diagnosis

R&B singer Nivea publicly revealed her recent leukemia diagnosis on an episode of the Atlanta-based performance and interview series “Cadillac Chronicles.”

In a conversation with host Brian Freeman, the 44-year-old Grammy-nominated artist said she was diagnosed earlier this year and is “grateful to God” for her health as she undergoes treatment.

“I’ve been going through treatment, and everything is going great so far, and I expect it to continue. Amen, amen, amen,” she said on Tuesday’s episode.

“Cadillac Chronicles” features Freeman riding in his 1974 Cadillac Eldorado with a musician, usually a hip-hop or R&B artist. In addition to discussing gratitude, Nivea also performed her hits from the car’s passenger seat, including 2002’s “Don’t Mess With My Man,” which earned her a 2003 Grammy nomination.

It seems the diagnosis hasn’t slowed her down. The singer also revealed she’s working on new music and going to school for audio engineering, which she said she’s “always wanted to learn.”

“I’m doing all the things I want to do,” she said. “Loving on my children, and just being grateful and taking every opportunity that comes my way.”

Nivea — born Nivea B. Hamilton — was married to singer-songwriter and record producer The-Dream from 2004 to 2008, and shares three children with him: daughter Navy Talia, born in 2005, and twin sons London and Christian, born the following year.

She also shares a son, Neal — who performs as Lil Novi — with rapper Lil Wayne.

Leukemia is a cancer of the blood that begins in the bone marrow, which varies based on the type of blood cell affected and the stage of the disease. The “Complicated” singer did not reveal which type she was diagnosed with, but said she maintains a “positive” outlook in all areas of life.

“I’m very grateful for life. It’s so cliche to say, you don’t know the time nor the hour, but it’s true, and it just helped me put a lot of things in perspective,” she said. “I live in gratitude religiously.”

As EastEnders’ king-hearted teen Barney Mitchell lands himself in hot water, let’s take a look inside the life of actor Lewis Bridgeman.

EastEnders has aired shock scenes for the teenagers of Walford this week, and Barney Mitchell could be hiding a very dark secret.

Actor Lewis Bridgeman arrived on the BBC One soap in the summer of 2024, alongside his dad, Teddy (Roland Manookian), and Harry (Elijah Holloway), and drama quickly followed.

It was soon revealed that self-confessed bookworm Barney is the product of an affair between his mum, Nicola (Laura Doddington), and Zack Hudson (James Farrar), leaving both Barney and Teddy devastated by the truth about his paternity.

Sweetheart Barney appears to be an innocent extension of the Mitchell family with a passion for friendship and education, but the schoolboy is now taking center stage, as he may be hiding a sinister side following a violent incident involving Joel Marshall (Max Murray).

In recent episodes of the BBC soap, Joel returned to Walford following a six-month prison sentence for violently attacking his step-mum, Vicki Fowler (Alice Haig), who was determined not to live under the same roof as the tearaway teen.

He soon realised he was not welcome in the Square and planned to leave without saying goodbye to his dad, Ross Marshall (Alex Walkinshaw). However, before Joel left the Square, he was attacked by Walford’s teenagers who tied him to a fence and soaked him in beer while making fun of him.

Lily Slater (Lillia Turner), Avani Nandra-Hart (Aaliyah James), Amy Mitchell (Ellie Dadd), Nugget Gulati (Juhaim Rasul Choudhury), Ricky Branning (Frankie Day), Denzel Danes (Jaden Ladega), and Barney Mitchell (Lewis Bridgeman) later went back to free Joel after Will Mitchell (Freddie Phillips) ordered to let him go.

But when they returned, Joel was found unconscious on the floor with a serious head injury. On Thursday (July 23), the group was sickened by the sight of his body, and the police soon arrived at the scene.

DC Craig Ingram (Matthew James-Bailey) assured the teenagers were not under arrest as their parents gathered at the station, though they were all witnesses to the assault.

The group later gathered in The Arches to get their story straight as Joel received treatment in the hospital, but Barney looked visibly sheepish.

Harry Mitchell (Elijah Holloway) arrived and told them to leave, saying that the garage owner, Phil Mitchell (Steve McFadden), would be furious if he knew they’d used his premises as a meeting point. It then transpired that Barney had taken his spare key.

With everyone gone, Barney asked his brother if he’d found anything. Harry pulled a carrier bag from his coat that contained a hammer and said he needed to know everything. Did Barney attack Joel?

Who plays Barney in EastEnders?

Barney Mitchell is played by actor Lewis Bridgeman. The 19-year-old actor was born in Maldon, Essex, and attended Plume School with aspirations to become a drama teacher or an actor from a young age.

In 2021, Lewis joined the National Youth Theatre, which allowed the soap star to participate in workshops and stage productions and opened up opportunities for professional acting contracts.

The young actor has since appeared in various theatre productions, including The Wind in the Willows and Goodnight, Mister Tom.

Lewis’ talents do not stop at acting, as the soap star is also very intelligent. At the age of 12, he took Mensa International’s acceptance test and passed, indicating an IQ above 132 and placing him in the top 2% of the world’s population.

Lewis has been diagnosed with autism and dyspraxia, and his mother, Jayne Bridgeman, was worried he would struggle at school.

“Lewis has wanted to become an actor since the age of six,” proud mum Jayne told Maldon Standard in 2021.

“He adores everything to do with theatre and film. I’m very proud, I love the theatre, and we geek out together on Star Wars and Marvel things.”

Lewis went on to achieve four grade 9s and studied drama at A-Level whilst attending Chelmsford Drama Centre at weekends.

He landed the role of Barney Mitchell in EastEnders in 2024, with his first scene airing the same summer.

EastEnders airs Monday to Thursday on BBC One and iPlayer

July 14 (UPI) — Chesley “Sully” Sullenberger, the pilot who safely landed an airliner in New York City’s Hudson River in 2009, announced Tuesday that he’s been diagnosed with Alzheimer’s disease.

He revealed the news in a post to his personal website. He described the condition as “the unwanted visitor at the door.”

“I recently found out that I have been diagnosed with Alzheimer’s Disease,” he wrote. “It is early stage. For now, this means a name may not come easily to me, I forget a story I have recently told, or I don’t sleep as well, but I am in the beginning of this long journey.”

