Spinal muscular atrophy18 Jul 2024Doctors failed to warn mother about pregnancy riskHull University Teaching Hospitals NHS Trust says steps have been taken to avoid any repetition.18 Jul 2024Hull & East Yorkshire1 Mar 2024'I knew Snowdon would be a challenge'A Race up Wales highest mountain in all terrain wheelchairs1 Mar 2024Somerset23 Feb 2024'Ticking time bomb' for service after staff changeCharities representing people living with neuromuscular conditions raise concerns about future treatment.23 Feb 2024Northern Ireland10 Dec 2023'Atlantic' challenge to fund toddler's treatmentTwo-year-old Oakley Moffatt has a rare muscle-wasting disease and needs specialised physiotherapy.10 Dec 2023Bristol6 Nov 2023Indians who need a $2.1m drug to fight rare diseaseMost people with rare genetic diseases are unable to access life-saving medicines due to high costs.6 Nov 2023India31 May 2023Twins forecast not to live past seven turn 18Sam and Alex Bolton plan to go to university and want to become TV presenters.31 May 2023Derby2 Sep 2022'Without an assistant I can only shower once a week'Baroness 'fears' disabled people could end up in care homes over lack of personal assistants.2 Sep 2022Disability3 Aug 2022India teen who died but raised millions to save brotherAfra Rafeeq, who died this week, had raised millions of rupees to help get a crucial drug for her baby brother.3 Aug 2022India4 Jul 2022Baby blood test 'could prove life-changing'A County Tyrone mother wants babies tested at birth so those with a rare condition are treated quickly.4 Jul 2022Northern Ireland