← LEADERSHIP TERMINAL

UK PARLIAMENT · SITTING

Debbie Abrahams

MP for Oldham East and Saddleworth · Labour · United Kingdom

IN THEIR OWN WORDS

“We cannot afford to march to the edge of action, only to falter when we have finally shown the collective action of the UK and our allies to be a powerful threat against breaches of international humanitarian law.”

House of Commons28 October 2026Contains Parliamentary information licensed under the Open Parliament Licence v3.0Source ↗

“As the name sets out, the Global Human Rights and International Humanitarian Law Sanctions Regulations 2026—I will just call them the new regulations—expand the former regulations so that serious breaches of international humanitarian law around the world now constitute designate-able activity.”

House of Commons28 October 2026Contains Parliamentary information licensed under the Open Parliament Licence v3.0Source ↗

“It is a pleasure to serve under your chairship, Mr Stringer. I, too, welcome these regulations on global human rights and international humanitarian law sanctions. We know that sanctions are a vital tool for the Government to use to promote our British values, particularly in relation to the rule of law, democracy and human rights.”

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“One of the chief catalysts for this action was the Israeli Government, under Benjamin Netanyahu, making a clear statement that they intend to bury the prospect of a Palestinian state, and with it the two-state solution, through illegal settlement expansions, particularly in the case of the E1 project.”

House of Commons28 October 2026Contains Parliamentary information licensed under the Open Parliament Licence v3.0Source ↗

“Although I wholeheartedly support the replacement of the previous regulations with the new ones, two questions remain, which I would like to put to the Minister. How will the Government monitor those who commit acts that may make them liable to designation? How swiftly will we act on reliable reports of such acts?”

House of Commons28 October 2026Contains Parliamentary information licensed under the Open Parliament Licence v3.0Source ↗

“Friend the Foreign Secretary was exactly right to say in his statement on 8 September: “If the occupation is illegal, do we want to maintain, at the level of principle, normal economic relationships? We say no.” —[ Official Report , 8 September 2026; Vol. 790, c.”

House of Commons28 October 2026Contains Parliamentary information licensed under the Open Parliament Licence v3.0Source ↗

The complete record

3,394 lines on record for Debbie Abrahams, in date order, each linked to its source. Free to read, without an account. Most recent 500 lines shown. Search to find more. Page 8 of 10.

This is not an official version of UK Parliament proceedings. It reproduces the published record and links to it; the official version is the one UK Parliament publishes.

  1. “Those facts may come as a surprise to many, including many commissioners, but I will focus today on two important inequalities in dementia: the inequality in dementia diagnosis rates between different parts of the country and different groups of people, and the inequality between those who do and do not have access to post-diagnostic support. First, I will share some information that hon. Members will hopefully find useful. When we talk about dementia, we are using a collective term covering the common symptoms associated with a range of brain diseases. Alzheimer’s disease is the most common of those, but they also include vascular dementia, which my mother-in-law had, Lewy bodies, frontotemporal dementia and many others. Each of those brain diseases has different pathology and as a consequence will have different therapies.”

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  2. “I was really reassured that the approval of lecanemab and donanemab is going through the regulatory cycle at the moment, and we hope to hear when they will be available in the next couple of months. The fact of the matter is that dementia is a monumental pressure on our health and social care system, but it is all too often an afterthought in commissioning. It is not commonly known that dementia is the leading cause of death in the UK. Nearly 1 million people have dementia, but of those one in three currently live without a diagnosis. Dementia costs the economy more than £40 billion each year, and more than 60% of that cost is borne by individuals and families.”

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  3. “Yesterday I had the pleasure of sponsoring the Alzheimer’s Society’s reception in Parliament for Dementia Action Week, where we welcomed many Members to hear about the importance of a dementia diagnosis and the transformative potential of new treatments for dementia. Back in January, I spoke in another Westminster Hall debate looking at the advent of new treatments, particularly lecanemab and donanemab. Those drugs have caused huge excitement, as they mark the first ever treatments for people in the early stages of Alzheimer’s disease and could change the way that we see dementia forever. However, even in that debate I highlighted the barriers to those drugs being delivered to patients and sounded a note of caution that they are neither a cure nor a quick fix.”

