thewhaleridingvulcan:

crystalsoulslayer:

I always hate it when people are all “so do you go to school, or are
you working, or” and I either have to

  • make up some lie, or
  • eventually get
    around to “I am not working because of depression/anxiety,” and
    subsequently have to deal with whatever bullshit-riddled and completely
    unsolicited opinions on mental illness this stranger feels obligated to
    share with me.

So my therapist was like, “You don’t have to do either.
You can just say you haven’t worked in a while because you’re recovering
from an illness.”

I tried it when the home inspector was here today, and it fucking worked.
He was like, “oh, I’m sorry, are you doing better now,” and I’m like
yeah, and don’t worry, it’s not contagious, awkward laugh, and we moved
on.

MY THERAPIST. IS A GENIUS. Because it is an
illness, so it’s not a lie to say that, and it’s also none of his
business to know specifically what it is, and I clearly don’t want to
give more details, so we should move on from this topic. MY THERAPIST IS A GODDAMN GENIUS.

Dude I needed this. I never know what to say when people ask if I work because I’m severely disabled and don’t work.

lowspoonsgourmet:

thecooingdove:

watchoutfordinosaurs:

homopositivity:

this book is worth more than a dozen restaurants that grow their own microgreens on the roof

ACCESSIBLE GARDENING FOR PEOPLE WITH PHYSICAL DISABILITIES

😍

I know this isn’t a gardening blog, but I feel like this would come in handy for those of you who want to grow your own food!
– Mod Aya

In light of everything going on…

withasmoothroundstone:

Could people, anyone capable of doing so, please do something every single time you see someone describe ableism as being about a list of words you are supposed to say and a list of words you’re not supposed to say?

Ableism is about going to a hospital and getting told by doctors that you’d be better off going home and dying than getting a feeding tube.

Ableism is about going to get SSI and getting told that if you can blog (or do some other random thing that is not gainful employment and will never be), you can work for gainful employment.

Ableism is about your own family believing you’re lazy or exaggerating or faking because you don’t seem like their idea of what a disabled person is (young white guy in a wheelchair from paraplegia, usually – who are actually usually among the more privileged and able to work of disabled people, not that they have it easy by any means, especially since able to work doesn’t mean able to get hired in an ableist workforce).

Ableism is about valuing people based on what we can do, rather than valuing people because we exist.

Ableism is about drawing a line past which people don’t count as disabled anymore, they just count as not even people, and not worth protecting.

Ableism is about there being entire books where people think it’s legitimate to debate whether people with intellectual or other cognitive or developmental disabilities (those are three totally different but overlapping categories, just so you’re aware) count as persons or not.  Both “philosophically” and under law.  Google Peter Singer if you don’t believe me (he also doesn’t think newborns are persons, but everyone loves him because he supports animal rights – by bringing down disabled human beings in the process, and everyone knows – because of ableism, of course – that disabled human beings don’t matter anyway, not as much as animals).

Ableism is not – at least not mostly – about whether ‘stupid’ is a slur.  It’s just not.  And it infuriates me both when disabled people treat it primarily that way, and when nondisabled people treat it primarily that way.  

Because when you do a serious discussion of racism, and then classism, and then sexism, and transphobia, and transmisogyny, and homophobia, and biphobia, and every other kind of oppression you can think of, large and small, and you give them in-depth coverage… and then you come to ableism.  And it’s always last.  And it’s always a footnote to all the other kinds of oppression.  And the footnote always reads “And ableism… don’t say stupid, or idiot, instead, say these other words that don’t actually form an adequate replacement for those first words at all.”  

Which diminishes the understanding of the power of actual ableist slurs such as retard (hint: a slur carries with it as part of the meaning, that the person being described by the slur is not a real person – an insult like ‘stupid’ can be used in an ableist or non-ableist way but is not necessarily a slur even when it’s ableist). And it also diminishes the understanding of what ableism actually is, by not taking seriously the fact that ableism kills people.  

And even this act of always putting ableism last, always treating it as less serious or possibly not even a real ism at all (possibly “political correctness gone amok”, possibly “(eyeroll) yet another group of people wanting to claim they’re oppressed and really stealing the idea of oppression from real oppressed people like people of color and taking their ideas and successes without crediting them at all”, however it’s phrased… that is one of the worst things about ableism in circles that claim to want to deal with oppression in all its forms.  Because it basically throws us to the wolves while claiming there are no wolves to throw us to and that we aren’t really dying in huge numbers everywhere and so forth.  There are ways in which ableism becomes worse, more deadly, because of being diminished in this way by all the “serious” anti-oppression people.

So – I don’t care if you call what you do social justice or anti-oppression or anything else.  I don’t care if you’re part of those circles or not.  I don’t care if you use ideas from those circles or not.  I just don’t care.  All I care about is that you take ableism seriously and that you take the danger disabled people are in right now seriously and part of taking it seriously is making sure that people understand it’s not about what words are politically correct or politically incorrect at this particular moment in time when it comes to disability.  

