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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 Health and all social media links are located here  

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 foundation to optimize their health.  You can find his podcast, The Grey Matters, here  Work with Josh: here Josh's Instagram: here

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 support groups here  Join us for our monthly epilepsy workshops to create your seizure first aid plan here  Download your copy of the BFF Guide to Epilepsy here

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 here Join us for our monthly virtual support groups here Join us for our monthly epilepsy workshops to create your seizure first aid plan here Download your copy of the BFF Guide to Epilepsy here

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 here Connect with Jamie: IG here Virtual 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 here I also host a support group bi-weekly!  Join us here Parents of kiddos with epilepsy?  Join us here

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 know what you think and if you can relate!  You can find Kristina at her website and purchase her book here

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 NHS South London & Maudsley Trust, on the SAC for Epilepsy Research UK, Council of Management for Epilepsy Action, on Patient Advisory Groups for UCB and EpiCARE, and an Ambassador for the UK Government Disability Confident – Yes I Can initiative. You can find her via Facebook: here and her Podcast: here

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 dynamics... it was an amazing and eye opening experience!    --- This episode is sponsored by · Anchor: The easiest way to make a podcast. https://anchor.fm/app

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 has a podcast, which you can find at the link below!  https://anchor.fm/felicia-waterfill5 

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 could benefit from learning about SUDEP.  For more information about SUDEP, go to http://.sudepactionday.org

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/1565021100319075

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 with epilepsy can and cannot do.

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/  --- This episode is sponsored by · Anchor: The easiest way to make a podcast. https://anchor.fm/app

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.instagram.com/fetchingstitches/