Advice on how to deal with epilepsy and seizures in schools, including how to recognise when a pupil might be having a seizure.

What is epilepsy?

Epilepsy can take many shapes and forms, but it can be summed up as the tendency to experience seizures. Seizures arise because of sudden bursts of excess electrical activity in the brain, causing disruption to normal brain functions. Seizures can affect people with epilepsy at any time. They usually only last for seconds or minutes, after which the brain generally returns to normal.

More than half a million people in the UK have epilepsy, which is around one in 100 people. Three quarters of sufferers experience their first seizure before the age of twenty. Around 80 per cent of children with epilepsy attend mainstream school. Most teachers, therefore, will teach a number of epileptic children during the course of their career, and can provide valuable support in helping to deal with the condition in a calm and reassuring manner, encouraging a positive and accepting attitude to the condition among other pupils in the class.

Epilepsy is a very individual condition, and every pupil with the condition will display different patterns and types of symptoms. In fact, the majority of children with epilepsy never have a seizure during the school day. It is because of this that it is particularly vital that a detailed individual health care plan is drawn up for every pupil with the condition. This should be devised in consultation with parents and medical staff, and should set out the particular pattern of the child’s epilepsy.

In particular, it would be useful to ask parents:

  • what type of seizures the child has
  • how long they last and what they look like
  • what first aid is appropriate and how long a rest the child may need
  • common triggers for the child’s seizures
  • how often is medication taken, and what the likely side effects are
  • whether there is any warning prior to the seizure, and if so, what form it takes
  • what activities might the parents or doctor place limits on
  • whether the child has any other medical conditions
  • to what extent the child understands their condition and its treatment.

It is important that as far as possible, children with epilepsy are included in all school activities. However, particular care may be required in specific areas, such as swimming lessons, technology or science practicals. In PE lessons it would be unwise, for example, to allow a child with epilepsy to climb ropes or wall bars. Any safety concerns should be addressed as part of the child’s individual care plan.

Recognising a seizure

There are about 40 different types of seizure, some affecting the whole brain, others only a part of it. Some seizures are easier to recognise than others. When only a part of the brain is affected, the child will remain conscious but might display such symptoms as twitching or jerking of a limb, sensations of pins and needles, or an unusual taste in the mouth. In cases where consciousness is affected, they might appear confused or start wandering around; they can also exhibit strange behaviour such as fiddling with objects or plucking at clothes. The child may subsequently have little or no memory of the seizure.

More serious forms of seizure, such as the ‘tonic-clonic’ or ‘grand-mal’ seizure, affect the whole of the brain and not just a part of it. Tonic-clonic seizures are characterised by loss of consciousness and convulsions that may last for a few minutes. Breathing may become difficult and the area around the mouth can turn a pale blue or grey colour. There may also be a loss of continence. Afterwards, the child is likely to be tired and/or confused. Some children will recover within a few minutes, but others may need to sleep for several hours.

The severity of the seizure is not necessarily dictated by the extent of the brain it affects. For example, if a pupil experiences an ‘absence seizure’, which affects the whole of the brain, there may be few visible indications that it is taking place, other than that an outward appearance that they are day-dreaming, looking ‘blank’ or staring. Such seizures can easily be mistaken for not paying attention in class.

Dealing with seizures

A number of factors may increase the likelihood of a child having a seizure. They can include:

  • anxiety or stress
  • tiredness
  • being unwell
  • flashing or flickering lights
  • certain geometric shapes or patterns.

Details of the types of triggers likely to affect an individual child should be detailed on their individual care plan so that staff can be aware of the need for care with particular activities. Most children with epilepsy do not have a problem using computers or watching television.

If a child has a seizure, teachers should observe the following guidelines, in addition to any specific advice given in the child’s individual care plan:

  • Remain calm and reassure others in the class.
  • Ensure that the child cannot harm themselves.
  • Only move the child if there is a danger of, for example, sharp or hot objects or electrical appliances.
  • Cushion the head with something soft, eg a folded jacket.
  • Do not attempt to restrict the child’s movements.
  • Do not put anything in the child’s mouth, including food or drink.
  • Loosen any tight clothing around the neck (care is needed not to frighten or alarm the child).
  • Once a convulsive seizure has stopped, place the child in the recovery position and remain with the child until they are fully recovered.
  • Re-assure the child and allow to rest and/or sleep as necessary, in a supervised, quiet place such as a medical room.

An ambulance should be called if:

  • it is the child’s first seizure
  • the child is badly injured
  • they are experiencing breathing difficulties
  • the seizure lasts for longer than the period set out in the child’s health care plan
  • the seizure lasts for longer than five minutes, and you do not know how long the child’s seizures usually last
  • there are repeated seizures, unless the child’s care plan states that this is normal for that child.

This information should be incorporated into the school’s emergency procedures as well as the child’s individual health care plan. This should also give background information and descriptions of the usual type or types of seizure experienced by the child and whether emergency intervention may be required. The plan should also set out whether the child should be sent home after a seizure.

In cases where the child tends to experience longer seizures, they may be prescribed rectal diazepam, or in some cases a solution of midazolam given orally or intra-nasally. In such cases it is vital that the school has clear procedures, drawn up in consultation with the child’s prescribing GP or paediatrician, on how and when it should be administered. Staff giving this medication must have received proper training from local health services, and the Department for Education (DfE) advises that it is best administered by two adults, at least one of whom is the same gender as the child. The NEU advises members to be particularly wary of volunteering to carry out such procedures, given the potential for accusations of abuse.


The majority of children with epilepsy are treated with anti-convulsants to prevent or reduce their seizures. It is not normally necessary for them to take this medicine during school hours. Where medication does need to be taken during the school day, reference should be made to the NEU health and safety briefing Administration of Medicines. Again, it is important to stress that where teachers have volunteered to administer any medicines, they should be provided with comprehensive training from appropriate health professionals.

Remember that teachers’ conditions of service do not include an obligation to administer medicines or to supervise a pupil taking them. The position may be different for support staff. It is for the management of a school to devise appropriate procedures to support children who need to take medicine at school.

If staff notice that a child’s seizures are on the increase, or that they appear sleepy, inattentive or hyperactive, they may need to have adjustments made to their medication. Such concerns should be discussed with the child’s parents who can take the necessary steps to inform the appropriate medical staff.

Reporting a seizure

Teachers and other school staff are in a comparatively good position to spot mild or sub-clinical forms of seizure which cannot be seen at all, but may be manifested by a drop in the standard of work or attainment by the child concerned.

Where any type of seizure is suspected, it should be reported immediately to the child’s parents. Such vigilance may not only help parents and medical staff to diagnose and manage the symptoms, it can also aid the child’s wellbeing and academic performance.

In reporting the seizure, the following information should be supplied:

  • What led up to the seizure (eg visual or auditory stimulus, anxiety etc)?
  • Specify any unusual feelings expressed by the child before the seizure.
  • Describe any parts of the body affected by the seizure, such as limbs or facial muscles.
  • Was the child unconscious?
  • Was there any incontinence?

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Epilepsy in schools

Advice on how to deal with epilepsy and seizures in schools, including how to recognise when a pupil might be having a seizure.