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Anyone experience semi-conscious dissociative state?

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In my case before fading away I can experiment many physical symptoms. Some of which are:

*Tingling in my head
*Spaciness/dizziness
*Sound is distorted
*Vision is distorted
*Environment starts to not look real, like in a dream-like way.

Then I feel tempted to just hyperfocus on one spot and if I give in all symptoms above tend to get worse, and I end up just fading away/going away.

To avoid this I try to forcefully look around making sure I'm moving my neck, take a sip of my iced drink, feel the fidget toy, hear my therapist, etc.

Another option is my protector getting activated and then it feels different, but that's a whole different story.
 
In my case before fading away I can experiment many physical symptoms. Some of which are:

*Tingling in my head
*Spaciness/dizziness
*Sound is distorted
*Vision is distorted
*Environment starts to not look real, like in a dream-like way.

Then I feel tempted to just hyperfocus on one spot and if I give in all symptoms above tend to get worse, and I end up just fading away/going away.

To avoid this I try to forcefully look around making sure I'm moving my neck, take a sip of my iced drink, feel the fidget toy, hear my therapist, etc.

Another option is my protector getting activated and then it feels different, but that's a whole different story.
Thank you! I share similar symptoms just before, except the tingling.
 
I am new to this website, and I am hoping to find people that have experienced in therapy what I have.

I am told I dissociate. My EMDR therapist with 24 years of experiences says my dissociation is the most severe he has seen.

When I dissociate, my T says that I go into a semi-conscious state where I am able to remember everything that I hear and see but I am unable to move or speak, but I am unable to recall what I was thinking or felt during this state. My psychiatrist calls this a dissociative form of "catatonia". I think it's some form of dissociative stupor. We are unable to find a trigger with my current and previous

You are not alone. Stopped EMDR cuz of it after two sessions. In my case, it was a response to bring overwhelmed. Also a way of protection. Reenactment of abusive situation where was being overwhelmed but forced to stay...no escape. It would happen at first during EMDR then when being *too* close to abuse details. At first no warning like flipping a switch. But T & I started backtracking and finding subtle signs. Worked out a signal I can give when getting close to that state. We back off & he approaches the issue differently. He is careful to allow me to be in control of confronting. Know that if start to go over the line, I hear positive reinforcing messages from him.
 
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I am new to this website, and I am hoping to find people that have experienced in therapy what I have.

I am told I dissociate. My EMDR therapist with 24 years of experiences says my dissociation is the most severe he has seen.

When I dissociate, my T says that I go into a semi-conscious state where I am able to remember everything that I hear and see but I am unable to move or speak, but I am unable to recall what I was thinking or felt during this state. My psychiatrist calls this a dissociative form of "catatonia". I think it's some form of dissociative stupor. We are unable to find a trigger with my current and previous T.

I am hoping someone here has experienced something like this and will be able to tell me more about their experience, and if and how they treated it.

Right now my T and P are doing damage control, trying to avoid me going into this state.


@LOTR741 When I would wake up in the morning, I evaluate my vision and alertness or dissociation-1-green (keep on going...stress level low-gonna be a good day), 2-vision not so clear, dragging a bit, moving slow, memory not sharp-in this state....I tend to essentials right away (protein shake, vitamins, medication, something cold, do the room senses activity (taste, touch, smell, hearing (make sure I put hearing aids on), and reread my list for the day, and see if there is anything I can cut to reduce stress in the afternoon if need be.....But a 3-red and foggy, memory is shit, (for you maybe 4 is catatonia). That red light, yellow light, green light way of tracking was easy.....

So, got a new T and I've been tracking my dissociation and rating it on a 0-4 scale. You can use whatever rating scale fits your situation with dissociative disorder.....but just use the same rating scale everyday. For me, at 4-I have tinitius so very loud that I can't concentrate or think and this is where I just want to go to sleep-hearing is so distorted....balance is poor, and attention to safety is severely impaired (kinda like tunnel vision.). Right now, to get a handle on grounding....I rate upon waking, and hr after meds, mid morning, lunch, an hour after lunch, mid afternoon, dinner time, hr after dinner time, two hrs. before bed and bedtime. It's a pain in the ars but the information is very helpful and noting the different triggers and activities throughout the day has been helpful. It is always a 1-2 when I walk in this new T's office, but my T is all about grounding first, trauma talk......only if I'm feeling safe....and not being grounded in her office....not a good thing. You are fortunate that your T realizes that grounding is an essential safety skill and wants you to feel grounded first. My last T didn't do grounding exercises, or teach me to ground at the end of the session, and I walked out of the office highly dissociated and had to cross the street......in a stupor. It wasn't safe. Sounds like you are doing good work!
I write what I'm doing at each interval, or write when anxiety(precipitator/trigger) increases as related to dissociation. If you use a numbered system, like a Likert scale, and it is divisible by 100 (rating scale of 0-4) then you can change it to percent.
 
What are your signs you’re about to fade away? For me it feels like an internal battle to stay conscious.

When mine would come - this sounds kind of funny, I know - but I would get "tingles in my butt". LOL (like the feel your skin gets when your arm or leg "fall asleep"). When this would start to happen to me, I would leave the room and go to the bathroom, or just signal my friend, who knew what is going on, and then she would watch me for problems.

I remember a party at a friends house. I was sitting on the floor and felt the "tingles". I always seem to lose my ability to speak first, so I used my signal to my friend to let her know that I was going to "step out " ( our code word). She saw me and simply said to everyone, "lets all go get a drink in the kitchen. So we're not all staring at her when she comes out of it."

When I finished, I got up and joined the party. She told me later that she just stayed by the doorway to keep an eye of me. To this day, she is the one who knows the most of what I went thru. It is such a relief that I don't get these "fade outs" any more. But, I do teach this signal to anyone close to me. So they know what to do -or not to do, if these were to ever happen again.
 
Sounds like you have a very nice friend. Glad you no longer have to go through that.
If you have someone to "know" even some, of what your going thru. I found that a "secret signal" was a good idea. It was kind of like having someone on my team. Someone who knew. A lot like when you and your best friend could signal each other across the classroom while the teacher was talking, and know where to meet at recess.

Mine was very simple. I would just tap the side of my head with my finger. Basically saying: "I'll be back in a moment. I have to step out." LOL (simple. quiet. not very noticeable to a stranger or anyone else. Yet, it gets the point across clearly.
 
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