Sullenberger was the pilot of US Airways Flight 1549, which made a safe emergency landing in the Hudson River after striking a flock of birds that disabled the plane’s engines. Aviation officials and the plane’s passengers credited Sullenberger with guiding the Airbus A320 safely to the surface of the water. All passengers and crew members aboard the flight survived, prompting observers to describe the incident as the “Miracle on the Hudson.”

In addition to working as a commercial airline pilot, Sullenberger served in the U.S. Air Force, an accident investigator and was the U.S. ambassador to the Council of the International Civil Aviation Organization.

He said the diagnosis has challenged what it means to live an act of service.

“And the answer is to speak up. It is my hope that by sharing this, other families living in the shadows with this disease will feel they too can step forward,” he said Tuesday.

“Over the years, when people would ask about the successful outcome of Flight 1549, I would say that ‘courage can be contagious,’ and on that day it helped everyone band together to get everyone off that airplane successfully. Now we need that courage to battle this disease. I am now part of a larger community with many of you, and we will be courageous together.”

NATALIE Imbruglia has opened up on receiving new mental health diagnoses while managing perimenopause.

The 51-year-old Aussie star who is best known for her hit single, Torn, revealed she was diagnosed with OCD (obsessive compulsive disorder) and ADHD (attention deficit hyperactivity disorder).

She was also dealing with the effects of perimenopause which made her “really angry” and would contribute to her anxiety before performing.

“You name it, there’s a sprinkle of it. They’re just labels. It’s not a negative, it’s my superpower,” she told The Sunday Times.

“But there’s a particular thing about my neurodiversity that’s hard for me to accept, which is how I get when I’m nervous before a show. Perimenopause made it worse.”

Natalie added: “Let’s just say it was a grieving process. I was really angry. I fell off a cliff. It felt like someone had taken some of my personality.”

read more natalie imbruglia

RED HOT

Natalie Imbruglia, 48, stuns as she strips down to a red bikini on holiday

AHOY THERE!

Natalie Imbruglia shows off her incredible curves as singer, 48, enjoys holiday

The singer and actress reached out to TV presenter Davina McCall, who has been a public menopause campaigner, for advice after battling feelings of “anger and anxiety.”

Natalie is now on HRT (hormone replacement therapy) which has helped her symptoms and she’s glad the topic has become less “shameful or taboo.”

Perimenopause refers to the time during which your body makes the natural transition to menopause, thus marking the end of a woman’s reproductive years.

A woman may begin transitioning sometime in her 40s. However, this transitional period happens at a different age for every woman, and it could happen as early as mid-30s.

Natalie rose to fame on Neighbours in the early 1990s and in 1997 kicked off her pop career with a cover of the Ednaswap song Torn.

Natalie has also appeared in the films Johnny English, Closed for Winter and Underdogs.

She has sold 10 million records worldwide, and is believed to have a net worth of around £10 million.

In 2019, Natalie revealed she had given birth to a son, Max Valentine whom she welcomed via IVF and a sperm donor.

Coronation Street have revealed a first look at Betsy Swain’s hospital dash that sees her given a life-changing diagnosis, and as her condition deteriorates, Dylan is blamed

A health battle will see Betsy Swain deteriorate on Coronation Street in upcoming episodes, resulting in a life-changing diagnosis.

The teenager will be rushed to hospital after collapsing at home. As she’s discovered, am ambulance is called and her mother Lisa Connor-Swain is left distraught.

As Lisa waits by her daughter’s bedside, she’s joined by her wife Carla Connor-Swain as they wait for news. There’s panic ahead, as Betsy’s condition worsens.

Soon, Betsy’s partner Dylan Wilson is blamed for what has happened to her. But what has he done, and why is Dylan facing accusations? All will be revealed when the scenes air, and Lisa wants answers.

A new trailer for the episodes released by the ITV soap has confirmed the moment Carla is told by Ryan about Betsy. She races to Betsy’s hospital room and finds a worried Lisa, but the trailer gives no extra information about what has happened.

It’s said that the scenes will see Betsy given a life-changing diagnosis, and accusations fly. As Betsy tries to come to terms with what has happened to her, her family will rally around her.

Spoilers released ahead of the trailer had teased the drama set to unfold. They revealed that Ryan Connor is the one who finds Betsy unconscious on the kitchen floor.

A nurse explains to a tearful Lisa that they are taking Betsy for an MRI Scan, and later, Dylan witness Betsy appearing to have a seizure. In the fallout, an upset Betsy begs Lisa not to blame Dylan for what has happened.

But Lisa soon confronts Dylan and blames him for Betsy’s collapse. After, Lisa calls at the station and tells the desk sergeant she’d like to report a crime.

As the week goes on, Betsy doesn’t want to see Dylan, and Lauren Bolton says her pal is in a bad way. Dylan is quickly arrested, and when he’s released, more than one resident make it clear they are against him.

Things take a turn when Dylan suggests Brody is responsible for what has happened to Betsy.

Coronation Street airs weeknights at 8:30pm on ITV1 and ITV X. * Follow Mirror Celebs and TV on TikTok , Snapchat , Instagram , Twitter , Facebook , YouTube and Threads .

JOHN Torode’s wife Lisa Faulkner has given fans an emotional update after revealing her shock breast cancer diagnosis.

The 54-year-old announced the news on Thursday and divulged that she had already undergone surgery and will be moving onto a course of radiotherapy.

She took to her Instagram stories today to thank her fans for all of their support over the last 24 hours.

Lisa penned: “Thank you for all of your support and your lovely messages. i promise I will read every word.

“So many of you going through this or someone who is. Your love and kindness has really touched me and I thank you from the bottom of my heart.”

The former EastEnders actress told her fans yesterday why she’d been quiet on social media.

READ MORE ON LISA FAULKNER

BREAST AWARE

The easily-missed signs of breast cancer after Lisa Faulkner’s diagnosis

END OF TORODE

John Torode’s ITV cooking show with wife set to be axed after BBC sacking

She divulged: “I know I’ve been very quiet on here, reason being I have had to have surgery for the early stages of breast cancer.

“I had surgery two weeks ago, it was quite a big op but it’s all good and I’ve my results back and they’ve got everything out.

“So it’s all clear and I just need now to have some radiotherapy in a few weeks.

