ā you will find a forest of curious light

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he wasn't even looking at me and he found me
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if i look back, i am lost
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@spiritwoods
ā you will find a forest of curious light
you know, i don't remember
"DID symptoms no-one talks about" but very specific this time:
Conflicts and arguments are harder because you're more likely to rapid switch and experience amnesia when you're emotionally distressed, so I often end up feeling like I'm contradicting myself, back-tracking, and don't remember enough of what transpired to be able to truly engage and communicate well. This can make me seem like a liar who is trying to manipulate others and dismiss accountability for their actions. The reality is that different alters have different opinions, feelings, and input, and one alter cannot explain another alter's thought process, so sometimes I say something and then seem to back-track and contradict myself, because I can't explain a thought process I previously had, no matter what, because it was an entirely different alter with that thought process who is no longer fronting.
I don't know if I have ARFID, but I've suspected it for a while, and I've suspected that part of my problems with eating and food could also be different alters having different food preferences. I've had a lot of experiences where I felt like I thought I liked a food, only to try it and it tastes completely different from how I remember it and food not tasting good to me anymore, even though I previously liked it. I'm not talking about the normal human "taste buds change" over the course of years - I'm talking about "I know I liked this weeks ago, but I hate it now", "I seem to sometimes like rice and soy sauce and it's delicious, but other times it seems to taste disgusting and nothing at all like I remember."
How different DID feels when you have little to no awareness vs much more awareness. Why does no-one talk about this? Before I've gained some more of the awareness I have now, I was totally unaware of switches and alters, and many people treated me like I wasn't describing DID symptoms or like I was describing OSDD instead of DID, all for reasons like me telling people "I don't switch" when the reality was actually that I was simply not aware of switches and discounted any time I thought a switch may have happened and I didn't know how to figure out if I had switched, so I BELIEVED that I didn't switch, and I BELIEVED other things too such as "my memory is fine" and would tell people these things - other systems - and they'd tell me that I wasn't describing DID symptoms or that I was describing OSDD instead. The reality was that I just had extreme denial and little to no awareness because my dissociation was so extreme. And I just have to say that DID feels completely different when you have actual more awareness of who your alters are, when you switch, of passive influence, internal communication, and more, and I never see anyone talk about it.
DID is not rare, but the entire world makes you FEEL like it is.
Dysphoria/dysmorphia (I'm unsure which word would be more accurate to use here) because your visual appearance doesn't match how you want to be/wish you were perceived. I've seen people talk about some weird experience of ""seeing yourself in the mirror and seeing someone who doesn't look like you"", and I assume that's the experience I'm talking about, but at least for me, it just feels more like this bone-deep discomfort with my appearance because I don't look the way I wish I did. And it can be like "I'm uncomfortable because we are wearing clothes that the current fronting alter doesn't feel comfortable in" to varying degrees of gender dysphoria experienced by different alters to "I look completely different from how I wish I could look, and that brings me great discomfort."
Honestly being surprised at times to truly think about some alters and see them as "Me" just another side of me. Like, sometimes I just think about some of us and it feels strange to really think about the fact that "that alter is Me, just other aspects of my personlity."
Stoat facts
a lot of things seem to happen to the guy whos body i happen to be observing through its own eyes although from afar
ē³äøē“ä¹ę° Junya Ishigami ā Water Garden, 2018, Nasu Mountains, Japan
There is this false narrative that Complex Dissociative Disorders are only caused by the most extreme trauma imaginable, when that isnāt true for most pw/CDDs.
Though it does happen, pw/CDDs do not usually have histories including the most horrific actions recorded in history, and this belief is often dangerous to people with the disorder.
Everyone with a CDD has severe trauma response. However, development of CDDs is not related to the severity of trauma, but instead to the complexity of trauma. This is why disorganised attachment to caregivers is common in pw/CDDs, because the shift of adapting from extreme kindness to cruelty is too complex for children to manage.
In most situations, dissociative responses to trauma are due to feeling like a situation is inescapable. Children may experience abuse, neglect or multiple āless horrificā traumatic events, and feel as though they cannot escape the situation, usually due to a combination of repeated trauma and lack of an adequate support system. Due to this feeling, children dissociate, since it is the only method of escaping the overwhelming feeling when other escape routes are not accessible. Missing a support system to overcome traumatic events or stressful feelings and situations is a recognised central cause of dissociative responses.
Itās also important to mention that children have a higher predisposition to dissociation, due to already having a less cohesive identity. For this reason, children may experience dissociative responses to situations that adults (without a history of dissociation) would not.
When adults experience complex trauma, for example domestic abuse, itās not uncommon for them to mention feeling as though they ālost themselvesā or āneed to rebuild themselvesā because they already have a cohesive self, but their trauma made them dissociate from that self. Children, however, do not have a cohesive self to āloseā and therefore the threshold for dissociation is lower.
Many people with CDDs do not recognise their trauma as being severe enough to qualify for a dissociative disorder. This is due to dissociation, and denial, but also because the false narratives about how CDDs appear, and what our trauma looks like, because people will often only listen to stories which can be turned into a spectacle for consumption. Your trauma is enough, regardless of what it may be, and you donāt need to doubt yourself.
TLDR ā Development of DID is not exclusively connected to severity of trauma, and not everyone with DID has experienced the most extreme, horrific actions of human malice. Its development is more connected to complexity of trauma, feeling of inescapability, and lack of adequate support systems. Your trauma is always valid, and enough.
(summary/information of the theory of structural dissociation) (pdf of the haunted self, book proposing the theory of structural dissociation)
Wishing there was more research on epochal divisions in DID.
I suspect (know) I experience this phenomenon and I have months and months of severe dissociation from the start of old parts going dormant/latent and the start and full formation of new parts.
