I have DID and feel paralyzed during the pandemic

This pandemic has done something to me that after almost an entire year of it, I still can’t really explain it. I wonder how many others with Dissociative Identity Disorder (DID) are in the same boat? I have moments of recognizing how my complex-PTSD affects me during the pandemic. But the DID, I don’t know.

Sadly, my therapist who is trying herself to survive this pandemic, is of little help to me as a therapist. She seems more like supportive friend material now. Maybe because our sessions are over the phone, it just doesn’t work well for most of me. I can also clearly hear her own stress most sessions as she deals with her own feelings through the pandemic.

I think the constant stress of the pandemic keeps me in fight/flight/freeze on a daily basis. There really isn’t anything to de-escalate it as the truth is the fear is real. None of us could have imagined our lives like this, and none of us know where we are headed. But, with this comes a constant cortisol surge. Part of why I know this is happening is because I am never tired.

If you are interested, I actually found a supplement that stops the Cortisol surge enough so I can at least sleep. I got the idea from an Amino Acids expert named Trudy Scott if you want to research it. The product name is Seriphos by InterPlexus. It is now a product I can’t live without, and more helpful than any psychiatric drug I have had.

Admitting there is little-to-no mental health help available to those of us who usually need a lot of it is an interesting thing. Honestly, I try really hard not to let my mind focus on that issue for longer than a split second. To do so is too reminiscent of a brutal childhood with no help and no escape. I can’t go there again.

I joked with my therapist the other day when she was expressing her pandemic fatigue that it was much easier for me because my DID gives me little sense of time. Intellectually I know how long we have been in this pandemic, but honestly, it feels like only weeks have gone by.

I am mostly coping without the help of my therapist. I am that child who got us through our childhood. That child who should not have survived, but somehow managed to. I keep my head down and keep pushing forward trying to get me and my family through this. It helps me understand how I might have survived something so horrific as my childhood. My auto-pilot survival part has taken over. Maybe those of you with DID have found this to be your experience too?

I made it 10 months before getting COVID. I was so careful, but one lapse in judgment, I let an electrician come into my home not wearing a mask because I mistakenly thought I was safe because I had on a mask. Never before have I let someone in my house without a mask. Perhaps the reason I did this is because this electrician was an abuser from my childhood. F-ing figures.

The very first symptoms of my COVID were 3 nights of very bizarre dreams. I was telling a friend about the strangeness of them the morning I came down with the full-blown symptoms. I knew something was wrong, but couldn’t pinpoint it.

When I got COVID, it attacked my brain, which was weird because I was so worried about my lungs before getting it. I know to the average person that may sound crazy, but I don’t really care. When I was in the emergency room, the doctor there validated me saying “we know that COVID gets into the brain because we have autopsies that show the virus is there.”

I believe the bizarre dreaming was the first sign it was in my brain. Then came the headaches. Then came the extreme head pain that felt more like brain torture going on in multiple places at the same time. Then I developed what felt like severe earaches that would come and go. Then everything turned surreal, in a way that was different than my regular dissociation, and I thought I was going to die.

I abandoned traditional medicine and went with a treatment protocol that the NIH had been ignoring, but my kids’ infectious disease doctor believed in (Marik COVID Protocol, if you are interested). I had already been taking the supplements, but when I got the Ivermectin my brain symptoms and high fever disappeared within a day. It was a miracle, but like DID, most people assume those of us who believe in it are just crazy. No matter, but I share it here in case it saves one other person.

I knew with the Adverse Childhood Events (ACES), my age, and the fact that I had asthma, I could die from this. Strangely, the only two things I told the ER doctor were 1. I don’t want to become brain damaged, and 2. I didn’t want to die. It was one of those DID moments where I was surprised what came out of my mouth. Internally, I marveled that that was what I found most pressing to say in the moment.

Anyway, I survived it. I am proud that I did. I had prepared for it with all the right supplements and medications. I still have some lingering symptoms, but I at least survived it.

The “experts” say that COVID will often attack what is already weakened in a body, so they say people with psychiatric symptoms will likely see a worsening of those symptoms. That’s a scary thought since I can’t imagine worse. But, it is true so far that I have moved from horrible, but medication managed insomnia pre-Covid, to severe horrible insomnia post-Covid.

