Category Entertainment News

Peter Andre has shared the one aspect of moving to the UK from Australia that he found challenging. He also offers encouragement to Brits trying to survive the “miserable” month of January.

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Peter Andre has admitted he used to struggle with winter when he moved to the UK. The Mysterious Girl singer, 52, spent his childhood in Australia but moved to the far colder climate in the early 1990s to pursue his pop career, and he has remained here ever since, but initially struggled to keep his spirits up as he adjusted to the vast difference in temperature.

What’s more, the star is also aware just how “tough” this time of year can be for so many people, and appreciates that they can find things “really difficult,” especially after the festive period is done.

Writing in his new! magazine column, he said: “January can be such a depressing month for a lot of people here in the UK. Not only do millions suffer from the cost-of-living crisis, especially post-Christmas, but it can also be cold and miserable. It’s a tough time for many.

READ MORE: Peter Andre addresses idea of becoming a dad for the sixth timeREAD MORE: Katie Price in major ‘turnaround’ as she finally joins Princess Andre’s ITV show

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“But Brits are resilient and always find a way to battle through tough times. I used to find it really difficult to deal with winter after I came over from the tropical parts of Australia. But there’s also a very beautiful part of this year, especially in the build-up to Christmas.”

However, the former I’m A Celebrity…Get Me Out Of Here! The contestant is pleased that he has a lot to look forward to as he prepares to head out on tour across the UK with The Very Best of Frankie Valli and wants others to remember that things will “improve” eventually, as he wishes them all the best for the coming year.

He continued, “Thankfully, I’ve had a really busy year so far, and it’s given me real focus.” I am aware that many people have seasonal affective disorder, which can really derail people at this time of year. But keep in mind that the days will get longer and the weather will start to improve, so enjoy a fantastic 2026 together.

Peter has been based in the UK for over 30 years. He married NHS doctor Emily in 2015, with the pair having three children together – Millie, 11, Theo, nine, and 21-month-old Belle. The reality star already has two children with his ex-wife, former glamour model Katie Price – they are parents to Junior, 20, and Princess, 18 together. It was recently reported that Peter has no plans to appear on the upcoming series of Princess’ reality show The Princess Diaries, despite having featured prominently the first time round.

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Elsewhere in his column, Peter spoke out about Adolescence star Owen Cooper’s plans to go leave education as soon as possible so he can focus on his career, noting that his father made sure he finished school, and he insisted his own children do the same before going into anything else. He said: “I do understand Owen’s point of view. He has had a lot of success with Adolescence, and has probably been given some great opportunities.

“I can’t recall when I was 16 when I was offered my recording deal. I was a guest on an Australian national talent show, and luckily, I was given a recording deal to record live on air. I had to resign from my job and enter it.

“But my dad told me to finish my education, and that is when I did that.” With my kids, I made the same decision. They had to complete their education before moving on to anything else.

But the singer recently revealed that he has no plans to have any more children and he is very happy with where he is in life now. He said: “George Clooney has been talking about how it was easier for him to become a dad later on in life – and for some people it is. Some people want to get a lot of their career done and then focus on children.

“I felt ready to start having kids,” I said. I could have waited a little longer, but you get older and you get more mature. At 52, you can’t stop growing up and you get more mature.

In preparation for her 31st birthday celebrations with her family, Nicola Peltz declares her love to her husband Brooklyn while he is still celebrating with her family.

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While declaring her love for Brooklyn Beckham, Nicola Peltz has abandoned her in-laws. Nicole is getting ready to celebrate her 31st birthday on January 9 and has already begun the festivities after missing a party with Brooklyn’s family due to a rumored feud.

While Brooklyn recently blocked his family on social media, he appeared to focus his efforts on making sure his wife had a magical birthday month. Nicola shared a sweet snap on Instagram drinking an iced coffee as she cuddled up to Brooklyn outside. She was also joined by her brother, Bradley, and captioned the snap: “I’m so grateful for my boys”.

She also shared images of her dad and daughter’s first birthday celebrations, including a ballerina-themed party, Brooklyn posing in front of the sunset, and her. She wrote, “So happy to welcome these beautiful people to the new year,” in one Story post.

READ MORE: Wicked Broadway star dies aged 46 leaving behind three-year-old sonREAD MORE: Nicola Peltz says she’s ‘grateful’ for Brooklyn after he shuts out family

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Brooklyn appeared to have cut his own family out of their lives while Nicola showed off her close relationship with her closest and dearest.

After a previous post that received jibes about Brooklyn and the ongoing rumored feud with the rest of the Beckham family, Nicola has now turned the comments off on her final two posts.

It came after Brooklyn blocked his father, Sir David and mum, Lady Victoria and brothers Cruz and Romeo from his social media accounts in the lead up to Christmas.

