Epilepsy Awareness: 1 in 26

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!