What is an individual healthcare plan?
Every young person with epilepsy in school should have an individual healthcare plan (IHP), setting out information about their condition and the support they need to be safe and included at school.
The IHP should describe their seizures, how their condition is best managed, and the impact it has on their learning and behaviour, including any anti-seizure medication side effects. A clear emergency protocol must also be included, including when an ambulance should be called.
The IHP should be developed jointly between the school, the young person, their parents or carers, and healthcare professionals. The responsibility for its implementation remains with the school and the IHP should clearly set out who will deliver which aspects of support.
As epilepsy can be a fluctuating condition, IHPs should be reviewed annually, or sooner if circumstances have changed. Parents should be reminded to keep the school informed of any changes in seizure activity, medication or behaviour.
An IHP is needed even if a young person’s seizures are currently controlled by treatment, because seizures may reoccur and epilepsy may still be having an impact on the young person’s learning and behaviour.