#Neurology and Brain Disorders
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nightmaretour · 2 months ago
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Constantly reminded that even a lot of disabled people don't trust people with brain damage to think for ourselves and hold opinions, let alone abled people. Constantly reminded that even the most otherwise progressive people often think that it would be better if I had died and will happily tell me that. Constantly reminded that being visible both online and offline as someone with noticeable brain damage is a sure way to get myself dehumanised or worse. Well fuck you I'm doing it anyway
(This is about physical brain damage, including ABIs. No your autism/ADHD/PTSD/depression/etc. is not brain damage. Non-brain damaged people can reblog but don't add anything.)
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incognitopolls · 8 months ago
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We ask your questions so you don’t have to! Submit your questions to have them posted anonymously as polls.
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headpainmigraine · 5 days ago
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If there's anything I'd like people to take away from this Migraine Awareness Month its
that a migraine isnt a severe headache
It's a complex neurological disorder
Its a cascade of neurological activity in an over sensitised brain, the main symptom of which is usually a severe headache.
It is disabling, especially when it's chronic (15 days a month, at least 8 of those with migrainous symptoms, for over 3 months)
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casestudytobe · 6 months ago
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Having a rare disorder or rare complications can be so incredibly lonely. Thinking of people who will never meet another person in person with their disorder or have difficulty even connecting with other people online with their disorder. Thinking of people with disorders or injuries that are common, but their age makes them a huge outlier. I feel alone, but I have to believe i'm not
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mindblowingscience · 11 months ago
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Researchers have discovered patterns in the brain that reflect the effectiveness of deep brain stimulation therapy for obsessive–compulsive disorder (OCD), potentially leading to improvements in the way that the condition is handled individually for each case. A team led by researchers from the Baylor College of Medicine in Texas used brain scans from 12 people with treatment-resistant OCD, who were undergoing deep brain stimulation (DBS) – a treatment that monitors and controls the activity of precise patches of neural tissue via implanted electrodes.
Continue Reading.
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dredgen-dumbass · 4 months ago
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(Disabled) player's guide to making D2 more accessible
because so far (correct me if I'm wrong) I haven't seen one on here, & maybe (hopefully) it'll help someone.
Alright, to get it out of the way, I'm disabled. I have neurological damage from a tbi, and more recently another concussion, and among many many other things it makes gaming a lot more complicated. It can (unfortunately) be difficult to find advice for disabled gamers online that isn't just "get good" or "then gaming isn't for you", so I figure this might be helpful, since it was for me.
I can't speak to other conditions, so this is more about adjustments for specific symptoms, but I can only really speak from experience. That said, I've had to learn quite a bit, so it's sharing time :)
(I play on Xbox. Some settings aren't the same between platforms, just a warning. For that reason, some of this post is going to be xbox-specific.)
This is divided up into menus & subjects of bullet points are bolded to be easier to skim.
Controller settings - (and explanations for some of them in case y'all don't know)
Test out different look sensitivity. The default is 3, I moved mine up to 5. I have issues with spacial awareness and saccades dysfunction, and this has made it easier for me to keep whatever I'm looking at on-screen.
ADS sensitivity- if you don't know, this is the speed when you aim down sights. The default is 1, I have mine reduced to .5, and I've found that the larger difference between the look & ADS sensitivity can really function as having two look settings available when using a weapon that doesn't have a very extreme scope.
The default sprint-turn scale is 0.4, I bump mine up to 0.8 for similar reasons to the look sensitivity increase. (Turning this up makes you turn faster, turning it down makes you turn slower.)
Alternatively, if you have more issues with overstimulation/visual clutter/quick movements/etc, you may want to turn everything down a bit to slow down your camera, but that may make combat harder to keep up with, especially pvp.
Axial & radial deadzone. This helps with stick drift. Stick drift is a pain for everyone but if you have fine motor issues, tremors, arthritis, etc, it's even worse. Finding what works best for your hardware will help make sure you're compensating less, which puts less strain on your hands.
