symptoms and stopping the cycle of incontinence, the drug has allowed them to return to work, to contribute to their communities, to pay their taxes—that is quite important—and, most importantly, to enjoy a fulfilling family life. This is a clear example of where the right medication does not just treat a disease but restores a person’s dignity and their place in society. It is a powerful reminder that when we invest in the right treatments and pathways, the system burden is reduced because patients are empowered to live independently. Despite those successes, the single biggest driver of poor outcomes remains the time it takes to get the initial diagnosis. At a meeting I attended at the Royal College of General Practitioners in December, bringing together UK-based healthcare professionals involved in trials, patient care and leading research into neuroendocrine cancer, I heard that, on average, it takes four-and-a-half years for a patient with a tumour to be correctly diagnosed. During that time, the average patient visits their GP 11 times. Because the cancers can occur anywhere in the body and the symptoms are often non-specific, they are frequently dismissed as more common conditions such as irritable bowel syndrome, asthma, the menopause or anxiety. I hope somebody somewhere is taking a list of all the conditions that get confused with menopause, because I think it is quite a long one. Many patients, including the three who came to visit my office, look perfectly well, even while harbouring the disease. The consequences are severe, however. Over half of all patients are diagnosed at stage 3 or 4, when treatment options are more limited and the cost to the NHS is significantly higher. Neuroendocrine Cancer UK estimates that it costs between £200,000 and £300,000 more per patient when treating at a later stage rather than at an early one. Currently, the UK has 13 accredited centres of excellence, including a specialist team in Edinburgh and an accredited centre in Glasgow. Those hubs deliver multidisciplinary, evidence-based care that is proven to improve survival rates—yet access remains a postcode lottery. Whether a patient is in rural Scotland or in a coastal town in England, the quality of care they receive should not depend on whether their local hospital happens to have a neuroendocrine lead. In Scotland we see a stark divide between our urban hubs and our rural communities, whereas in England the access issue is more related to the divergent priorities of different cancer alliances. In both cases, patients suffer because we do not have a standardised diagnostic pathway for everyone. The closest we have to a standardised service, which all neuroendocrine patients can access, is the one that is offered by Neuroendocrine Cancer UK. It provides a critical safety net, offering helplines, counselling and peer support, and it regularly steps up to fund the small-scale, early-stage studies or trials that are needed to get research off the ground. It is sobering that 95% of Neuroendocrine Cancer UK’s income comes from community generosity. It delivers system-critical services that support the NHS, yet it does so with almost no statutory resourcing. In closing, I ask the Minister to address five specific priority areas. The first is clinical awareness. May we embed neuroendocrine cancer into primary care training and early diagnosis initiatives to stop these patients being lost in the system for years, perhaps reducing the number of GP appointments needed before a diagnosis? The second area is clear pathways. As I mentioned previously, we need to tackle the postcode lottery when it comes to treatment, and the only way to do that is through a nationally recognised diagnostic and referral pathway to centres of excellence. Will that be considered? The third area is the guidance gap. Currently, the NG12 guidance is critical to cancer diagnoses in England and Wales. Neuroendocrine cancer is not included in that guidance. May we review whether there could be a way to include it? The fourth area is data and visibility. Neuroendocrine-specific cancer data is not routinely published. We need that to accurately track the incredible rate at which cases are rising and our response to that. May we also ensure that more data is published more regularly? The fifth area is research equity. The issue of funding for research into rare cancers was one of the key asks that charities raised with me when I was consulting on my Bill, which is now the Rare Cancers Act 2026. What more can we do to ensure that the Government are using all the mechanisms at their disposal to stimulate research in this rare cancer and all the others that currently fall through the cracks of major funding streams? In summary, earlier recognition, clearer routes to specialist care and access to life-changing drugs have the protentional to transform outcomes. I look forward to hearing the Minister’s plans to make that a reality.