I don’t know why I am writing all this kind of interconnected stream of thoughts down. Except that I know I need to write to try to get myself back.

I have felt paralyzed during this pandemic, and that scares me. It also keeps me alive. But I know it is a terrible way to live long-term, and I have no idea how to change it. I actually miss the challenge of living life as a trauma survivor. At the same time, I enjoy the luxury of it being socially acceptable to stay at home everyday and do I don’t know what. With my dissociative skills neatly intact, the days just blur right by.

But, paralysis with my DID means that most of me is missing. Those many, many parts who make me who I am are just not here the majority of the time. No, it’s not spontaneous integration. I haven’t become a singleton. It means I am so terrified I am locked into survival mode, repressing the majority of who I am. It’s lonely and I feel almost nothing for a year now. 🥺

Therapists, we need you to be courageous

It is hard for my brain to push forward with my usual coherent thoughts. Each day during the pandemic, I just keep moving forward in crisis mode and it never seems to end. If I slow down, I get consumed by depression and lack of energy, so I have to keep moving to survive.

I shouldn’t feel sorry for myself because I know just about everyone is struggling with the way we must live during the pandemic. Maybe this is why it is hard for me to put my thoughts or even words together on paper.

I am so tired. Probably because I am surging in cortisol and burning out my adrenals. I also recognize every day is like Groundhog Day. Nothing really changes. It’s stressful as hell, but I know the stress keeps me moving, and to not move will allow feelings of depression and suicide to creep in.

I am mad at my therapist, but not really mad because I don’t even have the energy to experience or express that feeling too much. I also know she is struggling through this pandemic too, but my irrational child parts feel so abandoned.

It is a fight not to quit therapy again. I don’t have the money to have wasted sessions with her, but I continue to do so because I am scared not to. I hate that she will only do phone sessions with me. I am also triggered by her feelings that I might be contaminated with COVID, although she has never directly said so. Still, it brings up childhood feelings that there is something bad about me.

Of course the big one is that I don’t matter enough to her when the chips are down and she needs to prioritize her own health. My adult brain understands what she is doing, but my child selves feel painfully abandoned.

Having DID and not being able to get in-person support is so hurtful. It’s as if the therapy world suddenly decided we are all doing much better than many of us are (I am happy for those of you who are doing well). Suddenly, our survival is not as important, perhaps we are just collateral damage to this pandemic.

Don’t get me wrong, I have a healthy fear of the coronavirus. It is not something to play with, but I also feel like I have learned how to function safely in the world with my mask, hand sanitizer, and social distancing.

This brings up the “if my therapist really cared about me, she would see me in person.”

I am struggling. Struggling with just about everything. So conflicted inside about whether I should just quit therapy or that is the dumbest idea in the world.

I hate that I can’t get the support I need. I hate that my therapist is so caught up in this stupid pandemic that I barely matter to her.

I know I have returned to trauma time almost 24/7. I can’t make decisions which is usually a pretty good indicator I am frozen in trauma time.

I just love how everyone pretends like those of us with DID and are in need of support don’t really exist anymore.

I guess it is our own fault for not screaming loud enough, or maybe it’s just because the whole world is fighting us for scream time.

Let’s stop pretending that those of us with serious mental illnesses are doing ok, and that the fact that our therapists have abandoned us is going just fine. I do understand their desire for self-preservation, but enough is enough.

Psychotherapy can be done safely with masks, social distance, and hand sanitizer. The restaurants and stores are making it work. It’s time for the therapists to get off their home couches and their teletherapy.

Some of us are dying out here for reasons outside the Coronavirus. Staying at home indefinitely hiding from the coronavirus is not the answer for anyone. The mental and physical cost is severe.

Therapists, it is time to start doing your job again, and not just for the people who get enough out of teletherapy.

It can be done safely. Be creative. Let go of your irrational fear that we can’t meet in person with appropriate safety measures to protect us all. Heck, have therapy outside if you need to, but stop ignoring those of us who don’t find help with teletherapy.

Model strength, creativity, and courage. We need you to do that as much as you need it for yourself.

Missing my life

I have been away a lot lately. It’s been a combination of extreme stress going on in my life and losing time.

