#adhd pain | Explore Tumblr Posts and Blogs

owlmylove · 7 months

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the flesh is unwilling and honestly, the spirit isn't too keen on the idea either

#disability slogan #we loveeeee chronic pain x ADHD bayBEY #disability #ADHD #chronic pain #owl post #best of

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quackquackquackin · 9 months

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since I have both adhd and anxiety i took both the creatures and combined them into one species.

I call it the “holy shit”

#artists on tumblr #art #artwork #digital art #drawing #anxiety creature #adhd creature #btw creature #yippee creature #idk creature #it’s in pain #send help #foaming at the mouth #it’s so silly #it screams

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kalethemonster · 9 months

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what neurotypical abled people cant seem to get into their heads is aids and medication dont stop people from being neurodivergent and/or disabled. hearing aids dont stop deaf or hard of hearing people from being deaf or hard of hearing, it just makes hearing easier mobility aids such as canes or crutches dont stop people with arthritis, chronic pain, or just general mobility issues from having arthritis, chronic pain, or just general mobility issues, it just makes getting around easier

pain medication doesnt stop people with chronic pain stop being in pain (specifically in the long term), it just makes pain management easier

fidget & stim toys and fidget & stim jewelry dont stop people with anxiety from having anxiety, adhd-ers from having fucked up exectutive function, and autistics not being able to automatically regulate emotions and sensory responses, it just makes dealing with them all easier

various adhd medications doesnt make people not have adhd anymore, it just makes it easier to regulate their executive function.

anxiety medication doesnt get rid of anxiety, it just makes it easier to deal with.

white canes and sight specific service animals dont stop blind people and people with sight impairments from being blind or having sight impairments, it just makes living with them easier.

trauma and emotional support specific service animals dont stop people from having trauma and emotional issues, it just makes dealing with them easier

anti-depressants dont stop people with clinical depression from being depressed, they just make it easier to deal with by stabilizing mood.

immune suppressants dont stop people with any autoimmune condition(s) (such as crohn's, psoriasis or psoratic arthritis, rhumitiod arthritis, myasthenia gravis, fibromyalgia, ect.) being affected in any way affected by their autoimmune condition(s), they just make living with the condition(s) easier.

medication and aids arent magic. they dont make the disabled and/or neurodiverse person not disabled and/or not neurodiverse, they dont entirely cancel out the thing they are used/pescribed for, they just make it easier to exist in a world where whats considered "normal" or "independant" or "a regular human being" doesnt automatically include them.

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enbycrip · 8 months

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ID: a tweet by mythical @mitskileaks

“I used to rebel by destroying myself, but realized that's awfully convenient to the world.for some of us our best revolt is self-preservation,”

#disabled #disability #disableism #chronic illness #chronic pain #chronic fatigue #autistic adult #adult adhd #trans #queer #nonbinary #trans nonbinary

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chronicsymptomsyndrome · 5 months

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Gentle reminder that your disability and/or chronic illness struggles are valid, even if others have it worse. It’s not like there’s one definitive Most Disabled Person In The World and they’re the only one entitled to accommodations or reactive emotions. That’s not how it works <3

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moonlit-typewriter · 3 months

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There’s an underlying bitterness in Percy’s tone in this scene, despite the fact that he’s making a “joke,” that couples with the way he doesn’t look at his mom while he says it but kind of just stares distantly. And also the way his eyebrows go up and down in a quick, wry — and almost judgmental, even — way.

This one singular line hit me so hard as a neurodivergent person because it’s all you need to see the way that Percy feels about his own inability to do “basic” things, like pay attention. He’s making a joke that’s also a dig at himself for “screwing up” in some way and it felt so relatable.

And the fact that it’s basically setting up him the next scene when he tells his mom that he thinks there’s something “broken” in his brain?

It hurt in all the best ways that seeing an accurate representation of yourself in a series that’s been your comfort series since the moment you picked it up 🥲

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ghostonly · 5 months

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Irritates the hell out of me when people respond to a post or comment like, "everyone does this, it's not just [disorder/illness/neurotype], it's called being a person."

Yeah and everyone coughs once in a while but it doesn't mean someone with pneumonia doesn't cough?? It doesn't mean pneumonia doesn't cause coughing??

Everyone gets dizzy once in a while but it doesn't mean vertigo doesn't exist??

