On SUDEP and New-Onset Refractory Status Epilepticus (NORSE)
Comedian and actor, Bob Dibuono, shares his family’s experience with SUDEP and New-Onset Refractory Status Epilepticus (NORSE).
Tips on how to 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.
World Health Assembly calls for global action plan on epilepsy
At #WHA73, Member States endorsed a resolution calling for global action plan on epilepsy and other neurological disorders. Learn more.
On being resilient when it all seems to be too much
Amanda encourages readers to remember we are resilient, as we manage the pandemic, seasonal changes and a chronic condition.
Three opportunities for researchers interested in developing neurotherapeutics
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.
On showing up for yourself despite your diagnosis
Lauren shares her experinence of “showing up for yourself” after her diagnosis of epilepsy.
The journey to practicing gratitude during difficult times
Recently Colleen was sick and hadn’t eaten in days. Jenny shares her experience with practicing gratitude during this difficult time.
Epilepsy in Kenyan Villages and why community matters
Rich shares his experience with epilepsy throughout Kenyan Villages. Despite fears and epilepsy myths, the community has agreed to form a Self Help Group where they meet once a month.