Disability and Accessibility

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All things disability and accessibility related, and advocacy for making those things better.

See also this community's sister subs Feminism, LGBTQ+, Neurodivergence, and POC.


This community's icon was made by Aaron Schneider, under the CC-BY-NC-SA 4.0 license.

founded 1 year ago
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Hi there,

I've been building a threadverse web app, "PieFed", for the last few months and recently put a bit of effort into making it more accessible. It is almost WCAG 2.1 AA compliant now.

However I have no lived experience of using the web with disability so any feedback in this area is most welcome. Please give it a try at https://piefed.social and let me know what you think, from an accessibility perspective.

Thanks!

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it is really hard (self.disability)
submitted 11 months ago by xuxxun to c/disability
 
 

Everytime I leave the house to do anything, I either

  1. get shit from people because I am wearing a mask -either minimizing and simply gaslighting comments, or plain agression
  2. when they seemy mask they decide to share their grief with me. It is so hard to listen to all the stories of people dying and becoming disabled from covid, shared by maskless people. I tell them masks work, and they should vaccinate. But it is so tiring. I am just trying to survive. I wish others would help each other survive. I am already tired from my chronic illnesses. Seeing the COVID numbers rise and no one masking or doing anything and staying in denial is horrible for my mental health. I am trying my best to hang on to my sanity. I wish you all that you stay sane too.
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submitted 1 year ago* (last edited 1 year ago) by dankeck to c/disability
 
 

How do you write alternate text for a work with visual artistic merit?

  • How you balance too many words versus sufficient details?
  • What details should come first?
  • How do you account for different audiences, their needs and preferences?
  • Should it be written by the original artist or a professional describer?

In a recent IAAP webinar, inclusive media expert Joanne Pak explained an initiative to answer these questions and more.

The Literary Image Description (LID) Best Practices Guide is a Canadian government-funded project aiming to:

offer a more vivid and engaging approach to writing image descriptions in an effort to make art and literature more accessible to all readers everywhere.

Visit the project website to download a well-researched and illustrated guide in EPUB or PDF. Then maybe next time you see a painting, sculpture, comic strip, or even clever set of visual instructions, you can take a swing at making your own image description*!

*But of course, don't publish unless you first talk to the author or do sufficient research into the intent!

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web.archive.org link -- excerpts follow.

The ACS uses a set of six yes-or-no questions—related to difficulty with hearing, vision, and other functions—to determine disability status. A respondent who answers “yes” to any of those questions is counted as disabled.

Now, bureau officials are recommending replacing those questions with a set developed by the Washington Group on Disability Statistics ...

Seltzer, for her part, agrees that the more comprehensive WG-SS could “potentially yield greater insights into disability” in the U.S., but worries that many policymakers will use the 8% statistic to cut funding to programs that help disabled Americans.

The proposed change will be open for public comment until 19 December, although the National Advisory Committee, which advises the Census Bureau on policy and research issues, will discuss initial comments on 16 November. Landes hopes policymakers will listen to the voices of disabled Americans and not move forward with the change. “The power of the disability community is strong,” he says.

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Cost of living payments for those receiving Pip have been quietly axed, forcing many to choose between charging their wheelchairs or staying warm

It’s getting cold, which means that many disabled people will, once again, have to choose whether to keep warm or charge their wheelchairs. Only this winter, they won’t be getting any additional help with the cost of living.

Last year, the government allocated cost of living payments to those on low incomes, and to disabled people who receive personal independence payment (Pip), the main disability benefit. And yet, as the next round of low-income payments start to go out this week, that separate disability payment has been quietly scrapped. If it wasn’t so nakedly cruel it would be absurd.

This is hardly the first cruelty. When the original payments were made last autumn and again in June this year, the disability-specific one was less than half the amount of the low-income one. And this despite the fact that disabled people face astronomical costs in order to make the world more accessible to them. The source of these costs varies from person to person; from care costs to taxi fares or prepared food.

In 2019, before Covid and the inflation crisis, the charity Scope found these extras amounted to £583 a month on average, rising to more than £1,000 a month for one in five disabled people. Now, Scope puts that figure at £975 a month for households that include one disabled child or adult, or £1,248 for households with two disabled adults. The charity’s research shows that disability-related extra costs are equivalent to 63% of a disabled household’s income, after housing costs. For those with the most complex needs, costs will be much higher.

In a crisis born of rising energy prices, it’s important to note the disproportionate effect soaring bills have on disabled people. A wheelchair user with a chronic lung condition may need to work from home to protect themselves from common illnesses – meaning that, if it’s cold, they have the heating on all day. If they get cold their breathing gets worse, so they put the heating on earlier in the autumn than most people, with the thermostat set higher. It’s not hard to see how their gas bill takes up a huge chunk of their income. Add in increased electricity bills associated with charging electric wheelchairs and other equipment, and those figures from Scope start to make a lot of sense. As do recent survey results from the Trussell Trust, which found three-quarters of people referred to food banks say that they or a member of their household are disabled. There is a real crisis here.

