diagnosis

Strictly Come Dancing’s Anton Du Beke devastation over wife’s ‘cruel’ diagnosis

Strictly Come Dancing judge Anton Du Beke has opened up about his wife Hannah Summers’ battle with endometriosis and the couple’s IVF journey to parenthood

Strictly judge Anton Du Beke has opened up about his wife’s agonising battle with endometriosis and how it affected their journey to parenthood.

The BBC favourite married marketing executive Hannah Summers in 2017, having first met at Wentworth Golf Club in Surrey back in 2012. The pair welcomed twins George and Henrietta soon after tying the knot, following IVF treatment.

But Anton revealed on Giovanna Fletcher’s Happy mum Happy Baby podcast that Hannah had doubts about their ability to conceive because of her crippling condition.

The professional dancer admitted he “couldn’t understand the universe” after witnessing Hannah’s bond with her nephews, before opening up about their IVF experience.

He said: “I knew I wanted to be with her, I saw her with her nephews. She’s so kind and so caring, I just couldn’t understand the universe.”, reports Lancs Live, reports Wales Online.

“And whoever is upstairs, if anyone’s upstairs, looking down and going ‘you are the most perfect person to have children, but I’m not going to let you have any children because I’m going to give you this’.

“And I’m going to say ‘you’re going to have this endometriosis, and you’re going to suffer with this all of your life, chronically, and I’m not going to let you have any children.

“I thought that was peculiar, cruel, and inexplicable and unforgivable. And if ever I go up to somewhere and meet this person I would say ‘I think you’re not OK with decisions like this, this doesn’t make any sense to me.”

Anton has candidly spoken about the hurdles he and wife Hannah encountered during their fertility treatment, which ultimately brought them closer together.

The couple were blessed when the treatment worked first time, resulting in the birth of twins George and Henrietta in 2017, with their nuptials taking place later that same year.

In an emotional chat with Giovanna, Anton admitted his previous lack of understanding about endometriosis and highlighted the urgent need for increased government funding in women’s health.

Reflecting on their journey, he shared: “Then we went through the process of IVF, well crying out loud. You girls are extraordinary. As much as I want to get involved, all I can do is hold your hand. It makes me emotional every time I talk about it. The injections, the stress, the anxiety. I have anxiety and stress but it’s not my body.

“She has these injections and the bruises in the bum, in the thigh, in the stomach. And you’re trying to help but what can you do? Whatever you want, tell me and I’ll do it but that’s all you have and it’s horrendous as a man to watch it.

“You feel so inadequate and you want to do so much more but I can’t do anything. And that’s why you girls are so extraordinary, you’re extraordinary that you do all this stuff.”

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Clare Balding’s weight loss transformation, cancer diagnosis and new life with famous wife

The BBC Sport presenter joins the likes of Tom Daley, Jonathan Ross and Alan Carr in taking part in the first series of The Celebrity Traitors

The inaugural series of The Celebrity Traitors hits our screens on Wednesday night, with a star-studded cast taking part in the spin-off of the popular BBC programme.

Following the same format as the regular version, the series will see 19 celebs becoming either ‘Faithfuls’ or, in the case of some, ‘Traitors’. The task for the Traitors is to work together to ‘murder’ their fellow contestants without being detected, while the Faithfuls are charged with successfully identifying and ‘banishing’ the Traitors by voting them out.

The celebrity line-up includes singer-songwriter Cat Burns, telly host Jonathan Ross, actress Celia Imrie and former Olympic diver Tom Daley. However, one contestant who’s been tipped to go the distance and bag the £100,000 charity prize is BBC Sport legend Clare Balding.

Over her 30-year career, the presenter has become one of Britain’s most esteemed broadcasters, having fronted massive sporting events such as the Grand National, Olympic Games and Wimbledon for channels like the BBC and Channel 4.

Balding will be hoping her authority, popularity and affability to take her far in the iconic Traitors castle, while she has grown used to the spotlight being cast over her, and particularly her life away from the cameras. As her stock has risen, particular attention has been paid her personal life, from her relationship with another presenter to her recent weight loss. Here’s what you need to know.

Ex-BBC presenter wife

Balding first met her wife, broadcaster Alice Arnold, in 1999 while they were both working for the BBC. While they were simply good friends at first, they began dating in 2002, after a national newspaper publicly revealed Balding’s sexuality.

The pair entered into a civil partnership in 2006 before getting married in a private ceremony in 2015, following the legalisation of same-sex marriage in the UK. Their marriage was subsequently back-dated to 2006.

Balding has described Arnold, who worked as a newsreader and continuity announcer at BBC Radio 4 for over two decades, as “fiercely loyal” and her “own little guard dog”.

Reflecting on their first meeting, the Wimbledon presenter confessed she was unaware of Arnold’s identity when she first noticed her at a BBC show, but added: “I saw her and thought ‘Oh, she’s really interesting and rather beautiful. We started chatting and she’s very funny. We were friends for at least two years.”

Balding recently spoke more candidly about her relationship with Arnold during an interview with Hello! Magazine, crediting her wife as the inspiration behind her debut novel ‘Pastures New’, which hit shelves in September.

“One of the things I wanted to write about in my novel was about falling in love because I thought ‘I know that’,” she explained. “I know what real, deep love is and meeting someone I want to grow old with. Lucky, lucky me.”

In the same interview, she revealed that she and Arnold are preparing to leave their long-time home in Chiswick as they look to fill the “canine-shaped hole” in their lives by getting a new dog.

“We’re looking to move out of London in the near future, and one of the main reasons for that is to have a bit more space and protection from the road so that it’s a good environment for a dog,” said Balding. “As soon as we’re settled, it’s definitely our plan – probably next spring. I just smile at the thought of having a dog back in our lives.”

On how she and Arnold spend their time together, she spoke about their love of golf, adding: “I’m not as good as Alice, who’s a seven-handicap golfer, but I’m working on getting better”. She also discussed the couple’s travel plans, explaining: “Alice and I are about to go from New York up to Quebec and back again and we’re going to Japan on a cruise next year. We love being on the water and then ending up in a new place.”

Balding’s relationship with Arnold came after she previously dated men, with one of her former partners even proposing to her. However, she turned down the proposal and never regretted the decision, explaining that he went on to “behave appallingly”.

“I had a few boyfriends, not like loads,” she recalled. “But I had one very serious boyfriend for two or three years. He asked me to marry him, and he was in the Army, and he was going off. And I thought, ‘He’s only asking me because he thinks he’s in danger and, according to romantic films, I’m meant to say yes at this point’.

“I knew I didn’t want to. I said, ‘Look, that’s a lovely thing to say but ask me again when you come back’. When he came back he didn’t ask me again, and I thought, ‘Thank God’. I thought, ‘I don’t trust you and I’ll never trust you’ – and funnily enough I was absolutely spot on as his ex-wife told me not that long ago.”

She added: “That relationship ended not very well with him behaving appallingly. I think I was damaged by that, but that doesn’t make you gay. I just think when I first fell in love with a woman, it was completely different.”

Cancer battle

In 2009, Balding revealed she had been diagnosed with thyroid cancer after spotting a lump on her neck while watching herself present on television.

Warning signs of the condition include a lump in the neck, a painful throat and swallowing difficulties that persist, and after heeding her family’s advice to consult a doctor, she was told she had cancer and needed an operation. Balding then underwent surgery to remove a cyst, her thyroid gland and a lymph node, followed by radioactive iodine treatment to halt the disease’s progression.

She later admitted to going through a “dark stage” after her diagnosis, as she feared the potential impacts of her illness on her voice and career. However, she received the all-clear at the end of 2010 and has since seen her career flourish.

During a recent appearance on the Stick to Rugby podcast, she opened up about her diagnosis, recalling: “It was an odd one because I hadn’t noticed feeling any different. I was doing the show jumping at Christmas when it was at Olympia and I recorded an opening link, and I was watching it back on the monitor as we were about to go live.

“I was looking at the mirror and I saw this lump on my neck, a big lump. I thought, ‘Wow, that’s really weird, where has that come from?’ I went home for Christmas and my sister-in-law’s Welsh grandfather was a doctor, and he looked at it. He was still a practising GP and he said that I’d better go to the doctor. He took Alice to one side and said, ‘Make sure she goes’.

“Between Christmas and New Year, when the doctor’s surgery was open, I went and the GP did some tests and he sent me to a specialist. They came back and said, ‘You’ve got thyroid cancer’ and they had to operate.”

Pointing to her neck, she added: “I’ve got a cracking scar there, they had to operate three times. I was most worried about my voice because of where the surgery is. I was thinking, please don’t hit my vocal cords. I came back and was commentating on the tennis for the radio and I couldn’t hit the notes, the vocal cords weren’t meeting properly.

“Anyway, it came back and I was all fine and I got my bass notes back – but that was all I was worried about. I then had radioactive iodine therapy, but that’s all right, because it’s not as bad as chemo.”

Body transformation

Today, Balding is healthier than ever, having shed one-and-a-half stone by eliminating a few food and drink items from her diet.

During her Hello! interview, the 54-year-old revealed that she had embraced a low-carb diet, ditching pasta and bread while also reducing her sugar consumption. She also modified her drinking habits, choosing gin and tonic over red wine.

After overhauling her eating habits, Balding says she not only “feels better” but has gained fresh confidence as she can now wear whatever she wants.

“I’ve worked hard at it and feel better,” she said. “I got into my 50s and thought, ‘I’m just going to be fat and happy’, but then a friend talked about a low-carb diet and the late Michael Mosley publicised this form of weight loss, too, and I thought, I’ll give it one more go – as I’ve tried so many diets over the years – and see if it works. And it did!”

