#any doctors diagnosis for me
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Not to tell you how to run your own blog but I loved the discussions full of nuance and would love to see them more often. But also on the other hand I know people who did that often enough that they ended up a target of hate too. Apologies for sending the super chaotic album analysis ask, I was running on fumes too, it was 5am and I hadn't gone to bed yet. The winter months come and I always have trouble waking up before the sun sets, and falling asleep before the sunrise.
Anyway I am not diagnosed with anything, never really could be with where I am, even more so as a woman (we don't even have ADHD meds, those with a diagnosis travel abroad just to buy them) but I have an inkling I might be ND because of many factors but mainly due to feeling like I'm an alien my entire life which no one seems to understand. I've thought about going abroad to get a diagnosis and then I read about what they were doing to ND people during covid and I went fuck that I'll stay wondering and alive. As for Taylor I think the biggest pointer for me was seeing her directing Me! and saying she needs to do less "dead face" or whatever she called it when looking at the footage. I went, oh I know that, it's the thing I also tell myself to do when surrounded by people. Later on I learned why that might be a thing I do lmaooo
the absolute dread i felt getting this anon notif like oh no...it begins
I appreciate the very valid concerns, ive seen how swifties can react to and treat blogs that post too much about subjects they don't like or see as valid. I also have mutuals ive seen get on the wrong end of swiftie harassment and it definitely seems overwhelming at the very least. I have a bit of luck/disguise on my end because ive kind of deduced that swifties seem to not care too much about me if they arent mutuals bc i am not technically a swiftie blog. She's definitely the special interest ive been talking about the most, but I don't post about her solely, I don't have her as my icon or in my url (girard <3) or mentioned anywhere that i'm a swift enjoyer except for me tagging her posts for mutuals who don't wanna see it. My actual posts that I write about her rarely get a Ton of notes and i make them pretty sparsely while also talking about and reblogging a ton of other random shit. I think this helps lessen the likeliness that I'll get someone who like...obsessively reads my blog to point out how stupid dumb and stupid my takes are and get attached to me in like a lolcow sense of trying to provoke me into arguing or entertaining them. If i do start getting some of that, I'll probably just turn off anon and asks for awhile and eventually theyll forget I exist or maybe even block me, imagine that <3
For the second part, I do encourage you to look into whatever neurodivergencies you think you may have even if a literal doctors diagnosis isnt a possibility! Part of the reason im pretty comfortable with tossing around words like autism is because I don't see professional diagnosis as a be all end all, nor do I think its bad to give yourself a "wrong" diagnosis while trying to understand yourself. Even if you don't end up identifying with autistm, I think being around autistic circles and learning about coping mechanisms and thought processes for other neurodivergencies can be so helpful for understanding yourself and your brain, and can bring really helpful. Like, I don't personally have DID or severe psychosis but talking to and reading write ups from mutuals has let me learn about them as like mundane mental health issues/NDs that anyone could have as well as issues i have had in the past with mild hallucinations or conceptions of personality. Most mental illnesses and NDs are treated very strangely and cruelly in general society and are considered aberrant or inherently bad or painful, but these are normal and often neutral (or positive! Which is often ignored or not considered) aspects of peoples lives.
If you are curious about self diagnosis, the most reliable and popular test online is the RAADS-R questionnaire which theres a great version of on embrace autism which i also definitely recommend scrolling through. They also have interesting articles, alternate tests and articles and tests for other neurodivergencies like OCD, which really opened my eyes to the likeliness that I've been suffering with undiagnosed OCD for pretty much my entire life. Theres also an autism forum if you want a broader spread of information and advice that might not be immediately accessible to you. I didnt touch on taylor much in this response (the dead face thing is extremely real, that and her talking about deciding to make the blood in anti hero purple glitter glue because she doesnt feel like a real normal human being in that directors on directors interview) but I do hope the other stuff is helpful and not too rambly <3 autism forever
#ask#anonymous#taylor swift#Theres a few reasons for professional diagnosis but the core point of it is so you know where to look for help and advice and community#and if the help and advice and community that is meaningfully helpful and important to you is in the autism community then thats as good as#any doctors diagnosis for me
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“Normal” test results are not the relief people think they are. When you wake up in pain and continue to be in pain for hours every day and your tests come back normal you don’t stop being in pain.
