ableism:

kelpforestdweller:

you can reserve a space on the train for your bicycle in the default online booking form.

to get a wheelchair space, i have to book the ticket then exchange several emails with the railway company, as if the concept of wheelchairs is entirely new to them. sometimes there’s no email address and they try to insist i call them, which is inaccessible to so many people. then they demand i show up half an hour early, at which point they typically act as if they’ve never heard of you or they have a wheelchair ready because no one told them i have my own. when i arrive at my destination, i cross my fingers that anyone has bothered to call ahead for someone to get the ramp out, and usually have to resort to asking another passenger to flag down a member of staff. i leave long after all the other passengers and crew. and don’t even get me started on airplanes.

now apply this principle to literally everything.

myautisticpov:

not-so-superheroine:

myautisticpov:

Every time I see a kid wearing ear defenders, I wonder whether that kid has the ability to consent to other people knowing that they’re autistic.

Like, you see a kid wearing ear defenders, you know that they’re autistic.

I, a complete stranger, now know this personal piece of information about that kid.

But did that kid have the ability to consent to whether or not I knew that information?

Like, ear defenders are a good strategy to stop kids from having meltdowns.

So are noise cancelling headphones.

So is not going to the shops when it’s busy.

Like, I’m not talking about kids wearing them to the park, I mean seeing kids being dragged around busy department stores on a Saturday morning.

The kid’s not there because they want to be, they’re there because the parents wanted to go to John Lewis instead of Amazon.

Was the kid given an option? Besides “ear defenders or meltdown and get shouted at for not wearing the ear defenders”, I mean?

And like, yeah, sure, kids shouldn’t be told to hide their autism and they shouldn’t be made to feel ashamed of it, but it’s still personal information. It should still be their choice whether or not I – a stranger on the street – know that about them.

Idk, I’ve been seeing it more and more often when I go shopping on the weekends and I can’t help but wonder…

Shopping is kinda a necessity. And not all parents have the ability to find/afford someone who can watch their kid while they go shopping. While parents should aim for a time where shops are not busy, again, it’s not always possible. Shops are busy because Saturday/Sunday is a time where many ppl do not have to go to work. 

I also think that while you and I would know that the kid was probably autistic, this is because we are autistic. Kid could also have SPD, or just be sensitive to noise. Unless the stranger was familiar with autism, I’m not sure they would know for sure. And the only way to completely hide a child’s disability would be not to take them out imho.  As long as the child isn’t uncomfortable, and the parents reasonable (not some ungodly long shopping trip/takes breaks/knows when to stop), I’m not sure why it would be bad. Especially if parents try to make the trip enjoyable.

I agree autonomy is totally important, so forcing your kid to go out unnecessarily. esp when it’s causing pain is a no-go. 

I guess my main problem is “why not headphones”?

And I must stress, I mostly see this in very obviously middle class families and I live in a big city with access to any number of cheap “we’ll deliver whatever you want to your house for you” services.

I live right on the edge of town and am broke and I can still get pretty much anything I want delivered to my house within 24 hours. Like, it’s literally cheaper than the bus fare to get into town and I can’t afford a car. Shopping, in this city, really isn’t a necessity unless you want some really boutique stuff.

When looking at those really middle class parents, I can practically hear “Oh well, we don’t want little Montague listening to music when we’re out because we don’t want him to have any electronics that might rot his brain, like an mp3 player or mobile phone. He’s going to be exposed to nothing but paper books and The Outdoors.”

Like, we can talk about expense all we like, but autism is mostly* diagnosed in middle class kids with the “I only feed my child organic” yummy mummys who think giving kids electronics is EEEVIIIIILLL.

So, yeah, I realise “John Lewis” is a local reference, but put it this way, I have never bought anything from there in my life because the price tags give me headaches, so when I see a mother with a “can I speak to the manager” haircut dragging around a kid with ear defenders on through there, it doesn’t exactly paint a picture of “poor woman didn’t have another option”.

*I do mean “mostly”, not “all the time” and again, it’s the middle class parents I’m seeing this with

(Where “middle class” in British terms would correspond to “upper middle class” some other places. Which might be obvious from some of the rest of the description, but yeah.)

As came up in a reply too, with this particular example I’m not sure that very many members of the general public would have the knowledge to associate a kid wearing ear protectors with autism. Unless they were autistic too, or close to someone who is. Possibly more likely to assume it is just some type of wireless headphones, otherwise.

