Richard Quigley

IN THEIR OWN WORDS

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291 held · 283 searchable for Richard Quigley. The searchable lines are below in date order, each linked to its source. Free to read, in full, without an account. Page 4 of 6.

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1. “Following the work of the eating disorders all-party group, I was horrified to hear that 19-year-old Lilly Cliff, who suffers from anorexia, has been placed on an end-of-life care pathway, after Rotherham, Doncaster and South Humber NHS foundation trust obtained a Court of Protection ruling to withdraw her treatment. The decision directly contradicts guidelines from the National Institute for Health and Care Excellence, and the statement from the Minister for Care in September that eating disorders are not a terminal illness. Will the Prime Minister urgently review that case to ensure that Lilly and her family receive the support they need, and that Lilly is given every possible chance to recover and live, and remind all integrated care boards, the NHS and hospitals, that suffering from an eating disorder is not a terminal illness?”

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2. “The Government’s pride in place programme presents a welcome opportunity for communities across the country to once again feel proud of where they live, especially after years of austerity and neglect under successive Conservative Governments. However, the Isle of Wight received none of that funding, which feels like an oversight, given the challenges our island faces, not least with cross-Solent transport. Will the Chancellor assure me that she is doing everything possible to ensure that islanders are not left behind and that they, too, can benefit from this programme and feel pride in our island once again?”

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3. “But we should demand more, because this is about protecting the NHS, which will ultimately pick up the bill when those clinics fail, and it is about protecting families like Zoe’s from the grief of a tragic and unnecessary death. I thank the Minister for her engagement, and I am genuinely encouraged by the seriousness with which her Department has adopted the issue. Zoe’s family has said that they feel they have got further than ever before over the past weeks, and that they feel listened to. I thank the Minister very much for that, but this can only be the start, and whatever form Zoe’s law eventually takes, we must not stop until we get there.”

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4. “If we combine them with specific melanoma training for all professionals who encounter skin lesions, and encourage GPs and others to take up that training, that approach could significantly improve early detection and reduce the need for costly and often unsuccessful late-stage cancer interventions. Cancer is not a place to cut corners. Although they are not mandatory, histology tests are already routine practice for benign moles and other lesions in both NHS and private dermatology alike. Zoe’s law would ensure that a similar safeguard is applied across the board, from NHS hospitals to private dermatologists and beauty clinics. That would demand more from the clinics that are currently the least regulated.”

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5. “NHS doctors order these tests as a matter of routine, and many good private dermatologists insist on including a biopsy before agreeing to treatment in the first place. The tests are relatively cheap, with lab fees around £100. To put that into perspective, the cost of Zoe’s cancer treatment could have funded over 650 biopsies. Using state-of-the-art technology, we could go further. Trials are under way for handheld equipment that can test for melanoma by using artificial intelligence systems to analyse high-definition photographs of skin lesions. If those trials prove successful, the cost of Zoe’s treatment could have funded thousands of pre-treatment checks. The checks are cheap, immediate and, with proper training, could easily be deployed in beauty clinics and other non-medical environments.”

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6. “We are not here today because Zoe’s family want to cast blame; we are here because Zoe’s family want to make sure that what happened to their daughter, their sister and their mother will never have to happen to anyone else again. The safeguard we are asking for is simple: that all healthcare providers must test the lesions they remove. This extra check—a “Zoe check”—would prevent tragedies like Zoe’s from occurring. Over the past months I have spoken with a range of doctors across the NHS and in the private sector, and reassuringly—although it is not mandated—what we are asking for is already standard practice in the NHS for GPs and dermatologists. To avoid that one in a 1,000 case, removed skintags, moles or blemishes, however harmless they look, are almost always sent for testing.”

