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Program Contents
The S.E.E. program is designed for persons with epilepsy, family members, and for parents of children with epilepsy. The program works for kids with epilepsy and their brothers and sisters over 12 years of age.
Since the information and skills taught in S.E.E. are award-winning and state-of-the-art, professionals who want to improve their knowledge, expand their clinical skills, and earn continuing education credit make up an important part of the audience.
The S.E.E. program has two basic goals: 1) No seizures and no side effects, and 2) Get your life back.
The S.E.E. program is designed to give you or your family member the information and skills needed to get the best chance of becoming seizure free – without letting treatment become part of the problem. By the time the Medical Aspects of the program is completed, you should feel so confident in dealing with epilepsy that you can spend more time and energy getting on with the rest of your life.
The Psychosocial Aspects provide the understanding and skills you need to get your life back. Epilepsy doesn’t just affect the body. For many, the emotional, family, and social challenges of epilepsy are worse than the seizures. The second part of the program shows you how you can take back control of your feelings, your family, and your future. It is filled with ways to cope that work.
To get an idea of how much the program offers and the new knowledge and practical coping skills you will receive, review the contents of the Medical Aspects of the program and the Psychosocial Aspects of epilepsy.
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