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#ive been trying to get this person to understand autism and adhd a bit better bc i am prodx with adhd and depression and so are they
20somethingnobody · 1 year
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Question / vent
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goatpaste · 2 years
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Hey, I’m the person who made the initial callout and I’m glad to see that you’ve changed. I apologize for spreading any misinformation and have edited my post linking to yours. I’m glad to see you’ve improved 👍
hey no worries, i understand why ppl would feel the need to let others know about my past post if they worry about who i am right now
but i want to restate, that is not the same person i am now. i dont want those old post to represent me as a person. they were wrong and bad, and people are allowed to not want to be around me because of it.
However who i am at this time and place is not that person anymore. I would like to at least be acknowledged for growing and changing from that point in time. I was 18, and yes i should have been old enough to probably know better but i was in a transition period in my life a lot going on and i think i was much more on the internet discourse and letting myself fall into these groups and ideas that really were productive or helpful or kind. I took me a bit but i did eventually realized what i was saying was hurting people and for a reason, that i was not being a good ally to others.
it has been 5 years since i basically even mentioned any of that discourse half because i dont feel that way anymore, and the few times i did good or bad always spiraled with the ask and my followers and just felt like ask bait after awhile. and when i get flustered i have bad adhd, dyxlexia and autism so i tend to spiral myself where i mistype and things i say are spelt out wrong or lose my footing on topics when i get overwhelmed. most of the time i wouldnt really answer ask about if i was an aphobe unless people directly Dm'd me, which they have.
I have tried to remove old post of me saying these things because i dont like the idea of ppl searching my blog to find old outdating mean spirited things iv said, but i also havent gotten rid of it all between not being able to find all the post and part that i worried it seem like i was attempting to hide myself when its more i wanted to kill and bury this older version of myself.
but yes, i have had people pinning me for being an aphobe since i chose to be stupid publicly online 5 years ago and its something i have to accept and live with as i move forward and know it will effect how ppl who see me and know me and know about this look at me. you making a callout post was just your trying to keep the people you know and care about safe with the information you had at hand.
but thank you for understanding and seeing the change iv tried to make as a person over the last few years. i do appreciate you come to me and letting me know.
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indigayghost · 1 year
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1, 3, 14 and 16
1. what disability/ies do you have? (and are they mental, physical, or both?)
Autism & adhd (also like anxiety/depression I don't know if those countashahaj), chronic pain due to crocheting very hard + fibromyalgia + something autoimmune probably (I'm going to the doctor tomorrow)
3. what, if any, disability aids do you use? (mobility aids, sensory aids, braces, communicative devices, IVs, etc. meds also count here). do you customize them/their containers/outsides?
I take lots of meds for depression/anxiety, adhd and fm but like I won't try to translate their names I'm sorry agshsjs and also lots of painkillers and I have a cute pink container for them and the extra boxes I put in a cute cookie tin! (also funny story I stopped writing this to go take my night meds and I LOST THE CONTAINER I had to search the whole house I wasn't finding it anywhere and then it was with my nail things that I used in the morning :/
Sometimes when I'm nonverbal I use an text to speech app, sunglasses for eye sensitivity, ear mufflers, lots of sensory toys! Wrist and arm braces, hot bags for The Pain™ and I'm starting to use a wheelchair when I'm outside
Also i bought a thingie to put in the hairdryer so I don't need to hold it because it hurts I'm counting that as a mobility aid
Something I don't have but it would be so so so helpful is a shower chair because my blood pressure is very low and I faint like 8 out of 10 showers haha
I'm counting the little salt bags as a disability aid too sue me if you will but these things saved me more times than I can count
14. has there ever been a time where you felt solidarity/community with another disabled person in a situation with you?
Oh yeah! There was this time in the train that I was seated in the preferential seat and a woman started to scream with me that I shouldn't be there and then the guy seating next to me was like HE'S AUTISTIC IF YOU DON'T LIKE IT FUCKING LEAVE and I was like thank you 😭 and he said it's fine I'm *insert here another invisible disability I don't remember sorry kind train man* we got to have our backs and I was like yeah!
