Epilepsy Blog Relay: Story of a mother and son with epilepsy and autism spectrum
Audra, who writes Our Life With Autism, shares the life and adventures of mother and son with epilepsy and autism spectrum.
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
FDA has approved Epidiolex for the treatment of seizures associated with two rare and severe forms of epilepsy, Lennox-Gastaut syndrome and Dravet Syndrome.
I suffered a series of tonic clonic seizures on the day my daughter graduated from college, which also happened to be my birthday.
When reviewing David’s son’s IEP, and earlier 504 plans the need for epilepsy awareness in education became painfully clear to this family.
Lili was diagnosed with Lennox-Gastaut syndrome (LGS), a rare and severe form of epilepsy, but therapeutic horseback riding was an activity she could enjoy.
Francesca’s Story: I have a type of epilepsy that was inherited from my mother’s mother. My grandmother was born with PCDH19 epilepsy.
Five helpful tips for adjusting to a medication change. I spoke with my doctor and we both decided that it was time to increase one of my medicines.