Juvenile myoclonic epilepsy

Juvenile myoclonic epilepsy (JME) is a type of epilepsy that begins typically in adolescence. It is characterized by sudden, brief muscle jerks called myoclonic seizures, often occurring soon after waking. Some individuals may also experience additional seizure types, such as absence seizures or generalized tonic-clonic seizures. JME is thought to have a genetic component and is usually managed with medication to control seizures. While it is a lifelong condition, proper treatment allows many people to lead active lives with minimal interruptions. Regular medical care and medication adherence are key to managing JME effectively.