#but they'd NEVER believe a self diagnosis
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Hello, I hope it's not rude but I'm REALLY REALLY fond of your art!!!!! I was scrolling through your blog from new to old and found that you have Bpd,,,. I only heard about this condition, what is it like? If it's ok to know,,,!
hello, thank u! uhm it's something? HAHAHAHA idk how to explain it đđł lemme try to be as direct as possible
I'm high-functioning, but there are points I seriously just start showing symptoms.
Emotions: INTENSE as it can get while FEELING 99 PERCENT EMPTY. Something just- keeps you so.. hungry (not literally). Sensory is also another factor, and honestly I burn out a lot, tend to get overwhelmed n meltdown like shit
Identity: I either have BEEF WITH it, feel GODLY, or be so LOW, really low. I live with both passion and hate. I'm very confused. But I can say I'm just tired!
Attachments: Relationships are so hard to maintain bc of how much I fear abandonment, like bro I can't even leave my family as much as I want to. I'm more scared of getting disowned or losing my name. Love is a concept I long to grasp at the same time scared of it, I don't understand jackshit about " love ".
> I tend to self-Isolate with or without reason
> ...I used to test other people whether they can handle me or not, whether they'd leave or not. Not anymore though, but the thought lingers.
> Very- paranoid- about.. perception, neglect and invalidity HAHA.
Mindset: They call it Black and White, or generally just two categories to label my perception of things. However, I try to understand AS MUCH AS I CAN about a situation, etc. See what's in-between before I decide. that's really hard for me to do LOL.
> I always do my best to think and be nice
> I can be so fucking bad at the same time, only to regret it the next second or so
> My mind is scattered all over the place, It's exhausting
Trauma: I have memory problems and a lot to connect with that. Hate and fear is what I'm accustomed to. I live with a fuck ton of active predicaments like hell. Old wounds keeps reopening, and new ones never closes.
Impulse: shows in speech more than in action (THANK GOD LMAO I'D DIE IF I LET MY INTRUSIVE THOUGHTS WIN)
Habits: uhm. Ranging from sunshine and rainbows to SELF-DESTRUCTIVE. I get obsessive, like.. really obsessive.
Coping mechanisms: Usually I have mood stabilizers and anti-depressants n shit, but I don't rely on them anymore (bc I can't keep buying). I don't have good coping mechanisms even for physical needs. It's so bad bro. So I just end up drawing. that's the only good one I can list.
Living with it: Exhausting and an internal war 24/7. Does it affect me physically? Yes. Does it come with other mental factors and conditions? Also yes! But as one of God's most tired soldiers, nothing I can do but keep walking.
What I'm confused about: dawg last time, i kept searching about how conditions co exists likeâ Thats normal?? N the last diagnosis I was in confirms it does and nothing to worry about. BLUD I AM DEF WORRYING. Autism n bpd? u mean my behavior and shit isnt meant to be invalid as most people perceive â u mean these fckass experiences built that bpd? â ď¸ WHAT AM I THENâ
(I'm having a hard time believing it bc as an adult, it's harder to process information like these)
#messyr#uhh HAHA! people n my environment -- is like- all fun and games until you actually start showing mentally ill shit yknow?#like whoa didnt know ur fkin crazy or like in a way theyll say or avoid bc they cant handle what theyre seeing#some stays to understand and help and i am VERY grateful for them.#bpd#no i dont mind answering questions like these#if anything i like sharing the experience bc ik other people are able to relate to it or have the same#at least they know they are heard and valid#comorbid conditions
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Damn Right. If they'd been properly diagnosed back in decades before, the rate probably would have remained about the same.
We should be celebrating that the "600%" of girls are Finally Being Properly Diagnosed & Seen For Who They Are, instead of having Devastating Debilitating & Wrong Mental Heath Diagnoses.Damn Right. If they'd been properly diagnosed back in decades before, the rate probably would have remained about the same.
It's not our fault we were told lies about how "Crazy" we were back when, instead of properly diagnosed. Living with the Stigma and backlash of being labelled with Severe Psychological/Mental Health Illnesses meant we missed out on being properly diagnosed.
That "600%" uptick means these girls don't have be in mental health institutions or live with improper Labelling or have CPTSD because of they way they were treated as kids with "bad behaviour", BPD and a wide range of other Personality Disorders, Depression & Hyper-Anxiety, Psychosis or Bipolar Disorder... To name a but a scant few.
Now, these correctly diagnosed Autistic girls are seen for who they are, understand themselves better, and don't have to grow up "knowing" they are "Broken beyond repair" and living with CPTSD.
I was 33yo when I was Finally diagnosed, and it came about almost by accident. A Social Worker came to visit me because I had been utterly debilitated by Severe Fibromyalgia, and was being assessed for whatever I might need for it. But even from the first phone call, this social worker [a human angel, for me] had an idea that I was Autistic. She broached it with me eventually, saying she believed I had "Asperger Syndrome" [as it was known then], and suggested I get an Autism diagnosis. I did it, in the end. Somehow, it turned out to be effectively a "No Brainer" to the Psychologist. He didn't even bother to specifically confirm and verify the Diagnosis with me; he just launched into "well, here's a copy of your letter and I've recommended CBT to your community Mental Health Team".... and I was like "Say what now?.... Am I Autistic?" This was met with him looking up and a clear "Are you kidding me"?" look, before deadpanning, "Yes, I have diagnosed you with ASD" [or something to that effect]. Guess I should be glad it was glaringly obvious to The Psychologist, at least?[!!] And the unfortunate fact of all this was that if I hadn't been disabled by getting Fibro, I would never have found out about it. And I Hate That.
The respect, self-respect, understanding, and knowing makes all the difference growing up. People knowing & ACCEPTING need extra support in school and WHY - that you're not "acting out for attention/Bad Behaviour to get out of school/other stupid "Assumptions"....
So, yeh. Celebrate it - don't vilify it. It's a good thing. Not an "epidemic" or "overly diagnosed". It just means that For The First Time, these girls are actually being SEEN for WHO they are. And that's not Just A Good Thing - it's AMAZING and GREAT.
