Case Study 4

22 July 2025

S has been with KEYFORT for four years, her condition is a genetic disorder part of deletion of chromosomes which includes; Type 1 diabetes, Hypothyroidism and Epilepsy. S’s condition is very rare and around 5 people in the UK has the same condition. KEYFORT started support after the pandemic so our aim and mission was to get S back out being a social butterfly again and accessing the community with supporting her nursing needs. S now accesses day centre twice a week socialising with her support team and friends around her.

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