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Questions about my DID… and the answers I sometimes wish I could give.

**Do you have a lot of parts?**

Yes.

**How many?**

Honestly, I don’t know exactly. And at some point, the number stopped being the most important thing.

What matters more is:

Who is here right now?

What does this part need?

And who is actually handling the taxes this year?

**Do all the parts listen to each other?**

No.

Because every part has their own experiences, feelings, and needs.

There is no inner boss with a megaphone saying:

“Alright, everyone does exactly the same thing now.”

Would be nice sometimes.

**Are there rules everyone has to follow?**

We try.

But imagine different parts of one person trying to organize everyday life together. With different opinions, fears, and needs.

Just in the same body.

And nobody volunteers for the cleaning schedule.

**Can handwriting change?**

Yes, sometimes.

My grocery list can look like several parts tried to leave a secret message at the same time.

Who did it?

No idea.

Everyone looks innocent.

**Do you have different music tastes?**

Absolutely.

Our playlist sometimes feels like someone accidentally connected a stranger’s phone.

Calm music one moment.

Then suddenly techno.

No transition.

No explanation.

**Do you have different preferences when it comes to food?**

Yes.

The fridge can become a little surprise box.

“Who bought this?”

“Why do we have five of these?”

“And why does this have a name written on it?”

The closet can be similar.

What feels perfect for one part can feel like a costume for another.

Sometimes it is less a closet and more a diplomatic negotiation table.

**Can people notice from the outside when someone switches?**

Sometimes.

Sometimes not.

Voice, body language, facial expressions, or behavior can change.

And then someone might think:

“Why is this person suddenly acting so differently?”

Short answer:

Shift change.

But not every DID system looks the same, and not every switch is visible.

**Do all the parts have the same age?**

No.

In a DID system, parts can have different inner ages.

Some are children.

Some are teenagers.

Some are adults.

The ID shows one number.

But different parts may have their own inner ages.

**Do you forget plans?**

Sometimes.

Not because we don’t care.

But because sometimes the part who agreed to something wasn’t the one who was present later.

Our calendar is less of a law and more of an optimistic suggestion.

**What about friendships?**

Sometimes they can be complicated.

Not every part likes the same people.

Some feel completely comfortable around certain people, while another thinks:

“Do we really have to?”

Friendship for us can mean bringing many different feelings together.

**Do you have different ways of speaking?**

Yes.

Sometimes it sounds like a job interview.

Sometimes like an annoyed teenager who just slammed the door.

People close to us have learned:

Don’t overanalyze it.

Just get to know us.

**Are there different fears?**

Yes.

Some parts are afraid of conflict.

Some of completely different things.

And sometimes a simple dentist appointment becomes a full internal production.

**Do you always know what the others have experienced?**

No.

Sometimes a memory feels like a message from an unknown number:

“By the way, that happened.”

And you sit there thinking:

“Okay… and who exactly was involved?”

The same can happen with things we have learned.

One part remembers every math formula.

Another wonders:

“Since when can we do that?”

**Are there parts that are difficult?**

This question comes up often.

Yes, sometimes there are parts that are difficult to live with.

Sometimes difficult for my bank account too.

But seriously:

Difficult does not mean dangerous.

Many parts developed ways of protecting us when survival was the priority.

Sometimes those strategies are no longer needed today, but they once had an important purpose.

Sometimes we have to learn together:

What helped back then?

And what do we need now?

**Can you just turn the other parts off?**

No.

They are not apps you delete when they are annoying.

They are parts of a system that developed to survive.

**Is DID dangerous?**

No.

Having DID does not make a person dangerous.

People with DID are not automatically a threat to others.

Many of us have experienced extreme things ourselves and fight every day simply to live our lives.

What is often missing is not safety.

What is often missing is understanding.

**And what is the craziest thing about DID?**

That many people think:

“There are multiple people living in one body.”

But DID is much more complex than that.

It is one person with different parts, different experiences, different feelings, and different needs.

At the end of the day, there is still one person.

A person with everyday life.

With humor.

With chaos.

With their own story.

Some questions about DID come from genuine curiosity.

Some come from ideas shaped by movies or social media.

And sometimes humor helps build a bridge.

DID is a serious trauma-related disorder.

But people with DID are not just their diagnosis.

We have everyday lives.

We have favorite songs.

We have fridge chaos and closet debates.

We laugh.

We argue.

We live.

Because behind every diagnosis is a person.

Not a cliché.

Not a spectacle.

A person.

#DissociativeIdentityDisorder #DID #Dissociation #Trauma #ComplexPTSD

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Hey there I’m new…

Taking a moment to say hello, I’m Erin I have #DID #CinicalDepression #BorderLinePersonalityDisorder2 #Agoraphobia #ChronicPain

I joined #mighty because I want to listen, support, share and learn. As well I am MTF Trans.

