UK boy is only person in world with deadly condition
Oli-Jay Morris, 2, is the only known person with a unique gene mutation. His family are fundraising £14,000 for a personalised treatment plan to save his life.
Oli-Jay Morris, 2, is the only known person with a unique gene mutation. His family are fundraising £14,000 for a personalised treatment plan to save his life.
A groundbreaking gene therapy developed in Manchester offers new hope for children with Hunter syndrome. Three-year-old Oliver Chu shows remarkable progress nine months after treatment.
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.
New research reveals how moderate daily activity can significantly reduce coronary heart disease risk and symptoms. Discover the life-changing benefits of consistent exercise for your heart health.
A mother reveals how her daughter endured cruel bullying for years before doctors discovered her weight struggles were caused by rare Bardet-Biedl syndrome, exposing the hidden reality of genetic disorders.
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.
Groundbreaking research reveals three major pathways causing ALS, offering new hope for targeted therapies that could slow or stop the devastating neurodegenerative disease's progression.
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.
Former New York Jets centre Nick Mangold reveals his private health struggle with kidney disease in an emotional interview, sharing his journey from NFL glory to facing a life-changing diagnosis.
A mother's terrifying ordeal as her healthy son suddenly develops rare neurological condition ADEM, sparking urgent NHS investigation into childhood illness.
Exclusive insight into the final moments of Isabelle Tate's life and the devastating impact of Charcot-Marie-Tooth disease that led to the Nashville 911 tragedy.
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.
Exclusive: British surgeons pioneer revolutionary robotic prostate procedures that take just 10 minutes, offering new hope for thousands stuck on NHS waiting lists. Discover how this medical breakthrough is transforming cancer care across the UK.
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.
Harry Moseley's heartbreaking story highlights growing fears over NHS treatment delays as young father dies after multiple postponed appointments during pandemic.
Groundbreaking therapy offering hope to multiple sclerosis patients receives NHS approval, promising to transform treatment outcomes across the UK healthcare system.
A British teacher has become the first UK patient to receive a revolutionary new treatment for multiple sclerosis, marking a significant milestone in neurological healthcare that could transform lives.
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.
Shocking new research reveals the UK's favourite smoothing hair treatment contains up to 5 times the legal formaldehyde limit, posing serious cancer risks to clients and stylists.
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.
Groundbreaking research reveals moringa powder's remarkable ability to combat gum disease, offering a natural alternative to conventional dental treatments.
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
A courageous cancer survivor shares her emotional journey battling the same rare appendix cancer that claimed her sister's life, revealing crucial symptoms everyone should know.