Which takes us to the other cruelty in government policy on disability benefits – one that existed long before the current decision on who gets cost of living payments was made: Pip isn’t fit for purpose. Not only is it unreasonably hard to claim the benefit, it doesn’t come remotely close to achieving its purported aim, which is to cover those exorbitant extra costs of disability to level the playing field – just a little – for disabled people. The truth is, Pip has never been enough and over time the proportion of the costs it does cover has fallen and fallen. Pip is generally increased each year in line with inflation, but the cost of disability-related essentials, such as energy, has been rising much faster than the average increase. We’re not so much levelling the playing field as we are leaving disabled people to scale a cliff face.

A series of exceptional cost of living payments over the next few months is not going to undo the decade-long devaluing of Pip. A payment of a few hundred pounds wouldn’t make up for the relentless inaccessibility, ableism and failure of government services that has created all those extra costs in the first place. But it wouldn’t hurt either.

If, as the continuation of payments to those on low incomes would indicate, we recognise that we are still in an acute cost of living crisis that requires at least some mitigation, we must recognise that disabled people are in desperate need of the same help.

-Lucy Webster is a political journalist and the author of The View From Down Here: Life as a Young Disabled Woman

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A newmembeer of the GNOME accesibility team talks about current issues and plans

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Time: 12pm noon
Date: Monday 30 October 2023
Place: Caxton House, 6-12 Tothill Street, London, SW1H 9NA
Hashtag: #NoMoreBenefitDeaths

Join Disabled People Against Cuts and allies to protest against the government’s proposals to tighten the Work Capability Assessment.

These proposals threaten to remove essential income from Deaf and disabled people and to subject many more of us to distressing and punitive work search activities and benefit sanctions.

Their argument is that Deaf and disabled people can work from home now. They want to remove assessment points for social anxiety, communication difficulties, mobility issues and bladder/bowel incontinence.

We know that working from home does not overcome these barriers.

Research has shown that disabled people benefitted less from home working than non-disabled people, because we are less likely to be in the kind of jobs that can be done from home.

If the WCA is tightened in the way they propose, many more Deaf and disabled people unable to find sustainable paid employment will lose benefits [ESA support group/Universal Credit LCWRA component] and lose protection from conditionality and sanctions.
Monday 30 October is the last day that the government’s consultation on their proposals is open.

The consultation will not only inform immediate changes to the WCA.

The consultation will also feed into the Tories’ long-term plans to:
– scrap the WCA
– remove ESA/Universal Credit LCWRA altogether
– replace them with a new Universal Credit health component that will be dependent on eligibility for Personal Independence Payment
– subject all Deaf and disabled people to conditionality and sanctions at the discretion of individual work coaches.

These plans will be a disaster for anyone who faces barriers to paid work.

They will unquestionably lead to a considerable increase in avoidable harm and more benefit deaths.

And we **cannot ** trust Labour not to keep any changes to tighten the WCA if elected.

Please support the protest however you can and let people know about the consultation and the government’s despicable plans.

For help with travel costs for DPAC members email: mail@dpac.uk.net

Consultation here: https://www.gov.uk/government/consultations/work-capability-assessment-activities-and-descriptors

Template response from DPO Forum England here: https://dpac.uk.net/2023/10/template-response-to-the-wca-consultation/
Government white paper setting out their long-term plans here: https://www.gov.uk/government/publications/transforming-support-the-health-and-disability-white-paper

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This Tuesday, 2023-10-24: Women Who Code Advocacy Town Hall moderated by AmyJune Hineline ( @volkswagenchick@drupal.community )

From the event description:

  • Hiring Process, Getting the Job, and Support at Work: Know the challenges and opportunities for individuals with disabilities throughout the hiring process, workplace support, and career growth.

  • Visible and Invisible Disabilities: Understand and define visible and invisible disabilities, and how they affect individuals in the tech industry.

Legal Rights and Responsibilities: Learn about legal rights and responsibilities in hiring practices and actionable ways to advocate for yourself and others.

  • How Allies Can Be Advocates: Explore how allies can play a role in advocating for individuals with disabilities and creating inclusive workplaces, and how technologists can develop with accessibility in mind.

  • Access to Resources: Gain insights into accessibility resources and how you can find more support

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Shared by @onsman@aus.social, a list of experts and organizations to follow for news and ideas on digital accessibility.

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Employees of the state of Minnesota in the United States have created a "Maps Community of Practice" to advance the accessibility of digital and print maps.

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Disabled People's Manifesto launched (www.inclusionlondon.org.uk)
submitted 1 year ago by xuxxun to c/disability
 
 

Interesting news from the UK

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Hi everyone thanks so much for accepting me. My disabilities include fibromyalgia, ROP (I was born at 24 weeks gestation.) I'm also autistic and have hyperacusis. I'm hoping to contribute to what looks like a wonderful community.

It's great to see other chronic illness suffers here. As I've noticed the broader disability community despite their best intentions can have a tendency to forget about us. I'm really encouraging thing was to hear an episode on Pushing Limits that covered chronic illness.

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