I've seen people recommend turning off controller haptics for the same reason- the vibrations make you grip the controller harder and can cause worse strain. Personally, I leave them on because the sensory input helps balance out the awareness issues, but maybe it's for you! (this one's a system setting, not a d2 one.)
Video settings
Brightness can be important if you have issues with eye strain. I would recommend changing this relative to the lighting in the room, not just your monitor. Turning it up may help with visual issues with the tradeoff of risking overstimulation. Again, all of this is very dependent on the person.
Motion blur- Evil, evil, evil, turn this off. Visual problems or not, it's harder to follow things on-screen with it enabled. Combined with any garden variety problem with eye movements or cognitive strain it's even worse.
Chromatic aberration- I turn this off. It's a nice vfx, but it can wind up just being added visual stimulus and if that's a problem for it's worth losing. It can also make the radar harder to read. Not worth it (personally.)
Film grain- off for the same reason. It's a smaller change, but a clearer view is worth it if it helps you.
Sound settings
If you have problems with your hearing/auditory processing, I highly recommend turning the sfx & music drastically down compared to the dialogue, and then just turning up your system audio.
Personally, I often play with music entirely off, but I know that can be a very boring experience to a lot of people, so take that as you will.
(my current settings: sfx 8, dialogue 10, music 1)
if you're playing with an Xbox party or in a discord call, etc, I really recommend messing with the mixing settings there when you first get on to balance out peoples mics, regardless of processing problems.
Gameplay settings
HUD opacity- I turn mine down to high, the default being full. Just another thing that makes it easier to keep track of stuff.
Radar Background Opacity- Opposite here. If you have problems with spatial awareness you're probably relying pretty hard on the radar instinctively, so the clearer it is, the better. I play with mine on medium, you may want to play around.
Subtitles- Are on by default, so that's nice. Let's check out their settings menu for a moment.
Turning on show speaker name can be really good for hearing/auditory processing issues.
You can also change the color for the speaker name/caption text if the clearer contrast will help you.
The best background style for visibility is box, but it won't look as nice. Another trade.
Background opacity may be easier to lower if you switch to box, since the faded style isn't even. A lower background opacity may help you follow things on-screen at the cost of caption readability
If you don't need captions but do need to reduce visual clutter, try turning them off!
Colorblind mode is, obviously, helpful if you're colorblind, but I have also heard it recommended because the color changes can help improve contrast. Not one I've tried, but worth including.
Full auto firing/Full auto melee- Does what it says. Turning this on might help in the same way as turning off haptics/messing with deadzones, ie by changing how much you need to click. You can still fire normally with it on, so if anything it just gives you another option.
Reticle location is slightly below the center on d2. I prefer to center it, though it takes some getting used to. More helpful if you frequently switch between other games that center theirs.
Neutral/targeted reticle color- The defaults are white and red respectively. I prefer black for targeted because I feel like it makes it easier to see what I'm actually aiming at, but you may want to leave it for contrast. To each their own.
Other
Brief overview of Xbox accessibility settings
Xbox has a narration setting. I would assume anyone who needs it is aware of this, but just in case.
If you need more assisted play, there's controller assist where you can combine two people's input
Turning off haptic vibration (as mentioned) is in accessibility -> controller
You can make the on-screen keyboard larger!
There are party chat settings for both text to speech and speech to text
There's also game transcription!
Games that have the function can also do their own read-aloud. I don't know if/how this applies to destiny
Mono output for audio may make things easier to understand depending on your audio setup
There's also high-contrast mode for both dark or light
Colorblind filters are here, too
Night mode! You can change how much it dims/filters your device. If you have problems with blue light or eye strain, or have to limit screens for medical reasons like me, this setting is a lifesaver. The filter will affect how your games look, but personally it's worth the tint. Same is available on most PCs.
Hardware, etc.
