How epilepsy can affect education
Last updated 08 Feb 2010, review date due 08 Feb 2012
There are many reasons why a child with epilepsy might have special educational needs (SEN). Some of these reasons are described below.
Seizures
Seizures can mean that your child loses learning time. This can be direct (for example due to absence seizures in lessons) or indirect (for example if your child needs to rest after a seizure). Partial seizures can distract a child from their task, or cause strange or repetitive behaviours, which might not be recognised as a seizure by school staff.
Difficulties with memory, concentration and skills
Epilepsy can interfere with the way the brain works. Many people with epilepsy experience difficulties with short and long term memory, and this can lead to difficulties in picking up skills and information.
Underlying damage to the brain and sensory impairments
If the epilepsy is a result of damage to the brain, there may be other effects such as changes to personality or behaviour, and learning difficulties or disabilities. This might include difficulties in specific skill areas such as language and memory. Some people with epilepsy have impairments to their senses.
Sub-clinical seizure activity
This is epileptic activity which disrupts brain activity, without a seizure happening. This type of activity is quite rare. It can impair the brain’s processes, although the person might appear not to be affected.
Anti-epileptic medication (AEDs)
The routine medicines taken for epilepsy can have side-effects including dizziness and sleepiness, and some can affect memory. Some AEDs can also cause changes to mood or behaviour, making children depressed, confused or hyperactive.
Psychological factors
The diagnosis of epilepsy can be a long and complex process. Being diagnosed with epilepsy can have a big impact on the child and their family, and this may affect the child’s behaviour. Some children with epilepsy feel isolated or different, and some feel angry or guilty about their condition. Relationships within the family may also be altered by a diagnosis of a long term condition.
Social factors
The attitudes and behaviour of others can have a significant effect on a child with epilepsy. This includes being treated differently by adults such as teachers and teaching assistants, as well as by other children. The attitudes of other children will be affected if a child with epilepsy is excluded from activities.
We can provide references and information on the source material we use to write our epilepsy advice and information pages. Please contact our Epilepsy Helpline by email at helpline@epilepsy.org.uk.
- Information for...
- Information on...
- Fundraise
- Donate
- Membership
- Campaigns
- Take epilepsy action campaign
- Automatic substitution of anti-epileptic drugs
- National commissioning of paediatric epilepsy surgery
- National Epilepsy Week
- Save our Sapphires, protecting all epilepsy specialist nurse posts
- Women's campaigns
- Epilepsy in England: time for change
- 'Epilepsy Aware' scheme for GP practices and pharmacies
- Campaign Supporters' Group
- Surveys
- News
- Research
- Our services
- Forum
- About us
Epilepsy advice and information
- What is epilepsy?
- Caring for a baby or young child when you have epilepsy: a detailed guide
- Children
- Depression and epilepsy
- Developing epilepsy in later life
- Driving and epilepsy
- Education
- Higher education
- Parents and carers in England and Wales
- Parents and carers in Northern Ireland
- Support available for young people with epilepsy taking GCSE and GCE exams at school or college
- Education professionals
- Entitlements and benefits for people with epilepsy
- Epilepsy and learning disabilities
- Epilepsy and Travel abroad
- Epilepsy information for prisons
- Epilepsy, osteoporosis and osteomalacia
- Epilepsy: diagnosis, treatment and healthcare in the UK
- Epileptic seizures explained
- Flu and epilepsy
- Identity jewellery
- Inheritance
- Me and my dad
- Memory
- Mobile phones and epilepsy
- Photosensitive epilepsy
- Safety advice for people with epilepsy
- Sports and leisure
- Stress and epilepsy
- Sudden unexpected death in epilepsy (SUDEP)
- Syndromes
- The Disability Discrimination Act
- The Equality Act and epilepsy
- Vagus nerve stimulation therapy in epilepsy
- Work and epilepsy
- Women and epilepsy
- Young people and epilepsy
- Epilepsy Action and the Information Standard
- The Epilepsies: You, Epilepsy and the NICE Guideline
- Epilepsy Action Information Reviewers (EAIRs)
- Technical editing/writing and copyright
Epilepsy Helpline
- UK freephone 0808 800 5050
- International +44 113 210 8850
- Email: helpline@epilepsy.org.uk
- Twitter: epilepsyadvice
- Txt msg: 0753 741 0044 info






