Creators to Follow: Epilepsy Advocacy Edition ♿️🧠✨
Celebrating Disability Pride Month means diversifying our feeds! Today I am highlighting three game-changing resources in the epilepsy space that focus on community care, humor, and raw honesty:
🎙️ The What the EF?! Podcast
Life with seizures comes with a lot of "what the...?" moments. This podcast brings together advocates, researchers, and everyday warriors to chat about everything from medication side effects to the funny stories no one else talks about.
🌴 @socal.epilepsy
An incredible grassroots account focused on bringing Southern California families together. They excel at breaking down complex neurological facts into accessible, beautiful graphics while hosting real-world community events.
💫 @lucca.epilepsy
Lived-experience advocacy at its finest. They showcase the daily realities, joys, and challenges of navigating a dynamic disability, putting a relatable human face on a highly stigmatized condition.
Swipe through to see content from them! ➡️
#DisabilityPride #ChronicIllnessSupport #LearnOnLemon8 #PodcastRecommendations #CommunityCare




























































