If you're chronically ill and that limits the activities you can do, which is a bigger problem for you:

- many activities are or have become impossible for my body to do at all

- many activities have short- or long-term consequences that may not show up until after the activity

So this is the thing, I think, that makes accessibility/accommodation conversations feel irrelevant for some people with chronic illness.

If you're disabled by the consequences of your own actions, there's often no way to make those actions safe.

And when I say this, I *do* think there are lots of structural changes that would make life better for Consequences people (mostly stuff that prevents burnout in the first place).

Also this, from a reply: https://twitter.com/bennessb/status/1274429597426343936?s=19