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Introduction

Hi

I am 45 years old, I like to read, and trying out all things in the arts and crafts area.

I live DID and C-PTSD as a result of highly organised and transgenerational severe abuse throughout childhood and adolesence.

Also diabetes 1 since I was a kid, fibromyalgia for as long as I can remember but diagnosed when I was 35, osteoarthritis in knees and hips diagnosed at the same time, and a few years after I developed psoriatic arthritis (no, that did not make either the diagnosis or the symptoms of fibro go away, and you're not the first to ask as this can just be confusing)

So I am used to living with fatigue, pain, nausea, thd fun package of 'self-regulation' that comes with diabetes type 1. And chaos, hypervigilence, etcetera in the mental department. I've long made my peace with that and try to make tomorrow a little better by coping well today (and then there's those days...)

But last Autumn I got a covid-19 infection and developed post covid/long corona. I have been told by thd medics that my autonomous nerve system has been affected by the virus during the acute infection state. That leads to different symptoms for everyone, fatigue being the most prevalent.

In my case the symptoms are that mild exercise or stress can cause severe illness that may last from hours to days (pem), palpitations when I stand for more than 10 seconds (oi/pots, shortness of breath, nausea and digestive problems, muscle tension and spasms, problems expressing myself, problems with concentration, coordination, memory, focus, language processing and reading. And of course the fatigue which is FAR worse than I am used to.

I feel powerless and lost.

I hope to find some peers here who know what I'm going through.

#Diabetes #Fibromyalgia #PsoriaticArthritis #DissociativeIdentityDisorder #DID #PTSD #PTS #CPTSD #postcovid #long_corona #Fatigue #PEM #post_exertational_malaise #POTS #BrainInjury #pais #post_acute_infection_syndromes

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Welcome to my page! About me:

I’ve spent most of my life surviving things people couldn’t see.
Autism. OCD. BPD. Dissociation. Panic. Grief. Exhaustion.
Things that don’t show up on scans, or fit neatly into one diagnosis code on the first try.

I wasn’t made for the systems I’ve been pushed through — and honestly, neither were most of us.

I’m writing this blog because I’m tired of having to explain my existence to people who only listen with a clipboard.
I’m writing it because other people like me — people who are neurodivergent, disabled, mentally ill, or just deeply sensitive — deserve to see themselves reflected somewhere.

This is going to be messy, personal, maybe a little angry, and definitely honest.
I want to talk about misdiagnosis. About shame. About masking. About how hard it is to just exist in a world not built for us.

Some days this space will be heavy. Some days it’ll be hopeful, or funny. Some days it’ll be a mix. And if that’s something you need — even just a little — then I’m really glad you’re here.

Welcome to Unfit by Design.
#Autism #MentalHealth #BPD #OCD #DID #DissociativeIdentityDisorder #ChronicIllness #audhd #PTSD

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I'm new here!

Hi, my name is rearips. I'm looking for anyone with DID, please. I'm a teenager and I have been diagnosed with DID. I'll be honest and say I had no clue DID was a thing- I thought it was fake. Only a few months after I got diagnosed I realized it was real and that's what my alters were trying to say. My therapist teaches me about terms like dissociation and switching and I learned more online. I don't know where to go because nobody is really... with me? I feel alone. I'm in the Middle East so basically learning about mental health is non existent. If you have this please talk to me. I never used this it automatically put some of these tags.

#MightyTogether #ADHD #AutismSpectrumDisorder #OCD #Grief #PTSD #DID #Dissociation #DissociationDisorders #DissociativeIdentityDisorder

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This is distressing…TW…abuse mentioned.

I have been dealing with a situation that has culminated in my son facing criminal charges as well as civil penalties involving vulnerable adult abuse against me. It is all finally coming to a head and hopefully the end is in sight without completely distorting our parent child relationship. My current situation is that the extreme distress has caused my first physically overwhelming consequences. A week ago today I broke out in hives that keep getting worse. Some of them started blistering yesterday. I am in an assisted living facility and a histamine diet is not possible. The residence claims they can’t do that and stay within state mandates. Benadryl is not doing anything. I don’t know what else I can do for some relief. Suggestions and ideas no matter how crazy they might be? I do not have a current physician that is familiar with MCAS. I have an appointment with a new allergist/immunologist but not for another 6 weeks! I have so many symptoms besides this both mental and physical health related. But this is the most urgent at this point. ANY and ALL suggestions are welcome… #PTSD #MastCellActivationDisorder #Histaminediet #vulnerableadult #Abuse # #Hives #BorderlinePersonalityDisorder #Anxiety #DID #MentalHealth #Insomnia #MajorDepression #HEDS #AutonomicDysfunction

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Disappointed #groups #MentalHealth #DID

I have to say that I’m really disappointed that many of the groups I joined aren’t really very active. This is such a great platform for support. I wish more people would use it consistently.

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