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7. “Zoe even paid for her mole to be tested after removal at the beauticians, yet it never was. There is no doubt that Zoe was failed by her GP, who sent her a letter of apology after learning of her diagnosis, and that Zoe was failed deeply by her beautician, who failed to recognise her cancer or even to send her mole for testing. Zoe’s concerns should never have been dismissed, she should never have been referred out of the NHS, and the mole, which was actually a melanoma, should never have been removed. I welcome the fact that the Minister has enacted Jess’s rule, meaning that on the third time of asking, Zoe’s concerns may have brought about a different outcome.”

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8. “She then realised that the small mole on her back was the root of her cancer. Zoe died just 55 days after that diagnosis, and in those 55 days she had to try to explain to a five-year-old and a seven-year-old that mummy would soon not be coming home, and would instead become an angel. I do not bring that up purely to cause upset, but to emphasise Zoe’s outstanding bravery at such a young age in ensuring her boys were prepared for the unthinkable. Zoe had not ignored her symptoms; she did everything right. She visited her GP on three separate occasions asking that her mole be tested, yet she was told that her pain was caused by the mole rubbing against her jeans, and that she was too young for it to be clinically concerning. On her third visit, Zoe was told that if it bothered her that much, she should get her mole removed cosmetically.”

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9. “Despite her age, Zoe made a remarkable impact on our community. She volunteered as a carer, and later trained to become a radiologist at St Mary’s hospital. That is what makes Zoe’s story so heartbreaking. While she was dedicating herself to caring for others, her own health concerns were repeatedly dismissed. On the morning of Zoe’s eventual diagnosis, she woke up in pain, but brushed off her concerns, telling her mum that she had been teaching her boys how to do roly-polies—which many Members will know is, as an adult, no mean feat—and must have hurt herself that way. But that evening Zoe was in such excruciating pain that she was taken to hospital where, upon being tested by her boss at St Mary’s, she was told that her liver was full of cancer. Doctors asked Zoe whether any moles on her body had been causing her concern.”

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10. “I beg to move, That this House has considered histological testing of excised moles. It is a great pleasure to serve under your chairship, Ms Jardine. Many of those present may not yet be familiar with the name Zoe Panayi. If they are, it is likely to be because of my hon. Friend the Member for South Norfolk (Ben Goldsborough), who spoke about Zoe at Prime Minister’s questions two weeks ago. For Zoe’s family, the five years since her tragic death have meant that their daughter, sister, mother and friend has come to represent something far greater—a legacy that continues to grow and touch lives beyond their own. I welcome Charlie, Zoe’s brother, to Westminster Hall today. Zoe was like so many other 26-year-olds. She was a devoted mother to her two boys, a loyal friend to many across the island and a young woman full of promise.”

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11. “I thank him for his commitment to this cause, and for the support and extremely generous amount of time that he has given me. We need to make this safeguard a reality so that what happened to Zoe is never repeated. Question put and agreed to . Resolved , That this House has considered histological testing of excised moles.”

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12. “That is a small step with a profound impact—one that could save lives, reduce the burden on the NHS and spare families unimaginable grief. The cost is not preventable: the technology exists and the reason is clear —cancer is not a place to cut corners. I know that all the contributions we have heard today mean such a lot to Zoe’s family, her brother Charlie, and mum Eileen watching at home. We must not forget the human tragedy behind this story: the children who have lost a mother, the family who have lost a sister and a daughter, and the community who have lost a friend. That is why Zoe’s law is so important. I urge the Department to continue working with Zoe’s family, with me and with my hon. Friend the Member for South Norfolk (Ben Goldsborough), who has shared so much of his own journey, making such a difference.”

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13. “I thank the Minister for her remarks. I do not think anyone would question her passion and commitment to this cause. I thank her for previously sharing her own diagnosis. It is important that people understand that cancer can affect anybody. I thank my hon. Friend the Member for Neath and Swansea East (Carolyn Harris) and the hon. Member for Bath (Wera Hobhouse)—and it would not be a debate without the hon. Member for Strangford (Jim Shannon) making some contribution. Zoe Panayi did everything right. She sought help and she trusted the system, and yet the safeguards that should have protected her did not. That is why this debate matters. Zoe’s law is not about blame; it is about prevention. It is about making sure that every mole removed is tested.”

