Chronic Lyme Disease: Medicine's Divided Opinion
Explore the heated medical controversy surrounding Chronic Lyme Disease as patients fight for recognition while doctors demand scientific evidence in this deep-dive investigation.
Category : Search result: rare disease diagnosis
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.
Italian TV Star Pamela Camassa's Health Battle Revealed
Beloved Italian television personality and model Pamela Camassa shares emotional journey through devastating health diagnosis that's left her fighting for her life.
Florida confirms first 'zombie deer' disease case
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.
Anne-Marie reveals son's rare genetic condition diagnosis
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.
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.
Colin Farrell's moving tribute to EB sufferer Emma Fogarty
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.
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.
Lewis Moody reveals Motor Neurone Disease diagnosis
Former England rugby captain Lewis Moody shares heartbreaking Motor Neurone Disease diagnosis while thanking fans for overwhelming support in moving social media statement.
Woman shrinks 4 sizes after rare illness diagnosis
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.
Britain's only patient with ultra-rare disease
Exclusive story of Dean Sims, the solitary UK case of Mandibuloacral Dysplasia, and his extraordinary journey through the healthcare system.
Motor Neurone Disease: Key Risk Factors Revealed
Groundbreaking research reveals the complex interplay of genetic susceptibility, environmental triggers, and lifestyle factors that contribute to motor neurone disease risk, as rugby legend Lewis Moody shares his diagnosis journey.
Rugby hero Lewis Moody diagnosed with motor neurone disease
Former England rugby captain Lewis Moody MBE announces he's been diagnosed with motor neurone disease, vowing to fight the condition with same determination he showed on the pitch.
Lewis Moody diagnosed with motor neurone disease
Former England captain Lewis Moody opens up about his motor neurone disease diagnosis, sharing his determination to fight the condition and raise awareness for research.
Rugby Star Lewis Moody Reveals MND Diagnosis
Former England rugby captain Lewis Moody MBE shares emotional MND diagnosis, joining fellow rugby stars in motor neurone disease battle while vowing to fight with characteristic courage.
Woman's flu diagnosis reveals rare Victorian disease
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.
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.
Toddler paralysed after cold triggers rare condition
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.
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.
Woman's 'cold' was rare Empty Nose Syndrome diagnosis
A woman's persistent cold symptoms turned out to be a rare and life-altering condition. Read her shocking story of diagnosis and adaptation.
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.
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.
UK teen allergic to water where even crying causes pain
Abigail Beck, 19, has a rare condition called Aquagenic Urticaria. We explore her daily battle where showering, sweating, and even crying trigger painful allergic reactions.
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