LCLilia Colledge

1. Article · Jul 9, 2026 · Lilia Colledge

   Family takes on year of challenges to raise money in memory of friend (opens the original)

   Excerpt · Positive tone · English

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   A family has taken on a year of physical challenges in memory of a close friend and colleague. The Carter family from Norwich are raising funds for the Motor Neurone Disease Association after the death of Tim Angell. Mr Angell died in November last year after being diagnosed with the condition. Following his death, the Carter family decided to dedicate a year to fundraising in his memory. The family on Scafell (Image: Submitted) Freya Carter, who worked with Mr Angell, said: "As a family, we hav

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2. Article · Jul 8, 2026 · Lilia Colledge

   Four-year-old girl known as 'social butterfly' faces life with rare genetic disorder (opens the original)

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   A young girl is facing life with a rare genetic disorder that has left her unable to walk. Four-year-old Libby Bevis, from Dereham, was diagnosed 18 months ago with CDG - PMM2 subtype, which affects her neurological development, mobility and balance. Her mother, Melissa Prince, said there was “a lot of guesswork” involved when early signs of global developmental delay became apparent. Libby is described as a “social butterfly” who loves playing pretend, especially with her dolls. She shares her

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