Alison Bennett MP: speeches

Speeches

• 11 Jun 2025 · NHS Funding: South-west · Hansard source

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  It is a pleasure to serve under your chairship, Dr Huq. I thank my hon. Friend the Member for Torbay (Steve Darling) for bringing forward this important debate. We have been reminded by hon. Members that the Conservative legacy is pensioners left in agony, waiting for hours for an ambulance that may not come in time; women forced to give birth in unsafe, overstretched conditions; and people having to pull out their own teeth—in the 21st century—because they cannot find an NHS dentist. We have heard from hon. Members that the south-west has some of the longest ambulance waits in the country, some of the worst repair backlogs, and waiting times for GPs and dentists that are simply unacceptable. That is not just a strain on our health services but a daily struggle for families, carers and patients across our region. The Liberal Democrats believe that people deserve better, and that they should be in control of their own lives and health. That means people getting the care that they need, when they need it and where they need it, without them having to fight every step of the way. Instead of lurching from one crisis to the next, as previous Governments have done, we have a plan. It starts with early investment in community health—in GPs, pharmacists and dentists—so that fewer people end up in hospital to begin with. We will finally fix the crisis in social care, so that people are not left stuck in hospital beds with nowhere to go. If we expect to rely on our NHS in future, we simply must invest in it. We need not just big grand schemes but investment in the simplest yet most important things. For example, in my own patch in Mid Sussex, the Princess Royal hospital recently had only one of its four lifts working over a weekend.

• 11 Jun 2025 · NHS Funding: South-west · Hansard source

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  My hon. Friend makes an excellent point about rurality, which is obviously a big issue in the south-west. It is also a serious issue in Sussex where we have things in common with the south-west, such as having an older than average population and all the challenges that come with that, as hon. Members have mentioned. Hospitals want to be able to sort those issues out, but they are left juggling priorities, barely scraping by with the current levels of funding. Things do not work if we do not look after them, and if we do not look after our health system, it will not be able to look after us or our loved ones. Although I am sure that the Minister will make the point about capital investment in the NHS, which is welcome, the future looks very uncertain and precarious for our ICBs, as a number of hon. Members have said. Soon after ICBs were first created, they had to cut their budgets by 30%. They have now been asked to cut their budgets by 50% on average. Indeed, for Sussex, the cut is more than 50%—it is 53%. It is no surprise that Sussex and Surrey have formally proposed merging their ICBs, which, by running at the same time as local government reorganisation and the creation of a mayoralty, means we will end up with an ICB that does not have the same footprint as the new incoming mayor.

• 11 Jun 2025 · NHS Funding: South-west · Hansard source

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  My hon. Friend makes a really good point. It is vital that when we look at per head of population funding, we think about the different factors that actually drive up the true cost of delivering healthcare across the country, which obviously varies by region. On ICBs, I will press the Minister on three points. First, on the timescale for cuts to be delivered by ICBs, they have to be completed by the end of 2025. The Sussex ICB had about three weeks to make that initial submission to the Department. Does the Minister think that those timescales are realistic and achievable? Secondly, what will the cost of the redundancies be for ICBs? Has that calculation been done? For Sussex, we are looking at more than half the workforce losing their jobs. Thirdly, what is the impact assessment for patients and the service that they will receive as a result of cuts to ICBs? For too long, social care has been treated like the back door of our public services. It has been overlooked, underfunded and taken for granted. That must change. That is why we must once again ask for more urgency on social care reform. I believe that personal care should be free at the point of use, just like the NHS—

• 9 Jun 2025 · Winter Fuel Payment · Hansard source

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  I have listened to the Minister’s statement and read the words, too, and nowhere can I see an explanation for why this decision has come now, 11 months after it was first announced. Why has this decision come now? Will we have to wait another 11 months for the Government to rethink their cuts to disability benefits?

• 3 Jun 2025 · Prisons: Rehabilitation · Hansard source

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  Dyslexia is vastly over-represented in the prison population. While 10% of the general population are dyslexic, it is thought that as many as half of all prisoners have dyslexia. Does the Minister consider rehabilitation programmes to effectively meet the specific needs of dyslexic prisoners?