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  4. “My other co-chair is Baroness Angela Browning, and like Angela I became involved in the APPG because I became a carer of a loved one who developed one of the brain diseases that cause dementia. In my case it was my mum, who was also called Angela. She was diagnosed with Alzheimer’s disease in 2002, when she was just 64, and I cared for her along with my stepfather and brother. After she died in 2012, I became the first MP to train as a Dementia Friends champion and was subsequently elected as co-chair of the APPG on dementia in 2015. This debate could not be more timely. As you know, Ms Rees, this week marks Dementia Action Week.”

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  5. “I beg to move, That this House has considered inequalities in dementia services. It is a pleasure to serve under your chairship, Ms Rees. I thank the Backbench Business Committee for granting me this debate to discuss the huge inequalities in dementia diagnosis and other services across the country. I also thank the Alzheimer’s Society for providing the secretariat to the all-party parliamentary group on dementia and for supporting our many inquiries, including the inquiry we conducted into dementia diagnosis last week, which was published in our “Raising the Barriers” report. My particular thanks go to Lewis and Connor for their briefings and for helping me to prepare for this debate. It is a real honour to have recently been re-elected as co-chair of the all-party parliamentary group on dementia, a position that I have held since 2015.”

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  6. “Returning to our APPG inquiry, we received input from more than 2,300 people and I thank them sincerely. Those people have gone through—either themselves or with a loved one—a dementia diagnosis process. They shared their experiences in our survey and we found that every part of the country produced different experiences of the diagnosis system. In Somerset, for example, people were most likely to report that they were satisfied with the time it took for them to receive a diagnosis but were least likely to say that they received satisfactory post-diagnostic support. In London, respondents had the best access to brain scans but found it most difficult to access GP appointments. I know that £17 million was invested in dementia diagnosis by the Government in 2021-22 and that part of that money was to develop best practice advice.”

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  7. “Alzheimer’s Research UK also undertook an analysis and published a report last October—“Towards Brain Health Equity: Tackling Inequalities in Dementia Risk”—and this highlighted research identifying vulnerable groups and the dementia risk that they face. That is also an inequality. It referred to research in England and Wales that showed that socioeconomic deprivation and ethnicity are linked to increased dementia mortality, younger age at death from dementia and poorer access to specialist diagnostics. A number of recommendations were made around that. We know that there are 12 modifiable risk factors associated with dementia, and the report focused on action around reducing air pollution, lowering smoking rates, healthy eating, tackling higher blood pressure and identifying and treating hearing loss.”

    House of Commons16 May 2024Contains Parliamentary information licensed under the Open Parliament Licence v3.0Source ↗

  8. “There are significant differences in the dementia diagnosis rates between integrated care system areas in England. The report referred to a recent Alzheimer’s Society survey of clinicians, clinical commissioning groups—the predecessors of the ICSs—and dementia support workers. Poverty and health inequalities were identified as major barriers to getting a dementia diagnosis. This was also borne out by analysis by the Office for Health Improvement and Disparities. I have to say I do not particularly like the title of that organisation; I think it should be the “Office of Health Improvement and Inequalities”. Similarly, there were lower rates of diagnosis in ethnic minority populations. For example, the City of Wolverhampton has an overall diagnosis rate of 70%, but just 35% for people from an ethnic minority community.”

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  9. “I am very grateful to my hon. Friend for his intervention. This is the absolute crux of the issues we are facing. First of all the target is not ambitious enough, but as he rightly says there are these inequalities. I prefer calling a spade a spade, so these are inequalities and we need to call them what they are. Although the national picture is poor, if we dig further into the data we can see that there is a huge regional inequality in dementia diagnosis rates. In my Oldham constituency, for example, the rate is above 75% and in Devon it is just 40%. Where you live has a massive impact on whether you get a timely, accurate and high-quality dementia diagnosis. A postcode lottery on this scale for a condition that will affect one in three of us is not acceptable. The APPG’s dementia diagnosis inquiry revealed several issues.”

