Tamu’s Journey with Myoclonic and Tonic Clonic Epilepsy
Tamu was diagnosed with epilepsy at 14. She experienced myoclonic seizures for a several years prior to this diagnosis, and had her first tonic clonic seizure in the summer of 2014… Read More
Danielle on living with epilepsy and cerebral palsy
I’m Danielle and I wanted to share a little about my experience living with epilepsy and cerebral palsy as well as some info on epilepsy and CP.… Read More
5 Tips to Live Well with Epilepsy
Epilepsy is a fact of life and it’s our challenge to live with it as best we can. I want to share 5 tips that help me live well with epilepsy.… Read More
Meet Natalie: STEPS Toward Zero Champion
STEPS Toward Zero is a movement developed by SK life science, featuring epilepsy advocate Natalie Beavers founder of Angels of Epilepsy.… Read More
Delta Variant: It’s time to stock up on a few more face masks
With the Delta variant and the rise in COVID-19 cases, is anyone else feeling like it’s time to add a new set of face masks to the wardrobe?… Read More
Sheri’s Story: Learning to Live All Over with Refractory Epilepsy
Sheri was diagnosed with refractory epilepsy in her late 20’s. She keeps a positive attitude, but transportation can be difficult.… Read More
Epilepsy Blog Relay: Finding a New Doctor while Living with Epilepsy
It was back to the drawing board for me. I was left wondering if I could get lucky twice when it came to choosing a new doctor while living with epilepsy.… Read More
Epilepsy Stigma: Afraid to tell others about epilepsy
Stigma is still an issue for those living with epilepsy. So, it’s understandable why we are afraid to tell others about our condition. Let’s talk about epilepsy stigma.… Read More