#or neurological

[skeleton-squid-b0y]

thinking about 'bad' rep of disabled people and how important it is. House is so important to me because he reacts correctly to chronic pain. that's what it feels like. that's the impact it has. im not saying it makes him a good person, but that is exactly how my chronic pain makes me want to act. in some ways it's the most realistic rep of chronic pain I've ever seen. he doesn't get better. he doesn't get a partner who cures him and he doesnt get a miracle drug and he doesnt heal from some trauma and then become functional. he gets cruel and desperate and worse. and its the only thing ive found comfort in when dealing with my chronic pain.

[nightmare-from-heaven]

Hey. Your brain needs to de-frag. Literally it needs you to sit there and space out.

If you want your memory or executive function to improve, stare out a window at the skyline or sidewalk or trees or birds on the electrical wires for like 20+ minutes per day. (With no other stimulation like a podcast or TV if you can manage but hey baby steps innit). If you're fortunate enough to have safe outside with any bits of nature, go stare closely at a 1 meter square of grass and trip out on the bugs and shapes of grasses and stuff.

Literally this will make you smarter. Our brains HAVE TO HAVE this zone out time to do important stuff behind the scenes. This does not happen during sleep, it's something else.

That weird pressurized feeling you get sometimes might be your brain on no defrag.

Give your brain a Daily Dose Of De-Frag.

[asexual-amanita]

Unpopular opinion

I don’t want a self driving wheelchair that can go up stairs. I want ramps elevators, and curb cuts.

I don’t want a solution in 20 years, I want it now. I wanna be able to go to the mall with my friends and not have to worry about stairs. I want to go the movies and actually chose where I sit. I want to go to a park without having to parkour my way through cracked pavement and curb drops.

I want accessibility and I want it today.

[ghostzzy]

the worst part about a migraine is that it is BORING

[nightmaretour]

"Brain damage" only sounds like a harsh and offensive way to describe brain injuries because people constantly use it as an insult. It's a totally neutral descriptor of what it is. I have brain damage. My brain is damaged. It's not ableist to call it that, it's ableist to call people you don't like brain damaged because you think it's an inherently bad thing to be.

(Yes abled bodied neurodivergents, that includes you)

[ID: a dark red banner with the words "This post is about physical disabilities, do not derail." in grey font. Either side of it is a lighter grey wheelchair user symbol with the user leaning forward with the arms raised and back, giving the appearance of wheeling fast. End ID.]

[love-me-love-my-weirdness]

Shout out to the ten year old who just got diagnosed. Shout out to the housebound fourteen year old. Shout out to the eighteen year old who can’t go to the university they wanted. Shout out to the twenty two year old who can’t get a job. Shout out to the twenty six year old with a caretaker. Shout out to the thirty year old who can’t buy their own house.

Shout out to young disabled people. We exist.

[pangur-and-grim]

I didn’t share this before, but I took this video on night before Belphie was diagnosed with FIP. he’d stopped walking. if I placed him somewhere, he’d just crumple. finally I managed to get this weird, wobbly walk from him with a meat gogurt.

compare this video to the one I posted earlier today, where he’s flinging himself into the air like a frog! I 100% believe he would’ve died that week without the medication, and now he’s thriving. now he gets to be a happy, chaotic kitten. now he gets to grow up.

[thattripleabattery]

This is a threat

[mindblowingscience]

Researchers have just discovered a process in fruit flies which links inflammation with impaired motor function, providing researchers with a potential target for treating the persistent muscle fatigue that follows many infections. Of long COVID's numerous symptoms, an intolerance to exertion could be considered one of the more debilitating. "This is more than a lack of motivation to move because we don't feel well," says Washington University developmental biologist Aaron Johnson. "These processes reduce energy levels in skeletal muscle, decreasing the capacity to move and function normally."

Continue Reading.

[the-messy-artist]

Has this been done yet

[genderqueerdykes]

on the topic of mobility aids i just want to throw out a non-comprehensive list of tips from someone who's been using mobility aids for 10 years

everyone has different needs and responds differently to certain mobility aids

if a cane isn't right for you, it doesn't mean you shouldn't look into other aids to see if they help

neurological conditions and things like strokes and brain aneurysms can cause someone to struggle with balance for life and are more than welcome to try out mobility aids

it doesn't matter if it's a genetic condition or an injury- consider an aid

wearing braces and using walkers, canes, and so on is very normal after injuries. please use them if you are in pain for a long time after an injury. injuries are serious too

if you buy a cane and it didn't work out for you, you're hurting no one

folding canes are helpful but have a lower weight limit generally speaking

crutches may be a good idea for you if you really struggle with balance and stability

your mileage will vary with each type of aid. you may benefit more from one aid at one time, and more from another in other situations. you may need several different kinds

if you need a rollator, wheelchair or scooter, it really is okay to get or try one. if your insurance won't cover it it's okay to buy or crowdfund one

walkers and rollators require low upper body strength, unless they need to be lifted up on to a curb in which case the user may need assistance

even the lightest and most well constructed wheelchairs are still heavy. they require a lot of upper body strength and mass to propel if you are doing it completely by yourself. you may also need assistance transporting them, getting them up or down hills, on to curbs, and so on

if you struggle to walk for extended periods of time (30+ minutes uninterrupted) you probably need some type of aid. if you have poor balance you may need some type of aid.

you're not hurting anyone if you end up not needing the aids. it's fine to try them

it doesn't matter if the pain or exhaustion or bad balance is related to your weight. you deserve to be as mobile as you want to and can be. its okay for fat people to use mobility aids. it's not embarrassing. being a fat person using a mobility aid in public isn't embarrassing. the people insinuating that are. fat people deserve quality of life

[average-emo-enigma]

Mutual sleepover time!! I’m bringing lemonade 🍋🍋🍋. Everyone yap about all your hyperfixations!!

We can all chat in the comments section eee

@magical-sweet-kitty @i-apologize-in-advance @raythepsychic @rayne3636 @evilrobertsmith @dem0lition-lov3r @failed-verification @geewaysgreendayhoodie @gerardksser @handsonpictureframes @chrissyhoffmannwtf @notyourmarshall @noelgruberfr @new-zee-land @mikey-way-stole-my-kidney

[a-sassy-bench]

do able-bodied people not understand that if disabled people call out of work every time they don't feel good that we would call out of work every fucking day?

like honestly. what do you think being disabled means?

[krispychickenbread]

Ayooo haven't posted in a fat minute.

Here's some droids from star wars enjoying nature like everyone should once in a while. (I spend all my life in a basement)

[stuffieautism]

if you didn’t realize, ableism is actually bigotry and systemic ableism and inaccessibility are really oppression and it’s not something disabled people brought on ourselves by having bodies&minds that you think are inferior and therefore not worth fighting for. disabled people’s lives and wellbeing matter. we don’t have to earn our worthiness by doing “enough” to deserve a good life. nobody does.