disability wrath month

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[doesnotcontain]

so you know this?

it's on stuff now

redbubble | ko-fi

[weird-and-unwell]

Happy disabled pride month to the undiagnosed. To those with no idea what it could be. To those who are pretty sure they know, but can't be certain yet. To those whose doctors are trying their best, and to those whose doctors aren't. To those with test results, and those without. To those whose prognosis isn't looking good. To those scared by the course of their symptoms, and with no idea what's going to happen next. Living undiagnosed is hard, and I wish you all luck.

[balaclava-trismegistus]

Just saw my doctor type "FUCKED FOR LIFE" on my chart then he turned the screen away and stopped making eye contact with me

[louisegluckpdf]

they won't tell you this in therapy but sometimes the best way to stop catastrophizing/anxiety is to interrupt your spiraling with "girl what the hell are you talking about"

[ytpreviews]

It's not a cure but you have no idea how many times this image has helped me with my OCD

[sometiktoksarevalid]

[batbetbitbotbut]

Video summary: Tiktok by @pippabarnes - clips of a person with alopecia applying colourful makeup and other decorations to a bald spot as part of very dramatic looks, narrating now her relationship to her bald spots has developed over time

[flowercrowncrip]

This disability pride month I would like the community to understand that Sometimes wheelchairs aren’t freedom.

Sometimes using a wheelchair means you can no longer get to the places that used to be important to you, and not because of man-made inaccessibility. I have sat with someone as they cried because they could no longer visit the place they had scattered a loved one’s ashes because not even the most expensive wheelchair in the world could handle the terrain. As much as I wanted to, my wheelchair meant that I couldn’t position myself in a way that would allow me to give them a proper hug. In that moment, our wheelchairs felt more like heavy weights than freedom.

And sometimes wheelchairs are like the legs of someone who can walk but would maybe benefit from a wheelchair themselves. Sometimes wheelchairs are exhausting and painful and you’re counting down the time before you’re able to be lifted into bed. Sure, like painful legs, you can do more with them than without, but constantly performing gratitude for something that hurts you is exhausting. And again, not because you need a better wheelchair, but because those are the limits of your body and the technology that exists.

Yes it’s important to challenge the idea that wheelchairs are always a tragedy. And yes, there are lots of people who have a positive relationship with their chair. But for a lot of people, including me, the pressure to love your wheelchair and see it as freedom is painful and feels like it erases huge amounts of my experiences with disability.

[airandangels]

These little-known bank accounts allow Americans with disabilities to save and invest

If you're an American with a disability who receives government assistance, you likely qualify for an ABLE account, or you may starting next

The age of eligibility for an ABLE account, allowing USAmerican disabled people to save up money without losing their government assistance for having “too much,” is going to go up to cover disabilities diagnosed by age 46 (currently it’s age 26), meaning a much larger number of people will be able to access them. As the article notes, many Americans don’t know these accounts exist, let alone whether they or someone they care for could qualify for one, so please share this information around.

It seems to me it would obviously be better if the “no more than $2000 a month” limit were simply removed and disabled people could have whatever savings accounts they chose, but this is heaps better than nothing.

[non-binarypal7]

Effective as of January 1, 2026, eligibility has expanded to folks whose disabled diagnosis was established prior to turning 46 years old

About ABLE Accounts An ABLE account is a savings and / or investment option for people with disabilities who qualify. It falls under Section

[helenvaughans]

[hellgrub]

free KN95 masks are being given out all over NYC right now.

Masks are available at all NYPD precincts, and public library branches across the five boroughs, including all Brooklyn Public Library and Queens Public Library locations

on.nyc.gov/freemask (shows distribution spots on google maps)

[werewolf-transgenderism]

my most lukewarm take is that I don't think there should be any exemptions for vaccines, etc., beyond documented legit adverse medical shit that makes it physically impossible. like they should be free and required and nobody should be allowed to just choose to leave their child and any immunocompromised person they interact with vulnerable to potentially deadly but entirely preventable diseases and other medical conditions.

[tharkuun]

my lukewarm addition to this is that i think refusing your child vaccines is child abuse, just like refusing to feed them

[normal-with-adhd-is-a-joke]

What people don't understand about "no excess physical activity/exercise" is that everything is physical activity.

I told the people at orthopedic urgent care that I can't do physical therapy because my condition doesn't allow for exercise. They gave me a list of things I could do at home. They were exercises. I was frustrated at first, but it made me realize how able bodied people can't conceptualize "no exercise" at all.

Walking down two hallways to get to my college class is exercise. Cooking and baking are exercise. Getting something from downstairs is exercise. Even typing is exercise. Each one of those things chips away at my ability to do simple things, like sit upright or speak or even just stay awake. When someone says they can't exercise for medical reasons, that means they can't, and pushing them to do physical activity because it "doesn't take that much energy" is dangerous. Everything takes energy.

