Long COVID symptoms hid deadly heart tumour
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.
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.
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.
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.
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
A mother's quick thinking led to the diagnosis of a life-threatening double aortic arch in her toddler after noticing unusual breathing patterns and a distinctive cough sound.
Exclusive: Mother's emotional journey as her son battles rare chromosome disorder and the family's desperate search for answers in the UK healthcare system.
The Biden administration makes unprecedented investments in Western rare earth companies to secure critical minerals and challenge China's market dominance in green technology.
A quick-thinking midwife's extraordinary observation during a routine appointment led to the discovery of a rare and life-threatening condition, saving an unborn baby from certain tragedy.
A young woman from Manchester lives in constant pain with a rare condition that causes her ribs to dislocate when she laughs, coughs or even breathes deeply, leaving her unable to work or enjoy simple pleasures.
Singer Anne-Marie opens up about her young son's harrowing health journey with a rare genetic disorder, sharing emotional details about hospital stays and the impact on family life.
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.
Diversity star Ashley Banjo opens up about his daughter's rare health condition and the emotional journey that changed his family forever in an exclusive tell-all interview.
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.
A newborn's swollen belly revealed an extraordinary medical mystery - doctors discovered he was absorbing his twin sibling in the womb in a rare condition called fetus in fetu.
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.
In an extraordinary medical case, Lisa Millar from Largs, Scotland, awoke from a two-week coma speaking fluent French despite barely remembering the language since school. Doctors are baffled by this rare phenomenon of Foreign Accent Syndrome.
Exclusive story of Dean Sims, the solitary UK case of Mandibuloacral Dysplasia, and his extraordinary journey through the healthcare system.
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.
Former England footballer and Strictly Come Dancing contestant Karen Carney opens up about growing up with Perthes disease and how it forged her resilience and determination.
A young woman suffers from an extremely rare water allergy that leaves her skin burning, cracking and bleeding after simple activities like showering or sweating.
Popular YouTuber Alfie Deyes reveals his shocking diagnosis with a rare swallowing condition called eosinophilic oesophagitis after suffering for years with what doctors thought was acid reflux.
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.