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Jamie Wissinger
Epilepsy Awareness: 1 in 26Episodes
Jamie Wissinger
Epilepsy Awareness: 1 in 26
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Episodes of Epilepsy Awareness
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Today I am joined by Tiffany Kairos, an epilepsy advocate who has made such an impact on our community! She shares her story, her rebranding from The Epilepsy Network (TEN) to Rise Above Epilepsy, and so much more. You can find her via WEGO H
Today I'm chatting with Josh Perry about his journey with multiple brain tumors, and how he's shifted and prioritized his health, and now helping others do the same. Coined The Optimization Specialist, he helps hundreds of people build a solid
In today's episode I'm sharing a podcast where I was a guest for the Mindful Inspiration Champion. We chatted about my epilepsy and how I was able to shift my mindset and become an advocate for the community. Join us for our monthly virtual
Today I'm chatting with Vanessa about what it means to be an advocate for her. Vanessa lives in Canada, works with Epilepsy Canada, and shares with us about her absence seizures. You can find her on Instagram hereJoin us for our monthly
Hey everyone! Happy Summer + let’s catch up!
Today I'm chatting with Sydney about her epilepsy and her experience with Epilepsy Camp! Connect with Sydney: IG hereConnect with Jamie: IG hereVirtual Meet Ups: Sign up here
Today I'm chatting with Mindy about her epilepsy + support systems- a huge concern is that adults do not get that type of support- so she created it! You can find her support group via Instagram hereI also host a support group bi-weekly! J
Today I'm chatting with Katy, and she shares what it's like to live with tonic/clonic seizures. She shares a bit about her hospital stay, from her family's perspective- and how she manages her Epilepsy.
Today I'm sharing an episode that I was a guest on: Y'all Should Be Friends with my dear friend, Kristina. This is the first time I've shared THIS part of my story, and I'm excited to do so. I can't be alone with this situation, so let me kno
Today I'm chatting with Torie about her advocacy work and how she's bridging the gap between patient + science. Torie is also the: Founder, Editor, Writer & CEO for Epilepsy Sparks, Podcaster for Epilepsy Sparks Insights, Governor for the NH
Today I chat with Kirsten from @brey_fighting_back on IG! She is a Momma to 3, and her advocacy shines bright for her 6 year old son Brey- who has Epilepsy. We talk about med changes, keto diet, neuro + developmental regression, family dynami
Today, I'm chatting with Felicia- who is a mama to 4 and LIVES IN THE SAME TOWN AS ME! SO awesome! We chat about all things mamahood, driving, pregnancies, doctors, and CBD. This episode is a little controversial, so buckle up! She also h
Today is World SUDEP Action day and I want to share a little bit about it. When I was diagnosed with Epilepsy, my doctor did not tell me about it- and this is SUPER important for us with Epilepsy to know! Tune in and share with someone who co
Hey girl! Today I'm sharing a little bit about my trauma and the healing that is associated with it. If this resonates with you, please join me in our community, Surrender and Shine on FB! xo, Jamie https://www.facebook.com/groups/156502
I’m happy to share the mic with Fran Turauskis, who is a Podcast Producer, and a Writer from London. In today’s episode she shares about adventure and how her diagnosis has impacted her life. Fran educates us on what adventure sports people wit
A Letter to Myself: 5 things I wish I knew when I was diagnosed with Epilepsy - this is a solo episode from your host, Jamie. You can find her on IG @jamiewissinger
On this episode, Jamie and Destiney chat via IG LIVE, with their kiddos in the background (thanks quarantine), about ambulatory EEGS and what that process is like!
Today I’m chatting with Sharon about her life with Epilepsy and the VNS device. You can find her on IG @be.brave.brains
Today I’m chatting with Kyle about his epilepsy and how he advocates for the community.You can find him on IG @epilepsylifestyleblog or his website: https://www.epilepsylifestyle.com/
Today I'm chatting with Kati on how she manages her Epilepsy living solo in the Windy City! She also chats about her small business, which we LOVE supporting. You can find her via IG: https://www.instagram.com/kati_anne/ https://www.instagr
Today I am chatting with Meghan, from the Daley Life on the joys of Epilepsy and how her diagnosis changed (or did not change) her mindset. IG: livefearlessly_akfFacebook: www.facebook.com/livefearlesslyfitWebsite: www.meghandaley.wordpres
Today I'm chatting with Dylan about her seizures, and how she has created an Epilepsy toolkit for your loved ones to be prepared when you have a seizure. You can find her on Instagram, @digidyla
Today I talk with Angelina about her journey with Epilepsy. https://www.instagram.com/amperrino/ and on YouTube: https://m.youtube.com/channel/UCLRDsVxtkWYFuIDEFZ6H11Q
Today we chat with Christalle Bodiford- an artist, advocate, writer, and adventure seeker. As an entrepreneur diagnosed with epilepsy, Christalle brings a unique perspective of empowerment that inspires others to embrace a positive mindset an
Today I am chatting with Amanda about her journey with partial seizures and how she's navigated through living in a small town with Epilepsy.You can find Amanda: @epilepticmom on IG@epilepticmomAR on Twitterhttp://www.epilepticmom.comhttps
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