[spontaneousmusicalnumber]

A frustrating part of the mainstream vegan “love all animals and protect the environment” mindset is the fact that things need to die in real-life ecology all the time but deer hunting season makes icky feelings and carp culls aren’t cottagecore

[spontaneousmusicalnumber]

The vegan “any animal death ever is morally wrong” mindset doesn’t hold up when:

We don’t have any of the large predators we used to (black bears, mountain lions, or gray wolves) but still retain large deer populations. If nothing is removing animals, they’ll quickly overload the carrying capacity of the environment and have massive losses to starvation and disease that can also pass on to livestock. Human hunters replace the large predators that our landscape can no longer support.

It’s kinder to euthanize an un-releasable hawk rather than try to find it a permanent home with humans. Wildlife rehabs have extremely limited space and resources and are usually run entirely on donated money and volunteer time. Only a few are large and stable enough to care for permanent residents long-term, and those spots are few and far between.

An invasive species poses a danger to threatened native wildlife. I will admit- Australian possums are adorable. But not in New Zealand, where they’re an invasive species that eats the eggs of ground-dwelling birds that previously had no such predators. The landowners I worked with replanting native bush, all native Maori, had no qualms about setting the dogs on them.

I don’t know how to end this except. Sometimes things just gotta die and acting otherwise just isn’t a realistic expectation.

[spontaneousmusicalnumber]

Highlights from the notes over the past 6 months include a lot of angry vegans saying “you’re blowing things out of proportion, no vegans actually think like this!” and a lot of people who work in conservation and education saying “Every day. I have to fight people who think like this.”

As a bonus this post was originally inspired by the vegan who called me racist for saying we should kill invasive species

[doesnotcontain]

as an experiment (and kinda just for fun) I shoved my meds into a spoonful of jello to see how well I could get them down that way, and it technically worked. it didn't taste good, but some extra mouthfuls of jello helped

[ryan-sometimes]

When people justify using gen AI by talking about how it allows them to do (insert creative hobby) it sends me into a blind rage. The whole point of the creative hobby is to use your brain. Having a machine do it for you defeats the purpose. That’s like saying you’re getting into running marathons then just driving the 42km

[rosslynpaladin]

"well what if I was disable-"

Shut up. I am disabled. My brain barely works any more and my hands don't do what I want, and I don't have the strength for singing the way I did,

and I'd rather never paint again, never sew again, never sing again

than have a computer steal other people's work and call it mine.

Keep our disabilities out of your mouth- we're not your PROP for arguments.

[lifeafterpsychiatry]

Like if the field of psychiatry was in any way apolitical and objective the gender/race discrepancies in who gets diagnosed with what definitely wouldn't look like they do

[lifeafterpsychiatry]

It is not a coincidence when the white boy is more likely to get diagnosed with autism or ADHD and the white girl is more likely to get diagnosed with anxiety and BPD and the black kids are more likely to get diagnosed with ODD and schizophrenia and it definitely isn't harmless objective science...

[antiadvil]

it's wild that popular discourse around migraines is that there are too many people who claim to have migraines but "just have bad headaches". this is the exact opposite of my experience? i'm still trying to convince several of my friends that their "bad tension headaches" that are unilateral, throbbing, cause light sensitivity, nausea, etc, are migraines lmao. migraine is underdiagnosed and undertreated by every metric i can think of.

this narrative is not harmless! it prevents people from getting treatment that could really benefit them. so i would like it to die. thank you.

[shamebats]

As a guy who went to see a neurologist only to "rule out migraines" because I thought I had "tension headaches at worst and also it's not that bad really" only to realize by tracking my headache days that I have very bad chronic migraines just with no aura (most people with migraines don't have them), I co-sign this 100%.

Just starting abortive medications already improved my quality of life so much and now that my doctor started me on preventatives, I might actually be able to have more than a handful of headache-free days each month.

Migraine is frequently misdiagnosed as chronic sinusitis or tension headaches according to research. Mostly because people have a very rigid (inaccurate) idea of what it actually is.

But even if it's not migraine, you still deserve treatment for your headaches. Just because someone else has them worse than you doesn't mean you don't deserve relief.

What Type of Headache Do You Have? | American Migraine Foundation

Learning about the different types of migraine and headache disorders can help you better understand your symptoms and discuss them with you

[roach-works]

yeah i found out awhile back that the 'pressure headaches' that i get that 'aren't that bad' (but still leave me feeling sick and dysfunctional all day) were migraines. i now take a low dose of a preventative medication and the number of shitty rain days i have per month has dropped from like ten to two. it's great.

[captaindibbzy]

In my experience anyone who has chronic pain of any kind ALWAYS under diagnoses it in part cause people who DON'T have chronic pain always tell them how it's Not That Bad Just Get Over It and it takes a lot of fighting to get anyone (including doctors) to do anything about it. Fucked if I know why. Everyone seems to think we're making it up. I've never met anyone who is making it up.

[creekfiend]

its really darkly funny that so many public figures keep dying "of cardiac complications after a brief illness" like wow y'all are Never ever going to say the word COVID huh.

[cosmictuesdays]

They used to say "complications from pneumonia" instead of AIDS.

[creekfiend]

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