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Life After ECT

Awareness – Advocacy – Education

FDA

Read more about the article The American Psychiatric Association (APA) opposed mandatory neuropsychological testing for patients receiving electroconvulsive therapy (ECT).
ECT / FDA - 2016

The American Psychiatric Association (APA) opposed mandatory neuropsychological testing for patients receiving electroconvulsive therapy (ECT).

The America Psychiatric Association (APA) advocated against mandatory neuropsychological testing in the 2016 ECT device reclassification.

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January 7, 2023
Read more about the article Excerpts from 1990 FDA ECT Dockets
1990 FDA Dockets / ECT / ECT Side Effects & Risks / ECT Stories / FDA

Excerpts from 1990 FDA ECT Dockets

Exerpts from ECT recipeints submissions the 1990 FDA dockets.

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October 18, 2022
Read more about the article Electroconvulsive therapy and FDA adverse reporting – our findings and future goals
ECT / ECT News / ECT Research / FDA

Electroconvulsive therapy and FDA adverse reporting – our findings and future goals

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. 

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October 12, 2022
Read more about the article ECT Device Reclassification Draft Guidance – Moira Dolan MD to the FDA, 2016
ECT / ECT Side Effects & Risks / FDA / FDA - 2016

ECT Device Reclassification Draft Guidance – Moira Dolan MD to the FDA, 2016

Moira Dolan MD to the FDA regarding ECT draft guidance for the 2016 electroshock device risk reclassifacation.

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September 18, 2022
Read more about the article The Controversial History of ECT — An Interview with Linda Andre
ECT / FDA / Podcast

The Controversial History of ECT — An Interview with Linda Andre

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…

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September 5, 2022
Read more about the article ECT Device Safety: Attorney Barry Kade to the FDA, 2009
ECT / FDA / FDA - 2009

ECT Device Safety: Attorney Barry Kade to the FDA, 2009

Attorney Barry Kade to the FDA, ECT device reclassification, 2009.

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June 17, 2022
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