• 15 Apr 2026 · Strategic Defence Review: Funding · Hansard source

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  I am proud to be part of a Government who are building ships in Scotland, whereas our Scottish Government colleagues are building ferries in Poland, Turkey and now China. Quite incredible. Mr Speaker, you will be pleased to hear that I always use security guards at my surgeries, and a young chap who attended my surgery last year in Oxgangs library had just left 3 Rifles. He said he had left because he had joined some years ago on the promise of travel and excitement but spent a lot of time in barracks because of the lack of funding in our armed services. The last time I visited 3 Rifles, they had just come back from Finland, and some were about to go back there to serve alongside our allies. Some were due to go to Iraq, but I understand that that trip might not have happened. They are all now better paid. Outside the barracks site, people can see their homes getting renovated, and I have to say that there is a bit of jealousy about the quality of the kitchens. Recently, just before the recess, I was able to give a tour to a young apprentice from one of our defence primes who lives in Balerno in Edinburgh South West. She was very clear that this was not an apprenticeship or a job; it was a whole career that she had before her, because of the scale of what is happening in the sector. When the Minister goes around our defence establishments and our defence contractors, what is the mood? Do they trust us to deliver against this budget commitment?

• 14 Apr 2026 · “For Women Scotland” Court Ruling: First Anniversary · Hansard source

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  I know this is a really important subject to the hon. Lady. Of course, the Government received the revised draft guidance only yesterday and they issued a statement today. It is important to remember that. The hon. Lady mentioned parkrun a minute or two ago, before the flurry of interventions. What does her vision mean for me, as a keen parkrunner? Would I have to submit evidence that I am a man to parkrun in order to run as a man? Likewise, would women have to do the same? How does she see that working?

• 13 Apr 2026 · Diego Garcia Military Base and British Indian Ocean Territory Bill · Hansard source

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  I thank the Minister for working over many months with our allies on this issue to reach agreement in our national interest and theirs. He has remained consistent on this issue and has given many updates on it. I wish I could say the same about the Opposition. Their short memory, their flip-flopping and their complete disregard for national security are very similar to the position they have got themselves in with Iran—very, very similar. They are laughing in the face of real threats to our national security. I am actually quite concerned, because it seems to me that the status quo is not in our national interest. What does being without a treaty mean for the long-term access to the base, for us and for our allies?

• 13 Apr 2026 · Statutory Menstrual Leave · Hansard source

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  The hon. Lady has done a great job of outlining the changes to workers’ rights in terms of sick pay. Can she confirm that her party voted against those measures? She has explained the benefit to women with these conditions, but the hon, Lady’s party absolutely opposed those measures.

• 13 Apr 2026 · Statutory Menstrual Leave · Hansard source

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  You will not be surprised to hear me say, Mr Mundell, that it is a pleasure to serve under your chairmanship. I thank my hon. Friend the Member for Colne Valley (Paul Davies) for the way in which he introduced this debate, and other hon. Members for the excellent speeches that followed. I recently met a constituent who lives in Chesser and has adenomyosis. During our meeting, she told me about the debilitating impact of the condition on her personal life and her work life, and it was a real insight for me. On some days, her pain is so severe that she struggles to walk or move around her home, even to reach the toilet. She also reminded me just how common endometriosis and adenomyosis are: given that around 10% of menstruators suffer from one of the two conditions, there could be thousands of people in Edinburgh South West who currently suffer from the regular and excruciating pain that they cause. Although my constituent now has an employer who understands and accommodates her health needs and allows her to work from home or take leave for her condition, that has not always been the case. She recounted the degrading experience of having to explain her health issues in detail to a former employer, just for taking time off. Despite that, she was still given a written warning. It is such inconsistency among employers that motivated her to sign the petition and to meet me to ask, very politely, that I attend this debate on her behalf. As we have already heard, up to one in six women with endometriosis have to leave the workplace due to their condition. For some women, that will be because they really cannot work due to the pain they suffer. Sadly, for other women, who can work and want to work, it may come down to a lack of accommodating workplaces. We have to be honest about that situation and say that it is discrimination. I recognise the Government’s position that the provisions of the Equality Act 2010 should ensure the flexibility that is required for women affected by these conditions to take leave or for adjustments to be made for them. However, laws are only useful if they are respected and enforced. None the less, I hope that the reforms introduced in the Employment Rights Act 2025, including statutory sick pay, will ensure that further accommodations can be made. I hope that the Minister will give some guarantee today that the Government will look at menstrual leave schemes abroad to inform the evidence-based best practice that we need in the UK. I also hope that the Government will do what they can to support businesses or organisations that decide to introduce such practice in the interim, simply because it is the right thing to do. I must be honest and say that I had not heard of the endometriosis-friendly employer scheme before, so it would also be interesting to hear what the Government are doing to support that scheme. The data from the schemes implemented abroad show that they are unlikely to be abused. Although the petition we are discussing today relates to the scheme in Portugal, the introduction of a similar menstrual leave policy in Spain has not led to an avalanche of sick days being taken as a result. Although I know there have been some concerns about how easy it is to access that scheme, the Spanish allowance has been used just 1,550 times. It will hardly have a significant impact on the Spanish economy, but it will be a huge benefit to the women who are able to access it. Equally, such schemes can help employees avoid having repeatedly to justify in detail absences that they require. With the Portuguese system of requiring only one initial confirmation of diagnosis, employees will likely be spared uncomfortable and degrading conversations with superiors and work colleagues about this medical condition. I hope the Government will look to the positive impact of those schemes abroad and build up best practice for the UK. I want to make one last point: when I spoke about this debate on my Facebook page, many women who responded said that they were keener for GPs to be better informed about the condition, and for diagnosis to happen much quicker. I could not believe it took just over nine months for a diagnosis to take place—