“I just wanted to say I’ve got a bit of healing to do but I’m good. I’m well and feeling so much better and I’m so grateful I went for my mammogram.

“I just wanted to say don’t put them off, go, because they found this and without that mammogram it wouldn’t have been picked up.

“Thank you to our wonderful NHS and the fact we can have these mammograms and we can get treatment early.”

Within moments of her sharing the difficult news, Lisa was inundated with support from her famous pals and followers.

Actress Tamzin Outhwaite said: “Love you Lise. You’ve got this my darling.”

Another added: “Sending so much love your way, lovely xx.”

Before a third said: “Sending love and hugs.”

Lisa is best known for her various acting roles and in recent years has become prolific as a TV chef.

Her famous telly husband John Torode has yet to comment on the gutting news about his partner.

It is the latest in a long line of blows for John who was sacked from his role on MasterChef following an investigation at the BBC.

He was given the boot from the programme following an investigation which was launched based upon the conduct of his co-star, Gregg Wallace.

“Lethal Weapon” star Danny Glover has revealed he has been living with Alzheimer’s disease for years.

In an interview with NBC’s Lester Holt that aired on the “Today” show on Wednesday, the 79-year-old actor and activist opened up about living with the disease. According to People, he received his diagnosis in 2023, which was not long after he was awarded an honorary Oscar in 2022.

“I could live with it, in a sense,” Glover says of his condition, which has been affecting his movement, speech and memory. “I’m sure as it advances, things are going to be different and changing.”

A neurodegenerative disease, Alzheimer’s is a type of dementia that affects memory, thinking and behavior and worsens over time, according to the Alzheimer’s Assn. Holt reports that more than 7 million Americans over 65 are living with Alzheimer’s, with Black men suffering at a rate double the national average.

Glover and his family say the Hollywood icon is sharing his story now to “have ownership of his life” and to help remove the stigma around the disease.

“They’ve got my back,” Glover says of his family’s support.

Besides his portrayal of L.A. police Det. Roger Murtaugh in the “Lethal Weapon” film series, Glover is known for roles in movies including “Places in the Heart” (1984), “The Color Purple” (1985), “To Sleep With Anger” (1990), “Angels in the Outfield” (1994), “Dreamgirls” (2006) and “The Last Black Man in San Francisco” (2019). He’s also been a vocal advocate for social justice and humanitarian causes both in the U.S. and abroad.

He was the recipient of the Academy of Motion Picture Arts and Sciences’ Jean Hersholt Humanitarian Award in 2022.

“I don’t feel like it’s the end of my life,” he said in his interview with People about living with Alzheimer’s. “There’s work to do.”

Chris Johnson, the former NFL running back who holds the record for most yards from scrimmage in a single season, has the degenerative neurological disorder amyotrophic lateral sclerosis, commonly known as ALS or Lou Gehrig’s disease.

Johnson shared the diagnosis during an interview with Michael Strahan that aired Monday on ABC’s “Good Morning America.” The 40-year-old father of four spoke in his own voice but didn’t use his mouth — instead, he used his eyes to trigger a device that generated sentences based on recordings Johnson made soon after he was diagnosed last year.

“It’s continued to progress much faster than I ever imagined,” Johnson said of the disease. “I want people to understand just how quickly ALS can attack your body. Just over a year ago, I was picking up my 7-year-old daughter so she’d make a wish with her birthday cake. Today, I couldn’t do that.”

There is currently no known treatment that stops or reverses ALS, according to the National Institute of Neurological Disorders and Stroke, and most people with disease die of respiratory failure within three to five years of noticing symptoms (although one in 10 survive a decade or more).

In addition to receiving the standard medication to help slow the disease’s progression, Johnson has been working with neurologist and leading ALS researcher Dr. Merit Cudkowicz. She told “Good Morning America” that Johnson has taken part in a clinical trial for a therapy “that decreases inflammation, and I think that helped him a lot.”

“At first, you’re in shock, then you realize you have two choices: You can give up, or you can fight,” Johnson said. “I chose to fight.”

Johnson’s wife Brittany told Strahan: “We’re still hopeful. We’re hopeful that a breakthrough will happen or … a miracle will happen.”

Selected by the Tennessee Titans at No. 24 in the 2008 draft, Johnson was an instant NFL star. He made the Pro Bowl in each of his first three seasons and was named the league’s offensive player of the year in 2009. Also that season, Johnson led the NFL with 2,006 rushing yards — earning the nickname CJ2K as one of only nine players to have rushed for 2,000 or more yards in a season — and set a record with 2,509 yards from scrimmage that still stands.

Johnson rushed for more than 1,000 yards in each of his six seasons with the Titans, then spent a year with the New York Jets and three more with the Arizona Cardinals before retiring after the 2017 season. He finished with 9,651 yards and 55 touchdowns rushing and 2,255 yards and nine touchdowns receiving.

Titans owner Amy Adams Strunk released a statement Monday morning after Johnson’s diagnosis was revealed.

“Learning this news is extremely difficult, and we will support Chris every step of the way throughout his journey,” she wrote. “We are holding him and his family close, and join our fans around the world in expressing our love for Chris.”

The Jets and Cardinals also released statements expressing their support for Johnson.

While Johnson’s body will no longer allow him to perform a task like gripping a cup, he said he wants people to know that with ALS, “your mind stays sharp.”

“People sometimes look at the physical disability and assume you’re not still the same person inside,” Johnson said. “I still think the same. I still dream. I still love my family. My body just doesn’t cooperate.”

Julie Hayden and Gail Gregory, the self-proclaimed ‘dementia rebels’, appeared on This Morning to share their experiences of living with dementia and challenge misconceptions about the condition

Two women determined to challenge the stigma surrounding dementia have shared their personal journeys living with the condition.

Julie Hayden and Gail Gregory, the self-proclaimed ‘dementia rebels,’ featured on Tuesday’s This Morning to mark Alzheimer’s Society’s Forget Me Not month.

Chatting to hosts Ben Shephard and Cat Deeley, Gail, from Lancashire, disclosed she had received her diagnosis in 2019 aged 54, and was informed at the time she only had six to seven years to live.