Given how easy it is to avoid trips to places like John Lewis, as you say, I am even more concerned about the levels of consideration for the child’s needs, getting dragged around shops while obviously uncomfortable for the parents’ convenience. Headphones or ear protectors aren’t likely to make the whole experience entirely non-stressful. Even if that’s enough to prevent full-on meltdowns in the store, that doesn’t mean the child isn’t still stressed.

That was one thing my family got mostly right, way back when, without knowing exactly what was behind the problem. At least before I got old enough to be expected to have learned better, they tried to keep shopping trips with The Meltdown Kid along necessary and to the point. Everybody was happier that way. That was also mostly doable (for working class people) even before it was nearly as easy to get so many things delivered at little or no extra cost.

If they had known to try noise reducing aids, and were maybe operating under the impression that this totally solves the problem? (I.e., usually prevents total meltdown behavior as the main perceived issue.) Who knows.

That said, while I’m not sure if in this particular example, people would see ear protectors and immediately think autism? This does raise some interesting points around children and privacy.

I mean, I grew up with very little reasonable expectation of having any say whatsoever over who was given access to what information, especially where health/disability issues were concerned. No matter how heavily stigmatized the thing might be, that did not get treated as my own personal info that I should have any say over whatsoever. (And still probably wouldn’t, after too many years as an adult.)

This is a way more common approach to respect for privacy than it should be. Especially where children and/or disability and medical stuff are concerned–even before they’re combined. It’s really not good.

So, I am usually even more inclined to err on the side of assuming a very limited need to know, dealing with another person’s privacy. And I can understand why this scenario might not sit totally right, from that standpoint. Complicated.

I’m extremely stressed right now, when I really ought to try to get some sleep.

The rain lately really hasn’t helped matters, but this is our patio right now.

This has been a problem for at least a week, with nasty drain water from our kitchen and upstairs’ coming up through the inspection cover thing back there. No clue exactly what might be wrong, but something is obviously blocked up. But, now it’s covering half the patio.

(Which was a wreck even before that, but I really don’t have the spoons to deal with any of the floating debris right now. At least that may drown some of the weeds I have just not been able to deal with this year.)

I’m really not in the best state of mind right at the moment, after finally putting on some boots and dragging waterlogged planters out of the flooded part. My garbage body enjoyed that about as much as you might expect.

But, what has me extra stressed right now is that he said he was going to call the British Gas Home Care thing to send a plumber out, actually last Thursday or Friday. That hasn’t happened yet. And I can’t do it instead.

Now instead of taking care of that this weekend, he’s heading off tomorrow toward Helsinki (via Stockholm) for Worldcon. Which runs through the 13th! So, over a week gone, all told.

The hotel has been booked since before Christmas and all, apparently. And I would feel like a complete jackass saying “NO, you are not going anywhere until this drain situation is dealt with. I am not staying here alone with a stanky flooded patio, to deal with any complaints about it too.” It’s still so tempting, though.

Especially since this is not the only neglected issue around here that I am the one who is mostly even at home to deal with, day to day. This is just close to the last straw right now.

He can’t help having executive function problems too. I can’t blame him for that. But, some of the apparent priorities there drive me up the wall sometimes. Not going to rant more about that right now, but yeah it can cause some problems. Which he doesn’t mean to do, but also often doesn’t even seem to register that there is a problem.

Even, say, slogging through smelly standing drain water to get in and out of the house 😩

(Another example of some of the stuff I have needed to vent about before, yeah. I am also frustrated again at the apparent denial that he even has any issues to work around, as long as he can get to work and pay bills on time. Limited spoons to keep on top of stuff is one thing, but some weird style of denial ain’t gonna help.)

Feds Find Fewer States Meeting Special Ed Obligations

karnythia:

aka14kgold:

blackraincloud:

autisticadvocacy:

Less than half of states are meeting their obligations to appropriately serve students with disabilities

If only “juvenile detention exists” and “poverty” were considered hostile learning environments…

Anyway, 22 out of 50 seems high. Like, I’m familiar with how low the bar is, and that still sounds high.

Virginia passes the test, but Southern Niece #1, who lives in Virginia’s wealthiest county/school district (one of the wealthiest in the country, in fact, and also one of the best), has been homeschooled for 2 ½ years now because the district can’t manage to place her anywhere that meets two basic requirements: 1) she isn’t placed in physically violent situations, and 2) she receives at least two hours of classroom time where her not-particularly-severe learning disabilities and not-at-all-uncommon psychological-behavioral issues are accommodated/not punished. 

