What the EF Podcast featuring DJ HAPA
What the EF podcast released its first episode today! Wanna stay motivated to keep those New Year’s resolutions? Take a listen to this heart-to-heart with DJ HAPA.… Read More
What the EF podcast released its first episode today! Wanna stay motivated to keep those New Year’s resolutions? Take a listen to this heart-to-heart with DJ HAPA.… Read More
What the EF is a podcast to share, laugh, and cry at all our epilepsy WTF moments. Laughter has made epilepsy survivable for me. My co-host, Lexi, agrees. Which is perfect because we met at an epilepsy conference, where I had a seizure and believed the pillows smelled like pickles. Lexi assured … Read More
If you are newly diagnosed or just now looking into connecting with others living with epilepsy, we may not have met. I’m Jessica K. Smith, founder and CEO of Living Well With Epilepsy and I was diagnosed with epilepsy after having several tonic clonic (grand mal) seizures the summer between seventh and … Read More
FDA offers renewed hope for families facing rare disease with the launch of the Accelerating Rare disease Cures (ARC) Program… Read More
According to a study presented at the 2021 American Epilepsy Society Annual Meeting, childhood-onset epilepsy accelerates brain aging by about 10 years.… Read More
Learn more about epilepsy and pregnacy as well as the latest research on the topic.… Read More
For the researcher interested in developing Neurotherapeutics who is looking for ways to network with experts in academia, industry, advocacy, and government here are three great opportunities.… Read More
Thank you to our media partner Dravet Syndrome Foundation Spain. They have shared their call for research projects in both english and spanish.… Read More