#processing disorder seems

[aitadjcrazytimes]

#lmao #for anyone who's curious the process went: #send ask to aita official #blog blows up #someone realizes its a chexer fic #i follow them bc they seem cool #i join their rvb server #their encouragement pushes me to finish the Actual Fic i was working on #i expand the fic to be more of a whole au after it comes out much better than expected #the next fic in the au that i work on has to do with a character's brain injury #this leads me to do research into brain injuries #''......huh. this sounds. a lot like the neurological symptoms that my doctors have been saying is just part of my anxiety disorder'' #think on that for a while #go to the ER for unrelated reasons #remember my theory #bring it up to the doctor #Doctor Immediate Concern #doctors orders a ct scan #''eeyup! that there's some atrophying and a chiari malformation! y'ever had a head injury'' #(i had had several) #''well! shit! time to refer you to neurosurgery :) see if we cant do somethin about all that memory loss and severe pain and shit'' #and now we are here #it also lead me to research osddid systems for the first fic #and now my therapist is having me tested for osdd because i did not know that those symptoms were not a thing everyone experiences #so like. thanks for helping me meet friends who could encourage me to engage with the things i like + learn more about myself #^ ^ <3 #im actually not gonna say ''ok last update fr this time'' bc idfk maybe something WOULD be funny to post on here

[lolexjpg]

obamacare website hates me and wants me to die

#'oh the website seems to be glitching lets just do it on the phone' ok itll take hours bc ill need you to repeat everything 10 times bc #i have audio processing disorder hope thats ok with yoU!!! i wanted to read it all for a reason #i just need to change my apartment number maybe YOU should change the system so i dont have to go through the entire application agian #she speaks

[julie-su]

gonna see spiderverse?

I'd love to! I've been told it's too flashy for me to watch, though, so I'll wait for DVD and try it on a small screen. Or perhaps, audio described. On that note.. Thank you to everybody who thought of me, and gave me the heads' up <3 I have to wait anyways for the subtitled showings; what a good thing I did ^^"

#not hoh but have auditory processing disorder diagnosed. #creates interesting dilemma... am legally blind. get to pick and choose whether it's harder to see or hear. and of course.. the epilepsy. #-siiiigh- most of these stem from only two disorders. It seems like I have a lot going on - but it's really just two disorders :P

[andromedasummer]

me 🤝 the person at the cafe counter 🤝 the person behind me = auditory processing disorder

#i was like 'im so sorry im taking so long to answer and not hearing things properly im autistic and i have auditory processing disorder'' #and then they were like ''no way me too its a part of my adhd'' #and the person behind me was like ''DUDE SAME'' #does not surprise me cos this cafe is very disability friendly #its a vegan + gf cafe that recently opened up and is owned by a chronically ill person #im p sure all their employees also have diff disabilities (physical/non visible) #all their food can be adjusted to peoples dietary requirements and the place is spaced so wheelchair users can easily come through #(its been very popular with wheel chair users i feel like everytime i go past theres someone chilling beside the lowered counter adjacent #table sipping some tea/eating sweets) #theres also a play area for kids and a bookcase full of board games/paper/pens and pencils/books #very good atmosphere all around and its so nice for people to understand that im not trying to seem disinterested or obtuse #i just cant hear things well when theres background noises of buses and cars and clinking cups and plates and cutlery and people chatting #because my ears will focus on like. pouring water or a car door opening and not the person talking to mes voice #ALSO you get a free mini square of brownie with any hot drink

[sharktholomew]

me wanting to play DnD but realizing numbers are involved

#and i also have audio processing disorder #and the only person i could play with is my dad #so no way i could get any accomodation #<- cause he's very ableist #which is weird cause he seems very neurodivergent himself

[sweetnessfollowsmp3]

wait a minute

#ok i think i might have auditory processing disorder?? #like i always assumed i didn’t because my brother does and he couldn’t really talk that well until he was like 9 #but i mean whenever i read about it it’s relatable as hell #like i literally do not hear words unless i really focus—it’s just sounds #and even when i am focusing i still miss stuff #i think everyone in my family just missed it because my brother has it so severely that my auditory processing seems normal but comparison #astrid.txt

[tinyredpoppies]

Eyyyy speaking of therapy I finally have insurance again lol.

