Tessa Munt MP: speeches

Speeches

• 27 Nov 2025 · Public Office (Accountability) Bill (Second sitting) · Hansard source

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  Q Who investigates those allegations? Chief Constable Guildford: That often depends on who makes the allegation and whether it is criminal or conduct related. If it is a criminal matter, it is reported to a police force or the IOPC. If any criminal or conduct matter is reported and it involves a chief constable, it goes to the IOPC under the law. If it is anybody below that level, it goes to the professional standards department in each of the police forces. It is then independently assessed, and given to an investigator, who is trained and accredited, and independent of the people who are complained about and the complainant.

• 27 Nov 2025 · Public Office (Accountability) Bill (First sitting) · Hansard source

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  I wish to declare that I am a director and vice-chair of WhistleblowersUK, which is a non-profit organisation.

• 27 Nov 2025 · Public Office (Accountability) Bill (First sitting) · Hansard source

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  Q Can I just say how sorry I feel for you? It sounds dreadful and I am sorry. The question I should ask you is, “How confident are you that this will change the culture in public authorities?”, but I sense from what I have heard that I ought to ask, do you have any confidence that the Bill will change things? Charlotte Hennessy: We are very confident. We have literally given 10 years of our lives, fighting to be here in this place. We have to acknowledge that Keir Starmer is the only Prime Minister who has endorsed the Bill. I would like to remind everyone that our Prime Minister made me a promise. He made a pledge to the public. It is now your duty to ensure that you fulfil that promise as well. If we were not confident in the Bill, we would not be sitting here today. Steve Kelly: Just touching on something that Seamus was talking about before, about changing cultures within authorities and so on, I would like to give you an example that has never left me. During the Hillsborough inquests, a man in his 40s or early 50s was giving evidence. He was an ex-PC—at the time of Hillsborough, he was probably a young PC. He was being questioned about the culture within the South Yorkshire police force at the time in 1989. I will never forget that man saying, “When you used to go Snig Hill, and you’d be walking along the corridor, you’d hold your head down when you’d see the bosses. You daren’t look at them, because we were frightened of them.” How could we encourage young officers like that to become whistleblowers? You couldn’t. We need a culture change. I thought that was a great point that this is something this law might do for not only policemen, but any public servants—anyone deserves support if they are trying to right a wrong. That young policeman must have taken that with him to those inquests. I remember looking at his face and thinking, “That’s the first time you’ve got that out.” The burden was on him all those years as well. It should not be like that. Hopefully, the Hillsborough law will support that. Sue Roberts: You are right; the culture changes have to be led from the very top—from the CEOs of these companies. Either they have to want to make this change happen or they need to move on.

• 27 Nov 2025 · Public Office (Accountability) Bill (First sitting) · Hansard source

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  Q What do you feel are the potential risks and benefits of requiring permission from the Director of Public Prosecutions to prosecute? Tom Guest: Let me explain how the DPP’s consent to prosecute works. In most criminal offences, a private prosecutor or the police can commence proceedings—so they get a summons or they charge someone, the suspect becomes a defendant and they go into the court system automatically. Where the DPP’s consent is required, that means that the permission of the CPS is required to prosecute. We apply our standard tests to that: “Is there sufficient evidence to prosecute?” and “Is a prosecution in the public interest?” They are the same tests that we apply to a prosecution. If we conclude that those tests are met, we take the prosecution forward ourselves. If we conclude that they are not met, the case does not go into the court system. The purpose of the DPP’s consent is to make sure that unmeritorious or vexatious prosecutions cannot get taken forward. Certainly, in terms of the misconduct offences, sometimes there are private prosecutors who wish to take forward unmeritorious prosecutions, so it is a check and balance on that. If it is a meritorious prosecution, however, we will go ahead with the prosecution ourselves.

