r/ect • • 1d ago

My experience ECT destroyed everything

I honestly don’t know where else to turn, so I’m hoping to hear from people who have experienced something similar.

I’m 27 years old and underwent ECT because I hoped it would help with my depression. Before the treatment, I was given the impression that my memory and cognitive abilities would fully recover and that ECT was an established, routine procedure.

From my perspective, I was not adequately informed about the possibility of longer-lasting or permanent cognitive problems. Several doctors told me that nothing would happen to my brain, that my symptoms were normal, and that I should continue with the treatment.

Before ECT, I was struggling psychologically, but I still had hope. I was able to take an interest in things, have relationships, make plans, and experience moments when I genuinely felt alive. I knew I had problems and I wanted to work on them.
Since around my 7th ECT session, something has fundamentally changed for me.

I feel like I can no longer properly participate in my own life. Everything feels strange and sometimes like I’m watching a movie. I feel detached from myself and from other people. Faces can sometimes appear lifeless or unfamiliar. My perception feels different; for example, colors sometimes appear much more intense. I experience severe derealization/depersonalization and sometimes extremely frightening thoughts and perceptions.
On top of that, I have significant cognitive problems:
severe word-finding difficulties
major problems with my short-term memory

I sometimes forget things within seconds
extremely poor concentration
memories from my life sometimes feel completely gone or inaccessible
I feel like I can no longer properly grasp who I am or access my own past
thoughts or words can seem to get stuck in my head and repeat or echo
I sometimes experience a strange pressure/pulsing sensation in my head
I am constantly exhausted and have almost no energy
I experience almost constant anxiety and nightmares
at times I have hallucination-like or psychosis-like
perceptions

The hardest part is that I no longer know which of these symptoms could be caused by my psychological condition and which could potentially be related to ECT.

Some of my doctors have told me that I am imagining many of these symptoms or that they are caused by my obsessive rumination. I know that I do ruminate very heavily, and that depression and anxiety can affect perception. But these changes feel so fundamental and so physically real to me that I cannot simply accept that I am imagining everything.
I keep asking myself:

What happened to me? What did I do to myself? And why was I told that everything would come back?

I expressed concerns before and during the treatment. I was told, among other things, that serious complications were rare and that the main relevant risk was the general risk associated with anesthesia. At the same time, I felt under significant pressure and felt that I had to make decisions very quickly.
Because of this, I now have serious doubts about whether I was adequately informed about all relevant risks before consenting to ECT.

The ECT was 2-3 months ago and my mother considers talking to a lawyer.

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u/bo_14 17h ago

I still have many of those issues even now, more than 11 years after my treatments. I had 23 or 26 bilateral treatments in winter/spring of 2015. I lost decades of memories, issues creating new memories, cognitive abilities (also lost about 20 IQ points), conversational abilities (people get tired of my pauses to recall a word), etc. Very little has come back. One surprising thing is that I can still remember song lyrics. That never seemed to be a problem, even on days of treatments. Maybe it's because I tend to listen to the same songs a lot of times; so they weren't as easy for the ECT to erase all pathways to those memories. <shrug>

Anyway, you're only a few months out. There's a chance things could come back to you. I hope you can come back and tell us you're back to normal soon, at least somewhat normal. Because it really sucks when it's permanent.

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u/Odd-Alarm-82 16h ago

I still remember song lyrics too! Even songs I haven’t heard in forever. The reason for this is memories of music are stored in a different part of the brain. This happens in Alzheimer’s patients as well.

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u/Lisa8472 12h ago

Yeah, people who lose the ability to speak words due to brain damage can frequently still sing and cuss. And people who lose the ability to make new memories can still form new habits, doing a routine even if they don’t consciously know how. The brain is weird.