Father and son die from same rare genetic syndrome
A mother from Kent shares her heartbreaking story after losing her husband and son to Alagille Syndrome. She now runs a bereavement group to support others. Read her powerful message.
Category : Search result: genetic disease prevention
Father and son die from same rare genetic heart syndrome
A mother from Kent speaks out after her husband and son died from Alagille Syndrome, a rare genetic disorder. She now runs a bereavement group to support others. Read her story.
Jesy Nelson twins diagnosed with rare genetic disease SMA
Pop star Jesy Nelson reveals her newborn twins have spinal muscular atrophy. Learn the early signs of SMA Type 1 and why early diagnosis is crucial for treatment.
Jesy Nelson twins diagnosed with rare genetic disease
Pop star Jesy Nelson reveals her newborn twins have spinal muscular atrophy. Learn the early warning signs of SMA Type 1 and why early diagnosis is crucial.
Jesy Nelson's Twins Diagnosed with Spinal Muscular Atrophy
Former Little Mix star Jesy Nelson reveals her eight-month-old twin daughters have been diagnosed with Spinal Muscular Atrophy. The singer shares her emotional journey and vows to be their ultimate role model.
Jesy Nelson's twins diagnosed with rare SMA disease
Former Little Mix star Jesy Nelson reveals her newborn twins have SMA Type 1. Experts explain the crucial early warning signs of this rare genetic condition that all parents should watch for.
Jesy Nelson's twins diagnosed with SMA
Former Little Mix star Jesy Nelson shares devastating health news about her eight-month-old twin daughters, diagnosed with the genetic condition Spinal Muscular Atrophy. Learn about SMA and the family's journey.
Jesy Nelson reveals twin daughters' SMA diagnosis
Former Little Mix star Jesy Nelson shares emotional health update after her eight-month-old twins, Ocean and Story, are diagnosed with Spinal Muscular Atrophy. Learn about the condition and the family's journey.
Gene editing breakthroughs need a new social contract
Rapid advances in gene editing, like the recent sickle cell treatment, require a new social contract to ensure equitable access and ethical governance. Read our analysis.
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.
GMB: Kate Garraway comforts guest after mum's kidney death
Good Morning Britain's Kate Garraway offered heartfelt support to guest Genieva Owens, who lost her mum to kidney failure linked to a genetic risk. The interview highlights urgent calls for APOL1 gene screening in Black communities. Read the full story.
'Rusting' Brain Flaw Found in Childhood Dementia
A single genetic error causing brain cells to 'rust' has been identified in devastating childhood dementia. This breakthrough offers new hope for treatments in Alzheimer's and other neurodegenerative diseases. Read the full story.
Food Mistakes Raising Cancer and Heart Disease Risk
A leading doctor reveals how simple dietary swaps, like choosing whole fruit over juice and grilled over breaded chicken, can dramatically lower your risk of chronic illness. Learn the facts.
UK boy is only person in world with deadly condition
Oli-Jay Morris, 2, is the only known person with a unique gene mutation. His family are fundraising £14,000 for a personalised treatment plan to save his life.
10 Deadly Genetic Diseases Risk, Warns GP
A leading GP reveals 10 deadly hereditary conditions many are unaware they risk. Learn your family medical history and how to take preventative action today.
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.
Daily Exercise Can Beat Heart Disease Symptoms
New research reveals how moderate daily activity can significantly reduce coronary heart disease risk and symptoms. Discover the life-changing benefits of consistent exercise for your heart health.
Stop condensation overnight with 50p hack
Discover the simple 50p hack that prevents condensation from forming on your windows overnight, saving you from mould and damp problems this winter.
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.
Late Nights and Chaotic Eating Increase Heart Disease Risk
Groundbreaking research reveals how irregular sleep patterns and unpredictable meal times could be silently damaging your cardiovascular health. Experts warn these common modern habits pose serious risks.
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.
NFL's Nick Mangold reveals kidney disease diagnosis
Former New York Jets centre Nick Mangold reveals his private health struggle with kidney disease in an emotional interview, sharing his journey from NFL glory to facing a life-changing diagnosis.
Wanted App: Retailers' New Weapon Against Shoplifting
UK retailers are deploying an innovative smartphone application that enables real-time sharing of shoplifter images and information, creating a powerful digital neighbourhood watch against retail crime.
Neck size may predict heart disease risk, study finds
Groundbreaking research suggests measuring neck circumference could be a simple yet effective way to assess cardiovascular health risks in British adults.
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.
Teen's death from rare Charcot-Marie-Tooth disease
The heartbreaking story of Isabelle Tate, a vibrant teenager whose life was cut short by the little-known genetic condition Charcot-Marie-Tooth disease, sparking urgent calls for greater awareness and research funding.
Tennessee HFMD Outbreak: Health Alert Issued
Health officials in Tennessee issue urgent warning as highly contagious hand, foot and mouth disease spreads rapidly through communities. Learn the key symptoms and prevention measures.
Tennessee HFMD Outbreak: Health Officials Issue Warning
Health officials in Tennessee report significant surge in contagious hand, foot and mouth disease cases, with schools and childcare centres particularly affected. Learn about symptoms and prevention.
Gum Disease Increases Dementia and Stroke Risk - Study
Groundbreaking research reveals how poor oral health could be silently damaging your brain, with gum disease sufferers facing significantly higher risks of dementia and strokes.
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