Negotiating participation in conversations about care planning between people living with mild neuro-cognitive disorders and their healthcare proxies: a single case analysis

and Implications: Our study contributes to understandings of how the epistemic rights of a person with MND to participate and provide information within interactions are constructed variably. This has implications for promoting the people with MND's individual and relational autonomy in interactions and decision-making and developing awareness-raising resources about how to improve the conditions of decisional autonomy of people with MND.