I know so many people with complex chronic illnesses who pretend to be healthier than they are. With ME/CFS this means they're making themselves sicker by performing health, but I almost never see this reality reflected *anywhere* other than private conversations or in ME/CFS-specific groups. Maybe someone has written an academic article about it, but this reality has not made it beyond the #disability community.
Access and Fandom: Disability Studies From a Feminist Science Fiction Perspective

No abstract available

Disability Studies Quarterly