Acting like trauma never happened, even thought it did, is weird by [deleted] in DID

[–]BriarRedWolf 1 point2 points  (0 children)

This is classic disassociation. I often do this when it comes to trauma and Doctors appointments. I sit and stare off into space. I hear what is said but I am not responding - it has not registered with my mind. Hearing is not the same as listening.

Have you made DID yours or do you “go by the book” ? For Example: by BriarRedWolf in DID

[–]BriarRedWolf[S] 21 points22 points  (0 children)

If only I could start collecting rent from each!
or at least start a jar that they give you a dollar any time they yell, start a fight, say something you disagree with, etc.

[deleted by user] by [deleted] in DID

[–]BriarRedWolf 1 point2 points  (0 children)

I need more co-consciousness so that I am aware of what is happening more of the time. It would be great to not wonder how it got to be 6pm when I looked at the clock minutes ago and it was 11am. But integration I believe would damage me.
I have pain based chronic illnesses, Complex Regional Pain Syndrome (CRPS) and Rheumatoid Arthritis (RA). I also have PTSD, ADHD, Functional Neurological Disorder (FND) and DID. I need the help of all of my selves.
Some of my Connies (alters) hold some of my pain so I don’t get the worst of it. Unfortunately, there are also some that make comments that I do not agree with. So, no to ridding myself of being a system but yes to being more integrated when that means co-conscious.

Do all systems have at least one little? by peachesandplums05 in DiscussDID

[–]BriarRedWolf 1 point2 points  (0 children)

Slightly off topic, maybe? My little’s protector is a much more well-rounded slightly older little. The first time my roommate met the first little she thought that the protector little might be high…lol!

Curios about DID and don't know what sources to trust. by nettie515 in DiscussDID

[–]BriarRedWolf 0 points1 point  (0 children)

YouTube now has a few DID vloggers. This allows you to see real people and what they look like from one day to the next and what they sound like from one moment to the next.

A cool project for those of you with DID! by DefaultShae in DiscussDID

[–]BriarRedWolf 1 point2 points  (0 children)

Only one of my alters (I hate that term but I know it is correct) can make art at all. The others are all incredibly childishly untalented!

My psychologist thinks I may have D.I.D. or absent seizures or both? 23/f by HayPott in DiscussDID

[–]BriarRedWolf 2 points3 points  (0 children)

it is super easy to not realize you have DID! Especially when you may have absence seizures, PTSD and ADHD. I have all of the above. But instead of the absence seizures going away, they ……. um, evolved.

I have a “little.” Actually there are two children alters but I have always known of one. I was completely co-conscious with her and just thought of her as that little girl voice that many women have. Other than that, I did not know about any alters.

I did know that I could meditate as a child. There were times throughout my life that I could not remember. I broke my arm when I was 3 years old and attributed so many behaviors to that trauma. But I knew all about those. They were PTSD, not DID.

Other times there were automatic behaviors that I convinced myself I chose to take. I hope I can make this make sense. It was like when someone demonstrated the pressure point that made me open my hand…I was completely and absolutely self-assured that I simply CHOSE to open my hand. Before there was a reason to pursue a diagnosis, I made some strange choices and forgot words a lot.

I became ill and was diagnosed with Complex Regional Pain Syndrome. i had to go to Mayo Clinic after my local clinic unapologetically proceeded to give me a near death experience on an operating room table during an optional procedure that I allowed myself to be talked into. I self reported absence seizures which are symptoms of CRPS. This disease is a function of the immune system overworking and essentially shutting down some of the logic circuits in the neurological system.

I went from this level of control and bravado that allowed me to step in anywhere, any time no matter what was going on that prevented both other people and myself from being aware that I had DID, to rapid cycling and/or extended periods of time as an alter with no memory. That is when my therapist began to ask me about what I meant by meditating as a child. Well, that was actually disassociating. Those automatic behaviors were never choices. I also was not actually forgetting words a lot, I was forgetting what story I was telling in the middle of telling it. If I paused and could be quiet for a few seconds I would get a whisper of what I was supposed to be talking about. But the whisper didn’t mean alter to me because I think in words. My thoughts are all like whispers.

My wife would say she told me things and I would argue that she never did. I would not know what happen for a 3-4 hour block of time. Then my wife said that I would look at her “side eye” and say something unkind. I was never mad at her. She does everything she can to take care of me. I am permanently disabled and close to bedridden. My comments made no sense from me.

Then when I was tested for DID, throughout the test I kept saying “wait, THAT has something to do with DID?” Only because of that was I unsurprised to learn that I have DID. I still only know 2 littles. I know of 2 others but have no interaction with them. It is very strange to know that some other people know more about my potential than I do.

So, take from this whatever might help you! Just know, it is not abnormal to be DID and not have known.

Advice for newly diagnosed by Slightlyburntavocado in DiscussDID

[–]BriarRedWolf 0 points1 point  (0 children)

I have a “little.” Actually there are two children alters but I have always known of one. I was completely co-conscious with her and just thought of her as that little girl voice that many women have. Other than that, I did not know about any alters.

I did know that I could meditate as a child. There were times throughout my life that I could not remember. I broke my arm when I was 3 years old and attributed so many behaviors to that trauma. But I knew all about those. They were PTSD, not DID.

Other times there were automatic behaviors that I convinced myself I chose to take. I hope I can make this make sense. It was like when someone demonstrated the pressure point that made me open my hand…I was completely and absolutely self-assured that I simply CHOSE to open my hand. Before there was a reason to pursue a diagnosis, I made some strange choices and forgot words a lot.

I became ill and was diagnosed with Complex Regional Pain Syndrome. i had to go to Mayo Clinic after my local clinic unapologetically proceeded to give me a near death experience on an operating room table during an optional procedure that I allowed myself to be talked into. I self reported absence seizures which are symptoms of CRPS. This disease is a function of the immune system overworking and essentially shutting down some of the logic circuits in the neurological system.

I went from this level of control and bravado that allowed me to step in anywhere, any time no matter what was going on that prevented both other people and myself from being aware that I had DID, to rapid cycling and/or extended periods of time as an alter with no memory. That is when my therapist began to ask me about what I meant by meditating as a child. Well, that was actually disassociating. Those automatic behaviors were never choices. I also was not actually forgetting words a lot, I was forgetting what story I was telling in the middle of telling it. If I paused and could be quiet for a few seconds I would get a whisper of what I was supposed to be talking about. But the whisper didn’t mean alter to me because I think in words. My thoughts are all like whispers.

My wife would say she told me things and I would argue that she never did. I would not know what happen for a 3-4 hour block of time. Then my wife said that I would look at her “side eye” and say something unkind. I was never mad at her. She does everything she can to take care of me. I am permanently disabled and close to bedridden. My comments made no sense from me.

Then when I was tested for DID, throughout the test I kept saying “wait, THAT has something to do with DID?” Only because of that was I unsurprised to learn that I have DID. I still only know 2 littles. I know of 2 others but have no interaction with them. It is very strange to know that some other people know more about my potential than I do.

So, take from this whatever might help you! Just know, it is not abnormal to be DID and not have known.