• 27 Nov 2025 · Public Office (Accountability) Bill (First sitting) · Hansard source

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  Q The duty of candour binds those who are in a direct contractual relationship with the public authority. I am interested in knowing how far down the line it would go to subcontractors and, indeed, subcontractors of subcontractors. Tom Guest: It is right to identify that the extension of liability is only to direct contractual relationships, so not necessarily further down the line. I would make two qualifications to that. First, we will look at the evidence and the precise contractual relationship—what the evidence of the contract is. Secondly, I think we are talking about clause 4(2) here, which would also cover a private contractor who had a health and safety responsibility in connection with the incident. Although it does not cover the contractual relationship further down the line, that is an alternative route to liability.

• 27 Nov 2025 · Public Office (Accountability) Bill (First sitting) · Hansard source

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  Q The Bill clearly has its duty of candour and assistance. You have already made comments about focusing on the chief executive or the senior leader in any organisation. Can I check with you whether you feel that that would be sufficient to enable cultural change within organisations? Pete Weatherby: No. The reason I have majored on command responsibilities is because that is a weakness in the Bill, but the Bill applies across the piece and to all public servants at all times, with the general duty as well as the duty of candour and assistance, which is the ancillary duty, if you like. So that is really important. We are very keen to underline that this is an empowering Bill. In many of the cases—Hillsborough is a particularly good example—ordinary, decent police officers tried to tell the truth and were not allowed to tell the truth. This is a Bill that imposes a duty of candour across the piece. Everybody knows about it. Senior officers required junior officers to tell lies—this is the evidence they themselves gave on oath. That has to be stopped, and this Bill does that. We have tried to build in it those empowerment things, including whistleblowing—enhanced whistleblowing provisions and the like.

• 26 Nov 2025 · 1994 RAF Chinook Crash · Hansard source

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  One of my constituents is a cousin of Master Air Loadmaster Graham Forbes, who was one of the four crew members who died that day. The bereaved families were never informed that the MOD had sealed those documents for 100 years, and it took a BBC investigation for that to be revealed. Will the hon. Lady comment on that? It seems utterly outrageous that the families were not informed in the first instance.

• 26 Nov 2025 · 1994 RAF Chinook Crash · Hansard source

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  Will the Minister give way?

• 26 Nov 2025 · 1994 RAF Chinook Crash · Hansard source

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  I have done quite a lot of reading and received information from the family, but it is not clear to me the date on which the documents were sealed or by whom. Can the Minister confirm that? Who made the request that they be sealed, who made the decision that they should be sealed, and when was that decision made? I do not expect her to be able to answer off the top of her head, so I am happy for her to write to me.

• 26 Nov 2025 · 1994 RAF Chinook Crash · Hansard source

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  rose —

• 26 Nov 2025 · 1994 RAF Chinook Crash · Hansard source

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  Exactly as has just been said, I asked earlier whether, and when, that practice had been changed. I would very much like to know the date on which that decision was made, the nature of the decision and its wording, which I would share with the right hon. Member for New Forest East (Sir Julian Lewis).

• 26 Nov 2025 · 1994 RAF Chinook Crash · Hansard source

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  I understand why they have been sealed. I would like to know who made the decision to seal the documents for 100 years, and on what date it was made. It was clearly not in June 1994, because it lasts for 100 years. Somebody made the decision after that date to seal those documents.

• 26 Nov 2025 · 1994 RAF Chinook Crash · Hansard source

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  When the Minister replies, I wonder whether she might answer this question, with which I am sure my hon. Friend will agree. When did the MOD stop allowing so many critical personnel on one flight? Those on board included members of MI5, RUC special branch and the British Army intelligence corps, as well as Northern Ireland security experts—almost all the UK’s senior Northern Ireland intelligence capability on one flight. We know that in the case of the royal family, the monarch and the heir are not allowed to fly together. Will the Minister explain exactly when the MOD stopped the practice of putting everybody on one flight? Has that actually happened?

• 24 Nov 2025 · English Devolution and Community Empowerment Bill · Hansard source

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  In Somerset, we were set back enormously by six years of council tax freeze during the early 2010s, under the Conservative-led council— [ Interruption. ] Council tax was frozen for six years, way in excess of what the Government had anticipated, leaving council finances in Somerset in dire straits.

