Shock and Suicide: The Poll Results

Thank you to all who participated in the shock and suicide poll! Here are the results!

13 responders had this to say about their experience with electroshock:

Did you experience any of the following from shock induced brain damage and/or disability?

shock and suicide multiple choice responses

Do you have any other thoughts you want to share with the public about electroshock and suicide?

“My story already posted in after-shock!”
“If I was told how I would feel, five, ten, fifteen years after shock. I would have said HELL NO to shock, HELL NO, I’d rather you cut off my right arm. Seriously. Also, I would like to ask Doctors who prescribe Shock or perform Shock, “Would you recieve shock if you were depressed, or would you suggest it for a loved one if they were depressed?” There is not enough told to patients about Shock, the permanent amnesia, BRAIN DAMAGE. I was told I would lose three months, before and three months after. Whole chunks and blocks of my memory of my whole life are gone. It’s infuriating as well as I feel a deep deep sadness, worse than any depression I felt before I was given Shock. I feel suicidal, daily. DON’T DO IT! I so WISH someone said that to me!”
“It is disgusting that there are shock docs today still advocating for and administering this lunatic procedure. They must be stopped.”
“I have never been that suicidal ever in my life before. But electroshock triggered a mania with psychotic tendencies and I became deeply suicidal and was so for almost three years when it finally lifted by itself. I have never before or after in my life been in such a state. It was traumatising along with the electroshock itself. I was very close to not surviving. Electroshock is very popular in Sweden – where I live – and they shock about 4000 people yearly here with a small population of 9,6 million. Numbers are increasing with about 200 people yearly. And no one is questioning this.”
“I think ECT patients should be required to have an MRI and neuropsychological testing done BEFORE the ECT is started and every year after for the following 10 years. This would be the best research. I’ve noticed that when people evaluate the effects of ECT, sometimes they’re looking at patients 3-6 months after treatment. At that time, patients are still in the thick of it and don’t know the damage the ECT caused. As someone with memory loss, you don’t know what you don’t know. You learn how much damage you start trying to work and live like normal and other people tell you what you don’t remember and you start struggling with work. Don’t survey the patient, survey their family. The family notices when you don’t remember your own life. As the one with memory loss, you don’t know what you don’t know. ECT causes memory loss, but also disability. It’s humiliating being on disability. It’s embarrassing meeting people you knew prior to ECT and having to tell them you have no idea who they are. After ECT, you’re still depressed, but now you have PTSD and shame from having a dark secret that you don’t want anyone to know, that you had ECT.”
This type of informal data collection is an example of ways survivors can take charge by helping create statistics without having to go through mental health organizations and without the sway of the psychiatric industry.
The form is still open for those who want to contribute. Scroll down to access it. I will update this post in a few months.
If wondering what all this is about, click here to read the accompanying article.
Thanks again to all who participated! Lets do this again soon 🙂
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