Not only are the experiences in the months affected by this severe dissociation not readily integrated into my sense of self but all past experiences/memories are basically alien to me or are forgotten and not reaccessed by any part until they can be recompartmentalized.
It resembles severe depression when it happens but I just lose my personality because past experiences are being sorted through and my brain is determining where they should be placed now. It's like mass reorganization, these parts should do this so they need to have have [x] memories. This is my best guess for what happens in these dissociated months.
I just want research done on this, new modern research so I can have an explanation for this that doesn't sound like I'm on some endo system reset bullshit. I don't choose these new alters, I have dozens and dozens of latent (or occasionally reformed) parts all from very specific periods in my life. I have no control over this and they don't immediately form. I know it's vaugely documented by Kluft by I haven't been able to find much else surrounding these divisions.
I just want actual and substantial medical documentation of this experience among systems. It isn't clear if these epochal divisions can only happen in DID and not OSDD or if it only happens in "polyfragmented" systems, which are also not well documented and there's no clear medical consensus of what polyfragmented really even means.
āBLACKTAILED DEERBATā KATE MACDOWELL // 2021 [hand-built porcelain and cone 5 glaze | 5 Ć 2 ½ Ć 3 1/2ā³]
Sharing your brain/body with other guys is cool and all but it comes with the secret side effect of making basic questions super hard to answer.
"What's your name?" Okay so my name or our name or the body I inhabit?
"What's your favourite colour?" This is going to start an hour long argument in my mind and the most you'll see that comes of it is me staring off into the distance unblinking.
"Do you want to go see a movie?" See here's the thing, I really do but there's a guy hanging around in here right now who hates movies and also is terrified of being surrounded by people in a movie theatre so I'm gonna have to say no even though I really want to.
"What are you gonna wear tonight?" This is yet another hour long argument, please don't start it.
"What's your birthday?" So. The body I inhabit, the day they discovered me specifically, the day that is my specific birthday, or the day that I formed???
"You like [food], right?" There's 100s of us and we may have strong opinions on the subject. One day I might say it's my fav and the next day I might rather eat cardboard.
hello! looking for some more currently active osddid focused blogs to follow, especially other polyfrag systems and/or systems of colour
pls like/reblog/reply if this applies to u! :D
p.s. : follows from a main + more info in tags
DID/OSDD Library
There was some interest in this earlier, so hereās a link to my google drive DID (and related trauma/disorders) library!
This library includes, but is not limited to:
Adult Children of Emotionally Immature Parents (Lindsay Gibson)
CPTSD: From Surviving to Thriving (Pete Walker)
Coping with Trauma Related Dissociation (Kathy Steele)
The Body Keeps The Score (Bessel van der Kolk)
The Haunted Self (Onno van der Hart)
Treating Trauma Related Dissociation (Kathy Steele)
Healing the Fragmented Selves of Trauma Survivors (Janina Fisher)
I can not personally vouch for anything in this drive. I havenāt read the majority of it, itās just the books / articles / PDFs Iāve happened to collect. Additionally, everything being shared here is being shared legally for educational purposes.
UPDATE: hyperfixated on this project for a few more hours today and added a ton of new stuff I previously had bookmarked. some of my fav new additions are:
My Life as a Dissociated Personality (B. C. A.) - a short autobiography published in 1909 by someone with DID. I canāt find very much info about it online, other than it exists, but the fact that itās over 100 years old interests me enough alone.
Many Voices (Lynn W.; in my āarticles/studiesā folder) - a DID newsletter by and for people with DID, featuring art and poetry. Currently, I have three issues uploaded (ranging from 1996 - 2000) but I may upload more later!
Worksheets! (in my ādiagnosis/treatmentā folder) - mostly self help worksheets, but thereās a few for loved ones as well, all from a variety of sources.
a reminder that the host isnāt the only person in the system who should be respected and made to feel comfortable.
the host is not āthe important partā, we are all completely conscious and capable of our own thoughts, feelings and our own boundaries. our brain created us because it decided that we are all important and needed.
the host is not the only member of a system you should care about.
I think a lot of people tend to think that blackout amnesia is super obvious, and that the experience is like cutting from one movie scene to another and being completely disoriented.
Blackout amnesia can be very deceptive, especially if you've had it nearly your entire life, because your brain starts getting really good at coping with it in basically any way it can. My brain often does this thing where I can remember remembering an event, but when I actually try to think about the event, I realise I don't actually know what happened. But the thing with memories is you're not constantly re-reviewing them to make sure you actually remember every single one- it was only when I started asking other people what happened during these events that I realised how little I truly remembered.
Coming to the front isn't always super obvious, because if we end up somewhere, it's fairly easy to orient ourselves just from virtue of having to do it all the time. You can get very good at spotting what type of building you're in, the people you're with, and how you most likely got there. The vast majority of the time, we're in places where we go to a lot anyways, so questions like "Where am I? Who am I with? How did I get here?" aren't even questions that would pop up. It can make it feel very much like you had a consistent string of memories, even if you really didn't. If you're wearing clothes you know you own, you'll probably think "Oh, I changed and forgot" or if you end up with food you like, you'll probably think "Oh, I must have gotten food and forgotten." It's natural to conclude normal forgetfulness over blackout amnesia.
Blackout amnesia isn't always as simple as ending up somewhere you don't recognize. It's not always as simple as ending up with things you don't own. Spotting blackout amnesia is extremely difficult- it's not as simple as just knowing what blackout amnesia is, but spotting the ways your brain has coped with it and what you could be missing these gaps. This isn't to say I've never been disoriented by my memory gaps. My memory gaps were pointed out by other people and had been aware of them long before I knew I had DID, but I had no idea I had blackout amnesia until I started looking more at what was going on. It can be easy to miss!
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