• 20 Nov 2025 · Business of the House · Hansard source

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  I would like to return to the listed places of worship scheme. Although departmental policy is to keep grant funding records for seven years, the Department for Culture, Media and Sport uses grant records only for the last three years, since 2022, as only that data is considered reliable. The Leader of the House will know that slots for Backbench Business debates are taken until the next King’s Speech, and there is a massive queue for Westminster Hall and Adjournment debates. However, in hope and endless optimism, may I ask him for a debate about financial record keeping? Neither the Secretary of State nor the Treasury can possibly assess the value, importance and impact of schemes like this if they have no idea where the money has gone, because record keeping is so poor, it is inaccurate, or the records have been lost.

• 20 Nov 2025 · Reoffending: Rehabilitation in Prisons · Hansard source

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  I thank the hon. Gentleman for presenting the Committee’s statement. With the chief inspector of prisons recently concluding that the outcomes for children in custody are not improving and the urgent notification issued to Oakhill secure training centre, and given that it is children we are discussing, does the hon. Gentleman agree that the conditions across the youth estate are completely unacceptable and, as recommended, the Government should produce an action plan for youth custody?

• 19 Nov 2025 · Myalgic Encephalomyelitis · Hansard source

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  Forgive me, but I am going to carry on. The final delivery plan rightly points to the need to build capacity in ME research, given the small UK research community and very few funded research projects. The University of Edinburgh’s DecodeME project has been a notable exception, recently reporting groundbreaking findings that revealed distinct genetic signals in people living with ME—medical, not psychological. This gives us a solid and compelling foundation for future research. Can the Minister explain what plans are in place for future funding to capitalise on this research? Again, the delivery plan is light on actions to build UK capacity in any research. A consensus recommendation for a post-infectious disease research hub was not funded. A joint showcase event was held earlier this month by the National Institute for Health and Care Research and the Medical Research Council, with the goal of stimulating research, yet it is not clear whether this will yield tangible results or how its outcomes will be monitored. Again, I ask the Minister what the plan is if, as seems possible, it is not a lack of information holding back capacity, but secure long-term finance to encourage researchers to build a career in the field. The final delivery plan gestured to HERITAGE and PRIME, which were effectively pre-existing funding announcements. The only genuinely new funding announced through the plan from the National Institute for Health and Care Research for research into repurposed therapies was capped to grants of £200,000. The Government’s response on this issue, including in the letter sent in response to concerns raised by the 72 Lib Dem MPs, tends to be that it is not usual practice to ringfence funds for specific conditions, and that researchers can apply for funding in open competition. Yet historical funding imbalances mean that it is not realistic to expect ME researchers to compete with researchers of diseases that benefit from more advanced research and much stronger institutional capacity. The UK Government do, in fact, set aside funding for specific conditions when they are considered a strategic priority. Just this June, £50 million of funding was announced for cardiovascular disease research to be awarded through open competition. In 2021, £50 million was committed to research into motor neurone disease. If we can award ringfenced funding through open competition for those conditions, why not ME? To echo a question asked at a recent research showcase event, why is ME not considered a strategic research priority? Can the Minister clarify that? The fourth and final point on which I would like the Government to go further is support from wider Departments, particularly the Department for Education and the Department for Work and Pensions. Children and young people are uniquely affected by ME. The condition disrupts and can derail key life stages and developmental milestones. Among educational professions, poor understanding of ME contributes to a lack of adjustments, limiting access to education and increasing school absences. The final delivery plan acknowledges the need for access to education and improved life chances among children and young people with ME, but while this is in theory a cross-Government plan, engagement from the Department for Education seems to have been extremely limited. Can the Minister outline what engagement has taken place so far and commit to speaking with colleagues in the Department for Education to ensure that they will engage with the delivery plan moving forward and ensure that children and young people with ME receive appropriate accommodations? Meanwhile, welfare benefits are the most common issue that constituents with ME raise with me. Many have struggled for years to access the benefits they are entitled to, feeling that they are fighting a system that works against them. Like most people living with disabilities, my constituents are terrified at the prospect of future welfare reforms and losing the support that they have and rely on to meet their basic needs. Looking at the current situation, I am indebted to a benefits adviser focusing on ME for her summary. “People with ME face intersectional and compounding barriers when interacting with the Department for Work and Pensions (DWP). These include structural flaws in benefit design, widespread misunderstanding of their conditions, systemic disbelief, inaccessible systems, poor-quality assessment practices, and the cumulative harm of being required to repeatedly prove their illness. The current benefit system and emerging reform agenda both fail to reflect the fluctuating, energy-limiting multisystemic nature of these conditions. And then, the Universal Credit Act 2025, together with the proposed abolition of the Work Capacity Assessment (WCA) and on-going threats to PIP eligibility, signals a fundamental shift in how disabled people meet entitlement to financial support.” I am particularly concerned about the proposals to replace the new-style employment and support allowance with a time-limited unemployment insurance and to abolish the work capability assessment. Replacing the new-style ESA would disproportionately harm individuals who are not eligible for means-tested support, for example because their partner works. Among other harms, that would increase the risk of domestic abuse while heightening financial dependence—a particularly pressing concern, given that ME is considerably more prevalent in women. Abolishing the work capability assessment removes critical safeguards in regulations 29 and 35 of the Employment and Support Allowance Regulations 2013 for those whose health would be seriously harmed by work or work-related activity. Those protections are vital for people with ME, who are at particular risk of harm and long-term health consequences if they push beyond their energy limits. Time prevents me from providing more detail, but I will conclude my observations by saying that, on the whole, what people with ME want most is to recover their capacity to contribute to their families, their community and wider society. They hate being ill. An appropriate benefits system must acknowledge that and treat them with dignity and fairness. The way to get people with ME and those caring for them back into work is not to take away crucial support, but to invest in helping them to get better. Many will be watching this debate from home, desperately hoping that we are doing everything we can to build them a better future. They deserve the assurance that the Government are committed to a clear, ambitious and, crucially, properly funded vision for change across healthcare, research and all forms of Government support. I ask the Minister for a meeting to discuss myalgic encephalomyelitis and the way forward for the 1.35 million people affected. I very much hope that today’s debate represents a big step forward in delivering that for them.

