The landmark may now also be able to open for a longer period, generating more income. It currently opens its State Rooms to visitors each summer and on selected dates throughout the rest of the year, the proceeds of which go to the Royal Collection Trust, a charity responsible for the care and conservation of royal art.

The King will continue to host a range of events at the palace, from state banquets and garden parties to receptions and audiences with the prime minister and new ambassadors.

“His Majesty retains huge affection for Buckingham Palace and a deep respect for its role in royal and public life,” said a palace spokesperson. “It will be a buzzing hive of royal activity in every other way.”

Norman Baker, former Lib Dem Home Office minister and a critic of royal funding, told the BBC that Buckingham Palace visitor ticket sales should instead go to the Treasury.

“They bring in millions every year, so what should happen is if they’re not living in Buckingham Palace, [they] should open it to the public and all the money from visitors 12 months of the year should go to the Treasury to help pay for refurbishment,” he said.

Graham Smith, CEO of Republic, which campaigns for an elected head of state, said: “The government agreed to spend £369m on refurbishing Buckingham Palace and now Charles doesn’t want to use it.

“But he’ll keep it under lock and key for when he does. Clearly, the palace needs to be fully open to the public all year round.”

The collision happened in the early hours of this morning

Two people have been taken to hospital following a serious crash in Co Fermanagh.

Emergency services have been at the scene of a serious road traffic collision on the Belfast Road in Maguiresbridge this morning, Friday, June 26.

Police earlier said the road was closed in both directions while officers dealt with the incident.

A PSNI spokesperson said: “Road users are advised the Belfast Road, Maguiresbridge is closed in both directions this morning, Friday June 26, due to a serious road traffic collision.

“PSNI officers are diverting traffic flow via the Boyhill Road. Please seek an alternative route for your journey at this time.”

In a statement, the Northern Ireland Ambulance Service said it received a 999 call at 01:29 on Friday, June 26, following reports of a road traffic collision on the Belfast Road area, Maguiresbridge.

“NIAS tasked two emergency ambulances to the scene. Following assessment and initial treatment at the scene, two people were taken to the South West Acute Hospital by ambulance,” a spokesperson added.

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Imagine a global political summit that shapes the future of our planet where one of the most populated countries in the world does not have a voice? This may seem unlikely, but currently 1.3 billion disabled people (nearly the population of China) do not have formal representation at policy talks held by the UN’s climate change body.

The United Nations Framework Convention on Climate Change (UNFCCC) hosts negotiations to limit global greenhouse gas emissions and address climate change. Yet, people with disabilities are two to four times more likely to die or be injured in climate-related emergencies such as heatwaves, flooding and storms.

People with psycho-social disabilities such as severe depression, schizophrenia, bipolar disorder or post-traumatic stress disorder are three times more likely to die during heatwaves. During the 2018 heatwave in Montreal, Canada, people with schizophrenia accounted for 25.8% of heat-related deaths, despite representing only 0.6% of the population.

The anti-psychotic medication used to treat symptoms makes patients less tolerant to heat. This increases the risk of heatstroke, severe dehydration and can prove fatal. A wide range of medications has similar effects.

These staggering statistics show the need to place disabled people, who are some of the most vulnerable, at the centre of climate change negotiations. In emergencies, additional barriers put disabled people at greater risk. These include inaccessible evacuation routes, power outages when electricity is required for equipment, and an increased risk of certain infectious diseases.

For five years, disability researchers, charities and advocacy groups, plus the International Disability Alliance (an alliance of 14 global and regional disability organisations) have been campaigning to change this. In February 2026, the UNFCCC finally recognised the Disability Caucus. This group of 120 organisations advocates for the rights of people with disabilities within climate negotiations. This year for the first time it could act as an informal group that coordinates advocacy campaigns to serve the needs of disabled people in climate negotiations.

Informal groups get allocated tickets for some events, such as opening ceremonies, and can have their meetings promoted by organisers during negotiations.

During recent climate negotiations in Bonn, Germany, we observed a growing momentum for disability inclusive climate action. This was largely driven by disabled delegates highlighting the needs of disabled people.

However, more action is needed. Here are three steps to ensure climate action is inclusive for disabled people, and their families.

1. Incorporate the best research

Research on people with disabilities and climate change is critical. Bringing together the best academic research and tools, developed by both disabled and non-disabled researchers, is vital to understand the consequences of climate change for disabled people.

This will support better preparation for climate emergencies and inclusive climate adaptation. Climate adaptation is the process of changing systems, actions and responses to reduce the damage associated with climate change both now and in the future.