#and my other therapist discharged me which is fine #she was nice and all but also a nun and didn't seem particularly knowledgeable in disorders beyond the standard garden variety #i experience frequent dissociation so uhhh that's wouldn't have worked for very long lol #so time to look for a better therapist! #tbf she did want me to be able to do emdr with her supervisor but like if i didn't trust her to process in between then what's the point #personal #k texts

[nomansgunssmoke]

hey guys! it’s unrealistic to assume everyone knows not to make cult jokes!

if you are going to inform someone, do it kindly. most people do not know what ramcoa means, let alone that it continues to this day.

sincerely, a cult survivor

#edit: especially if the individual in question is nd #nds greatly impact how people see the world #process it #etc #not to say nds are unable to entirely #but a lot of you seem to forget that theyre disorders & disabilities for a reason

[primrosebitch]

just realized that there's another disorder that i probably have to add to the list

#chronic illness #i have so many things wrong with my body #so many conditions #and it seems i find out about a new one regularly #this time it's auditory processing disorder #which in this case isn't like a surprise #it's just that i only now realized that it's a thing that can be diagnosed and added to the list #like i've always basically known i had it #but i didn't really think much into it #so i never looked into it #until now

[light-koe-pinsky]

.

#hey! a little update on my sis condition #the other tests came out and it seems she has something called dysautonomy #Dysautonomia is a nervous system disorder that disrupts autonomic body processes. These are automatic functions like your blood pressure #and heart rate. Having dysautonomia means these functions don’t work properly #causing disruptive symptoms. #i copy that from google #she was recomended to increase her salt consumption to eat better and to do yoga #but apparently shes gonna keep having black outs #if theyre too consecutevely shes gonna have to get a more detailed neurologic study #so far shes had like 3 more episodes #siiighhhhhhhhh #anyways Im trying to help everytime Im home and not at work I cook for her and try to distract her from stressful episodes bc it seems to #have to do a lot with anxiety #she has this sudden rush and anxiety sometimes but you can calm her by talking to her #she needs to keep checking her heart rate so my mom got her an oxymeter #shes very responsible and for someone her age shes really managing this very well despite the anxiety attacks #i was dueling on posting or not an update here it really doesnt matter and doesnt make much difference but i felt like it was weird to #never address it again lol #so here we are #supposedly that sickness regulates itself as you're getting older so lets hope thats her case #personal

[cocklessboy]

The biggest male privilege I have so far encountered is going to the doctor.

I lived as a woman for 35 years. I have a lifetime of chronic health issues including chronic pain, chronic fatigue, respiratory issues, and neurodivergence (autistic + ADHD). There's so much wrong with my body and brain that I have never dared to make a single list of it to show a doctor because I was so sure I would be sent directly to a psychologist specializing in hypochondria (sorry, "anxiety") without getting a single test done.

And I was right. Anytime I ever tried to bring up even one of my health issues, every doctor's initial reaction was, at best, to look at me with doubt. A raised eyebrow. A seemingly casual, offhand question about whether I'd ever been diagnosed with an anxiety disorder. Even female doctors!

We're not talking about super rare symptoms here either. Joint pain. Chronic joint pain since I was about 19 years old. Back pain. Trouble breathing. Allergy-like reactions to things that aren't typically allergens. Headaches. Brain fog. Severe insomnia. Sensitivity to cold and heat.

There's a lot more going on than that, but those were the things I thought I might be able to at least get some acknowledgement of. Some tests, at least. But 90% of the time I was told to go home, rest, take a few days off work, take some benzos (which they'd throw at me without hesitation), just chill out a bit, you'll be fine. Anxiety can cause all kinds of odd symptoms.

Anyone female-presenting reading this is surely nodding along. Yup, that's just how doctors are.

Except...

I started transitioning about 2.5 years ago. At this point I have a beard, male pattern baldness, a deep voice, and a flat chest. All of my doctors know that I'm trans because I still haven't managed to get all the paperwork legally changed, but when they look at me, even if they knew me as female at first, they see a man.

I knew men didn't face the same hurdles when it came to health care, but I had no idea it was this different.