• 19 Nov 2025 · Myalgic Encephalomyelitis · Hansard source

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  I beg to move, That this House has considered Government support for people with myalgic encephalomyelitis. It is a pleasure to serve under your chairship, Mr Mundell. Myalgic encephalomyelitis is a complex, chronic condition affecting multiple body systems. There is currently no cure or established treatment. The symptoms of ME go far beyond chronic fatigue or being very tired; the sickest patients lie alone in darkened rooms, sometimes unable to move or to speak—or, in the very worst cases, to swallow or to digest food. Even at the mildest end of this condition, people with ME who once had lives, hopes and dreams for the future live a shadow of their former lives. More than five years on from the start of the covid pandemic, it is timely to note how the numbers affected have increased. Approximately half of those with long covid go on to meet the diagnostic criteria for ME, so it is now estimated that 1.35 million people live with ME or ME-like symptoms. That includes healthcare workers, teachers and other key workers who kept our country running at the height of the pandemic. Add in carers, and even more are directly affected. Importantly, there is a gendered dimension, with women five times more likely than men to develop ME. Despite the devastating toll of the condition, people with ME have endured decades of substandard and sometimes downright unsafe healthcare, with pitifully little funding for research. In spite of the lack of robust evidence to this effect, ME is treated as though the condition is psychiatric.

• 19 Nov 2025 · Myalgic Encephalomyelitis · Hansard source

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  I accept my hon. Friend’s point. Most people I speak to say that ME has nothing to do with psychiatry. We now have evidence from Edinburgh, which I will go on to in a moment, to explain exactly why that is the case. Our counterparts in Germany have grasped the importance and scale of the challenge. Just last week, the German Government announced a national decade against post-infectious diseases, with a particular focus on ME and long covid. In Germany, an estimated 1.5 million people are living with ME or long covid. The German Government have rightly recognised post-infectious diseases such as ME as one of the greatest public health challenges of the 21st century. Last week, they committed €500 million—around £440 million—over the next decade into research to understand the causes of post-infectious diseases and to develop treatments. Will the Minister confirm whether Ministers in the Department of Health and Social Care have discussed that recent funding announcement and the logic behind it? I would love nothing more than to see the UK Government come up with a comparable level of commitment—or will the Government wait a decade for the German Government’s conclusions before taking action?