I find that I am losing time and not realizing it, which makes me sad.

Facebook is a big revealer of lost time. I look back at memories from past years to see sweet pictures of my kids, but lately noticing all sorts of writings that I have done over the years and have zero remembrance of and no idea what I am even talking about. It is not that I sound incoherent. I just have no understanding or even a remote memory to what I might be talking about.

Somehow I have been living in this cloud that has kept this losing time from me. I have been diagnosed a long time, and I like to think I have a good bit of co-consciousness, so normally I can figure out enough to understand what the heck I was talking about.

I know my system was designed to keep this stuff from me, but I also thought I was further along than I apparently am.

Yesterday, I got on my daughter’s phone to deal with some boys who had sent some inappropriate texts. It took me about 6 hours to realize it wasn’t me who did that talking to those boys and threatened to call the police on them.

I wonder how many times I do this subtle switching in a day. How much am I forgetting?

I belong to a secret FB group for survivors of DID and ritual abuse. I used to get support in that group, but I stopped because I realized I had all sorts of posts under my name that weren’t from me. They weren’t from child parts, but parts similar to me, but definitely different in some major ways. It became too overwhelming to see post after post that I didn’t recognize and didn’t have any sense of losing time.

I was thinking this morning that my biggest disabling part of DID is the memory loss, which is not news if you follow me. Yeah, I am suicidal and have attachment issues and CPTSD out the wazoo, but that is all manageable compared to the memory. Then I was thinking for me, do I really have a mental health problem as opposed to a neurological problem since my memory seems incapable of storing and being accessed correctly.

I know, it probably doesn’t matter to you what it is called or how it is classified.

It saddens me, though. To know I am living a life where I am missing so much of it. I guess it is a little like Alzheimer’s, but knowing you have Alzheimer’s which I think is more painful.

Now that I am getting older, people just attribute all the mental lapses as old age (though I am not that old). The neurologist who gave me an exam where I had to remember things was perplexed how severely I couldn’t remember the things she was testing me for, but in the end just attributed it to cognitive decline due to old age.

I was around my family over the holidays and I am hearing myself call my perpetrator brother my son’s name, and he call me his daughter’s name. We joke as if it is old age, but I know it is more likely that we are triggered and our parts are having trouble keeping things straight.

Anyway, why is Alzheimer’s a neurological condition and my similar memory impairment is a mental illness? Maybe someone can explain it to me.

Yeah, I am frustrated about my memory, but avoiding the tough conversation I need to have about something big I/we need to decide. Indecision is another curse for another day. If I remember.

The True Trauma Wound

Though I have been brutally abused both sexually and physically as a child, the pain of those instances is not what keeps me sick.

Those injuries play through my mind daily in one detrimental way or another for sure, but they are not what ruined me.

The psychological warfare done to me as a child has definitely left its mark, but still, it is not this that leaves me broken.

Abandonment.

I am sick, broken, and less than human because of abandonment.

My pain from, and fear of new abandonment, is what rules my days. It keeps me paralyzed, scared, and sad all rolled up into one messed up package.

I would like to think the blatant abuse by my parents and other adults is what has ruined me, but it is not.

The well of my pain stems from people turning their backs on me. People treating me as expendable. Instilling in me that I don’t matter, and that others are always more important.

This.

Recovering from humanity’s deep abandonment of my soul.

Surviving as either the walking dead or the walking wounded.

There is no beating it. It’s encoded in my DNA. Each and every subsequent betrayal reinforces the idea that I am only worthy of abandonment.

No matter how hard I try, I always find myself getting abandoned by those I need the most.

I try so hard to be “good enough” or “nice enough ” or “smart enough,” but I always land back in abandonment purgatory.

The therapists and spiritual philosophers always try to convince me I am not a bad person, and somehow this repetitive abandonment has nothing to do with me.

Of course, that’s not true.

It has everything to do with me, which is why it repeats over and over in my life.

If this is my final destiny, I am confused as to why I keep carrying on trying to prove it won’t happen again.

It always does, though.

Sometimes I see it clearly and try my best to stop the inevitable, and other times I am blindsided and never fully understand what happened.

