Celine Dion's Thanksgiving health update
Celine Dion delivers a positive health update on Instagram, sharing a heartfelt Thanksgiving message with fans while battling Stiff Person Syndrome. Discover her inspiring journey.
Category : Search result: rare neurological disorder
Jesse Jackson leaves hospital after neurological care
Civil rights icon Rev. Jesse Jackson has been released from a Chicago hospital following treatment for progressive supranuclear palsy. His family requests continued prayers during this time.
Rick Wakeman gives health update after brain surgery
Prog rock legend Rick Wakeman confirms successful shunt surgery for hydrocephalus. The 76-year-old plans to return to the stage for his 'Wakeman and Son' tour in March. Read his full recovery story.
Autoimmune Encephalitis: Body Attacks Brain
Discover how autoimmune encephalitis turns the immune system against the brain, causing severe symptoms. Learn about diagnosis challenges and treatment options for this rare condition.
Man's 'Year of Unraveling' from Brain-Attacking Immune System
A California man's immune system attacked his brain, causing memory loss and seizures. Discover his journey with autoimmune encephalitis and his path to recovery. Read his inspiring story.
Hitler's rare genetic sexual disorder uncovered
New DNA analysis reveals Adolf Hitler had Kallmann syndrome, a rare genetic condition impacting puberty. Discover the findings and what it means.
Footballer beats rare paralysis to run marathons
Relly Ladner was told she might never walk again after Guillain-Barré syndrome. Defying odds, she now runs marathons. Read her incredible recovery journey.
Woman lives normally despite missing brain part
Shocking medical case reveals woman living full life despite missing cerebellum - the brain region controlling motor skills, balance and coordination.
Woman born without cerebellum lives normal life
Doctors are stunned by a British woman born without her cerebellum who defied medical expectations to live a fully independent life, walking and talking normally.
Bullied for weight: Teen's rare genetic disorder revealed
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.
Mum with rare dementia forgets children's names
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.
Boy, 11, wakes up unable to walk or speak
A mother's terrifying ordeal as her healthy son suddenly develops rare neurological condition ADEM, sparking urgent NHS investigation into childhood illness.
Child's battle with rare disease stealing her ability to walk
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.
Teen's death from rare Charcot-Marie-Tooth disease
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.
Daughter, 21, dies after battle with rare neurological disorder
Isabelle Adora Tate's courageous battle against a devastating neurological condition ends at just 21, as her grieving mother pays emotional tribute to her 'beautiful warrior' daughter.
Hollyoaks star's real health scare mirrors soap storyline
Hollyoaks actress Jessica Fox reveals her terrifying real-life health battle with Functional Neurological Disorder, drawing parallels to her character Nancy Osborne's recent storyline.
Daughter's rare condition breaks hearts daily
Exclusive: The heartbreaking story of a family coping with their daughter's rare Cri Du Chat syndrome, revealing the daily challenges and emotional toll of caring for a child with complex needs.
Kelly Osbourne breaks down revealing health diagnosis
TV personality Kelly Osbourne breaks down while revealing her recent diagnosis with a rare neurological condition, sharing her fears and determination to raise awareness.
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.
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.
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