• 13 Apr 2026 · Statutory Menstrual Leave · Hansard source

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  Nine years—apologies. It took just over nine years for a diagnosis to take place, given the pain we have heard about. We have heard in this debate about the real human impact that delay causes. That must be impacting our economy too, so I hope the Government will commit to studying the effect of these conditions on the economy, and perhaps that will justify action in this domain.

• 24 Mar 2026 · Oil and Gas · Hansard source

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  Will the hon. Lady give way?

• 24 Mar 2026 · Oil and Gas · Hansard source

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  As ever, the hon. Lady speaks with great passion on this issue. She started by talking about Jackdaw. She must recognise that her party made a complete mess of that, which is why it is completely shrouded in uncertainty just now. She blames the Government and suggests that Labour is to blame, but it was her party, was it not? Is it not a quasi-judicial decision rather than a decision for the Minister?

• 23 Mar 2026 · Puberty Blockers Clinical Trial · Hansard source

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  I believe that a trial for puberty blockers is necessary, and I am hopeful that the issues raised between the MHRA and King’s College can be resolved to allow the PATHWAYS trial to go ahead. If not, I hope an alternative trial can be proposed. I believe that if we accept that trans people exist and have rights, which I think—or at least hope—everyone here does, such trials are a natural consequence. I understand the concerns the people here and outside this place have about the long-term medical impacts of puberty blockers. That is why we should act cautiously and it is why a trial is needed. We cannot possibly understand the short or long-term impacts without studying puberty blockers properly. The PATHWAYS trial came about because of a lack of conclusive evidence on the use of those drugs. The answer is not to allow their legal use again, but to undertake a trial into their benefits and consequences. Not long ago in my constituency, I met the parents of a trans woman. Their daughter struggled significantly with her mental health during her teenage years. At one point, she was hospitalised due to complications from a severe eating disorder, which was driven by her decision to reduce her calorie intake because she thought that would delay puberty. Her parents have told me that they believe a big cause of her issues was her inability to express her true gender identity. They have no doubt that puberty blockers would have saved her from some of the anguish that she has experienced. While I know life is not always easy for her, my constituent’s daughter has since medically and socially transitioned; she lives openly as a woman and is happier as a result. That story shows the profound impact that a struggle with gender identity can have on a young person. It is offensive to talk about young people simply needing love, to talk about trials being experiments, or to suggest that taking part would be an impulsive decision by anyone. People talk about trying to moderate language; we have a duty to bring people together on this topic, not create division.

• 11 Mar 2026 · Lord Mandelson: Response to Humble Address Motion · Hansard source

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  I thank the Minister for his statement and also for the tone in which he has brought it here today. It has been quite an open statement in terms of the discussion. As a Government, we are serious about the whole agenda of violence against women and girls, and I just cannot conclude that giving Mandelson £75,000 is compatible with that, so I hope that he repays it. Constituents in Edinburgh South West are really concerned about Epstein’s links into the British establishment, particularly given the allegations against Mountbatten-Windsor and Mandelson himself. I know that a live court case and investigation are under way, but can the Government commit to a public inquiry into Epstein’s links into the British state, once these court cases are over?