• 19 Nov 2025 · Myalgic Encephalomyelitis · Hansard source

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  I absolutely agree, and I thank the hon. Gentleman. The second area where I would urge the Government to go further is support for people with severe and very severe ME. It is estimated that around one in four people with ME are severely affected. ME is perhaps the only condition where the sicker someone becomes, the less care they receive from the NHS. The recent prevention of future deaths report focused on the tragic case of Maeve Boothby O’Neill, describing NHS care for severe ME as “non-existent”. In my work on this issue, I have collaborated closely with #ThereForME, a campaign founded by two women, Karen and Emma, who are carers to partners with very severe ME. It can be difficult to comprehend the depth of suffering that ME can bring in its most extreme forms. With his permission, Karen has shared details with me about of her husband James’s day-to-day life. Before developing ME, James, in his 30s, lived a full life and was a civil servant. Today he is completely bed-bound and spends 99% of his day alone in a dark room, unable to tolerate any noise, light or stimulation. He is hardly able to communicate and is so sensitive to touch that, despite his suffering, his wife Karen is unable to give him a hug or hold his hand. Despite an acute level of need, James is receiving next to no care from the NHS. Karen tells me that her biggest fear is that he deteriorates to the point of needing lifesaving care. She cannot feel confident that the NHS will provide it.

• 19 Nov 2025 · Myalgic Encephalomyelitis · Hansard source

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  Probably most of us have constituents in exactly the same situation. In just over a year, two prevention of future deaths reports have been issued related to severe ME. I have already referred to one of them, regarding the case of Maeve Boothby O’Neill; the other was on the case of Sarah Lewis. Neither report has yet resulted in satisfactory action. The risk of death, specifically from malnutrition, is real and ongoing. Earlier today I spoke with Dr Binita Kane, a private sector clinician with a special interest in ME and long covid. She told me about the case of a 25-year-old woman, a medical student, who developed severe ME after a viral infection in 2018. The young woman has been in an acute NHS hospital for 17 months with nutritional failure and has deteriorated to the point that palliative care is being instituted. Her family is being prepared for the worst—it is dreadful. She has been disadvantaged not because of the individual clinical decisions, but because she suffers from a condition for which there is no safe or established service model. There have been multiple missed opportunities to prevent her condition progressing to this stage. Sadly, that young woman is not alone. I have heard of many other cases today, and before today. What is being done to help patients like her? In the foreword to the final delivery plan, the Minister stated that “tragically avoidable deaths of people with ME/CFS, in England…must become never events.” However, the plan does not clearly set out what actions the Department will take to guarantee patient safety. No one is being held to account. The plan committed the DHSC and NHS England to “explore whether a specialised service should be prescribed by the Secretary of State for Health for very severe ME/CFS”. I hope that the Secretary of State will do the right thing and commission that service, but it is frankly astonishing that the option of leaving this group of patients without specialist NHS care, as they are now, is even on the table. I ask the Minister to clarify what progress has been made in commissioning such a service. That is not to mention that developing a new service from the ground up is, at best, a medium-term solution. It may take years. It is astonishing that no interim solution has been proposed to ensure that patients with very severe ME, whose lives are at risk right now across the country, do not become tomorrow’s mortality statistics. How many more preventable deaths will it take? I ask the Minister to commit to work with groups such as #ThereForME to rectify the situation immediately, for example by convening a national advisory group to advise in these cases and by undertaking a full review of the lessons learned from ME deaths. Will the Minister clarify what data is being collected to better understand the number of those with ME who are affected by life-threatening complications? The third area on which I would like to see the Government do much more is accelerating ME research. I spoke earlier about the need for investment in research and improving healthcare. For many patients, biomedical research represents their best hope of regaining their former life, yet the condition has historically received very low levels of research funding from the UK Government. Based on parliamentary answers and official announcements, I estimate that around £10 million has been invested in ME research over the past 12 years. To put that figure into context, on the current numbers that is about 60p per person living with ME per year. Four times as much was spent on a helicopter for the former Prime Minister as has been spent on ME. We spent £125 million—12 times as much—on a bat tunnel for HS2. We spent £10 billion—about 1,000 times as much—on personal protective equipment that turned out to be unusable. Money talks, and the record of the past decade makes it clear to people with ME that their collective futures have been valued by successive Governments at astonishingly little.

