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.
The heartbreaking story of Isabelle Tate, a vibrant teenager whose life was cut short by the little-known genetic condition Charcot-Marie-Tooth disease, sparking urgent calls for greater awareness and research funding.
A teenager's persistent itching that kept her awake for nights led doctors to discover a rare autoimmune liver disease that could have been fatal without treatment.
Health officials in Tennessee report significant surge in contagious hand, foot and mouth disease cases, with schools and childcare centres particularly affected. Learn about symptoms and prevention.
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.
A scarce 2009 Kew Gardens 50p coin has sold for over double its face value in a recent auction, sparking renewed interest in coin collecting across the UK.
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 courageous mother's relentless pursuit of answers revealed she was suffering from a rare autoimmune condition, not cancer as initially diagnosed, sparking calls for improved medical awareness.
Doctors were left baffled when a routine tummy ache complaint revealed a shocking parasitic infection rarely seen in Britain. The astonishing medical case highlights the importance of thorough diagnosis.
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
The Biden administration makes unprecedented investments in Western rare earth companies to secure critical minerals and challenge China's market dominance in green technology.
Beloved Italian television personality and model Pamela Camassa shares emotional journey through devastating health diagnosis that's left her fighting for her life.
Florida faces its first confirmed case of Chronic Wasting Disease in white-tailed deer, sparking urgent containment measures and raising concerns about the fatal neurological condition's spread.
Discover how a rare 2009 Kew Gardens 50p coin hiding in your pocket change could be worth a small fortune to collectors.
A heartbreaking story of love and resilience as a British man battles a rare neurological condition that has stolen his ability to show physical affection to his wife of 20 years.
Hollywood star Colin Farrell reveals his profound friendship with Emma Fogarty, who lives with the painful skin condition Epidermolysis Bullosa, in a powerful new book highlighting courage and resilience.
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.
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.
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.
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 three-year-old girl from the UK has been left paralysed from the neck down after a common cold virus triggered a devastating rare condition called transverse myelitis.
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.
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 seemingly healthy mother-of-two's legs suddenly failed, leading to a terrifying medical mystery and a rare diagnosis that changed her life forever.
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.