<p>this kind of experience has me thinking about how accommodations/access tends to be framed in terms of first order effects (in my case: RA symptoms) & not side effects of meds or how treatment itself (& adjusting to changes in treatment) adds new barriers. clinically i’m “in remission” so it’s not even clear i would qualify for anything ADAish (though i have low certainly about this & would be happy to be corrected)</p>
