Programs and Events

Through our website, phone and email/mail, we offer bilingual information, referral and resources to individuals and families affected by epilepsy in order to inform, support and empower in the fight against epilepsy and in pursuit of a better quality of life.

Local Helpline Services:
1.800.564.0445 | Email
9:00 a.m. to 5:00 p.m. (Mon-Friday, excluding Holidays)

24/7 Helpline Services:
1.800.332.1000 | En Español: 1.866.748.8008

Information Packet

Free Information Packet includes:

• Epilepsy info and resources
• Invitation to a program, event or group
• Seizure first aid and safety instructions
• Seizure Alert bracelet/necklace (on request)
• Pillboxes

Support Groups meet periodically for information updates and benefit from two-way sharing in an understanding, empathetic group setting. Each group meeting may have a different topic or focus but, over a period of time, participants will benefit from the education, socializing, self-help, and idea-sharing that occurs. Please join a Group if you desire to learn more and/or connect with others.

Throughout the year we offer activities and outings for adults with epilepsy and their guests to make and renew friendships, learn something new, and have fun together. Events vary depending on interest and funding.

Our supportive care program offers Family Events so families of children with epilepsy can connect with others in fun, social environments. The events offer a chance to meet and learn from others in a fun setting. Parents are able to talk to a specialist. Siblings are able to meet other siblings who understand, because we recognize the impact a chronic illness has upon the entire family.

We offer a Family Weekend Camp and Teen Retreat for children and their immediate relatives – siblings, parents/guardians – to connect with others and have fun in a safe and supportive environment. Activities include arts & crafts, woodshop, fishing, archery, boating, swimming, indoor/outdoor games, and much more!  

Families and individuals can obtain basic epilepsy information on the phone and/or by scheduling an “Epilepsy 101”. Attendees learn about epilepsy, treatments and tips+tools for living with epilepsy.

Families and individuals can obtain basic epilepsy information on the phone and/or by scheduling an “Epilepsy 101”. Attendees learn about epilepsy, treatments and tips+tools for living with epilepsy.

We are eager to educate our community about epilepsy. Schools, employers and agencies can request a presentation. We encourage the organizers to schedule a couple presentations on the same day or to invite all your employees and/or personnel from a wider region together for the presentation. There may be a presentation fee to help cover the cost of transportation and staff time. Limited scholarships for trainings are available.

From time to time we offer or partner with others to offer educational programs - conferences, webinars, seminars - with content of interest to those affected by epilepsy. They are designed to connect the community affected by epilepsy to information and to each other.

Epilepsy Foundation Kids Crew is a program for kids ages 14 and under of all abilities, with three areas in mind: 1. Creating epilepsy awareness to help educate family, friends, and your community. 2. Sharing your stories so that others can learn from your experiences. 3. Participating in Lemonade for Livy, the Purple Pumpkin Project, and local walks. Kids are some of the best advocates, make a difference, and can make a tremendous impact on the community with their experience.

Individual advocacy is when someone comes alongside to help you solve a problem or challenge or overcome a barrier in your life or in the life of your loved one with epilepsy. Based on our staffing and your needs, individual advocacy assistance may be provided in different ways: – Help advocate with and for you to address your need in the arenas of healthcare, school or workplace. – Refer you to another community, professional, legal resource or organization that specializes in your area of need, such as legal advocacy, individual (civil) or disability rights. – Invite you to a training on how to be a more effective self-advocate. – Provide epilepsy training in your school or workplace to help promote understanding, safety and accommodation. – Refer you to an experienced peer-mentor who can advise you.

Recognizing the need for a united voice for people with epilepsy in California, we helped create and continue to be involved as an active founding member of Epilepsy California.

Adults with epilepsy who need college or vocational training scholarships may request information about this scholarship program. Request information and forms

The Epilepsy Walk Los Angeles is a fun-filled community event – with a serious cause – that gives everyone an opportunity to share their story of epilepsy, learn more about epilepsy, and connect with others affected by epilepsy — all while raising funds.

The ultimate goal of Care+Cure is no child diagnosed with epilepsy. Until we achieve that dream we strive to ensure that all children with epilepsy can get timely access to specialty care and their families can have greater hopes for cures.

Nuestro personal bilingüe ofrece servicios a las familias de habla hispana. Estos servicios incluyen una conferencia anual, conferencias educativas, eventos sociales y materiales educativos que están a disposición de la comunidad hispana en general.