Ah, back to my parents, and the others who created the permanent scarring of my brain. The deep state of confusion I am always meant to live in.

That’s it, you know. The deep abandonment wounds that can never be understood.

Healing. No. That doesn’t exist for me.

Only the slow drip of confusion and pain serves as the morphine of my life.

Is healing from Dissociative Identity Disorder possible?

I was diagnosed with Dissociative Identity Disorder (DID) in my early twenties. I was in my Senior year of college when I suddenly started having significant psychiatric problems I hadn’t experienced before. Even though my life was actually going very well in the world, my internal experience was crumbling as I had my first Major Depressive episode, panic attacks, and suicidal ideation seemingly coming from nowhere.

I didn’t know what was happening, so I quietly went to the campus mental health center, where the psychiatrist gave me a bottle of Xanax to help me deal with whatever was happening.

It completely consumed my life rather quickly. The pills helped a little, but I was seriously suicidal for unknown reasons.

By some miracle, I had the wherewithal to find a therapist off campus. And then a psychiatrist, and quite quickly, I ended up inpatient at the local psychiatric facility for about six months.

During my time in the hospital, I was trying really hard to understand what was happening to me. I was a mystery to my treatment team, too, as I had so much going for me, why was I doing so poorly?

I started having outrageous transference with my therapist. I felt as though I couldn’t live without her. I would start to get better and approach discharge, and then my therapist would go out of town and I would find myself plotting to kill myself at the hospital. I never had feelings like this about anyone before.

I can remember sitting in a chair thinking in my head that I didn’t understand what was happening. And then I realized there were voices in my head commenting on things or expressing their despair about the therapist. I had always had these voices commenting in my head, but I realized for the first time it was like they were different people with different thoughts. I knew I was going crazy.

I started feeling like I wasn’t in control of my thoughts or behaviors sometimes. I tried to speak about it some to my primary treatment team members, but they didn’t take it too seriously as they knew I was not psychotic.

Back then, I didn’t have the words to properly express my experience of what I now know to be Dissociative Identity Disorder (DID).

When I finally discharged from the hospital, I had a crazy sexually abusive relationship with a counselor from the hospital, and then abruptly decided to get a job at another psychiatric hospital as I was suddenly interested in helping people (and ignored the fact that another part of me had already accepted a job offer from a big corporation).

While I was working at the hospital, I was still trying to figure out me, and would read every patient history, study the DSM, talk to clinicians, sit in on clinical meetings. During my research, I discovered a therapist who specialized in dissociative disorders and trauma therapy.

While still seeing my old therapist back in my college town, I decided to go see the therapist who specialized in dissociation and trauma, and asked her to help me figure out if I had DID.

In case you are wondering, my therapist who I adored and my psychiatrist did not believe in DID.

It is still common today, you have the believers and nonbelievers in the mental health community. It sucks for those of us afflicted.

But I knew I had these strange forces acting within me that I could not explain. I didn’t know anyone with DID back then, so I was really just doing research and grasping at straws to understand what was happening.

It is a blur, but my consultation with the dissociative disorder psychologist led me to a fairly quick diagnosis of DID, and I transferred to her to help me with therapy.

It was a balancing act. I would be in terrible shape during my therapy sessions talking about childhood trauma, and she would also see me as a high functioning successful person at the local hospital when she would come in to see her patients.

What I have found for myself is that if I am around someone who knows I have DID, my parts are more likely to show themselves. My parts found a safe place for them to be “out” and to express their feelings and traumas with the psychologist.

It was a lot. Coming to terms with the truth about my childhood, and learning about all these parts of me.

I managed for a few years to work at the hospital and do intensive outpatient therapy three times a week. Then, the train started coming off the track, and I began a journey of hospital-hopping and instability for the next decade. Sadly, I was so dissociative during this period that I have very little memory of it, so it saddens me to know I lost an entire decade of my life to this illness.

Quite honestly, this was in the 1990s, when there were treatment centers that specialized in DID, but in retrospect, they did not know what they were doing in their attempts to help people with DID. Still, they were important because they were places that understood who we were and what was happening to us, which is not an understanding we could find anywhere else in the world.