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  10. “National strategies should not just reflect the evidence and data for a national profile around dementia, so we should agree that that needs to change.”

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  11. “As I said before, 2,300 people filled out our online survey and shared their stories to inform our work. Sadly, just 5% of people’s stories were positive. Five per cent: that is awful, is it not? After a constituent came to see me regarding concerns about the delay for her mother’s diagnosis—it took her 15 weeks to get an appointment for her mother to attend for a dementia diagnosis, during which time she noticed a considerable decline in her cognitive health—I tabled some written questions on the proportion of people waiting more than 15 weeks for an initial dementia diagnosis and the average waiting time for an assessment. I was told in response on 22 January 2024 that those data were “not held centrally”. I find that extraordinary.”

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  12. “The hon. Member is absolutely right; there is less money going into research. On why there is not more done about it, the hon. Member really needs to direct that question to the Minister. I have set out all the evidence that says it should be a priority for the families and individuals affected and a priority for our society, and it should also reflect how we organise our care system, given that predominantly the people in the care system are those living with a diagnosis. The hon. Member will therefore have to direct that question to the Minister. Going back to my point about the investment made in 2021-22, can the Minister update us on how that is going and the improvements that she may not see immediately but which she hopes to see? Clearly, that is something we need to see as part of the levelling-up agenda.”

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  13. “Dementia is a monumental health and social care challenge, and will be the defining test of our system in the decades to come—I have absolutely no doubt of that. We have spoken in this place about planning for the next generation of dementia care in the context of the new, potentially transformative drugs that are currently under appraisal, but almost 1 million people are living with dementia in this country today, and much more can be done to get them the care and support they need and deserve at the earliest possible moment. I would like to thank the Backbench Business Committee and those who have joined us on a Thursday afternoon when a lot is going on in Parliament. I look forward to the Minister’s response.”

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  14. “First, what will the Department do to ensure that where someone lives, their socioeconomic status or their ethnicity do not negatively affect their likelihood of getting a dementia diagnosis? Secondly, what will the Department do to ensure that everyone with dementia has access to high-quality, post-diagnostic care, regardless of where they live? Thirdly, it was two years ago this week that the right hon. Member for Bromsgrove (Sir Sajid Javid) announced a 10-year plan for dementia, which was then folded into the major conditions strategy. However, we still do not know when that strategy will be published. Can the Minister update us on when we can expect publication of the strategy?”

    House of Commons16 May 2024Contains Parliamentary information licensed under the Open Parliament Licence v3.0Source ↗

  15. “The average cost of care for someone in the early, or milder, stages of dementia is about £28,000 a year; in the later, severe stages of dementia, it rises to well over £80,000 a year. Caring well for people with mild dementia can prevent falls and infections, which cause unnecessary hospitalisations and deconditioning, which increase the speed of deterioration in people with dementia. Early identification and increased spend in the early stages of dementia pay dividends further down the pathway. I would like to end by putting three questions to the Minister, and I would be grateful if she could address them in her response or in writing at a later date, if that is easier for her.”

    House of Commons16 May 2024Contains Parliamentary information licensed under the Open Parliament Licence v3.0Source ↗

  16. “The additional cost—I know it should not be just about cost, but there is an associated cost—is almost £6,000 per patient, which is far more than the cost of an occupational therapy appointment. I have to say that I just do not get why we are prioritising things in this way. I do not want to reduce health and social care decisions purely to finance, but the fact of the matter is that early intervention for people with dementia saves so much money. The Alzheimer’s Society reported on Monday that the cost of dementia to the UK economy is £42 billion a year, and that figure will skyrocket to £90 billion by 2040 because of our ageing population. The cost of dementia rises significantly as the condition progresses.”

