Influencer loses second daughter on Christmas day
Melissa Mae Carlton and husband Tom share devastating news of daughter Molly's death, a year after losing her sister Abi. Doctors suspect a genetic heart condition.
Category : Search result: genetic condition
Two sisters die months apart from suspected heart condition
A mother shares her family's devastating loss after both her young daughters died, suspected from a genetic heart condition. Read her heartbreaking story and vital warning to other families.
Girl, 13, completes wish list before going blind
Audrey Tyrrell, 13, is ticking off a 'visual wish list' after a diagnosis of Usher syndrome. The Essex teen aims to see the world before progressive vision loss takes hold. Read her inspiring story.
Christmas Disease: The Rare Bleeding Disorder Explained
Contrary to its festive name, Christmas Disease is a rare inherited bleeding disorder. Learn about its history, symptoms, and how patients can lead healthy lives with proper treatment.
Genome Sequencing Speeds Up Rare Disease Diagnosis in Kids
A breakthrough NHS study reveals whole-genome sequencing provides diagnoses for rare genetic conditions two years earlier, offering families crucial answers and access to care. Read the inspiring story of three-year-old Nathaniel.
Genome sequencing helps diagnose rare child condition earlier
A breakthrough NHS study reveals whole genome sequencing is diagnosing rare genetic conditions in children two years sooner, transforming care for families like Nathaniel's in London.
The £250k-a-year fight against an invisible illness
At 26, Caitlin Magagna battles cystic fibrosis, an invisible genetic condition. Her story reveals the high costs and daily struggles, offering hope with new treatments. Discover her journey.
Samia Longchambon's 20-year Raynaud's disease secret
Coronation Street actress Samia Longchambon opens up about living with Raynaud's disease for two decades. Discover her coping tips and how she manages the circulation condition.
Experts: No Evidence Gut Microbiome Causes Autism
Leading scientists refute claims that gut bacteria cause autism, urging a shift in research focus towards genetics. Discover the facts behind the debate.
Mark Riddell's tearful reveal about daughter's rare disease
Rugby league star Mark Riddell breaks down discussing daughter Ava's Ogden Syndrome, affecting just four children in Australia. Read his inspiring family story.
Boy, 4, diagnosed with rare childhood dementia
A Swansea mum is in a desperate race against time after her four-year-old son Tate was diagnosed with Sanfilippo Syndrome, a rare and terminal childhood dementia.
UK toddler first in world with unique genetic condition
In an extraordinary medical breakthrough, 19-month-old Oscar Sparrow from West Midlands has been identified as the only person worldwide living with a never-before-seen genetic mutation, offering new hope for rare disease research.
Bullied for weight: Teen's rare genetic disorder revealed
A mother reveals how her daughter endured cruel bullying for years before doctors discovered her weight struggles were caused by rare Bardet-Biedl syndrome, exposing the hidden reality of genetic disorders.
Adam Henson reveals daughter's genetic condition diagnosis
BBC Countryfile presenter Adam Henson opens up about his daughter's genetic condition diagnosis and how it's changed his family's perspective on life and farming.
Cancer detection breakthrough spots genetic risks early
Groundbreaking research reveals new method to identify cancer-causing genetic changes early, potentially revolutionising preventative care and saving thousands of lives through timely intervention.
Child's battle with rare disease stealing her ability to walk
The heartbreaking story of Isabelle Tate, a young girl from England fighting Charcot-Marie-Tooth disease, a rare genetic condition threatening her ability to walk and enjoy a normal childhood.
Daughter, 21, dies after battle with rare neurological disorder
Isabelle Adora Tate's courageous battle against a devastating neurological condition ends at just 21, as her grieving mother pays emotional tribute to her 'beautiful warrior' daughter.
Daughter's rare condition breaks hearts daily
Exclusive: The heartbreaking story of a family coping with their daughter's rare Cri Du Chat syndrome, revealing the daily challenges and emotional toll of caring for a child with complex needs.
Woman speaks with Thai accent after stroke
A Hampshire woman developed Foreign Accent Syndrome after suffering a stroke, causing her to speak with a Thai accent despite never visiting Thailand. Medical experts explain this rare neurological condition.
Mum's heartbreak as son battles rare chromosome disorder
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.
Mother's heartbreaking baby loss story to rare condition
Jade Millner shares her emotional story of losing two babies to Patau's syndrome and her campaign for better baby loss support in the UK healthcare system.
Anne-Marie reveals son's rare genetic condition diagnosis
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.
NHS screens thousands for hidden genetic disorder
The NHS is rolling out a groundbreaking genetic testing programme to identify thousands of Britons with undiagnosed hereditary haemochromatosis - a dangerous iron overload condition that can cause organ damage if untreated.
America's Most Inbred Family: The Whittaker Story
An investigative journey into the lives of the Whittakers, known as America's most inbred family, uncovering their isolated existence and the genetic consequences of generations of intermarriage.
Britain's only patient with ultra-rare disease
Exclusive story of Dean Sims, the solitary UK case of Mandibuloacral Dysplasia, and his extraordinary journey through the healthcare system.
Study: Intense Exercise May Increase MND Risk
Groundbreaking research from the University of Sheffield suggests vigorous exercise may accelerate motor neurone disease onset in those with predisposing genes, challenging fitness norms.
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.
Diabetes gene breakthrough could transform treatment
Groundbreaking research reveals how a specific gene disrupts insulin production in the pancreas, offering new hope for millions living with diabetes worldwide.
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.
Women genetically more vulnerable to depression - study
Groundbreaking research uncovers significant genetic differences that make women more vulnerable to depression, challenging long-held assumptions about mental health gender disparities.
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