#fibromyalgia#chronic illness#chronic pain#fibro#disability#mental health#asd#disabled#autistic adult#autistic girls#autitic females#autistic#diagnosis
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*might be sending this to a bunch of people with great blogs who I really like and appreciate
saw a claim made that ocd "can never be cured, like thatevery person who has ocd will always deal with it, "have it" and that's because ocd is caused by a "chemical imbalance in the brain" and that it's been "proven by research". so they say you can't deal with ocd for only a few months or years, if you say you have than it wasn't actually ocd you're lying or exaggerating. which I find ridiculous and insulting, but than they say something worse "research has proven it's chemicals in the brain" which sounds even more ridiculou (im anti-psychiatry all the way. but what can I say to that?! any thoughts?? is this person referencing any real research? or just made up pro psychiatry nonsense??
I'm afraid I might not have a satisfying answer to this ask, mostly because I'm 1) agnostic (at my most generous) to the "chemical imbalance theory" of "mental illness" (as it were). there is nuance to this: i don't think that we are somehow entirely unaffected by our brains, in terms of structure and contents etc. Rather, I think that the construction of "mental disability" is relatedly only tangentially to what our brains actually "do." That is, the construction of mental disability preceded and continues to exceed what is capable of being known about the brain "itself," because mental disability is first and foremost a social, medical, legal, linguistic construction. Little more evidence of this is needed than the fact that I have never had my brain scanned, yet have been diagnosed with myriad mental disabilities and institutionalized against my will. The brain is to mental disability what "sex" is to gender ââ a mythology of concreteness designed to (unsteadily) bolster the flimsiness of the diagnosis, the assignment.
While I am also uninterested in recovery as a paradigm, and in theorizing what it might look like to be "free" of a certain part of the way i move through the world (ocd included), I am interested in collective healing with and through self-determination and free association. What I know for sure, despite the murkiness of everything else, is that it is possible to substantially improve your quality of life in a wide variety of ways: some people find medications that help, some counselling (whether professional or informal). Others choose spirituality and meditation. Others self-direct using freely available therapeutic resources. Still more enlist the help of their friends and loved ones to keep track of types of behavior they'd like to avoid. And, of course, some don't do any of that, and it is their right to do so, so long as they are not endangering others, regardless of how shitty it feels (both for them and the people who care about them).
so: I'm giving you a non-answer. I don't believe in cure because I don't believe in disability-as-disease. I think people who are obsessed (haha) with figuring out the etiology of different diagnoses are at best naĂŻve and at worst eugenicist. (Note: i am not upset with you, nor do I think you're a eugenicist or any other genre of bad person! Thinking about these things does not make you bad. Asking these questions in good faith does not make you bad, either.) I think that we will be much better positioned to talk about living and improving together when we forget chemical imbalances or medical decrees of terminality or unrecoverability or treatment resistance, and start thinking about things we can do in our lives now that help us create better futures.
#antipsychiatry#ask#anonymous#if you think that my reasurance is excessive#please remember that i am assuming anon has some ocd-labelled shit going on (as do i) and responding with that in mind
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Guuuys i finally see a CRPS doctor this week!
Tw: brief mention of wishing self harm, and mention of medical abuse.
So for 4 years ive had undiagnosed chronic pain, its severe, ive been bed/house bound for 2 years and need a wheelchair when i leave the house.
I talk alot about my experience with being disabled, but i usually don't talk about my actual symptoms often.
I can't use a computer 90% of the time, on good days, which is now twice a week, but used to be never, i can play pc games in 20 minute increments, twice a day. I can't wash dishes, i cant walk without pain, i can't sit in chairs without pain. Im stuck laying in bed, all day, everyday. I usually can't make art, sometimes i can. Im just in bed, on my phone, in constant pain. Its a VERY difficult existence and i have often wished i didn't have limbs because the pain can be so intense.
So ive gone to countless doctors, rheumatologists, a pain specialist, an orthopedic, a neurologist. The reason im always saying stuff like "doctors are scum" is because every single doctor ive ever met has minimized this pain, lied to me and told me they'd do everything they can and didn't, and purposefully wasted my time. I even traveled to a different state to see rheumatologists, they saw me twice, i literally cried and begged these people to give me medicine for the pain, they gave me a shot that they said would help for 2 weeks, it helped for 30 minutes, when i asked them what to do they ignored me. They diagnosed me with fibro specifically so they could get me to leave them alone. I knew that diagnosis was incorrect. Last doctor i saw was a neurologist, i told her i needed to be tested for CRPS, because that was the only lead we had left. She scheduled a brain mri and nerve damage test, they came back normal. I brought up that there is no test for CRPS, she said i was right, and i could definitely have it, but she said she can't diagnose it and i need to see a pain doctor. I told her first time i saw her what i was looking for, and she mislead me into thinking she had experience with crps, and wasted my valuable time and money with tests that were irrelevant. My pain doctor wasn't an option because he doesn't treat crps because he doesn't believe it exists.
So i was lost
Every doctor i knew actively worked against me and none of them could refer me to a CRPS specialist.
But last week i simply googled "crps doctor near me", i found one close by, called them, they didn't require a referral, and the appointment was scheduled a week later. No 2 months wait time, no bullshit doctors approval. Just a phone call away. Im seeing them in 3 days. Wish me luck!
To others out there struggling to get diagnosed, im rooting for you.
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Self DX culture is your parents never believing you and being unable to go get a diagnosis on your own because you're a minor and no one would believe you and even if they did they'd probably need parental permission in order to diagnose you anyways
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Really sick reason to be happy but I can't stop smiling
TW/CW child abuse, mental illness, SH
One of my aunts calls our family "yours, mine, and ours", which is accurate. We've got me, my (step)brother, my dad, my stepmom, and my (half)sister. My brother is seven weeks younger than I am. Our parents got together when we were around four- "work spouses" who were both recently divorced- and our little sister came a few years later.
My bio mom and my brother's bio dad are a mess, somewhere between incapable and unwilling to parent full time. I've been in therapy off and on for most of my life and got my C-PTSD diagnosis at 15. My brother, god love him, just reached his first year of sobriety, having started drinking around the same age.
Naturally, every time we had a chance to say "This isn't normal" to our shared folks, we'd be told "Well of course you'd think that, you're used to your other parent!". The other person was a shovel used for digs: "This isn't their house!". They'd call me by my mom's name when I made them upset.
I assumed I was broken either because of my mom or because of the split. I can't know for certain, of course, but I think the cause of the C-PTSD was specifically that they traded custody daily, at my mom's request, until she moved out of state. She gives the silent treatment. My stepmom screams. The rules changed on me literally every 24 hours until I was 13.