As my life was in chaos, and I wasn’t making any progress in therapy, I had a shift in my internal world out of anger toward one of my therapists at the time. This part of me who had enrolled in graduate school to get an MSW had decided that she had enough of the mental health system and the craziness going on in our life.

After ten years of chaos and suicide attempts and more hospitalizations than I can count, with a simple, but determined decision, this part was able to put away the chaos of our lives (the endless number of parts), and we were suddenly living with only 5 parts.

This was manageable.

We had 5 parts who cooperated with one another and didn’t even need therapy or hospitals. The depression, anxiety, and suicidality was suddenly completely gone. We still were not able to sleep without medication, but found doctors to prescribe it for us. Other than that, no mental health care was required.

Our only symptom that we worked to hide every day was our amnesia. We couldn’t remember things that were current (and past important life events), like our neighbor’s first name, or how long it had been since we last spoke to our boss, but we were otherwise doing well.

I don’t want to make light of the amnesia we dealt with during this period as it created enormous anxiety in us everyday that we would be found out that we had a mental illness. But, we knew the skilled clinicians couldn’t help us with this problem, so we did what we do best, we hid our truth.

We lasted about 12-13 years in this fully-functioning (except for the amnesia) period of our life where we were successful in multiple careers, got married, adopted children, bought homes and lived what looked like a “normal” life.

Then my dad got sick with cancer. My family required me to come home to take care of him. It was an extremely messy situation that ended with his death (I am leaving out a tremendous amount of trauma that came with this experience).

While he was dying, voices started showing up again.

About 2 weeks after his death when I returned home, I started experiencing PTSD symptoms. Within weeks of that starting, I went to see a therapist to try to prevent myself from getting really sick again. The therapist had no idea I had DID as it wasn’t something I told people, as I certainly didn’t want to ruin the successful and public career I had at the time.

The therapist was a grief specialist, and was actually really good. Since she didn’t know about my trauma background, she didn’t know that her sitting down beside me on a couch in a therapy session would send me into a mute dissociative state.

It was the first time something like this had happened in over a decade. And the therapist recognized it as something significant, and would only work with me if I went to see a DID specialist and got cleared to see her. I reluctantly agreed, having a sense it was a bad idea for me.

Sure enough, I went to see the therapist in early 2015, and my system of parts exploded open with more parts than I even had before. I struggled mightily to hold onto my life and my career.

By 2017, I wasn’t able to work, and was in and out of hospitals with rageful suicidal ideation, debilitating amnesia, depression, anxiety attacks, and off the charts PTSD. My life was splintered into a zillion pieces again.

Now, it is 2019, and I have been working hard the past 3 years with a therapist who understands severe trauma. I am fortunate to have a therapist who takes clients that other therapists throw away.

I am coming to terms with the abuse I endured. I have just barely made it a full year without being in the hospital. I am still suicidal off and on rather frequently, but manage to get through these times a little better. Working on accepting my truth causes a lot of switching between parts on a daily basis, which in turn means I can’t remember easy things that I should remember.

My brain feels like a jumbled mess just about every day. It is frustrating. I accept my diagnosis and don’t hate or even dislike my parts. I accept my childhood abuse as true, but still, I am mentally incapacitated with amnesia and confusion.

I have come to wonder whether healing is actually possible. Maybe it is for some folks, but not for me? I don’t say that in a derogatory way, but maybe the truth is my mind is just too damaged?

These are the questions I am facing these days. It saddens me to think I might not be able to recover my mind the way it was intended to work.

The wreckage from my childhood may be a permanent part of my life. It doesn’t seem fair, but I for one should know life is not fair. 😔

When my Dissociation makes me feel lost

It has been a long time since I have written anything. I have been doing some better, but struggling more than ever with feeling lost.

There are moments when I forget about my Dissociative Disorder, and then I am talking to a good friend about his son and I can’t remember his son’s name.

These moments of amnesia make me afraid to pose as normal to the world. I have thought about trying to go back to work, then I feel this inner flooding of anxiety.

I ask inside to my other parts what we are so afraid of about going back to work. Apparently, they just don’t think we can do it.

It is possibly true. I know I may seem like I am ok sometimes, but then I look back on my day and realize I only accomplished 1-2 things. On an intense day, I might have struggled to get a 3rd thing done.

