Illinois
Seizure Safe Schools - Status
Select your state below for information about Seizure Safe Schools laws and legislation in your area.
The chart below shows the provisions of the model bill that were included in the legislation and enacted into law
| Seizure safe schools components | Illinois |
|---|---|
| Effective Date | July 1st, 2020 |
| School Type | Primary or Secondary Public, Private, and Charter Schools |
| Seizure Action Plan |
Yes: The plan must be submitted to the school by the parent/guardian in consultation with their doctor, and will also be provided to anyone who transports a student with epilepsy to a school-sponsored activity |
| School Personnel Training Mandate |
Yes: All staff must receive training in the basics of seizure recognition and appropriate first aid emergency protocols. Additional training must be provided to the delegated care aid who helps the student in accordance with their seizure action plan |
| School Nurse Training Mandate |
Yes: As part of the staff-wide mandate |
| Delegation of Rescue Medication |
Yes |
| Student Training Mandate |
No |
| Good Samaritan Clause |
Yes |
Please contact the national advocacy team at [email protected] or contact your local Epilepsy Foundation office with questions.
This summary was developed for informational purposes by the Epilepsy Foundation and reflects a review of data available as of January 2023. Information is subject to change. This law does not impact federal education laws like Section 504 or the Individuals with Disabilities Education Act (IDEA). This summary does not constitute legal advice. Please contact [email protected] with questions or the 24/7 helpline at 1-800-332-1000.
Currently, there is not an enacted law for your state. Many states are laying the groundwork for Seizure Safe Schools bills or have even introduced legislation. We are working alongside advocates and organizational partners to pass this legislation in all 50 states and Washington, D.C. If you are interested in learning more about your state’s legislative efforts on this issue or would like to become involved, please contact the national advocacy team at [email protected] or contact your local Epilepsy Foundation office.