The last time I saw my GP (a man, fairly young, 30s or so), I mentioned chronic pain, and he was concerned to see that it wasn't represented in my file. Previous doctors hadn't even bothered to write it down. He pushed his next appointment back to spend nearly an hour with me going through my entire body while I described every type of chronic pain I had, how long I'd had it, what causes I was aware of. He asked me if I had any theories as to why I had so much pain and looked at me with concerned expectation, hoping I might have a starting point for him. He immediately drew up referrals for pain specialists (a profession I didn't even know existed till that moment) and physical therapy. He said depending on how it goes, he may need to help me get on some degree of disability assistance from the government, since I obviously shouldn't be trying to work full-time under these circumstances.

Never a glimmer of doubt in his eye. Never did he so much as mention the word "anxiety".

There's also my psychiatrist. He diagnosed me with ADHD last year (meeting me as a man from the start, though he knew I was trans). He never doubted my symptoms or medical history. He also took my pain and sleep issues seriously from the start and has been trying to help me find medications to help both those things while I go through the long process of seeing other specialists. I've had bad reactions to almost everything I've tried, because that's what always happens. Sometimes it seems like I'm allergic to the whole world.

And then, just a few days ago, the most shocking thing happened. I'd been wondering for a while if I might have a mast cell condition like MCAS, having read a lot of informative posts by @thebibliosphere which sounded a little too relatable. Another friend suggested it might explain some of my problems, so I decided to mention it to the psychiatrist, fully prepared to laugh it off. Yeah, a friend thinks I might have it, I'm not convinced though.

His response? That's an interesting theory. It would be difficult to test for especially in this country, but that's no reason not to try treatments and see if they are helpful. He adjusted his medication recommendations immediately based on this suggestion. He's researching an elimination diet to diagnose my food sensitivities.

I casually mentioned MCAS, something routinely dismissed by doctors with female patients, and he instantly took the possibility seriously.

That's it. I've reached peak male privilege. There is nothing else that could happen that could be more insane than that.

I literally keep having to hold myself back from apologizing or hedging or trying to frame my theories as someone else's idea lest I be dismissed as a hypochondriac. I told the doctor I'd like to make a big list of every health issue I have, diagnosed and undiagnosed, every theory I've been given or come up with myself, and every medication I've tried and my reactions to it - something I've never done because I knew for a fact no doctor would take me seriously if they saw such a list all at once. He said it was a good idea and could be very helpful.

Female-presenting people are of course not going to be surprised by any of this, but in my experience, male-presenting people often are. When you've never had a doctor scoff at you, laugh at you, literally say "I won't consider that possibility until you've been cleared by a psychologist" for the most mundane of health problems, it might be hard to imagine just how demoralizing it is. How scary it becomes going to the doctor. How you can internalize the idea that you're just imagining things, making a big deal out of nothing.

Now that I'm visibly a man, all of my doctors are suddenly very concerned about the fact that I've been simply living like this for nearly four decades with no help. And I know how many women will have to go their whole lives never getting that help simply because of sexism in the medical field.

If you know a doctor, show them this story. Even if they are female. Even if they consider themselves leftists and feminists and allies. Ask them to really, truly, deep down, consider whether they really treat their male and female patients the same. Suggest that the next time they hear a valid complaint from a male patient, imagine they were a woman and consider whether you'd take it seriously. The next time they hear a frivolous-sounding complaint from a female patient, imagine they were a man and consider whether it would sound more credible.

It's hard to unlearn these biases. But it simply has to be done. I've lived both sides of this issue. And every doctor insists they treat their male and female patients the same. But some of the doctors astonished that I didn't get better care in the past are the same doctors who dismissed me before.

I'm glad I'm getting the care I need, even if it is several decades late. And I'm angry that it took so long. And I'm furious that most female-presenting people will never have this chance.

#transgender #queer #transmasc #lgbtqia+ #trans man #sexism #medical sexism #feminism #male privilege

[oscill4te]

damn. i love IFS (therapy module) as a theory and think it can be very invaluable form of therapy for many, but personally i just hate it in practice (for me).

