First things first: I think it’s important that blogs be accessible to persons with disabilities. My own (invisible) disabilities don’t hinder me from reading blogs, but I recognize that this is a real issue. It’s also a thorny one when you start asking how to make blogs universally accessible.
As so often, the devil’s in the details. A few days back, brownfemipower posted a most satisfying gripe about some instructions posted at Bitch Magazine for making one’s blog accessible to people with disabilities. For bfp, a big sticking point was that the instructions presumed totally linear thinking:
just the title alone (The Transcontinental Disability Choir: How to make your blog accessible in five not-very-complicated steps) should be enough to let most people in on why people with ADHD/ADD simply aren’t going to be able to incorporate any of those “easy” or “not so hard” steps into their blogging very easily. Steps and directions suck, quite simply. When a brain can make one particular “step” mean twenty five different things, “steps” are a goddamn nightmare for many of us. not easily navigated.
Her whole post was great, but her description of how her brain works differently than the so-called norm was especially illuminating to me, because I’m one of those people who usually likes instructions laid out in steps. They help me organized my scattered neurons, and I especially appreciated such scaffolding when I had cognitive problems after falling sick last winter. For me, it was a revelation that “easy steps” could become stumbling blocks instead.
My biggest issue with Bitch’s instructions was the amount of typing they require. I actually appreciated Bitch’s suggestion to give a brief description of pictures, especially if they’re relevant to the post and not just decorative. I know I’ve got one blind reader (hi, Reg!) and while I’m certain I can’t evoke the beauty of a perfect clematis blossom in words, I can try to be more consistent in at least identifying a photo’s subject and describing any substantive connection to the post’s content.
But transcripts! That’s where I balk. I’m a very very fast typist, and while I’ve got an old carpal-tunnelish injury as a souvenir of grad school, it rarely flares up anymore. The issue with transcripts is, quite simply, time and energy. Even before I got sick last January, both were at a premium. Now my energy is short enough that whenever I’ve got a little surplus, I want to invest it in writing my own words, not transcribing someone else’s. From both academic and purely mercenary endeavors, I know what a time and energy suck transcriptions can be. Fatigue has been one of my most debilitating, long-lasting symptoms, and this is true for lots of other bloggers who deal with a chronic condition.
I know that some feminist blogs make a big effort to do provide transcripts. Shakesville obviously stands out. I know how much work goes into it. I know that if I felt compelled to match their standard, you’d never see Jon Stewart on Kittywampus again. Too many words! We’d be stuck with silly cat videos forever.
Seriously, this is an area where disabilities can and will collide. In the comments at bfp’s, Quixotess said:
Disabilities conflict. There was a discussion on FWD/Forward a little while ago where a woman said she needed speakers at her events to look up and speak clearly, or she couldn’t hear them. People on the autism spectrum replied that they couldn’t do that. She said, I know, and I’m not going to tell you you have to when you can’t, but you still have to know that that excludes me.
So how to minimize these collisions? Quixotess says she’s willing to transcribe videos for others, and that’s incredibly cool of her. But because most blogs rely wholly or largely on volunteers, more unpaid labor can’t be the long-term solution. As Quixotess also remarked, disability activists are pretty sympathetic to bloggers’ limitations. But relying on their patience is no long-term fix, either.
The problem with all of these proposals is that they’re radically individualized. They demand herculean effort from individual bloggers (disabled or not) and from individual readers with disabilities. Those efforts are that are probably unsustainable over the long run, because even the most able-bodied, able-minded bloggers will tend to burn out if they try to do it all. (Transcription wasn’t even on Melissa McEwan’s long and frustrated list of what it takes to keep Shakesville afloat, and yet I know it’s a big time sink.)
