Jonathan Brash MP: speeches 2026

Speeches

• 21 Jan 2026 · Warm Homes Plan · Hansard source

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  Some 15% of my constituents live in fuel poverty, and many more go without in order to pay the outrageous energy bills they face. Many vulnerable people, children and elderly people are living in properties that are too cold and too damp. That is not acceptable to me, and I know that it is not acceptable to the Secretary of State. How will we ensure that the welcome measures in this plan reach the most vulnerable people in communities in Hartlepool and beyond?

• 21 Jan 2026 · Water White Paper · Hansard source

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  Hartlepool is a coastal community home to some of the most beautiful beaches in the north-east, but they are too often polluted by water companies to the detriment of my constituents. I absolutely agree with the Secretary of State that this Government have done more in 18 months to fix this mess than any other Government in history, but does she agree that once we have forced these failed water companies to get their house in order and clean up our waters, we should get them out of the ownership of foreign nationals, hedge funds and private equity, and reverse the worst privatisation in British history?

• 20 Jan 2026 · Mobile Phones and Social Media: Use by Children · Hansard source

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  It is clear that social media harms our children. I am firmly of the belief that when a child is being harmed, it is the Government’s duty to act. I support a ban, but even the most cursory engagement with Hartlepool residents shows me very clearly that there is a range of views among parents on this issue. Can the Secretary of State fathom what possibly could be the objection to listening to parents?

• 19 Jan 2026 · Sale of Fireworks · Hansard source

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  It is a pleasure to see you in the Chair, Ms Jardine. I thank the hon. Member for Keighley and Ilkley (Robbie Moore) for the expert way in which he opened the debate. I think the last time I spoke in a petition debate that he led, Members across the Chamber agreed about mandatory digital ID, so I am hoping for a similar outcome today. I thank the petitioners, Helen and Robert, everyone else who is in the Public Gallery here today, and the people across the country who have signed the two petitions. In my constituency alone, 361 people signed the petition calling for firework sales to be limited to council-approved events and 227 signed the petition calling for lower noise levels. I have also received 114 emails from Hartlepool residents, all calling for tighter controls or an outright ban on personal use. That tells us something very clear: this is not a niche concern. It is widespread and persistent across the country, including in Hartlepool. I want to be clear from the outset that I support public firework displays. When they are organised and well managed, they bring communities together. As a child, I loved attending the firework display at Ward Jackson Park in Hartlepool. Hartlepool is fortunate to have a major public display still at Seaton Carew, supported by Hartlepool borough council and sponsored by X-energy, and I am grateful that it continues. What my constituents are experiencing now, though, goes far beyond a few celebratory nights. Fireworks in Hartlepool begin in September, and intensify through October, November, December and into early January. For weeks at a time, there is no predictability and no break—and that has real consequences: children awoken night after night and elderly residents reporting fear and anxiety. In 2024, Hartlepool police was forced to issue a dispersal order on the Bishop Cuthbert estate where fireworks were being used as weapons, seriously injuring at least one young person. Pets suffer distress, and veterans and others living with trauma are affected by the sudden loud explosions. Calling for action is not being anti-fun; it is respecting others. There is nothing nanny state about protecting the most vulnerable in our society. Limiting sales to council-approved events would bring order and safety to communities such as Hartlepool. Reducing the maximum noise level to 90 dB is a simple, common-sense approach. Quieter fireworks already exist; alternatives are available. People in Hartlepool are not asking for celebrations to end. They are asking for balance and fairness. I urge the Minister, who I know has listened intently all afternoon, to listen to the petitions and to the messages from Members across the House and from the people of Hartlepool. The current system is not working and needs to change.

• 13 Jan 2026 · Topical Questions · Hansard source

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  T8. Currently, not a single NHS dentist in Hartlepool is taking on new patients, and many of my constituents are desperate. We have made real progress on urgent care, including a new urgent dental access centre, but it is not enough. What more will be done to fix NHS dentistry in Hartlepool and across the country?

• 13 Jan 2026 · Brain Cancer Treatment: Hartlepool · Hansard source

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  7. What steps he is taking to improve access to tissue freezing for brain cancer patients in Hartlepool.