Beckham family friends claim David and Victoria will “never give up” their fight for resolation. David “set out his love for his son for the record,” according to one source in a New Year’s message that one person described as “his boldest olive branch yet.”

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The England footy icon wrote, “I love you all so much,” in a sweet black and white photo of him and Brooklyn that Victoria shared.

Along with it, David wrote, “I love you all, love Daddy,” in a new black-and-white photo of him with Victoria and their entire brood. On to 2026″.

According to one source, David and Victoria will never give up trying to reconcile with their son. They live in hope, and nothing can change that. They will continue to keep their feelings open and honest with them forever.

On David’s birthday, according to legend, the family dispute started. Brooklyn was missing from a number of family gatherings as soon as people realized it. He also snubbed both of his parents’ birthdays on Instagram, something he had never done before.

Despite avoiding significant family events like Sir David’s long-awaited knighthood earlier this year, Brooklyn and Nicola remained unmoved. Without the presence of any of Brooklyn’s immediate family, the couple also renewed their vows.

Davina McCall, a panelist for The Masked Singer, spoke candidly about parenting and how Holly, Tilly, and Chester, the three of her children, have taught her important life lessons.

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TV legend Davina McCall opened up about the greatest lessons she has learned from being a parent – after her youngest daughter told her to stop doing one thing. The Masked Singer panellist co-wrote a book, titled Birthing, with midwife Marley Hall which was published last year and offers support and advice on every stage of birth.

The well-known presenter revealed that Holly, 24, Tilly, 22, and Chester, 19, have all taught her lessons as their own children have grown up.

She said, “I don’t know whether to have children or not, one of the reasons I would say have kids is because of what they make you look at,” according to the North Devon Journal.

My middle child, Tilly, has been the best at teaching me to stop being a micromanger. She says, “No, Mum, let me try this; don’t tell me what to do.” I am aware of what to do, and I will still be okay if something goes wrong.

You think, “Oh my God, I have to lead you through this one,” is the biggest fear parents have. They will have to make mistakes, but it’s going to be challenging.

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Davina, 58, claimed that every one of her “greatest gifts” in life have come from tragic circumstances, and that they will struggle to learn if they don’t allow their children to go through them.

She also advised parents to be as open as they can with their children, which is important because it makes them more open with you in return.

The mother-of-three believes that when a parent and child forgive one another for mistakes, it is simpler for them to do so.

Davina also discussed a different project she was planning to write while promoting the paperback version of the birthing book on Chris Evans’ Virgin Radio Breakfast Show.

She referred to the topic of death and how to end one’s life in a positive way.

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Her brain tumor ordeal, in which she had a 14mm colloid non-cancerous cyst removed in November of this year, partly influenced this.

Opening up about the health scare, and how it shaped her thinking about dying, she told The Guardian: “The best thing to come out of it is not being frightened of death any more. I wasn’t terrified of dying, but I didn’t want to die. I love life, love living, and definitely wanted to be around for my kids while they were young.

Although I didn’t want to leave my three children, I did think that you’d all be okay if I did. “I think if I had been sick when my kids were young, it would have been very different.

This evening at 6:30 p.m., The Masked Singer will be available on ITV.

As she begins work on her upcoming album, which she hopes to release in the following year, the Little Mix star has admitted she enjoys “weirding people out” with her music.

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Former Little Mix star Jade Thirlwall has said she looks forward to “weirding people out” with her new music, as she gets to work on her next record this year.

After her debut album That’s Showbiz Baby reached No3 on the Official Charts, the 33-year-old pop star established herself as a solo artist. However, the singer will continue to experiment with her upcoming material by admitting she isn’t feeling like a “first listen artist.”

The South Shields native hopes to have arena shows off of her upcoming album by setting her sights high. Before her ex-bandmate Jesy Nelson shared a heartbreaking update about her twins, Jade explained in a new interview that she didn’t think she was a first listener. “I don’t think I am a first listen artist. I like weirding people out. I like people listening to my music and feeling a little disoriented or like it’s a little too much, and then they have to listen again and dissect it,” she said. That’s something I really enjoy.

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As reported by the Daily Star, Jade added: “I did a theatre show which was nice and I actually really enjoyed a more intimate setting, but in my brain it was an arena show, I like all the bells and whistles. I love pop, I love putting on a show, so I’d love to keep getting bigger with that.”

As well as her music career, Jade is hoping to branch out into reality TV, revealing she plans to produce a documentary about her career. Alongside long-term boyfriend – who is best known as half of British hip-hop duo Rizzle Kicks – she has plenty of footage documenting her transition from Little Mix to solo fame.

Jade continued, “I would like to do, like what we touched on, the documentary idea,” in a statement on 33-year-old Jordan’s podcast Miss Me? The last year was very intense; I thought it had just started as a snowball, but it kept on going, sometimes I couldn’t keep up with it.

