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!
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!
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!
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.
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/
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.
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 and live with purpose.
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 Twitter
Destiney is a wife, mother, soon-to-be published author, and runner living with Epilepsy. In this episode we chat about all things family, job, and seizure related- and how Destiney turned from avoiding her diagnosis to embracing it.
You can find her online at @destineywendtrunning