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

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