Illinois Governor Pat Quinn signed the Danny Stanton SUDEP Act into law on Monday, August 12th. The law requires medical examiners and coroners to include an inquiry about a history of epilepsy and seizures as part of a standard autopsy, and, if an instance of Sudden Unexpected Death in Epilepsy (SUDEP) is determined, to report it to a national registry. Illinois State Senator Dan Kotowski, in collaboration with the Danny Did Foundation, spearheaded this bill.
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Illinois Governor Pat Quinn signed legislation on Monday, July 22nd, which requires the Department of Health and Family Services (DHS) to ensure that Medicaid patients with epilepsy do not require prior approval from the Department in order to receive anti-convulsant drugs.
Duke Medicine researchers have identified a receptor in the nervous system that may be key to preventing epilepsy following a prolonged period of seizures.
Researchers from UC San Francisco have discovered a way to reverse severe forms of epilepsy in mice with stem cells, providing a new sense of hope for patients who suffer from the seizure-inducing disorder.
Children born to mothers who took the anti-seizure drug valproate were five times more likely to be born with autism than those whose mothers didn’t take the medication, a Danish study found.
EFGC’s Debbie Flader receives the Sara Stubblefield Advocacy Award from the national Epilepsy Foundation
Debbie Flader of Hanover Park, IL received the national Epilepsy Foundation’s Sara Stubblefield Advocacy Award for her years of tireless service as the Epilepsy Foundation of Greater Chicago’s Director of Clinical Outreach. The award was given at the Epilepsy Foundation’s 2013 Public Policy Institute in Washington, DC.
President Obama will unveil a $100 million initiative to research the human brain, in hopes of unlocking further understanding of brain disorders.