“I was running my own business, and we’d noticed changes with my personality,” she explained. “I had an embroidery business like teddy bears and clothing, and we put personalised messages on, and I was taking a lot of information in which I wasn’t retaining. So when people were placing orders, I was having trouble retaining information, so I was making mistakes, which we put down to stress at the beginning because we had just moved.

“As you do, you put things off, and you think it’s going to get better, but it doesn’t get better, it goes worse, and so other things start to creep in,” reports Lancs Live.

Eventually, Gail chose to consult a medical professional and described the assessments she underwent at the doctor’s that proved challenging, such as drawing a clock face, “getting the numbers muddled up,” and attempting to recall an address.

Reflecting on that moment, she said: “You realise there’s something wrong. It’s then that it’s reality, that there’s something wrong. But what, you don’t know.

“Nobody tells you it’s going to be dementia, and you don’t imagine it’s going to be dementia, especially not at the age of 54.

“This is where the perception is wrong. Everybody expects it to be an older person in their later years, what they don’t expect is that people younger than me have been diagnosed, there are even children diagnosed.

“It’s that perception we need to change, because it’s not the end of life, it’s the beginning of a new one.”

Julie also revealed how she had been suffering from “life-changing” symptoms for more than five years when she was diagnosed, but was dismissed by the doctors.

She was told she was depressed and going through menopause, and it took Julie more than five years for a diagnosis.

Julie and Gail are now both supporting other people with dementia, particularly younger people, and fighting back against the stigma of people living with the condition.

As she urged for more training and information to support doctors, Julie said, “I can’t tell you what it’s like to live with cancer and go through the treatments because I’ve never been there. Nobody can tell you what it’s like to live with dementia unless they’ve actually lived with it.”

She added, “I had huge surprises as to what it was like, compared to how I thought it was going to be like when I got my own.”

Sharing her gratitude for the support they’ve both received from friends, family and those spreading awareness, Gail read: “A diagnosis of dementia, it can change many things but it should never, ever change our worth.

“We don’t need pity, and we don’t need to be pushed aside, because we need understanding and support and the opportunity to continue to live our lives with purpose, dignity, and connection.”

She added, “When I got my diagnosis, they said to me I would have six to seven years to live. I’m in those years now, and I’m still going, and what people should be saying to us is, go outside and live your life. Do the things that you want to do because that’s what life’s about at the end of the day, it’s about living.”

She continued: “I’m very grateful for dementia, because dementia has made me calm down. It’s made me appreciate the things that we have, like nature and things like that; it’s been wonderful. We get so many opportunities that we wouldn’t even dream of having, like coming here today, it’s wonderful.”

This Morning airs weekdays from 10am on ITV1 and ITVX.

For more information, visit https://www.alzheimers.org.uk/

The news presenter has shared his Alzheimer’s journey in his new Channel 4 documentary

Jon Snow’s wife has opened up about his health condition during a documentary about the star’s life.

The 78-year-old broadcaster has been flooded with support in recent weeks after sharing he was diagnosed with Alzheimer’s back in 2023.

Jon was the face of Channel 4 News from 1989 to 2021 and became one of the nation’s most trusted broadcasters before he decided to step down from his role after 32 years to focus on ‘longer-form projects’.

On Saturday evening (June 20), Jon shared his journey in an insightful Channel 4 documentary, Jon Snow: A Last Big Story, in association with the Alzheimer’s Society.

Jon’s wife, Dr Precious Lunga, starred alongside the veteran journalist on in the show. The 51-year-old is an epidemiologist and entrepreneur from Zimbabwe who left the country at 17 to study in the UK.

She graduated from the University of Edinburgh in 1998 with a degree in neuroscience, before completing a PhD in neuroscience at the University of Cambridge in 2003.

The couple first met in 2001 on the Caribbean island of Mustique, where they tied the knot nine years later in 2010.

They welcomed a child together via surrogacy in 2021, with Jon also having two children from his previous marriage.

In one scene of the documentary, the camera followed Jon into a doctor’s appointment, where he was accompanied by Precious, and informed that his health has been slowly declining.

Precious responded to the doctor by adding that she felt Jon’s health had recently changed, before opening up about his initial diagnosis.

“When we received a diagnosis, people were writing Jon off, and that’s when I realised how stigmatised Alzheimer’s is, and it made me so angry actually”, Precious explained.

“This is a progressive disease, but you can have Alzheimer’s and still will be a valuable member of society to contribute, if your loved ones are there to help you navigate it.”

Speaking about what the future holds, Precious bravely confirmed: “So, I want to give him as good a life as I can.”

Speaking about his diagnosis in the film, Jon says: “At the beginning I wanted to hide it, there’s so much prejudice. Any sort of hint of mental decay, you’re sort of dead.

“There are moments when it pops up, but it’s not an all-day, every-day condition, and that’s what I cling onto.”

He added: “I’ve witnessed a great deal, I hope I’ve learned something – but I’ve still got a huge amount to learn. We all have. There’s still more to do.”

Jon Snow: A Last Big Story is streaming now on Channel4.com

Following Jeremy Clarkson’s emotional cancer admission, questions are being asked about the future of Clarkson’s Farm, which has already been rocked by behind-the-scenes health battles

The latest episodes of Clarkson’s Farm have taken a devastating turn, with Jeremy Clarkson announcing his shock cancer diagnosis.

The former Top Gear host reduced farm manager Kaleb Cooper to tears as he revealed he’d known about the “aggressive” prostate cancer since May. Following treatment, Clarkson confided in Kaleb that he’d had “10 per cent” of his prostate removed via ultrasound, explaining: “The prostate, 10 per cent of it’s dead. The 10 per cent where the cancer is.”

In the season finale, Clarkson addressed viewers from his hospital bed, sharing that there had been complications during treatment. The 66-year-old told fans: “What I wanted to say was if this is all successful, I’ll see you for season six, and if it isn’t, I won’t. Take care, everyone.”

Over on Instagram, ahead of the new episodes dropping, an emotional Clarkson warned followers that a “really, really difficult watch” was in store.

Holding back tears in a candid post, Clarkson said on Tuesday: “Ordinarily, we try to keep the show bucolic and charming and cheerful. But the final two episodes, which drop in the middle of the night tonight, are none of those things really. They’re a difficult watch. They’re really, really, difficult.”

Fans of the hit farming show will know all too well that Clarkson is not the first cast member to share his health battles, with other stars being struck with serious illnesses throughout its five-year run.

