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Showing posts with label The Fraud of Psychiatry. Show all posts
Showing posts with label The Fraud of Psychiatry. Show all posts
Wednesday, December 14, 2016
Groundbreaking, Ceiling Shattering, Box Destroying . . . Dr. Bonnie Burstow's Toronto Public Library Talk on "Psychiatry and the Business of Madness"
If you really want to understand why psychiatry is such a threat to humanity, watch Bonnie Burstow's (Dec. 6, 2016) Toronto Public Library Talk on Psychiatry and the Business of Madness.
I believe that your future self will thank you for it.
Coalition Against Psychiatric Assault thank you for getting this video out!
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Thursday, March 3, 2016
Watch People Who Are Shock Survivors and Allies After 2011 FDA Shock Device Hearings
#FDAStopShockDevice
In 2011 the FDA held public hearings on the shock device that delivers electric shock treatment (electroconvulsive treatment, ECT). The panel voted in nearly all situations to keep the shock device a Class III Experimental Device.
Now, the FDA is proposing to down-classify the shock device to a Class II device with "special controls" that would put it in the same category as a pair of eyeglasses or a wheelchair specifically for people who are over 18, have a "major depressive episode" as part of "major depressive disorder" or "bipolar disorder" are deemed "treatment-resistant" or "require rapid response".
The FDA is proposing that since they held hearings in 2011 they do not need to hold hearings now. Not one of the members of the decision-making panel from 2011 is on the panel today.
Please get involved and tell the FDA not to down classify the shock device for any reason and to hold public hearings.
Psychiatry ought not be allowed to get away with this fraud! The FDA needs to be held responsible for the damage this will cause. Shock treatment will soar.
In 2011 the FDA held public hearings on the shock device that delivers electric shock treatment (electroconvulsive treatment, ECT). The panel voted in nearly all situations to keep the shock device a Class III Experimental Device.
Now, the FDA is proposing to down-classify the shock device to a Class II device with "special controls" that would put it in the same category as a pair of eyeglasses or a wheelchair specifically for people who are over 18, have a "major depressive episode" as part of "major depressive disorder" or "bipolar disorder" are deemed "treatment-resistant" or "require rapid response".
The FDA is proposing that since they held hearings in 2011 they do not need to hold hearings now. Not one of the members of the decision-making panel from 2011 is on the panel today.
Please get involved and tell the FDA not to down classify the shock device for any reason and to hold public hearings.
Psychiatry ought not be allowed to get away with this fraud! The FDA needs to be held responsible for the damage this will cause. Shock treatment will soar.
Sign the petition here: https://www.change.org/p/fda-stop-fda-from-down-classifying-the-shock-device-to-a-class-ii-device-stop-shock-treatment
Friday, December 4, 2015
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