• 3 Jun 2025 · Prisons: Rehabilitation · Hansard source

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  18. What assessment she has made of the adequacy of rehabilitative programmes in prisons.

• 22 May 2025 · Business of the House · Hansard source

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  Val Upton is a pillar of the community in the village of Lindfield in my constituency. Among the many hats she wears in her village is her involvement in the Royal British Legion. When I saw Val a couple of weeks ago at the 30th celebration of the Eastern Road nature reserve, she asked me to find out whether more notice could be given for celebrations and commemoration events for VJ Day than were provided for VE Day. Is that possible?

• 21 May 2025 · Parkinson’s Disease · Hansard source

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  It is a pleasure to serve under your chairmanship, Mr Stuart. I thank the hon. Member for Colne Valley (Paul Davies) for securing today’s debate. As hon. Members in the Chamber have noted, Parkinson’s does not just affect movement; it affects every part of life. It disrupts eating, swallowing, sleeping, mental wellbeing and independence. Although more than 40 symptoms are recognised, each person’s experience is different—as unique as their fingerprint. I want to focus a little on one group today: the experience of women with Parkinson’s is often more complex, more misunderstood and more neglected. That was brought to my attention by a constituent of mine in Mid Sussex, whose mother was diagnosed six years ago; it took her mother five years to get an accurate diagnosis. Women are more likely to be misdiagnosed, and more likely to be underdiagnosed. They are more likely to experience delays in treatment and to have their symptoms dismissed or attributed to anxiety or the menopause. Some research even suggests that women’s Parkinson’s symptoms may fluctuate more dramatically due to hormonal cycles, but we do not yet fully understand that because, historically, as in so many other contexts, women have been under-represented in clinical trials. Women with Parkinson’s are also more likely to carry the invisible burdens of being carers themselves, all the while struggling with a progressive neurological disease. We need gender-specific research, treatment strategies and clinical training. We need health professionals who understand that Parkinson’s in women is a critical gap in care that we must close. When I submitted a written parliamentary question about that recently, the response revealed that the National Institute for Health and Care Excellence has no specific guidelines for Parkinson’s that reflect those gender differences. We need, as a society, to realise how differently the disease can present in and affect women. Across the board, people with Parkinson’s face long waits for specialist care, delays in diagnosis and difficulty in accessing essential treatments. I recently talked to Richard, a constituent of mine in Mid Sussex who has Parkinson’s. He spoke of the profound difference that such treatments can make; he told me that they make life-changing differences to him. Yet for too many they are inaccessible due to postcode lotteries, which hon. Members have mentioned, and a lack of trained staff. What is perhaps worse is that some patients in hospitals are not even receiving their medication on time. For people with Parkinson’s, that delay can mean the difference between mobility and being bedbound, between clarity and confusion, and between dignity and indignity. We have to do better. We must also talk about mental health. Nearly half of all people with Parkinson’s experience anxiety and depression. As the disease progresses, up to 60% develop psychotic symptoms, and they are up to six times more likely to develop dementia. Those are staggering figures. What needs to change? We Liberal Democrats are calling for urgent reform, starting with a full review of the medicine supply chain, to ensure that no person has to live in fear of running out of vital medication. We want a faster approval process for new treatments through an expansion of the Medicines and Healthcare products Regulatory Agency’s capacity—not slashing it, as the Government have done by cutting 40% of its workforce. Every person with Parkinson’s or other long-term conditions needs access to a named GP, because continuity of care should not be a luxury. We also need to restore the importance of mental health in NHS planning. The Government’s decision to let the share of NHS funding going to mental health to fall and to scrap targets for dementia and mental health was wrong and totally short-sighted. We also know that family carers are at breaking point. I thank the hon. Members for Aberdeenshire North and Moray East (Seamus Logan) and for Strangford (Jim Shannon), as well as my hon. Friend the Member for Tewkesbury (Cameron Thomas), for raising the issue of the personal independence payment. According to the Government’s own assessment, 150,000 family carers are going to be impacted by 2029-30 as a result of the proposals on PIP, and that is on top of the 800,000 people losing PIP. Has the Minister pressed his colleagues in the Department for Work and Pensions on that point when it comes to conditions such as Parkinson’s? People with Parkinson’s should be supported not only to live, but to live with independence and dignity. Parkinson’s is cruel: it steals movement, independence and, far too often, hope. But we can fight back with the right policies, the right funding and the right political will. We can make a difference. Let us listen to the voices of people living with Parkinson’s—including women, whose voices and needs have been overlooked for far too long.

