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
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
People with epilepsy experience the impact of stigma everyday. In many cases this can lead to a sense of vulnerability and despair. Elaine shares how she deals with those feelings.… Read More
When it comes to nutrition and epilepsy, well, my comfort food is pizza. But now I have epilepsy, cancer, heart disease, & alzheimer’s hanging over me it can’t hurt to look into eating a little healthier.… Read More
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
We’ve taken a close look at epilepsy stigma and wanted to share the similarities and differences in how teens and adults respond to epilepsy stigma in real life… Read More
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
Early on, Soo’s family would not use the word epilepsy in their home. Now, she is an advocate and makes the most of her local epilepsy support group.… Read More
Karen on brain surgery for epilepsy: My life was going well, epilepsy didn’t stop me doing anything and I thought why take the chance?… Read More