It makes me feel both seen yet unseen at the same time. It is so hard to find a therapist comfortable working with the idea of the mind being split into parts!! And IFS is founded on the idea that all people, whether they have a dissociative disorder or not, have different parts that make them as a whole. But still, i find IFS uncomfortable as someone who heavily dissociates, the "parts" IFS describe feel different from what I experience. I was told a part cannot be both a firefighter and exile, yet that is exactly what I seem to experience with one of my alts. A part who holds integral shame , and holds traumatic memories (like an exile) and also self soothes through self-harmful actions (like a firefighter), does that not fit the definition of both? I asked if parts can have parts and was told no.. even though that is what i seem to experience. It makes me feel really weird for having these experiences that no T really understands.

Idk if this is a general IFS thing or just my T who askes this but: i really hate being asked where i "feel"a part in my body!! i feel so disconnected from my own body, i genuinely don't know what to sayn.

Apologies for the rambles i just have no outlet. I hope i can be brave and ask my T about this stuff. its been boiling in my mind like soup -_-

#i cant tell if my alts are self sabotaging or not bc one alt is pissed off and says therapy is useless #another alt has a healthy dose of skepticism and askes my T questions to see how much she knows about disso disorders. #i might honestly just ask her if we can drop ifs as it just seems to upset parts of me #osdd #ifs #text #i also am scared to tell her i think i could have osdd bc she seems to have skepticism to those who self dx #which i understand. but its not my fault i have these experiences and want to make sense of them. even if im wrong yknow? #i just feel like whatever i have is ruining my life. like #this isnt a life i cant even experience anything and im forgetting everything as time goes by. isolating and hiding and numbing #much of my teenage yrs are blanked out of my memory. hell childhood. hell even whoever i was before age 22.. #it feels gone. how can I process memories that my brain wont let me access yet still affects my nervous system #i guess i just feel stressed and like its hopeless to try but ik thats not true. i gotta keep trying idk

[metalheadsforblacklivesmatter]

Heat Intolerance

This disability pride month I'd like to talk about heat intolerance. Because honestly although it's not the first health issue that presented symptoms in my life. It was the first time I was like "I don't think my body works right".

And honestly given disability pride month is during one of the hottest months in the year. It seems fitting. Especially because there's a lot of disabilities and medications that cause it.

What is heat intolerance?

Simply speaking it's the inability for the body to regulate it's temperatures especially in hot settings to cool itself down.

Why is awareness important?

Because gaslighting people or worse not providing them a place to cool down just because you "feel fine" is extremely fucking dangerous.

What are the medicines that can cause heat intolerance?

Antihistamines (Allergy medications) . Decongestants (Sudafed or any medication that has the D at the end of it). Stimulants (ADHD medications. Steroids. Caffeine.) Beta-blockers (blood pressure medications). Overactive bladder treatment. Psychiatric medications (including but not limited to medications for depression and anxiety). Pain relievers. Antibiotics.

What medical conditions can cause heat intolerance?

EDS (Elhers-Danlos syndrome). Autism. ADHD. Migraines. Brain/spinal-cord injury. Sensory processing disorder. Chronic fatigue syndrome. Endocrin problems. POTS. Menopause. Hypothyroidism. Diabetes. Heart Disease. Multiple sclerosis. Mental health disorders.

What should I do if I suspect I have heat intolerance?

Reduce time outside during hot months. Keep your electrolytes up. Drink plenty of water. Stay out of the sun whenever possible if outside. Be aware of the symptoms of heat exhaustion and heat stroke.

Clothes that are best worn for heat intolerance. Loose lightweight breathable fabrics. Natural fibers. Long sleeves that protect from sunburn as sunburns will increase your risk. Light clothes that reflect light. Wide brimmed hats that shade the face and neck.

Cool. So what are those symptoms I'm supposed you be looking for?

Headaches. Excessive fatigue. Mood changes. Muscle cramping or weakness. Nausea/ vomiting. Rapid heartbeat. Excessive sweating or not sweating at all.

When should I do to the doctor?

If you suspect you have heat intolerance you can go to your PCP to discuss what medications you may be on and what you can do about it. Otherwise, please go to the emergency room if you have symptoms of heat stroke.

This is good information and all but why are you making this post?

To raise awareness. Not just for the people that have it but weren't aware of what it was called. But for all of the idiots that tried to gaslight me when I was in school because I was like "I don't think this is normal. Every time we do our mile run outside I vomit all over the place but other kids aren't doing that."

