District of Columbia
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 | District of Columbia |
|---|---|
| Effective Date | March 7, 2025 |
| School Type | All Public, Public Charter, and Private Schools |
| Seizure Action Plan |
Yes, must be submitted by a parent/guardian or student’s healthcare provider, kept as part of the student's record, and shared with relevant staff. |
| School Personnel Training Mandate |
Yes, the D.C. Department of Health must offer voluntary seizure awareness training 3 times per school year starting June 1, 2025. |
| School Nurse Training Mandate |
No |
| Delegation of Rescue Medication |
Yes, a trained employee or agent of the school may administer seizure treatment to the student in accordance with the student’s seizure action plan. |
| 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.