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.
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.
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.
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.
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.
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.
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.
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.
BBC Radio 2 presenter Zoe Ball opens up about her son Woody Cook's struggle with a rare medical condition that causes severe joint pain and mobility issues in emotional new interview.
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.
Married at First Sight favourite Emma Barnes gives a raw and emotional account of her debilitating health struggles, revealing how a rare condition has left her feeling trapped in her own body.
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.
Actress Sarah Parish and husband James Murray open up for the first time about the devastating loss of their eight-month-old daughter, Ella-Jayne, and their journey through grief.
GMTV legend John Stapleton opens up about his Parkinson's diagnosis, revealing the subtle sign he ignored for a decade and his mission to help find a cure.
A British man's life was turned upside down after a simple morning yawn dislocated his jaw and triggered a rare, life-threatening condition. This is his shocking story of survival and the vital health warning he now shares.
The astonishing true story of Ella Cate, a woman born with a rare parasitic twin, and her lifelong journey of medical challenges and ultimate triumph.
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.
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
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.
New research uncovers a startling link between a widespread eye disorder and a significantly increased risk of developing Parkinson's disease. Experts urge vigilance.
A woman with uterus didelphys, a rare congenital condition giving her two vaginas, shares how she earns over £150,000 monthly on OnlyFans by embracing her unique anatomy.
A comprehensive guide to transverse myelitis, a rare but serious neurological disorder causing spinal cord inflammation. Learn about its sudden symptoms, potential causes like infections and immune disorders, and the crucial treatment pathways for recover