• 20 May 2025 · Adoption and Kinship Placements · Hansard source

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  It is a pleasure to serve under your chairmanship, Mrs Harris. I thank the hon. Member for South West Devon (Rebecca Smith) for bringing this vital debate. I rise to applaud the work of Beacon House in Cuckfield in Mid Sussex, which serves people across the south-east, including constituents of my hon. Friend the Member for Chichester (Jess Brown-Fuller). I visited recently and met the incredible people who do incredible work there. Jigsaw in Burgess Hill also supports children who have been adopted. I thank the families in Mid Sussex who have taken on children in kinship care or have adopted them. That is an enormous commitment to make and is so important, as we have heard from a number of hon. Members. I also thank them for writing to me. As has been said, many of us do not know what it is like to be an adoptive parent or to take on kinship care; I certainly do not. Until a few months ago, I was unaware of the ASGSF and the vital provision it offers to families who have come forward to take on children. When considering the work provided by the ASGSF, we need to remember that we are talking about families, and because of that, a lot of what goes on is in private, behind closed doors and not very visible to the public. That is why so many hon. Members have come today from all parties to make the case for the ASGSF to be reinstated and properly funded. I thank my hon. Friend the Member for Twickenham (Munira Wilson) for her work in pushing the urgent question that came the day after last year’s funding expired, which resulted in ASGSF funding being secured. Details of the changes to how the funding is allocated were released during recess, and I think we were all deeply dismayed by that. As other Members said, this money gives people the courage to offer to adopt and take on kinship children, and prevents adoption breakdowns every single day. There is a great deal of cross-party support for getting this right, which is why after this debate I am going to the Backbench Business Committee to put in a bid for a Back-Bench debate on this matter, because we share the same strength of feeling. I urge the Minister to come back with a better answer than the one that I suspect she will be able to give this afternoon, although I do not want to prejudge where she is going to go.

• 20 May 2025 · Adoption and Kinship Placements · Hansard source

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  What is the Minister’s assessment of the reserves that local authorities and adoption agencies have available to boost that funding?

• 20 May 2025 · Night-time Economy · Hansard source

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  The Hop Tub in Hurstpierpoint, the Hop Sun in Haywards Heath and the Brickworks in Burgess Hill are three fantastic microbreweries serving the constituents of Mid Sussex. Given the pressures of national insurance and the challenges of business rates, what is the Treasury doing to support these innovative businesses?

• 19 May 2025 · UK-EU Defence and Security Agreement · Hansard source

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  15. If he will make it his policy to negotiate a defence and security agreement with the EU.

• 19 May 2025 · UK-EU Defence and Security Agreement · Hansard source

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  I welcome the news that the UK is deepening defence ties with the European Union, including participation in the €150 billion Security Action for Europe, or SAFE, defence fund. However, given that France has previously said that it wants the UK’s access to be limited to 15%, will the Secretary of State confirm what level of access has been agreed?

• 19 May 2025 · Mental Health Bill [Lords] · Hansard source

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  I thank the Secretary of State for giving way; he is very kind. I was interested, when he was talking about the impacts of mental health on society at large, whether he has given consideration to the Carers Trust proposal, which would amend the Bill so that when a parent has a mental health crisis, checks and safeguards are put in place to ensure that any young carers in that family are suitably cared for?

• 14 May 2025 · Carer’s Leave · Hansard source

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  I thank the hon. Member for that question. I agree there are some exemplar employers who lead the way. As the hon. Member for Strangford (Jim Shannon) said, the benefits to the economy of offering paid leave outweigh the potential costs. Carers are more likely to be women, more likely to be middle-aged and more likely to be juggling children and caring responsibilities. They are that sandwich generation. One in seven people in the workplace are doing just that. They deserve real action and real support. I say to every unpaid carer listening today that, whether they realise it or not, they are pillars of our society. We, here and everywhere else, must recognise that. Carers, we see you and value you; the Liberal Democrats are on your side.