• 13 Jan 2026 · Brain Cancer Treatment: Hartlepool · Hansard source

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  I thank the Minister for her answer, and for her positive response during a recent Westminster Hall debate on this issue. As she will recall from that debate, my constituent Trevor Jones died in September last year from glioblastoma. His widow, Samantha, learned only later that life-extending treatment options might have been available had his brain biopsy not been stored in paraffin blocks, but instead been flash frozen. Will the Minister recommit to examining how flash freezing can be made standard practice for brain biopsies across the NHS, and will she meet me and Samantha to discuss a way forward?

• 12 Jan 2026 · Topical Questions · Hansard source

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  In purporting to discharge their homelessness duties, some southern local authorities are bundling vulnerable people into taxis in the middle of the night and dumping them in Hartlepool because our housing is cheaper. They are acting in a vile way. I welcome the fact that the Minister has written to me and set out her belief that we need to ban this poor practice. Does she agree that we need to ban it outright?

• 7 Jan 2026 · Advanced Brain Cancer: Tissue Freezing · Hansard source

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  It is a pleasure to serve under your chairmanship, Mr Western. I start by saying how honoured I am to follow the hon. Member for Strangford (Jim Shannon), who demonstrates so ably that the high-minded ideals of representation, compassion and decency run right through this place, and perhaps more often than is fully recognised. I thank him for his contribution. I also thank my hon. Friend the Member for Caerphilly (Chris Evans) for securing this important debate, and his constituent Ellie for her campaigning—I can say without hesitation that you have another signed-up supporter of Owain’s law here today in me. As my hon. Friend demonstrated, MPs do not generally come to these debates to have abstract policy discussions, but to do our most important job: to be the voice of our constituents. That is where I want to start. I want to share the experience of my constituent, Samantha Jones, who came to see me alongside her father-in-law, Garry Jones, following the death of her husband, Trevor, from glioblastoma. Trevor was just 41 years old when he suddenly became ill on Christmas Day 2024. Until that moment, there had been no warning signs and no symptoms that anyone could reasonably have recognised. Tests revealed stage 4 glioblastoma, and he was given six months to live. He lived for nine months and died in September 2025. Like so many families confronted with this diagnosis, they were plunged into a world of shock, fear and urgent decision making. A biopsy was taken, which confirmed and sequenced the cancer, and at that point the family believed that everything possible was being done. It was only later, through Samantha’s own research and through conversations with an oncologist experienced in international practice, that they learned something that they found deeply troubling. There were treatments that may have been available to Trevor on the basis of his biopsy, but they could not be used because the tissue sample had not been flash frozen. Instead, the biopsy had been stored in paraffin blocks, which is standard practice in much of the UK, as we heard from my hon. Friend the Member for Caerphilly. By the time the family discovered the significance of that, it was too late: Trevor was too ill to undergo another biopsy, too unwell to travel and unable to take part in clinical trials. Samantha told me that in Germany brain tumour biopsies are flash frozen as a matter of course. That allows for far more advanced genomic and molecular testing, which can open the door to a wider range of treatments. In the UK, by contrast, flash freezing is done only if it is specifically requested, or if the patient is part of a clinical trial. For families who have just been told that their loved one has an aggressive and terminal brain cancer, that is not a realistic expectation. They are in shock. They are terrified. They are placing their trust in the system to do everything that it can, without knowing that one unmade request could close off future options entirely. That raises a simple but profound question, which I put to the Minister: why does the NHS not routinely flash freeze all brain tumour biopsies as standard practice? What can we do to change that here and now? I am not suggesting false hope. I fully recognise that glioblastoma remains a devastating diagnosis with limited treatment options, but when options are already so few, it cannot be right that patients are denied even the possibility of certain treatments because of how their tissue samples were stored. This is also an issue of fairness and equality. Access to the best possible diagnostics and research pathways should not depend on geography, chance or whether a family happen to know the right question to ask at the worst moment in their lives. Samantha and Garry came to see me not only in grief but with a determination—one reflected by Ellie, in the Public Gallery this morning—that something good might come from their devastating experience. They want other families to be spared the same sense of missed opportunity and unanswered questions. More broadly, brain cancers remain under-recognised and underfunded compared with other forms of cancer, despite their severity and poor outcomes. If we are serious about improving survival, treatment and research, we must be willing to look honestly at current practice and ask whether it is good enough, because I think the consensus is that it is not. I hope that the Minister will engage constructively on this issue and consider making the flash freezing of brain tumour biopsies standard practice across the NHS, because that could improve patient access to treatment, strengthen research and offer families reassurance that everything possible is being done. For Trevor, such a change has come too late, but for future patients it does not have to.