• 19 Nov 2025 · Myalgic Encephalomyelitis · Hansard source

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  I could not agree more. For far too long, patients have been dismissed, and that care element is incredibly important, because it affects so many people. In July, the Department of Health and Social Care published the final delivery plan for ME, a cross-Government strategy aiming to improve attitudes, bolster research and better lives. It included some positive steps: new small grants for research into repurposed medications, and the development of a new service specification for mild and moderate ME. However, overall, the consensus of the charities and patient advocates I have spoken to is clear: the delivery plan falls far short of what was needed.

• 19 Nov 2025 · Myalgic Encephalomyelitis · Hansard source

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  Thank you, Mr Mundell, but I have little to say. I am delighted to hear what the Minister had to say, and I will be holding her feet to the fire. I wish to continue this campaign, and I will work with others on it. One of the things I omitted to say at the beginning was that I am a member of the APPG on ME. I should have declared that, so I seek your forgiveness for not having said so. I am delighted by a number of the things that the Minister has been able to say. I thank everyone who contributed to the debate—I should probably have asked for a two or three-hour debate. In particular, I point to a phrase of the former Secretary of State, the right hon. Member for Godalming and Ash (Sir Jeremy Hunt), about digging for treasure, I think. It is so moving to have heard so many important stories of people who are suffering. We really have to do something about this.

• 19 Nov 2025 · Myalgic Encephalomyelitis · Hansard source

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  I agree. In fact, we do not just need specialists; we also need training for GPs and other healthcare workers. I will highlight four areas in which we need to see much more from the Government going forward. Given the gravity of the situation, I would appreciate it if the Minister could arrange for written responses to a number of my points. The first area is funding. If the delivery plan felt threadbare, that is because no substantive new funding was attached to it. Before the plan was published, all 72 Lib Dem MPs signed a letter expressing our concerns about the anticipated lack of funding, which of course came to pass. To put it bluntly, what patients need is transformed NHS care and a step change in research. Neither is likely to happen without investing some money. The case for investment is clear. I urge the Minister to see this not as a sunk cost, but as an investment in a group of people who are desperate to contribute to society. We know that one in five working-age adults are out of the workforce, many because of health problems, yet remarkably there was no modelling of the demography of those living with ME for the delivery plan exercise, and neither the Department of Health and Social Care nor the Department for Work and Pensions has an estimate of what the neglect of people with ME is costing our economy. I would like to look at some of the figures. The most recent estimate of the economic impact of ME was for 2014-15—10 years ago—and was carried out by 20/20health. The cost was then calculated at £3.3 billion annually, based on only 260,000 people living with ME. With many more affected following the pandemic and a decade of inflation, that cost will now be much higher. Even the most conservative estimate of current numbers living with ME, excluding cases linked to long covid, puts them at 404,000 patients. Does the Minister accept, using that conservative estimate and adjusting for inflation, the annual economic impact of ME today is likely to be at least £7 billion? If those living with ME-like symptoms following covid are included, we could be approaching an annual cost of £20 billion. Surely it is time for the Government properly to cost the impact of a condition that affects so many, rather than brush it under the carpet, and to invest accordingly.

• 19 Nov 2025 · Myalgic Encephalomyelitis · Hansard source

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  It is not only untenable, but completely absurd. In September 2024, on World Patient Safety Day, over 200 healthcare workers were so concerned about NHS care for ME, and particularly care for severe and very severe ME, that they wrote a letter to the Health Secretary calling for immediate action to save lives. That letter was sent 14 months ago. I am sorry to say that very little has changed since, and they did not receive a response.