Gayathri Kallukaran is a Junior Journalist with Eastern Eye. She has a Master’s degree in Journalism and Mass Communication from St. Paul’s College, Bengaluru, and brings over five years of experience in content creation, including two years in digital journalism. She covers stories across culture, lifestyle, travel, health, and technology, with a creative yet fact-driven approach to reporting. Known for her sensitivity towards human interest narratives, Gayathri’s storytelling often aims to inform, inspire, and empower. Her journey began as a layout designer and reporter for her college’s daily newsletter, where she also contributed short films and editorial features. Since then, she has worked with platforms like FWD Media, Pepper Content, and Petrons.com, where several of her interviews and features have gained spotlight recognition. Fluent in English, Malayalam, Tamil, and Hindi, she writes in English and Malayalam, continuing to explore inclusive, people-focused storytelling in the digital space.
Olympic swimmer Rebecca Adlington has recently revealed her diagnosis of coeliac disease and has called for greater awareness of the condition. In a video shared on Coeliac UK’s Instagram, Adlington discussed the importance of gluten-free prescriptions and urged the government to protect access to these prescriptions, which have been cut in some areas.
Her diagnosis shines a light on coeliac disease, a condition that affects approximately 1 in 100 people in the UK. However, due to the difficulty in recognising the symptoms, only around 36% of people living with the condition have been officially diagnosed.
If you’re unfamiliar with coeliac disease, here’s what you need to know:
1. What is Coeliac Disease?
Coeliac disease is a serious autoimmune condition triggered by the consumption of gluten. Gluten is a protein found in grains such as wheat, barley, and rye, which are common in many everyday foods.
For people with coeliac disease, consuming gluten causes their immune system to attack the lining of their small intestine, leading to damage that prevents the absorption of essential nutrients. This can cause a wide range of symptoms and, if left untreated, can lead to long-term health problems such as osteoporosis, anaemia, and, in rare cases, small bowel cancer.
Coeliac disease is not an allergy, as some people may assume, but a lifelong autoimmune condition that requires strict management through diet.
2. Symptoms of Coeliac Disease
The symptoms of coeliac disease can vary greatly from person to person, which makes diagnosis challenging. Some common symptoms include diarrhoea, bloating, fatigue, abdominal pain, nausea, and mouth ulcers. These symptoms can be persistent, recurrent, or even unexplained, which often leads to misdiagnosis.
One striking fact is that 1 in 4 people diagnosed with coeliac disease had previously been misdiagnosed with Irritable Bowel Syndrome (IBS). This overlap in symptoms can delay the correct diagnosis, and as a result, it takes an average of 13 years for adults to receive a proper diagnosis after their symptoms first appear.
3. The Importance of Early Diagnosis
Diagnosing coeliac disease early is crucial to preventing further complications. Damage to the small intestine caused by continued gluten consumption can result in nutrient deficiencies, affecting overall health and quality of life.
However, due to the complexity of symptoms and the fact that they can be mistaken for other conditions, many people live with the disease for years before being diagnosed. Rebecca Adlington's own diagnosis highlights the need for greater awareness, as even high-profile athletes and public figures can struggle with the condition.
4. Who is Affected?
While coeliac disease affects approximately 1 in 100 people, the number of people experiencing symptoms without diagnosis is much higher. According to Coeliac UK, an estimated 500,000 people in the UK are living with undiagnosed coeliac disease.
The condition can develop at any age, although more than 50% of people are diagnosed after the age of 40. Coeliac disease also tends to be more common in females, and studies show that if a family member has the condition, there is a 1 in 10 chance that a close relative will also develop it.
People with Type 1 diabetes are six times more likely to have coeliac disease than the general population, and the risk increases to 10 times for children with Type 1 diabetes.
5. Rebecca Adlington’s Advocacy
Since her diagnosis, Rebecca Adlington has been using her platform to advocate for the protection of gluten-free prescriptions. She explained that she quickly learned how vital these prescriptions are for managing the condition, yet some areas have seen these prescriptions cut.
Adlington has encouraged others to support a petition that gathered 22,826 signatures and was submitted to the government, calling for better access to gluten-free prescriptions. Her efforts are helping to raise awareness of the challenges faced by those living with coeliac disease.
6. The Only Treatment: A Gluten-Free Diet
At present, there is no cure for coeliac disease, and the only treatment is to follow a strict gluten-free diet for life. This means avoiding any foods containing wheat, barley, and rye. While some people may be able to tolerate very small amounts of gluten, most must avoid it completely to prevent symptoms and further intestinal damage.