• 9 Mar 2026 · Social Cohesion Action Plan · Hansard source

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  Thank you, Madam Deputy Speaker, I think we are easily confused. Yesterday I attended Open Heavens church in Wester Hailes, and a man told me how he had faced open racism from his colleagues and had been forced to resign, take his employer to court, and win his tribunal—a fantastic achievement. It was a shameful episode, but what made it worse was that he was an NHS consultant, and it was the NHS that he took to court. The point he made to me on the floor of the church was that too often society views hate as a series of events, rather than a culture. Will the Secretary of State confirm that what he has presented today will result in a change of culture, rather than simply addressing events? How will we measure that as we proceed through the remainder of this Parliament?

• 9 Mar 2026 · Middle East: Defence · Hansard source

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  I want to start by paying tribute to Edinburgh’s Iranian community. Despite being concerned about their families in Iran, they have taken time in the past week to host public events, which shared details of Iran’s rich culture and the barbaric nature of its regime. I want to ask a question about HMS Dragon. The maths are quite clear: the ship cost £1 billion, but the Conservatives cut the defence budget by £14 billion. Surely, if they wanted to see more destroyers in the Mediterranean, they should have built the things.

• 26 Feb 2026 · Eating Disorders Awareness Week · Hansard source

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  Before we move on to end-of-life care, I welcome the great offer that the Minister has given to reach out to the Department for Science, Innovation and Technology to better understand what they are doing on digital platforms. I expect that many of the people who are going to respond to the consultation around the banning of social media for under-16s will come from the healthcare profession, because of the connections between mental health and eating disorders and the use of these platforms. Will he be proactively asking for action to make sure that young people are protected? That would also mean more resources for people who have eating disorders, because hopefully fewer people would be coming forward.

