#disabilitypridemonth

70 posts · Last used Aug 03

Without looking it up, do you know what the disability tax is? For the purposes of this poll, you decide whether you consider yourself disabled or not. Remember that disabilities aren't just physical and aren't always visible. Please boost! :HeartDisability:#disability #disabled #ChronicIllness #poll #DisabilityPrideMonth

Without looking it up, do you know what the disability tax is? For the purposes of this poll, you decide whether you consider yourself disabled or not. Remember that disabilities aren't just physical and aren't always visible. Please boost! :HeartDisability: #disability #disabled #ChronicIllness

yes, and I'm disabled 41%
no, and I'm disabled 9%
yes, and I'm not disabled 31%
no, and I'm not disabled 19%

772 people · Closed

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Hey all, my friend Sabi is a disabled woman and the sole caretaker of her elderly mom who has dementia. They need $757 due Saturday to stay housed. https://paypal.me/SabiLewSounds https://linktr.ee/sabilewsounds Being houseless could be fatal for them so please boost and support, every amount counts. You can help! #Disability #DisabilityCrowdfund #DisabilityPrideMonth
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The risk of mycobacterial infections associated with inhaled corticosteroid use. "Oral corticosteroids increase the risk of systemic infection." https://publications.ersnet.org/content/erj/50/3/1700037.full Wanted to share this with you as some awareness. It can happen despite rinsing your mouth after each use, so please check regularly if anything changes in your mouth or if you get throat issues. Stay safe! #Disability #DisabilityPrideMonth
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My baby's been complaining about her tummy hurting off and on for a while yet still being hungry and I'm worried she has a food sensitivity. Both me and her father have food allergies, so it wouldn't surprise us, but that means testing. We're starting with gluten cuz she eats so much flour products cuz kids are picky. I can't fucking afford this but my baby needs to eat #FoodSensitivity #FoodAllergies #disability #DisabilityPrideMonth
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Many of us had to figure out our own queer/ neurodivergent identities, and or how to manage our disability(s). I figured its time we had a book bundle in which characters do that, by authors on the same journey(s). So I organised this fantasy & multi-genre bundle. https://itch.io/b/3781/figuring-it-out-queer-neurodivergent-disabled #QueerBooks #Neurodivergent #books #DisabilityPrideMonth #Disabled #DisabilityBooks #fantasy #Bookstodon #FantasyBooks #LGBTQIA
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Hey could anyone help me with some cash to pick up medical pot for breakthrough pain? My neck, hips, and shoulders have been falling out of joint constantly for the last few days and it hurts so much. I’ve already blown through my usual pain management solutions and supplies and could use all the help in the world. $0/50CAD 🙏​:boost_request:​​:boost_ok:​ #disabilitypridemonth Support me directly: https://paypal.me/arianagiroux https://ko-fi.com/eclecticmedia Subscribe to Zine Club for art every month! https://ko-fi.com/eclecticmedia/tiers But my music: https://eclecticmedia.bandcamp.com/music/ #mutualaid #disabilitymutualaid #transmutualaid #mutualaidrequest
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currently thinking a lot about how much less disabled I'd probably be if the general attitude in society to people – INCLUDING CHILDREN!!!! CHILDREN ARE PEOPLE!!!! – struggling or being slow or avoiding tasks would be to accomodate them and be patient, rather than to be annoyed or punish them. My earliest memories are of constantly getting chided for being slow. Sometimes it was good-naturedly, sometimes sternly, sometimes I was actually punished (slow at eating? not getting to eat my fill). At no single point did anyone wonder if I just needed more time than others and if this human variance, this diversity, might be tolerable. No, I had to be made to fit into the box, into the schedule. For no reason. Just 'cause. Was I already disabled or chronically ill as a kindergarten-aged child? Was that why I was slower than others, despite trying? It's possible. I don't know how I'd ever find out. But even without pathologising the way I have always been. I needed accommodations. And not getting them trained me to dissociate, to push myself past my limits on a daily basis as the default way to interact with anyone. It was fucking exhausting and everyone told me it wasn't. So I lost touch with my body's signals, distrusted them, actively faught them. A couple decades later my body is breaking down and no longer able to accommodate my rushing and pushing myself. I could compensate as a child, as a teenager. I stopped being able to in my 20s. I could still be part of society by living off benefits instead of having to work. Now, a few days before my 40s birthday, I can't take proper care of myself and can't even dream of participating in society beyond mastodon (and even then it's spotty). I deteriorated in a way that felt imperceptibly slow until it suddenly wasn't. And in hindsight, there was a steady progression. At no point did anyone (except Dion) consider encouraging me to slow down. To listen to my body and its limits. No. They all just assumed I needed to try harder, or that I'd always be miserable and pityable. It's not true though. I have turned the boat around, slowly. I am recovering now and am getting better. Slowly at first, I hope I will look back in a few decades and see as steady an incline from now on, as I had a decline before. Sure, I can't expect to be as spry as a 20yo when I'm 60, 70, 80. But I can be spry for my age. And I will get there by no longer trying so hard. By doing the actually hard work of allowing myself rest. #disability #DisabilityPrideMonth #ChronicIllness #ableism #AbuseCulture #adultism #AutisticBurnout #burnout
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ICYMI, you can still get my latest album for free for #DisabilityPrideMonth. This album was mostly recorded in the summer of 2025, when not on bed-rest for #longCOVID, #MECFS, #fibromyalgia. It's a response to the rising christian nationalism/dominionism in the US and the world. I was a worship leader for many years. I left that world for how it treated me and other queer, disabled folks. If you grew up in the church and have been burned, this one's for you. ❤️‍🩹
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Über 100 Menschen nahmen heute an einer antiableistischen Demo durch Bonn teil. Begleitet von einer Trommelgruppe zogen wir zu Parolen wie "Mad is not my burden, ableism is" oder "Krüppel, die kämpfen, sind Krüppel, die leben" durch die Innestadt von Bonn. Die Stimmung war toll. Das Demoende kam einem Aufruf gleich: "bis spätestens nächstes Jahr!" #DisabilityPrideMonth
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Hotel Past Due, we're incredibly close, please before they come ask what's going on $132 short https://paypal.me/SabiLewSounds Disabled people suffering #poverty face these kind of comments daily, I'm fortunate to be grounded in my content creation to know it adds to engagement even if it burrows into my trauma and pain but most can't access that fact when facing death by #capitalism#MutualAidRequest #DirectAid #DisabilityPrideMonth
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Martha Lillard, the last US polio patient using an iron lung, dies at 78 This month is Disability Pride Month and July was chosen because it was when the Americans with Disabilities Act was finally signed into law (1990). A number of the activists who helped pass ADA were people who'd been disabled by polio in the days before the vaccine was available (Judy Heumann, Ed Roberts, etc) https://www.youtube.com/watch?v=GodTgZf5zQY #Vaccine #DisabilityPrideMonth

Martha Lillard, the last US polio patient using an iron lung, dies at 78

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Replying to
es ist #DisabilityPrideMonth und die #merz-regierung würgt chronisch kranken eins rein, indem sie ab erstem tag eine AU haben sollen und psychisch kranken soll der eh schon beschissene zugang zu therapieplätzen noch unmöglicher gemacht werden – jackpot, wenn man zu beiden gruppen gehört. das leid kann man sich jetzt schon ausmalen. das ist struktureller #ableismus und der ist tödlich und: er ist gewollt.
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