Epilepsy Blog Relay: I’m tired of fighting within the epilepsy community
Frankly I’m tired of the fighting among members of the epilepsy community. The fact that the epilepsy community is so fractured is only hindering all our work.… Read More
Epilepsy Blog Relay: Epilepsy Stigma in Teens and Adults
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
Epilepsy Blog Relay: Taking on Imposter Syndrome and Epilepsy
Currently, Jamie is feeling a sense of imposter syndrome when it comes to her epilepsy. She’s come up with a few ways to tackle it.… Read More
Epilepsy Blog Relay: My beef with SUDEP Research
Before I started treatment for Cancer, I knew my “5-yr survival rate” was 39%. Yet it’s taken ~40 years to est. 29% of deaths in epilepsy could be from SUDEP.… 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: Developing a creative life while managing epilepsy
Caroline has found that managing her epilepsy has allowed her to be true to herself and focus on the creative work she is passionate about.… Read More
Epilepsy Blog Relay: A soon to be graduate searches for hope
Amanda’s passion has always been to be a writer, and more specifically a journalist. She shares her adventures and stressors when dealing with her epilepsy as this soon to be graduate searches for hope.… Read More
Epilepsy Blog Relay: A seizure while driving made her hopeful
If Epilepsy has taught me anything, it’s that changing my goals is not failing. I had an absence seizure while driving on the freeway. I am more hopeful because my best friend Emily loves me despite the accident.… Read More