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14. “T8. I welcome the changes in the GP booking system, but in many cases it is still very difficult to obtain a GP appointment on the Isle of Wight. A large factor in that is the difficulty of recruiting GPs to the island. Will the Minister assure me that he will investigate all options for improving GP recruitment to coastal, rural and island communities, like mine?”

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15. “The UK is committed to growing our wind energy manufacturing capacity, but this requires investment in innovation to develop the next generation of products that could be made in the UK, using expertise that exists in places like my constituency of Isle of Wight West. Can the Minister assure me that the Government are doing everything possible to provide the funding to not only create jobs but provide sovereign ownership of blade technology and development in the UK, so that we become a true energy superpower?”

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16. “The Government were elected with a phenomenal majority, winning places we never thought possible—including my own constituency of Isle of Wight West—on a platform of meaningful change. If we do not use this moment to do the right thing and acknowledge that children in mental health services need their parents more often than not, I fear that we may never get another chance.”

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17. “In fact, the cross-party support I have received, including from the right hon. Member for Salisbury, reflects how uncontroversial they are. The Minister and I have had robust and constructive discussions on the matter, but I ask him to confirm that he will do everything in his power to ensure the following. Parents must not be shut out of their child’s care, as evidence shows that regular parental contact enhances care outcomes. The placement of children on adult mental health wards under the Mental Health Act must be limited strictly to exceptional circumstances, and practitioners must be actively compelled where appropriate to involve themselves in the development and delivery of a child’s care and treatment plan. We have a duty to ensure that the tragic circumstances surrounding Ruth’s death are never repeated.”

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18. “I genuinely struggle to understand why our clinical consensus around mental health continues to support a model where already vulnerable children are isolated from their parents—the very people who know and love them most. Children on these wards are treated as wilful—they are not; they are children—and without empathy or sympathy. Many consultants we encountered opted not to apply the National Institute for Health and Care Excellence guidelines. Staff were poorly trained and in fear of psychiatrists, who ruled the roost and prevented people from speaking up. The private equity firms are focused not on long-term treatment but just on turning mental health into money. My amendments do not seek to undermine the Bill’s strengths, nor the important work undertaken by the Department.”

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19. “That is the problem with NHS-funded private provision: even at £900 a night, the operators plead poverty. My wife and I have two vivid memories of our youngest being prised from us without any warning. We thought that was normal. Six months of nasogastric tube feeding—we thought that was normal. Illegal restraint so bad that it caused post-traumatic stress disorder—we thought that was normal. Forgetting to feed our daughter 11 times—we started to realise that that was normal, but not acceptable. Instead of wishing to improve its practice, the hospital has accused me of making this up. If a child is facing any other physical illness such as cancer, or even something more short-term that requires a hospital stay, parental visits and involvement are quite rightly seen as a means of enhancing care.”

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20. “Ruth was admitted to an in-patient facility for treatment of an eating disorder, but instead of receiving the care she needed, her family were shut out and allowed only two two-hour visits per week. They spent more time travelling than they did with their daughter. Ruth was just 14 years old when she fatally self-harmed, just five months into her stay. Three months from that date, my family were faced with the same hospital, Huntercombe, as the only choice of a bed for our daughter. At that same hospital, when a child asked if they could have an extra type of jam for breakfast in the morning, they were told it did not have the budget, and when asked why Minstrels were no longer part of snack time, they were told that they were eating too many.”

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21. “I will speak to new clauses 28 and 36 and amendment 39, which I tabled not just as an MP but as a father. After what my family have been through, I believe that any parent would do the same. Yesterday, alongside the right hon. Member for Salisbury (John Glen), I had the privilege of hearing Dr Kate Szymankiewicz speak about her daughter Ruth. She shared not only the tragic circumstances of Ruth’s death but the type of person Ruth was: her dream of becoming a vet, her kindness, and how friends described her as a character straight out of an Enid Blyton novel. That is the Ruth her family remember and cherish. As parents, we became part of a world we never wanted to know. I am privileged to have met Kate, but we agreed that we wished our paths had never crossed because of what that meant.”