Because disabled people are often the first to die – or among the first – in situations like this. And this is not an accident.  It is because the people with power know that a lot of people don’t give a rat’s ass what happens to us, whether on the right or on the left.  It’s because they know that you don’t take our oppression seriously.  It’s because they know that our deaths will be considered inevitable.  Have you ever considered it inevitable that disabled people and old people end up in nursing homes, group homes, developmental centers, psych wards, and other institutional settings? – sad, maybe, tragic even, but inevitable consequences of disability?  Because that’s the same kind of thinking that makes our deaths inevitable.  (By the way, nursing homes are the cause of death for a lot of us, but our disability gets blamed instead and this is all normalized so much you probably can’t even see it.)  Have you ever considered it inevitable that disabled people contemplate suicide, and never thought it might be the result of the same forces that cause other oppressed people to contemplate suicide?  Have you ever responded almost reflexively to disabled people’s suicidal thoughts by saying that we ought to have the right to kill ourselves easily and painlessly (when you’d never say the same of, say, queer teenagers), without even thinking that maybe most of the time we’re suicidal for the same reason queer teenagers often are?  Have you ever thought that when we don’t get SSI and die on the streets, that’s just…. unfortunate but sort of inevitable?  That basically our deaths however and whenever they happen are unfortunate but inevitable consequences of being disabled, and you’ve never even thought of the way ableism plays both into our deaths themselves and into your own thoughts about them?

Because that’s why you need to get people to take ableism seriously immediately.  And that’s why I’ve always been infuriated by people not taking ableism seriously.  Because I’ve been that person in that hospital room being told by doctors that I would do better off to go home and die of a totally preventable pneumonia or starvation, rather than get the combination of feeding tubes that would prevent both?  

Oh and by the way – don’t quote me statistics about aspiration pneumonia and feeding tubes unless you know my exact disability, the exact cause of the aspiration pneumonia, and the exact configuration and type of feeding tubes I use and exactly how I use them.  I know that as a general rule feeding tubes don’t prevent aspiration and may even cause it, but in my particular circumstances that doesn’t apply.  There are dozens of reasons for feeding tubes, dozens of types of feeding tubes, and if you don’t understand all of this in-depth you have no basis for commenting.  I went from getting aspiration pneumonia seven times in the first few months of a year, to getting it once or twice a year at most, instantly, with the right combination of feeding tubes.  And I gained back roughly half of the 75 pounds I’d lost rapidly as a result of my stomach disorder.  

And I’m happy, and I’m fucking alive, which is more than I expected by now.  I didn’t expect to hit 34 or 35, and I’m now 36.  I might even eventually hit old age at this point, who knows.  But however long I lived, I deserved a chance to be alive.  And it took a lot of people calling the hospital and demanding I get treated right, to even get the feeding tube.  They couldn’t deny it to me – because I needed it – so they just tried every trick they knew to talk me out of agreeing to it.  After tumblr and other places resulted in enough phone calls to the hospital, I got my tube the next day, although my problems with ableism in that hospital were and remain far from over and the circumstances of getting the tube and the aftermath were something out of a nightmare scenario.  Not because they had to be, but because they could get away with it, because ableism is everywhere and practically unacknowledged by just about everyone, including especially the people who supposedly care the most about disabled people (family, caregivers, “helping professionals”, anti-oppression people, etc).

Anyway, this has gotten into a long enough rant I’ll be surprised if you could read this far – I probably couldn’t (I write better than I read). But hopefully you get the message.  Right now is a time when disabled Americans, especially those of us facing other forms of oppression (ever try to get proper medical care as a queer, genderless and visibly gender-atypical, poor person with developmental disabilities? …yeah) need people fighting ableism more than ever.  And that doesn’t mean tacking up a list of words that everyone can say instead of ‘stupid’.  And treating it like it does, is part of the problem that leads to us dying in circumstances like these.

thepryncess:

bitterbitchclubpresident:

laffytaffygaddaficomeatme:

dragonsatmidnight:

cometoruin:

kyuofcosmic:

erinkyan:

hmasfatty:

(x)

Some light in the darkness that is Gaming news right now

gaming is SO IMPORTANT for so many disabled people (myself included).  There’s not many hobbies that have the range of interactivity and engagement that gaming has, while still being something someone can do with little movement or motor control.

I’ve met a few people who were very disapproving of my gaming hobby (was literally told to “go read a book” in a snooty way by one of them) and it frustrates heck out of me that they can’t see how important and fun gaming can be.  Gaming isn’t passive like a lot of other hobbies recommended for disabled folks.  Gaming is something to get pumped about and something that you can get better at!  You can improve your gaming skills and feel accomplished!

if it weren’t for video games I would be a much, much more unhappy and unfulfilled person.

This is why its SO important to make gaming accessible to disabled people.

This new ‘trend’ of strobing when hit [Destiny/Assassins’ Creed to name a few] is very detrimental to anyone with a seizure disorder that is effected by strobing. A lot of people with motor disorders often have visual disorders too.

Developers really need to make flashy visual effects optional or toggled on/off in menus; not left as a fixed point.

Gaming is SO important to help with my motor skills and comprehension skills and making it inaccessible to some audiences is really detrimental. 

^^^Really important commentary

video games are sometimes the only thing that will help keep me sane.

