Aaron Chalmers' son diagnosed with rare Apert Syndrome
Former Geordie Shore star Aaron Chalmers and his ex-partner Talia Oatway reveal their son Oakley's battle with Apert Syndrome, a rare genetic condition.
Former Geordie Shore star Aaron Chalmers and his ex-partner Talia Oatway reveal their son Oakley's battle with Apert Syndrome, a rare genetic condition.
Scientists have identified key genetic markers linked to chronic fatigue syndrome, offering new hope for diagnosis and treatment.
A journalist recounts their unsettling encounter with the Whittaker family, known as one of America's most inbred families, revealing their struggles and the harsh realities of genetic isolation.
A rare genetic condition means some individuals never experience hunger, leading to unique health challenges and lifestyle adjustments. Discover their fascinating stories.
Actor David Suchet shares his family's journey with tuberous sclerosis, a rare genetic condition affecting his grandson, to raise awareness and support research.
Renowned actor David Suchet shares his family's journey with tuberous sclerosis, advocating for greater awareness and research into the rare genetic condition.
A shocking medical case reveals a patient who gouged out their own eye due to an unidentified neurological disorder. Doctors remain baffled by the rare condition.
Beloved actor David Suchet reveals his grandson's battle with a rare genetic disease, sharing the family's emotional journey and raising awareness for the condition.
A family's terrifying ordeal with heart attacks has prompted vital health checks, revealing a hidden genetic condition.
Pop superstar Justin Timberlake reveals his struggle with Lyme disease, detailing the physical and emotional toll it took on his life and career.
A woman shares her harrowing journey of suffering from an undiagnosed illness for years before doctors finally uncovered the truth behind her debilitating symptoms.
A baby boy's persistent crying was dismissed as colic before a devastating diagnosis revealed a rare genetic disorder. His parents share their emotional story.
Discover how the MyHeritage DNA test kit can help you explore your genetic roots with detailed ethnicity estimates and family matching features.
A father emotionally shares his family's struggle with his daughter's rare genetic disorder during an appearance on ITV's This Morning, raising awareness and touching viewers' hearts.
A father-of-two was left paralysed from the neck down after a sudden headache revealed a devastating spinal condition. Read his shocking story.
Strictly Come Dancing star Anton Du Beke reveals his wife Hannah's struggle with a rare and painful health condition, sharing their emotional journey.
A baffling new illness is causing severe neurological symptoms, leaving patients unable to speak or walk. Experts are scrambling for answers as cases emerge.
A celebrity chef opens up about his daughter's rare illness, shedding light on the family's emotional journey and raising awareness for the condition.
Spain's key player Aitana Bonmatí has been hospitalised due to a rare illness, casting doubt over her participation in the Euros final against England.
Brits are being urged to check their spare change as certain rare 50p coins could be worth hundreds, even thousands, of pounds. Discover which coins to look out for!
Groundbreaking research reveals why certain individuals avoided COVID-19 infection entirely, pointing to a remarkable genetic advantage that kept them safe.
A mother's harrowing 999 call reveals the NHS crisis as her 12-year-old son with a rare genetic disorder is left without a hospital bed for days.
A revolutionary genetic test may soon predict obesity risk years before symptoms appear, offering hope for early intervention and prevention.
After years of uncertainty, a determined mother finally uncovers the truth behind her daughter's baffling health condition—a rare genetic disorder that had eluded doctors for years.
A groundbreaking DNA test may soon help identify children at risk of obesity early, offering parents and doctors a chance to intervene before health issues arise.
The UK's groundbreaking mitochondrial donation IVF technique marks a significant but careful step in genetic innovation, offering hope to families affected by mitochondrial diseases.
A 10-year-old schoolgirl has undergone triple amputation after a seemingly harmless bruise led to a life-threatening condition. Doctors reveal the shocking truth behind the 'killer disease' that left her fighting for survival.
The UK has become the first country to officially approve a groundbreaking IVF technique that incorporates DNA from three individuals, aiming to prevent genetic disorders in babies.
A groundbreaking IVF procedure has successfully prevented mitochondrial disease in eight babies, marking a significant milestone in genetic medicine.
A grieving mother shares her devastating story after losing her daughter to mitochondrial disease, a rare and often misunderstood condition.