Also my cousins fiancé is disabled and everytime we're in a family dinner or something there's always one moment someone say something so dumb and we look at each other with so much understanding it's funny
And also obviously all the times I talk about an issue here there's always so many kind comment and helpful advice ❤️ to my disabled moots yall are awesome and you helped me understand and validate my experiences so so much I love you all
16. free space to talk about whatever disability issue or experience you want !
Uuuugh I'm so bad at free spaces!!!! I don't know what to saaaaaaaaay
Well I think like, my journey of accepting my disabilities is just beginning actually
Growing up autistic (and specially afab, autistic and fat) makes it very very hard for you to listen to your body and needs. Everytime I said something was wrong or that I didn't felt right people said it was nothing or that I was being a crybaby and it wasn't as bad as I was making it or that it was my fault because I was fat, so I'm still very bad at telling like how much pain I'm in and stopping doing something before it hurts me, but I'm learning and everyday I get a little bit better at stepping up for myself and my needs so that's cool!
I love how I found in the wwdits fandom not only other crazy people to scream with me because of gay vampires but also a really kind community full of disabled folks that make me feel so validated and free and looked out for so yeah I love you guys 💖
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ironmanstan · 3 years
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hi rohan how did u figure out u were autistic? p much all of my irl friends (who are nearly all autistic, if it's of any relevance) think i am, and i relate to all the diagnostic criteria, but i feel like i "can't" be because i don't know if i did some of the common autistic experiences (practicing facial expressions in the mirror, the feeling that everyone else got a manual on social stuff and you didn't, idk if i get meltdowns, not understanding figurative speech or idioms, etc) and i can't tell if it's because they presented differently in me or if i'm just not autistic. i know i have sensory issues, i know i stick to routines a lot (but i don't get anxious when they're interrupted? i don't like it, but i deal with it), i know my tone of voice is very flat, i know i shut down if i'm in a social situation where i don't know what i'm supposed to do (which doesn't happen often, but it has happened), i know i have intense, specific interests, but i also have adhd so they could just be hyperfixations, i know i relate to hyperlexia, though i don't enough about it to comfortably say i was hyperlexic, i know that, as previously mentioned, nearly all of my friends are autistic (and the ones that aren't are adhd) and so i definitely get along better with nd people than nt ones, i know my brother is autistic, if that's of any relevance, and i took a lot of the tests on embrace-autism and consistently scored past the thresholds, but i don't "feel autistic," i guess? there's a sense of alienation from my peers present, but i've lived in a very white area my entire life so it could just be from that, and i don't know that it's all that intense. i'm generally both easy-going and a bit oblivious, so i'm often "in my own world," plus my episodic memory is absolutely horrid, so i have no clue if i miss social cues. this is getting very long so i'm going to cut this off here, but if you have any advice, it'd be appreciated, and if you guess which one of ur mutuals this is, please give me the guise of anonymity. thank you and so sorry for the absolute monster this ask is
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(Dw anon I understand you’re on anon for a reason I would never try to discover your identity <3. [and sorry if you’re one of my mutuals i haven’t responded to dms for ive just been all over the place and busy latelykjhdkfdg])
Hellooo, thank you for the ask! This is a long ask and gonna be a long answer. I also haven’t edited this a whole lot outside of rereading it a few times, and I apologize if I have some very long blocks of text in this but I did my best to break it up, so ig buckle in for that lol. I'm not gonna get too personal bc again public tumblr post but i'll do my best to help ya.
Ig ill start by saying how i figured out i was autistic? And then my opinions on autism and diagnosis criteria of it and it being diagnosed in general bc I have a Lot of thoughts on this, I used to hyperfixate on psychology for a while lmao but I am a teen and I am no expert, I just feel my thoughts on some things alongside my thoughts on my own autism might be relevant here.
Honestly i relate to what you're saying a lot anon, I didn't feel a disconnect between myself and other people for a long time, and even when I did a lot of the time it could be chalked up to racism or being surrounded by people who treated me weirdly for being mixed, or it could be chalked up to me just being a gullible kid, or living in a toxic/abusive household and not knowing how to relate to people who didn't. For years and years I thought "oh this is just how it is."
