Seizures / Epilepsy

Sensory Needs, Social Care & Support, Behaviour & Mental Health, Parent Support

Types of Seizures in Children:
Children can experience various types of seizures, each with distinct characteristics. Here are some common types:

  • Absence Seizures: These seizures involve brief, sudden lapses in consciousness. A child may stare blankly into space for a few seconds, often without realising it. These seizures can occur multiple times a day and may be mistaken for daydreaming or inattentiveness.

  • Tonic-Clonic Seizures: Also known as grand mal seizures, these involve a combination of muscle stiffness (tonic phase) and jerking movements (clonic phase). The child may lose consciousness, fall to the ground, and experience convulsions. These seizures can last for a few minutes and may be followed by confusion or drowsiness.

  • Myoclonic Seizures: These seizures cause sudden, brief muscle jerks or twitches. They can affect the entire body or just one part, such as the arms or legs. Myoclonic seizures often occur shortly after waking up.

  • Atonic Seizures: Also known as drop attacks, these seizures cause a sudden loss of muscle tone, leading to the child collapsing or falling. They can result in injuries due to the sudden loss of control.

  • Focal Seizures: These seizures originate in one specific area of the brain and can cause various symptoms depending on the affected region. They may involve unusual sensations, movements, or behaviours. Focal seizures can be simple (without loss of consciousness) or complex (with impaired awareness).


What to Do If You Suspect Your Child Has Epilepsy:
If you suspect your child has epilepsy, it’s important to take the following steps:

  • Consult a Healthcare Professional: Schedule an appointment with your child’s paediatrician or a neurologist. They can conduct a thorough evaluation, including medical history, physical examination, and possibly diagnostic tests such as an EEG (electroencephalogram) to monitor brain activity.

  • Keep a Seizure Diary: Document the details of each seizure, including the date, time, duration, and any specific symptoms or triggers. This information can help healthcare providers make an accurate diagnosis and develop an effective treatment plan.

  • Ensure Safety: During a seizure, ensure your child’s safety by removing any nearby objects that could cause injury. Place them on their side to prevent choking and avoid restraining their movements. Stay calm and reassure your child once the seizure ends.

  • Follow Medical Advice: If your child is diagnosed with epilepsy, follow the prescribed treatment plan, which may include medications to control seizures. Regular follow-up appointments with the healthcare provider are essential to monitor progress and adjust treatment as needed.

  • Educate and Support: Educate yourself, your child, and other caregivers about epilepsy and seizure management. Support groups and resources can provide valuable information and emotional support for families dealing with epilepsy.


Seizure Passport: Purpose and Benefits

Purpose: A Seizure Passport is a vital document designed to provide essential information about an individual’s epilepsy and seizure management. It serves as a quick reference guide for caregivers, medical professionals, and emergency responders, ensuring that they have access to accurate and up-to-date information about the person’s condition. The Seizure Passport typically includes details about the individual’s seizure types, triggers, medications, emergency contact information, and specific instructions for managing seizures.

The benefits of a Seizure Passport include:

  • Improved Emergency Response: It ensures that medical professionals and emergency responders have immediate access to critical information, allowing them to provide appropriate and timely care during a seizure.

  • Enhanced Communication: It facilitates clear communication between the individual, their caregivers, and healthcare providers, reducing the risk of misunderstandings and errors in treatment.

  • Personalised Care: It provides tailored information about the individual’s specific needs and preferences, ensuring that they receive personalised care that aligns with their unique condition.

  • Increased Confidence: It empowers individuals with epilepsy and their caregivers by providing them with a comprehensive and easily accessible document that outlines their seizure management plan.

You must be logged in to view this content.