diagnosis

“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.

Hughton then moved into management, where he guided both Newcastle and Brighton to promotion to the Premier League.

He also had spells in charge of Birmingham, Norwich and Nottingham Forest, and was most recently manager of Ghana.

“I had very good advice and all the treatment options were given to me, and I decided to have my prostate removed. The recovery has gone really well,” he added.

“I’m one year post-operation and I feel good. It’s all gone very well. I’ve got a lot of energy.”

Prostate Cancer UK chief executive Laura Kerby said: “Chris’ story is ultimately a positive one. But it’s also a timely reminder of the dangers of prostate cancer and we thank him for sharing his story in the football community, and helping men.

“Prostate cancer is now the most common cancer in the UK, and it’s still the only major cancer without a screening programme. It doesn’t give you signs or symptoms in its earlier stages when it’s more treatable, so awareness is everything.”

JANE Fallon has given her fans a health update after having her second surgery following her cancer diagnosis.

The author, 65, who is the partner of Ricky Gervais, told fans earlier this month that she was suffering with breast cancer, despite having no symptoms before the diagnosis.

Posting a sweet pic alongside her cat Pickles on Instagram, Jane wrote: “Little update. So, my 2nd surgery went well.

“They got the clear margin they need on the original excision, which is great. 

“They did hit a new little patch of precancerous cells on the other side of the new bit they took out but, thankfully, everyone agrees more surgery would be overkill. 

“A huge % of pre cancer doesn’t develop into cancer. 

SECRET BATTLE

Gemma Collins reveals there’s ‘behind the scenes’ drama in I’m A Celeb feud

TEARFUL THOMAS

Adam Thomas breaks down in tears again as I’m A Celebrity sees star sobbing

“I saw the oncologist today & we’ve agreed the risks of radiation outweigh the benefits in my case.

“Which leaves Tamoxifen (or similar) or wait and see (my preferred option). 

“I’m very nervous about going the drug route, because I know the side effects can be hideous, but I’m taking all the info on board & luckily there’s no pressure to make a quick decision.

“So, all good & I’m just looking forward to getting back to normal.”

Jane’s followers flocked to support her, including author Jojo Moyes who wrote: “Well done for getting through another surgery.

“Wishing you some reassuring news very soon x”

A fan added: “Happy to hear the update and it sounds very positive … yes take your time to decide , & so all the research … as of course you will x”

Another said: “That’s such uplifting news , so pleased your doing well. onwards and upwards x And cats will always upstage.”

This comes just days after Jane slammed a fake obituary that was published online after she was revealed she had cancer.

She said: “I’ve taken the post about the obituary down, because I don’t want people to think I’m upset by it. I’m not. P***ed off yes.

“But more, I just want people to know that any photos you see of me in hospital, looking sad or with tubes sticking out of me are 100% fake – AI generated.”

Following her recent procedure, Jane told her followers she was feeling “remarkably fine” and in good spirits.

She assured people she wold update them once she had the medical all clear.

“Then 8-10 days wait for confirmation that they’ve got it all & the margins are clear (small % chance of more surgery if not),” Jane wrote.

She has been resting up at home with the support of cat Pickles.

When Jane announced her diagnosis, Jane asked fans not to “panic” and said her prognosis was “excellent”.

She has been with comedian Ricky for more than 40 years after meeting back in 1982.

Jane is the author of 14 bestselling books and has penned titles such as Getting Rid of Matthew, Got You Back, Queen Bee, Worst Idea Ever, and Faking Friends. 

Jess Warner Judd does not remember much about that night in Rome.

It has been a long and difficult journey since, but the 31-year-old speaks with admirable ease about the traumatic events which have led her to a London Marathon debut in 2026.

“I’m very lucky to have had sort of a second chance at running. It’s a second chance I just didn’t think I’d probably have,” Warner Judd tells BBC Sport.

“I remember having really horrible discussions after trying to restart my track season and it quickly not happening. The doctors, who were brilliant, saying that I would probably have to retire if I kept trying before I had therapy, because my body wasn’t going to cope.”

The distressing details of what unfolded at Stadio Olimpico are recalled vividly by her husband Rob, who witnessed it all from the stands alongside Warner Judd’s father and coach, Mike, in June 2024.

Less than 10 months had passed since Warner Judd celebrated one of her proudest achievements, placing eighth in the world over 10,000m, but it became evident early in the European Championship final that something was amiss.

The noticeable lack of co-ordination. The veering out into lanes two and three. The distress increasingly visible across her face.

“It got to the point around five or six kilometres in when Mike and I had got as close as we could to the track and were shouting at her to stop,” says Rob.

Warner Judd struggled on until, with 600m to go, she collapsed.