It is essential for all people with epilepsy to have ready access to quality care that appropriately suits their individual needs. Epilepsy California must ensure a full range of medication and treatment types are available to those that require any level of care.
To help prevent breakthrough seizures, Epilepsy California strongly encourages notification and informed consent of both patient and physicians before changing or replacing a patient's medication in any way. Antiepileptic drugs (AEDs) are very precise and establish a delicate balance for each individual with epilepsy. Any slight change to medications can cause breakthrough seizures. Because the therapeutic window is often very narrow for people with epilepsy it is critical that each individual have access to the medication that provides the best outcome for them.
Individuals with prolonged or clustered seizures sometimes are prescribed an emergency seizure rescue medication to be administered by a caretaker. Current State laws and regulations are not consistent and prevent children in schools and adults in residential care facilities from receiving the medication. Epilepsy California seeks to work with State education and health groups to develop a life-saving plan that will support our students and our resident adults.
Due to the varied nature of epilepsy, Epilepsy California opposes across-the-board seizure-free requirements, and endorses individualized evaluations of ability to drive. California remains one of six states that currently requires mandatory physician reporting. Epilepsy California will continue to support efforts to change state laws or regulation to reverse mandatory reporting.
Epilepsy California promotes the expansion of civil right laws to ensure that people with epilepsy have essential protections from discrimination based on disability in any part of life, including the workplace.