You both have changed our lives for the better by sharing your journey with your beautiful daughter. We were devastated when our daughter was diagnosed with epilepsy. You both open up your lives to help others was the beacon of light we were desperately looking for. I could never express our appreciation in words how grateful we are to you and the work you are doing. Thank you! Thank you for being the voice for those who live with epilepsy.💜

Thank you for this continued information! We need all the information about epilepsy. Not enough information out there and surprisingly...even in the medical field!

I love the informative and honest information in Seizing Life. As a parent to a child who has seizures, this is the first resource that makes me feel like we're not alone in this journey.

I have loved all these podcast episodes, and especially enjoyed the latest on epilepsy and genetics. My son has SCN8A epilepsy (IS, tonic seizures, developmental delays) and I was so excited to hear Dr. Millichap mention SCN8A on the episode. There are still only about 300 cases diagnosed worldwide and many neurologists are still not even familiar with it. I’m a parent volunteer for The Cute Syndrome Foundation, which raises funds and awareness for our SCN8A community. I shared your podcast with the foundation because I know lots of the other parents would enjoy it!

I am a mother of two who has had epilepsy since age six. I am 29 years old and it’s been hard but I am happy to hear about life with it. It’s a struggle with remembering medication to being able to function. Or even not being able to drive with epilepsy, but I’m happy to have a epilepsy podcast to listen to. Thank you so much

Great content! I am a host of another podcast about epilepsy, and I am so happy to see so much dialogue happening about epilepsy! 💜💜💜

Thank you guys for sharing yours and Adelaid’s story.

As a Mom with a child with epilepsy, this brings lots of hope:) Thank you for creating this podcast 💜