The Xbox Adaptive Controller is highly customizable and great for anyone with physical impairments that make the standard Xbox controller difficult to use. Find it here.
I've seen thumbstick extenders recommended for arthritis, might also be helpful for similar conditions
If you have arthritis/fine motor issues/muscle weakness/tremors/etc/etc/etc controller grips might make holding a standard controller easier
If any of those are the case for you, then you might also benefit from a lightweight controller (or playing with a standard controller plugged in & removing the batteries for a lesser weight adjustment)
evilcontrollers also has one-handed controllers and a one-handed controller customizer much like the standard controller customizers
evilcontrollers for hardware accessibility in general
If you play on PC and have muscle or joint issues then you may want to look into different keyboard/mouse shapes. Lightweight, vertical, and ball mice are all options, though there's apparently some argument about using them for gaming. I've also seen good reviews of the Azeron keypad from people with muscular/joint problems. There's also split keyboards, wave keyboards, one-handed, etc etc etc.
If you have problems with auditory processing I would HIGHLY recommend gaming with noise-cancelling headphones. (Hell, do everything with noise cancelling headphones.) I would recommend these for everyday, but they also work pretty well for gaming. The mic is mid, but it works well enough, and there's multiple sound modes + active noise cancelling.
Other other (oh no I forgot these, editing now)
Compression gloves !!!!!
Pause and do hand exercises after a while
20/20/20 rule for eye strain
may come back and expand this as I think of more things
There is a lot that Bungie could do to improve the game's accessibility without causing an imbalance with abled players, but I'll save that for another post. Feel free to reblog this with any other advice/anecdotal stuff/whatever, I'm considering this as opening a discussion.
I don't know of any clans specifically for disabled players but I'm sure they exist? If anyone has recommendations for community stuff, please do throw that in.
As always, my dms are open. Being a disabled gamer can suck sometimes and if you need a space to vent w/ someone who gets it, I'm your guy. If you're just curious how it impacts gaming, I don't mind being asked, I just don't feel like posting about myself that much unprompted.
I think that's all for now. Happy gaming :)
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zebulontheplanet · 2 years ago
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See posts from people saying things like "If i can do this, so can you!''
What if we can't? What if we can't learn a new sport, what if we can't be valedictorian of our school? what if we can't learn a new language? what if we can't excel in some areas? What if we can't?
Your posts about "Oh i did this so you can definitely too" are plain weird because i bet someone read that and CAN'T do the things you're saying they can. Stop it. Just stop with your takes. Maybe look at a bigger picture.
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fehck · 4 months ago
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lavellaned · 1 year ago
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Never not thinking about how the veil must be such a sensory overload for Solas.
Like he made the thing, it’s not naturally occurring, it’s just a big ol magic spell on a near cosmic level.
It’s a running canon joke that he’s constantly measuring and making comments on the veil, but it’s bc he’s never not aware of it. That’s sounds absolutely exhausting no wonder he’s either grumpy or disassociating 90% of the time.
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fenrichaita · 10 months ago
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Can we talk about how psychiatry has a pattern of using treatments for mental illnesses and disorders that cause brain damage and then labeling the direct effects of that damage as "healing"
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nightmaretour · 1 month ago
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So I got bored and made a server for people with brain damage. Idk how this is going to go with how Tumblr behaves towards brain damage and anything we try to have for ourselves, but it's worth a shot right? It's about time we had some form of unified community.
This server is specifically for people with physical brain damage.
Brain injuries of any kind and cause are welcome! TBIs and ABIs (neurodegenerative diseases if you want to classify yours that way, infection, stroke, drug overdose, birth complications, all are welcome!) of any severity belong here equally. This is intended to be a safe and welcoming space to connect with each other, share experiences and advice, and feel a little less alone with our disability.
