Epilepsy Blog Relay: Danny Did Foundation on SUDEP
The Danny Did Foundation (DDF) has worked tirelessly since 2010 toward its mission to increase awareness of Sudden Unexpected Death in Epilepsy (SUDEP).… Read More
4 Tips to help you track seizures
Jewel shares a few tips on how to keep track of your seizures. We hope this helps as you move through your own epilepsy journey. … Read More
Epilepsy Blog Relay: New epilepsy diagnosis after seven years
After seven years of struggling to get a proper epilepsy diagnosis, Laura found a neurologist who would listen. She’s now a year seizure free!… Read More
Epilepsy Blog Relay: On Recovery Days
I’m still struggling to deal with the concept that living with epilepsy means there are going need to be recovery days.… Read More
Epilepsy Blog Relay: On Epilepsy and Stigma
Okay so I’ll be honest the topic of epilepsy and stigma is a bit of a bugaboo of mine. But I promise to spare you the soapbox today and make it interactive.… Read More
Epilepsy Blog Relay: On the importance of questioning side effects
I now know I need to question all the potential side effects a medication causes, even the rare ones.… Read More
Epilepsy Blog Relay: How is epilepsy diagnosed?
The process of getting an epilepsy diagnosis can be slow. So dealing with this process requires patience, but here are a few things to expect.… Read More
Epilepsy Blog Relay: Does having one seizure mean you have epilepsy?
Does having a seizure have to mean you have epilepsy? Learn more about how the ILAE and doctors define epilepsy.… Read More