Marie Tidball MP: speeches

Speeches

• 1 Jul 2025 · Universal Credit and Personal Independence Payment Bill · Hansard source

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  In March 2020, when the Conservative Government looked like an outlier in appearing to pursue a strategy centring on herd immunity, I felt raw, hot fear. Thinking of my toddler and what might happen if I caught coronavirus meant that I sobbed deeply. After 10 years of austerity, I knew then that disabled people would pay an enormous price, and they did: almost 60% of covid-related deaths in that first wave were of disabled people. I vowed then that I would do all I could to create a country that treats disabled people with dignity and respect. The social security system was broken by the Conservatives’ legacy of austerity and their monumental mishandling of the covid pandemic. I am now one of the only visibly physically disabled Members of Parliament. I am proud that our manifesto committed to championing the rights of disabled people, and the principle of working with disabled people to ensure that our views and voices are at the heart of all we do. My communities nurtured me growing up, and they taught me the values of fairness, equality and community. It is with a heavy, broken heart that I will be voting against this Bill today. As a matter of conscience, I need my constituents to know that I cannot support the proposed changes to PIP as drafted in the Bill. Since April, I have been engaging relentlessly with the Government at the very highest level to change their proposals, making clear that I could not support the proposals on PIP. PIP is an in-work benefit designed to ensure that disabled people can live independently. Low-level support such as PIP helps to build the bridge to the deinstitutionalisation of disabled people, keeping us out of the dark corners of hospitals, prisons and social care settings. The concessions that the Government have announced are significant, including that all recipients of PIP who receive it will continue to do so. While that will come as a relief to my 6,000 constituents who receive PIP, 4 million disabled people still live in poverty in the UK. The proposed changes to be made in Committee are still projected to put 150,000 people into poverty. I cannot accept that or a proposed points system under current descriptors, which would exclude from eligibility those who cannot put on their underwear, prosthetic limbs or shoes without support.

• 2 Jun 2025 · Bus Services (No. 2) Bill [Lords] · Hansard source

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  Building better buses is in my blood. Growing up, my dad was chair of Barnsley passenger transport; South Yorkshire had a world-class bus service, thanks to our Labour county council. Labour knew then, as we know now, that buses are for the people. The Conservatives and Reform just don’t get it, as is demonstrated right now by those empty Opposition Benches. When they were in government, the Conservatives promised South Yorkshire a London-style transport system. Instead, after 14 years of their neglect, our constituency has lost 53% of its bus services, including the vital SL1 Supertram service link connecting Stocksbridge and Oughtibridge to Sheffield. The crucial number 57 and 57A was left frequently running late, or failed to turn up at all, and the cuts to the number 43 and 44 buses seriously affected my Dodworth constituents. The reality for our rural neighbourhoods is even more stark, as constituents at my community event on transport told me—villages such as Bolsterstone are entirely cut off, Ingbirchworth loses bus connectivity after certain hours of the day, and the number 21 from Penistone to Barnsley is a route crying out for urgent improvements. Our Labour Government know that buses are a lifeline that connects our families and communities across Penistone and Stocksbridge. That is why I am proud that through our better buses Bill, we are empowering communities by ensuring that buses serve local people rather than distant corporate interests. The Bill will remove barriers to public control and franchising, placing decisions over bus routes, times and fares back into the hands of communities. Our Labour South Yorkshire Mayor, Oliver Coppard, has been driving change locally. His franchising consultation involved nearly 8,000 people, with 75% strongly supporting it. The plans allow profits to be reinvested directly into better, more reliable services. That is why I am proud that our Transport Secretary has announced a landmark £1 billion fund to transform England’s bus services, including £17 million specifically for South Yorkshire. This issue matters deeply to local people in my constituency. Older and disabled constituents often tell me that they are left stranded, enduring painfully long waiting times due to unreliable services, and facing distressing situations including toileting issues and missed NHS appointments because buses simply fail to appear. That is unacceptable. That is why it is right that the Bill will deliver a more accessible and inclusive bus network, as well as introducing a £3 maximum cap on bus fares until 2026, to encourage more people to use public transport. After years of broken promises, our Labour Government are taking urgent action to rebuild Britain’s bus services, ending the postcode lottery and delivering a public transport system that is affordable, accessible and dependable, enabling South Yorkshire to bring back lost bus routes. I am committed to working with our Labour mayor and the leader of Sheffield city council to secure the return of the quick, reliable SL1 supertram link and our local hopper bus. We need bold bus solutions now, while we await the long-term infrastructure improvements I am advocating for, like the tram-train extension to Stocksbridge via Oughtibridge, Wharncliffe Side and Deepcar. Every single one of us has the right to use buses to travel to work and to see our families and friends. Public transport is fundamental to achieving social justice, so that young and old, in our rural areas—our towns and villages from Gilroyd to Grenoside, High Green to Hoylandswaine and Chapeltown to Ecclesfield—can depend on public transport for work, education and access to healthcare. I commend the Bill to the House.