    House of Commons16 May 2024Contains Parliamentary information licensed under the Open Parliament Licence v3.0Source ↗

  17. “This trend continues outside primary care and in allied health professions. Over half of people with dementia who have been signposted to mental health services report having to wait up to a year for treatment. Evidence shows that mental health treatments can be effective in treating depression and anxiety symptoms associated with dementia, but just 0.002% of referrals to NHS talking therapies are for people with dementia—that is 2,000 people out of 1 million referrals. A quarter of people with dementia wait for up to a year for occupational therapy after referral. Occupational therapy can help people to avoid dangerous falls and to live well in their own home for as long as possible. The average time spent in hospital for a hip fracture is seven days, but patients with dementia stay in hospital for up to four times longer a hip fracture.”

    House of Commons16 May 2024Contains Parliamentary information licensed under the Open Parliament Licence v3.0Source ↗

  18. “I turn now to the inequality between those who have post-diagnostic support for dementia and those who do not—or, perhaps more insidiously, the gap between what people with dementia are supposed to receive and what they actually receive. Guidance states that people living with dementia should be offered a review with a healthcare professional at least once a year. However, just 25% of people with dementia who were polled by the Alzheimer’s Society said that they or their loved one had had an annual dementia review within the last 12 months, and only 16% said that they had received enough support from local services in the last 12 months. In addition, more than half said that, even if they had received an annual dementia review, it did not help them feel more able to manage their condition.”

    House of Commons16 May 2024Contains Parliamentary information licensed under the Open Parliament Licence v3.0Source ↗

  19. “I am very grateful to the hon. Member for that intervention, and I absolutely agree. All of that underlines the importance of improving the dementia diagnosis pathway and making it work better for people living with dementia and their loved ones. The APPG has developed a series of recommendations across the core themes of dementia diagnosis, data, workforce, and public health messaging. Collectively, these recommendations outline how dementia pathways can be strengthened to enable access and quality care across all settings, communities and regions in England. I would be grateful if the Minister could say what work the Department is undertaking in those areas to reduce inequalities in the experience of dementia between localities and population groups.”

    House of Commons16 May 2024Contains Parliamentary information licensed under the Open Parliament Licence v3.0Source ↗

  20. “I will be very quick because I know that people have trains to catch, but I want to reiterate the Minister’s thanks to everybody for taking part. This has been a particularly nice debate in its collaborative approach, and I thank her also for saying that she will follow up on the data and whether it could be retained centrally. I also hope that there is evidence that has been supplied here and elsewhere that will help to strengthen the dementia aspect of the major conditions strategy. We have not spoken about type-specific diagnoses, so I ask the Minister to ensure that that is included, because access to the therapies will not be available without that. Question put and agreed to. Resolved, That this House has considered inequalities in dementia services.”

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  21. “I also rise to present a petition on behalf of my constituents, which calls for the implementation of the recommendations of the second interim report of the infected blood inquiry—in particular, the payment of interim compensation to those who have been infected and affected, whose families have suffered enough. The petition states: The petition of residents of the constituency of Oldham East and Saddleworth, Declares that people who received infected blood and who have suffered as a consequence have, along with their families, waited for too long for redress. The petitioners therefore request that the House of Commons urges the Government to implement the recommendations in the Second Interim Report of the Infected Blood Inquiry without delay. And the petitioners remain, etc. [P002982]”

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  22. “The United Nations has found that the Government have breached the rights of sick and disabled people, including their rights at work, and the UK’s own equality watchdog has said that the Department for Work and Pensions has discriminated against sick and disabled people. Given that only 2.7% of participants in the Government’s work and health programme have a successful job outcome, what meaningful proposals do the Government have to reduce the 29% disability employment gap?”

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  23. “8. What recent discussions she has had with Cabinet colleagues on compliance with international humanitarian law in relation to the Israel-Palestine conflict.”

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  24. “The ICJ ruling also declared that there was a “plausible right” to be protected from genocide, and following the urgent question to the Deputy Foreign Secretary on Tuesday I cited United Nations international law relating to that. When there are concerns about a potential genocide taking place, those are the circumstances in which the sale of arms should be withdrawn. Can the Attorney General tell me, and my constituents—as this is a massive issue for thousands of people across the country—exactly when the Government will come out and recognise both international law and the risks that we take in breaching it?”

