Epilepsy at School

Elementary school aged boy with glasses and a backpack walks down a path to school.

Use these tips to make sure your child with epilepsy is safe and supported during the school day.

Parents often feel a mix of excitement and worry as a new school year begins. “Back to school” time may be a lot different for many families this year, depending on where you live.

Parents of students with epilepsy and seizures often have extra concerns about safety. As your child with epilepsy returns to school, use these tips to keep them safer during the school day.

1. Make a Seizure Action Plan.

A Seizure Action Plan contains the essential information school staff may need to help a student who has seizures. It includes first aid steps, parent and health care provider contact information, and medicines that may be needed during the school day. See an example of a Seizure Action Planpdf iconexternal icon from the Epilepsy Foundation.

2. Help school staff get trained.

CDC partners with the Epilepsy Foundation to deliver free training programs to school staff. Talk to your child’s school to see if school personnel could participate in these programs.

The Epilepsy Foundation also offers a free, online Seizure Recognition and First Aid Certificationexternal icon program that anyone can take to learn how to recognize a seizure, provide first aid, and when to call for help. This program is helpful for families, friends, caregivers, and others your child may interact with before and after the school day.

3. Help other students understand epilepsy.

Teen girl smiles as she sits in a classroom, writing on a piece of paper.

Use these tips to make sure your child with epilepsy has the support she needs to stay safe at school.

Teachers can find resources on CDC’s Body and Mind (BAM) website. There, they can learn more about epilepsy, what a seizure looks like, stigma and bullying, and how to provide seizure first aid.

4. Find Support

If you have questions about epilepsy, want to find others to talk to online or in a local support group, or want to find community events, visit CDC’s Find Support page.

Parents of teens may have specific concerns about how to manage epilepsy as their children become more independent. CDC’s You Are Not Alone Parent Toolkit can help! Learn from other families as they talk about driving, dating, medicine, stress, school problems, and other important issues. Parents can use the toolkit on their own or lead a support group.