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22. “It is also important to realise that any imposed switch-off would not have a limited impact; it would be deeply felt across our communities. The reality is that some people would be left behind, and many people would feel a greater sense of entirely avoidable social isolation. This shift is not just a technical one, but a social one. If we move too quickly or without providing proper support, we risk entrenching inequality, whereby access to media and public service content becomes a privilege available only to those who can afford it. Terrestrial TV helps to level the playing field. It ensures that everyone, regardless of their income or their location, can stay connected to other people around the world—and that is worth protecting.”

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23. “Additionally, I worry that any decision to switch off terrestrial TV could further exacerbate the cost of living crisis and deepen existing inequalities in our communities. I know that not everyone on the Isle of Wight has the means to afford high-speed internet or multiple streaming subscriptions. For many households, especially those on fixed incomes or struggling with rising bills, terrestrial TV is not just a preference; it is a necessity. Asking such families to transition to online-only services could mean they face additional costs of hundreds of pounds a year, not only for subscriptions but for upgraded devices and internet packages. That is a burden that many of those families simply cannot bear, and it is imperative that we do not impose it on them.”

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24. “For such households, terrestrial TV is not a back-up; it is their primary connection to news, entertainment and public service content—and not just reruns of “Mrs Brown’s Boys”. That is especially true for older residents, those in rural areas and families facing financial pressures. As hon. Members have already said today, terrestrial TV is free, reliable and accessible. It does not require expensive subscriptions or high-speed internet. It just works. At a time when loneliness and isolation are growing, it plays a vital role in promoting wellbeing, inclusion and a sense of community. Three quarters of people say that terrestrial TV has helped to reduce loneliness, and among those aged 65 and over the figure rises to 87%.”

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25. “It is a pleasure to serve under your chairmanship, Mr Twigg, and I thank the right hon. Member for Dumfriesshire, Clydesdale and Tweeddale (David Mundell) for securing this important debate and for the hard work that he has already put into this area. I am very pleased that broadband coverage in my Isle of Wight West constituency is improving—it was at 94.2% in 2022 and is projected to reach 99.4% by 2040—thanks to our very own fibre company, WightFibre. However, actual take-up tells a different story, and it is one that we cannot ignore. Only 63.5% of households were using high-speed broadband in 2022, and even by 2040 only 76.1% of households are expected to be using it. That means that in 15 years’ time, nearly a quarter of households still might not be online.”

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26. “Does the hon. Gentleman acknowledge that, under the Tories, a pub closed every 14 hours? That was 10,000 in total, so whether it is 14 hours or 14 years, the Tory party cannot be trusted with the economy.”

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27. “Unlike most, if not all, of the Conservative Members listed on the Order Paper as supporters of the motion, my wife and I own two successful hospitality businesses. We welcome the increase in national insurance contributions and the improvements in workers’ rights because they are good for our employees, our businesses and our customers. Does the Minister agree that the Tories only know how to race to the bottom and not how to give workers a leg up?”

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28. “We all know by now that the pandemic has taken a wrecking ball to children and young people’s mental health, but we cannot pretend that these issues do not predate 2020. Since the mid-1990s, eating disorders have been found to carry the highest mortality rate of any psychiatric illness. However, in the UK, we are unable even to quantify the true havoc that eating disorders cause, because of the lack of a national register for eating disorder deaths. The most recent year with confirmed data from the Office for National Statistics is 2019, when 36 deaths were recorded. However, a US study suggests that the real figure in the UK could be closer to 1,860 deaths, which I am sure people in this room would more than agree with.”