Also because people always blame me for over heating if I wear long sleeves or pants. I always like to take notes from what people in the middle east wear because they literally live in the excessive heat and spend long hours in the excessive heat. Often in clothing that covers most of their body. They've gotta know what they're doing, right?

I have some type of xenophobic comment about why people from the middle east cover up

Shut the fuck up 😊

-fae

#disability pride #disability pride month #disability awareness #heat intolerance

[bitternanami]

something i think is really interesting about dungeon meshi is the cast's respective views on food as the story progresses. the way many adventurers get through the dungeon is to eat when they Must, but mostly rely on healing magic to keep going when they're tired or beaten down. death is something you can buy your way out of, here.

having these lower stakes when it comes to running yourself too hard has made a lot of people in this setting kind of devalue food and what it does for you.

im not all the way through the manga yet, but so far i really like how it goes about debunking that mindset.

long post under the cut, cw explicit discussion of disordered eating. textual depiction of unhealthy methods of dealing with it. please be cautious!

it seems like to most folks, food is either a decadent luxury, like when the governor offers mr tance a feast as a show of power and wealth, (although he is the only one who actually eats in that scene as he talks about his ambitions);

[id: the governor and mr. tance talk politics and hierarchies, while the governor eats from a bowl. mr. tance's meal is not visible behind a speech bubble.

"so you believe the sorceror is an elf?" he asks.

"i can't say with absolute certainty," mr. tance replies, "but the spells are not ones dwarves and humans typically use." /end id]

like the painted-royal feasts laios tries to partake in that never actually nourish him...

[id: laios, fresh out of the living painting feast, surprisedly holding his grumbling stomach /end id]

or, to the working class, it's pretty much exclusively fuel. i'm thinking about the scene where kabru's party, ostensibly intended to be our view into how adventuring Typically goes for most people, is shown preparing to go to the dungeon by like. walking up to someone and ordering 'a weeks' worth of rations.' purely functional.

[id: kabru enters a store, and the merchant says "welcome!"

kabru says "i need a week's worth of rations for six, and two days' worth of water."

"sure thing." the merchant then reaches behind him and grabs a large cube-shaped package, wrapped in nondescript cloth and tied in place. it thumps onto the counter in front of them both. /end id]

when kabru hands mickbell his food for the trip, he complains about how heavy it is on his back. it's a necessary liability.

we also see chilchuck, in an early chapter where there isn't much food to go around, grumbling about how he used to be better at not noticing when he was hungry. he's frustrated that he's more attuned to his bodily needs, now that he's starting to fill them with regularity.

[id: chilchuck, the only one awake, sits in his bedroll and glares at the timekeeping-candle burning down in front of him while he listens to his stomach growl. moving to find his canteen and fill himself with water instead, he thinks to himself, "my stomach has gotten weaker. i used to be able to go two days without food." /end id]

(like im not even gonna lie this is a big mood. the healing process is really really annoying)

even laios, early on, working out the logistics of going back for falin, considers his expenses and ultimately the thing he decides to save money on is their food supply. like, even the guy most invested in eating as an experience kind of just assumes he will Figure It Out. its what hes eating, not how hes eating it that matters to him at that point.

[id: marcille looks down at the ingredients they've gathered, the walking mushroom and the scorpion in an unappetizing heap on the ground, and asks laios "so how exactly do we eat them?"

he responds "let's just cook them, like normal." /end id]

but its here that senshi introduces the idea of food as art and as healing. its exciting and its fascinating for laios, getting to taste the creatures hes been reading about and fighting, but i dont think it would ever really help him feel full if not for this.

[id: three panels of laios tasting the scorpion hotpot, looking stunned, and then excitedly telling senshi "delicious!"

senshi matches his energy, asking "isn't it? isn't it?" /end id]

pictured: guy who had resigned himself to kind of just doing his best rediscovers the joy in something tasting really fucking good

what they did last time isnt going to work. falin is gone, and constantly anesthetizing their pain and healing through their weakness is no longer a realistic option for the party. in order to make it through they must all relearn how to eat well, one by one and as a group over and over again, because its either that or nothing.

one of my favorite depictions of this idea thus far is when marcille is seriously low on health and mana, and both of these problems are mitigated by taking care of herself, and trying to get iron and protein