• 26 Feb 2026 · Eating Disorders Awareness Week · Hansard source

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  The workforce plan is key to resolving that, although I do not know an area in the NHS that has too many staff and wants to redistribute them. It is a huge challenge and we have to address it. Again, the starting point is to acknowledge that there is an issue and offer staff support where we where we can. I raised this issue with NHS Lothian’s chief executive because—this was partly me exploiting my position— I had a close family member who had been dealing with an eating disorder. She was given an appointment to meet the service, and I was so frustrated, because it was months and months into the future. I waited patiently— I am a patient person—and my hope built up and up as we got closer to that day, but when we reached it, and my loved one went to the appointment, it was merely an assessment of whether a person needed proper support. I felt completely deflated. Hopefully, people are not still going through that. In these times of crisis, it is all too often communities and families who are left to step up to provide what care they can. I have met parents in my constituency who are doing their absolute best for their children. I met one woman—another anecdote, I am afraid, Ms Vaz—who told me that her daughter was so weak that she had to phone an ambulance to take her to hospital. When her daughter arrived at the hospital, the medics said she was too weak to be removed from the ambulance and had to treat her there. The nature of the condition can often be secretive and very hidden until it is—hopefully not—too late. Parents doing their absolute best is not enough, and professional medical help is required. Both the UK Government and the Scottish Government must go further to ensure that treatment is more readily accessible for those who can no longer rely solely on the support of their loved ones—I will come back to that. However, when considering the idea of community around eating disorders, we must also consider the online world and its ability to create a space for more dangerous communities. Pro-eating disorder content, as referred to by the hon. Member for Bath, exists across the internet, from independent forums to social media sites that we all use daily. Those groups or posts provide “thinspiration” and tips on how someone can starve themselves or make themselves throw up. They glamorise the awful illness that eating disorders are, introducing them to previously well children and young people who might not have considered them, exaggerating conditions and sometimes normalising them. This became particularly concerning during the pandemic, where we also saw a massive growth in eating disorders among the male population, as many young people were left isolated from their peers, turning to online communities. Instead of support, all too often they found content that damaged their mental health and isolated them further from the people around them. It is hard to understand just how disturbingly common such content is. Figures from April 2025 show that more than a quarter of young people have been exposed to eating disorder content online, which is likely an underestimation. That sits alongside the one third of children who have seen self-harm and suicide content online. Social media sites are feeding young people this content from a never-ending algorithm, which we also heard about from the hon. Member for Bath. More children are likely to consume the content because of social media and its algorithms. The more they continue to see such content, the more they consume it, and the more they consume it, the more they continue to see it, creating a greater relationship with those harmful online communities. The proliferation of this content is the result of passivity from tech firms, and in part, their profit motives. One study shows that Meta derives an annual $2 million in profit from pro-eating disorder content on Instagram. With content creating such profits, it is hard to see why social media sites would have ever self-regulated to ensure that content was hidden from children. I met Meta this week, not to talk explicitly about eating disorders but to talk about the proposed ban on social media for under-16s. I can see that it is something the company feels challenged by, because it is concerned about a loss of income—not from people under 16, but from losing them as users as they move into adulthood. I hope, perhaps blindly, that there is an opportunity to work with those companies to ensure that the ban works properly. I support a ban on under-16s’ access to social media, and I know that my constituents do as well. We must also work with charities in this sector to make sure that the ban works. I welcome the Online Safety Act and its commitment to ensuring that children see less harmful online content. Many constituents have contacted me since the summer raising concerns about the Act and what it means for their use of the internet as adults—often men, as hon. Members may not be surprised to hear. I understand the wider flaws, which I think were raised by the hon. Member for Bath when she spoke about their impact. While it is not perfect for eating disorders and suicidal ideation content for children and young people, it adds quite a lot of friction and makes it harder for young people to access that content. The Act is not perfect, but it is definitely a step in the right direction, and is a key part of protecting young people and reducing their exposure to harmful content, including eating disorder content and other negative influences. I have only one more anecdote, you will be glad to hear, Ms Vaz. When I googled content about eating disorders and the Government policy on the train this morning, I was pleased to see Google was good at putting a warning in place, telling me that I might want to phone a particular helpline or contact a particular service to talk about eating disorders if that was why I was googling them. I was impressed by that and it is a good example of how tech companies, while they are quite often the bad guys, can do good stuff in this space as well. We must continue to ensure that communities supporting those with eating disorders are supported by proper medical care where necessary, and do all we can to remove harmful content. I am sure this is not the first time that the Minister has attended a debate in Westminster Hall, or even in the main Chamber, in which the Government have been asked for a strategy, more staff and greater clarity about what they do. I know that he cares about this subject and that the Government are doing work in this area, but the calls for a strategy make sense because it would help to pin that work together and give us clarity about the next steps. I look forward to hearing the Minister sum up.

• 26 Feb 2026 · Eating Disorders Awareness Week · Hansard source

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  You will not be surprised to hear that it is a pleasure to serve under you in the Chair, Ms Vaz. I thank the hon. Member for Bath (Wera Hobhouse) for the way she introduced the debate and for her leadership of the APPG on eating disorders. I join her in thanking Hope Virgo for all the work that she does. In many ways, eating disorders can be a hidden condition—even a secretive condition—but Hope really does give the topic the publicity that otherwise it would not get. Hope has been through a lot, and I would not wish what she has been through on anyone, but we are lucky that she is the campaigner she is.

• 26 Feb 2026 · Eating Disorders Awareness Week · Hansard source

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  Absolutely. I do not attend the APPG as much as I should, but when I do people tell amazingly personal stories about what has happened to them, not only as survivors but as people who have lost loved ones. It can be very emotional for people, but it is important that we share the stories and experiences. I thank my hon. Friend the Member for Isle of Wight West (Mr Quigley), because he has been a fantastic champion in the House of Commons. I am surprised that he is not here, but I expect he has a good reason. Maybe he is watching. I want to focus on the role of community. We are trying through the APPG to create a sense of community. We all accept that proper community support is hugely beneficial to those with mental health issues generally. Through my membership of the APPG, and my work as an MP more widely, I have become much better informed about what community looks like for those with eating disorders. The support of a community, whether it be family, friends, school or a support organisation, is a wonderful thing for anyone struggling with their mental health. It is so often the first support network that someone will reach out to, and families and friends are there to catch their loved ones in the most difficult times. Community care is often the best approach to eating disorder care. Beat’s “There’s No Place Like Home” report highlights the importance of expanding access to intensive community and day treatment for eating disorders. In many cases, it could be a lifeline for those struggling, allowing them to access a support network nearby, rather than being sent to treatment facilities sometimes hundreds of miles from their homes. However, effective community care can seem a long way off when the existing services for eating disorder treatments are so stretched right across the UK. I want to talk a little bit about Scotland, given that my hon. Friend the Member for Glasgow South West (Dr Ahmed) is the Minister. The crisis in young people’s mental healthcare in Scotland is acute. CAMHS in Scotland are overwhelmed, and constituents contact me every week about their difficulties accessing services. My staff have to tell me to be careful not to raise people’s expectations, because the service is so overwhelmed. I have met staff who work in CAMHS and they are working so hard. I pay absolute tribute to them. They just need more resources. I spoke to the chief executive of NHS Lothian specifically about the support for people with eating disorders, and she was very frank. She had just come into post and said that she thought the service was at the absolute minimum acceptable level. Perhaps I should not have welcomed that, but I did, because the starting point for fixing a broken system is to accept that it is not working. I welcome the fact that she did not try to gloss over it.