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

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  One of the reasons I stood for Parliament was to work hard to create a society that values disabled people, that treats us with dignity and respect, and that ensures there is nothing about us without us. It is right that this Government will fix the broken system to ensure that we give mental health the same attention as physical health. I am pleased to see the four key principles from the independent review of the Mental Health Act at the heart of the Bill: choice and autonomy, least restriction, the principle of therapeutic benefit and, most importantly, treating people as individuals. After 14 years of a Conservative Government, over 2,000 autistic people and people with a learning disability are in mental health hospitals in England. Some 92% of those people are detained under the Mental Health Act 1983, and the average length of stay for in-patients is almost five years. This is a human rights scandal, as the Joint Committee on Human Rights concluded in 2019. The current situation is simply wrong. Autism and learning disabilities are not mental health conditions, and yet under the current Mental Health Act, autistic people and people with a learning disability can be detained in mental health hospitals indefinitely. In my 15-year career working with autistic people and those with learning disabilities, along with autism organisations up and down the country, including the National Autistic Society and the Autism Alliance, I have seen the tragedy of autistic people cycling through the mental health system because of those measures and the failure of public services to provide adequate social care on discharge from hospital orders. As an MP, I know from my constituency that too many people are still being detained who could be supported to live well in our communities by organisations such as Greave House Farm Trust and Action for Autism Barnsley which are on my doorstep. The most significant change in the Bill is the removal of autism and learning disability from the definition of mental disorder under section 3 of the existing Act. This vital change means that autistic people and people with a learning disability cannot be detained for treatment unless they have a co-occurring mental health condition that requires in-patient mental health care. The Government have said that “the proposed changes to the detention criteria for people with a learning disability and autistic people will only be switched on when systems are able to demonstrate a sufficient level of community support”. It is crucial for that to happen quickly, through the Government working closely with autistic people and those with a learning disability, as well with as advocacy groups, to publish a plan to build sufficient support in our communities up and down the country. My book on the treatment of autistic people in the criminal justice system demonstrated that ensuring that there is an appropriate level of services in the community is essential in preventing the needs of autistic people and people with a learning disability from becoming too complex, leading to admission to mental health hospitals. It also demonstrated the need to support safe discharge out of hospital. Critical to reducing the numbers of those currently detained in hospital under the current law are care, education and treatment reviews for adults and children who are autistic or have a learning disability, which will help speed up discharges, prevent admission and ensure that the person is being given appropriate care. I am delighted that the Bill will make those reviews statutory in in-patient settings. The responsible commissioner, clinician, integrated care board and local authority must have regard to the recommendations arising from them. As chair of the all-party parliamentary group on autism, I am aware that recommendations are often not followed in an expeditious manner. Therefore, there is an opportunity to strengthen the duty on responsible parties to follow recommendations from those reviews. The Health Secretary has been moving mountains to work on our 10-year plan. I therefore hope that the Bill’s 10-year implementation period for the changes to detention criteria will align with his important work. He is also doing an incredible job to move to a prevention-led health system, and that provides an opportunity for an integrated approach to community support, including working with the Ministry of Housing, Communities and Local Government to ensure there is adequate housing in every integrated care system. The exclusion and marginalisation of autistic people and those with learning disabilities through their institutionalisation in hospital perpetuates their exclusion from our society. I am proud that our Government are tackling these issues so early on in this Parliament, alongside their commitment to the mental health investment standard, the recruitment of 8,500 mental health workers, and work to deliver a long-term plan for the reform of adult social care. Society is an order of equality and non-discrimination. It is all the richer where autistic people and people with learning disabilities are included within it to fulfil their potential. I commend this Bill to the House.

• 8 Apr 2025 · National Wealth Fund: Regional Growth · Hansard source

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  There is currently no tram network from central Sheffield to Oughtibridge, Wharncliffe Side, Deepcar or Stocksbridge, and no operational train service to those areas. My constituents want the Sheffield tram network to be extended to Stocksbridge and to connect those rural communities with jobs, education and hospitals, as well as supporting the advanced manufacturing district and the steel plant in Stocksbridge. Will the Minister meet me and the Mayor of South Yorkshire before the spending review to discuss the next steps to establish the Stocksbridge extension to the Sheffield tram-train service?