Revealing she no longer eats bread or pasta and as little sugar as possible, she added: “And if I want a drink, I have a gin and tonic instead of wine, so I don’t feel like I’m depriving myself of things.

“I’m never going to be stick thin – that’s just not me. I’ve got massive bones. But I can now put on a pair of trousers with a belt and my shirt tucked in and I went for years without being able to do that. That feels great.”

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‘I felt like my brain was falling out’ says Love Islander as he reveals 18-month health battle & devastating diagnosis

A LOVE Island star opened up about his secret 18-month health battle, saying ‘I felt like my brain was falling out’.

Chris Williamson, 37, featured on the ITV2 dating show’s first series in 2015.

Chris Williamson reclines in a brown leather chair, wearing a black t-shirt, with medical equipment attached to his arm.

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Chris Williamson opened up about his secret 18-month health battleCredit: Youtube/Chris Williamson
Chris Williamson receiving an IV drip, sitting in a chair.

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He posted a YouTube v video updating his subscribersCredit: Youtube/Chris Williamson
Chris Williamson talking to another man in a Love Island villa.

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Chris appeared on Love Island back in 2015Credit: ITV2

He entered the villa on Day 1, however, he was ultimately “dumped” on Day 19.

Speaking in a video posted on his YouTube channel, Chris discussed his health with subscribers.

In particular, his experience facing toxic mould exposure, Lyme disease and EBV.

In a clip recorded in September 2024, Chris said: “Struggling, yeah, in the last week.

“Five episodes in three days in New York. Two episodes in two days in Florida, plus travelling. Plus a bunch of meetings.

“It’s felt like my brain is trying to fall out of my ears the entire time.

“Memory is really rough, thoughts are very muddy. Getting confused in the middle of sentences.

“So it’s probably the worst that my mind’s been – just disheartening as I’ve been working on trying to get out of all this.

“Mould, EBV, Lyme, whatever it is, stuff for six months, more.

“It’s disheartening. I’ve no idea how far along I am, it feels like I’m going backward.”

I was on the first series of Love Island but quit reality TV and am now worth millions thanks to new job

Chris also appeared on dating show Take Me Out and has completely reinvented himself following his reality star days and is now a millionaire.

He earned the bulk of his fortune through his podcast, Modern Wisdom.

Chris does not look back fondly on his time on Love Island, stating in a chat with Sadia Khan he was “pretty bored” and having an ‘”existential crisis” while in the villa. 

He told the BBC: “I was living this persona of the professional party boy – the big name on campus, the guy with the hair out front [of the club], that wanted people to need him, that thought he had found the culture and industry he belonged in.

“Then I got on to Love Island and had nowhere to hide from people who were the person I was pretending to be.

“I was there with people who were genuinely extroverted, outgoing, party people. And I was just playing a role…

“I’d convinced myself [Love Island] was something that made me finally belong. And I didn’t belong.”

Love Island airs on ITV2 and ITVX.

Chris Williamson on a couch, talking.

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Chris has reinvented himself since Love IslandCredit: Youtube/Chris Williamson

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The real reasons why autism rates have shot up over the decades

This week, the Trump administration announced that it was taking “bold action” to address the “epidemic” of autism spectrum disorder — starting with a new safety label on Tylenol and other acetaminophen products that suggests a link to autism. The scientific evidence for doing so is weak, researchers said.

Health and Human Services Secretary Robert F. Kennedy Jr. said federal officials “will be uncompromising and relentless in our search for answers” and that they soon would be “closely examining” the role of vaccines, whose alleged link to autism has been widely discredited.

Kennedy has long argued that rising diagnoses among U.S. children must mean more exposure to some outside influence: a drug, a chemical, a toxin, a vaccine.

“One of the things that I think that we need to move away from today is this ideology that … the autism prevalence increase, the relentless increases, are simply artifacts of better diagnoses, better recognition or changing diagnostic criteria,” Kennedy said in April.

Kennedy is correct that autism spectrum disorder rates have risen steadily in the U.S. since the U.S. Centers for Disease Control began tracking them, from 1 in 150 8-year-olds in 2000, to 1 in 31 in 2022, the most recent year for which numbers are available.

But physicians, researchers and psychologists say it is impossible to interpret this increase without acknowledging two essential facts: The diagnostic definition of autism has greatly expanded to include a much broader range of human behaviors, and we look for it more often than we used to.

“People haven’t changed that much,” said Alan Gerber, a pediatric neuropsychologist at Children’s National Hospital in Washington, D.C., “but how we talk about them, how we describe them, how we categorize them has actually changed a lot over the years.”

Defining ‘autism’

The term “autism” first appeared in the scientific literature around World War II, when two psychiatrists in different countries independently chose that word to describe two different groups of children.

In 1938, Austrian pediatrician Hans Asperger used it to describe child patients at his Vienna clinic who were verbal, often fluently so, with unusual social behaviors and at-times obsessive focus on very specific subjects.

Five years later, U.S. psychiatrist Leo Kanner published a paper about a group of children at his clinic at the Johns Hopkins Hospital in Baltimore who were socially withdrawn, rigid in their thinking and extremely sensitive to stimuli like bright lights or loud noises. Most also had limited verbal language ability.

Both Asperger and Kanner chose the same word to describe these overlapping behaviors: autism. (They borrowed the term from an earlier psychiatrist’s description of extreme social withdrawal in schizophrenic patients.)

This doesn’t mean children never acted this way before. It was just the first time doctors started using that word to describe a particular set of child behaviors.

For the next few decades, many children who exhibited what we understand today to be autistic traits were labeled as having conditions that have ceased to exist as formal diagnoses, like “mental retardation,” “childhood psychosis” or “schizophrenia, childhood type.”

Autism debuted as its own diagnosis in the 1980 third edition of the Diagnostic and Statistical Manual of Mental Disorders, the American Psychiatric Assn.’s diagnostic bible. It described an autistic child as one who, by the age of 2½, showed impaired communication, unusual responses to their environment and a lack of interest in other people.

As the decades went on, the DSM definition of autism broadened.

The fourth edition, published in 1994, named additional behaviors: impaired relationships, struggles with nonverbal communication and speech patterns different from those of non-autistic, or neurotypical, peers.

It also included a typo that would turn out to be a crucial driver of diagnoses, wrote cultural anthropologist Roy Richard Grinker in his book “Unstrange Minds: Remapping the World of Autism.”

The DSM’s printed definition of autism included any child who displayed impairments in social interaction, communication “or” behavior. It was supposed to say social interaction, communication “and” behavior.

The error went uncorrected for six years, and the impact appeared profound. In 1995 an estimated 1 in every 500 children was diagnosed with autism. By 2000, when the CDC formally began tracking diagnoses (and the text was corrected), it was 1 in every 150.

Reaching underserved communities

In 2007, the American Academy of Pediatrics recommended for the first time that all children be screened for autism between the ages of 18 and 24 months as part of their regular checkups. Prior to that, autism was diagnosed somewhat haphazardly. Not all pediatricians were familiar with the earliest indicators or used the same criteria to determine whether a child should be further evaluated.

Then in 2013, the fifth edition of the DSM took what had previously been four separate conditions — autistic disorder, Asperger’s disorder, childhood disintegrative disorder and pervasive developmental disorder — and collapsed them all into a single diagnosis: autism spectrum disorder.

The diagnostic criteria for ASD included a broad range of social, communication and sensory interpretation differences that, crucially, could be identified at any time in a child’s life. The term was no longer limited only to children whose development lagged noticeably behind that of their peers.

Since that definition was adopted, U.S. schools have become more proactive about referring a greater range of children for neurodevelopmental evaluations. The new DSM language also helped educators and clinicians better understand what was keeping some kids in disadvantaged communities from thriving.

“In the past, [autism was] referred to as a ‘white child’s disability,’ because you found so few Black and brown children being identified,” said Shanter Alexander, an assistant professor of school psychology at Howard University. Children of color who struggled with things like behavioral disruptions, attention deficits or language delays, she said, were often diagnosed with intellectual disabilities or behavioral disorders.

In a sign that things have shifted, the most recent CDC survey for the first time found a higher prevalence of autism in kids of color than in white children: 3.66%, 3.82% and 3.30% for Black, Asian and Latino children, respectively, compared with 2.77% of white children.

“A lot of people think, ‘Oh, no, what does this mean? This is terrible.’ But it’s actually really positive. It means that we have been better at diagnosing Latino children [and] other groups too,” said Kristina Lopez, an associate professor at Arizona State University who studies autism in underserved communities.

The severity issue

An autism diagnosis today can apply to people who are able to graduate from college, hold professional positions and speak eloquently about their autism, as well as people who require 24-hour care and are not able to speak at all.

It includes people who were diagnosed when they were toddlers developing at a noticeably different pace from their peers, and people who embraced a diagnosis of autism in adulthood as the best description of how they relate to the world. Diagnoses for U.S. adults ages 26 to 34 alone increased by 450% between 2011 and 2022, according to one large study published last year in the Journal of the American Medical Assn.

Kennedy was not correct when he said in April that “most cases now are severe.”

A 2016 review of CDC data found that approximately 26.7% of 8-year-olds with autism had what some advocates refer to as “profound autism,” the end of the spectrum that often includes seriously disabling behaviors such as seizures, self-injurious behavior and intellectual disability.

The rate of children with profound autism has remained virtually unchanged since the CDC started tracking it, said Maureen Durkin, a professor of population health science and pediatrics at the University of Wisconsin-Madison. Indeed, the highest rate of new diagnoses has been among children with mild limitations, she said.