I am not sure why I can’t get more done in a day, except for this damn amnesia and feeling confused and lost so much.

I have been trying my best to be present for my children as they both have issues going on and need me. Some moments I am good about that, other days I feel inner parts distance themselves from the children and contemplate suicide.

The therapy is a struggle lately. My child parts are so hurt and don’t understand why we are seeing the T less often. Our insurance would rather pay for hospitalization than outpatient care. Brilliant business people.

The therapist wants us to trust her, but the younger parts feel like she doesn’t care about us. The T struggles with this because she says she doesn’t understand what she can do to show parts she cares about them.

Then, the parts reveal that because she is not abusing us, she doesn’t care about us.

She says she is never going to abuse us, so she is never going to care about us?

Then there are older parts who say we should just stop going to therapy. This doesn’t go far because the Little’s surface and put us in a Little hurt state of mind.

Anyway, like I said, I am feeling lost. Don’t know what to do about much. Contemplating giving up my career and going to work for a low paying job or no job at all. Can’t seem to make any decision about that or anything else.

Lost. That is me.

Hiding from my truth

I was getting too close to acknowledging the intense pain of my childhood abuse. It was coming for me. I got really scared.

As someone with Dissociative Identity Disorder, I managed to dissociate it from my awareness, and eventually switch to an Identity that doesn’t experience abuse and lives in the here and now.

My system is mad that this Identity went to therapy this week and basically “wasted” the session by talking about mostly nothing.

Our experience seems normal on the outside. We are taking care of the kids and participating in life to some degree.

Our memory is still severely impaired. My son asked me my neighbor’s name, who I know well, and I couldn’t remember it. So, so frustrating.

I don’t know how long we can hold out in this safer position. I feel sadness and suicide creeping around nearby tonight.

I read an article about Designer Kate Spade’s suicide at age 55, and found myself jealous. She left a note to her 13 year old daughter telling the daughter it wasn’t her fault. My children have always kept me from doing it.

I have a mostly good life, yet I selfishly want to end it. What is wrong with me besides the obvious?

My journey has changed

Some of you may have noticed that I have been missing in action for the past month or so.

I was really not doing well and needed intensive inpatient help with managing the symptoms of my DID and PTSD, particularly the level of suicidality I was experiencing.

I decided to go inpatient and it lasted longer than I expected. If I wouldn’t have really pushed to get out, I still easily met the criteria of someone who needed to be inpatient. But alas, I always feel terribly restless and triggered when I am inpatient, so a month was as much as I could do.

I am now happily home with my family and working to transition back into my real life. Still figuring this out and hope to share it with you as I uncover the new path of my journey.

I experienced incredible levels of amnesia and confusion while inpatient, but I was still able to gain some important insights into a new direction for my life.

I plan to share these new plans with you as I unpack myself back into the real world and my real life.

For now, I can say I realize I do have a life to live while doing this work, and I don’t have to “fix” my life before I can start living it.

I am also happy to say I am not currently feeling suicidal, which is remarkable because that is my typical normal. I know better than to get overly excited about this as I know it can change on a dime, but I do feel a sliver of hope that it is currently absent.

Speaking of hope, I did manage to gain some hope despite the incredible amnesia, confusion, transference, and uncomfortableness I experienced staying in this inpatient unit. Nothing like being locked up and power taken from you as a survivor that is seemingly required for inpatient treatment.

I am feeling well today and I am looking forward to sharing my new journey with you, and my experience during my inpatient stay.

Thank you from the bottom of my heart for all the support I received from you all.

With love and hope to you all,

Kathy

Lost and alone

I have been quiet lately, feeding off my mom’s voice in my head that if I don’t have anything nice to say, I shouldn’t say anything at all. So, I am breaking the rules.

Lost would probably best describe how I have felt most of the time lately. I can’t remember things, much more so than usual. My sense of “time” is completely off. Can’t tell you if it has been one week or 2 months since things have happened.

I am living day-by-day, not knowing if I will make it through the day.

I plan for my future and my demise all in the same hour.

I am suffering from wicked thoughts of suicide that are in my brain but don’t feel like my thoughts. It’s confusing.