• 3 Apr 2025 · UK-US Trade and Tariffs · Hansard source

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  I am pleased to hear the Secretary of State’s commitment to steel. Stocksbridge Speciality Steels in my constituency is a strategically significant site with world-class, unique capability for creating specialist parts that will be essential in increasing our defence capacity and net zero infrastructure. Last week, I held a community listening event on the Government’s excellent steel strategy. The message was clear: let us ensure that British-made steel is best. Does the Secretary of State agree that today’s news further demonstrates why it is so important that this Government are committed to a £2.5 billion plan for steel?

• 25 Mar 2025 · Terminally Ill Adults (End of Life) Bill (Twenty-ninth sitting) · Hansard source

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  I beg to move, That the clause be read a Second time. This is the final new clause of the Committee. As I said in support of new clause 25 and associated amendments last week, I want to strengthen the voice of disabled people in the Bill. New clause 35 would require the voluntary assisted dying commissioner to establish a disability advisory board that would report annually on the implementation and impact of the Act on disabled people. The new clause has been designed to ensure that disabled people have a voice at the heart of the Bill and an ongoing role in monitoring its impact. The disability advisory board model reflects a structure that was used at the Department of Health to implement the Autism Act 2009 and monitor the implementation of its provisions, statutory guidance and strategy. It was a highly effective body. Including a disability advisory board structure on the face of the Bill would entrench the board in the work of the commission, enabling a long-term and iterative structure in which disabled people could report on the reality of the impact of the Bill on disabled people across this country. This reflects comments made by Dan Scorer of Mencap in oral evidence. He said that if the Bill was passed, “We would want to see strong representation from patient groups…as well as from people who have been involved in the process, such as family members, advocates and clinicians, to make sure that if serious issues are being raised, they can be picked up early and addressed.” –– [ Official Report, Terminally Ill Adults (End of Life) Public Bill Committee, 30 January 2025; c. 280-81, Q367.] The board must therefore consist of “(a) people who have a disability under the Equality Act 2010, (b) representatives from disabled people’s organisations, and (c) other such persons or organisations as the Commissioner considers relevant to the impact of the Act on disabled people.” The commissioner would, within six months of being appointed, have to appoint a programme board to advise on the implementation of the Bill, and annually thereafter report on the impact of the Bill’s operation on disabled people. The clause reflects the learning of Dr Greg Mewett, the specialist palliative care physician from Australia who gave oral evidence to the Committee about the Australian implementation taskforce, which includes a strong disability advocate. My new clause would go further, by including a rigorous reporting process that requires the advisory board to report to the Secretary of State and the commissioner within six months of the commissioner being appointed, and annually thereafter. It also provides: “The Secretary of State must, within three months of receipt of any report under subsection (3), lay the report before both Houses of Parliament.” In the oral evidence sessions, I asked witnesses for their views on what structures or mechanisms could work to facilitate the opportunity to hear the voices of disabled people in monitoring the implementation and impact of the Bill were it to pass through Parliament. Dr Miro Griffiths said: “I think there needs to be further robust action around how to collect data and allow it to be analysed, to see the trends that are occurring in why people are pursuing this option and how that may play into broader political and socioeconomic issues, such as a lack of services elsewhere or frustrations for disabled people and their families in trying to access particular services…I would therefore encourage their representation on any form of advisory council. I would also request that disability studies scholars, who are often left out of the discourse around disability policy, are part of any form of mechanism to advise or scrutinise.” –– [ Official Report, Terminally Ill Adults (End of Life) Public Bill Committee, 29 January 2025; c. 145, Q183.] Subsection (2)(b) and (c) would provide for this. Professor Tom Shakespeare corroborated the benefits of such an advisory board, calling it a “very good idea.” Importantly, Fazilet Hadi, from Disability Rights UK, stated: “Should the Bill go through, it would be good to see a monitoring mechanism. I cannot say what that should be, but it would be good to see disabled people shape it. Some 45% of older people are disabled people, so disabled people are going to be very affected by the Bill.” Poignantly, she went on: “It is often our experience that we are the last people who are spoken to; maybe that is what is behind the question. We should of course be at the table now in respect of whatever mechanisms, and in the shaping of any implementation, should the Bill be passed.” –– [ Official Report, Terminally Ill Adults (End of Life) Public Bill Committee, 29 January 2025; c. 175, Q227.] There is, and there should be, nothing about us without us. As a disabled Member of Parliament, I am grateful to my hon. Friend the Member for Spen Valley for inviting me to sit on this Committee. Through this new clause and my earlier new clause 25, I have worked hard to put together a structure that ensures that disabled people are firmly at the table in the process of monitoring the implementation and impact of the Bill. I urge members of the Committee to support new clause 35.

