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Trending Reels

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#Raseing Reel by @thecameronboycefoundation (verified account) - 🚨 New podcast! How do we use social media for good? This episode welcomes Dr. Jessica Lowe, a double board-certified neurologist and epileptologist w
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@thecameronboycefoundation
🚨 New podcast! How do we use social media for good? This episode welcomes Dr. Jessica Lowe, a double board-certified neurologist and epileptologist who is nationally recognized for her innovative public education efforts as @doctorbrainbarbie Also joining the conversation is Miles Levin! His film @underthelightsfilm has become a movement to break the stigma surrounding epilepsy. This episode explores how social media can help reduce stigma, share reliable information, and build community for people living with epilepsy — while also navigating its challenges responsibly. Thank you to @ucb_usa for making this podcast possible!
#Raseing Reel by @herkindofbrave_podcast - EPISODE DROP 🎙️ In this episode of Her Kind of Brave, Olivia shares what life looks like living with epilepsy and navigating chronic illness - incl
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@herkindofbrave_podcast
EPISODE DROP 🎙️ In this episode of Her Kind of Brave, Olivia shares what life looks like living with epilepsy and navigating chronic illness - including the parts that often go unseen. She speaks candidly about resilience, self-advocacy, and learning how to move through the world when your body doesn’t always follow the rules. This conversation sheds light on invisible illness and the strength it takes to keep showing up, even on the hardest days. 🎧 This episode is now live. Make sure you listen on Spotify, Apple & Amazon. 🔗 Link in bio. . . . . EpilepsyAwareness ChronicIllness InvisibleIllness BraveWomen AustralianPodcast FemaleVoices
#Raseing Reel by @thebarrierofficial - Hear her voice It was a lovely day to be invited to go and speak at @youngepilepsy he's her voice event. Being able to go hear about other peoples st
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@thebarrierofficial
Hear her voice It was a lovely day to be invited to go and speak at @youngepilepsy he’s her voice event. Being able to go hear about other peoples stories @leos_angelz was truly inspiring and has given “The Barrier” film lots to think about. Truly inspiring, well advocated and brilliant panel
#Raseing Reel by @cureepilepsy - What is this, a crossover episode? We sat down with What the Ef?! podcast host Landis Wiedner to get her perspective on life and love with epilepsy. F
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@cureepilepsy
What is this, a crossover episode? We sat down with What the Ef?! podcast host Landis Wiedner to get her perspective on life and love with epilepsy. Full episode now available on your favorite podcasting platform! #epilepsy #podcast #clips
#Raseing Reel by @cureepilepsy - Epilepsy affects more than 50 million people worldwide, with the vast majority living in low-resource settings where treatment gaps exceed 75%. Share
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@cureepilepsy
Epilepsy affects more than 50 million people worldwide, with the vast majority living in low-resource settings where treatment gaps exceed 75%. Share this clip from the Seizing Life podcast to spread awareness about the international need for better epilepsy care. #InternationalEpilepsyDay #IED2026
#Raseing Reel by @iconradioke - Today on The Breakfast Jam, we focused on breaking down some of the most common myths and misconceptions about epilepsy - because misinformation is of
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@iconradioke
Today on The Breakfast Jam, we focused on breaking down some of the most common myths and misconceptions about epilepsy — because misinformation is often the biggest barrier to dignity, inclusion, and proper support. 💜 With insights from Peter Nyette, psychologist, the conversation reminded us how deeply false beliefs shape fear, stigma, and silence. Common Myths We Debunked • Myth: Epilepsy is a mental illness or a curse Truth: It is a neurological condition caused by unusual brain activity — nothing supernatural and nothing to be ashamed of. • Myth: People with epilepsy cannot live normal, productive lives Truth: With proper management and support, people with epilepsy thrive in school, careers, relationships, and leadership. • Myth: You should restrain someone during a seizure Truth: Restraining causes harm. The focus should be on safety, calmness, and allowing the seizure to pass. • Myth: Epilepsy is contagious Truth: Epilepsy cannot be passed from one person to another — fear of “catching it” is pure misinformation. • Myth: Only children get epilepsy Truth: Epilepsy can develop at any age, including adulthood. • Myth: People with epilepsy should be sheltered or excluded Truth: Overprotection can be just as damaging as neglect. Inclusion builds confidence and independence. Key Reflection Stigma doesn’t come from epilepsy — it comes from ignorance. When communities are informed, fear disappears and compassion takes its place. Thank you to our listeners for the thoughtful questions and honest engagement. These conversations matter, and they save more than time — they save dignity. 💜 Let’s keep unlearning myths and spreading facts. Watch here: https://www.youtube.com/live/_ctV2sOoIAA?si=kym08NQvUlsZO7kK #InternationalEpilepsyDay #EndTheStigma #EpilepsyAwareness #TheBreakfastJam #IconRadioKE MentalHealthMatters
#Raseing Reel by @herkindofbrave_podcast - She lives with epilepsy. But this episode goes deeper than most people realise. This week, @livmiles opens up about SUDEP - Sudden Unexpected Death i
