The Difficult Journey of a Child with Dravet Syndrome: Perspectives from a Parent and the Neuropaediatrician.

The Difficult Journey of a Child with Dravet Syndrome: Perspectives from a Parent and the Neuropaediatrician.

Publication date: Sep 19, 2025

Dravet syndrome (DS) is a rare and severe form of epilepsy, characterised by recurrent seizures that begin during the first year of life, leading to motor, cognitive and behavioural impairments. This article provides the perspectives of a parent of a child with DS (‘Ethan’) and the treating neuropaediatrician. Ethan’s seizures began when he was 9 months old, and were a mixture of focal seizures and status epilepticus. Numerous treatments were tried, including standard anti-seizure medications (such as levetiracetam, clobazam and fenfluramine), other medications (cannabidiol) and nonpharmacological approaches (ketogenic diet), with little success. When Ethan was 3 years old, a prolonged episode of status epilepticus precipitated by coronavirus disease 2019 (COVID-19) led to brain damage. Rehabilitation allowed Ethan to regain some of his previous functioning and, at the age of 38 months, combination therapy with clobazam, sodium valproate and stiripentol was begun and has successfully controlled Ethan’s seizures. Ethan’s father describes the stress that the diagnosis of DS, interactions with the healthcare system, and the search for effective treatment imposed on the family. Since Ethan’s seizures have been better controlled, the family has been able to lead a more normal life, and is now focused on supporting Ethan and looking to the future. Ethan’s neuropaediatrician outlines the approach she takes to the diagnosis and management of DS, including the importance of the clinician-parent relationship in imparting the diagnosis and making initial and ongoing treatment decisions. The preferred first-line treatment is sodium valproate, which is followed by sodium valproate-clobazam-stiripentol combination therapy, topiramate or a ketogenic diet as second-line options. In children > 2 years, cannabidiol and fenfluramine can also be considered. The aim of maintenance treatment (which will invariably be polytherapy) is to reduce the number of seizures, particularly status epilepticus, given the significant impact of this seizure type on patients and caregivers.

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Concepts Keywords
38months Caregiver perspective
Coronavirus Dravet syndrome
Neuropaediatrician Epilepsy
Old Status epilepticus
Seizures

Semantics

Type Source Name
disease MESH Dravet Syndrome
disease MESH epilepsy
disease MESH seizures
disease MESH status epilepticus
drug DRUGBANK Levetiracetam
drug DRUGBANK Clobazam
drug DRUGBANK Fenfluramine
drug DRUGBANK Cannabidiol
drug DRUGBANK Spinosad
disease MESH coronavirus disease 2019
drug DRUGBANK Stiripentol
drug DRUGBANK Tropicamide
drug DRUGBANK Topiramate
disease MESH Syndrome
disease MESH shock
disease MESH emergency
disease MESH tremors
disease MESH uncertainty
disease MESH anxiety
drug DRUGBANK Coenzyme M
drug DRUGBANK Midazolam
drug DRUGBANK Diazepam
drug DRUGBANK Etoperidone
drug DRUGBANK Water
drug DRUGBANK Medical air
drug DRUGBANK Trestolone
drug DRUGBANK Thiopental
disease MESH coma
disease MESH panic
drug DRUGBANK Nonoxynol-9
disease MESH infection
disease MESH live births
disease MESH death
disease MESH SUDEP
disease MESH febrile seizure
disease IDO blood
drug DRUGBANK L-Valine
disease MESH recurrence
drug DRUGBANK Isoxaflutole
drug DRUGBANK L-Phenylalanine
drug DRUGBANK Phenobarbital
disease MESH sequelae
pathway REACTOME Release
drug DRUGBANK Ibuprofen
drug DRUGBANK Pentaerythritol tetranitrate
pathway REACTOME Reproduction
drug DRUGBANK Ilex paraguariensis leaf
disease MESH chronic disease
disease MESH encephalopathy

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