• 12 Mar 2025 · Points of Order · Hansard source

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  On a point of order, Madam Deputy Speaker. I would like to correct the record and make a declaration of interests. In my excitement while making my first intervention during proceedings on the Employment Rights Bill yesterday, I did not point Members to my entry in the Register of Members’ Financial Interests or mention my proud membership of the Community, GMB and Unison unions. I would like to ensure that that is on the record as well as in the register.

• 6 Mar 2025 · Business of the House · Hansard source

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  Flooding has caused heartache for families and communities in my constituency. In order to be protected from extreme flooding, they desperately need Sheffield city council’s excellent proposals for the upper Don flood alleviation scheme, including work on the Clough Dike culvert and Whitley Brook improvements. Despite widespread local support and the importance of that scheme, the Conservatives never actually allocated funding to it. Will the Leader of the House allow time to debate flood alleviation schemes, to ensure that the appropriate funding is allocated in the forthcoming spending review?

• 30 Jan 2025 · Terminally Ill Adults (End of Life) Bill (Seventh sitting) · Hansard source

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  Q Dan, I am really keen that we ensure that if the Bill passes, the voices of disabled people are continually involved in understanding its impact, particularly on the issue that you have just raised. Earlier, we heard evidence about implementation taskforces that are used in other jurisdictions. I am considering tabling an amendment on an advisory council. How might we ensure that the voices of people with learning disabilities can be included in such a body? Dan Scorer: There are a couple of things that I would like to say in response. One is about clause 31, on guidance from chief medical officers. Immediately, I would say that people with a learning disability should be involved in the development of that guidance from chief medical officers. That guidance will be key to many of the issues that we have discussed. Clause 35 is about the review of the Act. The lived experience of people is absolutely vital to that. The Bill says that it will be five years until we have that review. Our view is that that is far too long. If the Bill becomes law and if there are really serious issues and discrimination taking place against people, we will want to know that a lot earlier than in five years’ time, and we will want action to be taken. Our suggestion is that review should be earlier. We would want to see strong representation from patient groups across that, as well as from people who have been involved in the process, such as family members, advocates and clinicians, to make sure that if serious issues are being raised, they can be picked up early and addressed.

• 29 Jan 2025 · Terminally Ill Adults (End of Life) Bill (Fifth sitting) · Hansard source

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  Q With respect, my question was about whether you think that, should the Bill go through Parliament, there should be some kind of body, possibly an advisory council, that disabled people in particular should be involved with. Your other point speaks to some evidence that we heard yesterday and earlier about the anchoring, where there is assisted dying in the legal system, of the quality and level of provision of palliative care. I would be grateful if you could speak to the point of my original question, which was about the need for some kind of advisory body that includes disabled people, should the Bill pass. Baroness Falkner: Had there been a Public Bill consultation on the Bill, you would have heard from the different players that need to be consulted. We do not have an opinion on the kind of advisory body, because we would find it difficult to see where it would fit in with the provisions of this particular Bill, but a public consultation in advance of the Bill being written would have been the way to deal with that.

• 29 Jan 2025 · Terminally Ill Adults (End of Life) Bill (Fourth sitting) · Hansard source

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  Q This question is for Professor Tom Shakespeare and Dr Miro Griffiths. One of the amendments I am backing would establish an advisory council on the impact of the Bill on disabled people, because I am passionate that we monitor the impact on that group of people, should the Bill pass through Parliament. What structure or mechanism do you think could work to facilitate that? Dr Griffiths: This plays into a broader issue around the reporting mechanisms associated with the Bill. I think there needs to be further robust action around how to collect data and allow it to be analysed, to see the trends that are occurring in why people are pursuing this option and how that may play into broader political and socioeconomic issues, such as a lack of services elsewhere or frustrations for disabled people and their families in trying to access particular services. This goes back to a point that Tom made. While we may see popular opinion within disabled people’s communities, it is worthy of note that no deaf and disabled people’s organisation—these are organisations that are representative of disabled people who engage critically with the issues facing disabled people’s communities—has been in support of this. I would therefore encourage their representation on any form of advisory council. I would also request that disability studies scholars, who are often left out of the discourse around disability policy, are part of any form of mechanism to advise or scrutinise. Professor Shakespeare: I think the council is a very good idea. It should reflect the range of views, as Miro says. In Oregon, disabled rights advocates have not, as I understand it, opposed the Act that they now have. Of course, it is mixed, but some disability groups are definitely in favour. There is a difference between organisations of disabled people and disabled people on this. Politically, the disability rights community are against assisted dying—they always have been. That does not mean that they reflect what ordinary disabled people want, and that is what is important. I think you should be interested in what people want, and they want this.

