Gain insight as you read the stories of women living with epilepsy-- told in their own words. Women discuss the impact of epilepsy on their roles as mothers, wives, and individuals, and express their concerns about how epilepsy will affect pregnancy outcome, the health of their babies, and parenting. They share candidly how epilepsy impacts family planning, fertility and sexuality.

A collection of personal stories from friends, family members, and co-workers of people with epilepsy in which they describe their observations and feelings about witnessing seizures and about the person with epilepsy. Epilepsy in Our View shed light on the social consequences of epilepsy while increasing understanding of what's happening when a person has a seizure.

This collection of frank, first-person narratives by people with epilepsy from 21 countries offers unique perspectives on the personal and social aspects of seizure disorders. Reflecting a diverse array of cultures, the narratives reveal many common concerns and show the distinct ways that people around the world affected by epilepsy react to the diagnosis and cope with their families, friends, and communities. The book includes chapters on the Global Campaign Against Epilepsy and a physician's firsthand experience in East Africa.

This enlightening book presents the firsthand personal accounts of children with seizure disorders and their parents. In their own words, these children and parents vividly describe the experiences of handling the crisis of the initial seizure, adjusting to the diagnosis of epilepsy, coping with seizures, managing medications and side effects, and dealing with health care providers, teachers, schoolmates, siblings, and friends. Reveals the terror, uncertainty, and frustration felt by children and parents after an initial seizure or a diagnosis of epilepsy. Documents the ongoing trials,...

The book reveals, for the first time, the wide range of emotions, challenges and triumphs experienced by those who work with epilepsy patients and their families. The book also records the profound, uplifting and often heartbreaking experiences of practitioners with seizures who have come to understand, first hand, the perspective of patients with epilepsy.

In Our Words: Personal Accounts of Living with Non-Epileptic Seizures shows those diagnosed with PNES that they are not alone, and how others have courageously managed to come to terms with their seizures. These heartfelt personal accounts will also allow family, friends, healthcare providers and researchers to gain more understanding of the condition and work to provide a better quality of life to those living with PNES.