Indeed, I think this is a to-do list area (even if they are ignored it is a line in the sand on it being proper ethics) to have some documents noting specific things that are not OK or required for ME/CFS-based studies and underlining that not doing this is taking advantage and a welfare issue.
JUst so that these terms are actually said somewhere and we stop getting the 'yeah, yeah as if a survey harms someone severe' taunt from the same people who are doing something disingenuous but just trying to do the laugh it off reply when they get pulled up on what is plain obvious.
And yes, if they'd do this for other vulnerable populations too then at least hopefully we've done something good for them because it shouldn't be happenning, and them not being aware of it is cringe-worthy lack of empathy in the basic 'put yourself in the shoes' theory of mind reality of that term (not their misinterpretation of it as sympathy/fake fawning words).
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