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Epilepsy Foundation of San Diego

Camping with the Epilepsy Foundation of San Diego County

The Epilepsy Foundation of San Diego County invites our epilepsy community to share their thoughts as we explore partnerships with San Diego-based organizations to develop two unique camping experiences—one for kids & teens ages 8–17 with epilepsy, and another for families impacted by epilepsy.

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We’re excited to partner with the YMCA of San Diego County to explore a summer overnight camp experience for children and teens ages 8–17 living with epilepsy.

Important: All camps will have on-site, trained medical staff available to assist with seizures and any other medical needs, so families can feel confident and supported.

Camps would run Sunday through Friday and may be hosted at YMCA Camp Marston or YMCA Raintree Ranch. Camp Marston—San Diego’s oldest and best-known overnight camp—offers a classic outdoor camp experience, while Raintree Ranch is a western-themed paradise with a special focus on horseback riding and animal care.

Campers would enjoy outdoor adventures, group activities, and meaningful opportunities to build friendships in a supportive, inclusive environment where they can be themselves, try new things, and grow in confidence.

Help us plan a camp experience for kids & teens in 2026! We’re committed to developing a camp experience fitting for our community. If your child or teen may be interested in attending a summer overnight camp in 2026, please fill out our Kids & Teens Camp Interest Form.

NOTE: This form is not a registration, but your responses will help guide camp planning and offerings.

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We’re also excited to explore the opportunity to offer a Family Camp weekend experience for families impacted by epilepsy, in partnership with the YMCA of San Diego County or the Boys to Men Mentoring Network.

This Friday–Sunday outdoor camp experience will be designed to bring families together for connection, rest, and fun in a supportive and inclusive environment.

Family Camp offers a chance to step away from daily routines, build meaningful relationships with other families who understand the epilepsy journey, and enjoy shared activities that strengthen family bonds.

Camp sessions will either be hosted at YMCA Camp Marston or the Boys to Men Mentoring Mt. Palomar property—both beautiful settings focused on community, confidence-building, and belonging.

Help us plan a family weekend camp experience  in 2026! If your family may be interested in attending a weekend camp experience in 2026, please fill out our family camp interest form.

NOTE: This form is not a registration, but your input is incredibly valuable. We look forward to exploring this opportunity together and imagining what Family Camp could become for our community.

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Epilepsy Foundation of San Diego

Epilepsy Foundation of San Diego County on Transportation Access and Innovation

SAN DIEGO – “Safe, reliable transportation remains one of the greatest barriers for many individuals living with epilepsy. For those who cannot drive, getting to work, school, or a doctor’s appointment can take hours – multiple transfers, delays, and limited routes turn simple errands into exhausting journeys. For someone managing seizures, that unpredictability can be overwhelming.

Many in our community depend on public transit because they have no other choice and are often left out of the conversation. MTS is an essential service, but it simply isn’t meeting the needs of riders living with epilepsy and other disabilities. Long waits and inconsistent schedules can mean missed medical care, lost income, or trips abandoned altogether.

The constant possibility of a seizure also turns crowded public settings into a source of anxiety and stigma. Experiencing a seizure on a packed bus or busy station can be traumatic, for the individual and for those who may not know how to respond. More options mean fewer risks, fewer barriers, and greater independence.

Waymo’s arrival in San Diego matters because it represents possibility – shorter and more affordable trips, safer travel, and greater autonomy. It offers dignity, choice, and access to the everyday moments many take for granted.

This is not an either/or issue. We applaud efforts to strengthen MTS while expanding access to new mobility solutions. When San Diegans living with epilepsy have multiple transportation options, they gain opportunity – employment, healthcare, education, and true connection to their community.

We look forward to what this progress will bring and encourage local leaders to prioritize accessibility and innovation for those who need it most.”

