The NHS is rolling out a groundbreaking genetic testing programme to identify thousands of Britons with undiagnosed hereditary haemochromatosis - a dangerous iron overload condition that can cause organ damage if untreated.
Discover how a rare 2009 Kew Gardens 50p coin hiding in your pocket change could be worth a small fortune to collectors.
Two-year-old Ivy's constant hunger battles a rare genetic disorder called Prader-Willi syndrome, leaving her parents in a 24/7 vigil against life-threatening complications.
An investigative journey into the lives of the Whittakers, known as America's most inbred family, uncovering their isolated existence and the genetic consequences of generations of intermarriage.
Love Is Blind's Danielle Ruhl reveals her rare Ehlers-Danlos Syndrome diagnosis and how it threatens her vision, sharing an emotional journey of invisible illness awareness.
A woman's mysterious health battle led to dramatic weight loss and a shocking diagnosis. Discover how she fought back against the life-threatening condition.
Exclusive story of Dean Sims, the solitary UK case of Mandibuloacral Dysplasia, and his extraordinary journey through the healthcare system.
Conservative commentator Charlie Kirk's alarming claim about Utah's DNA collection practices sparks debate over genetic privacy rights and government overreach in criminal investigations.
EastEnders actress Kellie Bright opens up about her family's emotional journey navigating her son's rare genetic disorder and the daily challenges they face.
Struggling to tell COVID-19 from seasonal flu? Our comprehensive symptom checker reveals the key differences and when to seek medical help.
A routine flu diagnosis turned into a medical mystery when a British woman discovered she'd contracted a rare Victorian-era illness doctors thought had disappeared from modern Britain.
After being dismissed by doctors for years, Megan Hogg finally received a life-changing diagnosis that explains why she spent four years bedbound with debilitating symptoms.
A UK family shares their emotional journey as their newborn son battles a rare neonatal disease, facing months of uncertainty and fighting for answers in the NHS system.
A luxury Royal Caribbean cruise ship has been struck by a significant norovirus outbreak, leaving more than 70 passengers suffering from severe vomiting and diarrhoea symptoms during their holiday voyage.
The emotional journey of a family who fought for answers after noticing developmental delays in their son, culminating in a rare MICPCH syndrome diagnosis.
Discover how four rare 50p coins featuring iconic British designs could be hiding in your pocket change, with collectors paying hundreds of pounds for these sought-after pieces.
Exclusive: The heart-wrenching story of a mother's battle to save her daughter, Arianna, from the ultra-rare GRIN1 gene mutation, a condition so uncommon it affects just a handful of people globally.
A woman's persistent cold symptoms turned out to be a rare and life-altering condition. Read her shocking story of diagnosis and adaptation.
The parents of a baby girl born without eyes due to an incredibly rare genetic condition share their emotional journey and determination to give their daughter the best life possible.
An East Sussex mother's heart-wrenching account of her son's ultra-rare GRIN2B condition, which causes extreme violence, property destruction, and a desperate fight for support.
Steve Martin halts 'Dukes of Funny' tour performances in Dallas after Martin Short falls ill. Full refunds issued as fans await health updates on the comedy legend.
Jade, 33, went for a routine blood test expecting nothing unusual. Weeks later, she received a life-altering diagnosis of Hereditary Angioedema (HAE) - a rare genetic disorder with no cure. Her story highlights the importance of recognising unusual sympto
A landmark study from the Natural History Museum reveals how British DNA is reshaping our understanding of African genetic history, uncovering centuries of migration and diversity.
Exclusive: A teenager's life has been defined by unimaginable pain and hospital isolation due to the cruel genetic condition sickle cell disease, robbing her of a normal childhood and future dreams.
A seemingly ordinary 1p coin, minted with a unique error in 1983, has just sold at auction for a staggering £127,000, making it one of the most valuable modern coins in the UK.
A rare 2009 Kew Gardens 50p coin, discovered in everyday change, is set to fetch up to £50,000 at auction, stunning its finder and captivating coin collectors nationwide.
A heroic preschooler from the UK becomes a lifesaving donor for her baby brother after a rare medical emergency. Their incredible story of bravery and family love will inspire you.
A UK mother's extraordinary bond with her newborn daughter has captured hearts worldwide after the baby was born with an identical facial birthmark. This rare genetic phenomenon defies odds and celebrates the unique beauty of family connections.
A rare Kew Gardens 50p coin has sold for a staggering £285 on eBay. Discover why this specific coin is so valuable and how to check your spare change for a hidden fortune.
A UK teenager's life changed forever after waking up paralysed from the chest down. This is the shocking story of a rare condition that struck without warning.