Ultimately, there need to be collective solutions. They need to be universally available, especially if they involve specialized technology, as they almost certainly must. I know that Reg has special equipment that lets him surf the web, write his own blog, Tangentville, post comments, play clips, etc. without needing to “see” what he’s doing. This is the model I think we need to be demanding, and we ought to expect public monies to pay for it, just as a surtax on telephone services funds telecommunications for the deaf. I’m still enough of an idealist about the Internet to insist that everyone ought to enjoy equal access. The voices of differently abled people, those who are aging or just plain old, non-native English speakers and immigrants, folks with limited literacy – we’re all a crucial part of the conversation. Or we all should be, in a just and reasonable world.
Patron cat of Kittywampus (1985-2001)
I would not consider myself a blogger, per se, but I do have a Live Journal account. Live Journal offers a tool where you can phone in a journal update, and the audio will be available to your readers along with a computer generated transcript. Your readers are invited to transcribe, or to correct errors in previous transcriptions. The machine transcriptions are sometimes fine, sometimes entertainingly bad, but they provide a starter set that can be manually corrected pretty easily. It works well.
I wonder if a similar solution could be used to provide transcriptions of other things? Maybe someone will build it for us eventually. I am not disabled but I really appreciate the transcriptions.
Yeah, I definitely appreciate transcriptions, too, although my hearing is just fine. If a clip isn’t entertaining or dramatic or otherwise compelling to watch, I’d often rather skim a transcription than take the time to watch the clip. Sometimes, the transcription catches my interest and persuades me to watch the clip after all. In any event, transcriptions are wonderful.
Voice recognition systems are still pretty primitive. My husband gave them a very serious go a couple of years ago, when he lost the ability to use his left hand. (Long story.) He’s found it’s more efficient to type with six fingers rather than fight with the errors that got transcribed. Based on the number of customer service lines that take voice cues, I’m hopeful that voice recognition technology is still improving.
[...] Have you seen this yet? Really excellent post about the problem of accessibility and multiple disabilities interacting with each other… The problem with all of these proposals is that they’re radically individualized. They demand herculean effort from individual bloggers (disabled or not) and from individual readers with disabilities. Those efforts are that are probably unsustainable over the long run, because even the most able-bodied, able-minded bloggers will tend to burn out if they try to do it all. (Transcription wasn’t even on Melissa McEwan’s long and frustrated list of what it takes to keep Shakesville afloat, and yet I know it’s a big time sink.) [...]
Hey! First, thanks for the link! And second, I really really love your suggestion of making collective demands for collective accessibility instead of individual demands–I mean, I’m still going to do what I can to make something more accessible to readers–but I agree totally that if there is the technology to make accessibility happen–then it needs to be available to all–just like how high speed needs to be available to all…
really good post!!!!
Of course, we live in a country where collective responsibility will be derided as big government, coddling the poor, etc. etc. – but it’s still the right thing, and it’s still a good idea. I recall France doing something like this with a gadget called the Minitel in the early 1990s or so. It was a bare-bones terminal that was handed out to pretty much everyone in France, with the goal of getting everyone online. It still exists but must be a dinosaur today, since it was geared to the pre-WWW Internet. But the *idea* of guaranteeing everyone access is more important than ever.
I want to second what you say about the availability of high speed for all. I just spent a couple weeks at my mom’s house, mostly reliant on her dial-up, and I pretty much stopped blogging. Even reading blogs was well-nigh impossible.
Thanks for the kind words and the link back to me – as a small-potatoes blogger, I appreciate it! I really did like your post, too.
came over from flip flopping joy, and just want to tell you that you rock! thank you thank you thank you for this post!