Now questions have emerged about the future of Clarkson’s Farm, which has been running since June 2021, with Prime Video yet to issue a formal statement on its continuation.

At present, the show has not been officially recommissioned. In February, Clarkson himself confirmed that, while some recording for the upcoming series had already taken place, some pausing had been required due to the weather.

In his column for The Sunday Times, the presenter wrote: “There’s no filming happening on the farm at the moment. Or farming. It hasn’t stopped raining since the beginning of the year, so I can’t plant anything, and I can’t do anything with my cows either because we are still locked down by TB.”

But planning documents submitted to West Oxfordshire District Council reportedly suggest that season six is in the works. According to The Independent, part of it reads: “Season five will air this year and season six has been commissioned and will air in summer 2027.”

Clarkson’s enthusiasm for the farming show shows no sign of waning. Speaking previously with The Sun, he said: “We’ll definitely do six – Amazon want to (do series six), and I want to. I’ve got a good idea for six. I said I’ll stop doing them when there are no more ideas. But I’ve got two quite good ones, so we’ll do six, and then we’ll see…”

The beloved farm has been plagued by setbacks and personal health struggles. Back in 2024, during the show’s third series, farmhand Gerald Cooper revealed he had prostate cancer.

The fan favourite, known for his distinctive mullet, has since confirmed that he is thankfully cancer-free. Discussing his diagnosis with Prostate Cancer UK, Gerald shared: “It was a shock – but everyone has really supported me.”

He added: “I received tremendous support from family, friends and Prostate Cancer UK – which was also a lifeline. I made it through, and I’m now cancer-free.”

Wanting to do something “joyful” following his recovery, the 77-year-old went on to launch a racehorse syndicate to help raise some all-important awareness of prostate cancer. The horse itself is, of course, named ‘The Mullet’.

Then, in June 2025, it was revealed that castmate Alan Townsend – aka Alan the Builder – was awaiting heart surgery. While carrying out building work on the Farmer’s Dog Pub, Alan confirmed to Clarkson that he had a “quadruple bypass coming.”

When asked whether he had any fears about the procedure, Alan admitted: “Oh, [I’m] frightened to death. I don’t even like thinking about it. That’s why I keep going to work — keep out of the way. They told me to really just take it easy and stay at home. But if you stay, you’ll be worrying to death about it.”

In the latest season, fans were delighted to see Alan back at work after undergoing a gruelling procedure. Opening up to Clarkson about returning to normality, Alan confirmed that the op had been “very painful”, adding, “I don’t want to show you on camera, but it’s a nasty cut.”

Alan shared that he’d been hospitalised because of issues with the arteries in his heart. He explained: “One had collapsed and curled itself up, and the others were about 85-90 per cent blocked. Horrible. I had a bit of a problem with the lungs, I lost 36 per cent of the lungs.”

Coincidentally, Alan and Clarkson had been neighbours at the same hospital, with Clarkson undergoing follow-up heart check-ups at the same time.

The presenter underwent a heart procedure in October 2024, after experiencing a tightness in his chest. Medics revealed he’d been mere days away from a heart attack, in a scare that led to him having a stent fitted.

Opening up about his brush with catastrophe on the first episode of season five, Clarkson blamed his health woes on the pressures involved in launching The Farmer’s Dog. He told Kaleb, “I’m back and not dead. The Grim Reaper will have to wait. It was f***ing close, though.”

Clarkson’s Farm season 5 is on Prime Video

Do you have a story to share? Email me at julia.banim@reachplc.com.

Follow Mirror Celebs on Snapchat , Instagram , Twitter , Facebook , YouTube and Threads.

The farmer was visibly upset, breaking into tears, when Jeremy Clarkson announced his cancer diagnosis in the latest episodes of the TV show Clarkson’s Farm

Jeremy Clarkson’s devastating cancer diagnosis left farm manager Kaleb Cooper in tears.

The 66-year-old shared the news in the final episodes of his series Clarkson’s Farm, as he sat down to chat with Kaleb Cooper and Charlie Ireland.

“I’ve got cancer,” Clarkson said during a conversation about the farm’s harvest.

Kaleb replied, “No, you haven’t. Where?”

The former Top Gear host has continued: “Where it is, is of no concern of anybody. I’ve known since May.”

“I had a medical, you remember back in May? I disappeared off the other week and I had a biopsy and it is cancer and it’s aggressive, but it’s really early so the treatment will be, you know…

“I was praying we could get the harvest done and then I could go and get some treatment but it’s going to be slap bang in the middle.”

Kaleb, wiping away tears, then said, “Look after yourself, you go and do… if you need anything just ring.”

Later in the show, Clarkson spoke about how the year had been challenging while talking to Kaleb, his girlfriend Lisa, and his two other employees.

“We started the year and I had coronary heart disease and ended it with me with cancer,” he explained.

“We can dwell as much as we like on all the bad things that have happened on the farm, but I think it’s better now, at the end of the year, to focus on things that have happened that are good.”

Kaleb asked, “When will we know the treatments worked?”

In response to Kaleb’s tears, the Who Wants to be a Millionaire host jests at him to “cheer up”.

“Not for another few weeks. Come on cheer up, it probably did work.”

The emotional episode has now been added to Prime Video.

Ahead of the episodes the TV star warned fans that they may be “a difficult watch”.

He posted on Instagram: “Ordinarily we try to keep the show bucolic and charming and cheerful. But the final two episodes which drop in the middle of the night tonight are none of those things really.”

In the clip, he took a deep breath and added: “They’re a difficult watch. They’re really, really difficult.”

After he announces the news to the farmers, Clarkson is later seen in a hospital bed set to undergo surgery.

However, Clarkson appears to maintain a positive attitude as he says he hopes to be back for a sixth season, before joking that if the treatment isn’t successful ‘take care everyone’.

PERRIE Edwards has spoken out on ex-bandmate Jesy Nelson and shared her heartbreak over her twins’ diagnosis. 

Jesy, 34, previously shared the devastating news that her baby girls Story and Ocean had been diagnosed with SMA1. 

Now Perrie, 32, has shared her support for her former friend, after Jesy quit Little Mix in 2020 and sparked a bitter fall-out among the girls. 