Naturally gluten-free foods include rice, potatoes, corn, plain meat, fish, eggs, fruits, vegetables, and dairy products. People with coeliac disease must learn to identify which foods are safe and navigate the complexities of avoiding gluten in processed or packaged foods.
7. Support from Coeliac UK
For those living with coeliac disease, Coeliac UK provides valuable resources and support. Their website offers information about maintaining a gluten-free diet, as well as details on local support groups, volunteering opportunities, and ongoing campaigns.
If you or someone you know has been diagnosed with coeliac disease or is experiencing symptoms, Coeliac UK’s helpline (0333 332 2033) is available Monday to Friday from 10am to 4pm to provide further assistance.
The Department of Health said the rollout would reduce missed days at nursery and school, cut time parents take off work, and save the NHS about £15 million a year. (Representational image: iStock)
CHILDREN in England will be offered a free chickenpox vaccine for the first time from January 2026, the government has announced.
GP practices will give eligible children a combined vaccine for measles, mumps, rubella and varicella (MMRV) as part of the routine childhood vaccination schedule. Around half a million children each year are expected to be protected.
The Department of Health said the rollout would reduce missed days at nursery and school, cut time parents take off work, and save the NHS about £15 million a year. Research estimates chickenpox in childhood leads to £24 million in lost income and productivity annually.
Minister of State for Care, Stephen Kinnock, said: “We’re giving parents the power to protect their children from chickenpox and its serious complications, while keeping them in nursery or the classroom where they belong and preventing parents from scrambling for childcare or having to miss work. This vaccine puts children’s health first and gives working families the support they deserve. As part of our Plan for Change, we want to give every child the best possible start in life, and this rollout will help to do exactly that.”
Dr Gayatri Amirthalingam, Deputy Director of Immunisation at the UK Health Security Agency, said: “Most parents probably consider chickenpox to be a common and mild illness, but for some babies, young children and even adults, chickenpox can be very serious, leading to hospital admission and tragically, while rare, it can be fatal. It is excellent news that from next January we will be introducing a vaccine to protect against chickenpox into the NHS routine childhood vaccination programme – helping prevent what is for most a nasty illness and for those who develop severe symptoms, it could be a life saver.”
Amanda Doyle, National Director for Primary Care and Community Services at NHS England, said: “This is a hugely positive moment for families as the NHS gets ready to roll out a vaccine to protect children against chickenpox for the first time, adding to the arsenal of other routine jabs that safeguard against serious illness.”
The eligibility criteria will be set out in clinical guidance, and parents will be contacted by their GP surgery if their child is eligible.
By clicking the 'Subscribe’, you agree to receive our newsletter, marketing communications and industry
partners/sponsors sharing promotional product information via email and print communication from Garavi Gujarat
Publications Ltd and subsidiaries. You have the right to withdraw your consent at any time by clicking the
unsubscribe link in our emails. We will use your email address to personalize our communications and send you
relevant offers. Your data will be stored up to 30 days after unsubscribing.
Contact us at data@amg.biz to see how we manage and store your data.
WHEN broadcaster and journalist Naga Munchetty began speaking openly about her experiences with adenomyosis and debilitating menstrual pain, the response was overwhelming.
Emails and messages poured in from women who had endured years of dismissal, silence and shame when it came to their health. That outpouring became the driving force behind her new book, It’s Probably Nothing, which calls for women to be heard and to advocate for themselves in a medical system that has too often ignored them.
“For so long, so many women haven’t been listened to by the world of medicine,” Munchetty said. “I knew this from my own experience of not being given adequate pain relief, or waiting years for a diagnosis. My motivation was to help women and people who love women to advocate better for women’s health.”
The book blends Munchetty’s personal journey with the voices of other women who have faced similar struggles, alongside expert insights from medical professionals. Its purpose, she said, is clear: to empower people to fight for their health.
“We need to be unafraid of saying how we have been weakened by our symptoms,” the BBC presenter said.
“Too often, we try to keep afloat, keep our head above water, but we don’t want to seem weak. That needs to change.”
Munchetty’s candour is striking. She describes the shame of being told her excruciating periods were “just normal,” leaving her to feel weak and whiny for struggling.
“You might as well have told me people have heart attacks while I’m having a heart attack,” she said. “Debilitating pain is serious — it may not be lifelimiting, but it is life-impacting.”
Her determination to challenge that culture led to her giving evidence in parliament, contributing to what became a Women and Equalities Committee report, published in December 2024.
The report made headlines for its stark conclusion: medical misogyny exists.
For Munchetty, seeing that phrase in black and white was transformative. “It was almost self-affirming,” she said. “We now know it’s there, so we can challenge it. Women can say: I know my body, I know there’s not enough research, and I am entitled to push for answers.”
