A Blantyre mother has spoken out over the difficulties her disabled daughter has faced accessing financial support, prompting an apology from the government.
Lisa Devine, 43, is the full-time carer for her 18-year-old daughter Erin (pictured), who was born with microcephaly, a neurological condition affecting brain development. Erin also has cerebral palsy, scoliosis and learning difficulties, requiring round-the-clock care and assistance with everyday activities.
However, Blantyre Telegraph has learned following an application for Universal Credit, the family was told that medical evidence from their GP was insufficient and that Erin would need a further assessment to determine whether she was capable of working.
Lisa has expressed her frustration at having to repeatedly demonstrate her daughter’s lifelong disabilities, describing the process as unnecessary and deeply stressful.
The Department for Work and Pensions has apologised for the difficulties faced by the family, confirming that work-related requirements have been suspended while Erin’s circumstances are assessed. Officials say they are working to progress her case as quickly and sensitively as possible.
The situation has raised wider concerns about the challenges facing families caring for young adults with significant disabilities, particularly when transitioning into adult benefits.
For Lisa, the priority remains ensuring Erin receives the financial support and protection she needs without further unnecessary delays.
Should families caring for young people with lifelong disabilities have to undergo repeated assessments to prove they need support?
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