I’m crying : ’ ). Videogames are important for all ages and degrees of abled people. My grandma definitely has kept a somewhat sharp mind since she plays golden sun and pokemon feverishly, though apparently she was stuck at the Sky Pillar in Ruby for two months (arthritis problems).

i just wish we could get more games that relied less on violence and fighting but Diablo fuckin rules and i’m so glad this person found a way to make it work for them.

we need to make sure all the disabled have the tools and support they need to live the lives they want to.

There is a charity called Able Gamers that helps people with varying disabilities and gives them the chance to play video games. They work both with caregivers, gamers themselves and video game developers (both indie and mainstream)to help make video games more accessible on a software level as well as through assistive technology like Ken here is using. I urge everyone to check them out and donate if possible or spread the word about their foundation!

The AbleGamers Charity

vastderp:

the-future-now:

PlayStation employee builds a customer controller for gamer with cerebral palsy

Peter Byrne of South Amboy, New Jersey, has been gaming since he was a
kid and had no issue with previous PlayStation controllers, but found
the manufacturer’s latest edition to be troublesome.

Alex Nawabi, a retail marketer for PlayStation, responded immediately saying he would look into it,
and after initially saying that the problem would be impossible to fix,
the PlayStation employee mailed Byrne a care package which included a
new modified controller and a powerful personal letter.

Follow @the-future-now

cooooooool!

If someone isn’t available during your most crucial time, then their presence any other time is useless.

neurotoxinsonline:

mymindsecho:

This isn’t realistic for adults. I’m sorry it’s just not.

Don’t fall into believing that, “if they’re a true friend they’ll drop everything and run to be by your side!” crap.

As a responsible adult there will be times that your friends are hurting and you won’t be able to go to them.

There are times that you will have to go to work, or take your sick kid to the doctor, or do many other things that will prevent you from being there for your friend.

When your friend calls you and they’re falling apart and it’s ten minutes until you have to leave for work, you’re not a bad friend for saying, “Look, I love you. I’m sorry this is happening, but I have to go. I’ll call you back tonight when the kids are asleep.” Or “I’m so sorry this is happening. I love you and I want to be here for you but I’ve got to get to work. I’ll call and check on you during my lunch.”

Adult life is hectic and busy with important things all the time and unfortunately it’s also full of shitty things happening to people we love.

Do your best to be there for the people you love and ask for support when you need it but be understanding when being a responsible adult comes before helping you.

The idea that people need to be there any time you need them is really damaging and unhealthy, too. You can’t place value on a person or a relationship based solely on whether or not they’re available, no questions asked, whenever you need them.

In addition to the above: sometimes, someone simply does not have the energy to help. Maybe they’re coming out of a rough patch themself, maybe they have been busy all day,maybe a chronic illness is flaring up. There are a myriad of reasons someone may not be able to be there.

Obviously, if someone is taking you for granted, and never seems to care how you’re doing, that’s an issue. But to write someone off because their life and your life didn’t line up quite right at a given point in time, or maybe even on more than one occasion, is not a healthy way to handle things.

divinghoe:

vanetti:

arguingvitality:

dilfweed:

cosmic-noir:

trxylerhxwellter:

onlyblackgirl:

ntbx:

kingofhispaniola:

Awwwww

My sensitive self can’t take this. this is beautiful 😫😢💕

I love Gordon.

She’s blind and he was making all the points about the pie in a way she could respond to: sound. He is an amazing man

Not to mention Christine won Master Chef that year.

I reblog Gordon Ramsey every time he appears

i reblog this every time it comes on my dash and i will until the day i die or this hellsite does

I can’t believe I’m crying over an apple pie

fullyarticulatedgoldskeleton:

chavisory:

queenshulamit:

ozymandias271:

reading a paper on quality of life among 45-to-70-year-olds with Down syndrome:

“Individuals expressed a desire to be allowed to go to bed when they wanted to.”

😦

Imagine.

I lived in a room and board that failed the burrito test. (”If you’re not allowed to get up in the middle of the night to microwave a burrito, you live in an institution.”) No one stopped me from going to bed, but they did tell me I had to have my lights out by 10, and that I had to be out of the house by 10 the next morning. When I complained to my outpatient program that I needed more help than I was getting, they threatened me with board and care, where my cell phone would be taken away and I would lose contact with the outside world. My case manager sounded so damn smug, like he had caught me out, when he said, “if you’re really as helpless as you say, then you need to be in a board and care.” Like my only options were struggling to do things I couldn’t do, or surrendering my life to an institution.

When I tried to talk about these things with other people, they always rationalized it away. (I told my dad once that my caseworker was reading my e-mails as I wrote them, demonstrating extreme disrespect for my privacy, and he said, “Well, she’s probably making sure you don’t use the internet to goof off.” I was 22 years old.)

 People tend to mock the idea that telling an adult when to go to bed, when to eat, etc., is a human rights violation, even though they would find it outrageous and absurd if anyone came into their lives to do the same thing to them.

And this is what people seem to think when they tell disabled activists we’re just not disabled enough to understand that some people really do need to be locked up and deprived of all autonomy.