I think making friends was a real turning point for me, because those were people who acknowledged my weirdness but didn't turn me away because of it. Unsurprisingly, most of my closest friends and partners are/have been neurodivergent in some way, which I think chalks up to me being more comfortable around people who I'm understood by. And me, having autism, ig being less put off by people not conforming to social rules and being "weird" bc that's how i am, and if anything, i think it makes it easier for me to connect to others.
The biggest thing after gaining friends that pushed me into realizing I was autistic, was learning what masking is. Masking is the act of hiding your symptoms and presenting yourself as neurotypical in social situations so as to not alienate yourself and to keep up with a situation that does not accommodate you. A lot of autistic people mask without realizing it, thinking that everybody has to work harder to pick up on social cues, everybody studies social situations even in the most minor of ways, everybody mirrors the people around them to try and keep conversation flowing without issue, everyone has responses to conversations mapped out in their head, almost like a script, everybody jokes constantly because having a reaction of laughter and being seen as quirky and eccentric is better than getting told you're too quiet or you're weird, everybody feels extremely anxious in new social situations because they have no plan for this and don't have a mask prepared.
Right?
Social issues are also present in ADHD but whilst social issues in ADHD stem from a lack of ability to focus on conversation and invest in something that may or may not give the dopamine hit ADHD forces you to seek out, autism is the act of being thrown in water and being told to swim without experience. Some of us remain calm and realize we can float, even if it takes all our stamina, and some of us sink to the bottom, needing help and accommodation to pull us out. Autism is a spectrum and not having some symptoms or presenting them in different ways from other autistic people doesn't always mean you are not autistic.
I think the idea that you must feel a sense of disconnect between yourself and others socially heavily relies on having ties to others in the first place. Someone who has no close friends growing up is not going to be able to weigh this accurately. The other issue is that a lot of the time you never look at yourself and think you are socializing incorrectly because the way you socialize is going to be what you think is normal. I didn't realize my voice can be largely monotonous at times when I forget to mask until my friends pointed it out. Now I know I don't mask my voice when I'm most comfortable. I only fake having a "normal" voice due to being seen as unfeeling, cold/angry, and emotionless by people who do not enjoy my "weirdness".
Figuring out the social differences between yourself and others I think is the hardest thing to weigh. You have to look at yourself very hard and unravel layers of: questioning if you are masking, figuring out who you as a person truly are and how you truly act when you are you're most comfortable, and then questioning if how you act is how society believes most people act, or if you fall on the wayside.
I also think unconsciously, neurotypicals can notice when somebody isn't like them, which leads to a lot of autistic people being bullied or othered or seen as extremely weird whether it be for showing affection "strangely", or emoteing "strangely". For example there's often a sentiment autistic people are either not emotional enough, or overly emotional. Or both, depending on the situation (someone having a meltdown or autistic shutdown and being overly emotional vs that same person in their day-to-day not knowing how to express gratitude outside of a monotonous "thank you"). On the flipside, I think autistic people also sometimes get a sense that neurotypical people are different from us, and if we get this sense, it leads us to over-perform, trying to live up to this same status of baseline ability everybody else seemingly already knows how to get to. We as autistic people do not know how to be neurotypical though, leading some of us to be overly observant of other people's behaviors, even if we interpret them incorrectly. This over-observance alone is something I think most neurotypical people would not do, what reason do they have to study their social partners? A more concrete example of this (which's a little funny to me) is how when I was younger and didn't know how to speak to people online I once lurked in a discord server of people who I'd later become friends with, for a year straight, because it was the first real space where i could actually see other people have conversations and bond, and I could figure out how they did it so I could follow in their footsteps and do the same. This line of actions and thought is where the "born without the same manual everyone else was given" sentiment comes from, though it isn't a required experience.
Even sensory issues aren't a required experience, but a lot of us still have them. Sensory issues, stims, tics, things like dyscalculia and dyslexia, flat affects, general monotony. All comorbidities common with autism but not required. Thank you actually for bringing up hyperlexia bc that was a term I did not know prior to this lmao.