The parliamentary report went further than acknowledgement. It called for ring-fenced funding for women’s health hubs, better training for GPs, and greater investment in research into reproductive conditions like adenomyosis and endometriosis.
It highlighted how symptoms are routinely dismissed as “normal,” delaying diagnosis and disrupting women’s careers, education and daily lives. Munchetty wrote in her book — referencing the report — that medical misogyny is not about blaming individual doctors, but about challenging a system built on insufficient research into women’s bodies.
“It gives women the language and the confidence to not just be heard, but to insist on being taken seriously,” she wrote.
Her book also tackles the additional barriers faced by women from minority communities, who may be discouraged by stigma or embarrassment from speaking about menstruation or menopause. To them, Munchetty has a clear message: “You are so much more valuable than you realise. If you don’t prioritise your health, you are lessening your ability to hold up everyone around you.”
Those featured in the book are friends, colleagues, charities and everyday women who contributed their stories, many for the first time. “I was surprised at how many friends are in that book with such powerful experiences,” Munchetty said.
“It told me all the more that we’re not speaking about it, and that it is sadly so very common.”
At a launch event for the book, contributors, family and experts filled the room with what Munchetty describes as an “electric and inspiring atmosphere.”
She said, “It was full of joy, of women who felt safe to speak up and be heard. This is not a whiny book — it’s a positive book. People felt they were part of making things better, part of this women’s health revolution.”
For Munchetty, writing the book was exhausting, but transformative, she said.
“I never thought I’d be an author. I’m a journalist. But this is journalism — facilitating people’s stories to be told powerfully and truthfully. People trusted me, and I’m proud of that.”
And Munchetty’s aim is for the book to be a tool for change: arming women with the language, confidence and strategies to advocate for their health.
“It’s not easy to admit you need help, and it’s not instinctive for women to prioritise themselves,” she said. “But this book will help you do that. It’s the silent friend who has your back and gives you strength.”
It’s Probably Nothing - Critical Conversations on the Women’s Health Crisis is now available in all good bookshops
Keep ReadingShow less
Williams explained that her weight challenges began after the birth of her first daughter
Serena Williams reveals she has lost more than 31lbs using a GLP-1 medication
The tennis legend says the treatment enhanced her existing healthy lifestyle
She stresses that weight loss should not change self-image or self-confidence
Serena Williams has revealed she has lost more than 31lbs after turning to a weight-loss medication, saying the treatment has transformed both her body and her mindset.
The 23-time Grand Slam champion, 43, told PEOPLE that using a GLP-1 medication — a type of injection that works by regulating appetite — has helped enhance the healthy lifestyle she already maintained through diet and exercise.
“I feel great,” Williams said. “I feel really good and healthy. I feel light physically and light mentally.”
Postpartum struggles
Williams explained that her weight challenges began after the birth of her first daughter, Alexis Olympia, in 2017. Despite training intensively and eating healthily, she found it difficult to return to her preferred weight.
“I never was able to get to the weight I needed to be, no matter what I did, no matter how much I trained,” she admitted. “It was frustrating to work so hard and not see results.”
She experienced the same plateau after giving birth to her second daughter, Adira River, in 2023. Although she initially shed weight quickly, progress soon stalled. “I never lost another pound,” she recalled.
Turning to treatment
Determined to try a new approach, Williams consulted doctors through Ro, a direct-to-patient healthcare company, and began a GLP-1 course once she had finished breastfeeding. The medication, also known as a glucagon-like peptide-1 receptor agonist, is commonly marketed under brand names such as Ozempic and Mounjaro.
“I did a lot of research before I started,” she explained. “I wanted to know if it was a shortcut or if it could really help me. In the end, it felt like the right decision.”
Williams, who is now a patient ambassador for Ro, said the injections made a noticeable difference. “I lost over 31 pounds and was really excited about that weight loss.”
Feeling better than ever
The Olympic gold medallist says she now feels stronger and more energetic.
“I can do more. I’m more active. My joints don’t hurt as much. Even simple things like moving around are easier. I feel like I have a lot more energy.”
She emphasised that GLP-1 was not a substitute for discipline but a way to support her existing healthy habits. “GLP-1 helped me enhance everything I was already doing — eating healthy and working out, whether as a professional athlete or just at the gym every day.”
Confidence and body positivity
Despite her transformation, Williams stressed that her self-confidence has never depended on her size.
“Weight loss should never really change your self-image,” she said. “Women are judged about their bodies at any size, and I’m no stranger to that. I’ve always loved myself at every stage. The difference was that my body didn’t feel good carrying that extra weight after having children.”