Life evened out a lot when she did move away - but not entirely. I wound up in screamland 90% of the time rather than 50. I couldn't figure out why it didn't feel right or why it kept happening to me, but I believed my folks: I wasn't used to it because my mom's "parenting" is different and worse. I felt sickened to be involved with my mom at all. I thought that if only she wasn't waiting in the wings, I'd be entitled to a normal childhood, but because of her influence, I deserved everything I got.
Anyway, I have been texting my little sister about Christmas gifts for our brother, and out of nowhere, earlier this week, she tells me she's going to therapy for the first time... because she's realized it's not normal for your mom to scream at you literally all day and your dad to not intervene.
I haven't been home for more than three days since I moved out over a decade ago. I had a chance to pass through the town earlier this year, didn't do it, and still had panic attacks for two weeks straight. I can't hack it as someone's daughter; it makes me physically sick.
But that isn't a me problem.
Not a one of them could hack it as parents.
I've stopped hearing my mother's doubts in my head - I cut her off when I moved away. I've never been quite able to shut off my stepmom's. The screamer versus the silence... it fits.
I'm not a poser if I can't create when I don't have a comfortable space to work. I should not self-reject because I'm frightened. In the absence of an abuser, I'm finding that holding ideas in also hurts a lot.
I'm not stupid or useless or gearing up to be a failure for needing the introvert rest period and knowing my limits. It will not hold me back in life.
It isn't normal to want to hurt yourself. It isn't normal for people to laugh it off and talk about themselves when you tell them you want to hurt yourself.
The mandatory insincerity I grew up around has thankfully faded a lot - I don't think I could summarize that anymore if I tried.
I'm heartbroken that my little sister is going to need to learn these things - but ecstatic that she will, and is actively moving towards it. Had a similar conversation with our brother a few years ago, but of course, he has his dad in the wings; it hits differently now knowing that it would have happened no matter what. Children in that home are screamed at, hit, and not defended. Simple as.
I'm not what they wanted me to be.
I'd say that's "fine" but that doesn't even begin to cover it. It's exemplary.
#em can#farther beyond that#em will#cw sh mention#cw mom mention#cw child abuse#tw verbal abuse#tw mommy issues#tw sh implied
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It's especially bad when it comes from other autistic people, like you of all people should understand how shitty it is to not know what the fuck is wrong with you. I'd be in a significantly worse place right now if i didn't self diagnose, i wouldn't know who i am, i wouldn't know why i do any of the things that i do, i wouldn't know that stimming is okay, and and and (german expression we should totally bring into the english language)
I brought up a hypothetical child in an argument once, they're autistic but not getting diagnosed because their parents don't believe in autism. Would you rather
A. The child think it's broken and have to wait until it's at least 18 and financially stable enough to finance a diagnosis, which may never happen if it's poor, or even with the money they might not get diagnosed because they're part of certain minority groups like racial minorities or not a cis man, or the doctors around them brush off people above the age of 7 because "autism is a childhood disease"
B. Self diagnose and FINALLY find out who they are and that they're not broken before the age of whenever they'd be able to be diagnosed
C. You think autism starts when you're diagnosed? (Why would you think that)
And what's even the big bad thing that could happen if someone self diagnoses and is wrong????? Literally what??????? People will say "Think of the accomodations they're taking away from actually diagnosed real autistic people!!!" What accomodations???
âYou shouldnât self-ID as ADHD/autistic, youâre turning a very real mental condition into a trendâ Ok then stop saying delulu. Stop speculating on which cluster C personality disorder the criminals you hear about on the news have. Stop saying âschizopostingâ and âacousticâ and âis it restarted?â Stop using âpsycopathâ and âsociopathâ as catch-all ways of calling someone a bad person. Stop saying âthe intrusive thoughts wonâ when you bleach your hair and then turn your nose up at people who suffer from very real, very scary urges of physical/sexual violence. Stop saying âIâm so OCDâ as a way of calling yourself neat. Stop treating BPD/ASPD/Bipolar as inherently abusive. Stop saying âOP I am living in your wallsâ without tagging for unreality. Stop diagnosing complete strangers youâve never met on r/AITA with NPD.
You first. If you donât want our disabilities to be treated like trends then stop belittling and minimising them. Iâll NEVER judge a person for trying find labels for their symptoms when an apathetic, racist, sexist, ableist healthcare system refuses to. But I will absolutely judge a hypocrite. Which a lot of you are
#autistic rage#autism#it's like how people want severe and debilitating dysphoria to be a requirement for calling yourself trans#like what if I'm a happy whimsical little guy who's happy?#why do i have to suffer first to be allowed to call myself the thing????#be for fucking real
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The Billeted Pachyderm Dilemma
I'll be treading into some murky waters with this entry. I'm not a psychologist, I'm not an expert on mental health, and I know armchair diagnosis is a dangerous area to get into. But all that said, I needed to try to understand how I ended up being treated the way I was in my relationship if I was going to start recovering. I wanted to be able to look at Anagram's behaviour and see if it made some kind of sense. And it was while talking to a friend of mine who works in the mental health sphere that I started to pick up on things I recognised from my time with Anagram. Mental health had always been the elephant in the room between us; I was aware that I had my issues and tried to be upfront about them, but we could never seem to talk about what was going on in Anagram's head without them taking it as a personal attack. It's only been after the breakup and with me coming to terms with the abuse that I've given this some consideration. I've done some reading, talked to my friend, watched some videos. I have a theory - which is all it is, but I think a strong one - about what Anagram has been dealing with. In some ways it makes me more sympathetic to them even as I wish they'd been able to face it themselves and avoid hurting me.