Appearing on Jamie Laing’s Great Company podcast, she said: “I mean, when I think everything we’ve been through as a group, and even though it ended in ways that I wouldn’t have wanted it to, and we’re not that close anymore and we’re not in each other’s lives, I still feel everything that the girls feel and I think they’re the same. 

“We’ll always have that weird connection. And seeing Jesy go through that, it broke me.

“Because you wouldn’t wish that on anyone. It’s literally wild. And as much as we’ve got our issues and, you know, I think I don’t want to see her go through that.

perrie’s pain

Perrie Edwards hints Zayn Malik cheated amid ‘hellish’ split & ‘breakdown’

wedding bells

Perrie Edwards finally reveals when she’ll marry Alex after 4 year engagement

“I don’t want to see her hurt and I don’t want to see any of that. It’s heartbreaking.”

In her recent documentary Life After Little Mix, Jesy made some bold claims about Perrie, Jade Thirlwall and Leigh-Anne Pinnock. 

Recalling how she attempted to take her own life before quitting the group, she said: “I sat ­everyone down to explain how I was feeling and I remember one of the responses being, ‘Are you done now? Is that it?’

“She [one of the girls] was like, ‘Can I go now?’”

Fighting back tears, Jesy added: “That made me feel really alone. I felt like there was no point. That no one cared.”

And in her chat with Jamie, Perrie had her say. When he asked if she envisioned repairing her friendship with Jesy, she said: “If I’m being completely transparent, part of me wanted to until the documentary. And then part of me withdrew again. 

“I’m not a horrible person. I haven’t got a bad one in my body, but I can cut you off.

“There’s personal things, there’s public things, there’s everything. I don’t have the capacity for somebody like that in my life anymore. And that might make me sound like a bitch, but I just don’t have the energy for it.

“And as much as I will always love her, I don’t think I can hack that energy in my space.”

EastEnders’ Denise Fox, whose symptoms began with fatigue, will discover she has acute myeloid leukaemia following a bone marrow biopsy – Yvonne Gabriel knows exactly how she feels

EastEnders’ Denise Fox is all alone today when she receives the shattering news that she has blood cancer. While partner Jack Branning gears up for the upcoming World Cup, Denise, whose symptoms began with fatigue, will discover she has acute myeloid leukaemia following a bone marrow biopsy.

And Yvonne Gabriel, 58, will know exactly how she feels. The retired deputy head teacher was also by herself when told she had AML, in July 2018. She says: “It was such a huge shock. I wrongly thought adults couldn’t get leukaemia. The whole thing was a blur. But I remember the doctor saying it was treatable and I hung on to those words for the whole of my cancer journey.”

Yvonne went back to her home in Wallington, Surrey, and told her civil partner Annette, 63, a lawyer, and daughter Leanne, 38, a graphic designer, the awful news. She recalls: “My partner and daughter kept reiterating that the cancer was treatable and curable.

“I am usually the person that looks after people so it was really hard to feel I was causing the upset. They held themselves together for me.” EastEnders worked closely with the charity Blood Cancer UK on Denise’s storyline, starting today on World Blood Cancer Day, which in many ways mirrors Yvonne’s.

Yvonne and Denise, played by Diane Parish, 56, are both Black and, according to the charity, Black or mixed-race blood cancer patients with leukaemia have only a 37% chance of finding a 10/10 matched unrelated stem cell donor, compared to 72% for white patients.

Yvonne began treatment in Sutton’s Royal Marsden Hospital within days of diagnosis. She had three courses of intensive chemotherapy, requiring hospital stays, and finished that November. She says: “It is fantastic that EastEnders are running this storyline. It might mean viewers watching it get help if they have symptoms or even understand a little more what people with blood cancer are going through.”

Yvonne also recommends staying active, as it helps the body to cope with the harsh treatment. She adds: “I lost my hair and if Denise has chemotherapy this will probably happen to her. I was very emotional on the day I shaved it.” But she adds: “It will come back and it’s a sign the treatment is working. You can adorn yourself in different ways – wear jewellery or colours that make you feel like you.”

Yvonne has now trained to do massage therapy after benefiting from it herself as a patient. She says: “It was life-changing. It helped me physically and emotionally.”

Matthew White, director at Blood Cancer UK, says: “Many people with blood cancer have to visit their GP multiple times before they are diagnosed. Seeing blood cancer spotlighted on such a popular programme like EastEnders is a powerful platform that can help make a ‘hidden’ cancer more visible.”

*Blood Cancer UK provides trusted advice for people with blood cancer and funds research into better and kinder treatments that will transform lives. bloodcancer.org.uk

May 22 (UPI) — Tulsi Gabbard resigned as director of national intelligence Friday to support her husband, who has been diagnosed with a rare form of bone cancer.

Gabbard said in a resignation letter, which she posted on X, that after her husband Abraham Williams’ recent diagnosis she will “step away from public service to be by his side and fully support him through this battle.”

The principal deputy director of national intelligence, Aaron Lukas, will take over as acting DNI after Gabbard departs June 30, President Donald Trump said in a post on Truth Social.

“I am deeply grateful for the trust you placed in me and for the opportunity to lead the Office of the Director of National Intelligence for the last year and a half,” Gabbard said in her letter.

Gabbard, who told Trump that she is resigning during a meeting in the Oval Office on Friday, was a controversial nominee for the position.

Nearly all Republicans voted to confirm her on a party-line vote, but former Senate Republican leader Sen. Mitch McConnell voted against her because she had “failed to demonstrate” that she was ready for the position.

Before she was named DNI, Gabbard served in the U.S. House of Representatives and the Hawaii House of Representatives dating to 2002.

The decision to resign, Gabbard said, is the balance of her husband’s dedication to her career, dating to her time in the military, and that she “cannot in good conscience ask him to face this fight alone while I continue in this demanding and time-consuming position.”

In his post, Trump said that Gabbard “has done an incredible job, and we will miss her.”

“She, rightfully, wants to be with [Abraham], bringing him back to good health as they currently fight a tough battle together,” Trump said. “I have no doubt he will soon be better than ever.”

“Further tests, specialist reviews and medical processes are still ongoing, and my doctors are continuing to assess my condition.

“On medical advice, I am not currently medically cleared to train or play at the required level, and I will be stepping away from those duties while I focus fully on my health, treatment, and rehabilitation.”

