Learn why team Walk4Joshua walks at Epilepsy Walk LA on April 28.
"We walk for our sweet grandson, Joshua James Godfrey, who was diagnosed with epilepsy at 1 ½ years old and passed away from SUDEP (Sudden Unexpected Death in Epilepsy) at age 6.
By walking, we hope to bring awareness to epilepsy and SUDEP to keep his memory alive, find a cure and help save lives."
The fight to END EPILEPSY is personal. Who or what inspires you to take action? Share your reason for walking to END EPILEPSY and tag us with #ShareMyShoes. 💜
Support, donate, and take action at EpilepsyWalkLA.org
Learn why team Walk4Joshua walks at Epilepsy Walk LA on April 28.
"We walk for our sweet grandson, Joshua James Godfrey, who was diagnosed with epilepsy at 1 ½ years old and passed away from SUDEP (Sudden Unexpected Death in Epilepsy) at age 6.
By walking, we hope to bring awareness to epilepsy and SUDEP to keep his memory alive, find a cure and help save lives."
The fight to END EPILEPSY is personal. Who or what inspires you to take action? Share your reason for walking to END EPILEPSY and tag us with #ShareMyShoes. 💜
Support, donate, and take action at EpilepsyWalkLA.org
THANK YOU @jcrew! 🛍️ This Saturday, April 20 from 12pm - 3pm - head to J.Crew in Century City for a special event! Shop in-store and 10% of your purchase will support Epilepsy Foundation Los Angeles and the fight to End Epilepsy! See you there!
For more info: https://jcrewxepilepsyfoundation.splashthat.com/
THANK YOU @jcrew! 🛍️ This Saturday, April 20 from 12pm - 3pm - head to J.Crew in Century City for a special event! Shop in-store and 10% of your purchase will support Epilepsy Foundation Los Angeles and the fight to End Epilepsy! See you there!
For more info: https://jcrewxepilepsyfoundation.splashthat.com/
Learn why team Cat Walk joins us at Epilepsy Walk LA. 💜
"The Cat Walk team strides in honor of our beloved Cat Tana-Acosta, fondly known as "Katana" for her keen ability to cut through life`s illusions and guide us towards what truly matters. Cat confronts a severe form of epilepsy, more profound than Dravet Syndrome. Despite being four years old and not yet taking her first steps, she instills in us the courage to stand up for others. Though she communicates without words, she emphasizes the significance of listening. Above all, she embodies unconditional love. Cat, both our daughter and our mentor, represents the millions affected by epilepsy. We walk to celebrate her and all those impacted by this condition, extending an invitation for you to join us."
The fight to END EPILEPSY is personal. Who or what inspires you to take action? Share your reason for walking to END EPILEPSY and tag us with #ShareMyShoes. 💜
Support, donate, and take action at EpilepsyWalkLA.org
Learn why team Cat Walk joins us at Epilepsy Walk LA. 💜
"The Cat Walk team strides in honor of our beloved Cat Tana-Acosta, fondly known as "Katana" for her keen ability to cut through life`s illusions and guide us towards what truly matters. Cat confronts a severe form of epilepsy, more profound than Dravet Syndrome. Despite being four years old and not yet taking her first steps, she instills in us the courage to stand up for others. Though she communicates without words, she emphasizes the significance of listening. Above all, she embodies unconditional love. Cat, both our daughter and our mentor, represents the millions affected by epilepsy. We walk to celebrate her and all those impacted by this condition, extending an invitation for you to join us."
The fight to END EPILEPSY is personal. Who or what inspires you to take action? Share your reason for walking to END EPILEPSY and tag us with #ShareMyShoes. 💜
Support, donate, and take action at EpilepsyWalkLA.org
We want to give a special thanks to Platinum Sponsor @waymo for their support to Epilepsy Walk LA on April 28 at the Rose Bowl! Their ongoing support means a lot to us and is helping us make this event possible! ✨ Together, we`re creating positive change and empowering our epilepsy community.
We want to give a special thanks to Platinum Sponsor @waymo for their support to Epilepsy Walk LA on April 28 at the Rose Bowl! Their ongoing support means a lot to us and is helping us make this event possible! ✨ Together, we`re creating positive change and empowering our epilepsy community.
🗓️ Just TWO WEEKS until the big day! 🚶♀️ Can you feel the excitement building? Lace up your shoes, gather your team, and join us as we take strides towards the fight to End Epilepsy. Together, we`re making a difference! Register now and let`s walk for everyone living with epilepsy.
