Mum Fears All Her Children Could Die Before 35 After Genetic Test Results Were Missed Friday, May 22, 2026 genetics friedreichsataxia autism diagnosis childhood nhs genetictesting caregiving raredisease family Sarah Bingham, a 39-year-old mother from Weston-super-Mare, is grappling with the devastating news that her 14-year-old son Caleb has been diagnosed with Friedreich’s ataxia, a rare and progressive genetic condition that … Read More
Mother Fears All Her Children Could Die Before 35 After Missed Genetic Test Results Friday, May 22, 2026 genetics friedreich’sataxia autism meningitis diagnosis healthcare neurodegenerative caregiving family nhs Sarah Bingham, a 39-year-old mother from Weston-super-Mare, faces a heartbreaking reality after discovering her 14-year-old son Caleb has Friedreich’s ataxia, a rare progressive genetic condition that could limit his life … Read More
Somerset Woman’s Ultra-Rare Blood Frozen to Save Lives for Up to 30 Years Friday, March 13, 2026 blood rarity donation nhsbt transfusion frozen raretype sicklecell pregnancy genetics Mina Stoddart-Stones from Bridgwater, Somerset, is recognized as a VIP blood donor due to her extraordinarily rare blood type. At just 26 years old, she is one of only nine donors in the UK with a unique combination of blood … Read More
Bath Dad’s Inspiring Mission to Raise Awareness for Ultra-Rare Genetic Disorder Affecting Only 3,500 Worldwide Monday, August 11, 2025 phelan-mcdermid genetics raredisease awareness fundraising charity disability autism cureshank jenson Tom Giles, a father of three from Bath, has undertaken an extraordinary journey to raise awareness about Phelan-McDermid Syndrome (PMS), an ultra-rare genetic condition diagnosed in just 3,500 people worldwide. His son … Read More
Bath Dad's Epic Run to Raise Awareness for Ultra-Rare Phelan-McDermid Syndrome Monday, August 11, 2025 phelanmcdermid genetics raredisease awareness cureshank bath fundraising autism genetesting charityrun Tom Giles, a father of three from Bath, has undertaken an extraordinary mission to raise awareness about Phelan-McDermid Syndrome (PMS), an ultra-rare genetic disorder affecting only around 3,500 people worldwide. This … Read More