• 14 May 2025 · Carer’s Leave · Hansard source

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  It is a pleasure to serve under your chairmanship today, Mr Stringer. It is also a great pleasure to speak on behalf of the Liberal Democrats in this debate, given that it has been secured by my hon. Friend the Member for North East Fife (Wendy Chamberlain). I thank her not only for securing the debate, but for all the work that she has done on this issue over a number of years. We are all grateful to her. Listening to hon. Members’ contributions, I was struck by the thought that we have represented all the countries of the United Kingdom—from Scotland to England, Wales and Northern Ireland. That makes it clear that this issue is of national importance, but it is also a very personal and specific problem, which many millions of individuals are dealing with in every constituency throughout the country. I think of my Mid Sussex constituent Fe, whom I met a few weeks ago. She is probably about my age, and has basically been a carer for the past 20 years—first for her mother, who sadly passed away, and now for her father, who has recently gone into a care home. Because of that 20 years of caring she has often been unable to work, and has at times been in employment that does not reflect her qualifications or the complexity of the work that she can do. Effectively, Fe has been impoverished by caring for her mother, and now her father. Now that her father is in a care home, the family home—her home—has had to be put on the market. When it is sold, Fe will find herself homeless. The hope is that there might be some money left over from the care home fees, but that may not be the case. Fe is looking at a bleak future: she has not paid into a pension and has been unable to build up a nest egg to look after her future after a lifetime of caring for others. Despite the enormous contribution that they make, unpaid carers like Fe live in financial hardship. As other hon. Members have said, the carer’s allowance, which is the main form of Government support, is just £81.90 a week—the lowest level for a benefit of its kind. That is not just unfair; it is also unsustainable. As our population ages and more people live longer with more complex needs, demand is only going to grow. How can we expect people like Fe to keep caring if they are pushed to the brink financially, emotionally and professionally? I do not see how we can. Worst of all, many carers have been punished for simply trying to make ends meet. As everyone here is probably aware, if a carer earns just £1 over the threshold of £150 a week they lose their entire carer’s allowance.

• 14 May 2025 · Carer’s Leave · Hansard source

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  I thank my hon. Friend for that powerful intervention. I absolutely agree that there should be an amnesty on those overpayments. They were accrued through no fault on the part of the people who received carer’s allowance. It came about through a failure of the Government, the Department for Work and Pensions and His Majesty’s Revenue and Customs to communicate with each other, convey information and follow up on debts as they accrued. This is a scandal. Many of those carers had no idea they were being overpaid. That is why I and Lib Dem colleagues are fighting for a better deal. In our manifesto, we pledged to increase the carer’s allowance by £20 a week, which would have raised it to £101.90—an extra £1,040 a year. We would also raise the earnings threshold to £183 a week, in line with 16 hours on the minimum wage. Crucially, we would taper the allowance gradually, instead of cutting it off entirely. That is fair, and means that carers will not be penalised for working a few extra hours to support themselves. Our vision for carers goes beyond financial support. We would introduce a statutory guarantee of regular respite breaks, because everyone needs time to rest, including carers. Many local councils already offer a respite service, but they have been stretched and pushed to the brink. Those councils do not have the resources to meet the demand for something so vital. We would make it a legal right to support respite care by introducing free personal care and pushing for long-term sustainable funding for social care, which is something I would like to see the Government act much faster on. We must support carers because they are frankly being let down. My Liberal Democrat colleagues and I would introduce paid carer’s leave, building on the Carer’s Leave Act 2023. The coming into force of that landmark law means that 2 million carers have the right to take unpaid leave. Our next step is to make that paid leave, because caring for a loved one should not come at the cost of someone losing their job or income. All of that is rooted in one simple belief: no one should have to choose between caring for a loved one and having a decent life of their own.