For many researchers and advocates, the Trump administration’s focus on autism has provoked mixed emotions. Many have lobbied for years for more attention for this condition and the people whose lives it affects.

Now it has arrived, thanks to an administration that has played up false information while cutting support for science.

“They have attempted to panic the public with the notion of an autism epidemic as a threat to the nation, when no such epidemic actually exists — rather, more people are being diagnosed with autism today because we have broader diagnostic criteria and do a better job detecting it,” said Colin Killick, executive director of the Autistic Self Advocacy Network. “It is high time that this administration stops spreading misinformation about autism, and starts enacting policies that would actually benefit our community.”

This article was reported with the support of the USC Annenberg Center for Health Journalism’s National Fellowship’s Kristy Hammam Fund for Health Journalism.

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Bjorn Borg on prostate cancer diagnosis, John McEnroe rivalry & struggles with drugs and alcohol

Borg won 66 singles titles, spent 109 weeks as world number one and claimed a record 41 successive wins at Wimbledon.

His retirement at 25 – a time when tennis players are starting to peak – was a shock.

“I had enough. I lost the interest and the motivation,” he said.

“If I knew what was going to happen in the years after, I would continue to play tennis.”

In his autobiography, Heartbeats: A Memoir, co-written with his wife Patricia, the notoriously private Borg speaks about his post-playing career struggles.

“I had no plan. People today, they have guidance. I was lost in the world,” he said.

“There was more drugs, there was pills, alcohol, to escape myself from reality.

“I didn’t have to think about it. Of course it’s not good, it destroys you as a person.”

Borg was hospitalised after an overdose, external in Milan in 1989 – an incident which made him reassess retirement.

He returned to the tennis tour from 1991 to 1993 but failed to win a single match.

“I was close to dying many times,” Borg added.

“I fixed my life. I’m very happy with myself.”

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Cabaret to end Broadway run early as Billy Porter exits production after sepsis diagnosis

The Kit Kat Club is closing its Broadway doors early on Sept. 21, as current “Emcee” Billy Porter battles a “serious case of sepsis,” according to the production team.

“It is with a heavy heart that we have made the painful decision to end our Broadway run,” said producer Adam Speers in a statement. “On behalf of all the producers, we’re so honored to have been able to bring this version of John Kander, Fred Ebb, and Joe Masteroff’s important masterpiece, ‘Cabaret,’ to New York and to have opened the doors to our own Kit Kat Club for the year and a half we have been here.”

“Cabaret at the Kit Kat Club” — as this revival is titled — opened on Broadway in April 2024, with Eddie Redmayne and Gayle Rankin in the lead roles. Following their September 2024 departure, duos Adam Lambert and Auli’i Cravalho, and Orville Peck and Eva Noblezada played the titular roles.

Porter stepped into the role of the Emcee, alongside co-star Marisha Wallace as Sally Bowles, in July. The duo was expected to lead the production’s final 13 weeks — originally scheduled to end on Oct. 19 — before Porter’s illness sidelined him.

“Billy was an extraordinary ‘Emcee,’ bringing his signature passion and remarkable talent,” said Speers. “We wish Billy a speedy recovery, and I look forward to working with him again in the very near future.”

As of Sept. 21, the production will have played 18 preview performances and 592 regular performances. Marty Lauter and David Merino, the production’s longtime alternates for Emcee, will share the role for the final two weeks of performances. Their exact performance schedules — opposite Wallace as Bowles — are forthcoming.

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Stranded on Honeymoon Island bride reveals show led to life-changing health diagnosis

DAVINA McCall’s dating show has proven life-changing for one bride after it unlocked a hidden disorder. 

Gorgeous Millie Thompson, 30, has been diagnosed with autism and ADHD after taking part on Stranded on Honeymoon Island having realised her OCD was so intense she considered smuggling in a pair of socks. 

Millie Thompson on a rooftop in London, wearing a floral corset dress.

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Millie Thompson, 30, has been diagnosed with autism and ADHD after taking part on Stranded on Honeymoon IslandCredit: instagram/@millie_thompson
Woman wearing number 14 contestant badge on Davina McCall's dating show.

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Millie realised her OCD was so intense she considered smuggling in a pair of socksCredit: instagram/@millie_thompson
Bride and groom pouring champagne at their outdoor wedding ceremony.

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Millie tied the knot with her groom Jordan after only a brief speed dating meetingCredit: BBC

One of the DJ and model’s quirks was she cannot bear to be barefoot, so she thought about sewing a secret set into her wedding dress. 

The BBC show sees singles marooned on a deserted beach in only their wedding attire. 

Millie told The Sun: “Coming back from the show, I ended up getting tested for ADHD and autism and I found out I have both. 

“I have learnt so much about myself, someone described it as being ‘neuro spicy’ and I love that for me.

Read More on Davina McCall

“It’s lifechanging really.

“I always knew things like I couldn’t be without a pair of socks, I always have to be wearing a pair, but being on the show made everything clear. 

“This sounds crazy but I was contemplating sewing some socks into the boob bit of my wedding dress, I was like ‘can I smuggle in some socks?!’ but then I was like, no they’ll be disgusting. 

“Now I know that’s why I am how I am. 

“I’ve changed so much from it but in such a good, positive way and everyone has noticed.”

Millie was so conscious of being without her comforts, she had her wedding dress custom made with the experience in mind. 

Davina McCall hosts new reality show Stranded on Honeymoon Island

She included a bodysuit she could wear like a onesie, and a skirt she could detach and use as a mosquito net. 

Millie, from Cheshire, added: “I am such a girly girl, I was combing my hair extensions with a fork. 

“But the experience makes you strip everything back and I thought I’d struggle because I’m so OCD but I actually coped really well.”

Viewers saw her struggle with the show’s dramatic jump into the sea that kicks off their stranded experience. 

“With Love Island there’s other couples and you can escape, but there’s nothing like Stranded for this, you’ve just got each other.”

Millie Thompson

After meeting at the altar, the couples then take a boat out to their deserted beach and then plummet into the sea ahead of a swim to land. 

But poor Millie can’t swim and she had to fit a life vest over her gorgeous wedding dress. 

She said: “That was a massive thing for me because I literally will not get in the water, I can put my feet in but that’s it, so to have to do that was massive.”

But she reckons being out of her comfort zone kickstarted a connection with her groom Jordan in a way that could never happen on Love Island.

While she can’t give away what happens on her journey, Milile added: “You are on a beach with absolutely nothing, you are relying on each other for everything.

Top dating trends of 2025

  1. Swamping: When you find someone you can comfortably share your ‘swamp’ with and let go of the pressure to be anything but your true authentic self.
  2. No-habiting: When you choose to wait longer to move in with your partner because you value your personal space.
  3. Fiscal Attraction: When you won’t settle for less and you’re seeking a match who is financially secure and who you find attractive.
  4. Rejuve-dating: When you cast away the blues and grow from past experiences so you can fully embrace the future of your dating journey.
  5. Thrift-matised: When you like to go on dates but hit that sweet spot between being cheap and frugal. Hidden gems, loyalty cards – these are all your type on paper.
  6. Loud-dating: Cutting to the chase, being open and to the point with what you want so you don’t waste your time.
  7. Marmalading: When you literally put your other half ‘before anything else’, much like Britain’s most beloved bear’s love for marmalade.
  8. Digital Ex-pression: The stage after a break-up when you are done grieving and turn to social media to share how you are healing to confidently get back out on the dating scene.
  9. Fine-wining: Proactively finding people to date who are older than you and who’ve aged just like a fine wine.

“With Love Island there’s other couples and you can escape, but there’s nothing like Stranded for this, you’ve just got each other.”

Stranded on Honeymoon Island continues on BBC One tonight at 9pm, then returns next week on Wednesday, Thursday and Friday. 

Headline: EXCL Stranded on Honeymoon Island bride reveals show led to life-changing health diagnosis,

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Millie couldn’t swim so had to get over that fear to jump into the sea to get to the islandCredit: BBC

The first episodes are already available to stream on BBC iPlayer.

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‘Fastball’ test you can do at home detects early Alzheimer’s clues years before diagnosis in just 3 minutes

A BRAINWAVE test could detect early signs of Alzheimer’s disease in just three minutes – years before clinical diagnosis would even be possible.

Researchers say the test, nicknamed ‘Fastball’, could even be used at home and serve as a cheap tool for those who struggle to get a diagnosis.

Older man wearing a brainwave-reading device, sitting on a couch with a younger man.

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Dr George Stothart (right) from the University of Bath, with volunteer John Stennard trying the FastballCredit: PA
EEG headset on newspaper and tablet.

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It records the electrical activity of the brain by placing small sensors on the scalpCredit: PA

Fastball measures patients’ brain waves through the use of a headset that uses electroencephalogram (EEG) technology.

It records the brain’s automatic response to a series of flashing images displayed on a screen.

Its inventors, from the universities of Bristol and Bath, say it can detect subtle changes to brain waves during the very early stages of dementia.

A £1.5million funding boost from the government will allow it to be tested on 1,000 patients in Bristol to find out if it can be used for mass screening.

Researchers hope the test could slash five years off the average age of diagnosis.

Dementia is often diagnosed too late, they said, up to 20 years after it has started to develop and when it’s already damaged the brain beyond repair.

Currently, diagnosis relies on tests to assess people’s memory, which researchers have previously said can be limited and may be impacted by a person’s education, language skills and whether or not they’re nervous.

They claimed Fastball swerves these issues as the test assesses patients ‘passively’, without requiring participants to follow instructions or recall information.

Dr Liz Coulthard, from the University of Bristol, said: “Patients can wait a long time for diagnosis and some of our current tests can be inaccurate and stressful for them. 