From the start, it was clear Anagram had a fear of abandonment. They had felt neglected by their parents, who even before divorcing had been kind of neglectful of Anagram and their siblings. As an adult, they seemed like they were always expecting friends or partners to leave them, and I think this resulted in ending friendships first to avoid that. With me, there were often threats to leave me followed by demands that I not give up on the relationship. With me and with other people, Anagram's opinion could change on a dime; one moment someone would be an amazing person who only brought joy, and then the next they'd be an irredeemable asshole who was more or less dead to them. (I was particularly either "beautiful" or "a piece of shit" depending on the mood of the day.) Anagram, despite claiming to not be an angry person, would fly into rages where they'd lose all sense of control or proportion. Sometimes this anger led to periods of dissociation, and they'd forget things they'd said or done during this time, absolutely refusing to believe me when I described any of the things they'd done. Outside of anger, their moods would seesaw wildly. Sometimes they would self-harm, which they generally kept from me as much as possible. Sometimes it seemed like Anagram had a really strong sense of self; other times, it seemed like they were completely unsure who they were at all. But beyond anxiety and a certain amount of depression, which they claimed to have under control, Anagram never admitted to any particular mental health issues.
It was only when my friend started talking about someone else we knew going through some of the same things that I started reading about Borderline Personality Disorder (BPD). There are nine diagnostic criteria for this condition, and a person only needs to meet six to be diagnosed with it. The more I looked into it, the more I was convinced that this was what Anagram had been going through. Again, I'm not a psychologist, so I can't say anything definitive here. But it did feel like the elephant in the room had a name that fit.
I want to be clear here that I don't think BPD made Anagram an abuser. Them abusing me is a choice they made, that they were perfectly able to not choose. Mental illness affects everyone who has it in a number of ways, but it doesn't create or excuse violence. And I understand that the person who suffered most from Anagram having BPD - if that is the case - is Anagram themselves. As I said, I have some sympathy for them having to experience this. I don't believe they knew this about themselves, and I certainly didn't at the time, so neither of us was able to help Anagram in the way they needed. (I am told that BPD is a highly treatable condition when people are aware they have it.) Anagram was suffering, and I wasn't helping. Their anger is understandable, even if taking it out on me was inexcusable.
I know there are a lot of people out there with BPD and other personality disorders like it. All of them deserve sympathy and understanding, most especially from their romantic partners. I'm probably not the sort of person who's equipped to be in a relationship with anyone who has BPD, which I can realise about myself now. I don't know if I could have helped Anagram if we'd both had this knowledge at the time. Perhaps it would have just been the trigger for us to break up, peacefully, a lot sooner.
Still, I'm upset that simply not knowing what was going on another person's head left me vulnerable to being so deeply hurt. If nothing else, it's taught me to be so vigilant about my own mental health issues, and the responsibility I have to see how they affect me, how my behaviour then affects other people. Especially now, as the pain and anger I feel interferes with my ability to regulate my mood, I keep watch over my interactions and keep prepared to apologise when I cross lines with the people around me. All I can do is remember my fear and shame as I tried to protect myself from an attacker, and promise myself that I won't ever do that to someone else.
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I'm going to yap here, and if you disagree that's completely fine, just please read what I have to say first.
A friend posted that you shouldn't self diagnose, and part of me agrees with that. There are serious disorders that, if they exist in you, need to be diagnosed and treated by a professional. There are other disorders that have now been stereotyped to high hell because of people lying. But, in other situations, getting treatment or even just diagnosed can be nearly impossible, but maybe you want to have a community.
For me, I've been able to tell something was wrong since 2020. I just was able to get put in for testing, and that's only for the intake. We don't even know what they'd test me for. Meanwhile, I can identify my symptoms, when the symptoms started, the cause of the symptoms, and the most likely mental illness that causes the issue. Like, I'm sorry but if it looks like an orange, tastes like an orange, feels like an orange, smells like an orange, and you can't get scientific confirmation that it's an orange for God knows how long, just call it a fucking orange until you get confirmation that it's an orange.
Another problem is, some people don't want to get the diagnosis because people are quick to discriminate against them. I didn't want to get diagnosed with anything for years because I already got discriminated against for being AFAB, you think I want people to know that I'm plural and that I'm (most likely) autistic along with all the other issues I probably have? There are places where being honest about that isn't even safe. I'm only opening up to it because I feel safe with the professionals I'm already working with. If I didn't? I would never get that diagnosis.
Over-all, I believe it's someone's choice if they get diagnosed or not 99% of the time. Of course I also believe that sometimes a diagnosis is necessary, but we should look at things case by case. And the fact that people discriminate against people that are public about having conditions like DID and then also go "you need a diagnosis!" Make me want to bash my head into a wall. So you're saying you want them to get the diagnosis for the issue you've shown to be a problem in society?
Of course, if we ended discrimination entirely that would be amazing, but I'm not stupid. We've got a long way to go, so let's just try and make others feel safe, no matter what they're dealing with, and encourage them to get help if they're a danger to themself or others.
#mental health#im sorry i just needed to get that out there#it pisses me off#especially with how hard it is to get a diagnosis?#it feels like gatekeeping a mental illness#im not sure if thats the right phrase#im also prepared to get a lot of hate on this#plurality
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RE: your question about whether it's a good idea to make alters separate or something along those lines:
Considering you're still questioning OSDD/DID, it would not be a good idea to try and force separation (barriers i think you said), because you may not have DID/OSDD and you could end up losing your entire identity if you are to learn you aren't a system. I wish I remembered who they were, but a person once described how entirely they'd become a void of a person with no idea of even what music they liked because they had forced separations between what they thought were alters but later learned were just facets of themself after they learned they had a different non-DID/OSDD disorder. Iirc, they talked about working so hard to make each part completely unique & ended up mimicking other systems' parts because "they were doing it right" and in the process lost whatever had made them their own person by the time they realized they'd gotten their self-dx wrong.
For us, we tried very hard early in our diagnosis to create distinct separations between us, popular systems like dissociatED and the entropy system on YouTube were, at the time, pushing that kind of alter separation to be a good way to build communication within a system/collective. They were the kind of systems who would dress differently depending on who was fronting & that kind of thing. For us, doing that made us so much more unstable & we were losing time much more frequently as well as the fact that our memory for daily life things got much worse.
We started only working with whoever decided to be around at the time when we went in for therapy, never forcing anyone to switch or talk or write, not even giving them a name unless they wanted one, just let people move fluidly. It's kind of like when you have a roommate and y'all live in the same house but are always doing your own things. Sometimes you're both in the kitchen and you talk for awhile, but you both go back to doing your own stuff.
In sessions, if someone new switched in, our therapist would work with them to resolve any trauma they remembered, ask them a little bit about themselves, and "built" them a room in the innerworld shop they had their own stuff and their own place to live. For a lot of them, that was all they needed, and also, for a lot of them, they don't really front anymore. They're happy where they are and what they have. There are 350+ of us, so we've never taken care of all of them in this, but we still do this for "new" or rediscovered parts.