• 12 May 2025 · Immigration System · Hansard source

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  The announcements today will deepen social care workforce shortages and risk harm to those who receive care. Have the Government considered the impacts on the sick, the frail and the elderly who rely on care workers to provide vital support? Will the Government publish an impact assessment setting out the effect of their reforms, and what will they do for the quality and availability of care and about the work of the Casey commission?

• 7 May 2025 · Data (Use and Access) Bill [Lords] · Hansard source

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  Yesterday, I spoke to a local author in Mid Sussex, Chris Bradford. He has written a number of brilliant children’s books, including the “Young Samurai” series, which my own children enjoyed a few years ago. Going back to the point made by the hon. Member for Gosport (Dame Caroline Dinenage), Chris told me that he is not against AI—he can see that it has uses—but that what we are seeing is blatant theft. Does the hon. Member for Perth and Kinross-shire (Pete Wishart) agree that the creative industries are part of the answer to growing our economy?

• 6 May 2025 · Victory in Europe and Victory over Japan: 80th Anniversary · Hansard source

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  In 1945, after six long years of hardship, sacrifice and loss, peace returned to a continent torn apart by conflict. When the news broke in Mid Sussex—in our towns and in our villages—people gathered for street parties, shared cups of tea at “bring your own cup” celebrations, held thanksgiving services and lit bonfires that could be seen for miles. There was joy, yes, but there was also reflection, for while victory brought peace, it could never undo the human cost. I recently met a wonderful charity working hard to highlight the work of a specific group during the war: the Photographic Reconnaissance Unit, who were an essential part of the war effort. Among those who served and died in the PRU was William Comber, a constituent of Mid Sussex at that time. Flight Lieutenant William Edward Comber, the son of William and Emma Comber, was born in Cuckfield. On joining the RAF, he was posted to 680 Photographic Reconnaissance Squadron, operating in the Mediterranean. He was taken ill on 5 December 1943 and was taken to the No. 63 general hospital in Salonika, Greece, where, despite the use of an iron lung, he died of polio on 10 December. We thank him, and I ask the Minister to support a national memorial to the Photo Reconnaissance Unit. We also thank the countless others who served and gave everything for their country.

• 6 May 2025 · Victory in Europe and Victory over Japan: 80th Anniversary · Hansard source

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  I thank the hon. Member for her intervention and for her additional insight into the work of the PRU. Coming from an Army family—the kind that took me, aged seven in 1984, on a tour of the D-day beaches as a holiday—we remember our war dead. Our war dead must be remembered, and doing so matters to me. Their strength and sacrifice paved the way for the freedoms we enjoy today. That is why this anniversary matters. It is not just a historical milestone, but a powerful reminder of the values that we must continue to uphold: courage, unity, resilience and an unshakeable belief in the importance of peace. It is fantastic that Mid Sussex is once again coming together to commemorate VE Day in the same spirit shown all those years ago: from a reflective service at the Burgess Hill war memorial to community street parties and parades. With the lighting of beacons in Victoria Park in Haywards Heath and St John’s Park in Burgess Hill, this anniversary will be marked with pride, with dignity and, I know, with heart. VE Day is not just about looking back; it is about reminding ourselves of what was fought for—freedom, democracy and peace—and about recognising how vital it is that we protect those values today. Sadly, we live in a world that still faces conflict and uncertainty. There are dark, divisive forces that seek to disrupt peace, incite hatred and push to the side the lessons that were learned 80 years ago. So on this 80th anniversary, let us remember, let us honour and, above all, let us ensure that the legacy of those who gave everything lives on—not just in our words but in our actions.