Understanding how mental health is affected by climate is clearly highlighted by the Belém Health Action Plan, announced during the UN climate summit, Cop30, in Brazil in 2025. More than 20% of the world’s poorest people have some form of disability and are the population group most affected by climate change.

At the UCL Warning Research Centre, we have recently developed a Mental Health Vulnerability Index. This first-of-its-kind tool has been developed by a disabled researcher to help reduce mental health inequalities that emerge during climate change. Without formal disability representation in global climate change discussions, such initiatives struggle to gain attention.

Climate discussions must include research about the effect of climate change on disabled people, led by disabled researchers and their allies, to ensure the protection of the health and wellbeing of the people most affected by climate change.

2. Make equal opportunity official

While the Disability Caucus was officially recognised by the UNFCCC in February 2026, the “caucus” status is still not classed as an officially recognised observer organisation, otherwise known as a constituency.

This means the voice of the disabled community does not have an equal opportunity to engage in the negotiations.

The caucus has been supported by the Women and Gender and Youth Constituencies, but disabled people need their own voice to be recognised. Granting full constituency status to the Disability Caucus is essential. Without a formal opportunity to participate equitably, disabled people still cannot contribute to the negotiation process.

3. Create accessible climate policy

Despite the work of disability organisations to improve climate policies by including disabled people, there is still a lack of disabled people negotiating policies or attending as observers. Even when disabled people attend negotiations, there can be barriers to participation.

During the UN climate summit in Glasgow during 2021 (Cop26), venues were not accessible by wheelchair.

Some accessibility barriers could be overcome by providing comprehensive sign language interpretation, braille and transcriptions, and simplified text versions of negotiations or presentations. Low sensory spaces, such as a meditation room at a conference venue, can offer respite to those suffering from sensory overload by providing a low-light, quiet and calm space.

Incorporating research on how climate change affects people with disabilities, led by disabled researchers and their allies, is a crucial part of devising effective policies. Granting the Disability Caucus constituency status is the next key step needed to address accessibility barriers to attending climate negotiations. These three simple actions would finally make climate action inclusive to all disabled people globally.

A supposedly unsinkable ship, an iceberg and a catastrophe that circulates through popular culture – the Titanic disaster is one of the most retold events in modern history. But familiarity comes at a cost. Repeated retellings tend to simplify what happened and reduce the real people involved to a basic story.

Retellings of the Titanic disaster often focus only on the sinking itself and forget what happened afterwards. Many lives were deeply affected by the disaster long after it ended, including people who were not even on the ship.

One such life is that of Helen Melville Smith, daughter of Captain Edward Smith, the man who commanded Titanic on its maiden voyage. While researching my new novel Daughter of the Titanic, I became increasingly struck not by the scale of the disaster itself, but by the quieter afterlives that followed it. Melville was 14 when her father went down with the ship in April 1912. Overnight, she inherited not only personal grief, but a public identity she had not chosen: the captain’s daughter, permanently attached to a disaster she did not witness but could not escape.

What followed has often been framed through the language of fate. Over the next decades, Melville’s husband died in an accident, her mother was killed in a road incident, her son died during the second world war and her daughter died of polio.

Taken together, these events could be interpreted through the language of a “Titanic curse”. As recently as July 2025, a Daily Mail feature revisited Melville’s life through this logic, treating unrelated tragedies as part of a doomed narrative arc.

Psychological research and research into narrative meaning-making have long shown that humans are predisposed to look for patterns, particularly after traumatic events. As psychologist Jerome Bruner has argued, we make sense of experience through narrative, organising events into stories that impose coherence. When multiple tragedies occur, we connect them into meaningful sequences.

The Titanic intensifies this impulse. Because the disaster occupies such a prominent place in public memory, it exerts a kind of narrative gravity. Lives connected to it are drawn into its orbit, interpreted through its lens and reduced to extensions of its story. The Titanic has become, in many ways, a modern myth: a historical event transformed into symbolic narrative, through which later lives are interpreted.

But Melville was not defined solely by catastrophe. She learned to fly aircraft at a time when aviation was still new and dangerous. She drove fast cars, moved within social and artistic circles and remained famous in ways that complicate the image of a life overshadowed by tragedy. Photographs from later life show a poised, fashionable woman who continued to participate in public life despite the losses she had endured.