Yeah, being blurry a lot of the time while everyone adjusted was frustrating, but eventually, everyone got used to it & there were no more possessions or fugue states. In fact, as the current host, we didn't even know I wasn't the previous host until 3 months after I got here. That's how relaxed we've been!
So I suppose my advice would be to endure the blurry state for now, let whatever part(s) you think are around write to the system or do activities they might like, etc. But we believe it would be detrimental in many ways to force barriers. The goal of a lot of systems in treatment is to reduce dissociative barriers as much as possible, anyway. Either to reach final fusion or functional multiplicity (neither of which is better than the other, just to each their own). And if you learn you're not dealing with DID/OSDD, you will still know who you are in the end.
âLCS
hey thank you anon, this makes a lot of sense. i really don't wish to lose my sense of identity even more, so much that in my head it was better to have multiple distinct identities than none at all.
I'll try to take things easy. sometimes it feels like im standing with a shovel at the edge of my mind, just waiting for the opportunity to dig in deeper. i probably shouldnt. not knowing what's in my head is a huge pain for me, but I'll try to pull through, at least until i have professional treatment.
thanks again :)
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Yep, that latter.
For me it was, my parents never told me about my sister's ADHD diagnosis because they didn't believe it was true/real. Because that would have made them address their own milder ADHD symptoms that they'd dismissed as "laziness" that they'd overcome with "hard work" (because that was all we needed to do, right?)
I struggled for years thinking that I was just really lazy and that if I was a good, organized, responsible person like my parents, I wouldn't have so many problems with procrastinating on assignments, inability to keep my room/clothes clean and organized, losing things, forgetting things, etc. etc.
(My sister and I almost certainly have the exact same brand of ADHD, but because I am much more naturally bookish than she is, I didn't have the same struggles at school that she didâI loved reading and my half-assed-stayed-up-till-3-the-night-before-the-deadline bullshit papers were generally still good enough for an Aâand so mine was never diagnosed)
My self-esteem still sucks. I have to consciously remind myself that I do have an actual fucking disability, the fact that I can work a full-time job and run a household is enough, I don't need to be down on myself for occasionally screwing shit up and not volunteering for a hundred different causes like my mom.
Not telling your kid they have a learning disability, chronic illness, mental illness etc. so they can âfeel normalâ actually does the opposite. They will not feel normal if they do not have the context to understand that their normal will be different from that of their peers.
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it's sad that being late diagnose autistic and having everyone* gaslight my autoimmune conditions for a decade because they've been so misunderstood for so long (even with all the massive amounts of information coming out on all my conditions in the last 5 or so years people still don't wanna take it seriously) that I obsess over these false ideas of being a "good human" that aren't as important as being a "good person".
being a "good human" is ableist and about our mechanical and cognitive abilities. being a "good person" is about doing our best be respectful and understanding of others and doing what we believe and know is right even when we we may have disabilities and struggles that make it hard to function in social dynamics and society.
it's hard to let go of the internalized ideas of I'm a failure or putting ideas of morality on my meltdowns. it's hard to not feel like I'm broken garbage. I would never feel that way about anyone else who is autistic or disabled in any other way but that internalized trauma of not being truly recognized as a disabled person with my cognitive disabilities (autism, adhd, complex ptsd) and my physical ones and instead being labeled as "weak", "failure", "making it up", "attention whore", "faking it", "manipulative", and so much more.
There were many people from childhood to early adulthood that did recognize my disabilities, but not with compassion, they looked at me "useless garbage taking up space" and "polluting the world". they believed people like me should be aborted or euthanized for being disabled and not being useful enough to society.
Although I think all this shit is wrong and false. I was so programmed to hate myself and not even recognize myself as disabled. A lot of what I've learned is disability I associated with just being stupid or useless and other harmful shit because everyone* around me did.
In meltdowns and complex ptsd episodes or any other time I'm struggling with metacognition it's hard to recognize that these things are disability symptoms and to have compassion with myself without falling back into those old timelines of being told I should hate and blame myself for being a "bad human". It's hard to remind myself that I am disabled not a pos and that I am still worthy of love.
it sucks because I don't have these beliefs of other disabled people, because I've never believed or agreed with this shit. But the problem is my image of self and having internalized the ableist trauma shit for almost 2 decades before I was finally validated for my cognitive and physical disablities. Even when I had diagnosis or all the symptoms of my disabilities (like going above and beyond minimal requirement for diagnosis) I was gaslight by professionals and doctors for my age. Which is inane because you'd think that with me being so young and being physically disabled they'd take it seriously ??? but no. and if doctors did take it seriously they'd be like you're too young for any treatment options but then gaslight me for my falls and needing a cane at 17.
My disabilities have often been framed as some kind of "choice" or "attempt for attention" â which is so fucking hilarious to me considering I HATE BEING PERCEIVED AND WOULD LOVE TO DISAPPEAR.
but not being able to recognize and validate the fact that I am cognitively and physically disabled for about 2 decades really fucked up myself worth and image of self, and it kept me stuck in cycle of internalized ableism without even realizing because I didn't even know it was ableism. Sometimes I still forget. I think the reason I've had such a completely different view of my own disabilities and others with disabilities is I recognize others as legitimately being disabled while gaslighting myself on being disabled at all because other people did it so much. and being undiagnosed autistic we fall into masking of letting everyone else define who we are and what we should be in order to survive in normie culture. So until finding people who love and accept me for my disabilities I haven't been able to even accept I am disabled until the last year really. And accepting I am disabled is the key to loving myself. I don't think there's anything wrong with being disabled. but when I can't recognize I am disabled, it becomes about some other idea of "morality" on myself that I was trained to develop through trauma. and it's hard because in these rougher states I fall backwards and the people who love me try to validate that I am disabled and there's nothing wrong with it. But I don't even think it's disability, I equate it to some of there idea of being a "good human" because trauma.
I honestly want to draft this like most my expressions of self but I also know that I need to for myself be open with the struggles of being disabled because I believe it's important for disabled people to share our stories and struggles and to be seen in the world. and I need to stop being ableist to myself like I never would be to others.
but being seen and being disabled is often traumatic. because you're seen through a lens of ableism and other misperceptions, rather than being seen for the reality of your multitudes and who you are as a disabled person.