[id: marcille, looking sickly, wakes to laios saying, "marcille, marcille, can you sit up? we've got something nice for you."

she watches senshi grill pieces of kelpie liver on a low fire, while laios ties a bib around her neck. /end id]

and drinking a bunch of dead water spirits. she gets the idea, she's supposed to get in nutrients and it'll help her feel better, but in aiming for the quick, inefficient fix, namely chugging that shit down like she heard it was good to Stay Hydrated and decided that would be the thing that fixes her,

[id: marcille throws back a cup of boiled undine-water, her face red. laios asks, "do you really need to drink it that fast?"

she gasps out "...the magical energy stored in nature spirits is actually quite hard to absorb. even if you drink a lot, the majority of it is excreted without being absorbed," and takes another drink. "that's why i need to drink as much as i can."

laios says weakly "you'll get water poisoning," but marcille only stops when senshi puts a hand on her shoulder and says,

"it's easier to absorb nutrients if ye digest them with food. that's a fundamental rule of nutrition."

marcille says, "senshi..." contemplative

and he holds out a bowl of tentuclus and a thumbs up. "let's get cooking!" /end id]

she doesn't immediately realize the answer is that she needs more than that. she's been working hard. she needs care, and she needs nourishment.

once she gets that, though, she makes her boiled water into a stew, and she works to make that stew as good as she can, and everyone can have some.

because in dungeon meshi, to feed yourself or allow yourself to be fed is treated as performing a kindness for yourself. food is what propels you, but there is also an art and a joy inherent to the process of making it; in the way you feel when you've had enough to eat.

[id: senshi watches as chilchuck and marcille eat and excitedly hash out plans.

"i've got a good feeling about this! maybe it'll work out!" chilchuck says

marcille responds, "well it's easier to feel optimistic on a full stomach!"

senshi smiles, proud. /end id]

^^^ i want to put this image on my wall

when you're working through disordered eating habits, you really do have to keep learning this shit. (in my experience, learning about cooking is one of the best ways to do so.)

i'll have to see if my thesis holds up as i continue, but i think one of the reasons the portrayal here resonates with me so hard is that ryoko kui puts most of her characters at eye level with me on this. they're all working at it, too. the text and i are both commiserating, and encouraging each other, 'have some more, you'll feel better.'

#its late -_- idk if this fullly gets across what i mean but ive been thinking about this for weeks #dungeon meshi #recovery #cooking tag #disordered eating cw #im on chp 31 atm but im like. squinting and steepling my fingers looking for this theme as i go now

[snapscube]

Would you be alright to ask how you found out that you had executive function disorder?

Basically my entire life I have been known as a serial procrastinator without any real explanation. When I was a kid I had a lot of trouble taking care of basic things, and I would constantly shirk chores and school assignments and really anything in between, but if you actually asked me why that happened it was never because I didn't want to do them. It even extended beyond obligations. I still remember not quite understanding why I couldn't ever finish drawing a comic, or start a long-term project and see it through to the end. I would start fanfiction and then just leave it within the first few paragraphs. I literally had no reason, and in fact it always sincerely frustrated me that I just couldn't bring myself to do things that should be really easy. I genuinely believed for my entire childhood that I was just kinda lazy and I held on to a lot of guilt for that. Of course, the problem really started to settle in a new way once I realized that I was in my early 20s, living on my own, with every reason to have grown out of it by now, but it still never got any better. I still struggled with doing things that I knew would only take a couple of minutes, I still ached over projects that I had no reason to not just start making but couldn't quite pull myself over the barrier towards actually doing it. And I still had no explanation that wasn't just "I am fundamentally broken and unexceptional". So, once I was living on my own and the problems really started to compound (since, yknow, not getting anything done holds A LOT MORE WEIGHT when you're an independent adult), I decided to look for other people who were going through these things and see how they managed it. I eventually ended up on a YouTube channel called How To ADHD where the host made a plethora of videos that all just instantly clicked with me and seemed to explain so much behavior stretching back all the way to my childhood that I NEVER had an explanation for. Everything she talked about was like, one-to-one my experiences. So then I basically immediately started the process of actually getting an official ADHD diagnosis, which I have now since gotten Twice.