Anna Bird says the decision by some NHS integrated care boards to impose a two-year minimum wait is harmful to young people and their families

Blocking assessments of children with neurodivergent conditions for over two years is cruel to children, deeply damaging to families and ultimately more costly to taxpayers (NHS bodies in England impose two-year minimum wait for ADHD and autism assessments, 25 September).

Imagine the long-term harm inflicted on a six-year-old child forced to wait two years for an assessment of a physical condition. Waiting for a diagnosis of autism or ADHD is no different. That’s a quarter of a child’s life, and ultimately their potential, put on hold by state bodies that should be supporting all children. It prevents young people receiving the medical and practical assistance they need to learn, make friends and achieve the ordinary things that other children can every day.

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