(I hope my grammar is right and this says what I mean, I just got out of a meltdown and needed to rant and brain not doing so good)
#vent post#autistic experiences#autoimmune disease#chronically ill#chronic disability#reminder to self#healing journey#disabled experiences
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Gary Goldsmith isn't the solitary wife abuser linked to Kate, her spouse William is as well!
By Stanley Collymore Â
Kate's major hospital operation is no more authentic than Charles' so-called fucking cancer diagnosis is. Both a deceitfully lying and dishonest part of a desperately contrived, concerted and an utterly self-serving artifice to save Kate and William's pathetic asses and what's miserably left of this odiously dysfunctional family. The reality is that William, who is effectually a cowardly bastard, like all of his kind are, in addition to the egregiously bullying, utterly selfish, socio-psychopath and delusional, quite inured racist, white supremacist, master race, Aryan white Caucasian that he innately but highly stupidly and equally ludicrously believes that he is, is also a violently nasty wife beater, who quite literally has been knocking the living shits physically out of his convenient Stepford wife Kate Middleton. I've personally no sympathy whatever for Kate and actually on the information that I've been evidently  rather assiduously confidentially and also trustworthily given, this white racist Karen is unquestionably essentially no different from the detritus piece of human shit that William likewise it.
Which brings the UK and other onlookers to the present situation that they're in and that the key players, the Palace, their quite bribed media acolytes and cronies, along with their own trolls assume they can get away with, and invariably do because they genuinely know they're dealing with a very intellectually challenged bunch of plebeian and serf sycophantic morons.
Kate and William aren't together and quite actually haven't been for some time. Also, while she lives in Windsor William actually lives in Kensington Palace in London. Not indistinct from Charles and Camilla living in separate homes 100 miles apart and as is well known was the situation with Philip and Liz Windsor. Notwithstanding all that, William who is most unquestionably so, a very closet Philip Schofield and undeniably lacking the balls as Philip Schofield did to own up to what he really is, in undeniably in the situation where he absolutely can't stand Kate, putting him in the very same situation as his father was with his mother Diana.
The principal difference being that Diana, the aristocrat that she was could, and if the Windsors didn't murder her as they did, would absolutely certainly in her own right carry on and independently like her son Harry do what she genuinely and honestly wanted to do. Kate, however, in marked contrast the stalking, gold digger trollop who has simply never actually done an honest day's work in her life and also is equally work shy, having gotten hold of the Christmas hamper that she connivingly got through marrying William, is not at all about to surrender it voluntarily. And as such, he William - and how very ironically that would bearing in mind the murder of his mother - his dad Charles and the rest of them can't actually embark on another risibly, "accidental" murder involving Kate, just as they'd also like to murderously and racially dispose of Meghan, they can't truly embark on that either; not realistically! So instead William, the psychopathic bully as he was with his brother Harry takes his ire and frustration out on Kate Middleton.
The problem is that ultimately like all very odious bullies this time William has simply literally gone too far; forcing Kate to flee to her parents with the children. A laughable state of affairs for me, as the Middletons, on their part, and distinctly from any really conscionable family simply can't or won't say and do anything because of whom the Windsors are; and most ironically as well, because of the undoubtedly principal role that Kate's mum Carole played in blatantly and sickeningly orchestrating the charade of social climbing and naturally rather self-serving interests that Carole contrived! A difficult situation to escape from let alone publicly explain, when your own, obviously evidently and distinctly sinister connivance does clearly turn on you and very viciously bites you on the ass! Â
As for Charles pathetic and desperately so, cancer charade; cancer is, unquestionably so, rather commonplace nowadays, as to be almost meaningless unless the bearer or sufferer of it specifies what precisely it actually is; something that Charles rather categorically hasn't done! And the obvious reason is that Charles fucking well hasn't got cancer! It's a sympathy garnering ploy callously and quite calculatedly conjoined with the Kate Middleton situation to simply milk as much sympathy as they can really get over the odiously evil, egregious, also malevolent and undeniably racist and still ongoing vendetta they've waged against Meghan, for essentially being an African American woman who reciprocally clearly fell in love with Harry who actually married her instead of some white and delusionally very perceived English rose broad, crucially and primarily because he essentially loves Meghan and rather cognizant of what was evilly done to his mother Diana intelligently doesn't sensibly indulge in the precept of a Stepford Wife and broodmare. But likewise in addition was equally well aware that the collective antipathy you all had and still do against Meghan wasn't simply just related to her very discernibly racial origin but the equally obnoxious and actually abysmally contemptible notion that clearly Meghan's own presence as well any children that she produced with Harry would quite distinctly and likewise discernibly; undeniably, contaminate the biological, societally perceived and as well the divine matrix of the actual British so-called monarchical family!
I personally, actually don't believe that you have cancer Charles, and basically couldn't give a fuck if you really do as the minimum respect that I had for you, has quite clearly long dissipated. In 1989 I distinctly wrote a journalistic article, effectively so while on a sabbatical year in Barbados, suggesting in it, obviously, that Barbados which has had a continuous link with England since 1625, and was clearly instrumental in catapulting the then obviously, European backwater of England into the global empire, which it so subsequently became - please, actually go and quite accurately check up on your real history man - should actually cease to be a realm and essentially become a sovereign republic. The article predictably generated much debate generally, within my cultural homeland Barbados, where it was written and published and my very close friend the Prime Minister rather laughingly said when I raised the issue generally with him "we've actually far more important things to do in Barbados than worry about white racists in Britain".
But a crucial torch had effectively, been lit by me, and interestingly influential friends of mine; similarly also, former local pupils as well as students I'd taught; members of the political establishment; and crucially a general cross section of the distinctly very astute and similarly politically well versed Bajan public, discernibly enthused by what I'd written, were in full agreement. On then leaving Barbados at the end of my official sabbatical session I essentially returned to Germany and my academic engagements but was nevertheless kept fully appraised significantly of what was going on back in Barbados politically, as I've always actually made sure was the case and still do!
