Children and adolescents with epilepsy experience significant long-term socioeconomic consequences and higher personal health care costs. The findings come from a study that followed young epilepsy patients until 30 years of age.
The study--which included more than 11,000 Danish youths with epilepsy and more than 23,000 controls--found that people with epilepsy, even many years after diagnosis, are neither able to compensate nor catch up with their peers in relation to overall health, education, and social status.