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
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
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
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
5 things my cancer diagnosis taught me about how to live better with epilepsy. … Read More
FDA offers renewed hope for families facing rare disease with the launch of the Accelerating Rare disease Cures (ARC) Program… Read More
Chantal has been battling epilepsy for 19 years with the help of VNS. She shares a recent letter to her epilepsy.… Read More
Accepting epilepsy as a part of my everyday life only happened when I felt the slightest bit of control and ownership over this new obstacle.… Read More
When warmer weather rolls around I begin to wonder does hot weather affect epilepsy? Well, turns out I wasn’t the only one wondering.… Read More