Low and high empathy, two of these common things found in autistic people, are funny. Because the way they are measured is always measured against a neurotypical sense of empathy. Like, with low empathy, it strikes me as similar to loveless aromantics being contrasted against alloromantic people. With loveless aromanticism you have that wedge between yourself and the term “love”, even though you may still care for people and even be affectionate towards them, you do not see “love” as something required or necessary because you experience attachments different to most people or you've been ostracized for feeling love but not in a romantic sense. Empathy in autistic people I feel is similar. Empathy is something I can feel in some ways, in small doses, in specific situations, but I feel a strange disconnect with it. And I think a lot of neurotypical people take this as a sign of coldness, detachment, emotional unavailability, and conveniently forget sympathy exists. Or even just do not process that not having empathy, or sympathy, isn’t a bad thing or something that makes you lack the ability to care about others and want them to be doing well (which leads to the demonization of people with ASPD/sociopathy).
It’s even funnier to me considering this, that a lot of autistic people are aromantic or asexual. I think that fact is less due to us just straight up “not understanding social situations to the point of being aro/ace” because that’s just not how that works. Instead I think it’s similar to how a lot of autistic people are also trans. Because we do not understand social norms we feel less beholden to them, and discovering our neurodivergence means being introspective already, and introspection and being okay with what you find is what’s necessary to discover you’re something most of society will misunderstand. And aro/aceness is something that is both heavily misunderstood, and not widely spoken about. Aro/aceness not only breaks down the social norm of heteronormativity, but also allonormativity.
The difference between hyperfixation and special interests are also something not widely known about, with a lot of people conflating the two. Over time I think I've come to understand the difference, but not every autistic person will agree with me and some may view it as completely different from how I see it, which is perfectly ok, we all have our own views and I'm not against hearing those alternative to my own.
To me, hyperfixations are fixations that are destined to leave eventually, and aren't necessarily part of your identity. I think the confusion usually stems from how a lot of people say spins (special interests) are something lifelong that can fade and pop back up, and are core to your identity, when hyperfixations can mirror this in a way. With hyperfixations, I think any interest you have is in some way going to stick with you forever. You are typically going to look at a show you liked as a kid and still feel some fondness or attachment to it. But that doesn’t necessarily mean it will become a core part of your identity. Hyperfixations are also something that people get for different reasons than spins I think. Hyperfixations source from the brain’s need for dopamine, and so it finds something to cling to, getting that hit of dopamine, and then dropping it for the next thing. If the hyperfixation happened to be something in line with your other interests, it makes sense to come back to it or have it crop back up over and over as a fresh hyperfixation.
With autism, I feel spins line up more with how I think autistic people are more likely to kin characters. I think a lot of autistic people struggle with recognizing their autism because even if we are introspective, a lot of the time it’s hard for us to understand what we find in ourselves, especially if we have no tangible example to relate our experiences to. I think this is why a lot of people who kin tend to be autistic, understanding the traits we see in ourselves when they are represented in a character we like makes understanding ourselves that much easier. It also I think makes some of us feel strange seeing other people kin characters we kin, because in a way it loops back around, and we end up feeling personally bonded to or related to that character, since we see ourselves so strongly in them. It’s the same with spins in a way, I feel. The distinction I make with spins is that even if they fade, they will always come back at one point or another, because they are core to my identity. JJBA, I think classifies as a spin for me, between the art style being something I heavily enjoy, comics being something I’m heavily interested in, and the characters being either relatable to me or just causing me immense pain lmao, all these things make it a very core interest of mine where, if you know me, you’ve 100% heard me talk about it at least once. Hyperfixations may leave lasting effects sure but spins I’ve always seen as something core to you, something that relate to who you are as a person and what you enjoy and often stick with you forever because of that, unless somehow you change into an entirely different person or simply grow out of the things that made it a spin for you in the first place.
