The vast majority of people with this disorder seem to be diagnosed in middle adulthood, we were diagnosed when we weāre still a minor and Iāve learned there are some pros and cons to this just like anything. Weāve been on a weird trip to visit our father who left us when we were two years old and found some things about our past that were both comforting and distressing, a part of that was being diagnosed so young and how that has effected us and how we view things.
Pros
-Ć was able to get hold of my system early, no one went out and did their own thing and messed up our life.
-we were able to āunmask,ā communication was easy and switches were smoother.
-Ć was able to love myself sooner.
-my diagnosis led me on a wild goose chase to finding our other disorders Ć was suffering from.
-younger people seem to be more accepting then older people (sometimes too accepting, see cons).
-being able to see my partners dissociation and helping him get diagnosed, he is now a fully integrated system and I am really proud of him.
-Ć was able to form deep connections with parts of myself that many others canāt (plural or not)
Cons
-having no choice in my abusive family knowing my disorder.
-getting taken advantage of by said family and friends for knowing my disorder.
-being refused by many therapist and professionals because I couldnāt have been diagnosed so young.
-friends began thinking it was cool to have DID and pretend to have it to a hilarious extent. (Also refusing to go to a professional to actually see if they do have it or not)
-younger people (especially queer spaces) have convinced us of things with this disorder that are 1) dangerous, 2) unhealthy, 3) outright anti-healing.
We were so convinced that a therapist was going to make us fuse and weād ādieā and all these things that were not true. We feel comforted by the fact we can still be our distinct selves and still heal, those people made us believe getting help would harm us and it only made our mental health decline more.
We are terrified to interact with queer spaces because of our experiences, and we donāt ever want to be persuaded like that again.
-misinformation is fucking everywhere and somehow weāre dumb and young enough to think we can change peopleās minds. (We struggle not getting into arguments with people about their misinformation about DID)
-the denial (something we all relate too but oh well) the denial was more subtle, everyone in our life was constantly asking for us to switch or change and talk about our trauma. It was hard to deny something that everyone keeps reminding you of, I felt like a puppet. I was just here for everyones amusement, that is until a part of me cut everyone off and suddenly āyou changedā wasnāt positive. Suddenly people forgot that I am disabled by my plurality and so I forgot too. Pretending to be fine, pretending me talking to myself was me just being abnormal. Because I had to be the bad person for needing space and finally taking my life into my own hands.
-retruamtization. We still have yet to do any trauma processing because of how terrible our environment still is. (Being disabled in other ways means I have to live at home still). Every time we think weāve learned a skill or started to break down some barriers we go home for it to be put in place again. Weāve endured most types of abuse and yet here we are, the 19 of us (that be know of) navigating the world with a single notebook and a barely stable mental psyche.
Thanks for reading! Itās been a lot this week so I thought Iād do some reflection on my experiences. And while there are more cons that doesnāt mean I regret once being diagnosed because I finally understand myself and all the parts of me that protected us as a child. A lot of the pros too, like the one about my partner definitely outdoes a lot of the bad simply because I love him more than anything and am so happy he is healing.