Take Action: EpilepsyWalkLA.org
🗓️ Just TWO WEEKS until the big day! 🚶♀️ Can you feel the excitement building? Lace up your shoes, gather your team, and join us as we take strides towards the fight to End Epilepsy. Together, we`re making a difference! Register now and let`s walk for everyone living with epilepsy.
Take Action: EpilepsyWalkLA.org
Learn why Team Super Xavier joins us at Epilepsy Walk LA again. 💜
"We are walking again this year as a community to support Team Super Xavier and the Epilepsy Foundation of Los Angeles. This is our 5th year participating in this event! The Epilepsy Walk LA event has brought our family community together to show support. We feel the love and support from family, friends and co-workers who generously donate to our team, keep us in prayers, and join our squad each year. Our son Xavier was diagnosed with epilepsy in 2016 at the age of 1. He underwent cranial surgery at CHLA in 2022. We are happy to say that he has been seizure-free since then. We are very grateful for the extended community that we have through the Epilepsy Foundation of Los Angeles, which has allowed us to connect with other parents, normalize emotions, share experiences, and not feel alone in this journey."
The fight to END EPILEPSY is personal. Who or what inspires you to take action? Share your reason for walking to END EPILEPSY and tag us with #ShareMyShoes. 💜
Support, donate, and take action at EpilepsyWalkLA.org
Learn why Team Super Xavier joins us at Epilepsy Walk LA again. 💜
"We are walking again this year as a community to support Team Super Xavier and the Epilepsy Foundation of Los Angeles. This is our 5th year participating in this event! The Epilepsy Walk LA event has brought our family community together to show support. We feel the love and support from family, friends and co-workers who generously donate to our team, keep us in prayers, and join our squad each year. Our son Xavier was diagnosed with epilepsy in 2016 at the age of 1. He underwent cranial surgery at CHLA in 2022. We are happy to say that he has been seizure-free since then. We are very grateful for the extended community that we have through the Epilepsy Foundation of Los Angeles, which has allowed us to connect with other parents, normalize emotions, share experiences, and not feel alone in this journey."
The fight to END EPILEPSY is personal. Who or what inspires you to take action? Share your reason for walking to END EPILEPSY and tag us with #ShareMyShoes. 💜
Support, donate, and take action at EpilepsyWalkLA.org
🌟 A heartfelt THANK YOU to our Leading Sponsor @olitasuncare for your unwavering support and commitment to Epilepsy Walk Los Angeles on April 28 at the Rose Bowl! Your generosity is making a real impact, and we`re deeply grateful for your partnership. Together, we`re creating positive change and empowering our epilepsy community.
#EpilepsyWalkLA #EndEpilepsy #EpilepsyLosAngeles
🌟 A heartfelt THANK YOU to our Leading Sponsor @olitasuncare for your unwavering support and commitment to Epilepsy Walk Los Angeles on April 28 at the Rose Bowl! Your generosity is making a real impact, and we`re deeply grateful for your partnership. Together, we`re creating positive change and empowering our epilepsy community.
#EpilepsyWalkLA #EndEpilepsy #EpilepsyLosAngeles
Learn why team Sparks Stripes Walks 💜
"We are the Sparks family. We walk for Kyllian who was diagnosed at 8 months old due to her rare neurological condition. The symbol for rare medical conditions is a zebra and that is why we are team Sparks Stripes. Please join us to end epilepsy and advocate for all rare seizure types and diagnoses."
The fight to END EPILEPSY is personal. Who or what inspires you to take action? Share your reason for walking to END EPILEPSY and tag us with #ShareMyShoes. 💜
Support, donate, and take action at EpilepsyWalkLA.org
Learn why team Sparks Stripes Walks 💜
"We are the Sparks family. We walk for Kyllian who was diagnosed at 8 months old due to her rare neurological condition. The symbol for rare medical conditions is a zebra and that is why we are team Sparks Stripes. Please join us to end epilepsy and advocate for all rare seizure types and diagnoses."
The fight to END EPILEPSY is personal. Who or what inspires you to take action? Share your reason for walking to END EPILEPSY and tag us with #ShareMyShoes. 💜
Support, donate, and take action at EpilepsyWalkLA.org
The Assembly Transportation Committee on Monday approved Senate Bill 357…
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Senator Portantino Bill Protecting Drivers with Epilepsy Approved by Senate Judiciary Committee
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The Senate Transportation Committee on Wednesday approved Senate Bill 357.
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