#chronic pain#I guess#cripplepunk#crip punk#<— correct me if that’s overstepping#what do I tag this with#I obviously didn’t get a diagnosis#personal but I’m also really scared of needles#and having to go through the fear and pain and crying and screaming#for nothing#doesn’t feel good#people tell me it’s not “nothing#but I know exactly what I did before the tests#which is nothing!!#and I didn’t have to go through that pain for that!!!#also å few months ago I genuinely thought it was completely normal#later I realised that spending hours each morning warming up my hands to feel usable might be more pain and stiffness than other people#experienced#I genuinely didn’t expect all of my friends to say they didn’t feel ANY pain at all#and now I’m just hyper aware of how not normal this is#and I’m still in pain#and now I’m not gonna get any help other than a “try heat therapy from the doctor#which is what I was already doing#like no im not crying cause I’m not sick#it would be great if I wasn’t sick#but clearly something’s wrong
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hi my darlings 🤍 sorry for disappearing on you — a lot happened at once. often i turn to writing when life gets tough, but now i’ve just needed a breather.
i’ve just been hospitalised for a while because of my chronic illness and disability, which was hard, but at least i’m getting the help i need. i’m officially back on the streets! the downside is i’m now too ill to work and am scrambling to get some sort of financial support to pay my rent lols:,)
my lovely lovely dog and companion also passed away. she is one of the best things to have happened to me 🫂 i will miss her always.
i’m alright and will be back whenever i get my bearings — i just had to get off any and all social media for a while. i’m doing better and have thankfully been able to defer my exams, so i’ve only got to crank out some essays, which i can do from my bed 🙏
genuinely from the bottom of my heart, thank you to all the people who reached out! and to the people who kept interacting as if i was here<3 it truly means the world to be faced with persistent compassion like this, all my love goes out to you<33 take care of yourselves 🫶 big hugs xx
#carina chats#it’s been a Month#we’ve also gotten my best friend’s terminal diagnosis more under control and we’re now mostly secure that he’ll live to see his wedding#i’m crossing all my fingers for it#it meant the world to me to finally get my ehlers danlos diagnosis in writing#previously i’ve had doctors be like “yeah that’s gotta be what you have” but no more#weight off my shoulders to finally have it figured out#i’m doing relatively alright mentally all things considered#and seriously. the few times i’ve popped in here it’s truly made my day to see any dms or asks<3#just noticing someone’s gone or sending them a little love can make such a difference#thank you and i love you 🫶#i hope everyone else is thriving#big hugs
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will wood miku and shayfer james teto
#will wood#will wood art#hatsune miku#kasane teto#shayfer james#the doctor saw that i draw shit like this and gave me an official autism diagnosis without doing any tests#art
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It’s moments like these that I fear I’m not built for this whole college thing
#I’m so burnt out#and one of my classes genuinely makes me anxious just thinking about#which is great#and getting any accommodations requires proof of diagnosis and a note from a doctor#problem is that one of the major things I need accommodations for is autism and I’m not diagnosed with that because an assessment costs#thousands of dollars and there’s currently two whole people in the entire state I’m in that does them#and then there’s the fact that contacting doctors seems to be impossible for my brain at the best of times#so getting a note from my neurologist saying I can miss class without failing because of migraines has been not happening for a while now#but also idk what to do if not study ecology and get a job in that field#like despite the fact that it was really overwhelming and I was in a ton of pain at the end of the day#working in an aquarium last summer was the only job I’ve had that didn’t make me feel like I needed to crawl out of my own skin#anyway that was a lot and now it’s going into the void of tumblr#j rambles
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the crazy thing about gettin diagnosed with shit is that it doesn't even help you unless you're trying to get some sort of very specific accommodation and it usually just makes your life harder/worse! so when ppl get mad at you for not being professionally diagnosed with whatever mental health problem, just remind them that RFK is trying to make a big list of autistic people in the US, and man that cannot be for a good reason!
