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and that constantly putting the onus on the people who have to live with these illnesses to simply "get better" is an incredibly shitty thing to do

and that it's not "toxic" for chronically ill and disabled people to feel down, and occasionally talk about how down they feel, in a world which continually disregards their suffering and makes their lives much more difficult than they need to be, sometimes deliberately

and that telling these people that they continue to be ill only because they haven't tried a certain exercise, supplement, therapy or diet will only further damage their health by causing them stress

and that doctors are not only not infallible magic-workers, but are very often actively prejudiced against their patients; especially female patients and patients who belong to marginalised and minority groups

please just understand this and accept that the chronically-ill and disabled people you speak to know more about their health and their limitations and what works or doesn't work for them than you ever could

We need to start commenting under other people's posts about how to properly warn for flashing lights and eyestrain. We need to be emailing and calling companies about their possibly triggering advertisements that could induce seizures. We need to stop tolerating ableism and start speaking up for the more vulnerable.

Also, stop putting epilepsy warnings. That's like saying "warning: schizophrenia" on a post including unreality or "warning: dyslexia" on a post with a typing quirk. First off, the disability mentioned isn't the only group of people that this could trigger. Second, it doesn't truly get the message across and instead makes it worse for those with the disability-- scrolling through the epilepsy tag on Tumblr should get you to view the content of other epileptic people, but no, you just get a bunch of flashing lights and eyestrain, even though you could instead tag for, oh I dunno, flashing lights and eyestrain.

I dont care if 9/10 of the people who use the wheelchair ramp arent actually in wheelchairs. As long as the 1 person who needs it has access to it.

I dont care if 9/10 people who use the automatic push button on the library door can actually push the door open themselves. As long as the 1 person who the door is too heavy for gets to use it.

I dont care if 9/10 people who buy the can tab opener, or the little guitar clamp that holds the chords for you, or the hand grip that helps you hold chop sticks, don't need any of it and just get it to "be lazy". As long as the one disabled person who needs it gets access to it.

I do not care. Oh my GOD I do not care. As long as there's a disabled person on this planet who the accessibility device will benefit, the accessibility device is necessary.