Flying and motoring were associated with modernity, glamour and risk, and her enthusiasm for both suggests someone drawn to experience rather than retreat. The picture that emerges is not simply of a bereaved daughter, wife and mother, but of a woman who remained curious, socially engaged and determined to continue living fully.

While public narratives may attempt to fix people in place – particularly those connected to major historical events – they continue to reshape their lives in ways that exceed those frameworks.

Melville’s story is therefore not simply one of loss, but one of negotiation between private experience and public expectation, between inherited identity and self-determined action.

The afterlife of disaster

Melville’s life also points to a wider problem in how we tell history. Disasters do not end when the immediate crisis is over. They continue to shape meaning long afterwards, influencing reputations, identities and interpretations across generations. Yet popular retellings tend to focus on the moment of impact rather than its aftermath. Titanic is repeatedly reconstructed as spectacle – the sinking, the heroism, the failure – while quieter, long-term consequences are marginalised.

When we privilege the event over its aftermath, we reduce history to a series of dramatic moments rather than recognising it as a continuing process. Melville’s life offers a corrective, shifting attention from the disaster itself to its enduring effects.

Why are we so drawn to narratives of fate, curse or inevitability when we encounter repeated loss? And what happens when those patterns are imposed on real lives?

In Melville Smith’s case, the idea of a Titanic curse imposes coherence where there may be none, compressing decades of lived experience into a single, legible narrative. In doing so, it recasts survival itself as misfortune.

This is not a neutral process. Historians, journalists and novelists like myself shape how lives are remembered and, in some cases, reduced. With that comes an ethical responsibility: to resist imposing patterns that make lives appear more coherent or narratively satisfying than they were, and to remain attentive to contradiction, complexity and reality.

Melville’s life resists that kind of closure. It contains independence, persistence and contradiction that sit uneasily alongside the narrative imposed upon her. To take that seriously is not only to recover an overlooked figure, but to recognise the limits of the frameworks through which we understand her.

The story of the Titanic disaster continues in the lives shaped by it – lives that cannot be reduced to the tragedy alone without losing what made them human.

He said he considers himself “one of the lucky ones” because he was able to walk away, but that had not come without its hardships

A bid by the Government to ban conversion practices sends a “clear signal” to LGBT+ people that they are “not broken, you don’t need to be cured”, a former Traitors contestant who once faced such so-called therapy has said.

Matthew Hyndman said he was asked in his 20s to “publicly repent” for being gay or leave his evangelical Christian community behind.

Hyndman, who was also known as Matty during January’s series of the gameshow, said no to going through counselling and has now backed a ban on such practices which could see people fined or imprisoned for carrying them out.

Speaking at an event in London as a draft Conversion Practices Bill was published on Thursday, he said he had been an evangelical Christian missionary on a ship sailing around the world as he wrestled with his sexuality.

He said: “I was so embarrassed that I was gay. I was so deeply embarrassed and ashamed, and I didn’t tell a soul. This was not something that I was willing to even utter, because as far as I was concerned, it was the worst sin.”

He said he had for a long time been “completely in denial about my sexuality”, but when it became known he was gay, he was confronted with the prospect of conversion practices.

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“I was basically given a choice to publicly repent in front of the entire ship’s community and agree to go through counselling, or go.”

He said he considers himself “one of the lucky ones” because he was able to walk away, but that had not come without its hardships.

“In order for me to walk away, in order for me to say no, there was such a huge risk,” he said. “The risk was that I would lose everyone I know and love. My vocation, my community, everything was so intertwined, particularly when you have a faith, it’s so intertwined.

“So for me to say no was for me to reject the belief of my entire community and walk away. And I did, thankfully. I consider myself one of the lucky ones because I did, I walked away, and I said ‘no, actually, I think I know who I am’.”

He spoke of his belief in the importance of a ban on such practices – which are aimed at changing someone’s sexual orientation or transgender identity and can involve anything from exorcisms to prayers.

Hyndman added: “I think it (a ban) just sends a really clear signal, as well.

“Anyone who is currently experiencing this, anyone who has, they’re hearing from the highest point that this is wrong and that it should not be happening to you. You’re not broken, you don’t need to be cured.”

The draft Bill covers England and Wales only and was a Labour manifesto commitment from 2024.

Hyndman, who is originally from Northern Ireland, appeared at the Alliance Party conference in March to back the party’s bid to ban conversion practices there.

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The pair have been jailed

Two men have been jailed and are due to be deported after a ‘large-scale’ cannabis grow was discovered in Bolton. Neighbourhood officers raided a property on Newport Street back on December 23 last year, after receiving intelligence.

