Epilepsy Foundation of Idaho

Safety and Seizures

When people are told they have epilepsy (often called a seizure disorder), they often think the worst. They feel somehow "different" and think their lives must change.

They may be told a lot more about what they cannot do than what they can do. They (or their loved ones) may worry about the risk of injuries from seizures, brain damage, or even death.

We all live with risks in our daily lives, and having epilepsy may increase those risks, at least for some.

However, epilepsy and seizures affect people in different ways. Some people may have to make several changes in their lives to live more safely. For others, very few changes will be needed.

A lot depends on the kind of seizure each person has, how often they happen, and the kinds of things that are important in that person's life.

If you have a seizure disorder, this information is to help you think about any risks you may face and to offer ways to help you live a safe and active life.

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Disclaimer

This information is based on common experience. It does not reflect the level of risk or need for safety measures of any individual. People vary in their need for safety measures and readers with seizures are warned not to base lifestyle changes on this material without first consulting a physician.

Epilepsy Foundation of Idaho

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