Routine is also something not necessary to the autistic experience, but I think a lot of people misunderstand what routine means in an autistic context. Routine to most usually means doing things on a schedule, certain things at certain times. To someone with autism though, routine can be a plethora of things. Routine to me is when I, in the back of my head, tell myself that I will work for a few hours and then play games for a few hours so I can keep myself on track and get something done when I am low energy/do not have enough spoons. Routine to me means having rituals and orders in which I do things because I’m used to them and doing something different feels unnecessarily strange and kind of uncomfortable. It means cleaning my room and getting water every time I call somebody because it just makes me feel more comfortable and if I don’t get a chance to do this I feel strange. It means going to the same places in video games constantly because they’re familiar. It means watching the same movies over and over when i feel bored because familiarity, routine, is what I know and what is comfortable. It means getting stressed when I don’t talk to the people I regularly talk to for too long, it means getting stressed when new people or people I don’t usually talk to start messaging me. It means feeling stressed when my cat passes away because now my routine at night has changed, she will not sleep next to me and I do not need to make a space for her by my side (even then, unconsciously I still do sometimes). It means eating the same foods for a week straight because you need something to cling to and nothing else feels right except for this and everything else feels off or bad or just not up to par. It means listening to the same song for a week straight not even for the sensory input anymore but because you need something you know so you don’t need to expect something new. It means planning out calls with friends or outings because not knowing what to expect stresses you out. It’s doing the same things in a stupid way over and over again even if something else is more efficient because doing something else means changing and change is stressful and sometimes harder than whatever you’re already doing.
Routine is something that exists because it helps ground us. Not because all autistic people particularly need to have schedules or something (though some do), but expecting something to happen helps ease us out of the pain change brings with it. It also doesn’t necessarily mean shutting down or melting down when change does happen. Personally, since I also have PTSD which also affects my mood, I’m more likely to get angry, anxious, and frantic, when change happens, whilst someone else might be mildly annoyed, and someone else could be upset to the point of tears. Autism is a spectrum.
Autism also isn't something to be gatekept. Autism has been under-diagnosed in afab people and people of color and largely only been studied in white amab people, leading most autism diagnoses to be delivered with this in mind, making it extremely hard for non-white non-amab people to be officially diagnosed. There's also a large sense of… idk what to call it… purity culture? On tumblr. Which i believe (amongst other tumblr dramas, such as slur discourse and the like) is caused by white people. What I'm talking about is the opinion that doctors know best above all and doing such things as seeking a second opinion or believing what you think, over a doctor, is some heinous crime. Meanwhile black afab people and indigenous people are often medically abused by their doctors, an act steeped in a lot of history people like to forget about. (tw in the link for anti-black racism and details about medical operations and malpractice)
All of this leads to my next point, this artificial difficulty around receiving a diagnosis, and the discrimination that you can go through for having a diagnosis, leads me to believe autism is something that isn't bad to self diagnose. I think self diagnosis often gets the stereotype of being attributed to young teens who want to be quirky, but nobody seriously keeping up with saying they have a disorder is going to fake it for years. Teens have said stupider things and done stupider things than lie about having ADHD on twitter. If autism sounds like something you genuinely have and you do not have the privilege to get diagnosed (bc i didn't even mention the costs for diagnosis) and if recognizing the issues you have and finding coping mechanisms or at least a sense of community would help you reclaim this piece of yourself and help you move forward in your life feeling like you know yourself better, than i think by all means, claim the label. Labels can change, people can be misdiagnosed even officially, it's your life, do not let anyone but yourself dictate how you should see yourself. I hope this helped ^__^ good luck <3
Also, an edit: autism and other neurodivergencies are extremely genetic. If you or a sibling is neurodivergent, chances are one of your parents or grandparents is. Therefore the chance of you also being neurodivergent in some way significantly raises. A lot of the time when a child is diagnosed with ADHD its recommended for their parents to get screened for it because of how likely it is that one of them has it, that stays true for autism, I don't know to what extent however.