Frankly Charles, and even with a palm full of salt I don't actually believe your clearly, quite ludicrous, obviously lying and rather pathetic story that you really have cancer. For starters you're very evidently because of who you are a very prominent and also discernibly a noted public figure. I'm also quite fully cognizant however that while it is both infra dig and equally also, likewise illegal for one's personal doctors or other medical staff to publicly disclose private, medical information pertaining to literally any patient; if, however, such a patient of their own volition publicly decides to truly disclose what's actually, medically wrong with them and that patient is a prominent figure like you are Charles; it's not actually breaking the bounds of ethics or basically confidentially, let alone going into the real realms of illegality if that quite prominent person and, no less so, the King of Britain had their very trusted medical consultant alongside them to just obviously confirm that particular ailment that the patient did voluntarily tell the public that they actually have. But no doctor, even to the ultra-rich is publicly going to openly lie, knowing that if he's really caught out he'd be struck off! And that's distinctively why none are really backing your ludicrous cancer story!
You have not requested that, Charles, and literally with spurious reasons, because it's obvious to anyone that isn't a fatuous serf, vacuous plebeian or a basically discernibly puerile, brownnosing sycophant that you're bloody well lying! There are irrefutably obviously, evidently manifestly loads of things quite literally rather undeniably wrong with you Charles Windsor which if you were not purportedly considered to be Homo sapiens you would basically have already been put down! For really how the Hell is it even feasible let alone possible for a man your age apparently wracked with cancer, quite essentially, one of Britain's major killer diseases to have his wife sauntering off just as he's actually milking his own quite dubious public support, in distinct tandem with Kate's own mysterious illness, actually on a tropical sunshine holiday alone, in the rich and full awareness that all her needs will be amply fulfilled while she is actually there.
In the meantime, you Charles, Camilla, William, Kate and obviously the rest of your lot see your rather sick stratagems against Harry and specifically Meghan, and even their children quite miserably fall apart, but all the same you crucially but rather asininely still persist in what you're so evidently quite vile and evilly doing; as you effectively desperately get your media and equally palace flunkies to simply offload your quite numerous failings onto Meghan, even though it's abundantly clear those stratagems just aren't working. But that's the nature of the white supremacist, delusional and white master race beasts, who like their routinely racist scum are so irrefutably dumb and cowardly they literally can't even take ownership of their own sick racism, which they always manifestly and emphatically most lyingly deny!
In a recent conversation I had with an American colleague, he succinctly very laudably effectively outlined the views on this very subject matter that I share. Brits, and basically white ones, he aptly emphasized, this guy is definitely white by the way, have rather unquestionably become very submissive while actually still remaining the feudal serfs and vile plebeians they've obviously, essentially always have been. Discernibly, he went on, you have this unquestionably quite solitary, incestuously inbred hereditary family sponging off you, yet effectively not regarding you with any dignity, to even tell you the most basic truth about Kate, William, or even Charles himself, pertaining to their actual situations. A state of affairs which you've every right to ask about and truthfully know, quite taking into account, that you pay taxes to permit them to live in and effectively enjoy the sumptuous lifestyle that they do have. Yet if you go against the actual grain and asked for answers you have prized sycophantic and arrogant cunts like Rebecca English purportedly editor in chief hack of the Daily Mail, while in her odiously sick and rather malevolent and simply egregious role most happily engaged in fostering, and undoubtedly poisonously promoting all the vitriolic crap she can muster against Harry, but specifically Meghan and their children, has the bloody audacity to vociferously berate those who sensible and similarly intelligently question the palace's lying narrative for which they handsome pay the likes of Rebecca English to support!
(C) Stanley V. Collymore 9 March 2024.
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it's been almost a year since i've sat down to write one of these holy shit. i don't know if that's a good thing or a bad thing? there's so much to say but i don't even know where to start? i went to the blue ridge rock fest this year and it got canceled because of weather after like 3 days. which, i'm not exactly complaining? it was a blast while it lasted but also a little bittersweet since it was something that i knew you would've LOVED and it was starting to hit me in the feels. now i'm just vibing out in nashville which is also something you would've loved lmao.
i've been sober for like a year and a half now. from narcotics, not alcohol lmao. ya girl still needs her tequila. sometimes, on the shitty days when i'm ready to cave, i can hear you go all "don't you fuckin DARE." it's insane how you're still my voice of reason sometimes. idk... this is the first time in my life that i've felt like i'm actually doing decent? i've been doing a lot of work on my inner self, trying to unlearn shitty habits... and i still have a lot of work to go. but like, progress is progress, right?
there's so much shit happening right now but i'm just kinda taking it a day at a time. my momma got a breast cancer diagnosis a few weeks ago and i'm also dealing with some health shit myself that i'm still coming to terms with. then there's just shit with my 'father' and i'm like what the actual fuck is happening rn. it is what it is i guess and i'll just keep dealing with it but sometimes i'd like a break.
once i get back home, i gotta go see your parents. they told me i could decorate their house again for halloween and i'm so excited. i feel like i haven't been able to see them as much as i'd like because i've been so busy but they've always been understanding about it. tbh, sometimes i'd wish they've just get mad about it but i know that'll never happen.
our girl is in highschool now and z is a full grown adult. it's kinda hard to believe. i'm glad that they're healthy and thriving but holy shit i wish they'd stay smol. kenzi still finds ways to bring you up in our conversations and it makes my heart happy knowing that you were so so loved. not only by me, but by literally everyone who knew you. i just wish you could've seen it before it was too late.
until next time, fly high nerd. i love you.
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This is going to be long, I apologize in advance.
I'd say my experience started when I was just out of high school (18-19 years old). My mom was working as a bouncer at a lesbian bar, her shift would end around 11pm, and she'd stay and drink until the bar closed, then call me to come pick her up. By the time I'd get there, she'd be waiting out front with several of her friends who were regulars at the bar. These friends (the youngest of whom was 38, the others all in their 50s) had a running bet on which one of them would be the first to "have" me and how many it would take to "make a good lesbian out of me" the 38 year old even offered that if my mother would get me to marry her she would "fix me" and "make sure I stayed a woman".
Before starting t I was told over and over again by a variety of people, including other queer people and even other trans people, that I shouldn't go on t, or I shouldn't want to go on t because it was bound to turn me into a monster or a rapist.
In an intake interview to get in to see a gender therapist to get my letter to start t. The therapist, who very clearly lacked even basic trans competency, diagnosed me with bipolar disorder, based on a bad reaction I'd had to a medication that subsequent doctors agreed I should never have been prescribed in the first place, 4 years earlier. This diagnosis was used to delay my appointment with the gender therapist until I had a minimum of 8 weeks with a different therapist, I don't believe this diagnosis is accurate, and I suspect it was to delay my transition.