No, depression, PTSD, ADHD, etc. are not brain damage. Not everything that affects your brain is brain damage. There are plenty of specific and nonspecific spaces for all manner of neurodivergencies, we deserve a space of our own. If you don't have physical brain damage, this particular space isn't for you and that's okay. I will not tolerate arguments about this, neither on Tumblr nor on the server.
🏳️‍⚧️This server is trans inclusive, terfs and other transphobes are not welcome.
🇵🇸This server is anti-genocide and supports a Palestine free from war and violent occupation.
EDIT 8/6/2025: Updated with a new invite link!
EDIT 22/6/2025: Updated the invite link again, this one shouldn't expire (hopefully)
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deplcythebattery · 4 months ago
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everyone: oh you're so lucky you get to stay home all the time!
me, chronically ill: ah. yeah. haha. lucky. i get to stay home. i don't get the fun parts of that though! i can't partake in my hobbies for more than an hour every two to three days :) i do get to watch a lot of tv though! oh you think that gets boring after a few hours? haha. yeah it fucking does. imagine that being the only thing you can do and then tell me how lucky i am
#cfs/me#fibromyalgia#chronic illness#functional neurological disorder#chronic pain#wrote 1k words in two sessions (15 min each) and then dared to take a full hour to start painting the back patch of my battle vest yterday#body didn't like that! it's also raining today so not only is the arm i painted with excruciatingly painful but so is the rest of my body!#staying home is so so so so so so fun haha isn't it when you literally can't do anything to alleviate the boredom!#i can't do shit i love all day every day. stay home for a week doing nothing and then tell me how lucky i am.#having a really rough day. yesterday was good so apparently i can't have more than one good day a week.#i also have to keep taking language classes if my residency gets sorted to receive aid even though we're moving#so what little i have to put towards things i enjoy i now have to divide towards class work too.#i've cried three times today i'm just so fucking tired and sad and it's so unfair i can't even do the stuff that brings me joy#brain so fried today i couldn't listen to music with my new headphones i've lived in for almost week. i'm that fucking spent today.#isn't that fun isn't it so fun to deal with this rather than going to work#god#i'd give fucking anything to not be like this i just want to not have to figure out what to spend my energy on#and i don't want to have to sacrifice the time i could put towards things that bring me joy#this is not living. for three years it's been oh i can do this when i get better or i could do that when i get better#doesn't seem like i'm getting better any time soon and in the meantime i can't even do things that make me happy.
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halloweeneva · 10 months ago
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I remove my mask (ADHD) only to reveal a second smaller mask underneath (Chronic Fatigue)
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chronicsymptomsyndrome · 1 year ago
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Me: Your place is so much nicer than mine I’m so dysfunctional lmao
Friend: no my house is such a mess I have adhd too dude
Me: Sure but your place is still way better than mine
Friend: stfu everyone always says that
Friend entering my home: oh dang. fair enough. how are you living like this
Me: lol dissociation
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helltiervriska · 2 months ago
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this is meant to be said in the most loving way possible. but it absolutely amazes me how few people with DID/OSDD are aware that 1) you cannot control the creation and subsequent formation of an identity that an alter takes because a coping mechanism is a coping mechanism is a coping mechanism. and 2) you have to be nice, kind, and accepting to persecutor alters that consistently lash out because, shockingly, being cruel to alters that have already experienced intense cruelty will not make them submit, itll make them lash out more. the cycle of abuse literally continues in headspace, its not secluded only to the real people around you. "let yourself cope" and "be nice to yourself" shouldnt be like revolutionary thoughts but you would be shocked the amount of friends ive had that are completely blind to it (again. loving way. for the most part lmao)
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bigticenergy1 · 25 days ago
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PANDAS/BGE awareness photo set? Don’t mind if I do 👌🏻
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I spread awareness of this condition because I lived with it for over a decade before I was properly diagnosed. The delay in diagnosis has made my case more difficult to manage and treat as my immune system had been damaging my brain for so long. More awareness will hopefully lead to early diagnosis or more successful treatments.
(I realize that I put Catatonia twice lol)
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