– Rick Burritt, President and CEO
Epilepsy Foundation of San Diego County
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Epilepsy Foundation of San Diego

SUDEP Community Conversation: Bringing Awareness with Compassion

Sudden Unexpected Death in Epilepsy (SUDEP) is a fatal complication of epilepsy, occurring without warning and often in individuals with uncontrolled or frequent seizures.

If you’re unfamiliar with SUDEP, you’re not alone. It’s a topic that’s often overlooked or not openly discussed, even within the medical and epilepsy communities. It isn’t the easiest topic to talk about but that’s exactly why we need to talk about it.

During a virtual support session hosted on Thursday, October 2, we were honored to have Dr. James Grisolia, neurologist and epilepsy specialist, alongside a courageous family, Lynnette and Kent, who shared their lived experience of losing their son, Tim, to SUDEP.

Their stories and expertise helped us understand more about:

  • What SUDEP is and who it affects.
  • Risk factors and preventive strategies.
  • How to have meaningful conversations with care teams and loved ones.

This meaningful conversation brought SUDEP into the light but with compassion, honesty, and community—giving families the tools, information, and confidence they need to make informed decisions, reduce risk, and feel supported.

For those who were unable to attend the workshop or would like to review SUDEP materials, please review the SUDEP Facts and Dare to Say SUDEP documents by tapping on the following buttons.

If you or anyone else you know has been impacted by SUDEP or any epilepsy-related loss, we host monthly bereavement groups to help support families in their time of grief. Please reach out to Sarah Waters, MSW, ASW, at sarah@epilepsysandiego.org if you’re in need of support.

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Epilepsy Foundation of San Diego

Many Thanks to the Mattei Family

We are honored and deeply grateful to share that the Epilepsy Foundation of San Diego County (EFSDC) has been named as a beneficiary of the Lee E. Mattei Family Trust, receiving a generous gift of approximately $175,000. We are also receiving an additional $47,000 from Ruth Mattei’s IRA, bringing the total impact of this contribution to over $220,000 in support of our mission.

Half of this remarkable contribution will support the Foundation’s ongoing charitable programs, while the other half has been used to establish a permanent endowment—the Epilepsy Foundation / Lee E. and Ruth S. Mattei Fund. The income generated from this fund will be used in perpetuity to further the charitable mission of EFSDC, helping to ensure long-term support for individuals and families affected by epilepsy.

Ruth S. Mattei, who passed away at the age of 101, met her husband Lee Mattei in San Diego. They were married for over 60 years until Lee’s passing in 2011. She was preceded in death by their only son, Gary. Together, Ruth and Lee built a successful development company responsible for many residential and commercial projects that helped shape San Diego’s historic growth.

Their legacy of building community continues through this incredible gift, and we are proud to honor their memory by carrying their generosity forward.

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Epilepsy Foundation of San Diego Our Programs

Empoderando a Nuestras Comunidades Hispanohablantes

En la Fundación de Epilepsia del Condado de San Diego (EFSDC), estamos comprometidos a garantizar que las personas y familias de habla hispana tengan acceso a los recursos, la educación y el apoyo que necesitan. A través de nuestro Programa de Alcance en Español, colaboramos con organizaciones comunitarias locales para conectar directamente con clientes hispanohablantes y aumentar la concientización sobre la epilepsia.

Nuestros objetivos incluyen:

  • Reducir el estigma que rodea a la epilepsia en las comunidades de habla hispana.
  • Ofrecer capacitaciones en primeros auxilios para crisis epilépticas en español para empoderar a familias y cuidadores.
  • Aumentar la concientización sobre la frecuencia de la epilepsia y su impacto.
  • Ampliar el acceso a los programas, servicios y grupos de apoyo de EFSDC disponibles en español.

Al fortalecer estas conexiones, ayudamos a que más familias se sientan informadas, apoyadas y empoderadas mientras navegan los retos que implica vivir con epilepsia.

Para más información, contacto Marie Picazo, (619) 296-0161 x114 o Marie@epilepsysandiego.org.