#17.txt#also as a professionally diagnosed schizophrenic allllll of your mental health providers will instantly not trust you#and treat you terribly because they “know whats best for you” better than you do!#hope you like antipsychotics because conivincing your doctor to take you off ANY MEDS is actually impossible!#sorry this has been on my mind recently#thinking about getting a DID diagnosis and realizing that it would do jack shit for me to actually have that on paper
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hm. after all this time i still get angry about this so i think it’s about time i make a comic about how i feel about personality disorders
#yapzone#i used to make comics about b/pd and even though i dont identify with that dx anymore and had it wiped from my record#the diagnosis did impact me in a PROFOUND way#tl;dr of my feelings is that a PD is majorly an excuse for a doctor that ignores your pain#or considers the source of it not enough to justify the way you cope#like. in retrospect i think some of the incredibly angry and unstable ways i reacted in relationships#were pretty justifiable considering how fucking awful it was to live in the world without the meds i’m on now#well. not ‘justifiable’ but it was understandable how i came to cope the way i did#of course the world feels unsafe and everything takes x3000 times the effort and the way people talk to you is unclear#and you’re pushed into being an outcast for reasons you can’t understand#like of course i get sent into a panic every time something bad happened in a relationship. i HAD to be hypervigilant.#i could only figure out facial expressions by looking at individual facial features and desperately clinging to tone#i had people say to me they think they have some symptoms of bpd and it’s like of course you do!!! of course you fucking do!#it is a trauma response that doctors deem you had no right to develop because they don’t believe you#and then make it a pathological problem#so every time you have a relapse you go down the pit x10 more because you just got dx’d with Bad Person Disorder#like fuck!!!!! fuck!!!!!!!#it was all bullshit and i should’ve known when my psych who diagnosed me said that ‘people outgrow this disorder’#THEN IS IT A DISORDER ? why do we treat people with a cluster B dx like they’re just bad people who are like that#idk for fun?#it’s dehumanizing. it’s a great way to say ‘it’s hard to treat this patient and i don’t like their tone so they’re just fucked for#some reason. throw them in inpatient’#idk i think we should notice how some of these PD’s very easily are explained by other dx’s but doctors are like#‘nah you’re [minority] you can’t have that you’re just irrational’#i don’t knowwwew i don’t knowww!!!!#the programs they put me in to treat my bpd made me so much worse and ruined my relationships with people because#the whole message was just ‘you’re inherently irrational and can’t trust yourself in any way’#so i never learned to communicate. i learned to keep everything down and let people walk over me. i gave them that permission by saying#oh no i have bpd im irrational my feelings dont matter. you’re fine you can never do anything wrong to me#and if im upset with you and i dont like you and if you make me feel unsafe then that’s my problem i need to fix
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The Healthcare horrors persist
Hhhhhhhhhhhhhh
#Updates on this whole mess:#Im insured under my dad#he has Healthcare option 1 which is government provided since he is retired millitary and option 2 due to his new job#after his retirement option 1 went funky for me and changed things around meaning i was no longer able to be seen by my pcp#Im also unable to log in to any of my accounts for 1 so im not sure whats going on there and what plan of 1 i have specifically#so i switched to a new pcp which accepted option 2 (which was super hard to find) literally last week#made an appointment with her for next month so i can finally get answers about my funky blood test results#(which is still don't know what specifically is wrong with it! for all i know i could just have high cholesterol-#or i could have markers for rheumatoid arthritis instead of my prior fibromyalgia diagnosis!)#(i also do not get refils for my anxiety medication until i have an appointment with my new doctor)#crisis averted right? WRONG!#I just got a call from my Dad saying he is switching jobs so I am no longer insured under 2#meaning...#1) i need to call option 1 and figure out how to get into my accounts and what my insurance is#2) check that this pcp acceprs said insurance#3) find yet another pcp if she doesnt and make an appointment for god knows when#and here is the kicker:#since option 1 is government and millitary based it is going to take FOREVER to get anything done#And Im not sure if they are going to want me to renew my millitary dependent ID or not#because that shit is EXPIRED and i was under the impression i can no longer renew it due to his retirement#but also in order to make any acoount with option 1 they require a benefits number which expires alongside the ID#Then on the other side of things i also have my wisdom teeth surgery to schedule (through my mom thank god)#and school starting again in a few weeks#going to defenestrate myself istg
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begging USians to realize their experiences are not only not universal, but extremely rare in comparison to basically the rest of the world. Brits too, actually. specially regarding disability and chronic illness.
#'wellllll in the us you wouldn't have a rare illness so it's actually well known and any doctors could treat you!'#my country hasn't stopped using medical terms from fucking 1950.#but it's really nice to see how nice it is for y'all when i can't get a fucking diagnosis#because there is ONE doctor here who could diagnose me#and i can't go fucking see them#i had to spend 6 years changing doctors and getting tests and changing doctors again#(because multiple of them said they couldn't help me. they were recommended for people with issues like mine)#to get diagnosed with *fucking fibromyalgia*#but sure. yeah. in the US things are easier. why didn't i think of that.#cripplepunk#cpunk#dyspunktional#disability#actually disabled#chronic illness#either pay so i can go to a hospital that ~knows~ and can treat whiny bitches with 'common' conditions like mine#or like. shut up.
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Here's how I'm asking my doctor for a wheelchair at my next appointment: "I need a wheelchair inside my home so that way I can continue to not need one outside my home"
Maybe that will get them to realize how serious my symptoms are and how stupid making me leave the house with a rollator I have said doesn't help multiple times is.
