In gratitude for my epilepsy
So much has happened in my world with a family health crisis during a pandemic, I wanted to share a little about my perspective on gratitude.
COVID and our Epilepsy Superheroes
As our world has dealt with the reality of being confined to home due to COVID – many of us felt the pressure in unique ways. But perhaps those of us with epilepsy also found some freedom.
Emily’s Perspective: Newly diagnosed with epilepsy or epileptic seizures?
Are you new to Epilepsy? Have you had a recent diagnosis of epileptic seizures in your family? Maybe I can help ease the anxiety with this column.
Epilepsy experience creates a whole new family of supporters
After Stephanie (known as Alyrical) was diagnosed with epilepsy the dynamic between her friends and family and loved ones changed. The road to being diagnosed with epilepsy was a difficult one that lead to major changes in her life affecting not only her health.
Virtual Epilepsy Education Conference to Celebrate Purple Day
The virtual epilepsy education conference to celebrate Purple Day will take place March 24-26. The free conference will include educational and advocacy sessions as well as a virtual expo.
Global Epilepsy: Helping Those with Living with Epilepsy in Uganda
Gideon Ronie shares an update on his work helping people living with epilepsy in Uganda. He gives insight into how the pandemic has affected the community.
Social Connections and Epilepsy: Discovering the impact of sharing one’s story
By sharing my story I discovered the social connections within the epilepsy community. Speaking about how I overcame the fear of uncertainty of having seizure was a different kind of exposure for me.
Patience and Epilepsy: A great ally when it comes to managing stress
Patience has been Justin’s best ally when it comes to epilepsy. By recognizing side effects and memory loss can help helps to reduce stress.