“A quick, easy-to-administer memory test, like Fastball, could transform that.”

Common painkiller used for back pain ups risk of dementia by 29%, scientists warn

A new study, led by experts from the universities of Bath and Bristol and published in the journal Brain Communications, included 52 patients with mild cognitive impairment (MCI) and 54 healthy older adults.

MCI refers to a decline in memory and thinking. Not all cases progress to Alzheimer’s disease, but it can be an early sign and risk factor for the condition.

As well as the Fastball test, patients on the trial also completed a number of neuropsychological assessments that tested their memory, their ability to pay attention and general cognitive function.

Researchers found Fastball could reliably identify memory problems in people with MCI.

Photo of Dr. George Stothart and volunteer John Stennard; John is wearing a device to test brainwave activity.

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Researchers said the test could be used at home and detect brain signal changes in indicative of Alzheimer’s in minutesCredit: PA

Patients with amnestic MCI – which involves significant memory loss, such as forgetting appointments and recent conversations – showed significantly reduced responses to the Fastball test compared to healthy patients and those with non-amnestic MCI.

Researchers re-tested the group after one year and found Fastball “showed moderate to good test-retest reliability” in healthy older adults.

The study also demonstrated for the first time that the test can be performed in patients’ homes.

Researchers now say the Fastball could also be used in GP surgeries and memory clinics to speed up diagnoses.

Lead author Dr George Stothart, a cognitive neuroscientist in the Department of Psychology at the University of Bath, said: “We’re missing the first 10 to 20 years of Alzheimer’s with current diagnostic tools.

“Fastball offers a way to change that – detecting memory decline far earlier and more objectively, using a quick and passive test.”

Alzheimer’s Society estimates there are around 982,000 people with dementia in the UK, but more than a third do not have a diagnosis.

The number is expected to rise to 1.4 million by 2040.

What are the early symptoms of cognitive decline?

WE all notice a natural decline in memory and thinking as we age.

This will be more pronounced in some people, as they experience memory and thinking problems that are mild but still noticeable.

This is described as mild cognitive impairment (MCI). Unlike dementia sufferers, people with MCI can still get on with day-to-day life.

Research suggests that two out of 10 people over the age
of 65 have MCI, according to Alzheimer’s Research UK.

About one in 10 people who’ve received an MCI diagnosis will go on to develop dementia.

Symptoms of MCI include:

Memory – Misplacing items or having trouble
remembering recent conversations.

  1. Attention problems – finding it difficult to concentrate,
    e.g. while watching a TV programme or carrying out
    duties at work
  2. Disorientation – confusion about time, date or place
  3. Thinking skills – problems with planning or completing
    tasks, e.g. managing money, or cooking a meal
  4. Problems with communication and finding the right words
  5. Mood and behaviour changes – becoming irritable, anxious,
    or feeling low

These symptoms may affect someone with MCI all the
time, or they might come and go.

There are steps we can take to keep our brains as healthy as possible. These include:

  • Not smoking
  • Doing regular physical activity
  • Staying mentally and socially active
  • Eating a healthy balanced diet
  • Limiting the amount of alcohol we drink
  • Having your hearing checked regularly
  • Keeping blood pressure, blood sugar and cholesterol
    levels in check

Dr Stothart added: “There’s an urgent need for accurate, practical tools to diagnose Alzheimer’s at scale. Fastball is cheap, portable and works in real-world settings.”

Chris Williams, chief executive of BRACE Dementia Research, which supported the study, said: “Fastball is an incredible tool that could offer anyone who, for whatever reason, cannot access a dementia diagnosis in a clinical setting.”

Reacting to the findings, Sir John Hardy, professor of neuroscience and group leader at the UK Dementia Research Institute at UCL, said: “Identifying individuals early for cognitive decline is going to be of increasing importance as therapies for Alzheimer’s and other dementias are developed and this protocol Fastball seems as if it may be helpful in this regard.

“What it does not do, and does not claim to do, is distinguish early Alzheimer’s from other causes of decline and this latter is also important.

“Because of this, it is likely that additional tests, biomarker or imaging, would also be needed for this second important aim.”

Dr Julia Dudley, head of research at Alzheimer’s Research UK, added: “Too many families face dementia without answers, with one in three people with the condition living without a diagnosis.

“Therefore it’s encouraging to see studies exploring potential ways to detect memory problems earlier.

“This study, in a small group of people, suggests that it can be used to measure mild memory impairment, which for some people can be an early sign of diseases like Alzheimer’s.

“However, as participants were only followed up one year later, we don’t know if those people will definitely go on to develop dementia.

“Longer-term studies in larger, diverse groups of people are needed to find out if this technology can predict how memory problems will unfold over time.”

Barriers to diagnosis

The trial results come as a new report by the Alzheimer’s Society warned that one in five people impacted by dementia receive no support.

A survey, carried out for the charity by Walnut Unlimited, included almost 3,500 impacted by dementia, such as patients, loved ones and unpaid carers.

Just a third said their experience of diagnosis was positive, while 52 per cent faced long wait times and 41 per cent had to see multiple healthcare staff.

Professor Fiona Carragher, chief policy and research officer at Alzheimer’s Society, said: “Almost a million people are living with dementia, yet its scale and the day-to-day realities often remain hidden.

Early signs of dementia

It’s not unusual for your memory to lapse a bit as you get older.

But dementia is different from ‘just getting old’ as it will cause noticeable – rather than gradual – changes to mental abilities and make managing everyday tasks and activities increasingly difficult.

The symptoms of dementia may be small to start with, but get worse over time.

Below are some examples of possible signs.

Memory loss

Memory loss is a key sign of dementia. This can include:

  • Forgetting something you were only recently told. You may ask for the same information repeatedly – for example, ‘Are the doors locked?’
  • Putting objects in unusual places – for example, putting your house keys in the refrigerator.
  • Being unable to learn new tasks, like how to use a new washing machine.

Planning and decision making issues

People with dementia can have difficulty with planning and decision making. This can include:

  • Getting very confused when planning or thinking things through.
  • Struggling to stay focused on a single task.
  • Not making informed, careful decisions when dealing with money or looking at risks.
  • Finding it hard to manage regular payments, budgets or monthly bills.

Problems with language and understanding

In people with dementia, this can manifest as:

  • Having frequent problems finding the right word or regularly referring to objects as ‘that thing’.
  • Finding it hard to take part in conversations.
  • Regularly being unable to follow what someone is saying even without distractions.

Losing sense of time and place

Dementia can cause problems with orientation, including:

  • Losing track of the date, season or the passage of time.
  • Getting lost in a place that is familiar or that should be easy to find your way around – for example, a supermarket.
  • Regularly being unable to follow what someone is saying even without distractions.

Problems with vision and perception

This can mean having problems making sense of what you see.

For example, having difficulty judging distances on stairs, or mistaking reflections or patterns for other objects.

Mood and behavioural changes

Finally, dementia can also make people act differently or shift their mood. This can mean:

  • Becoming withdrawn and losing interest in work, friends or hobbies.
  • Feeling unusually sad, anxious, frightened or low in confidence.
  • Getting easily upset at home, at work, with friends or in places that usually feel comfortable or familiar.

Source: Alzheimer’s Society

“These findings tell us that far too many people are going without the help they need, whether it’s support after a diagnosis, trained care professionals, or someone to turn to when things get hard.”

The charity also found more than a third (35 per cent) of people living with dementia are scared of getting diagnosed, while 31 per cent are apprehensive about talking to healthcare professionals.

Professor Carragher said: “An early and accurate diagnosis is vital to enable people living with dementia to access the care, support and treatments they so desperately need.

“Those who have been able to access these treatments experienced benefits, but we simply aren’t diagnosing people early or accurately enough to see current and prospective treatments rolled out widely.”

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Gordon Ramsay reveals skin cancer diagnosis, undergoes surgery

Gordon Ramsay has a message for you this holiday weekend: wear sunscreen.

The Michelin-starred celebrity chef posted Saturday on Instagram that he was diagnosed with skin cancer and had the basal cell carcinoma removed from the side of his face.

Ramsay shared two photos, one of a bandage stretching from his cheek to his neck. Another, a close-up, showed stitch marks directly below his earlobe.

“Grateful and so appreciative for the incredible team at The Skin Associates and their fast reactive work on removing this Basal Cell Carcinoma thank you! Please don’t forget your sunscreen this weekend,” Ramsay wrote in the caption.

His post was not without humor: “I promise you it’s not a face lift! I’d need a refund …” he said.

Ramsay — the host, most recently, of the reality TV show “Hell’s Kitchen” — has not been shy about sharing his health issues on social media, as well as offering cautionary advice to his followers. Last year he posted a video on Instagram after he was in a bicycle accident in Connecticut. In the video, the Scottish-born restaurateur lifted his white chef coat and pointed to expansive bruising on his torso. He urged his followers to “WEAR A HELMET.”

Skin cancers are among the most common cancers diagnosed worldwide, according to the World Health Organization’s International Agency for Research on Cancer. More than 1.5 million new cases were estimated in 2022.

Basal cell carcinoma in particular, which Ramsay was diagnosed with, is a type of non-melanoma skin cancer and the most common overall, says Elizabeth Bahar Houshmand, a double board certified dermatologist based in Dallas.

“But the good news,” Houshmand says, “is there’s a less than 1% chance of metastasis, meaning it would spread to other organs, regions. But it is a skin cancer and needs to be addressed promptly. Usually the treatment is surgical excision and that’s what Gordon Ramsay had done.”

Early detection of basal cell carcinoma, Houshmand says, is key. As are preventative measures, such as wearing sunscreen and SPF clothing.