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  25. “I am sure the Leader of the House, as a former Minister for disabled people, is as concerned as I am that it is now two years since the Equality and Human Rights Commission issued a section 23 notice against the Government with regard to their discrimination against disabled people. That was followed by the report from the UN Committee on the Rights of Persons with Disabilities investigating a second set of breaches of the convention by this Government, which was published a couple of weeks ago. Can we have a debate in Government time about why there has been this discrimination by the Government against disabled people and what the Government are going to do about it?”

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  26. “We should add to the Chancellor’s statistics that we have the widest economic inequalities in Europe. Last week, Professor Sir Michael Marmot published new analysis showing significant increases in health inequalities—how long we live, and how long we live in good health—and that is particularly the case between the north and south-east England. That is of course driven by the economic inequalities that I have just referred to. What assessment has the Chancellor undertaken on the loss in productivity directly as a result of that increase in health inequalities?”

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  27. “On a point of order, Mr Speaker. The Chancellor, in answer to my question, said that economic inequalities actually increased under the previous Labour Administration. A House of Commons Library publication released last month shows that that is categorically not the case. Would he like to take this opportunity to correct the record?”

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  28. “Like most people here, I want to see an immediate ceasefire, the release of all hostages and access to humanitarian aid, but quite frankly I have been absolutely gobsmacked by the Deputy Foreign Secretary’s response. I see no levers that the Government are using to influence the Israeli Government’s behaviour, and I see the playing with words around what our obligations are under international law in relation to our arms licensing process. As I am reading it here from the UN, if there is a “plausible risk of genocide” we should not be supplying arms to any country. The ICJ has already ruled that there is a plausible risk of genocide, so will the Deputy Foreign Secretary stop dancing on the head of a pin and do something about this?”

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  29. “I, too, welcome the increase to 2.5%. The world has definitely become a more dangerous place over the last 14 years. I can only suppose that the announcement was not made in last month’s Budget because it would have come under scrutiny from the Office for Budget Responsibility, but could the Defence Secretary say exactly what proportion of the 2.5% will be spent on cyber-security and armed services personnel?”

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  30. “In January, Professor Sir Michael Marmot published “Health Inequalities, Lives Cut Short”, which confirmed that between 2011 and 2019, driven by political choices, 1 million people in 90% of areas in England lived shorter lives than they should. The inequalities were amplified by Covid. These lives cut short are matched by shorter lives in good health. Does the Secretary of State believe in evidence-based health? If so, does she accept the overwhelming evidence that current levels of ill health reflect 14 years of escalating poverty, services that have been run into the ground, including the NHS, and the Government’s failure to do what they promised in 2019: level up?”

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  31. “I too am speaking on behalf of a constituent, who lost a brother and sister-in-law and whose nephew was left to be brought up by the family. I want to raise the urgency of this. I appreciate the Minister’s sincerity about what he is trying to do, and the fact that he has been in post for only a few months, but it is over a year now since Sir Brian Langstaff brought forward his report and said that interim payments were absolutely essential. I am trying to understand exactly where the block is. If this was a priority for the Government, it would have been done in that year, so where is the block?”

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  32. “Fundamentally, though, it ignored the sovereignty of Parliament. When can we expect the Government to bring the matter to the House so that we can question the Prime Minister on his assertions?”

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  33. “On a point of order, Madam Deputy Speaker. Last Friday the Prime Minister made a speech, not to this House, but to the press, describing what he referred to as a “sick note culture”, and implying that people who are economically inactive due to ill health or disability are not genuine, but malingerers. That was grossly offensive not only to people who are unable to work because of ill health but to the clinicians caring for them, as it questioned their professional integrity. It ignored the overwhelming evidence from epidemiologists such as Professor Sir Michael Marmot, which shows that over the last 14 years we have become a sick nation, living shorter lives and less of our lives in good health. It is certainly not the compassionate approach that the Prime Minister said he was going to preside over.”

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  34. “In her response, I hope the Minister or her officials can explain why those sorts of statements would be included in a bundle to a medical adviser on the first-tier tribunal, which are questioning somebody who is caring for somebody else, and who also happens to be in receipt of disability benefits?”

