#Disabled community
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"Mental health issues are also physical health issues because the brain and the body are connected" and "being neurodivergent and being physically disabled are not all the same and do not share exactly the same experiences" can and should coexist, actually.
#actually autistic#cripple punk#mad punk#neuro punk#disabled community#physically disabled#neurodivergent
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Happy Disability Pride Month! 🩶💚❤️🤍💛💙🩶🌈 (x)
#disability pride month#disability pride#disability#disability rights#disabled community#disabled women#wlw#wlw history#sapphic#sapphic history#sapphics#lesbian#lesbian history#black history#lgbt#lgbt history#lgbtq#lgbtqia#lgbtqia+#history#herstory#photography#vintage photography#b&w#b&w photography#bw#bwphotography#debra st. john#1990s#source: pinterest
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#yemen#jerusalem#tel aviv#current events#palestine#free palestine#gaza#free gaza#news on gaza#palestine news#news update#war news#war on gaza#disability rights#disabled community#disability justice#genocide#gaza genocide
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IM GOING TO CRY THEY MIGHT INCREASE THE SSI ASSETS LIMIT TO $10,000.
it's a bipartisan bill too! and for anyone unaware, people on SSI (which is different from SSDI), can only have $2,000 in assets (unless they have an ABLE account, which comes with its own rules). this assets limit has been in place for FORTY YEARS and is a giant part of why being on SSI keeps people incredibly impoverished.
i've also heard they might remove the marriage penalty but i don't have the spoons to read or explain it so someone else please add on!
this is huge! please spread the word and do what you can to help ensure this happens!
#softspoonie#disabled#disability#disability rights#disability advocacy#disability activism#disabled rights#disabled community#marriage equality#equality#usa#us politics#us congress#usa politics
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friendly reminder you dont need a diagnosis to be in disability spaces, as an example im in constant pain and fatigue, have migraines every week and my joints hurts to a point I can't write, but since familiar gaslighting/medical trauma and the fact that im an indigenous, brown skin fat man a diagnosis is fucking hard (but im in my way! :)) , but i still deserve a safe space to talk about my experiences and to feel valuable and supported.
never feel like youre interrupting someone's space or that you shouldn't be here cause you dont have a diagnosis, disabilities existed before diagnosis
#fatphobia#disabled pride#disabled community#actually disabled#pro self dx#pro self diagnosis#chronically ill#chronic migraine#chronic illness#chronic pain#chronic fatigue
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QUICK PSA FOR THE DISABLED COMMUNITY
If you take any daily medication, do not eat grapefruit or activated charcoal unless you know for a fact they won’t affect your medication.
Both Grapefruit and Activated Charcoal will cancel out medication.
‘Where would you ever eat activated charcoal?’ You may be asking
Well
Halloween eve is here y’all and if you want a black cocktail or cupcake, it was probably made black with activated charcoal! So please double check before consuming!!
#actually audhd#actually autistic#audhd#autism#actually neurodivergent#autistic adult#adhd#autistic things#actually adhd#disabled#disability#actually disabled#disability community#disabled community#spoons#spoonie#chronically ill#chronic illness#chronic pain#chronic fatigue#psa#meds
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in honor of disabled pride month, i want to give a shout-out to all disabled fat people who had to roll their eyes who have been told "you're not disabled, just fat" or "thats because you dont eat well/exercise"
#anti fatphobia#fat#fat acceptance#fat liberation#fatphobia#disabled#disability justice#disabled community
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I know its kind of silly to say “don’t feel bad for canceling because of pain, fatigue, etc” because I know guilt is a reflex you can’t easily refrain from. But you can reason with yourself so instead I’ll say this:
Nobody can feel what you’re feeling but you. Nobody knows the severity of what you would be putting yourself through if you were to “tough it out.”
If you do “tough it out,” the purpose for you doing the thing will most likely not be fulfilled anyway. You probably will not be mentally present or engaged. You probably will not have a good time or get much out of it. Etc.
If people really have such a problem with it, thats a huge red flag. Being transparent about your needs and boundaries is a great way to weed people like that out of your life.
If you have any kind of chronic illness or disability, remember that you probably have a very warped judgement of what is “reasonable” to endure in terms of pain, fatigue, burnout, etc.
You didn’t ask for this, you don’t deserve this, there is no reason you should have to bear the weight of it alone. I bet if someone else was in your position, you wouldn’t mind helping accommodate for them?
Low energy days are truly sacred, take them seriously. Please respect your body’s signals. “If you do not choose times to rest, your body will choose for you” or however the saying goes
It is so much pressure to have to deliberate what sacrifices are necessary for proper self care. Give yourself extra credit for having to deal with that stress on top of whatever is putting you in that position in the first place. Thats a lot at once
You are leading by example and showing others that you would never expect them to hurt or overextend themselves for your benefit. Putting yourself first always inspires other to do the same.
Please be proud of yourself for even considering canceling and putting your needs first. That is so strong of you <3
#rants & reflections#chronic pain rant#chronic pain#disability advocacy#disability community#disabled community#disability rights#chronic illness vent#undiagnosed chronic illness#chronic illness community#chronic illness rant#chronic illness#chronic pain problems#undiagnosed chronic pain#fibromyalgia#dysautonomia#spoonies#physical disability#chronic fatigue#ehlers danlos syndrome#pots#postural orthostatic tachycardia syndrome#craniocervical instability#migraine#cluster headaches#tmd#heds#neck pain#back pain#chronic headaches
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New favourite thing to do is to remind people of how much they hated lockdown when they say they wish they could stay home as much as I do.