“It’s generally slow-growing and rarely spreads to other parts of the body, and with early detection and treatment the cure rate is very high,” she says. “Always see your dermatologist if you see an irregularity that’s not going away. Don’t wait. And protect yourself — I like an SPF of 50 or greater and apply it 15 minutes before going outside.”

So if you fire up the grill this weekend — even attempting one of Ramsay’s barbecue favorites — still, make sunscreen the main course.



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Monica Seles: Nine-time Grand Slam champion reveals myasthenia gravis diagnosis

Nine-time Grand Slam champion Monica Seles has revealed she was diagnosed with myasthenia gravis – a neuromuscular autoimmune disease – three years ago.

The 51-year-old has chosen to go public with the rare long-term condition, which causes muscle weakness, to raise awareness before this month’s US Open.

Seles first noticed symptoms of the condition, which can affect most parts of the body – including the muscles that control the eyes, around five years ago.

“I would be playing [tennis] with some kids or family members, and I would miss a ball,” former world number one Seles told The Associated Press.

“I was like, ‘Yeah, I see two balls.’ These are obviously symptoms that you can’t ignore.

“It took me quite some time to really absorb it, speak openly about it, because it’s a difficult one. It affects my day-to-day life quite a lot.”

Seles decided to reveal her condition in the hope of using her platform to educate people about the disease, for which there is currently no cure.

The American won eight major titles by the age of 19, after capturing her first aged 16 at the 1990 French Open.

But she won just one more after she was stabbed with a knife by a fan during a match in Hamburg in 1993 and took time away from the sport to recover.

Seles played her last match in 2003 having won 53 tournaments and spent 178 weeks at number one.

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Bay Area sports broadcasting legend Greg Papa reveals cancer diagnosis

Greg Papa, the legendary sports radio voice in the Bay Area, is stepping away from his broadcasting duties while undergoing treatment for cancer, he announced Friday.

Papa, the radio voice of the San Francisco 49ers and a longtime host on KNBR (680 AM), did not specify the type of cancer he is battling in a statement released by the radio station but said he expects a full recovery.

“As I fully focus on my treatment and work toward a full recovery, I’m stepping away from my broadcasts but look forward to returning soon,” Papa said. “Thanks to everyone for your prayers and good wishes as I begin this fight.”

Papa, 62, began his career doing radio play-by-play for the Indiana Pacers in 1984 but launched a decades-long career in the Bay Area when hired by the Golden State Warriors in 1986.

He transitioned to television in the ‘90s, calling games for the San Antonio Spurs. He also called baseball games on TV, beginning with the Oakland Athletics before jumping to the San Francisco Giants in the mid-2000s.

When play-by-play announcer Dave Flemming’s microphone went dead for 10 seconds after Barry Bonds hit his 715th career home run to pass Babe Ruth on the all-time list in 2006, Papa took over the broadcast and explained what had transpired.

“To lose a mic like that, I’ve never seen it,” Papa said. “I’ve never been a part of something like this.”

Flemming was distraught but took it in stride with Papa’s help.

“I think it’s the last gasp of the curse of the Bambino,” Flemming joked. “Now, I’m starting to rethink my whole world.”

Papa’s coworkers rallied to support him when the diagnosis was announced.

“Greg is not just our teammate at The Sports Leader, he’s one of the most iconic play-by-play men in the history of our beloved Bay Area,” said Brian Murphy, the popular longtime KNBR talk show host. “Nobody else has done the Warriors, Raiders, Giants, A’s and 49ers like Greg, so he has every Northern California fan base rooting hard for him to come out healthy and get back behind the mic.”

Papa, a three-time winner of the California sportscaster of the year award, has been the radio play-by-play announcer for the San Francisco 49ers since the 2019 season. His contract with the 49ers extends through the 2028 season.

“The 49ers family extends our unwavering love and support to Greg Papa and his family following his recent cancer diagnosis,” the 49ers said in a statement. “We wish him a speedy recovery and look forward to welcoming him back to the radio booth as the ‘voice of the 49ers’ whenever he is ready.”



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Justin Timberlake reveals Lyme disease diagnosis amid world tour

As Justin Timberlake bid farewell to his Forget Tomorrow world tour, he got candid with fans about his health.

The “Mirrors” and “SexyBack” pop star, 44, on Thursday revealed in a heartfelt Instagram post that he powered through his circuit of live performances as he battled a “relentlessly debilitating” bout of Lyme disease. The singer, who faced backlash for his low-energy performances in recent weeks, said in his lengthy caption that sharing his health issues was to help him “shed some light on what I’ve been up against behind the scenes.”

The Grammy-winning singer and actor went in depth about the disease’s mental and physical toll. Although he said he was “shocked” by the diagnosis, he said it provided some clarity.

“At least I could understand why I would be onstage and in a massive amount of nerve pain or, just feeling crazy fatigue or sickness,” he continued. “I was faced with a personal decision. Stop touring? Or, keep going and figure it out.”

The Mayo Clinic defines Lyme disease as an illness “caused by borrelia bacteria” that humans can get if they are bitten by an infected tick. Symptoms of Lyme disease can include joint stiffness, muscle aches and pains, fever and headache. Antibiotics are used to treat the disease.

Timberlake, amid the “fleeting stress my body was feeling,” said he opted to continue with his tour. “I’m so glad I kept going,” he said.

Pushing through with the tour, which began in April 2024 in Vancouver and ended Wednesday in Turkey, allowed Timberlake to prove his “mental tenacity,” he said. The singer said he would also work to be “more transparent about my struggles” with fans.

Throughout his tour, Timberlake faced a handful of personal and public obstacles. In October 2024, he announced the postponement of several shows to recover from bronchitis and laryngitis. That same month, he also abruptly called off a concert in Newark, N.J., because of an injury.

Notably, the former ‘NSYNC frontman carried on with his slate of shows last year after his DWI arrest in the Hamptons in June 2024. He pleaded guilty to a lesser charge of impaired driving, his driving privileges were suspended and he was sentenced in September to 25 hours of community service at a nonprofit of his choosing. He was also required to make a public safety announcement about the dangers of impaired driving.

After sharing his health update, Timberlake reminisced on his touring experience, continuing his post in his own comments section. He thanked supporters for their “energy and love” and the crew and artists who joined him on the road. Though performing live is “sacred” to the “Suit & Tie” music star, he said the status of his stage career remains unclear.

“I honestly don’t know what my future is onstage but I’ll always cherish this run! And all of them before,” he wrote. “It’s been the stuff of LEGEND for me.”

He ended his post sending love to his actor wife Jessica Biel and their two children. His caption accompanied a carousel of behind-the-scenes photos.

Former Times staff writer Nardine Saad contributed to this report.

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Billy Joel shares health update after brain disorder diagnosis

Billy Joel reassured fans about his health on Monday.

The 76-year-old musician had previously canceled all of his scheduled concerts after announcing in May that he was diagnosed with normal pressure hydrocephalus (NPH). NPH occurs when excess cerebrospinal fluid accumulates in the brain’s ventricles, with patients experiencing cognitive decline, difficulty walking and urinary incontinence, according to the Alzheimer’s Assn.

Joel’s recent concert performances worsened his symptoms, leading to hearing, vision and balance problems, he shared in a May 23 statement. While on Bill Maher’s podcast, “Club Random,” the “Piano Man” crooner said he often feels like he’s on a boat, but otherwise, he’s doing just fine.

“I feel good,” Joel said, seated at a piano. “They keep referring to what I have as a brain disorder so it sounds a lot worse than what I’m feeling.”

Joel noted that the condition is idiopathic, meaning no one knows the cause.

“I thought it must be from drinking,” he said, adding that he doesn’t drink anymore. “I used to, like a fish.”

Joel finished his decade-long residency at Madison Square Garden in July 2024 after 104 monthly shows at the venue. His now-canceled tour included dates across the U.S. and performances with Stevie Nicks, Rod Stewart and Sting.

The first installment of Joel’s documentary, “Billy Joel: And So It Goes,” premiered Friday on HBO. The two-part series takes a deep dive into the pianist’s journey from a bullied kid in Long Island to a legendary hitmaker, and features appearances from Paul McCartney, Bruce Springsteen, Pink and Sting.

Part 1 “is notable in how it reframes the narrative around his relationship with his former wife and manager Elizabeth Weber, explaining how she was instrumental in guiding his career and helping him become a superstar — and how songs like ‘Big Shot’ and ‘Stiletto’ were inspired by the rocky times in their marriage,” wrote Times television editor Maira Garcia. “It’s a compelling and nuanced portrait of an imperfect person who created timeless music and whose influence continues to reverberate.”

Part 2 of “And So It Goes” premieres Friday on HBO and HBO Max.

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Dermot Murnaghan’s health woes in full from pitbull horror to cancer diagnosis

Former Sky News journalist Dermot Murnaghan has opened up about his journey with stage four prostate cancer, with an important message for other men. And it’s not the first time the sporty broadcaster has shared details about his health

Dermot Murnaghan has been diagnosed with stage four cancer
Dermot Murnaghan has been diagnosed with stage four cancer

Dermot Murnaghan has today revealed he has been diagnosed with stage four cancer. The 67-year-old broadcaster told how he’s undergoing treatment for prostate cancer, and urged other men to make sure they get themselves tested.

Praising his “outstanding medical team”, former Sky News reporter Dermot issued a statement via social media platform X, writing: “Some personal news……I’ve been diagnosed with Stage IV advanced prostate cancer I’m fortunate to have a simply outstanding medical team looking after me, who I can’t thank enough – they are administering the best possible care with expertise, compassion and sensitivity.”