Greater Manchester Police says it uncovered a ‘substantial and fully operational’ cannabis farm at the property, which had been ‘professionally adapted’ – including the illegal bypass of the electricity supply to power the grow. CCTV footage was observed as part of enquiries which identified a black van attending the property in the days before the raid.

Two men were captured on camera accessing the secured building, and the vehicle was subsequently traced to Leonard Tota. The now-26-year-old was arrested the following day at his home address, where Ridgan Taga, 26, was also located.

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A search of the address uncovered additional cannabis plants, sophisticated growing equipment, a significant quantity of cash, mobile phones, a suspected debtors list, and keys linking both men directly to the Newport Street premises. GMP says the investigation highlighted a coordinated and organised effort to cultivate cannabis at scale.

Tota, of St George’s Road, Bolton, pleaded guilty the production of cannabis, while Taga, of St George’s Road, Bolton, pleaded guilty to production of cannabis, being concerned in the supply of cannabis and possession of criminal property. Tota was sentenced to 14 months’ imprisonment, while Taga was jailed for a year. Both are due to be deported following the completion of their custodial terms.

Police Sergeant Jessica Prudence, of Bolton town centre neighbourhood policing team, said: “This is an excellent result and demonstrates the dedication and effectiveness of our neighbourhood officers in tackling serious drug-related crime. By acting on intelligence and carrying out thorough enquiries, the team has successfully removed a significant cannabis grow from the community and brought those responsible before the courts.

“We rely heavily on information from the public, and the intelligence you provide plays a vital role in enabling us to take action like this. Drug supply is not a victimless crime – it is often linked to wider, harmful criminality that can have a serious impact on our communities. We would continue to encourage anyone with concerns or information about suspected drug activity to come forward and speak to us.”

Spectacular thunder and lightning storms lit up the sky throughout the night in Scotland

Incredible footage captured by Scots across the country shows spectacular thunder and lightning storms illuminating the night sky during the early hours of Friday, June 26.

The dramatic display unfolded as a powerful storm swept across East Central Scotland between midnight and 3am, with repeated strikes of lightning lighting up the skies above Edinburgh, Fife and surrounding areas. The intense flashes, accompanied by rolling thunder, turned the darkness into daylight in a breathtaking overnight display.

Scots across the country took to social media to share videos and photographs of the extraordinary scenes, with many describing the storm as “crazy” and unlike anything they had ever witnessed before. Meanwhile others said the lightning, which lit up the sky every few seconds in some areas, was some of the most impressive strikes they had ever seen.

Stunning snaps taken over Fife in the early hours of Friday morning show spectacular bolts light up the night sky. The photos, shared by Fife Jammer Locations, are just some evidence of the spectacular weather event that was experienced across Scotland.

In one video which was posted onto X, formally known as Twitter, a huge bolt of lightning strike across the Edinburgh sky, illuminating the landscape for a split second and flooding the room where the person filming is sitting with bright white light.

The powerful fork of lightning cuts diagonally through the sky, while the low rumble of thunder can be heard rolling moments later. An accompagning caption read: “The thunder storm has been hovering over Edinburgh & Fife for the last 30 minutes. I managed to capture a lightening bolt.

Making a light hearted reference to the ancient Greek god of the sky and thunder, she joked: “Zeus is wide awake.”

Meanwhile another clip shows the lightening clatter over Edinburgh Castle. In what looks like it could be a scene from a film, the bolts light up the castle for a few seconds showing the beauty of the capital city. The strikes almost look like they are hitting directly into the castle grounds.

At times the lightning appears to strike extremely close to the castle grounds, while deep rumbles of thunder can also be heard echoing over the city.

It comes as a yellow thunderstorm warning remains in force across large parts of Scotland after the Met Office extended the initial weather warning, which was in place in till 23:50 tonight, to 3am on Saturday, June 27. The extension is due to slower clearance of rain across the far north of the country.

Forecasters warns that thunderstorms and heavy rain may cause some disruption throughout large parts of Scotland.

The Met Office states: “Spells of heavy rain and thunderstorms initially over northwest Scotland are likely to become more widespread during Friday morning.

“Further thunderstorms and spells of heavy rain are possible in the afternoon before becoming confined to more northern areas of Scotland later in the day.”

The forecast continues: “Rainfall amounts will be highly variable but narrow corridors of 20-30 mm falling in 1 hour and potentially 30-50 mm in 3 hours is possible. Frequent lightning, large hail (2-4 cm diameter) and locally gusty winds with stronger storms.”