Thanks for visiting, and thanks for saying nice things! A few years from now, when my children are teenager, I will remember that at least one person, once upon a time, said that I rocked.
well, i think i understood your “collective responsibility” differently than some readers did. i mean, we all kind of interpret something based on our own needs and pre-thoughts on a matter. so what i was thinking of when you wrote of there being collective responsibility, i didn’t think for one minute that it precludes individual responsibility, but that collective responsibility supports individuals to be responsible, either by providing a culture of responsible actions in this regard or by providing resources that individuals can use. so, for example, i used the WAVE site on my blog and it came back saying there are 2 accessibility issues. but i can’t make any sense out of it, because it doesn’t clearly list what those two issues are, much less any advice on how to fix them. in two places where this issue is being discussed, i have raised this issue – i want to be individually responsible, but if i don’t have the skills or, in this case, even the comprehension, of how to be accessible, shouldn’t someone(s) be offering me some assistance on how to make my blog more accessible? that’s part of what i think “collective” responsibility will mean – collectively designing and providing the tools that we all need to be more accessible, and not just telling people “you need to be more accessible/you’re not accessible” but giving concrete ways that people can be more accessible and the means with which to do something about it. and one other thing, as bfp brought up in her post and you reiterate in yours, is that we all have different accessibility needs. when the assumption is that the person writing the blog doesn’t have disabilities and therefore “shouldn’t” have any difficulty enacting all accessibility measures… that’s a little problemmatic. and while i agree to an extent that disabled people can be very understanding, hey, we are human too. it gets tiring trying to get people to understand our accessibility needs and why they should care. i have certainly known plenty of disabled folks who were not very understanding. i think we should save our anger for places that just refuse to get with the times and meet our needs, but the reality is that i’ve been turned on too. and at best, i’m just ignored. so eventually, someone will come to my blog and complain about an accessibility issue that could possibly have already been resolved, if only we had a collective conscience and those in the know would actually help those who don’t have the knowledge or ability.
I really like your formulation of collective responsibility as *supporting* individual responsibility.
I think the Bitch post was actually well-intentioned in this respect. It was trying to provide some tools and guidelines. It’s possibly quite helpful for folks that have the tech savvy and the time/energy to follow those guidelines. Problem is, as you mention, lots of people don’t have the tech expertise to follow them.
And I agree 100% that we should save our ire for people who just don’t get a rat’s patootie about accessibility. For me, that’s part of shepherding my energy.
Interesting post.
I do agree that disabilities collide a lot of the time. I personally have trouble relating to hearing people with low vision – Deaf people with LV are easier for me to relate to for some reason – and I’m not sure how to reconcile differences like that…
My blog is mostly about accessibility as it pertains to the Deaf, and Deaf cinema…. if you want to check it out.
Thanks for your thoughts, Daniel.
While I could click through to your blog based on the info you provided when you commented, that link isn’t available to the wide world, so here it is: Moving Hands – I’m glad you pointed out. Since you posted here, you had a guest post on captioning of online videos, which I think will interest anyone who’s still following the discussion here.
Thanks for linking to bfp’s post, very instructive. I have also been stymied over “photo descriptions” — since I describe them all, more or less. But I choose them based on what bfp says, a certain emotion or concept I believe they communicate. But that’s TO ME–you might not see it at all.
If I included MY observations, I would be forcing my interpretation of the photo on others, and I don’t necessarily want to do that.
Examples:
I picked THIS photo (first one) because they were both talking at once, and it summed up their relationship during the campaign.
I picked THIS photo because he looks calm (i.e. not like some raving atheist wacko), intelligent and authoritative… the microphone in front of him denotes the fact that many ARE listening to what he has to say.
I picked THIS photo because The Emperor in Tarot represents govt power. Also, I think the concept of “The Emperor” communicates the “absolute power” of the presidency. To explain all that would detract from the main point of the post; you don’t need to see the Emperor to understand that I am saying that in the post, too. (And you might believe the tarot is crap anyway.)
Etc.
I don’t think it’s necessary to understand photos or see them to appreciate the writing, so I admit, have not made that a priority… I often have NO IDEA why people use the photos/graphics they use, and how they go with the concepts. I figure other bloggers are as arbitrary about that as I am.
Great post, great analysis.
Those are all good illustrations, and I get what you’re saying about The Emperor. I don’t believe in tarot (though I sort of get why it’s fascinating) but that image really works anyway.
