Epilepsy Storylines App puts control back your hands Living Well With Epilepsy has now launched Epilepsy Storylines on the App Store℠ for iPhone® and iPad®. Epilepsy Storylines is, an app that lets users track seizures, medication side-effects, moods, appointments and much more on their smartphone. They can then share any information within … Read More
This personal story is Part 1 of a series of posts where Scott will chronicle his experience beginning with long-term monitoring and culminating in a brain surgery to manage his epilepsy. I hope you enjoy getting to know Scott’s story and benefit from his experience as much as I have. Scott’s Story … Read More
On Thursday 26th March 2015, I had the incredible opportunity to attend the Young Epilepsy Champion Awards at the London City Hall to represent Living Well With Epilepsy. I write monthly columns for Living Well with Epilepsy and it was an honor to attend the awards on behalf of the founder, Jessica … Read More
Living Well With Epilepsy has launched a new mobile and web app just in time for Purple Day. The app, called Epilepsy Storylines, is designed to help people living with epilepsy as they manage their daily routines and communicate with their caregivers. This app is possible thanks to a partnership with Self … Read More
Anticonvulsant medication can control seizures in most people with epilepsy, but for about 30% of patients, they either aren’t effective or are intolerable. There are other options to consider in these cases. They include: Epilepsy Surgery, Diet, Nerve stimulation, and Counseling. Option 1: Epilepsy Surgery What is epilepsy surgery? In some cases, … Read More
If you missed the broadcast, check out the recording of Jessica Keenan Smith, founder of Living Well With Epilepsy, as she talks about epilepsy on WHYY.… Read More
This personal story was contributed by Debbie Fincher, mom to Noel and Board Chair and Founder of the Angel Wings Foundation, an organization which is creating a new housing model for people living with epilepsy in need of long term support. … Read More
I was born in 1952, and back then, it was still illegal for a woman with epilepsy to get married. When I was young, all I could think about was getting married and becoming a mother.… Read More