Newborn's fight against rare HLH disease after sudden fever
A newborn baby's life turned upside down by a rare autoimmune disorder. His parents share their story and hope as he prepares for a bone marrow transplant. Read their emotional journey.
A newborn baby's life turned upside down by a rare autoimmune disorder. His parents share their story and hope as he prepares for a bone marrow transplant. Read their emotional journey.
The NHS has issued crucial guidance for millions taking amlodipine or ramipril for hypertension. Learn about the risk of low blood pressure and essential medication interactions to discuss with your GP.
Millie Fairley, 13, from Eastbourne, needs a stem cell donor after being diagnosed with aplastic anaemia. Her family and DKMS urge people to register as donors.
Millie Fairley, 13, from Eastbourne, has aplastic anaemia. Her family's urgent plea for a stem cell donor could save her life. Find out how you can help.
Millie Fairley, 13, from Eastbourne, has aplastic anaemia and needs a stem cell donor to survive. Her family and DKMS urge people to register as donors.
Annaliese Holland, 25, shares her decision for assisted dying after a lifelong battle with a rare autoimmune disorder. Read her powerful story of pain and peace.
Health experts reveal how adding beetroot to your winter meals can improve blood circulation, regulate blood pressure, and keep your extremities warm. Discover delicious recipe ideas today!
Celine Dion delivers a positive health update on Instagram, sharing a heartfelt Thanksgiving message with fans while battling Stiff Person Syndrome. Discover her inspiring journey.
Coronation Street star Samia Longchambon shares her 20-year experience with Raynaud's disease, offering practical tips for managing the painful circulation condition. Discover her story and advice.
Money expert Martin Lewis was unable to donate blood due to a minor medical issue but is now urging the public to support the NHS. Find out if you're eligible to help.
New DNA analysis reveals Adolf Hitler had Kallmann syndrome, a rare genetic condition impacting puberty. Discover the findings and what it means.
Relly Ladner was told she might never walk again after Guillain-Barré syndrome. Defying odds, she now runs marathons. Read her incredible recovery journey.
Hollywood actor Jesse Eisenberg makes heartfelt plea for NHS blood donors after discovering his family's life-saving connection to UK health service.
British families warned after teenager's shocking medical case reveals dangerous complication of severe chest infections. NHS doctors share crucial symptoms to watch for.
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.
Exclusive investigation reveals dozens of children in India contracted HIV after receiving contaminated blood transfusions, exposing critical gaps in medical safety protocols.
A major healthcare failure in India's Madhya Pradesh state sees a thalassemia patient contract HIV after receiving contaminated blood transfusion, sparking nationwide outrage and investigations.
The US Food and Drug Administration proposes lifting restrictions on blood donations from British citizens, marking a significant policy shift for American healthcare safety protocols.
The devastating story of Sarah, a mother with rare dementia who can no longer recognise her own children, as her family fights for access to revolutionary treatment that could save her.
A revolutionary stem cell treatment has successfully cured a British patient's rare blood disorder, marking a significant breakthrough in medical science through the Anthony Nolan registry.
A mother's terrifying ordeal as her healthy son suddenly develops rare neurological condition ADEM, sparking urgent NHS investigation into childhood illness.
Victims of the NHS infected blood scandal demand Chancellor Rachel Reeves overhaul compensation rules that could cost them millions in lost payments and tax liabilities.
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.
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.
Exclusive: Cabinet Office faces mounting criticism as HIV and hepatitis victims continue waiting for compensation amid ongoing public inquiry revelations.
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.
A scarce 2009 Kew Gardens 50p coin has sold for over double its face value in a recent auction, sparking renewed interest in coin collecting across the UK.
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.
Former Geordie Shore personality Aaron Chalmers reveals his young son Oakley faces unexpected hospital procedure while battling rare genetic condition that requires ongoing medical care.
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.