I’m just curious about this. As someone with a chronic illness, I pretty much never hear anyone talk about things related to the sorts of difficulties and discrimination I and others might face within society. I’m not aware of companies or governments doing anything special to bring awareness on the same scale of say, pride month for instance. In fact certain aspects of accessibility were only normalized during the pandemic when healthy people needed them and now they’re being gradually rescinded now that they don’t. It’s annoying for those who’ve come to prefer those accommodations. It’s cruel for those who rely on them.
And just to be clear, I’m not suggesting this is an either or sort of thing. I’m just wondering why it’s not a that and this sort of thing. It’s possible I’m not considering the whole picture here, and I don’t mean for this to be controversial.
Those of us with chronic disabilities tend to have to be very careful about how we spend our energy. Obviously it varies from person to person, disability to disability. But a lot of us just…can’t. We can’t lobby our local politicians or run for government positions, we can’t go to protests or rallies, we can’t volunteer for campaigns–we just can’t. Or at least, not much. Again, it’ll depend on the person.
And even organizing can take a lot of energy. Someone would have to organize all of us together, across all of these many different disabilities. How do you find them all and reach out to them, let alone manage to do all of that organizing despite your disability?
I know it can happen and that’s how the ADA was created, but the hurdles are great.
Totally fair, and I think that’s why allyship and solidarity are so important. I can’t speak to what it feels like to have a chronic disability, but I can amplify the voices of those who do and help to organize broader coalitions in support of accessibility.
I appreciate the hell out of you, thankyou.
This is exactly it. Many days I can’t even get out of bed. Very little I can do from there.