Dr. Wonder Cripple ♿️🏳️🌈 @wonder_cripple
CP, GAD, OCD | I ❤️ disability 🧵| Telehealth Therapist - BOOK W/ ME @ LINK! | She/her | Profile photo by @_ChaosSoda_ calendly.com/drkuznetsova/s… NY Joined August 2019-
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Sending love to all my friends with chronic pain ❤️ That stuff HURTS
Sending love to all my friends with chronic pain ❤️ That stuff HURTS
Life with chronic pain is like "my body is on fire but I guess I'll function anyway"
Can we please not shame chronically ill and disabled people for canceling plans at the last minute? Trust me, we would love to “just do the thing”. Sometimes, we think we can do the thing until it’s time to do the thing, and then we realize that we can’t actually do the thing.
YES. At least to the first part. I won’t say the thing b/c every time I do, someone always ends up missing the point — which is the exact problem. But the thing is quite necessary so I appreciate people who do it for me. Anyway. People need to learn to listen #DisabilityTwitter
I wish abled people understood that it will always be more annoying for us to explain why we can’t do a thing than it will be for them to do the thing for us or without us.
I don’t get how other disabled people who act like it’s easy to get to the doctor and then get mad at me when I can’t go for my INFREQUENT epilepsy. I’ve also been accused of not being a real disabled person because I’m not at the doctor’s office often #DisabilityTwitter
Can we all agree that disabled people deserve better
Don’t I know it. This attitude is why people don’t really take me seriously when I express longterm concerns about myself. I look fine. But because my rare disease hasn’t given me a mobility aid *for* getting myself around, all I get is to feel frustrated #DisabilityTwitter
This is your semi regular reminder that disability doesn’t always look like someone sitting in a wheelchair. That’s an ableist and harmful angle to take.
One of the hardest things about being disabled is living in a world where everyone thinks you're useless if you're not breaking your back trying to prove that you deserve to exist. I'm tired, y'all. #NEISVoid
My SSI was cut in half without warning yesterday, probably because I work. I make $75 a week, before tax. I'm a psychologist and building a caseload has been incredibly difficult. Tell me how making PENNIES a week means I need LESS support?? We’re set up to die. #Disability
Reminder that the disabled experience is not always a pleasant one. Some days you'll wake up and wish it wasn't yours. And that's OK. I'm with you.
I eat. I poop.
Ended a long friendship over lack of local accessibility. She also thought I was annoying/spoiled for not knowing who to call, etc. But then after being cut off for 8 mo. from what I needed, she said that I needed to think of the abled people. Not how it works #DisabilityTwitter
It's just pain.
Abled people don’t have the right to tell disabled people what we need. Just FYI.
My immune system decided screw it, less mobility and viral defence, more osteo tissue and useless matrix.
The Tweedy Mutant @the_tweedy
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1 Followers 337 FollowingThe Modify Movement �.. @modifymovement
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318 Followers 324 Following Woman (She/Her) who lives life with Cerebral Palsy. Subscribe to m Youtube for lifestyle & disability living content https://t.co/CyjtlwRgPc Tik Tok Blemi86Sending love to all my friends with chronic pain ❤️ That stuff HURTS
Life with chronic pain is like "my body is on fire but I guess I'll function anyway"
YES. At least to the first part. I won’t say the thing b/c every time I do, someone always ends up missing the point — which is the exact problem. But the thing is quite necessary so I appreciate people who do it for me. Anyway. People need to learn to listen #DisabilityTwitter
I wish abled people understood that it will always be more annoying for us to explain why we can’t do a thing than it will be for them to do the thing for us or without us.
I don’t get how other disabled people who act like it’s easy to get to the doctor and then get mad at me when I can’t go for my INFREQUENT epilepsy. I’ve also been accused of not being a real disabled person because I’m not at the doctor’s office often #DisabilityTwitter
Can we all agree that disabled people deserve better
@wonder_cripple It’s also worth to keep in mind that disability can happen to anyone at any time.
@wonder_cripple Allo Doc. Haven't seen you about for a while. Hope you're good.
@wonder_cripple Preach! Also, love your handle. :)
Don’t I know it. This attitude is why people don’t really take me seriously when I express longterm concerns about myself. I look fine. But because my rare disease hasn’t given me a mobility aid *for* getting myself around, all I get is to feel frustrated #DisabilityTwitter
This is your semi regular reminder that disability doesn’t always look like someone sitting in a wheelchair. That’s an ableist and harmful angle to take.
@wonder_cripple That goes both ways from so many people here.
I eat. I poop.
Doing this again because it's been years. Describe your disability badly. I'll start: My brain keeps telling my muscles to "talk to the hand". #DisabilityTwitter #Disability
@wonder_cripple My body keeps telling itself that I've got something attacking and it must fight back. It's looking in a mirror.
Ended a long friendship over lack of local accessibility. She also thought I was annoying/spoiled for not knowing who to call, etc. But then after being cut off for 8 mo. from what I needed, she said that I needed to think of the abled people. Not how it works #DisabilityTwitter
Abled people don’t have the right to tell disabled people what we need. Just FYI.
It's just pain.
Doing this again because it's been years. Describe your disability badly. I'll start: My brain keeps telling my muscles to "talk to the hand". #DisabilityTwitter #Disability
My immune system decided screw it, less mobility and viral defence, more osteo tissue and useless matrix.
Doing this again because it's been years. Describe your disability badly. I'll start: My brain keeps telling my muscles to "talk to the hand". #DisabilityTwitter #Disability
Sometimes my brain says to my ears, “You’re not going to be able to hear hardly at all for 2-3 hours. Just turn up your headphones until you actually *might* damage your hearing! Toodles!” This has been happening with frequency again lately. I hate it. #DisabilityTwitter
Doing this again because it's been years. Describe your disability badly. I'll start: My brain keeps telling my muscles to "talk to the hand". #DisabilityTwitter #Disability
My nervous system stoped developing when I was 3.
Doing this again because it's been years. Describe your disability badly. I'll start: My brain keeps telling my muscles to "talk to the hand". #DisabilityTwitter #Disability
The muscles of my feet look like a Big Mac bun and keep me from standing or walking for more than five minutes
Doing this again because it's been years. Describe your disability badly. I'll start: My brain keeps telling my muscles to "talk to the hand". #DisabilityTwitter #Disability
My vertebra thought it would be fun to fuse themselves together and then deteriorate, and my spinal cord attached itself to something it wasn't supposed to and now my nerves can't get their shit together.
Doing this again because it's been years. Describe your disability badly. I'll start: My brain keeps telling my muscles to "talk to the hand". #DisabilityTwitter #Disability
A small part of my brain didn’t receive blood for a brief amount of time. That part decided to be super dramatic about it and die. Now I have a natural pimp walk
Doing this again because it's been years. Describe your disability badly. I'll start: My brain keeps telling my muscles to "talk to the hand". #DisabilityTwitter #Disability
My brain and nerves never learned how to function together.
Doing this again because it's been years. Describe your disability badly. I'll start: My brain keeps telling my muscles to "talk to the hand". #DisabilityTwitter #Disability