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uiruu · 4 years
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because i grew up hanging around straight white boys in school in the US, i was exposed to a lot of stereotypes of what autistic people are like, and mockery of people like that, using that as an insult towards people who are neurotypical to show that theyre stupid or weird or whatever.... etc. i wish i could say i didnt participate in that, but i probably did more than i realize, cause i was like 11 or 12, i didnt really know what i was saying, you know? though, i’ve never really been a confrontational person in real life, so i didnt really engage in a lot of insulting other kids in general, though i had some stereotypes and stuff thrown at me i think. i mean they didnt use the word “autistic”, im not sure the kids i went to school with even knew what that meant at the time, im not sure i did either, but they’d use words and slurs that of course are about behaviors and things that autistic people do, you know what i mean. the r one and the one that starts with sp- and the other one that starts with sp- that is short for special education... you know. those. 
so like, ive absorbed and internalized a lot of that, i think. i catch myself doing and saying things online that make me react to myself like “woah, i really sound like...” and “i should try to rephrase things to be more normal, i dont want people to be weirded out by me, i dont want them to think im being too much of a...” that kind of thing. i dont actually think those in words lmao but you know, that’s the subconscious gut feeling. but like... having those thoughts also conversely makes me appreciate and be proud of thinking and saying things that are “too autistic” or whatever lol. i havent been diagnosed with autism, i dont know if i have it, but i have been diagnosed with adhd and there’s a looooot in common. much more than you would think if you just know adhd for what that acronym stands for (its kind of a bad name for the disorder, it’s not even close to the whole truth). adhd and autism often overlap and occur together too, because the lines when defining what does or doesnt count as a given disorder arent so clear when everyone’s brain is different. i’ve thought about trying to see if i actually am autistic, i’ve wondered it, but idk, it’s not really necessary i dont think, treating and managing adhd covers most of it anyway, for me. sort of. anyway
so now, as a 24 year old with a better understanding of this kind of thing (though still not perfect, im learning all the time), when i catch myself being too weird or alienating or saying something that suggests i think about things in a different sort of way from most people, it stops me for a sec, but then it’s kind of a source of pride and fascination for me lol, i like the way i think and i like discovering all the ways that i think, if that makes sense. it also feels good to have the thought that i need to tone myself down occur to me, and then actively say “no, im not gonna do that” and just carry on not toning myself down at all haha. so what if people see what i say and go “wow you think about that mundane thing in too much detail, why are you thinking so hard about something so meaningless, why do you need to invent systems and routines and stuff in order to conceptualize stuff, is it really fun for you to see the world like its all data”? so what if people see me and go “wow theyre a bit of a..., god you’re being a little too...”? i think the way i see the world is in and of itself an interesting thing to conceptualize and collect data about lol. and like whatever, im enjoying myself, i know i’m not the only person with adhd/autism, so i dont see the point in trying to consciously try to type as if i dont lol. i get wildly absorbed into stuff that seems pretty meaningless to most people. it’s what i do. it has a lot of downsides, but i like feeling proud of the upsides too :)
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Personal Update
Hiiiiiiiiiii……….. iiiI have absolutely no idea how to start this, but i guess the beginning is a pretty good start.
(Im not gonna lie i am absolute shit when it comes to talking about things in my life especially my health but im trying to work on that and hopefully use it to help educate in the future)
Il'l be honest this last year and a half-two years has been rough, no one ever tells you the sheer difference between just knowing about something and coming to terms with it being reality.
Growing up we always knew i had ADHD and even got that tested/medicated very quickly. But we also always knew i had Autism to some degree, unfortunately living in the south in the late 90s there weren’t many people willing to test/label a girl with that (things are ass backwards down here what can i say). What they don’t realize is its essentially social suicide by not getting me tested then because being the outcast of the outcast and not be able to offer explanations that does thing to people. But, At least we knew about it early on because i was able to do my own research over time and even found ways to work with people on the spectrum to better understand my own problems.
Now flash forward to the summer in between my 2nd and 3rd year of college, i can’t explain it but its like reality was playing catch up to the point that the DAY before my junior year was supposed to start I dropped out. Although i will admit at the time my reasoning was because of my mom having surgery and someone need to keep an eye on her for a bit. What I didn’t know however was giving my mind room to breathe finally would start sort of a domino effect of problems.