She added that she encourages her daughters to embrace body confidence too. “It’s important to teach them to be confident at any size, just as I try to be. Looking back, whether I was smaller or heavier, I always felt confident — and I looked great too.”
Looking ahead
Williams says she plans to continue with the weekly GLP-1 injections as needed, alongside training for a half marathon. The gym remains her “favourite place to be” — and she intends to keep sharing her workouts with fans online.
“I just feel pretty good about it all,” she said.
Keep ReadingShow less
Seles first began noticing symptoms around five years ago
Nine-time Grand Slam winner Monica Seles diagnosed with myasthenia gravis three years ago
The 51-year-old revealed her condition ahead of this month’s US Open to raise awareness
Disease causes muscle weakness and has no known cure
Former world number one Monica Seles has revealed she was diagnosed with myasthenia gravis, a rare neuromuscular autoimmune disease, three years ago. The 51-year-old, who won nine Grand Slam singles titles, went public ahead of the US Open to raise awareness of the condition, which causes muscle weakness and can affect multiple parts of the body.
Symptoms and diagnosis
Seles first began noticing symptoms around five years ago when she experienced double vision and struggled with coordination. “I would be playing [tennis] with some kids or family members, and I would miss a ball. I was like, ‘Yeah, I see two balls,’” she told the Associated Press. These symptoms eventually led to her diagnosis, which took time for her to come to terms with.
Living with the condition
The former tennis star described the impact of the disease on her daily life as “significant” and said it was initially difficult to discuss openly. Myasthenia gravis currently has no cure, but treatments can help manage its effects. By sharing her experience, Seles hopes to use her platform to educate others.
Career highlights
Seles rose to prominence as a teenager, winning her first Grand Slam at the 1990 French Open aged 16 and claiming eight majors by 19. Her career was interrupted in 1993 when she was stabbed by a spectator during a match in Hamburg. She returned to the sport and won one more Grand Slam before retiring in 2003, having spent 178 weeks as world number one and capturing 53 career titles.
NexGen knee implant linked to high failure rates was used in over 10,000 UK operations.
Concerns flagged as early as 2014; withdrawn from UK market in 2022.
Hundreds of patients required corrective surgery, with costs running into millions.
Manufacturer Zimmer Biomet says patient safety is its “top priority” but will not cover revision costs up front.
Implant used despite early warnings
A knee replacement implant used in thousands of NHS operations was known to have a concerning failure rate eight years before it was withdrawn, a BBC File on 4 Investigates report has found.
The NexGen implant, made by US manufacturer Zimmer Biomet, was fitted in more than 10,000 patients between 2012 and 2022. Concerns were first raised by the National Joint Registry (NJR) in 2014, though insufficient data at the time made it difficult to draw firm conclusions.
The model in question included a modified “stemmed option tibial component” or “tibial tray”, lacking a layer of plastic found in earlier versions. It was marketed as a cheaper alternative for the NHS.
Patients left in pain and needing further surgery
Patients have reported severe complications after their implants slipped out of place, damaging bone and causing lasting mobility issues.
Debbie Booker, from Southampton, experienced severe pain a year after her 2016 surgery, eventually requiring a second knee replacement. She says the failed implant left her addicted to strong painkillers and caused long-term health problems, including the need for a hip replacement.
Another patient, “Diana”, had her implant fitted in 2021. When it slipped and began wearing away her shin bone, her consultant told her she was “standing on a broken leg”.
Surgeons raised repeated concerns
Irish knee surgeon Prof Eric Masterson reported a surge in corrective surgeries after switching to the NexGen implant in 2012. He says his concerns were dismissed by Zimmer Biomet representatives, a view echoed by NHS surgeons.
UK knee specialist Prof Leila Biant said she and colleagues raised warnings as early as 2017, but the company was slow to engage in evaluating affected patients.
Recall and high revision costs
By 2022, NJR data suggested patients with the NexGen implant were almost twice as likely to require corrective surgery compared with the average knee replacement. Zimmer Biomet recalled unused units from the UK market that year.
Studies have estimated failure rates for the tibial tray component between 6% and 19%. Hundreds of patients have undergone revision surgery, with more expected.
Each corrective procedure costs between £10,000 and £30,000, according to Southampton University’s Prof David Barrett, meaning the total bill is likely to run into millions. Zimmer Biomet has told sales staff it will not cover diagnostic, follow-up, or revision costs up front.
Official responses
Zimmer Biomet says it is “committed to the highest standards of patient safety, quality, and transparency” and acts in line with regulations when new data becomes available.
NHS England has confirmed it is “currently reviewing the case involving Zimmer Biomet NexGen knee implants”.