Just about every symptom or group-common trait is going to be experienced by people who don't belong to those groups or have that disorder. It's about the frequency and intensity with which that symptom or trait comes up.

#disability #adhd #autism #asd #nd #actually adhd #neurodivergent #actually disabled #disabled #pots #pots syndrome #postural orthostatic tachycardia syndrome #fibro #cfs #chronic pain #chronic illness #chronic fatigue #chronic fatigue syndrome

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audhd-space · 6 months

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Alt Text / Image Description below

To do or not to do?

Pacing and Activity Decision Chart*

A. Will it cause so much pain or fatigue that I can't function for days?

If NO then :

B. Given current symptoms will I be able to complete the task?

(If you answer YES to question B go to D, if NO then go to C)

If YES then :

C. Can I make it manageable by:

Splitting the task into smaller sections?

OR

Using an adaptation or aid to make it easier?

OR

Asking for help with challenging parts of the activity?

(If you answer YES to C go straight to D)

D. Is there enough recovery time between now and when I next need to function?

If you answer YES/PROBABLY to D then LET'S DO

THIS THING!

If you answer NO to both question C and D then:

Best not. It's OK for an emergency, but not for routine tasks.

Disclaimer:

*A simplified version, The full version would fill a book. Process varies between individuals.

**Most activity can aggravate symptoms, so it's not about avoiding pain and fatigue, but trying to keep them manageable. Trial and error is required to find this level and it can change over time.

StickmanCommunications.co.uk (HMSA)

#infographic #decision chart #chronic illness #spoonie #disability #chronic pain #neurodivergent #audhd #autistic #autism #adhd #actually autistic #executive dysfunction

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theadhdravenclaw · 2 years

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help, my brain will not cooperate

i am aware that this is going to seem hilarious but this is serious and merlins beard please help me, my brain refuses to brain properly and I have a massive research project I need to work on Friday and now i just, i like can't , you know?

so please help me.

and yes i have taken all my meds and yes i have had a coffee and yes i did totally hyperfocus on this before and i do totally love this project and enjoy it and just aarrrgh

help me

please

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worms-in-my-brain · 4 months

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Shoutout to people with bad work histories due to disability.

People who can’t stay at one job.

People who can’t get a job or work.

People who can only work part-time or need a lot of sick days.

Our value is not determined by our ability to work.

#actually disabled #disability #disabled #mobility impaired #chronic pain #autism #actually autistic #actually adhd #actually antisocial #actually dissociative

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eggings · 10 months

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happy disability pride month to anyone who has a disability from a condition that “usually isn’t a disability”. happy disability pride month to people with disabilities that aren’t often understood by able-bodied people. happy disability pride month to people who don’t have any official diagnosis yet. happy disability to people whose “labs look completely fine”. wishing you peace this july.

#first sentence is phrased a little weird but i’m mainly referring to adhd #and the amount that it is not taken seriously even when it majorly affects someone’s life #anyways sorry if i phrased anything bad these are all based on personal experiences #actually adhd #actually autistic #adhd #autism #ocd #pots #heds #fibromyalgia #disability pride month #chronic pain #sleep disorders

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ithinkimauggie · 1 month

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Mm, yes... The one you call Benrey...

I've been advised by my employers that, his true nature is on something of a "need-to-know" basis...

And you, Doctor Freeman, do not need to know...

ayo fuck this painting lol have another cropped vers

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enbycrip · 10 months

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One common experience of disability all across the board - relating to everything from learning/intellectual disability to neurodiversity to physical impairment to chronic illness - is the way that “one little thing” can make everything - work performance, school performance, ability to communicate etc - go right off the rails and collapse.

This is an issue I frequently see abled doctors, therapists, psychologists, teachers, social workers etc speaking about in terms of “poor flexibility”, “need to teach resilience” etc etc, focusing on this as an issue *with the disabled person.*

And that illustrates absolutely *perfectly* why a) disabled people are the experts in disability, not abled “specialists”, and b) why the social model of disability *needs* to be taught and centred.

The issue in such circumstances is not some sort of “innate preference for rigidity” (you may laugh, but that’s a phrase I sadly *still* see used about autistic folks far too often) or even “innate widespread lack of capacity” in the disabled person. It is a symptom of a system - in this case, a disabled person’s *life* - that is under immense strain and operating without spare capacity available to be used to respond to unforeseen circumstances.