MND affects nerves in the brain and spinal cord, which tell your muscles what to do.

This leads them to weaken and stiffen over time and usually affects how you walk, talk, eat and breathe.

Scientists are not sure what causes MND, but it is likely to be a combination of the genes – or biological traits – you get from your parents when you are born, and other lifestyle factors.

Fellow former Queensland player Carl Webb died of MND at 42 in 2023, while former England rugby league half-back Rob Burrow died in 2024, five years after diagnosis.

Former Scotland rugby union international Doddie Weir died in November 2022, and World Cup-winning former England international Lewis Moody was diagnosed in September 2025.

“Thank you for the support I’ve received over what has been an incredibly difficult and uncertain period in my life,” said Arrow.

“Over recent months, my symptoms have affected different parts of my everyday life.

“I want to sincerely thank everyone at the South Sydney Rabbitohs for the personal support they have shown me and my family throughout this process.

“The South Sydney Rabbitohs, my team-mates, staff, and everyone behind the scenes have made an incredibly hard situation much easier to face.

“What I need right now isn’t sympathy or sadness. What I need is support, understanding and privacy while my family and I navigate this difficult time.

“This is only part of my story, and when the time is right, I’ll share more. But for now, I ask everyone to respect my privacy while I continue working with my doctors and my family.”

Arrow made his NRL debut in 2016 for the Broncos, before joining the Titans in 2018. He joined South Sydney in 2021, for whom he made 98 NRL appearances.

“We all know how difficult the past few months have been for Jai, but we also know that he will fight this illness with the same bravery, passion and character that was the hallmark of his playing career,” said Rabbitohs CEO Blake Solly.

“Jai and his family will always be Rabbitohs and they will be part of this club for many years to come.”

May 13 (UPI) — Kate, princess of Wales, visited Italy on Wednesday in her first official overseas trip since she announced her cancer diagnosis in 2024.

She is visiting Reggio Emilia, a city in north-central Italy that’s known for a unique child-centered approach to early childhood education. Kensington Palace said the princess is very interested in early childhood education and nurturing approaches.

Kate was greeted by crowds cheering and vying for photos of her, the BBC reported.

“Catherine is very popular here in Italy,” more so than other royals, said Paolo Rosato of the local paper, Il Resto del Carlino, to the BBC. “They see Kate as a story that follows Diana.”

Michael Cocchi, who visited from nearby Parma, brought flowers.

“I think the royal family still has an important role in British culture,” he told the BBC.

“Undoubtedly this is a huge moment for the princess,” an aide to Kate said. “There will be many highlights of 2026, but this being her first official international visit post her recovery, this is a really significant moment for her.”

Kate launched The Royal Foundation Centre for Early Childhood in 2021. It explores the impact of adult problems, including addiction and mental health issues, on early childhood.

She plans to meet with parents, children, educators and others at Reggio Emilia to learn from them.

“It’s the first time she’s out officially,” Richard Fitzwilliams, a British royal commentator, told The New York Times. “And she’s obviously grown in strength.”

King Charles III, who announced his own cancer diagnosis weeks before Kate announced hers, recently traveled to the United States, showing he can handle a rigorous trip. He announced late in 2025 that his treatments were going well.

Kate announced her diagnosis in March 2024, then announced her cancer was in remission in January 2025. She never said what type of cancer she had.

In the two-day visit, Kate will learn about the Reggio Emilia approach to education, and she visited the Loris Malaguzzi International Center. She will visit two local schools to see the learning in action.

The city of Reggio Emilia allocates 13% of its budget to preschool services, said Marwa Mahmoud, the city’s councilor for education.

“We’ve always maintained that education — as well as health and healthcare — should not be viewed as costs,” said Marco Massari, mayor of Reggio Emilia, The Times reported. “It is right to evaluate them in terms of efficiency and waste reduction, but they are not costs – they are investments in the present and the future.”

“She actually asked to meet the teachers, the children and their parents, and participate in an everyday situation,” said Maddalena Tedeschi, president of Reggio Children, a center that researches and promotes the approach.

Kate’s aide told the BBC that the visit is part of a broader tour.

“She wants to look at other models around the world and really create a global conversation,” the aide said.

JOHN Lennon’s son Julian has revealed his devastating health diagnosis while sending a warning to his fans.

The son of the iconic singer from The Beatles has opened up about being diagnosed with coronary heart disease and pre-diabetes.

The 63-year-old musician, who followed in his father’s footsteps and had the hit Too Late For Goodbyes, opened up in a recent social media post.

Taking to social media, Julian said in a post: “After being diagnosed with Coronary Heart Disease & a Pre-Diabetic, I urge you all to get checked out sooner rather than later.

“You never know what hidden health issues you may have, even after exercising and eating as much ‘good/healthy’ food as possible.

“Nip it in the bud! As they say…

Read More about The Beatles

BEATLES GET APPLE BACK

Beatles’ plans to turn iconic London building into fan experience

LOATHE ME DO

Guitarist who played with John Lennon slams ‘horrible’ Beatles biopics

“Even with these ailments, I’ve managed to catch them early enough, to be able to reverse some of the damage and will hopefully be able to live a healthy long life!

“Please get checked out, before you’re checked out…

“And last but not least, thanks to all the Doctors who have helped and guided me on this new journey so far… Truly.”

Fans rushed to support Julian amid his health woes.

“Be well Julian! I’m on the same journey,” said one fan.

“Dear Julian, You are very thoughtful to share this, especially for our benefit. Good luck with your new healthier journey. Please keep us updated,” added a second.

“Good advice. Trying to be better at it now. Take good care,” penned a third.

This isn’t Julian’s first health concern.

In 2020, the musician revealed he had to undergo an emergency operation to remove a cancerous growth from his head.

The singer had visited his dermatologist, who noticed a lump on his head which he had had all his life “looked and felt a little different”.

After having a biopsy, the results showed that the mole was cancerous and Julian got it removed immediately. 

Writing on social media at the time, he said: “She urged me to have a Biopsy 2 days ago, which I obliged…

“Only to learn, 24 hrs later, that it was malignant/cancerous, and that her recommendation was to get it removed immediately, which is what happened today…

“Hopefully we managed to remove all that was cancerous, but the mole is being sent off again, for a further/deeper analysis, and I’ll have those results next week.”