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@herkindofbrave_podcast
She lives with epilepsy. But this episode goes deeper than most people realise. This week, @livmiles opens up about SUDEP - Sudden Unexpected Death in Epilepsy - and the reality so many families are never properly educated about. It’s raw. It’s confronting. And it’s incredibly important. An educational conversation that will truly open your eyes — not just to the risks, but to the resilience, advocacy and strength behind her journey. If you or someone you love lives with epilepsy, this episode matters. 🎧 Listen on Spotify, Apple & Amazon. Episode dropping soon! 🔗 Link in bio. . . . . #HerKindOfBravePodcast #EpilepsyAwareness #SUDEP #WomensStories
#Raseing Reel by @epilepsy_india - What if epilepsy had a voice? 🎙️ And what if a PWE could finally talk back? 🗣️ This reel captures the invisible conversations people with epilepsy
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@epilepsy_india
What if epilepsy had a voice? 🎙️ And what if a PWE could finally talk back? 🗣️ This reel captures the invisible conversations people with epilepsy have every day, between fear and control, uncertainty and strength, stigma and self-trust. Epilepsy is not just about seizures. It’s about navigating emotions, identity, relationships, and resilience, often in silence. Let this be a reminder: PWE are not their condition. They are living, adapting, and showing courage in ways the world rarely sees.💪🏻 💜 Awareness begins with listening. Follow for more honest conversations around epilepsy & mental health. 🤍 [epilepsy awareness, people with epilepsy, PWE mental health, epilepsy stigma, living with epilepsy, chronic illness psychology, invisible illness, emotional impact of epilepsy, psychosocial support, support groups for epilepsy] #EpilepsyAwareness #PWE #LivingWithEpilepsy #InvisibleIllness #ChronicIllnessAwareness MentalHealthMatters EpilepsySupport BreakTheStigma Neurodiversity HealthPsychology SupportGroups
#Raseing Reel by @iconradioke - Today on The Breakfast Jam, one of the most important clarifications we made around epilepsy was about age - and the guest was clear: there is no defi
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@iconradioke
Today on The Breakfast Jam, one of the most important clarifications we made around epilepsy was about age — and the guest was clear: there is no defined age for developing epilepsy. With Peter Nyette, psychologist, we addressed a common misconception that epilepsy is only a childhood condition. The truth is far more nuanced. Key Clarifications from the Conversation • Epilepsy can develop at any stage of life. Childhood, teenage years, adulthood, and even later life — there is no age limit. • A diagnosis can come unexpectedly. Some people develop epilepsy after illness, injury, or for reasons that are never fully identified. • Late diagnosis does not mean late support. Regardless of when epilepsy appears, early understanding and proper management remain critical. • Age should never define capability. Whether diagnosed at 7 or 47, individuals can still pursue education, careers, relationships, and full lives. • Psychological adjustment matters. An adult diagnosis can be emotionally challenging, making mental health support just as important as medical care. Why This Matters When we tie epilepsy to a specific age, we delay diagnosis, dismiss symptoms, and deepen stigma. Awareness helps people seek help sooner — and without shame. Thank you to our listeners for engaging so thoughtfully and asking the right questions. Education remains our strongest tool. 💜 Let’s keep the conversation going. Watch here: https://www.youtube.com/live/_ctV2sOoIAA?si=QUfum6nuCv9EvIvO #InternationalEpilepsyDay #EpilepsyAwareness #TheBreakfastJam #IconRadioKE #EndTheStigma MentalHealthMatters
#Raseing Reel by @thezicast - There's nothing tougher than battling what's in your own head , but you can stay positive and control the controllable. 🎙️ For more insight into liv
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@thezicast
There’s nothing tougher than battling what’s in your own head , but you can stay positive and control the controllable. 🎙️ For more insight into living with epilepsy, catch Will Mella on Episode 107, available wherever you get your podcasts! #EpilepsyAwareness #mentalhealth #StayPositive #podcastlife #healthjourney
#Raseing Reel by @rxradiosa - Today is International Epilepsy Day and RX Radio would like to celebrate by bringing awareness to this day. Therefore, [LISTEN] to our reporters with
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@rxradiosa
Today is International Epilepsy Day and RX Radio would like to celebrate by bringing awareness to this day. Therefore, [LISTEN] to our reporters with epilepsy and their doctors sharing some words of encourage. For more stories from our reporters, please go check out our YouTube channel. #InternationalEpilepsyDay #wordsofencouregment #RXRadio #ByAndForChildren
#Raseing Reel by @misscassjohnston (verified account) - Here we go again!!! 💜 Epilepsy Awareness Month. This month means so much to me. This year, my focus is clear: funding research Living with epileps
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@misscassjohnston
Here we go again!!! 💜 Epilepsy Awareness Month. This month means so much to me. This year, my focus is clear: funding research Living with epilepsy has taught me many things, but one thing I know for sure is that research changes lives. It improves treatment options. It brings answers. It gives families hope. Every dollar makes a difference. Every share matters. Every conversation helps reduce stigma. If you’d like to be part of it, the link to donate is in my bio. Thank you for supporting something so close to my heart 🤍

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