#neurologi

[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

[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?

[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.

[chaoticbooklesbian]

Human: *crying, in pain, experiencing minor neurological symptoms* This is delicious, what's in it? Alien: ...our strongest, deadliest poison. Human: How much for a bottle to send home? My mom would absolutely love it. Alien: If you let a team of our finest scientists deliver it and study her reaction, it's free. Human: Sweet, I'm sure she'd be up for that, let me give her a call--

[aitadjcrazytimes]

[positivelyqueer]

give love to people with traumatic brain injury, acquired brain injury, stroke, neurological condition, worsening mental health, trauma, PTSD and all other brain based conditions that make you feel conflicted about your identity. About whether or not you’re the ‘same person’ you were before your injury or illness. People constant evolve and change but can be more difficult when changes more sudden, pronounced, and noticed by others. I hope you are doing well and are able to find some peace, support and love.

[nightmaretour]

Anyway, people with brain damage I love you. People who have had strokes I love you, especially if you're told you were "too young" to have one. People who acquired your brain damage by less common means such as infection, lack of oxygen at birth or degenerative disease, I love you. People with moderate and severe brain damage, I love you. People who lost their sight or hearing or ability to speak because of their brain damage, I love you. People who have paralysis from their brain damage, I love you. People with amnesia and severe cognitive issues from their brain damage, I love you. People with rare and unusual symptoms from their brain damage, I love you.

You are not a punchline, you haven't lost your humanity, your thoughts and opinions are as valuable as anyone else's. We deserve respect.

[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]

Sometimes I don’t think people get that chronic means chronic. It means forever. I’m going to be stuck with this for the rest of my life and I’ve had to learn to make peace with that myself. Telling me ‘hope you get better soon’ and ‘it won’t always be like this’ is pointless because you’ve completely ignored the definition of chronic illness.

[forystr]

NEW/NORMAL : a comic about becoming disabled in your twenties

My name is Fraizer, and I'm the artist behind forystr. I have Functional Neurological Disorder.

[neuroandhemo]

this is my oc neuro, its a neuron and i wanted to make it look like a diagram ^_^

its meant to be a cat looking thing

woah htis is geting attentoin thank yall1!! follow if u wanna see more o f this gober.. an its friends..!