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  35. “The tribunal may wish to explore this further.” Although that might not look particularly threatening on its own, given the context of the other arguments that the Department is looking to put forward, it is basically saying: “How can you be caring for somebody if you’re also disabled?” That is what it is saying, and unfortunately that was also the gist of the Prime Minister’s speech last week—“If you’re genuinely in receipt of social security, of course we’ll support you. But there’s a question mark over how many and what proportion of people in receipt of social security are genuine.” That really gets to the core of this, and it makes me quite angry. Most people have worked and are doing the right thing. To imply that they are not genuine is an absolute disgrace.”

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  36. “As we have heard, the problem with overpayment is exacerbated by the unfair cliff edge and the administration of these ridiculous rules, which really need to be reformed. I was contacted by a medical adviser, a retired GP who is providing medical advice to first-tier tribunals for PIP appeals, who also happens to be in receipt of carer’s allowance. This retired GP contacted me because she was concerned by the statement from the Department included in her bundle over the past six months, which said: “Although (Ms X) has identified a high-level of personal restriction he/she is entitled to Carer’s Allowance. To be entitled to Carer’s Allowance a person must provide at least 35 hours of care to another disabled person each week.”

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  37. “Again, I refer Members the Select Committee’s report on benefits in the UK. We have the lowest level of out-of-work support since, I think, 1911, so carer’s allowance is even less than that in real terms. It is just appalling. We have been doing a mini-inquiry, and we have a follow-up session on Wednesday, which the Minister is attending. If she wants to hear about the experience of those caring for loved ones now, she should reflect on the evidence they gave a couple of weeks ago. We have also heard about the Department for Work and Pensions’ appalling, draconian treatment of people—the utter lack of compassion shown to those who make, often, innocent mistakes and are then criminalised by the DWP. I feel quite ashamed, to be honest, that that is happening.”

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  38. “As we have heard, given the Prime Minister’s statement in his speech last week about the mental health impact on so many young people, we might also have expected a message about the impact on young carers. Many of those caring for their parents or siblings are as young as eight or nine. It really is appalling. I had a glimpse of being a carer: my mother had Alzheimer’s disease for 10 years, and I provided support to my stepfather, who cared for her during that time. We were not reliant on carer’s allowance, but we felt the strain, day in, day out, 24/7. This is a really significant gift that people are giving to their loved ones and society as a whole. We have heard how inadequate carer’s allowance is, at £81.90 a week—its lowest level, even compared with jobseeker’s allowance.”

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  39. “Friend the Member for Wirral West (Margaret Greenwood) shared the costs that carers save society—it would cost £162 billion a year if we were actually able to pay carers. That is the cost they save. I want to make a few points, many of which have already been made, on the lack of adequacy of carer’s allowance —as we have already heard, a quarter of those caring for loved ones are living in poverty—and on the issue of the rules: the cliff edge, the earnings limit, and the administration of those rules and the lack of common sense and compassion. I find that unforgivable, quite frankly. I worked very closely with young carers in my public health days.”

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  40. “It is a pleasure to see you in the Chair, Mrs Cummins. I will start by congratulating my hon. Friend the Member for Neath (Christina Rees) on bringing this debate to the Chamber, and on her excellent speech. I agree with her that carers are not only the backbone of society, but represent the best of us in the selflessness that they display. We should be championing them, and we know that is not happening. Last week, many Members will have seen Oxfam’s report on carers, which was called “Valued”—a little bit of a contradiction, because it gives case study after case study where people are not valued, and shows how little people, and society as a whole, value carers. My hon.”

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  41. “Could the Minister respond to my query about medical advisers to first-tier tribunals, and the statements that are included in their bundles?”

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  42. “Why have they been so ineffective and what will they do to make sure that Israel adheres to our requests?”