So now lets jump to the spring of 2016. I’ve had a lot going on both mentally and physically my whole life (especially right now) but for some reason one night as im sitting at a music festival camera in hand waiting on the main act to start i look around and for the first ever I felt like i was at home. You’d think that’d be a good thing right? Almost but not quite. Following that little realization i FINALLY got someone to get me tested and sure enough right in the middle of summer not even a week after Warped Tour, i got the answers I’d been waiting ages for. Not only did we finally have definitive diagnosis of Level 1 ASD we also found several things that had been lurking in my minds shadows (i.e. More anxiety, depression, insomnia, bi-polar, slight manic) which was fine but also felt like the entire floor had ripped out from under me with no warning.
Now, Ive dealt with depression off/on my whole life but it is TERRIFYING to be in an all out mental free fall and not even be aware of it at first. Im not even joking when i say i felt like i was going insane. I can say now though that I completely get why people love New Years. After months of trying to understand things and recalibrate meds we’d finally found a combo that works, and even driving that point home with me having a huge mental break through happened on New Years eve. As im typing this right now i can tell you my mental state is miles better than it was at the beginning of this year, theres still a lot of work to be done on my end but my self awareness and recognition has increased exponentially for someone late to the show here.
Oh, But wait! Theres more……….
Remember me saying there were physical problems occurring too? Well, around late 2015-all of 2016 I started having intestinal issues again which as someone who’s had ulcers before thats not something you want to feel again, ever. Except it wasn’t ulcers and after a shit ton of test we did determine it wasn’t my gallbladder either (s/o to my genetics), in the end it just kind of got chalked up to anxiety considering i had also been dealing with what we had thought was the start of TMJ (thanks mom).
And really that was pretty much the running theory up until February of this year happened. When i tell you my body has impeccable timing im beyond serious because literally TWO DAYS before my umptienth visit with the oral surgeon my jaw……well long story short, my jaw had been partially dislocating itself for a year until it finally just decided popped back into place on its own. Which yeah great that answers that problem, but the gut issues han only gotten significantly worse at this point. Spareing some details and numerous appointments, about mid spring this year we found out I actually have what is known as Auto-immune Pancreatitis, Sounds bad right? Because it is. Sad part is it would’ve been found a lot sooner too if it wasn’t for my almost inhuman pain tolerance. Even funnier is both EDS (associate with my jaw problem) and Pancreatitis are fairly common in Autistic and ADHD people (Story of my life at this point).
Were, still not done though!
Ontop of ALL of this ive also been getting significantly more frequent migraines, again not new in my life but it is something thats finally being paid proper attention to (kind of). Migraines aside, another problem being that my whole life i’ve always had a higher resting heat rate than most people, again very common in adhd people and athletes. Whats not common about it, is for my average to be 115bpm while sitting perfectly still and then jumping on its own all the way to 170bpm without me having moved an inch (bare in mind 115 for me is what 60 would be for most people so 170 is probably more like 130 in normal people).
Which bring me to the last couple of months here. Technical jargon and process aside we(my cardiologist) have fortunately found that it’s not a valve and it’s not a rythm problem but it is an electrical problem known as Sinus Tachycardia or laymens terms; my heart beats way to fast naturally and randomly speeds up on its own without any outside prompting. At this point in time the main goal is to figure the why i have some sort short circuit in my system and then the migraines and other things i haven’t mentioned can be dealt with.
And that “self tanner” photo (on insta), that is from me havin a LINQ montir placed in my chest so that my heart can be monitored 24/7. No i can’t feel it, yes i was awake, yes i mean my boob, no it doesn’t stay in forever it only has a battery life of about three years……
As for what this means in terms of the future of my photography: I’m not giving up on Beyond the Barricade I actually even have several ideas to make it so much better than what i originally had planned. But for right now i have to raise the caution flag and take a step back from basically everything in music. As much as i dont want too my health comes first and even if mentally im in a much better place physically its hard to even just get out bed most day and getting this sorted is my number one priority. Yeah, I might be down at the moment but i will be damned if i let life count me out. I’m still here I promise.
-JT
Insta: https://www.instagram.com/thiggy_/
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