Having Epilepsy can affect a child in different ways and the impact can vary, depending on their age and the type of seizures the child has. For some children, having a diagnosis of Epilepsy will not affect their day-to-day lives. For others it may be frightening or difficult to understand. They may feel embarrassed, isolated or different in front of their peers.
Encouraging your child to talk about their concerns may help them to feel more positive.
Seizures are often focal and include twitching, numbness or tingling of the child’s face or tongue, and may interfere with speech and cause drooling. Sometimes they can progress into a tonic-clonic seizure. Seizures usually happen in early stages of sleep. Medication is not always needed.
Some children’s seizures happen in response to triggers such as stress, excitement, missed medication or lack of sleep. Keeping a diary of their seizures can help to see if there are any patterns to when seizures happen. If you recognise triggers, avoiding them as far as possible may help to reduce the number of seizures your child has.
Getting enough sleep and well-balanced meals, will help keep your child healthy and may help to reduce their seizures.
For some children, having Epilepsy and taking AEDs will not affect their behaviour. However, some people may notice a change in their child’s mood or behaviour such as becoming irritable or withdrawn. Some children may be responding to how they feel about having Epilepsy and how it affects them.
For more information: https://www.epilepsy.org.au/