Empowering Our Spanish-Speaking Communities

At the Epilepsy Foundation of San Diego County (EFSDC), we’re committed to ensuring that Spanish-speaking individuals and families have access to the resources, education, and support they need. Through our Spanish Outreach Program, we’re partnering with local community organizations to connect directly with Spanish-speaking clients and increase awareness about epilepsy.

Our goals include:

  • Reducing stigma surrounding epilepsy in Spanish-speaking communities.
  • Offering seizure first aid trainings in Spanish to empower families and caregivers.
  • Raising awareness about how common epilepsy is and its impact.
  • Expanding access to EFSDC’s programs, services, and support groups available in Spanish

By strengthening these connections, we’re helping more families feel informed, supported, and empowered when navigating epilepsy.

For more information, contact Marie Picazo, at (619) 296-0161 x114 or Marie@epilepsysandiego.org.

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Epilepsy Foundation of San Diego Events

Sharon’s Ride.Run.Walk. in April will help spread awareness and raise money for San Diegans with Epilepsy.

SAN DIEGO (KUSI) – Feb. 14 is International Epilepsy Day. Epilepsy is the worlds 4th most common neurological disorder.

On April 24, 2022, Sharon’s Ride. Run. Walk. will help educate, spread awareness, and raise critical funds to make a difference for the 50,000 San Diegan’s living with Epilepsy.

During this event you can either choose to bike ride 15 -miles or run/walk the 5k.

Registration is open now! Register or fundraise for the event at: https://www.epilepsysandiego.org/

On Good Morning San Diego, KUSI’s Paul Rudy talked with Wendy Urushima-Conn, President & CEO of the Epilepsy Foundation of San Diego, about the Ride, Run, Walk coming up in April.

1 In 10 People Will Have A Seizure In Their Lifetime
1 In 26 Will Be Diagnosed With Epilepsy

This article was originally published by KUSI News.

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Epilepsy Foundation of San Diego

National Epilepsy Awareness Month

Living with epilepsy can have its challenges. Some people with epilepsy hide their disorder, which can lead to feelings of isolation, helplessness and even depression. Adults with epilepsy oftentimes experience changes in their quality of life, such as mobility, relationships, employment, and social interactions. Children and teens with epilepsy find themselves feeling isolated and misunderstood; they may lose friends, may not be invited to birthday parties, or may be ostracized or even teased or bullied at school.

Epilepsy affects everyone. Everywhere. Period. Thanks to YOU, we have upped our game to better serve YOU.

The Epilepsy Foundation provides programs and education to make a safer place for YOU. The Epilepsy Foundation raises awareness and funds to provide help and serve YOU. The Epilepsy Foundation advocates for new laws to address issues that affect YOU. The Epilepsy Foundation invests in research and innovation to bring new therapies and technology to YOU faster than ever.  Let’s take action together and make November the loudest and purple-est National Epilepsy Awareness Month ever for YOU! This November, be everywhere. Educate everyone.

Get involved and help spread awareness:

Join us at our Upcoming Events

Take Action for Everyone Affected by Epilepsy

Share your action with your friends, family and followers to help them better understand epilepsy and inspire our community. Create a social media post telling us why it is important to take action for epilepsy.

#MyNEAMAction #NEAM2022

Fundraise Your Way to Help Fund Our Programs & Services

Start a Fundraiser on Facebook on behalf of the Epilepsy Foundation of San Diego and help raise awareness and critical funds for the San Diego epilepsy community.

#MyNEAMAction #NEAM2022

Get Seizure First-Aid Ready to Help Save a Life

Did you know that 1 in 10 people will have a seizure in their lifetime?

Make sure you are prepared to help a loved one, coworker, peer, or someone else in your life. Learn #SeizureFirstAid basics this November by taking our 30-minute, on-demand #SFAReady course HERE or contact us for personalized training at no cost. #MyNEAM Action

Donate to the Epilepsy Foundation of San Diego

Make a direct impact on the no-cost programs and services our foundation provides including training programs on seizure recognition and first aid, college scholarships, as well as access to specialty and suppotive care for the more than 50,000 people living with epilepsy here in San Diego.

