When a Husband Becomes Epilepsy Caregiver
My husband, Pete, and I met before my diagnosis. But, when I was diagnosed with Intractable Seizures, Pete became my life-line.… Read More
My husband, Pete, and I met before my diagnosis. But, when I was diagnosed with Intractable Seizures, Pete became my life-line.… Read More
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.… Read More
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.… Read More
Avi shares 5 tips to make living with epilepsy easier from her own personal experience.… Read More
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.… Read More
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.… Read More
Amanda encourages readers to remember we are resilient, as we manage the pandemic, seasonal changes and a chronic condition.… Read More
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.… Read More