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29. “From the moment someone becomes a parent, their instinct is to protect and nurture their children—often, admittedly, much easier said than done—yet nothing can truly prepare anyone for the overwhelming sense of powerlessness that comes when their child develops an eating disorder. Eating disorders, in all their destructive forms, are one of the few types of illness where the person affected does not want to recover and they actively work against you. Watching your child struggle not only with the illness but with the very treatments meant to help them is truly something I would not wish on any parent, yet it is the reality faced by thousands of parents, families and friends up and down the country.”

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30. “I beg to move, That this House has considered the matter of the prevention of deaths from eating disorders. It is a great pleasure to serve under your chairship, Sir Desmond. I thank all hon. Members for attending this debate on a topic extremely close to my heart. As hon. Members may know by now, I am the very proud Member for Isle of Wight West and do my utmost to champion the island in this place, but I have brought forward this debate not only as an MP, but as a father who for some years was genuinely fearful as to whether I would see my child reach their 18th birthday.”

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31. “I agree entirely. We are fully aware of the political situation and the condition that the NHS was left in under the previous Government, but the point of today’s debate is not to make cheap political attacks; it is to focus on the matter in hand, which is eating disorders, so I thank the hon. Member for his intervention. With widespread under-reporting, misclassification and inconsistencies across the country, many of these deaths are wrongly recorded as organ failure, masking the true role of eating disorders and preventing us from fully grasping the scale of the crisis, especially among otherwise healthy young people.”

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32. “I thank my hon. Friend for that important point—it does. The loss of a loved one is harrowing enough without the true cause not being recorded. That is why we are calling for a confidential inquiry into eating disorder deaths. Given the concerns about under-reporting and inconsistencies in the data, it is even more alarming to read the findings from the Health Service Journal that revealed that between 2018 and 2023, 19 deaths related to eating disorders could have been entirely avoided. These tragic outcomes are attributed to severe failures in care, including missed or poorly managed safety risks, a lack of specialist knowledge among healthcare professionals and unacceptable delays in accessing appropriate treatment. If I were to ask for a show of hands in this room, I am sure many would be raised on that point.”

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33. “I thank my hon. Friend for his extremely pertinent point. Early intervention saves not only lives but a huge amount in costs to the NHS. I know the vast majority of NHS staff go above and beyond to support patients, often under immense pressure, and many of us here would like to put on record our thanks to them. However, these failures point to a systemic issue.”

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34. “It is true that a lack of understanding among professionals about the severity of the problem contributes to the situation. To have it put down to a lack of collaboration would be infuriating for that parent, as well as truly tragic. We know well by now that early intervention is crucial for identifying and supporting recovery in patients with eating disorders. However, as a parent of someone affected, I must say that has not been my experience on the ground. Hospital admissions for eating disorders have surged, exceeding 30,000 for the first time in 2023-24, which is a 60% increase compared with pre-pandemic levels. While the NHS struggles to meet this growing demand, private equity firms are profiting from the crisis by owning many of the in-patient units the NHS depends on.”

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35. “With integrated, well-resourced and evidence-based treatment, recovery is possible, even in the most severe cases and after many years of suffering. Despite that, coroners, families and communities continue to see too many lives needlessly lost. That should not happen, and it does not need to be that way. Although the facts I have set out today are difficult and harrowing, they must be heard. I also believe, however, that there are reasons to remain hopeful. I know at first hand that the Department, right up to the Secretary of State, is committed to improving outcomes and getting this right. As a Back Bencher, and more importantly as a father, I see it as my responsibility to push for this change to go further and faster.”

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36. “I do not wish to pre-empt the response from the Minister, who I know is keen to make improvements in this area, but I believe that eating disorders must be included in the suicide prevention strategy if we are to meaningfully tackle this worrying trend and stop patients from falling between the gaps in the already patchy world of child and adolescent mental health service provision. The eating disorders APPG and campaigners from Dump the Scales are urgently calling for a confidential inquiry into avoidable deaths of eating disorder patients. Eating disorders are treatable illnesses. They are dangerous and life-threatening when untreated, under-treated or poorly treated. The risk to life is entirely preventable; deaths from eating disorders are not inevitable.”