• 26 Feb 2026 · Eating Disorders Awareness Week · Hansard source

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  I thank the hon. Member for giving way—I have to say that she is one of my favourite Tories. Does she agree that there is a real inequality here? A one-hour car drive is a challenge, but if someone does not have a car, it is even more difficult. If they have a child, they might have to take a day off work to take them somewhere. So getting services, or capacity in the community, closer to people should absolutely be the ambition, shouldn’t it?

• 25 Feb 2026 · Post Office Green Paper · Hansard source

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  In a previous statement, I learned that the directly managed post office in Wester Hailes in Edinburgh South West was to close. It was a really concerning time for the community, but Mohammed Arshad and his sons Aamir and Adam stepped up and absorbed the service into their shop, Plaza News. Residents now have longer opening hours in which to access services, and they can do their banking, pay bills and get their passport checked. It is the most British of places; people queue to send their parcel via Royal Mail, Parcelforce, DPD or, if they are feeling brave, Evri, while browsing wool, knitting needles and knitting patterns in the aisle. It is a fantastic place. While news of the transition was concerning, particularly when it first broke, I really think that the community has ended up in a better place. Can the Minister reassure Mohammed and his sons that what has been announced today will enable them to serve their community more, rather than less?

• 24 Feb 2026 · Gaza Healthcare System · Hansard source

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  I thank the hon. Gentleman for giving way under time pressure. He has mentioned Hamas twice. It is an absolutely awful organisation and I want to see the end of it, but he must accept that Netanyahu has some role to play in the crisis and has to take ownership of the problem as well.

• 24 Feb 2026 · Online Harm: Child Protection · Hansard source

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  It is not just impractical; it is also anti-democratic. As Bills proceed through this place, there is interaction with our constituents who want to influence how we are thinking and how we are voting, so it is important for us to have time to discuss these matters with them as well as in the Chamber.

• 24 Feb 2026 · EU Membership Referendum: Impact on the UK · Hansard source

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  I thank the hon. Member for Arbroath and Broughty Ferry (Stephen Gethins) for the way in which he introduced the debate. He did forget, though, in his recollections, that we could have had a customs union if he had not abstained on that decision, along with his 35 SNP colleagues. That is a simple fact. Perhaps he can address that in his winding-up speech. One of the challenges we face as a country is that so many people in the UK feel left behind. They still feel the impacts of the banking crisis and of covid. Both were once in a lifetime but have been exaggerated and amplified by Brexit. The Brexiteers told us that all we needed to do to set our country on a wealthier path was to get rid of the Europeans. I have to say that it is very similar to the argument we hear from Donald Trump about Mexicans and also the argument we hear from the SNP about getting rid of the rest of the UK. All three are wrong for exactly the same reasons. Now the same Brexiteers tell us that all we have to do to set our country on a wealthier path is to get rid of immigrants—to other them. Again, that is not correct, particularly when we remember that there are about 350,000 immigrants working in our NHS. We all know that the route to prosperity is to work more closely with our biggest trading partners, and for us that is the European Union. I am proud that this Government have taken us in that direction. I do hope that one day we rejoin the EU, but I do recognise that, as others have hinted, that has to come after a manifesto commitment and a referendum. It is not something that any of us want to rush into right now, but I welcome the fact that, day by day, we are getting closer to our European partners.