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May is officially recognized as Women’s Health Month. This month, we’re taking the time to highlight women’s unique health issues and the importance for women of all ages to make their health and well ...
At the age of 9, I became 1 in 26. My journey began unexpectedly at an out-of-state diving meet, where I woke up surrounded by paramedics. From that moment on, my life shifted into a whirlwind of EEGs ...
The 118 undersigned organizations – representing people living with epilepsy; caregivers and loved ones; physicians, care providers, and epilepsy centers; epilepsy researchers; and others – are united ...
GRIN2A is a gene found on chromosome 16. It provides instructions for making a protein in the brain called glutamate ionotropic receptor that forms a subunit of the NMDA (N-methyl-D-aspartate) ...
Some concerns faced by people living with epilepsy include taking medications properly, having healthy habits, keeping in mind seizure safety guidelines, and avoiding medications that may worsen your ...
Familial focal epilepsy with variable foci (FFEVF) is a rare syndrome of focal seizures with varying degrees of severity and symptoms of seizures in different family members. Each family member will ...
Xiyan Yi MD, Ushtar Amin MD, and Selim Benbadis MD, of the University of South Florida’s Comprehensive Epilepsy Program answer frequently asked questions about seizures and epilepsy post-stroke.
I was first diagnosed with generalized epilepsy at 9 years old after I had three seizures. As a child, I didn’t understand what this meant aside from having to take medication every morning and night.
Tuberous Sclerosis Complex (TSC) is a genetic disorder that occurs in 1 out of 6,000 people and can involve multiple organs in the body, including the brain, heart, kidneys, lungs, eyes, and skin. The ...
The epilepsy syndrome of self-limited neonatal-infantile seizures used to be known as benign familial or non-familial neonatal-infantile seizures. Seizures begin in the first several months of life in ...
Photosensitive occipital lobe epilepsy is a very rare condition with an estimated occurrence in 0.7% of childhood epilepsies. This syndrome was formerly known as idiopathic photosensitive occipital ...