In the News

Our President & CEO Wendy Urushima-Conn talks about National Epilepsy Awareness Month and our Gingerbread City fundraising gala on KUSI’s Good Morning San Diego.

Challenges of Epilepsy: Stats

 
  • 150,000 new cases of epilepsy occur each year in the U.S.

  • 470,000 children have epilepsy

  • 336,000 kids have at least one seizure annually.

  • 30% of people with epilepsy do not gain full control of their seizures and continue to struggle day-to-day with the threat of imminent seizures.

  • 32% of adults with epilepsy can’t work, compared with 7% of adults without epilepsy who can’t work.

  • 29% of adults with epilepsy can’t use a car or public transit to get places, compared with 8% of adults without epilepsy.

  • 21% of adults with epilepsy can’t pay for medicines vs. 9% without epilepsy.

  • 4 in 10 kids who had at least one seizure in the past year live in homes at or close to the poverty level.

  • 3 in 10 kids who had at least one seizure in the past year live in homes without enough food.

Our Mission

With your help, The Epilepsy Foundation of San Diego County improves the lives of people affected by epilepsy through education, advocacy, research, and connection. 

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Epilepsy Foundation of San Diego Events

The Epilepsy Foundation of San Diego County hosts the Gingerbread City Gala

SAN DIEGO (KUSI) – The annual 28th Gingerbread City Gala hosted by the The Epilepsy Foundation of San Diego County will take place at the San Diego Air & Space Museum in December.

CEO of the foundation Wendy Urushima-Conn goes on to tell us more about the event on December 9th.

The Epilepsy Foundation of San Diego County offers various services for those affected by the neurological disorder. They offer support groups, counseling, scholarship, first-aid, and more..

If you are interested in the event, you can buy tickets on their website: Epilepsy Foundation of San Diego.

This article was originally published by KUSI News.

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Epilepsy Foundation of San Diego Events

Epilepsy Foundation to Host Gingerbread City Drive-Thru Event at Liberty Station

‘Tis the season for giving and helping others and the latter may be especially important this season due to the extra hardships brought upon countless communities by the coronavirus pandemic.

In typical years, year-end galas and holiday fundraisers would be held to help those in need. This year, however, has organizations shifting to virtual events or modifying their plans to keep attendants safe. The Epilepsy Foundation of San Diego County will be one of those organizations as they host their annual fundraising event but this time, with a twist.

The organization’s Gingerbread City will be a drive-thru affair at Liberty Station that will feature awe-inspiring (and delicious) gingerbread structures. The sweet aroma of the holiday classic cookie will be accompanied by festive music and decorations.

The event takes place this Saturday from 11 a.m. to 4 p.m.

And the best part? You’ll safely be in your car the whole time there.

“We have 11 gingerbread artists joining us this year and when I say artists, it’s not like me building a little house from Michael’s,” said Wendy Urushima-Conn, President & CEO, of Epilepsy Foundation of San Diego County. “They are these incredible pastry creations so we have a working mom who is an incredible artist on the side. We also have someone who has been on the Food Network and has won in their pastry challenge.”

The Epilepsy Foundation has been serving the San Diego community since 1954, offering personal advocacy and counseling, seizure first-aid training, and various services like expressive arts therapy and camp.

All of these services are free and available to anyone whose life is touched by epilepsy. That number may be more than you think; 50,000 San Diegans are impacted by the disorder.

Those who are interested in supporting The Epilepsy Foundation with this festive event can purchase tickets online.

Tickets start at $25 per car and the event is expected to sell out due to limited capacity. There are VIP upgrades available that include getting a family photo with Santa and a take-home wine and cheese package.

All of the money raised goes back into the foundation and the services it provides.

This article was originally written by NBC 7 San Diego.