He continued: “I’m responding positively to their excellent treatment and feeling well. I’m blessed to be fortified by the monumental love and support of my wife, family and close friends. Needless to say, my message to all men over 50, in high-risk groups, or displaying symptoms, is get yourself tested and campaign for routine prostate screening by the NHS.”

READ MORE: Dermot Murnaghan sends plea to men after devastating stage four cancer diagnosis

British Broadcaster, Dermot Murnaghan trains in preparation for the Sport Relief All-Star Games: Birmingham 2022
The journalist is known for his active lifestyle(Image: Getty Images)

Journalist Dermot went on to share that, going forward, he hopes to participate in Sir Chris Hoy’s fundraising charity bike ride in Glasgow this September, encouraging followers to make a donation if they can.

In a previous interview with the Mail Online, keen cyclist Dermot opened up about his health, describing himself as “fairly fit”.

He shared that his father had “lived till the ripe old age of 86”, before offering his own thoughts on the prospect of “living forever”. He reflected: “Only if everyone else I knew could. Being old without your loved ones could be very lonely. “

The Devon-born media personality also opened up about his healthy diet, which he supplements with immune-boosting vitamin C and zinc tablets, and spoke about his “worst illness or injury”, telling the publication how he was injured after a dog lunged at his bike.

He said: “A few years ago, I broke four ribs when a pitbull knocked me off my bike. The charming owner then had the audacity to reprimand me for scaring his dog. They can’t do much for broken ribs, you’re just sent off with strong painkillers. For eight weeks, sleeping was very uncomfortable and sneezing, coughing or laughing could aggravate it. Even now, when I turn to my right side, I often feel a twinge.”

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This, unfortunately, isn’t the only time that Dermot has found himself in peril while on the road. In 2017, the newsreader shared photographs of his bruised face after he was injured in a hit-and-run incident. He told fans at the time: “Here’s why I haven’t been on air for 2 days. A hit and run in Kentish Town yesterday. Police were fantastic.”

Delving into the incident in more detail on Sky News, Dermot explained: “Having worked on Breakfast TV for 10 years in two stints, I’ve become a bit of an early bird. So last Thursday I woke at 6am, put on my hi-vis cycling jacket got on my bike to meet my mates for a few healthy miles before work.

“Twenty minutes later, I was lying by the side of the road with a broken cycle helmet and a hobbled bike, still spinning, lights shining – and a variety of cuts, bruises and abrasions. But thankfully, no broken bones.”

He added: “On an empty road in north London, a guy in a car on a mobile phone pulled out from the side of the road without indicating. I swerved that. But a millisecond later, he U-turned into me and wiped me out.

“The Good Samaritan who saw it says the driver then sped off. I didn’t catch his name in the muddle, so if you read this, thank you from the bottom of my heart. The perpetrator was too interested in his phone to bother to stop and would have left me lying in the road.

“Police were there within five minutes and were absolutely fantastic. Took all the details and went to check the CCTV. Then drove me and my crushed bike home. Professional through and through. “

Do you have a story to share? Email me at [email protected]. Like this story? For more of the latest showbiz news and gossip, follow Mirror Celebs on TikTok , Snapchat , Instagram , Twitter , Facebook , YouTube and Threads .

READ MORE: Sky News’ Dermot Murnaghan diagnosed with Stage 4 prostate cancer



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Erin Moriarty of ‘The Boys’ shares Graves’ disease diagnosis

Erin Moriarty, the outspoken and righteous Starlight of “The Boys,” is speaking out about her health, specifically her ongoing battle with an autoimmune disorder.

Moriarty, 30, revealed to her Instagram followers on Friday that she was diagnosed last month with Graves’ disease, an autoimmune disorder in which the thyroid becomes overactive. In the caption of her post, Moriarty expresses the positive effects of treatment but reveals the disorder could have been identified earlier “if I hadn’t chalked it all up to stress and fatigue.”

The “Jessica Jones” and “One Life to Live” actor shared a carousel of photos including text message exchanges with her parents. In one screenshot Moriarty tells her mother “I really need relief” as she details her discomfort. “I can’t live like this forever,” she writes.

“It’s not just fatigue — it’s an ineffable, system wide cry for help and I don’t know how long I can remain in this state,” Moriarty continues in her text to her mother.

Moriarty did not reveal too much about her symptoms, noting in her caption that “autoimmune disease manifests differently in everybody/every body.” According to the Mayo Clinic, symptoms of Graves’ disease can include “feeling nervous or irritable,” slight tremors of the hands or fingers, weight loss, menstrual changes and heart palpitations. Wendy Williams, Daisy Ridley and Missy Elliott have also spoken publicly about living with Graves’ disease.

“Within 24 hours of beginning treatment, I felt the light coming back on,” Moriarty said in her caption. “It’s been increasing in strength ever since.”

She did not reveal the details of her treatment, but Moriarty told her father in a text message, “I already feel a world of a difference” and that she has since been thinking, “‘Damn, this is how I’m supposed to feel? I’ve been missing out!’”

Since “The Boys” premiered on Prime Video in 2019, Moriarty has starred as superhero Annie January, a.k.a. Starlight, who possesses the power to fly and manipulate light. Without spoiling too much about the series, it now seems Moriarty knows what it’s like to lose her spark on- and off-screen — and how to get it back.

She concluded her post by urging followers to listen to their bodies and seek medical attention when something feels off. “If [your light] is dimming, even slightly, go get checked,” she said.

“Don’t ‘suck it up’ and transcend suffering; you deserve to be comfy. S—’s hard enough as is.”



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Holly Willoughby ‘wrote herself off’ after hidden dyslexia struggle before diagnosis

Former This Morning host Holly Willoughby spoke about her experience with dyslexia in the new documentary Jamie’s Dyslexia Revolution which aired on Channel 4 last night

Presenter Holly Willoughby has opened up about feeling “different” when she was younger in a new documentary that she has described as “important”. She’s suggested that she ended up “writing herself off” due to a challenging experience.

Holly, 44, has previously spoken about being diagnosed with dyslexia shortly before her GCSEs. She once shared whilst hosting This Morning that she felt “shameful” about struggling with spelling for years, but also revealed on the ITV show that she’s since become proud to have dyslexia.

She’s now further discussed her experience with the learning difficulty at school. Holly opened up in the documentary Jamie’s Dyslexia Revolution, which aired on Channel 4 on Monday, with her among the participants in the project.

The one-off special saw chef Jamie Oliver, who has spoken about his own experience with dyslexia, explore the challenges faced by pupils who have dyslexia. It also shows him campaigning for more support for those affected by dyslexia.

Like other participants, including Jamie Laing, Holly makes brief appearances in video messages shown during the documentary. She’s seen talking about her experience, including sharing that she felt “different” when she was at school.

Holly Willoughby in a white top in a video being shown on a whiteboard in a classroom.
Holly Willoughby spoke about her experience with dyslexia in a documentary that aired last night(Image: Jamie’s Dyslexia Revolution/Channel 4)

Opening up about her difficulty with spelling, she said in her first appearance: “I definitely was terrible at spelling.” She continued by sharing with viewers: “I knew that because in spelling tests I’d always get really poor results.”

Holly later said that she was “always” expecting feedback on her homework to include “silly mistakes” being brought to her attention. She said in the documentary: “I always knew that when I’d get my homework back, there would be red pen all over it where there would be ‘silly mistakes’.”

She said: “I felt like I was working really, really hard with not getting much results. So I felt different.” She later added: “The school system is made for a certain type of learning and it’s so hard when you don’t learn like that.”

Holly suggested that it had an impact on her even after she had left school. She said: “When you then write yourself off at school as being ‘non-academic,’ that does shape your future somewhat.”

Jamie Oliver in a blue top and suit at an event in June 2025.
She featured in Jamie’s Dyslexia Revolution, fronted by Jamie Oliver, which aired on Channel 4(Image: Getty Images)

Following the broadcast of Jamie’s Dyslexia Revolution, Holly responded to the documentary and a post made about it by Jamie. He had reflected on the reaction to the project in a post on Instagram this morning.

He wrote: “I’ve been completely blown away by the response to Jamie’s Dyslexia Revolution. The stories so many of you have shared- about your own journeys, struggles, and strengths – have been powerful, emotional, and deeply moving.

“If you’ve got something to say about dyslexia or neurodiversity -whether it’s your own experience, a frustration, or a big idea -please share it with [Secretary of State for Education] @bridgetphillipsonmp with the hashtag #ComeOnBridget and let her know that change is needed! If you missed it last night on @channel4 hit the link in my bio to catch up #ComeOnBridget.”

Holly later shared the post on her Instagram Story and wrote in her caption: “Well done [Jamie] such an important documentary! Just the beginning of this conversation.”

Jamie’s Dyslexia Revolution is available through Channel 4.

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READ MORE: Molly-Mae says this affordable moisturiser is so good she’s been using it for a year



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The 4 signs of skin cancer beyond moles as Atomic Kitten’s Natasha Hamilton reveals diagnosis after ‘itch on her back’

ATOMIC Kitten’s Natasha Hamilton opened up about her skin cancer battle, revealing she was diagnosed with the disease after getting a persistent itchy spot on her back.

In an emotional Good Morning Britain interview, the singer, 42, revealed she’d had basal cell carcinoma (BCC).

Natasha Hamilton of Atomic Kitten discussing her skin cancer diagnosis on Good Morning Britain.

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Atomic Kitten’s Natasha Hamilton revealed she was diagnosed with basal cell carcinomaCredit: ITV
Natasha Hamilton smiling after being evicted from Celebrity Big Brother.

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The singer got an itchy spot on her back after it got burnt on holidayCredit: Getty
Atomic Kitten filming a music video.

