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10 articles
Waiting for a neurology appointment can feel like an uncertain interval with no clear task. This calm, UK-focused guide sets out how to keep a useful record, prepare focused questions and recognise when to seek urgent help, without trying to diagnose yourself or step outside NHS pathways.
Photosensitive epilepsy is a specific seizure trigger, not a general sensitivity to screens or blue light. This guide separates genuine risk from everyday screen fatigue and sets out practical UK steps for gaming, streaming, workplace displays and cinema in 2026.
A suspected first seizure can leave people with more questions than answers. This guide explains how UK first seizure clinics work in 2026, what tests may or may not be needed, and how to prepare for a calm, useful appointment.
A school epilepsy healthcare plan is most useful when it is treated as a working agreement rather than a form filed once. This guide sets out what UK parents and carers can reasonably ask for in 2026, from staff training and rescue-medication protocols to reviews around trips, exams and transitions.
Sleep and epilepsy influence one another in ways that are easy to miss during a busy week. This guide explains why night-time seizures and sleep deprivation matter, how shift work complicates the picture, and how UK patients can build a calm routine and know when to ask for a sleep assessment.
The move from paediatric to adult epilepsy care is rarely a single appointment. This UK guide for young people and parents explains what to ask before the handover, how to keep records and medication summaries clear, and how families can shift responsibility without stepping away.
Wearables and apps that claim to detect seizures can offer useful reassurance, but the evidence is uneven and the limitations matter. This calm review sets out what UK users should ask before relying on alerting technology in 2026.
A seizure diary should make neurology appointments more useful, not turn daily life into a data-entry task. This guide sets out a practical minimum record for UK patients and carers, how to spot patterns sensibly, and how to share information securely with a clinician.
Most seizures stop on their own, but some need urgent help. This guide explains the red flags that should prompt a 999 call, what to do while waiting, and how a personal epilepsy care plan can make decisions clearer for families, carers and workplaces.
Epilepsy care in the UK is rarely delivered by one clinician alone. This practical guide explains who typically does what, how to keep records and messages connected, and what to do when a referral or medication review appears to stall.