The America Psychiatric Association (APA) advocated against mandatory neuropsychological testing in the 2016 ECT device reclassification.
Exerpts from ECT recipeints submissions the 1990 FDA dockets.
This spring, Life After ECT launched a comprehensive FDA reporting guide for injured electroconvulsive therapy (ECT) recipients. This post is a progress update and an overview of our future reporting goals.
Moira Dolan MD to the FDA regarding ECT draft guidance for the 2016 electroshock device risk reclassifacation.
ECT survivor activist and author Linda Andre talks about her book, Doctors of Deception, What They Don't Want You to Know About Shock Treatment, with…
Attorney Barry Kade to the FDA, ECT device reclassification, 2009.