#and to get them to realize i want to prevent instead of react to symptoms#im so fucking tired#even with a wheelchair i know Im still going to need it part time in my house as well#but i have been using my rollator every time i leave the house#and its not prevented any symptoms yet#and yes i have tried tonexplain that to my doctor#at this point walking is suffering and i dont wanna do it anymore#disability#disabled#chronic illness#dysautonomia#inappropriate sinus tachycardia#possibly me/cfs but still in the process of a diagnosis
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Things probably are not supposed to be this difficult actually. I think something is wrong with meeeee
#husband has been suggesting i pursue another diagnosis lately lol#ive always kinda wondered if i have something more up with me than adhd and depression and anxiety and ptsd but every doctor/therapist ive#talked to about it tells me thats all. ive even specifically mentioned bipolar and borderline and no one wants to diagnose me soooo .....#idk. ¯\_(ツ)_/¯ i guess.#hes been saying lately though that its like theres two of me and he's never really sure which one hes going to be dealing with at any given#time. maybe i should make him come with me and tell my therapist about that and see if it changes the diagnosis opinion. idk#also though: THEN what? a diagnosis alone wont really change anything.
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should i just spend the 40 bucks and speak to a psychologist or councelor or whatever and get over myself -_-
#i dont trust the 40 dollar 'you pay' estimate but ill clarify on the phone. i dont understand co pay versus what i actually pay#esp w like behavioral health stuff like do they start tacking on charges with certain questions#'get over myself' means get over my nauseating fear of mind doctors who are out to get me and make me unable to get a job w#a diagnosis (i do not have any symptoms that would require this at all i am just paranoid)#alas. spent an hour planning on what to say and wrote over four pages of symptoms and insite. can i just fax this to someone and the can#send follow up questions#expode. anywyas it is rough lately in weird ways compared to normal. like the normal stuff is at a low point its other things that are#getting at me lately.
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I have been diagnosed with autism yayyy!
#autism#the tism#the doctors basically just told us a load of stuff we already knew#but in a more patronising way lol#kind of said everything in a way that made me feel like there was something wrong with me?#i think that's just because of the language they used#but there was shit like “rosie is very bad at eye contact” and “she did not express any interest in making small talk with the examiner”#which is true but like#since when was i expected to make small talk with a complete stranger who was studying me like a praying mantis?#since when is that normal for anyone?#still it's good that i've finally got a diagnosis after like 2 years
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why... why am i just not good enough anymore? For the past few years, none of my art has won. For the past few years, I haven't had any friends. For the past few years, no one will actually give me an actual official diagnosis on a mental/physical problems. Is every facet of me not good enough? Am i just not good enough?
#unityrain.txt#i just... i don't understand#all the art i've submitted to things that didn't win... they weren't even bad things! i was really proud of them!#but i didnt win the art festival. i didn't win the nengajō competition (either level). i didn't even get in the top three of the jotun loki#design contest、which only had like 14 submissions.#given my streak i highly doubt i'll win the sonatina composition contest i entered either#with friends、i have none.#i used to have someone i was really really close with、but they left. And even though i've tried desperatly to make other friends、#no one seems interested#i do have some friendly acquaintances#but they don't seem to want anything more than that#i don't even fit in with my own family either#i'm very very lonely#with diagnosis、#my therapist (when i had one) said i definitely had anxiety depression and ocd、but that she couldn't actually diagnose me#also the general doctor i went to seemed to accept it and even offered medication that they don't usually give ppl my age#but if you actually look in my medical record it says nothing#and then i've had awful menstrual problems、and thought i probably had endometriosis、but when i went to the gynocologist#they said it wasn't that、but they didn't really seem to want to give me an actual specific diagnosis of whatever else it was either#they just said it was bad dysmenorrhea (medical term for cramps)、gave me a medication prescription、and then didn't put any diagnosis on my#record.#i just... why#vent#tw vent#vent in tags
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The pain has been bad. I dreamt I was diagnosed with cancer and I celebrated. Things are looking grim.
#it’s not that I want to get a deadly diagnosis I just want any diagnosis no matter how bad#because how am I supposed to fight something I can’t see#but I don’t believe any doctor will figure it out#I get why people do hard drugs#if something to dull the pain was offered to me rn I think I’d take it#I’m seeing my psych next week#maybe I can up my meds
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sort of sad and angry to find that I can't even do pushups because of my stupid wrist
#I broke it while bikeriding in early 2020#doctors didnt detect any fracture in the wrist initially so it spent 2 years necrotising while they fucked around#and tried to give me an arthritis diagnosis!!! in one wrist!!! at the age of 18!!!!#I got reconstructive surgery eventually but it cost 6k out of pocket and it was in a cast so long I lost most of my range of motion#I absolutely despise doctors sorry not sorry
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