DNA Database Controversy Sparks Privacy Concerns
Conservative commentator Charlie Kirk's alarming claim about Utah's DNA collection practices sparks debate over genetic privacy rights and government overreach in criminal investigations.
Category : Search result: rare genetic condition
MAFS Emma Barnes reveals heartbreaking IVF journey
Married at First Sight favourite Emma Barnes opens up about her devastating fertility struggles and genetic condition discovery while trying for a baby with husband Matt.
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.
Karen Carney reveals childhood health condition battle
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.
Woman allergic to water suffers burning skin
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.
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.
Zoe Ball's son battles rare condition causing severe pain
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.
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.
MAFS's Emma Barnes: 'My Body Is a Prison'
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.
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.
Sarah Parish on trauma of losing baby daughter
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.
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.
Morning Yawn Nearly Killed Me: UK Man's Ordeal
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.
Woman Born With Four Legs Shares Incredible Medical Journey
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.
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
British DNA study transforms African ancestry understanding
A landmark study from the Natural History Museum reveals how British DNA is reshaping our understanding of African genetic history, uncovering centuries of migration and diversity.
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.
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.
Baby born with identical birthmark to mother in rare genetic show
A UK mother's extraordinary bond with her newborn daughter has captured hearts worldwide after the baby was born with an identical facial birthmark. This rare genetic phenomenon defies odds and celebrates the unique beauty of family connections.
Woman with two vaginas earns £150k monthly on OnlyFans
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.
Mum's heartbreak over keeping daughters apart
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.
Kate McKinnon Diagnosed With Rare Auditory Processing Disorder
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.
Teen's 13-Inch Growth After Agonising Surgery
Exclusive interview with the British teen who underwent groundbreaking but agonising limb-lengthening surgery to correct a rare condition, gaining over a foot in height and a new lease on life.
Conjoined Twins Abby & Hensel Announce Baby on TikTok
Abby and Brittany Hensel, the renowned conjoined twins, have delighted fans by announcing they are expecting a baby. The groundbreaking news was shared through heartwarming TikTok photographs, marking a new chapter in their extraordinary lives.
Young rugby star's career halted by rare disease diagnosis
Promising 19-year-old rugby talent Cody Tamou faces the fight of his life after doctors discover an extremely rare and dangerous vascular disease, putting his sporting future on hold.
Mother's 18-month fight to diagnose son's rare disease
A mother's harrowing journey to uncover the truth behind her son's mysterious illness, battling a healthcare system that failed to recognise a rare genetic condition. A story of resilience, love, and the fight for answers.
Doctor: Trump's Health Condition "Cannot Be Reversed"
Exclusive medical analysis reveals the former US President faces an irreversible health condition that could impact his political future, according to leading physicians.
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