Epilepsy Blog Relay: Kat takes on temporal lobe epilepsy
Kat takes on living with temporal lobe epilepsy from a personal perspective
Living Well With Epilepsy’s, Epilepsy Blog Relay™ is an epilepsy awareness movement to designed to maximize collaboration and eliminate stigma. Thanks as always to our generous sponsors and partners!
Kat takes on living with temporal lobe epilepsy from a personal perspective
Audra offers some tips on creating a 504 and an IEP plan to safeguard your child with epilepsy at school.
Living with epilepsy, I’m finding self-care to be more important than ever
Our wedding was perfect, we said the vows, danced to some favorite songs, and enjoyed our ranch dressing fountain. Just a month later, I had a tonic clonic seizure. It was the first one in over a decade, and the first one my husband has had to witness.
On 6/30 at 7pm ET, we will host our next #LIVINGWELLCHAT. We will hear from the community on what the new marijuana-based epilepsy drug could mean for families affected by LGS and Dravet Syndrome.
Maternity leave found Shonet longing to go back to work. But a baby and a relapse in seizures made her rediscover her creative side to keep her mind active.
Audra, who writes Our Life With Autism, shares the life and adventures of mother and son with epilepsy and autism spectrum.
This post is part of the Epilepsy Blog Relay™, which will run from June 1 to June 30, 2018. Follow along! Elaine’s Story I was diagnosed with epilepsy at age four. At that time, early 1960s, one of the few medications available for epilepsy was phenobarbital. Concerned about negative side effects for … Read More