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Natasha was part of Atomic KittenCredit: Getty

BCC is the most common skin cancer type in the UK.

It begins in the basal cells — a type of cell within the skin that produces new skin cells as old ones die off – and is more likely to develop on skin regularly exposed to the sun, like the face, head or neck.

The cancer often tends to appear as a pearly lump, but it can also develop as a scar-like patch on the skin or rough, scaly growths.

Natasha initially mistook the diseased patch of skin as a mosquito bite.

She told her hosts Kate Garraway and Rob Rinder that she developed an itch after catching a bit too much sun while on holiday in Majorca.

Natasha said: “So I had been on holiday, I wasn’t actually in the sun a lot, my baby was only about five months old and I was breastfeeding.

“One afternoon I had her on my lap, my back was in the sun and I burnt.

“I don’t know if it was later that day or the next day, I had an itchy spot on my back.

“I felt it, I went “oh mosquito bite”.

‘It wasn’t until four weeks later when I was at home and it was itching I was like ‘hang on a minute, that seems a bit long for a mosquito bite’.

‘I asked my husband to have look and he went “oh that’s not a bite,” he took a picture.

Natasha revealed: “Originally it had just been a dark freckle that I’d had on my back for many years.

“It wasn’t even raised, it wasn’t a mole, it was just a freckle.”

The star sought specialist help and was diagnosed with BCC.

Close-up of a non-melanoma skin cancer.

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BCC can start as a pearly-looking lumpCredit: British Skin Foundation
Close-up of non-melanoma skin cancer.

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Cancerous patches can be a range of colours, including purple, brown and redCredit: NHS
Close-up of a non-melanoma skin cancer.

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Some growths may be bumpier, rough or crustyCredit: NHS

She was able to have the cancerous skin removed and is now living cancer-free.

But she revealed: “Now I have to be really vigilant, I have to check my skin all the time.

“Since then I’ve had a few things appear where I’ve had to go back to the dermatologist, they’re on the ‘watch list’.  

“This is probably something I am going to have to keep an eye for the rest of my life,” Natasha said.

The 4 signs of BCC

When you think of signs of skin cancer, a mole probably comes to mind.

This is usually the case with melanoma, the deadliest form of the disease.

But non-melanoma skin cancer – which includes BCC – can manifest in other more subtle ways.

According to Macmillan Cancer Support, a BCC might have some of these features:

  1. A smooth, firm lump that may be pearly, pink, red, brown or black – on black or brown skin, it is more likely to be pearly, brown or black
  2. A lump that is sunken in the middle like a crater
  3. A flat patch of scaly, crusty or irritated skin
  4. A scar-like area of pale, shiny skin

This type of skin cancer tends to be painless but it can cause itchiness or bleeding.

Close-up of a non-melanoma skin cancer lesion.

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Sometimes skin cancer may start as a flat discoloured patchCredit: NHS
Close-up of a non-melanoma skin cancer lesion.

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The patches may be darker on brown or black skin.Credit: NHS
Close-up of a non-melanoma skin cancer lesion.

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Sometimes the patches may look crusty and feel rough or itchyCredit: NHS

Over time, a BCC may develop into an open sore that does not heal.

Any part of your skin can be affected, but it’s most common in areas exposed to the sun, such as the:

  • Head, face and ears
  • Neck and shoulders
  • Back
  • Hands
  • Lower legs

BCCs mainly people with fair skin, but those with other skin types may also be at risk, according to the British Skin Foundation.

Those with the highest risk of developing a basal cell carcinoma are: 

  • People with pale skin who burn easily and rarely tan
  • Those who have had a lot of exposure to the sun, such as people with outdoor hobbies or outdoor workers, and people who have lived in sunny climates
  • People who have used sun beds or have regularly sunbathed.
  • People who have previously had a basal cell carcinoma

Almost all cases of BCC can be cured and it’s almost never a danger to life, according to the charity.

However, if a BCC is not treated early, it may get larger and may be more likely to come back.

Treatment can include surgically removing the affected area of skin.

Melanoma vs. non-melanoma skin cancer

There are two main types of skin cancer – non melanoma skin cancer and melanoma skin cancer. 

Non melanoma skin cancer includes:

  • Basal cell skin cancer – this is also called basal cell carcinoma (BCC)
  • Squamous cell skin cancer – this is also called squamous cell carcinoma (SCC)
  • Some other rare types

Non melanoma skin cancers tend to develop most often on skin that’s exposed to the sun. There is a high cure rate for these cancers.

Most people only have minor surgery and don’t need further treatment.

Melanoma skin cancer is when abnormal cells in the skin start to grow and divide in an uncontrolled way.

It starts in skin cells called melanocytes. These cells are in the deep layer of the epidermis.

Around 17,500 people are diagnosed with melanoma skin cancer in the UK each year. The number of people diagnosed has increased over the last few decades.

Melanoma skin cancer is the fifth most common cancer in the UK.

Source: Cancer Research UK

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Billy Joel cancels all shows after brain disorder diagnosis

Billy Joel has canceled all upcoming concerts, revealing he has been diagnosed with a brain disorder that causes physical and mental issues.

Joel, 76, has normal pressure hydrocephalus, or NPH, according to a statement posted Friday on the piano man’s social media. “This condition has been exacerbated by recent concert performances, leading to problems with hearing, vision and balance,” the statement said.

“Under his doctor’s instructions, Billy is undergoing specific physical therapy and has been advised to refrain from performing during this recovery period.”

Symptoms of NPH — in which cerebrospinal fluid accumulates in the ventricles of the brain but pressure doesn’t increase — include difficulty walking, according to the Alzheimer’s Assn. Sufferers walk with a wide stance and their bodies leaning forward, as if they were trying to maintain balance on a boat.

The association’s website says that another symptom is cognitive decline, including slowed thinking, loss of interest in daily activities, forgetfulness, short-term memory loss and difficulty completing ordinary tasks. Later in the disease, bladder control can become an issue.

NPH is one of the few causes of dementia or cognitive decline that can be controlled or reversed with treatment, the association’s website says. Surgical treatment usually involves placement of a shunt. The condition is often misdiagnosed as Alzheimer’s or Parkinson’s disease.

Danny Bonaduce of “The Partridge Family,” radio and wrestling fame was diagnosed with NPH in 2023. The 65-year-old said in a 2024 interview that he initially thought he’d had a stroke, while doctors thought it was early-onset dementia or Alzheimer’s. It took “the better part of a year” for him to get a correct diagnosis, he said.

Bonaduce’s memory loss appears to have been serious: He showed the interviewer a photo of himself in a wheelchair checking out the house where he and his wife now live. He said he has no memory of visiting the place multiple times before moving there.

Billy Joel’s message Friday follows his mid-March announcement that he would postpone his upcoming tour to manage his health after surgery for an unspecified condition. At the time, the singer expected a full recovery after physical therapy.

Now, the statement said, Joel is “thankful for the excellent care he is receiving and is fully committed to prioritizing his health” and “looks forward to the day when he can once again take the stage.”

“I’m sincerely sorry to disappoint our audience, and thank you for understanding,” Joel said in Friday’s statement.

In late February, the “Just the Way You Are” singer fell after performing “It’s Still Rock and Roll to Me” in Connecticut. He quickly recovered; it’s unclear whether that incident was a symptom of the disease or simply coincidental.

Times staff writer Alexandra Del Rosario contributed to this report.



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6 doctors on Biden’s cancer diagnosis and his treatment options

President Biden’s weekend announcement that he has an “aggressive” form of prostate cancer that has metastasized to his bone sparked the usual sympathy from supporters — and sharp suspicions among detractors.

The announcement comes amid fresh reporting on Biden and his inner circle hiding the degree to which his mental acuity was slipping during his presidency and campaign for reelection last year, and the advanced stage of his cancer drew immediate accusations from the right that the former president was also hiding problems with his physical health.

President Trump said he was surprised the cancer “wasn’t notified a long time ago,” suggested the public wasn’t being properly informed and said that “people should try and find out what happened.”

The Times spoke to six doctors who are experts in prostate cancer. They said the information Biden’s office has shared about his condition is indeed limited, but also that many of the assumptions being made publicly about the progression of such cancers, the tests that can screen for them and the medical guidelines for care among men of Biden’s advanced age — 82 — were simply off base.

The cancer

In its statement Sunday, Biden’s office said the former president was seen last week “for a new finding of a prostate nodule after experiencing increasing urinary symptoms,” and on Friday was “diagnosed with prostate cancer, characterized by a Gleason score of 9 (Grade Group 5) with metastasis to the bone.”

Dr. Mark Litwin, chair of UCLA Urology, said that description indicated Biden has a more advanced and aggressive form of prostate cancer than is diagnosed in most men, but that it was nonetheless “a very common scenario” — with about 10% of such cancers in men being metastatic at diagnosis.

Dr. Howard Sandler, chair of the Department of Radiation Oncology at Cedars-Sinai, agreed.

“It’s a little unusual for him to show up with prostate cancer that’s metastatic to bone at first diagnosis, but not extraordinary,” he said. “It happens every day to elderly men.”

That’s in part because of the nature of such cancer, the modern screening guidelines for older men, and the advanced treatment options for such cancer when it is found, the doctors said.

Prostate cancer in small, slow-growing amounts is prevalent among men of Biden’s age, whether it’s causing them problems or not. Most prostate cancers can be slowed even more dramatically — for years after diagnosis — with medical intervention to block testosterone, which feeds such tumors.

For those reasons, many doctors recommend men stop getting tested for prostate-cancer-related antigens, through what’s known as a PSA test, around age 70 or 75, depending on the individual’s overall health.