• 28 Jan 2025 · Terminally Ill Adults (End of Life) Bill (Second sitting) · Hansard source

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  Q Professor Ranger, may I pick up on the points that Glyn Berry made about the different circumstances in which patients find themselves? The barriers to healthcare as a result of health inequalities, access to education and disability are well documented. How could your members help to remove the barriers for such groups in access to the provision of assisted dying? Professor Ranger: It is vital that any of those barriers be removed and that we always maintain outstanding care at the end of someone’s life. The reality is that the majority of palliative care is given by nursing staff, whether it is in the community, in someone’s home, in a hospice or in a hospital. It is key that it be an expertise and a specialist practice in which someone has extra training and extra education. The skills of listening to patients, advocating for them and ensuring that they are pain-free at the end of their life—these are skills that nurses have now, and it is vital that our nursing members maintain them. They are often the one a patient will speak to at 3 in the morning when no one is there. As Glyn said, it is vital that the wider team be included in the Bill. The Bill talks about the guidance and recommendations being for the chief medical officer, but I think it is absolutely vital that the chief nursing officer be a key part of the guidance and the drawing up of any care, because even in these circumstances it is nursing staff who will give the majority of the care.

• 23 Jan 2025 · Topical Questions · Hansard source

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  Two weeks ago, my constituency was hit by the worst snow in 15 years, leaving vulnerable and older residents, schools and GP surgeries blocked in by the snow. I commend the Barnsley council team, who were out 24 hours a day, eight days a week solid, but because resources are stretched, their gritters can cover only the council’s primary and secondary roads. Does the Minister agree that much more should be done to improve national resilience in extreme and exceptional circumstances where snow is prolonged by cold temperatures, by giving local authorities that cover rural areas such as mine increased gritting resources and access to snow ploughs?

• 17 Dec 2024 · Employment Rights Bill (Thirteenth sitting) · Hansard source

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  I draw your attention to my declaration of interests, Mr Mundell. I am a member of the Community union, Unison and GMB. I found it difficult to hear, in anything the shadow Minister just said, any rationale for getting rid of this body all those years ago. I missed three years of school as a child because of the surgeries I needed. Incredible classroom teaching assistants helped me to build my confidence and learn to mix with other children again when I returned—making education and learning an escape, a way to express myself, to overcome people’s assumptions about my disability and to feel free. I stood in my constituency because I wanted to use my skills and experiences to give back to the communities that gave me so much. To know that, because of this Bill and the clause before us now, teaching assistants and other school support staff like the ones who made school a less daunting place for me will once again have a collective bargaining system for pay and conditions—which will ensure that those staff are finally valued and recognised for their vital work—is a very great privilege indeed. The reinstatement of the school support staff negotiating body in England, previously scrapped by the coalition Government for reasons that still remain unclear, will be key to providing professional recognition for a group of staff who have been overlooked for far too long. As Unison, of which I am proudly a member, has highlighted, the proposals in this clause “demonstrate that the Employment Rights Bill isn’t just tackling worker’s rights—it holds the key to tackling long standing public policy failures that have been ignored because they affect workers and service users whose voices are too often neglected by decision makers. Tackling this neglect and allowing trade unions to engage in constructive social partnership and better represent their members is long overdue”. This clause therefore empowers that group of working people, who have been so long overlooked by the Government, to have a better life at work. It will help trade unions to raise standards and pay across the labour market.

• 26 Nov 2024 · Employment Rights Bill (Second sitting) · Hansard source

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  I refer again to my declaration of interests and to my membership of the Community union, Unison and the GMB.

• 26 Nov 2024 · Employment Rights Bill (First sitting) · Hansard source

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  I also refer to my declaration of interests. I am a member of the Community union, Unison and GMB.