The argument that image descriptions are impossible/useless because no description can be perfect is a strawman that fundamentally misunderstands the function of image descriptions. The rule of thumb with image descriptions is to give a first-glance impression of the image--not every single detail, not down to the tiniest letter in a gigantic diagram. A perfectionist image description wastes not only the time of the person writing it but also that of the screen reader user who must either skip over all that text or sit through the whole thing if they want to glean any understanding of the image at all.
No one is demanding you devote your life to describing the tiniest detail of every picture; interpreting image description requests and reminders that way and thus an intrusion on your precious freedomz is simply pathetic, turning willful ignorance into an excuse to attack and mock disabled people. Don't be this kind of turd.
As proof that adequate descriptions of even the most complex images are fully possible (which is not the same thing as being easy or feasible for everyone), I will use the very image that was used to argue image descriptions are useless.
Try reading the image description of the attached image. Sighted people can compare it to the original image. Does the description give you an idea of what the image is about? Can you understand the gist of it? For sighted people, is the description comparable to an understanding most sighted people would have at a first glance?
If the answers to these questions is "yes," then it's a useful image description that proves that even complicated and inscrutable images can be described, if only to convey the complicated nature of the image. And I promise you, very few if any sighted people can take in, completely understand, or even read an image like this in its entirety at most display settings.
Why the cancellation of the new NICE guidelines matters, MECFS
To people outside the #MECFS community who might not know why this matters... The old guidelines included so-called treatments (GET - Graded Exercise Therapy & CBT) that have been proved, at the least, to do nothing, but at the worst, have caused serious damage to a lot of patients with ME. The new guidelines acknowledged & removed them.
By not publishing the new guidelines, doctors etc, can continue to push these damaging treatments. The DWP can continue to push patients to undertake these treatments and deny anyone who refuses, their benefits. And research into ME continues to be stymied, by both stopping people researching the physical causes of ME, and stopping investment in research.
We thought we were finally seeing the end of the BPS (biopsychosocial) model that GET & CBT are based on. Instead, they are continuing to maintain their control over people with ME.
This will also impact on people with #LongCovid, which has a lot of similarities to ME, and who the BPS lot, are now going after.
it's a good video tho, nicely explaining the physics behind falling forces/slowdown https://www.youtube.com/watch?v=WyExE2qH4Fs
fucking hell I can up the video settings to best with 20 chunks render distance and still be at 150+ fps except close to my tree farm lol
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