• 1 May 2025 · Parkinson’s Awareness Month · Hansard source

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  I thank the hon. Member for Dunfermline and Dollar (Graeme Downie) for bringing forward this important debate, and I thank all Members who have contributed. Everyone has made excellent contributions that were thoughtful and moving. Right now in the UK around 153,000 people are living with Parkinson’s, and that number is set to increase to 172,000 by 2030. Richard from Burgess Hill in my constituency is one of those many thousands. I count Richard as a friend; he is someone I greatly admire for his courage and tenacity. I was lucky enough to speak to him recently and get a brief insight into his life with Parkinson’s. He told me that something he has noticed since his diagnosis is increased anxiety. He says that he now gets anxious about everyday things in a way that he never used to. He also said that the part of experience he has found most depressing is knowing that it is, in his words, “a one-way street”, where his condition can only be managed by using ever-increasing levels of medication. From even a short conversation with Richard, it is clear just how complex people’s experiences can be. It is also clear to me that we need to do better, as many hon. Members have said, and that we have solutions already but we just need to get on with it. Parkinson’s is the fastest-growing neurological condition in the world. It is progressive, it fluctuates, and it affects everything from movement, swallowing, sleep and speech through to mental health. There are over 40 symptoms, and each person’s experience is unique. Half of those living with the condition, like Richard, experience anxiety or depression, and up to 60% can develop psychosis. They are also six times more likely to develop dementia. Parkinson’s UK has identified some of the major failings in care today. They include long waits for specialists, a lack of access to expert multidisciplinary teams, people not getting their medication on time in hospital, and limited mental health and dementia support. There is also a postcode lottery when it comes to advanced treatments such as Produodopa and deep-brain stimulation. Those failings have consequences: unplanned hospital stays, severe complications and worsening mental health. Parkinson’s costs the UK an incredible £3 billion a year. In England alone, unplanned hospital admissions cost £277 million. So this is not only a health crisis but one with significant economic impacts. I and my Liberal Democrat colleagues believe that the system must change urgently and that the Government have to act. First, we have got to fix the basics. To do that, we need to review the medicines supply chain. People with Parkinson’s must get their meds on time. We also need to expand the MHRA’s capacity, reversing the 40% workforce cut, and reducing the time for treatments to reach patients. Secondly, we need to put care and support front and centre. We can do that by giving people with Parkinson’s access to a named GP—someone who knows their story and their condition—and by making mental health a priority, not an afterthought. That means regular mental health check-ups, easier access to services through walk-in hubs and restoring the mental health and dementia care targets that the Government have abandoned. Thirdly, the Government must step up and support carers. Behind every person with Parkinson’s, there is often someone else who cares for them; someone who is quietly exhausted. We must provide respite breaks and ensure that carers have access to paid leave. We need to fix the broken social care system once and for all. It is time for those cross-party talks—no more delays. As I have said in this place before, we will clear our diaries to get those talks happening. This issue is simply too important for diary clashes. I wonder whether the Minister can give us any clarity and a date on those vital talks. Finally, we have got to help people live and work with dignity. I and my Liberal Democrat colleagues are campaigning for: a new right to flexible work; better accessibility standards for public spaces; a stronger blue badge framework; the incorporation of the UN convention on the rights of persons with disabilities into UK law; and the closing of the disability employment gap. We can do that if we implement a dedicated strategy for disabled workers, simplify the application process and introduce adjustment passports so that workplace support follows the person, even if their job changes. This is a health issue, an economic issue and a social justice issue. As others have said, it is about human dignity. We owe it to people living with Parkinson’s that we must do better, not some day but now. Let us build a future where those with Parkinson’s like Richard get the proper help and support they deserve.

• 1 May 2025 · Rural Businesses · Hansard source

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  11. What steps his Department is taking to support businesses in rural areas.

• 1 May 2025 · Rural Businesses · Hansard source

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  I thank the Minister for his answer. I am encouraged that his Department is working with other Departments. There are brilliant vineyards in Mid Sussex, such as Bolney wine estate, which produce high-quality English wine. They form a vital part of the rural economy and they also entice domestic and international tourism. With the end of the wine duty easement on 1 February causing significant concerns across the sector, what steps is the Minister taking to ensure that the English wine industry is not damaged by that and instead can continue to grow and go from strength to strength?

• 30 Apr 2025 · Energy Grid Resilience · Hansard source

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  Will the Minister expand a little on a question put to him by my hon. Friend the Member for Thornbury and Yate (Claire Young)? The PSTN, or public switched telephone network, switch-off means that by the end of 2027 all landlines will require an electricity supply. This means that the mobile network becomes ever more vital for people who require their mobile phones for medical care or even to make a 999 call in the event of an emergency. What assessment has been made of the resilience of the mobile network in the event of power outages? What more needs to be done to make sure we are ready for that kind of situation?