I try not to act on any of the suicidal plans, yet at times I find myself getting up to go do whatever is my demise of the hour. Most times I catch myself when I am getting up and am able to stop myself. Sometimes I haven’t been completely lucky with that strategy.

Some days I feel morbidly depressed. I have resorted back to hiding in my bedroom as much as possible. I spend countless hours staring out the window, and suddenly I have an extreme depressive feeling, which follows with a graphic idea of killing myself.

I don’t know where these graphic suicidal ideas are coming from as I am much more practical than to think of these ways if I was suicidal.

I imagine there is extreme anger and pain behind the graphic ideas about my demise.

As I said, it gets so confusing. I think parts of me are “leaking” into me in a way that I cannot distinguish me from them. As such, their thoughts seem to make perfect sense to me.

Yes, I should stab myself with a butcher knife and lie down in my bed to bleed to death over night.

That is so not me, but yet it is me.

I would never do that to my children, but in my head it feels as though I will.

The world is so lonely for me right now. I am fortunate to have a spouse, therapist, and friend who know about some of this and are trying to get me help.

But, I worry no help exists.

In my life in the mental health system, there have been times when I know if I just went and worked on “x” I would stabilize or feel better. Honestly, I have no idea what x is for me this time.

Lost, pushing through each day hoping to gain some clarity the next day. It doesn’t come.

I am wasting my life, lost, never feeling grounded to this earth and my life.

The clock ticks, and ticks, and ticks. My dilemma stays the same. My fragility about my life continues.

I must have some hope hiding in me somewhere, but it is well hidden. The confusion in my mind keeps it from coming to surface. It is amazing to see the mind work so intensely against itself.

I plan for the future. I plan my demise. I don’t know how this will play out. I hope for the best, whatever that turns out to be.

DID is NOT a party

Lacking a consistent voice makes me confusing to those outside and inside of me.

At night, I often write things, whether a blog article, letter to someone, or a quick text. Sometimes I shop on Amazon while others are sleeping in my house. The difference for me is when I wake up in the morning it is a gradual unfolding of what I did the night before.

I see e-mails from Amazon alerting me to a purchase I don’t remember, and often don’t need.

I sometimes get an emergency call from my therapist before I have even awoken asking me if I am alright. That usually means some part of me has been texting or emailing her.

I almost never remember blog posts that have been written under our Mistaken Survival blog. I read them over and over, each time feeling like the first time I have read it, even though it was authored by this shared mind of mine.

I have learned to shrug and stay quiet in response to other people’s reactions to something I have done that wasn’t me. I kind of freeze because I know it was me, but it also wasn’t me. What’s the protocol for that scenario?

The mind is so adaptive. It is amazing I get through the days, but somehow I do.

It feels a lot like being lost, then found, then lost, then confused, then found, and on and on.

Unfortunately, this makes for a really spotty memory. And though I get by with the adaptive skills of my brain, it leaves me empty on the days I have the capacity to think about how little I remember about my life.

I read earlier today someone writing about how they don’t think of Dissociative Identity Disorder as a disorder at all. They see it more of a blessing and an alternative way of living.

Though I try my best to respect other’s differing opinions, it pisses me off to hear someone who has this disorder glorify it and act like it is a positive.

Here is the one true thing most people believe about DID (though not all parts inside of me agree with this opinion): if you have DID, it helped you survive as a young child when your life was so traumatic and overwhelming that your mind would not have survived otherwise.

If you truly have DID, it means there is major distress going on in your life. You can’t get the diagnosis if you are not impaired in some way.

Though I love all parts of me, even those I disagree with or can’t understand, there is nothing wonderful or great about the way we live.

I wouldn’t wish this chaos and confusion and missing life on my worst enemy. It sucks. It is not fun.

Some people describe elaborate parts who have hobbies and like to play like children. Those parts for me are hurt and damaged, and they are not having fun. They are mostly terrified every minute of their experiences.

Carrying around trauma on a daily basis and trying to survive is not fun. My life is extremely difficult, and profoundly sad due to the lack of connection I feel to the world and those in it.

This is no party. For me, it is a serious ordeal of surviving a life of torment and confusion.

I’ll let you have your opinion, and do my best to be respectful, but I can’t make that promise on a bad day.