Disabled people are, almost universally, *master* adapters. Incredibly adept at adaptive thought; incredibly resilient and incredibly dogged. We are that way because we *need to be* to survive in a world that is incredibly ill-adapted for our needs. The reason we are *perceived* as “inflexible”, “rigid”, “fragile”, “incapable” etc etc is because we are, very very frequently, *already* operating at the limits of our capacity just to survive in a world that is incredibly hostile to our needs and to our existence.

The medical model of disability judges all people to exist in the same world under the same circumstances, and thus judges the disabled person to be “lacking” when we struggle. Thus the onus is put on *us* to “correct” this “lack”. “You need to build resilience”.

It is the exact same mindset that blames people living in poverty for their lack of available resources, and suggests “budgeting classes” or “stopping spending money on avocado toast and Netflix” instead of recognising the need to raise wages to liveable levels in low-paid work and provide genuinely affordable housing. Focusing on, and *blaming*, the individual rather than recognising the systemic injustice and the desperate need for systemic change.

“Resilience” as long-term quality more or less means “having the resources to put into dealing with unexpected difficulty while still maintaining other functions.” Whether those resources are time, energy, money, family or community support - if a person does not have access to enough of them, the system - in this case, their life - *will* become overstretched, and they *will* fail on one, or, very often, on multiple points.

That does not represent a personal or moral failure. It represents having access to insufficient resources to meet needs. It is genuinely that simple. And that is what needs to be addressed for disabled people to live and thrive.

#disabled #disability #disableism #ableism #chronic illness #chronic pain #chronic fatigue #autistic adult #adult adhd #learning disability #physically disabled #systemic disableism #intersectional disability

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crippledpunks · 1 day

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my heart goes out to you if you're a disabled person who has a complicated or negative relationship with sleep. if you need to sleep a lot but can't due to life circumstances, or sleeping extra causing other symptoms to flare up. if you can't sleep enough due to pain, or nightmares, or psychosis, or bipolar, or depression. if you sleep way too much and find it hard to stay awake. if you can't fall or stay asleep. if you need medication in order to be able to sleep. if you don't feel rested from sleep. if you wake up a lot in the night. if you have bladder or bowel accidents while asleep. if you twitch or convulse or move too or get injured in your sleep. if you can't control your sleep schedule no matter what. if you can't sleep during "normal" sleeping hours. if you can't sleep for 8+ hours straight but can sleep for shorter amounts of time. if sleep is what you need but for one reason or another you just can't or refuse to do it.

i care about you. your disabilities deserve to be seen and acknowledged

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thedisablednaturalist · 3 months

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Sometimes terms mean certain things and belong to certain groups of people and are not meant to apply to people outside that group. And that is on purpose and valid. You can make your own terms to describe your own experiences, you don't get to take terms from other people, especially people more vulnerable/less privileged than you. If multiple people tell you that the term is not for you, respect that.

When terms get used for many different situations they get diluted and trivialized. Remember "trigger"? It was a specific medical term and is now used to mean "something that pissed or upset someone". Brain fog is now turning into abled people just being a little sleepy or out of it, not literally a clinical term for brains not functioning correctly due to various illnesses. I tell someone I have brain fog and they say lol me too XD no you fucking don't. "Spirit animal" was taken from indigenous peoples so white people could make funny haha relatable t-shirts. Two spirit almost got taken by queer white people as well (although I think most people have backed off on that hopefully).

Not everything needs to apply to as many people as possible. You don't need to and can't relate to everyone. We can still support each other while respecting differences.

(Edited ver)

#wrenfea.exe #this is about people using nonverbal for selective mutism btw #and about mentally ill abled people using cripple #like if ambulatory wheelchair users can come up with our own term then you can too #idk if its not as concise or it takes effort to get it to catch on #you dont get to steal the work other people have done to spread awareness of their term and its meaning #disability #nonverbal #selective mutism #spoonie #chronic disability #chronic pain #chronic illness #cripple #cripple punk #autism #adhd #readying my inbox for a wave of the stupidest people who've never seen any of my posts to flood the gates #i saw someone throwing ambulatory wheelchair users under the bus to justify why they should be able #to use the term nonverbal #pls correct me if you are from the relevant communities #i updated this to make it more accurate bc funnily enough brain fog made me forget about chronic illness triggers

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