Inside America's Most Inbred Family
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 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.
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.
A Southern California resident turned to sewing during lockdown, discovering a therapeutic hobby that transformed her life.
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.
A recent court ruling has upheld the use of isolation booths in schools across England, sparking debate over student welfare and disciplinary measures.
Groundbreaking research highlights how untreated hearing loss may accelerate cognitive decline and social isolation, urging early intervention.
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.
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.
A groundbreaking pilot scheme in the UK is testing whether football match tickets prescribed by GPs can help combat depression and social isolation.
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.
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.
A 12-year-old girl was reportedly put in isolation at her school for wearing a skirt deemed 'too short'. Her parents are outraged, calling the decision 'ridiculous' and demanding answers.