Mother's instinct saves toddler from rare heart condition
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.
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.
A young mother's persistent tingling sensation led to a shocking diagnosis of multiple blood clots, prompting urgent medical warnings about postpartum health risks.
A grieving family shares their heartbreaking story after Lee Clarke tragically died from a blood clot caused by falling asleep in his chair, warning others about the dangers of prolonged sitting.
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.
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.
Medical experts share groundbreaking advice on reducing thrombosis risk through easy daily habits that could save lives. Discover the two key lifestyle adjustments backed by scientific research.
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.
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.
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.
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.
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 mother reveals her agonising decision to keep her two daughters separated after one was diagnosed with a rare and life-threatening condition. The family's story is one of love, sacrifice, and a desperate plea for understanding.
Saturday Night Live alumna Kate McKinnon opens up about her diagnosis with a rare auditory processing condition, sharing her lifelong journey with sound sensitivity and communication challenges.