Why was July chosen for #DisabilityPrideMonth? Because the Americans with Disabilities Act was signed into law on July 26, 1990.
What does it mean that laws are being distorted and torn apart in the US right now? Well, 34 years post-ADA, most places in the US still aren't accessible. Things are better than in 1989, but a "compliance" based approach doesn't work as well as an approach of viewing disabled people as part of your community.
You can make a difference by volunteering accessibility! Don't wait to be compelled by law. Now more than ever, offer accessibility because you want to.
When abled people become temporarily disabled and heal again, most forget the #ableism they noticed.
When this high school student actually spoke up, at least partly because of a school project on accessibility, she got a taste of how fiercely systemic ableism trains us to defend it.
This doesn't suddenly get better in higher education - it often gets worse.
Nothing says "We care about accessibility and equity for disabled people in STEM like 'Go to Google and let their AI handle it"" #Ableism#DisabledAndSTEM
@ml and the point is not that it is a "zero effort" solution or "not done by human professionals", the point is that AI-generated captions are not good enough in quality to provide sufficient accessibility, and therefore using AI as only accessibility measure is a fucking poor excuse.
🧵 What is this? After pushing UC for 4 years now to quit designing buildings where inaccessibility is the default, a main entrance to a building is wheelchair accessible?
Ah, there's the UC Davis we know. Unnecessary steps because you weren't specifically PAID to do your duty under Section 504 of the Rehabilitation Act nor to actually make a public university accessible to the public.
Are there places in the Fediverse where folks who are longtime disabled (i.e. having done some of the work of dismantling their internalized ableism) and are into pan-disability activism are hanging out exchanging ideas and tactics?
Most of what I see is discussion within silos of one's own disability group (ME, blindness, autism, etc.) or COVID discussion [all of which is great, but I'm looking for more pan-disability stuff to supplement].