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.
5 Ways Epilepsy is Life-Changing plus 5 Tips to Make it Easier
Avi shares 5 tips to make living with epilepsy easier from her own personal experience.
Living an Active Life with VNS
John has been living with epilepsy for the past 12 years. He’s had to give up triathlons. But he’s looking for advice on living with VNS and doing endurance sports.
Employment, Epilepsy and Equality: To tell or not to tell?
When it comes to epilepsy, equality, education and employment, it is my firm belief that we are all allowed to dream regardless of abilities or disabilities.
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.
On showing up for yourself despite your diagnosis
Lauren shares her experinence of “showing up for yourself” after her diagnosis of epilepsy.