Code Vein 2 Preview: A Polished Anime Soulslike Sequel
Our hands-on preview of Code Vein 2 reveals a sequel focused on refining its unique formula. With deep customisation, a partner system, and a new story, it's set to launch on 29 January 2026.
Our hands-on preview of Code Vein 2 reveals a sequel focused on refining its unique formula. With deep customisation, a partner system, and a new story, it's set to launch on 29 January 2026.
Verity Went, 28, woke from a nap slurring her words and speaking with a thick Geordie accent. Diagnosed with rare Foreign Accent Syndrome, she now says the new voice is the 'real' her. Read her incredible story.
A Scottish mum's extreme fatigue, including sleeping for 24 hours, led to a life-threatening Addison's disease diagnosis after years of being told she had anxiety. Read her fight for answers.
A father from Corby issues an urgent warning after his healthy daughter, Sienna, 4, was diagnosed with Acute Necrotising Encephalitis following the flu. She faces a long hospital stay, missing Christmas.
Mikey Strachan, 13, has an undiagnosed condition requiring 24/7 care. Through the Mirror's Christmas appeal for Lifelites, virtual reality technology lets him play football and explore worlds.
Top surgeon Dr Rema Malik reveals how 'gravity and time' damage veins. Learn the three simple daily habits that can prevent serious circulatory issues like DVT and varicose veins.
A 95-year-old woman declared dead was found cooking in her kitchen six days later. Doctors diagnosed an 'artificial death'. Read this astonishing medical mystery.
A breakthrough NHS study reveals whole-genome sequencing provides diagnoses for rare genetic conditions two years earlier, offering families crucial answers and access to care. Read the inspiring story of three-year-old Nathaniel.
A breakthrough NHS study reveals whole genome sequencing is diagnosing rare genetic conditions in children two years sooner, transforming care for families like Nathaniel's in London.
Matthew Pascoe, 33, battles gastroparesis, vomiting up to 90 times daily. His life-saving device needs a £15,000 battery, but the NHS won't cover the cost. Read his story and learn how you can help.
The NHS urges the public to call 111 if they notice a throbbing pain or swelling in just one leg, a potential sign of a dangerous blood clot. Learn the symptoms and risks of DVT.
Coronation Street actress Samia Longchambon opens up about living with Raynaud's disease for two decades. Discover her coping tips and how she manages the circulation condition.
Rugby league star Mark Riddell breaks down discussing daughter Ava's Ogden Syndrome, affecting just four children in Australia. Read his inspiring family story.
A Swansea mum is in a desperate race against time after her four-year-old son Tate was diagnosed with Sanfilippo Syndrome, a rare and terminal childhood dementia.
Emmy-winning actress Ruth Wilson opens up about her debilitating mystery illness and the frustrating five-year search for answers that led to a rare disease diagnosis.
Meet baby Ezra, the courageous infant born with amniotic band syndrome whose incredible survival story is capturing hearts across Britain after beating overwhelming medical challenges.
In an extraordinary medical breakthrough, 19-month-old Oscar Sparrow from West Midlands has been identified as the only person worldwide living with a never-before-seen genetic mutation, offering new hope for rare disease research.
Medical experts reveal why swollen feet during flights isn't just uncomfortable - it could signal a life-threatening condition. Discover the simple £10 solution that could save your life.
A British woman's persistent dizziness and blackouts were initially dismissed as Long COVID, until a shocking diagnosis revealed a rare and potentially fatal heart tumour that required emergency surgery.
The devastating story of Sarah, a mother with rare dementia who can no longer recognise her own children, as her family fights for access to revolutionary treatment that could save her.
A runner's persistent leg pain turned out to be a life-threatening deep vein thrombosis, revealing how easily DVT can be mistaken for sports injuries.
Ben Miller opens up about his daughter's life-changing diagnosis that forced him to leave the hit BBC series and prioritise family during their darkest hours.
Afshin Ghaderian, recognised as the world's shortest man at just 65cm tall, has passed away at age 27 after refusing to let his rare condition define his life's ambitions and dreams.
The heartbreaking story of Isabelle Tate, a young girl from England fighting Charcot-Marie-Tooth disease, a rare genetic condition threatening her ability to walk and enjoy a normal childhood.
A teenage girl's life has been shattered after NHS doctors repeatedly dismissed her symptoms as growing pains, only to discover she had a rare spinal condition that may leave her permanently unable to walk.
TV personality Kelly Osbourne breaks down while revealing her recent diagnosis with a rare neurological condition, sharing her fears and determination to raise awareness.
Discover how to protect your circulation and overall health during extended car journeys with expert advice from vascular surgeon Dr. John Campbell.
A Hampshire woman developed Foreign Accent Syndrome after suffering a stroke, causing her to speak with a Thai accent despite never visiting Thailand. Medical experts explain this rare neurological condition.
After two decades of being dismissed by doctors, a woman's persistent rash turned out to be a rare pre-cancerous condition requiring life-changing surgery.
A British woman shares her extraordinary medical journey after discovering a mysterious 2-inch growth on her body that doctors identified as a rare condition. Her story highlights the importance of trusting your instincts when something doesn't feel right