The bill safeguards physician-directed care in a school setting and helps school personnel manage students living with ...

The latest edition of the Foundation Quarterly captures a defining theme, Turning Hope into Action. This issue highlights powerful personal stories, the dedication of volunteers raising awareness, and ...

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 ...

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 ...

Join the epilepsy community for Purple Day® on March 26, a global initiative to raise epilepsy awareness and support the millions of people living with epilepsy worldwide. Approximately 65 million ...

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.

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 ...

Neurofibromatosis type 1 is one of the most common neurocutaneous disorders. It is a neurodevelopmental disorder affecting about 1 in 3000 individuals. It is inherited in an autosomal dominant fashion ...