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37. “That reversal highlights not only the fallibility of such decisions but the danger in labelling eating disorder patients as beyond help. We cannot ignore the fact that eating disorder deaths are most likely to occur due to suicide. Following an evidence session of the eating disorders all-party parliamentary group, one expert stated that their research found that anorexia sufferers are 18 times more likely and bulimia sufferers seven times more likely to die from suicide than the average patient, due to a combination of pre-existing and untreated mental health conditions, early discharge and the physical effects of eating disorder recovery triggering suicidal ideation.”

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38. “Our approach to mental health treatment, especially eating disorders, remains stagnant, outdated and alarmingly resistant to progress. Another deeply concerning issue is how we respond when patients with severe anorexia refuse treatment and are subsequently diagnosed as terminally anorexic, a classification that holds precedent in UK Court of Protection rulings. In such cases, treatment may be withdrawn entirely, resulting in preventable deaths, such as that of a young patient known as BG who tragically died aged 19 in 2022. For those who may argue that treatment will be withdrawn only when a patient is terminally ill, I point to the case of Patricia, previously deemed untreatable by the Court of Protection, only to have the judgment overturned last month—August 2025.”

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39. “My hon. Friend is entirely correct. Our experience of private equity is that it is selective in terms of the patients accepted. It profits from misery. We were put in the awful position of having to choose to send our youngest child to a hospital that had just seen the tragic death of Ruth Szymankiewicz—I take this opportunity to pay tribute to Ruth’s parents. Our second trip to a private equity-run hospital led to them forgetting to feed my daughter 11 times. My hon. Friend’s point is, unfortunately, well made. More concerning still is that I do not believe that our approach to treatment is changing year on year to confront the heightened demand. If these admission increases were associated with a disease such as cancer, the treatment would quite rightly adapt.”

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40. “In many parts of the UK, the treatments available to patients are not supported by evidence and can even be harmful, rather than providing integrated and evidence-based care. Underfunded services and poorly trained staff often leave high-risk patients institutionalised or without any meaningful or appropriate support. The system currently fails to listen to those who matter most—the patients, their families and supporters. Too often, it fosters a harmful culture of patient blaming rather than delivering compassionate, personalised care that supports recovery. We now know that eating disorders do not discriminate, and neither should our services.”

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41. “No matter how much they pleaded for help, it was a constant battle and they never received the support Zara so desperately needed. Zara should never have died of this illness. There was a whole world out there for her and she had so much to give, but ultimately she felt everyone had given up on her. She was only 24 when she died, but she was exhausted and did not know any other way to keep going without support. Unfortunately, Zara’s story is just one of many, and it is a story unfolding for countless others across the country. Behind these tragedies are systemic failures, often overlooked and hidden behind a lack of national data, questionable legal decision making and cost-saving agendas.”

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42. “With each admission, her eating disorder and mental health deteriorated further. During that time Zara was restrained daily, often by a minimum of six people holding her down. She received very little therapy; instead there was a culture of patient blaming and shaming. In the last two years of her life, Zara was crying out for help but no one would listen. The eating disorder unit eventually discharged her completely, handing her over to the community mental health team. Her mum, who is with us today, spent nearly every day taking ligatures off her neck, lifting her down from a wardrobe when she was nearly unconscious, and performing CPR when she was found unresponsive in the shower. Zara’s mum states there was little to no support from the community psychiatrist; her family were left to cope alone.”

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43. “I thank my hon. Friend for her excellent intervention. I agree that this is a family-wide illness. We must reach the point where no one in the UK dies from an eating disorder, where every individual—man, woman, girl, boy—regardless of age, location or clinical classification has access to the support they need when they need it. I want to finish with the story of a young woman called Zara. She was diagnosed with anorexia nervosa in May 2013 and was admitted to an eating disorder unit almost immediately. Instead of being good news for her recovery, that was when the nightmare began. From May 2013 to June 2021, Zara endured 13 in-patient admissions across seven different units, including three years as a continuous in-patient, nearly two of which she spent without leaving one of the units or going outside.”