That advice is based in part on the idea that finding a slow-moving prostate cancer and deciding to act on it surgically or otherwise — which many alarmed patients are inclined to do when they get such news — can often lead to worse outcomes than the cancer would have caused if simply left alone. That includes impotence, incontinence and life-threatening infections.

Also, if an older patient does start experiencing symptoms and is found to have a more advanced prostate cancer, modern treatments are capable of stalling the cancer’s growth for years, the doctors said — often beyond the point when those patients are statistically likely to die from something else.

Even when older patients are tested and show somewhat elevated PSA levels, it is not always of immediate concern, and they are often told to just keep an eye on it, Litwin said. Simply put, doctors “typically don’t get too exercised about a diagnosis of prostate cancer in an 82-year-old,” he said.

Dr. Sunil Patel, a urologic oncologist and an assistant professor of urology and oncology within the Brady Urological Institute at the Johns Hopkins University School of Medicine, said that’s because the average life expectancy for an American man is under 85.

“And so most men at that time, at 75, they’re like, ‘OK, well, if it’s not going to kill me in the next 10 years, I’m going to leave it alone,’” Patel said. “That’s a really shared decision between the patient and the physician.”

When advanced, aggressive prostate cancers are found, as with Biden, the prognosis — and treatment plan — is of course different, the doctors said. “He is for sure going to need treatment,” Litwin said. “This is not the type that we can just observe over time like we often do.”

But that doesn’t mean Biden’s doctors dropped the ball earlier, he and others said.

The diagnosis

Biden’s office has not said whether he was receiving PSA screenings. A letter from Biden’s White House physician in February of last year made no mention of PSA testing, despite other recent presidents’ medical assessments including that information. Biden’s aides did not respond to requests for comment.

The doctors The Times spoke to had no special insight into Biden’s medical care, but said his diagnosis did not make them feel any less confident about the caliber of that care or suggest to them any nefarious intent to hide his condition.

For starters, “it would be considered well within the standard of care” for Biden to have forgone testing in recent years, given his age, Sandler said. “Certainly after 80.”

Litwin said he believes Biden probably was still tested, given his position, but that doesn’t mean he was necessarily hiding anything either. Some forms of aggressive prostate cancer don’t secrete antigens into the blood at levels that would be flagged in a PSA test, while others can grow and even metastasize rapidly — within a matter of months, and between routine annual screenings, he said.

Patel said he has personally found “very aggressive disease” in patients who had relatively normal PSA levels. “I don’t think anyone can blame anyone in terms of was this caught too late or anything like that,” he said. “This happens not too infrequently.”

Dr. Alicia Morgans, associate professor of medicine at Harvard Medical School, a genitourinary medical oncologist and the director of the Survivorship Program at the Dana-Farber Cancer Institute, agreed. Even if a patient is diligent about getting screened annually, “there will be some cancers that arise between screening tests,” she said.

Morgans said things gets even more complicated as men get older, when their PSA number may increase and start getting monitored before it is considered a clear indicator of cancer.

“Maybe it’s up a while. It was not cancer before, it hasn’t really changed that much. Now it has become cancer. It’s not the fault of anyone,” she said. “You can do everything right and things like this can happen.”

The treatment

Biden’s office said his cancer appeared “to be hormone-sensitive, which allows for effective management.”

The doctors The Times spoke to were relatively bullish about Biden’s short-term — and even medium-term — prognosis. “It’s not curable, but it’s highly treatable,” Morgans said.

“Without meaning to sound glib, there’s never been a better time to have metastatic prostate cancer in the history of medicine,” Litwin said — in part thanks to Biden’s own cancer “moonshot” initiative and the funding it sent to institutions such as UCLA, which has helped develop new drugs.

“There are numerous, very effective treatments for a patient in his situation,” Litwin said.

The standard and most likely course of care for Biden will be ADT, or androgen deprivation therapy, which involves a pill or shot that will shut down testosterone production, the doctors said.

“Now, an 82-year-old doesn’t have the same testosterone production as a 22-year-old anyway, so there’s not that far to go. But we shut it off,” Litwin said. “And by shutting it off, it cuts out the principal hormone that feeds the prostate cancer. That alone can be very, very effective.”

Dr. Geoffrey Sonn, urologic oncologist and associate professor of urology at Stanford Cancer Center, said Biden’s cancer is serious, but the ADT treatment “will make prostate cancer cells shrink down, stop growing, at least temporarily, in the vast majority of guys.”

“That is, it’s not a permanent fix, in that those cells will eventually figure out a way to grow even with low levels of testosterone,” Sonn said. “But that can take several years, and sometimes longer.”

Recent studies have shown that adding additional medications to an ADT regime can extend life even further, Sonn said, to “four, five, seven, 10” years or more after a metastatic prostate cancer diagnosis.

Dr. Mihir Desai, a urologist with Keck Medicine of USC, said with modern advancements, prostate cancer is just different than other cancers.

“If you find, say, colon cancer or pancreatic cancer or liver cancer are metastasized, then the deterioration is fairly fast and the outcomes are very poor,” he said. But with previously untreated metastatic prostate cancer, “there are many lines of treatment that can, if not cure it, certainly keep it under control for many years, with good quality of life.”

Sandler, who focuses on radiation oncology, said ADT treatment can cause loss of bone density or muscle mass, so Biden will likely be encouraged to stick to a fitness regimen or take medications to counter those effects.

He may also receive radiation to more heavily target specific pockets of cancer, including where it has metastasized to the bone, but that would depend on the number of metastatic sites, Sandler said — with radiation more likely the fewer sites there are.

“If there’s cancer all over the place, then there’s probably no benefit,” he said.

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Biden’s cancer diagnosis renews transparency debate, as Trump cries coverup | Health News

Former United States President Joe Biden’s cancer diagnosis has rekindled questions about whether he deceived the public about his health while in office, with his successor, Donald Trump, adding his voice to those suggesting a coverup.

Speaking to reporters at the White House on Monday, President Trump cast doubt on the timing of Biden’s advanced cancer diagnosis amid renewed scrutiny of the former president’s physical and mental fitness during his tenure.

“I’m surprised that the public wasn’t notified a long time ago,” Trump told reporters at the White House.

“Why did it take so long? This takes a long time, it can take years to get this level of danger,” Trump added.

“So, look, it’s a very sad situation, I feel very badly about it. And I think people should try and find out what happened.”

Trump also said that the doctors who had examined Biden while in office were “not telling the facts”.

“That’s a big problem,” he said.

Biden’s office said in a statement on Sunday that the former president was diagnosed with an aggressive form of prostate cancer that had spread to his bones.

The statement said Biden was diagnosed on Friday after experiencing “increasing urinary symptoms” and that he and his family were reviewing treatment options.

Doctors graded Biden’s cancer with a score of 9 under the Gleason classification system, according to the statement, indicating it is among the most aggressive kinds.

Late-stage prostate cancer has an average five-year survival rate of 28 percent, according to Johns Hopkins Medicine.

Biden earlier on Monday expressed gratitude to well-wishers for their words of support and encouragement.

“Cancer touches us all,” Biden wrote on social media.

“Like so many of you, Jill and I have learned that we are strongest in the broken places. Thank you for lifting us up with love and support.”

The news of Biden’s cancer diagnosis came as the former president’s health was already under renewed scrutiny ahead of the publication of a new book detailing the alleged coverup of his physical and mental deterioration by his inner circle.

Original Sin, written by CNN anchor Jake Tapper and Axios correspondent Alex Thompson, contains various damning accounts of Biden’s alleged decline, including an incident in which the then-president was reportedly unable to recognise Hollywood actor George Clooney at a 2024 fundraiser.

In his comments on Biden’s diagnosis on Monday, Trump drew a link between the former president’s cancer and the alleged concealment of his mental acuity.

“If you take a look, it’s the same doctor that said Joe was cognitively fine, there was nothing wrong with him,” Trump said.

“There are things going on that the public wasn’t informed of, and I think somebody is going to have to speak to his doctor,” he added.

Some doctors have publicly questioned the account of Biden’s cancer diagnosis provided by his office, pointing out that such advanced cancer would have had to progress over a period of years.

“For even with the most aggressive form, it is a 5-7 year journey without treatment before it becomes metastatic,” Steven Quay, a pathologist who is the chief executive of biopharmaceutical company Atossa Therapeutics, said in a post on X.

“Meaning, it would be malpractice for this patient to show up and be first diagnosed with metastatic disease in May 2025. It is highly likely he was carrying a diagnosis of prostate cancer throughout his White House tenure and the American people were uninformed.”

Howard P Forman, a professor of radiology at Yale University, said it was “inconceivable” that Biden’s cancer was not detected before he left office, as it would have been picked up by a blood test known as a prostate-specific antigen (PSA) test.

“Gleason grade 9 would have had an elevated PSA level for some time before this diagnosis. And he must have had a PSA test numerous times before. This is odd,” Forman said in a post on X.

However, Daniel W Lin, a prostate cancer expert at UW Medicine in Washington state, said that while Biden has “very likely” had cancer for years, it is possible he was not given a PSA test.

“There are screening controversies with the use of PSA, and many medical groups do not recommend PSA testing after 70 or 75 years of age, although others recommend based on life expectancy or state of health rather than age cut-points,” Lin told Al Jazeera.

Lin said it was also possible that Biden has a rarer form of cancer that is not detectable by the test.

“This situation is less common, but not considered overly rare. Additionally, when this situation occurs, it is more common in high-grade cancers, such as former President Biden’s case,” he said.

“Playing the odds, he does not fall into this category, however, it can definitely occur.”



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