There’s a good tutorial now up on how to do those alt tags, which bfp linked at her place. It turns out that even having a blank tag is more helpful for a vision-impaired reader than no tag at all. But Blogger and WordPress don’t include that blank tag by default, which is just ridiculous, because it means that to do it “right” you’d need to edit the code every time you’ve got an image, even if it’s purely decorative and not essential to understanding the post. (I don’t know if I’m making sense, or if this is only comprehensible if you’ve looked at the linked tutorial …)
At any rate, here’s again a situation where a sensible solution would require a centralized change, which would be very easy for the big platforms to implement, and which individual bloggers could then customize where appropriate.
[...] 16, 2009 at 2:48 pm (Uncategorized) Via BFP, from Sungold at Kittywampus, comes this continuation of the discussion about when disabilities collide: The problem with all of [...]
One of the things I’ve been doing in the background is contacting people who are often linked ’round the progressive sphere for their video blogs and asking them to provide closed captioning for videos. They’re not really done off the cuff – they’re done with scripts and stuff – so it shouldn’t be a huge drama to provide such a service in a way that will be of benefit to a lot of people, such as those who have difficulty hearing words clearly, people for whom English is a second language, people who can’t process videos very effectively without having the text, folks who read blogs at work and don’t like to have the sound on, stuff like that. There’s a whole variety of reasons that closed captioning on videos would be a huge boon to a lot of people.
I just finished the very time-consuming stuff I’ve been doing offline, so that particular project is becoming something I can actually dedicate real time to, and hope to make a more visible project in the new year – because this *is* a collective issue. It’s part and parcel of similar issues we’ve linked to and discussed at FWD/Forward, where we don’t have such a narrow mandate of discussion topics. Marlee Matlin is championing an internet captioning crusade for American providers of content, such as Hulu & iTunes. Fandom folks have put together instructions on how to subtitle a vid, which could be useful for people like Jay Smooth, say, who is often linked ’round the sphere. There’s the whole “better captioning campaign” being run here in Canada, which argues for consistent and good captioning to be done by providers of content.
I mean, there’s a serious ongoing discussion about balancing conflicting needs and conflicting ways of processing things that needs to continue, and needs to be highlighted, because it’s not a simple problem that can be solved easily with the wave of wand.
[bfp, I was going to comment on your initial post, but I saw my cobloggers were in there and I was going through an "omg all criticism of my stuff is criticizing me as a human being!!!" phaze and wasn't very coherent about it. I'm feeling a lot more functional as a person now (yay!), so I can actually read this stuff for content instead of reacting like I everyone essentially wrote "Anna is evil and should be shunned forever." Oh, mental health condition, you're so awesome.]
So wait, are you the same Anna who wrote the post at Bitch? If so, thanks for getting the ball rolling. You are awesome, not evil.
You provided a great service.
I am so glad to hear that you’re working on closed captioning. I absolutely agree that it would be swell for a lot of non-disabled folks too. I don’t have any issues with hearing, myself, but I spent ten years living in Germany, and I absolutely get how helpful captions and subtitles are for non-native speakers! I had really rudimentary skills at first, and I was always so grateful to *see* the words because my reading abilities were better than my oral comprehension.
It’s also wonderful that you’ve got a famous spokesperson giving the issue some attention. I know change can still be slow but it’s great that you’re pushing for collective solutions.
Anna–I’m sorry that I wrote that when you were feeling that way. please know that like i said in the original post, that was something that was brewing for at least two years, if not more. it wasn’t all, ERGH that ANNA SUCKS! it was, ok, I’m strong enough to take it when somebody tells me I’m a stupid fuck because I can’t figure out how to caption a photo!
again…I’m sorry.
Oh gosh no!
You know how 8 million things are going that all warrant being upset, and then one thing happens that isn’t really a huge deal and THAT is what sets you off? Oh yeah, I was there.
I really felt what you had to say in criticism of that post was very spot-on.