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44. “I thank the Minister for his response and all hon. Members for their thoughtful contributions. It has been truly heartening. This is the main message I hope to leave today: one death from any eating disorder is one too many. These deaths are not inevitable; they are preventable, yet far too many lives have already been lost, and far too many people continue to suffer needlessly. I am pleased that the Minister and the Department have committed forcefully to improving the area, and to working with members of the APPG and me. We look forward to launching our report, at the end of October, on preventing eating disorder deaths. I hope to see many of my colleagues there when we do. Lastly, I pay tribute to Zara’s mum, to Debs and cousin Tricia, and to all the parents fighting for the wellbeing of their children. Question put and agreed to.”

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45. “Eating disorders cost the UK an estimated £9 billion each year, yet research into these serious conditions receives just 1% of all mental health research funding. That is despite eating disorders affecting around 9% of people with mental health conditions, the consequences of which are delayed diagnosis and treatment and often lengthy hospital admissions. Will the Minister agree to meet me and the eating disorder charity Beat to discuss how the Government can break this cycle and ensure that eating disorder research receives the attention and investment that it urgently needs?”

    House of Commons22 July 2025Contains Parliamentary information licensed under the Open Parliament Licence v3.0Source ↗

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46. “T8. Thank you, Mr Speaker. I am so delighted to have two questions on health this week that I am not even going to mention ferries! As my hon. Friend will know, the process for securing an education, health and care plan is complex and can lead to delays in accessing vital support. That can have a serious impact on the health and wellbeing of young people and children. What steps is the Minister taking to improve the health element of EHCPs for families navigating the process, including those in my constituency?”

    House of Commons22 July 2025Contains Parliamentary information licensed under the Open Parliament Licence v3.0Source ↗

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47. “While the facial expressions of Opposition Members are worth an intervention all on their own, does my hon. Friend agree that this Bill provides stronger financial oversight and increased fan involvement, promotes equity and inclusion, protects club heritage, and increases transparency and accountability? The reason the Opposition oppose it is because those are alien concepts to them.”

    House of Commons8 July 2025Contains Parliamentary information licensed under the Open Parliament Licence v3.0Source ↗

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48. “T2. While it could be said that the Conservative party could fit into a children’s paddling pool, we in Isle of Wight West take swimming—as well as our issue with ferries—very seriously. [ Laughter. ] I thought hon. Members would like that one. West Wight sports and community centre is an excellent community-run facility that needs to replace its swimming pool after 50 years. Will the Minister meet me to discuss how it might access grants to do so?”

    House of Commons3 July 2025Contains Parliamentary information licensed under the Open Parliament Licence v3.0Source ↗

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49. “It will be an important chance to get Isle of Wight students and SMEs in the same room. A working-class child from the Isle of Wight may never have met a scientist, but they could go on to become a great one. It is our responsibility to ensure that every child has that opportunity.”

    House of Commons19 June 2025Contains Parliamentary information licensed under the Open Parliament Licence v3.0Source ↗

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50. “Research by the Edge Foundation shows that SMEs are typically far more hesitant to offer work experiences, not due to a lack of willingness but due to limited time and resources, which prevents them from tackling the logistics of arranging work experience placements. The Edge Foundation recognises the crucial role that SME brokerages play. I want to put on record some of the excellent work that Isle of Wight organisations are doing, particularly the Solent Careers Hub, the Isle of Wight Youth Trust and Island Careers Partnership, which are working in concert with careers advisers and businesses across the island. Those organisations are absolutely crucial to opening doors to SMEs. I am pleased to say that a youth partnership event will be taking place in Newport on 1 July.”

    House of Commons19 June 2025Contains Parliamentary information licensed under the Open Parliament Licence v3.0Source ↗

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