Even then, I’m sure the district passes – sure,

we can’t place a kid with Tourette’s anywhere that she doesn’t end up being traumatized by violence, despite having 150 elementary schools serving 100k students, but hey! We tried a couple times!

There is no bar. None. IEPs may as well not exist for the most part. Accommodation requires multiple people – and taxpayers in general – to give a shit about someone who isn’t them, and that’s a pipe dream. In any case, technically everyone should fail, because starvation begets hostile learning environments and now we’re trying to take away free school lunches. 

My state combined the special ed funds with general funding & immediately acted like having to provide services to my kid was a burden. You don’t want to know how many people I have had to curse smooth the fuck out at his IEP meetings. This year they said in the meeting that his autism makes any bullying he receives his fault because of his limited social skills. I almost jumped over the table. States are literally pushing the idea that kids with IEP’s are greedily hogging the funding that they deserve to meet their needs & it is maddening. 

Feds Find Fewer States Meeting Special Ed Obligations

kalany:

ffsshh:

for some disabled ppl their disability is a gift that they feel they’re a better person for having & they wouldn’t change it for the world
for some disabled ppl their disability is the worst thing that ever happened to them & they’d give anything not to have it
for most disabled ppl their disability is neither or both. their feelings are somewhere inbetween or all over the map. completely neutral or shifting between the extremes
all of these are perfectly valid relationships to have w/ your disability. none of them are wrong or right or inherently healthy or unhealthy. they just are what they are. if you wanna improve your relationship w/ your disability that’s fine. if you don’t that’s fine too.
the only thing that’s not fine is telling someone that their relationship w/ their own disability is wrong

Also? If you are abled, or have a markedly different disability? Your feelings about someone else’s disability are not important and are not welcome.

(I mean, competing access needs exist, and that’s worth recognizing—if for example someone’s stimming is an overload trigger for you, by all means, vent to someone else, try to find a way out of the situation, whatever. Maybe even discuss it with them if you can do so respectfully. But I sincerely do not give two fucks what some abled person feels about my disability. I don’t care. I don’t want to know. I just want to exist in peace.)

girlgrowingsmall:

qjusttheletter:

dysfunctionalqueer:

telegantmess:

pragnificent:

betheothergirl:

outsider-my-ass:

via [x]

[Loni (Literary_zealot) Tweeted: “It’s a privilege to just laugh with your friends and say, ‘There’s always Canada’. Not everyone has that option.”

Coffee Spoonie replies:  Literally, Disabled folx cannot immigrate to Canada.
They don’t get that I cannot ‘lol move to Canada!’, bc Canada doesn’t want my crip ass.”]

This is something a lot of people are not aware of. Canada will deny people permanent residency on the basis of certain health conditions if they cause ‘stress’ on the healthcare system (or if they are a danger to public health or safety). It’s an attempt to prevent people taking advantage of Canada’s universal healthcare, but unfortunately even if someone is immigrating for legitimate reasons, there’s a good chance they’ll be denied (it may be overlooked at times, but that doesn’t change that a family of refugees could be denied immigration if a kid has down syndrome)

We’ve still got a lot of shit to work on here

Many countries have similar laws. 

New Zealand does.

iirc so does the UK

“an attempt to prevent people taking advantage of Canada’s universal healthcare” i know people will argue economics and all but if someone has a need to “take advantage of” this country’s healthcare, they have a need to immigrate here. healthcare is a right, despite the way it’s treated as a privilege.

Holy shit, this is huge news for me. I’m planning to move there in 2-3 years. I need to do some research. Thank you for posting and sharing this info.

mathbalnase:

allthecanadianpolitics:

Meanwhile in Brad Wall’s Saskatchewan…

At the same time Brad Wall is doing this he gave millions in tax breaks to rich corporations.

Here’s the full article, and there’s more than the above coming in cuts for social assistance:

Changes coming for thousands of Sask. people on income assistance

Those ‘admissions to hospital’ are not only ‘costlier’, they are also riskier.  They involve (and produce) more ‘complications’ than preventive healthcare like nutrition support.

PEOPLE WILL DIE BECAUSE OF THIS.

Austerity KILLS.