Like no you dont you were miserable when you were forced to stay home all day everyday for the good of your health. Thats my entire existence as a disabled person so pack it in.
#disabled#chronically ill#chronic fatigue#chronic pain#disability#actually disabled#chronic disability#disabled community#spoonie problems#disablity
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Disabled people deserve to fall in love. Disabled people should be able to marry without repercussions, without losing anything. It's almost 2023 and why is this still a hot take.
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Be nice and don't mock tumblr users that communicate differently.
Examples:
1.) Typing quirks
2.) No punctuation
3.) Random Capitalisation
4.) Long run on sentences
5.) Frequently misspelled words
6.) Missing spaces between words
7.) Repeating words and sentences
8.) Posts audios and videos instead of typing
9.) Express themselves through custom emojis
10.) Use an AAC (Augmentative and alternative communication) device
Some users have intellectual disabilities, use speech to text, struggle with grammar, have hand tremmers, have high support needs, etc.
Regardless of how they communicate and their reason why, they still deserve respect. They are trying their best.
#intellectual disability#disability#communication styles#disabled community#communication#aac user#aac device#autism awareness#disability awareness#typing quirk#disability advocacy#poor grammar#grammar nerd#actually neurodivergent#actually neurodiverse#its the neurodivergency#neurodivergent#neurodiversity#autistic#autism#disability community#neurodivergent community#judgment free zone#no judgement#adhd#adhd brain
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#spoonie#chronic illness#chronically ill#chronic disease#invisible disability#disabled#disabled people#disability#mentally disabled#actually disabled#disabled artist#disabled girl#disabilties#disabled pride#disabled representation#disabled community#disabled life#disabled rights#disabledcreator#physical disability#physically disabled#disabledandcute#psychology
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once again thinking about how fucked up it is that special ed used me and other disabled children as unpaid, coerced labor. i worked enough to be making $100 a week. i was "paid" in fake money redeemable only at the school cafeteria, which i worked at, and was forced to do things that distressed me. they gave us $1 a week, if they remembered to give it to us at all.
this was while i would sometimes go the entire day without eating because i didn't have the money to buy food and the free food was not sensory safe. we also worked outside the community - grocery stores, warehouses, shoe stores security tagging items. all under the guise of job skill development, we did $100 of labor a week without ever getting paid. and we were demeaned while we did it. and we were just teens.
so no, i don't want to hear about how special education is good. not with the way me and my peers were treated and taken advantage of. death to institutionalization, in all forms.
#softspoonie#disabled#special education#special ed#disability#disability rights#disabled community#neurodivergent#special needs#autistic#autistic spectrum#autism spectrum disorder#autism spectrum#autism#neurodivergency#ableism#sanism#systemic ableism#unpaid labor#labor rights#workers rights#anticapitalism#anticapitalist#working class#leftist#leftism
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Becaise I'm tired of seeing this happen to other bloggers & also frequently myself:
If someone talks about being unable to do something without assistance due to a disability, and how that influences their life, how that dependency on others is scary and can be exploited etc. And your only response is "I experience this except I end up doing the thing by myself because no one helps me". and then they tell you "hey, you deserve to get support for this when you need it. but this is actually not the same as my experience because if i do not get help i absolutely can not get it done by myself. Like I'm fully unable to do this." And your response is to get mad / accuse them of trying to be "divisive" / telling them they're dismissing your struggles / blaming them for your feelings about this response essentially / calling them ableist for literally just pointing out the fact that there is a difference between these situations / etc, then you are the problem.
Just for a minute try to imagine what it's like. That you can not do something without assistance. Let's say you absolutely can not drive a car even if your life depended on it. You completely rely on being driven around. You can not do anything that requites a car without another person being physically there the entire time and holding the steering wheel. And tons of people see you talk about that and join in with "yeah I also can't drive in theory, but I still do it because I have to because my life depends on it". That does not feel good. That is a constant reminder that hey! Other people can totally do this even though its hard! If your support vanishes you can not do this thing your life depends on no matter how hard you try! The voices of people who actually experience the same thing as you get drowned out in the flood of these "I totally get it"s from people who do in fact, not totally get it. Because In reality, one of you is sitting behind a wheel and the other isnt and Never Will.
Acknowledging differences is not the enemy. We are not arguing about emotions here. We are literally begging people to see that two physical realities are different. And no matter how often we say that you still deserve support and that we acknowledge that things are hard and exhausting for you and sometimes even dangerous, that isnt enough for you? Every time I try to get one of these people to see reason I tell them: I know this is hard for you. I know this is exhausting for you. I acknowledge your reality. But that's not what they want to hear. So, what more do you want? For me to lay down and say "yeah actually we experience totally the same things" and then watch as the healthcare system out to save every penny tries to dismantle my support system because well, if I try really hard I'll probably get it done myself?
#actually autistic#autistic adult#autistic community#medium support needs#actually disabled#disabled community#inspired by recent events but this feeling had been building up for months at this point
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I found a guide for a no tape, easy to unwrap wrapping tutorial to make Christmas a little more accessible, wish I just found it sooner
#christmas#disabled#disability#disabilties#accessibility#gift wrapping ideas#physically disabled#spoonie#chronically ill#chronic illness#disabled community#disability awareness
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