After receiving the Freedom of the Borough, Jade described it as the “highest honor my hometown can bestow” and received a prestigious award from her hometown a few weeks ago. The proud North-East native acknowledged that she wished her late grandparents and great aunt had been present, despite the accomplishment.

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She shared a number of photos from the event on December 17, writing on Instagram: “I’m so proud to come from South Tyneside and couldn’t be happier to receive this alongside South Shields legend Richard Ord MBE – owner of @colmansfishandchips.”

Before going into her own honor, she praised the owner of the chip shop, saying, “Over the years, the Colmans family has been so kind and helpful to me. There is no other person who would be more kind and worthy of this award.

I wrote down a little something about how important it is to me to be a Sand Dancer on my way to the event from London to South Shields. I was very nervous because I don’t usually like to speak in front of groups, but as I looked around the room, I remembered that people I care about are surrounded by people who have led me to where I am today.

What an honor it was to have my family and friends by my side; my only wish was for my grandparents and great aunt to be present, ensemble, and celebrating together. They might be. “

She then thanked those who helped make the day happen, saying, “Never mind if I walk my cattle around town.” Your Honorary Freewoman of the Borough x “, I love you so much.

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Two parents who are well-versed in the importance of early screening are pushing for change in the NHS as Jesy Nelson opens up about her twins’ spinal muscular atrophy (SMA) diagnosis.

Jesy Nelson revealed today that her twins may never be able to walk despite their heartbreaking diagnosis of spinal muscular atrophy (SMA). Unfortunately, she is not the only mother who has SMA, which, if left untreated, can be fatal in just two years.

Following a challenging pregnancy and an emergency procedure, Jesy, 34, and her partner, Zion Foster, 27, welcomed their daughters Ocean Jade and Story Monroe Nelson-Foster into the world on May 15. Unfortunately, the baby girls’ health problems increased as a result of discovering they were carrying SMA Type 1, a severe form of the disease that eventually destroys the muscles in a person’s body.

Opening up to followers on Instagram, Jesy shared: “When they assessed the girls at Great Ormond Street, we were told they were never going to be able to walk. They would probably never regain their neck strength. They will be disabled. The best thing we can do right now is to get them treatment and hope for the best. Thankfully, the girls have had their treatment, which I’m so grateful for. If they didn’t have it, they would die.”

READ MORE: Jesy Nelson’s boyfriend Zion breaks silence with hopeful message and new photo of twins

Messages of support have flooded in for Jesy, including Rosie and Wes, who have shared their own personal experience of raising two children with SMA, with very different outcomes. Taking to their Marley’s Journey, Facebook page, the parents, from Driffield, East Yorkshire, wrote: “Sending so much love and strength to Jesy & her beautiful family with their twin girls’ diagnosis of SMA type 1.”

Marley and Meadow, age five and six months old, are the parents of Rosie and Wes, who spoke to BBC News about their children’s diagnoses in November and stressed the importance of early screening. While young sister Meadow, who was tested at birth, is meeting all of her developmental milestones and has the ability to undergo gene therapy right away, young Marley, who was diagnosed at five months, is unable to walk or talk and needs assistance with breathing.

Rosie said, “Your life turns around the earlier you learn about the newborn SMA.” Marley requires constant care and complex needs. Meadow will hardly need any breathing assistance because she will live a completely normal life.

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Rosie and Wes are now supporting a campaign by the charity SMA UK, which wants to add this condition to a blood test that already screens newborns for ten uncommon but severe conditions. SMA screening is currently only performed on babies who already have a brother or sister who are affected by the condition.

An estimated 47 babies in the UK were born with SMA in 2024, according to SMA UK, despite the fact that one in 40 people have the SMA-related gene that can cause it. When Marley was five months old and given the diagnosis of SMA, Rosie and Wes’ world “came “crashing down.” He received a healthy copy of the affected gene with the life-enhancing gene therapy drug Zolgensma at the age of 16 months.

The nervous system may already have suffered irreversibly negative effects, so timing is everything when it comes to this treatment. Rosie blasted the difficulties Marley faces daily, describing how “Marley needs to have respiratory support every day. He is fed via a tube because he can’t swallow orally. At night, he uses a ventilator. He is unable to speak or walk.

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The baby girl can roll over like other girls her age, which makes it a different story for her. She received the drug at just a few weeks old. Rosie is aware of how drastically different the two siblings’ lives will be, despite Marley’s enormous leaps in his progress and his physiotherapy and medication. “I think the guilt that eats me and my partner, as well as other SMA families, is enormous,” Rosie said. It gets better if you’ve had a child with SMA.

