Rare 50p Coin Sells for £113 at Auction
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.
Category : Search result: rare neurological disorder
Woman speaks with Thai accent after stroke
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.
Aaron Chalmers' son hospitalised with rare disorder
Former Geordie Shore personality Aaron Chalmers reveals his young son Oakley faces unexpected hospital procedure while battling rare genetic condition that requires ongoing medical care.
Mum's heartbreak as son battles rare chromosome disorder
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.
US Bets Big to Break China's Rare Earth Monopoly
The Biden administration makes unprecedented investments in Western rare earth companies to secure critical minerals and challenge China's market dominance in green technology.
Woman's ribs pop out when she laughs due to rare condition
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.
Rare 50p Coin Could Be Worth Over £500
Discover how a rare 2009 Kew Gardens 50p coin hiding in your pocket change could be worth a small fortune to collectors.
Husband's agony as condition stops him kissing wife
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.
FND: The hidden paralysis crisis in the UK
Functional Neurological Disorder affects thousands in the UK, causing debilitating symptoms like paralysis and seizures while facing widespread medical misunderstanding. Discover the truth about this life-changing condition.
Girl's constant hunger battle with rare genetic condition
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.
Gene Therapy Breakthrough for Autism & Epilepsy
British scientists pioneer revolutionary gene therapy treatment showing remarkable results in children suffering from debilitating SYNGAP1 syndrome, a rare genetic condition causing severe autism, epilepsy and developmental delays.
FND: The invisible illness paralysing thousands
Discover the shocking reality of Functional Neurological Disorder affecting thousands in the UK. Learn about symptoms, diagnosis challenges, and one woman's journey from paralysis to recovery.
Woman wakes from coma speaking fluent French
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.
Potential cure found for misophonia sound disorder
Groundbreaking research reveals a neurological basis for misophonia and identifies a promising treatment approach that could help millions suffering from sound sensitivity.
EastEnders Star Reveals Son's Rare Condition Struggle
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.
Christmas electric shocks warned of woman's MS diagnosis
Paula Adamson's bizarre electric shock sensations during Christmas festivities masked a terrifying neurological condition that left doctors baffled. Discover how one woman's strange symptoms led to a life-changing diagnosis.
YouTuber Alfie Deyes diagnosed with rare swallowing disorder
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.
Baby's rare disease battle: Family's 5-month diagnosis wait
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.
Toddler's mystery illness diagnosed as rare genetic disorder
The emotional journey of a family who fought for answers after noticing developmental delays in their son, culminating in a rare MICPCH syndrome diagnosis.
Rare 50p coins worth £1,000 found in circulation
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.
Mother's battle against daughter's ultra-rare GRIN1 disease
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.
Huntington's Disease: New Drug Slows Progression in Trial
A revolutionary new drug, pridopidine, has shown significant promise in slowing the progression of Huntington's disease, offering new hope to UK families affected by the genetic condition.
Baby Born Without Eyes in Ultra-Rare Genetic Condition
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.
Son's Rare Disorder Destroys Home: Mother's Plea for Help
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.
Chris Kamara's powerful health battle confession
Football legend and broadcaster Chris Kamara gives a raw and emotional account of his ongoing struggle with apraxia of speech, detailing the initial fear, his diagnostic journey, and his inspiring resolve to adapt and raise awareness.
Routine blood test reveals incurable genetic condition
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
Mum's legs suddenly stopped working - rare diagnosis revealed
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.
Teen's decade-long battle with agonising sickle cell disease
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.
Rare 1p Coin Sells For Astonishing £127,000
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.
Rare 50p coin discovered in change could fetch £50,000
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.
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