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  43. “We continue to call for the immediate release of all hostages, for an immediate ceasefire, for unhindered humanitarian aid, for adherence to international law and accountability for any breaches, and for immediate international efforts for a two-state solution. On aid and international law, between 6 and 12 April, 41% of UN co-ordinated missions to northern Gaza, where famine is under way and children are dying by the minute, were denied. The Israeli authorities’ obligation to facilitate humanitarian aid is a matter of law. It is not just about access; it must also be able to get to where it is needed. I appreciate the difficulties in which the Minister has found himself today but, again, why are the Government so ineffective in getting support? We have had months upon months of saying that things will happen, and they never do.”

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  44. “While I acknowledge the role that Pakistan has played in hosting Afghans after Operation Pitting, we need to recognise that many of the people being returned from Pakistan will be at significant risk. On top of that, many Afghans were incorrectly advised about which scheme to apply for and, as a consequence, may not even be in the process, so in addition to those who have started the process, there will be another cohort who have not started it because of the poor advice that they were given. Given that the ACRS is not even open—there is no phase 4 open at this moment—what numbers of people are expected? I have a constituent for whom this is really important. Can the Minister tell us the number of people she is expecting who are not in the process and who need to be accommodated?”

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  45. “I am struck by how reasonable Lord Hope’s amendment seems in setting up an independent body to assert that Rwanda is a safe place, as the Minister says. What could possibly be wrong with that?”

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  46. “Similarly, polling by the think-tank Compassion in Politics showed that four out of five people have no respect for politicians, and that 40% of parents would be concerned if their child expressed a desire to become a politician, which is worrying if we want our democracy not just to survive but to thrive.”

    House of Commons16 April 2024Contains Parliamentary information licensed under the Open Parliament Licence v3.0Source ↗

  47. “Last year, a King’s College London study of 24 countries found that the UK fares poorly in people’s confidence in the Government, political parties and even Parliament. Added to that, there is a marked difference by generation. Young people have experienced some of the biggest shifts in attitude: confidence in the Government among millennials in Britain has halved since 2005, falling to its lowest level on record, and generation Z has very low confidence in a wide range of other institutions, too. In the Hansard Society’s audit of political engagement series, which was carried out between 2004 and 2019, people reported an increasing sense of powerlessness and disengagement over time.”

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  48. “I beg to move, That this House has considered citizens’ assemblies and local democracy. It is lovely to see you in the Chair, Ms Vaz. I am absolutely delighted to lead this Westminster Hall debate on how citizens’ assemblies can be used to enhance public engagement in political decision making, bringing benefits to our democracy and society as a whole. As hon. Members may know, last month I introduced the Standards in Public Life (Codes of Conduct) Bill to Parliament. Many people across our great country and nation states feel that the UK Parliament—including MPs and Ministers who sit in this place—is disconnected from them and their lives. It is not just the poor behaviour of a few bad apples affecting how people feel; there is a much deeper malaise. People have a growing lack of trust and confidence in politics and politicians.”

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  49. “Of course, that is the situation we find ourselves in at the moment. There are other good reasons for greater public engagement and deliberative policymaking, including through citizens’ assemblies. Before I was elected to this place, I served as a public health consultant and academic. My work was focused on tackling health inequalities and their main determinants—inequalities in income, wealth and power. It may surprise hon. Members to hear that there is an independent and universal effect on our health and wellbeing that relates to our status in a hierarchy. The process of engaging people in decision making and sharing that power has a positive impact on their health and wellbeing, in addition to leading to the development of better politics based on lived experience and consensus.”

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  50. “I was not specifically aware of the citizens’ assembly in Northern Ireland, although I am aware of many across our nation states and in other countries. They are seen as a mechanism by which elected representatives can maintain contact with their constituents on various policy issues throughout a political cycle. Polling from the Institute for Government recently showed that two thirds of constituents do not think that the current Government behave to high ethical standards. Likewise, polling from the UK Anti-Corruption Coalition found that two thirds of voters believe that UK politics is becoming more corrupt. We know that when socio- economic inequalities are narrow, trust between different communities and groups increases, and the reverse is true when the inequalities widen.”

    House of Commons16 April 2024Contains Parliamentary information licensed under the Open Parliament Licence v3.0Source ↗