Back in 2018, the UK National Screening Committee (NSC) recommended against SMA screening for SMA, due to limited evidence of long-term treatment outcomes, as well as cost-effectiveness for the NHS. Over the past few years, however, the NSC has conducted an external review of the decision, on account of “significant developments”, such as new drugs. Going forward, additional evaluation work is scheduled to be carried out within the NHS.

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READ MORE: Jesy Nelson inundated with support from pals including ex Chris Hughes after diagnosis

Spinal Muscular Atrophy has been identified in the baby twins of Little Mix singer Jesy Nelson. Although early treatment is necessary, the NHS does not routinely offer testing.

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With some genetic conditions that affect newborns, time is of the essence, and early diagnosis can mean the difference between life and death.

Spinal Muscular Atrophy is one of those illnesses, and today, Little Mix star Jesy Nelson shared the heartbreaking news that her twins have both been diagnosed with the rare genetic condition and may never walk. The 34-year-old singer and her musician fiancé Zion Foster, 27, welcomed daughters Ocean Jade and Story Monroe Nelson-Foster in May after a difficult pregnancy.

Fighting back tears, she shared a video to Instagram to say her girls had the most severe form of the disease which kills muscles in the body over time. SMA causes floppiness in the limbs, difficulty breathing and swallowing as well as delayed motor skills.

Prior to 2019, babies with SMA type 1 often wouldn’t survive until their second birthday, and infants with the milder type 2 would never walk, facing life in a wheelchair as well as multiple surgeries and respiratory infections. In the past five years treatments have been approved for use on the NHS that can stop the disease in its tracks – the earlier the treatment is given then the less the damage will be.

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However the tests need to be started within the first weeks, or even days, of life. Babies in the UK aren’t tested for SMA, for many the diagnosis comes too late for this. Campaigners and senior experts are pushing for that to change. Testing for all babies is due to begin in Scotland in 2026 under a two-year pilot programme. Portia Thorman, from SMA UK, believes it would be ”ethically wrong” not to introduce screening throughout the UK. “I think facing a diagnosis now, you can be filled with hope,” she says.

In the meantime, parents should contact SMA UK, as well as their treating hospital, for guidance as not all private tests will be suitable for babies and results are always best interpreted by a trained professional. Costs to go private range between £413 to £900. Private Blood Tests London offers an SMN1 deletions/duplications test for £924 with results back in 10 days. No GP referral is needed. A similar test by Synnovis has a price tag of £413 but will need to be arranged through your NHS hospital. Results come back with in three days. Harley Street’s Medical Express Clinic charges £567 with results in 10 days.

After her mother noticed that the twins weren’t moving as much as they should for their age, Jessica first visited her GP. Jesy claimed she told herself not to “compare” the babies to other babies of the same age because she had been warned that they would develop more slowly as they were premature. Jesy’s twins were diagnosed with SMA Type 1 after asking for help.

Jesy shared the news with you guys on Instagram, saying, “I wanted to come on here to share some news. With this video, I’m not exactly sure where to begin.

My mother noticed that the girls’ legs weren’t moving as much as they should. At the time, I didn’t really care about it. Your babies are premature, so don’t compare your babies to other babies, advice I received right away when I left the NICU. They simply accept them as they are, despite not achieving the same goals. ‘

It didn’t really ring the alarm, I thought. I was instructed not to compare them to my first child because they are my first. The girls’ health care providers reaffirmed that everything was alright and that the girls were healthy.

Later, there were some indications that the girls were having trouble consuming enough food. We would take them to the doctor and say, “Our babies are not feeding as frequently as they should. They said it was fine and to give it a restraint. “

The girls have been given the most exhausting three to four months and interminable appointments, according to Jesy, who continued, “Long story short, they have been given the diagnosis of SMA Type One, a severe disease.” Every muscle in the body, from the legs to the arms to swallowing, is affected by spinal muscular atrophy. It eventually causes the body’s muscles to become dead. Your baby’s life expectancy won’t exceed two if it isn’t treated in time.

Time is of the essence with this disease, Jesy said, “Once the girls got treated, it was a very quick process.” We were told that the girls at Great Ormond Street would never be able to walk when they were surveyed. They’d probably never be able to use their necks again. They will be disabled.

The best thing we can do at this time is to treat them and hope for the best,” she continued. “I’m so grateful that the girls received the care they needed.” They would perish without it if they didn’t have it. “

Although there is no known cure for (SMA), there are options for treatment and support to ensure that people have the best possible quality of life. If one in 40 children has a carrier gene for the condition, then the child is born with SMA.

Jesy described how her life has changed in the past four months as “I am grieving a life I believed I was going to have with my kids.”

“It has become my second home,” I said. Within two weeks of receiving the diagnosis, I feel like I must start nursing. Nothing a mother should have to do to their child should have to do.

Because the last three months have been my life’s most heartbreaking experience, I made this video. “