#actual physical pain

[panties-on-boys]

the fact that anytime something scary happens, richie always calls out for eddie :(((( and only eddie :( god help me

how he touches eddie’s arm when he gets cut for the blood oath i’m fucking crying

eddie’s fucking blood circling richie’s ring finger like a wedding band. EDDIE’S BLOOD CIRCLING RICHIE’S RING FINGER LIKE A WEDDING BAND!!!!!!!

he’s still in there we can still help him eddie!!! EDDIE!!!

[birdsofash]

.

*googling how to feel negative emotions without amplifying them more than the situation calls for and having your entire body physically hurt and feeling 10x more suicidal*

*also googles how to not obsessively ruminate about every little thing that annoys me when I could usually let them go because of eczema flares and current events are shortening my patience to 0*

[crippledpunks]

i wanna say fuck you to anyone who shame disabled, chronically ill & neurodivergent people, especially homebound folks, for "spending too much time on their phone/on the internet/etc." when it's the only (Somewhat) accessible way for them to experience the world. many people don't get to get out much even if they want to because of their disabilities. shaming someone for trying to connect with the world, make friends and engage with hobbies in ways that are accessible to them is beyond cruel and unnecessary

[minimallycreative]

autism "i need my routine and the routine was already ignored yesterday" vs chronic pain/disability "good fucking luck dude. you got no bones today"

[tinylambnursery]

to the people who struggle with hygiene, kinda smell bad, have rooms filled to the brim with trash and dirty clothes, or can’t properly take care of themselves for whatever reason i love you a lot and i care about you a lot. able bodied and mentally well/stable people have no right to be commenting on our lives, they know nothing. go at your own pace, no matter how slow that pace may be.

[schizoaffectively]

You are well within your right to be angry about the help you didn't get and should have gotten.

You are well within your right to be angry about having your needs neglected.

You are well within your right to be angry.

[pumpkinspicedmochi]

Dear parents

Pretending that your kid isn't disabled and getting mad at them for needing more help and support than your other kids and wanting them to "try harder" and also pretend that THEY aren't disabled by ignoring their OWN needs as well doesn't make them less disabled by the way

[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?

[tam-is-damned]

i think a lot of people don't realize that when you are in extreme and acute pain you don't have the ability sometimes to reason or communicate clearly. It's harder to understand things and be able to rationalize and communicate and articulate yourself well when your pain is impairing that function. Please be patient with people in acute pain, it takes way more mental energy to come up with a coherent thought or phrase when your body is fighting with you.

[cr-pplepunx]

if youre considering using a mobility aid, youre probably thinking about getting a cane. even if it seems like youre issues arent bad enough, you should probably still consider other mobility aids. please look into the pros and cons of several different mobility aids, especially in conjunction with your specific disability/diagnosis/needs.

i got a cane at first because i thought my issues were "mild" and therefore i needed a "mild" mobility aid. but canes are moreso for stability than support. i damaged my wrist and worsened my scoliosis by deciding to use a cane without an educated opinion.

i now use forearm crutches primarily, a rollator for longer outings, and a wheelchair for worse days and longer events. dont make the same mistake as 16-year-old me. dont choose your mobility aid based on palatability, consider your needs and address your internalized ableism if need be.

[stellaltumi]

stop villanizing disabled people. stop assuming we're just being lazy. stop assuming we could be trying harder. stop assuming that we'll "feel better" in a few weeks. stop assuming that we have the same energy levels as everyone else. thanks for coming to my ted talk.

[tumble-tv]

"You're always so chipper and excited even though you're in pain, I could never."

Bethany, if I wasn't chipper and excited about the most mundane things like bees and dice, then I would literally be bedrotting all day every day, sobbing because my entire life is falling apart because I have no answers or relief to pain that doctors think is fake. So I will take joy in my trinkets and rollerskating while my body allows because one day I won't be able to.

[viktorgf]

bro i didn’t even laugh once

guys we are not surviving act three of arcane

[crippleddetective]

everybody supports disabled people until we’re inconveniencing them.

everybody supports people with chronic pain conditions until we have to cancel plans because we’re in immobilising pain.

everybody supports people with brain damage until we need extra support, until we have memory issues and forget basic information, until we have immobilising migraines.

everybody supports disabled people until we are disabled.

[love-me-love-my-weirdness]

I think the reason why people want to know what's "wrong" with disabled people is because they want to reassure themselves.

They want you to say you were in a horrific accident or that you have a well known and treatable disease because they think they can stop it happening to them.

They think their health is a given because they aren't a dangerous driver/ an alcoholic/a drug user/obese/an unhealthy eater etc. Obviously this isn't true but it's easier for them to think of it like that.

Until one day they meet someone who did nothing. They're not really asking "what's wrong with you". They're asking "what went wrong" because they think they can avoid it.

So when they meet someone who made all the right choices, who was healthy, who was safe and one day woke up sick and never got better, it scares them because some part of them realises that it could happen to them.

They can exercise and eat a balanced diet and be as careful as possible and it doesn't do a thing and they can't do a thing about it. That terrifies able bodied people.

People like to look for something or someone to blame and they hate it when there's nothing there.

[mori-is-missing]

shoutout to all my people with invisible disabilities

shoutout to people who don’t feel disabled enough

shoutout to people who have been denied care because they don’t look disabled

shoutout to people who thug it out every single day because the world doesnt stop when you’re disabled no matter how much you wish it would

shoutout to people with no diagnosis but still have symptoms because you don’t need a diagnosis to have symptoms