Articles

  • 1 month ago | bbc.com | Seb Cheer |Oliver Day |Georgey Spanswick

    'Only 60 people in the UK have our daughter's genetic condition'Seb Cheer, Oliver Day & Georgey SpanswickBBC/Seb CheerThree-year-old Autumn is "one in a million" because of her rare genetic conditionThe family of a three-year-old girl with one of the UK's rarest genetic conditions are faced with the prospect of relocating to another city in order to get treatment for her. Autumn, who lives near York, has Hyper-IgE syndrome, which affects her immune system and requires daily antibiotics.

  • Mar 26, 2025 | bbc.com | Hayley Coyle |Seb Cheer

    Customers warn of cafe closure 'social impact'Hayley Coyle & Seb CheerBBCAdrian Haigh Hutchinson says the closure in Elland will cut him off from some of his peersThe supermarket giant said a raft of changes announced on Monday would redirect cash to other parts of the business, with 365 employees now at risk of redundancy. The BBC spoke to shoppers in Elland to hear how the move would affect them.

  • Dec 8, 2024 | yahoo.com | Seb Cheer

    Nishath and Kenya said the anonymous surveys offered an opportunity to raise issues [BBC]Generate Key TakeawaysData from one of the world's largest health studies is helping teachers understand how they can better support their pupils. Born in Bradford has followed the lives of more than 13,500 babies born in the city between 2007 and 2010, with findings influencing local decision-making.

  • Dec 1, 2024 | yahoo.com | Grace Wood |Seb Cheer

    The Rob Burrow Centre for Motor Neurone Disease will receive a sapling grown from the Sycamore Gap tree as part of the Trees of Hope project. Following the felling of the famous tree on Hadrian’s Wall in Northumberland in September 2023 the National Trust has awarded 49 saplings to charities across the UK. Ian Flatt, who has motor neurone disease (MND), put the application forward for the Leeds centre to receive a tree.

  • Nov 26, 2024 | msn.com | Julia Bryson |Seb Cheer

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