Disease-modifying drugs for Alzheimer’s offer a meaningful glimpse of hope for many people who fear dementia. Alzheimer’s disease is the most common cause of dementia, but dementia itself is an umbrella term for symptoms such as memory loss, confusion and changes in thinking.

Unlike older dementia drugs, which help with symptoms but do not change the underlying disease, disease-modifying treatments are designed to slow the disease process itself. So far, these treatments appear to delay symptom progression by several months rather than years. They also carry a small but serious risk of side-effects, including swelling and bleeding in the brain. At present, they are suitable only for some people in the early stages of Alzheimer’s disease, meaning that many others will still face dementia with no cure on the horizon.

The fact that scientists are now achieving some degree of disease modification has generated enormous interest in dementia research. That attention is essential if these advances are to continue. But public excitement can also narrow the conversation, drawing attention towards the biology of dementia and away from the lives of the people experiencing it.

For many years, social scientists have argued for a broader understanding of dementia. Dementia begins with changes in the brain, but it affects the whole person. It can change how someone remembers, communicates, relates to others and makes sense of the world.

That means dementia care has to do more than slow biological decline. It also has to ask what helps a person feel recognised, connected and still themselves. Even when medicine cannot offer a cure, care can still reduce distress, support identity and create moments of meaning. Music, poetry, storytelling, theatre, visual art, dance and museum work can give people with dementia ways to respond and connect, especially when ordinary conversation becomes difficult.

The value of this work can be hard to measure. A person singing along to a familiar song, recognising an image, laughing at a shared joke or becoming briefly more engaged with others does not fit neatly into the same evidence framework used to assess a drug.

As these interventions become more common, and increasingly extend beyond the very early stages of the disease, they make visible the humanity of people living well into the dementia process. Such work can challenge harmful stereotypes in print and social media, where dementia is often portrayed as a “living death” and people with dementia are reduced to “zombies” or “empty shells”. Language like this encourages the idea that a person with dementia has already disappeared, even while they are still alive, responsive and capable of connection.

Yet there is a further risk. If public attention focuses mainly on people who can still speak, sing, paint, perform or respond in recognisable ways, those with very advanced dementia may be treated as unreachable. They are already frequently considered unsuitable for research, and sometimes even unsuitable for creative or relational engagement.

In dementia, this can create a damaging divide between those who can still communicate in familiar ways and those whose communication has become harder to understand.

In a recent publication, we explored the limits and possibilities of engaging with people living in the very late stages of dementia. The paper examined two ideas that can help us think about this problem: narrative dispossession and critical fabulation.

Narrative dispossession means being deprived of control over your own story. As dementia progresses, people may become less able to explain themselves, describe memories, correct misunderstandings or tell others what matters to them. Their life does not stop being meaningful, but their ability to narrate that life in conventional ways may become diminished.

This creates a serious ethical problem. How should carers, researchers, artists or family members respond when a person can no longer tell their own story clearly? What should we do with the fragments that remain: a gesture, a glance, a touch, a sound, a facial expression, or even an absence of response?

Critical fabulation offers one possible approach. The term comes from work on history, archives and silence. It describes a careful form of imaginative reconstruction, used when direct evidence is partial, missing or impossible to recover. In dementia care and research, it can help us think about how to engage ethically with the inner lives of people whose communication has become profoundly limited.

At its best, critical fabulation is tentative and restrained. It allows us to ask what a person might be feeling, remembering or communicating, while remaining honest about the limits of interpretation.

That interpretation must be humble. A caregiver may know a person’s history, habits, preferences and fears better than anyone else. This familiarity can deepen understanding, but it does not guarantee accuracy. Even those closest to a person with dementia must remain alert to the risks of projection, over interpretation and reading their own assumptions into another person’s experience. Or, even, taking over someone else’s story entirely.

If we refuse all imaginative engagement, we may leave people in the latest stages of dementia in silence. That silence can become a form of erasure.

For this reason, critical fabulation in dementia care and research must remain anchored in restraint and relational care. It means examining our own assumptions, motives and power, and requires us to ask what this person might be experiencing, but also what right we have to narrate that experience.

New drugs may help some people stay in the earlier stages of Alzheimer’s disease for longer. But dementia care also requires us to think about those for whom these drugs will do little or nothing, and those who are already far beyond the point at which they can tell us their stories in familiar ways.

Their lives still require attention. Their silence should not be mistaken for absence.