If you& #39;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& #39;re disabled by the consequences of your own actions, there& #39;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">https://twitter.com/bennessb/...