Julian is the son of John Lennon and his first wife Cynthia, who sadly died in April 2015.

May 12 (UPI) — Polycystic ovary syndrome, known to more than 170 million women suffering from the condition worldwide, was renamed polyendocrine metabolic ovarian syndrome Tuesday by patients and medical organizations.

PMOS causes fluctuations in hormones, with impacts on weight, metabolic and mental health, skin and the reproductive system.

“For too long, the name reduced a complex, long-term hormonal or endocrine disorder to a misunderstanding about ‘cysts’ and a focus on ovaries. This contributed to missed diagnoses and inadequate treatment,” a press release from the Endocrine Society said.

Professor Helena Teede, director of Monash University’s Monash Centre for Health Research & Implementation and an endocrinologist at Monash Health in Melbourne, Australia, led the name change process after spending decades researching the condition and seeing the patient impacts firsthand, the release said.

“What we now know is that there is actually no increase in abnormal cysts on the ovary, and the diverse features of the condition were often unappreciated,” Teede said in a statement. “It was heart-breaking to see the delayed diagnosis, limited awareness and inadequate care afforded those affected by this neglected condition.

“While international guidelines have advanced awareness and care, a name change was the next critical step towards recognition and improvement in the long-term impacts of this condition.”

While the name change was published Tuesday in The Lancet, it took 14 years of collaboration between those who live with the condition and experts.

Teede led the name change process with Professor Terhi Piltonen, president of the International Androgen Excess and Polycystic Ovary Syndrome Society from Oulu University and Oulu University Hospital, Finland, and AE-PCOS Society Executive Director Anuja Dokras from the United States and Chair of Verity Rachel Morman. There were 56 other patient and professional organizations involved.

“It was essential that the new name was scientifically correct but also considered across diverse cultural contexts to avoid certain reproductive terms that could heighten stigma and be harmful for women in some countries,” Piltonen said in a statement. “This made a culturally and internationally informed consultation critical to getting it right.”

JESY Nelson today shared an emotional update about her twins, months after their SMA diagnosis.

The former Little Mix star, 34, has been keeping fans up-to-date with how her daughters, Story and Ocean Jade, are doing as they battle Spinal Muscular Atrophy Type 1.

The tots’ devastating diagnosis is a genetic condition that weakens the muscles by damaging motor nerve cells in the spinal cord.

Today, Jesy shared a new update with fans where she revealed how Ocean and Story had tried eating in their specialised feeding chairs for the first time.

In the heartmelting moment, the singer could be seen feeding her daughters some fruit purée.

Speaking to Ocean as she gently spooned food into her little mouth, Jesy said:: “Excuse me, you’re supposed to eat it, not spit it out.”

jesy’s pain

Jesy Nelson offers £10k reward after car with twins’ hospital equipment stolen

NEW FELLA?

Jesy Nelson sparks romance rumours with mystery man after split from Zion Foster

She then turned her attention to Story, who was seen enjoying her dinner,

Jesy previously revealed how she got emotional when the special chairs arrived back in February.

“So the girls need special feeding chairs that came yesterday and I couldn’t help but burst into tears yesterday when I saw them,” she said at the time.

“It just made me feel so sad as it’s just another reminder of another obstacle we have to tackle.”

Meanwhile, Jesy’s latest update comes after she revealed last week how Story, who is just 11-months-old, had said the word “muma” for the first time.

SMA1 patients typically have limited or no spoken speech with communication usually made through eye movement and guttural sounds.

But Jesy’s baby girl is fighting against all odds, and managed to very clearly get out her first word, in a video posted on Instagram.

Story was wrapped up in a blanket, laying down on the sofa when she gave her mum quite the shock.

Jesy could be heard shouting with happiness: “Yeahhhhhh! Yesss clever girl.

“Storyyy good girl, you’re such a clever girl. Wow well done. Yeah do it again.”

The Boyz singer wrote the words, “Story said muma for the first time my life is complete,” over the top of the clip.

Jesy captioned the post: “My heart is so full.”

The star bravely revealed the twins SMA1 diagnosis back in January and has since been keeping fans updated on their battle via social media.

Both the girls have had feeding tubes fitted into their noses to clear their chests.

TV star Jesy has also shared some of the stretches she’s been doing with the girls to help strengthen their legs.

SMA1 leads to progressive muscle wasting, and if untreated, the life expectancy of a baby with the disease is just two years.

Jesy and her ex-fiancé Zion have been told it’s unlikely the girls will ever walk, and may face serious breathing and swallowing difficulties.

The 34-year-old has opened up on her hopes to use her platform – of over 10 million followers – to raise awareness of SMA1 and shine a light on the realities families face when caring for children with the condition.

Jesy previously said that if sharing her story helps even one other parent feel less alone, it will be worth it.

Spinal Muscular Atrophy: Signs and symptoms

Spinal muscular atrophy is a disease which takes away a person’s strength and it causes problems by disrupting the motor nerve cells in the spinal cord.

This causes an individual to lose the ability to walk, eat and breathe.

There are four types of SMA – which are based on age.

• Type 1 is diagnosed within the first six months of life and is usually fatal.
• Type 2 is diagnosed after six months of age.
• Type 3 is diagnosed after 18 months of age and may require the individual to use a wheelchair.
• Type 4 is the rarest form of SMA and usually only surfaces in adulthood.

What are the symptoms?

The symptoms of SMA will depend on which type of condition you have.

But the following are the most common symptoms:

• Floppy or weak arms and legs

• Movement problems – such as difficulty sitting up, crawling or walking

• Twitching or shaking muscles

• Bone and joint problems – such as an unusually curved spine

• Swallowing problems

• Breathing difficulties

However, SMA does not affect a person’s intelligence and it does not cause learning disabilities.

How common is it?

The majority of the time a child can only be born with the condition if both of their parents have a faulty gene which causes SMA.

Usually, the parent would not have the condition themselves – they would only act as a carrier.

Statistics show around 1 in every 40 to 60 people is a carrier of the gene which can cause SMA.

If two parents carry the faulty gene there is a 1 in 4 (25 per cent) chance their child will get spinal muscular atrophy.

It affects around 1 in 11,000 babies.