When I started testosterone, the physicians assistant that was supposed to show me how to do the injection refused to do so, claiming that if I didn't already understand how to self administer an intramuscular injection then I clearly was not competent to be making this decision. The only thing she did tell me was that I didn't need to measure a dose because each vial was one dose. As I'm sure anyone on injectable testosterone knows, that is absolutely not accurate. This led to my t levels being way too high. Before that test came back, the doctor took me off t because I'd gained weight (~7 pounds, a perfectly reasonable amount for the first 8 weeks on t). Then, once my hormone test came back showing such high levels, all my future appointments were canceled, and I was told testosterone was clearly not a viable option for me. Luckily, a friend of mine urged me to get a second opinion, and I've been safely on t for 2 years.
Shortly after starting t, a trans fem nonbinary person who I had considered a friend prior to this, called me in the middle of the night claiming to need help. I went to their house immediately and discovered they'd lied about needing help. It turned out that they'd seen me post on Instagram earlier, and based on the post, they assumed that I was drunk and would be easier to take advantage of. They spent an hour or so telling me how it's such a shame I'm a man and I would be so much better off being nonbinary because they "don't like men but they like me". They then asked if they could practice knot tying on me, I agreed, and they bound my hands together, pushed me back on the couch, climbed on top of me, and said I should "just let them fuck the man out of me".
Ive sat through trans support groups where it was explained that trans men shouldn't want to be men but since we are we have a responsibility to be good allies to women by never going out in public after dark, never speaking to women in public, etc. Because it could be taken as a threat. I've sat through trans support groups in which it was explained that because all fetuses initially develop as female, that trans femininity is a developmental issue, but trans masculinity is a mental illness, and therefore it makes sense that I'm both trans and autistic because "all trans men are retards". I've sat through trans social groups where one person explained to another that "t boys make the best fuck dolls and you don't even have to treat them like people".
I tried to join a queer mens group and was told that it's for queer men, not "delusional little girls."
My mothers believe I was manipulated into thinking I'm trans (and gay) because the lgbt center I went to "hates lesbians"
I could probably go on but this is long enough as is.
âď¸âď¸ This is asked entirely in good faith. This post is intended to open dialogue and help with solidarity and understanding. âď¸âď¸
I would like to hear specifically from trans men and trans mascs how the system of [whatever the fuck you call the intersection of transphobia, misogyny, and specifically your gender- whether transandrophobia, isomisogny, antitransmasculinity, transandromisia, transmisandry, or any that I have missed as there are a lot of words to describe similar concepts] uniquely targets and affects you. Things that you feel other demographics do not experience. Reblogs and replies are very encouraged! If you would prefer, you could dm or send an ask to be added anonymously by me.
This is in the spirit of wanting to understand. I am listening. I encourage all non-trans-mascs to not speak on this topic and let trans mascs and trans men do the talking here. Reblog the post to spread it, but please say nothing.
Any and all people who identify as trans men and/or trans mascs are encouraged to participate.
This is not bait to start a fight. I will block without hesitation anyone who is actively being a shithead on this post. I want to hear and uplift your voices by getting it directly from you.
Click this to access the trans fem and trans women version of this post.
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Okay so I readily acknowledge that I know jack shit about politics/how to run a community or society/whatever, and I donât generally like to get involved with that for this reason, but I hope your self-sustained anti-capitalist anarchist future vision contains some kind of method for caring for those who cannot care for themselves other than just âthe community will do it!â because I promise you they wonât. Or at least they wonât do it well. If I canât get people to listen to the fact that I canât garden now, when there is no real reason for me to be gardening, they sure as fuck arenât gonna listen to me in a solarpunk future.Â
Some people need synthesized medication that you cannot replace with herbal meds or be synthesized outside of a lab. Some people need 24/7 care that only specialized workers can provide. Some people need care that the average person is not equipped or trained to handle. Some people will physically not be able to handle living in a self-sustained fashion without outside help. Some people will simply forever be the weird one out, the one that everyone avoids because they have tics or they stim or they talk weirdly or not at all or they see things that arenât there or for a variety of reasons, and when they start flagging, they community is just as likely (if not more likely) to ignore them as they are to help them. Disabled people arenât gonna disappear just bc capitalism did.
So unless you want all disabled people to go extinct in your new utopia, youâre gonna have to plan around that, and until I see someone discuss this in depth, Iâm not gonna be very down with whatever future vision you got.Â
#for the record this is not vaguing about a specific idea or specific person or whatever#i'm sure more established utopian ideas like solarpunk or whatever have at the very least /thought/ about this#but i never see anyone discuss this in any meaningful way and from a lot of the attitudes coming out of those communities i uh#start questioning how well this is going to function for disabled people#because i basically see a lot of people go gaga over the idea of living in small self-sustained communities#and that's valid and all that but like. if that's the way i grew up i would've been fucking miserable#i'm pretty much always tired to the point where chronic fatigue is the only way i can properly describe it#which would've prevented me from doing much of anything to consistently contribute to the community#i'm bad at communicating with people and would've been even worse if i hadn't gotten therapy for it#meaning that in a small community with presumably no resources for evaluating autistic children i would've been fucked#constantly left out and derided for everything and forced beyond my limits even more than i am now#bc nobody would believe that my limits actually existed without a fucking diagnosis of some kind#i'd probably still have massive anger issues that very well might've led to me seriously injuring someone#not to mention that i can't be around people 24/7 but in a commune like the way people often describe that this would be mandatory#it would lead to a mental breakdown that neither i nor anyone in the commune could have any way of dealing with#and i would be lucky; i'd be capable of going on; even miserable; but many others would probably straight up die#like the system now is by no means perfect but all those anarchist ideas i've seen thusfar basically disregard how necessary#a comprehensive and at least somewhat standardized health care system is#like i've had a LOT of interaction with people who want a self-sustaining anarchist anti-capitalist future of some kind#and NONE have talked about what they'd do with people who need specialized equipment you can only find in hospitals#or people who need to take pain meds or anti-depressants or insulin or anti-psychosis meds like#i'm just saying it's a fun idea to live off the land in large communes but you need to make sure that disabled people can do it too#my posts
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