| Abstrakt: |
Mostly based on Belgian and French-language source material (such as hospital archives, medical ethics, Catholic nursing manuals, etc.), this article sheds light on the way that information around serious illnesses was managed in the late 19th and early 20th century. It is suggested that information-giving practices were largely defined by the paternalistic nature of pre-mid-20th century medicine and although these practices aimed to the same objective, their content varied greatly according to the medical professionals or caregivers involved (doctors, catholic nurses, priests). The patients' and their families' reactions are examined as well. With the ambition to better flesh out the history of the therapeutic relationship, we argue that the interactions between patients and the various actors of the medical world were in continuity with the broader social dynamics of the time. [ABSTRACT FROM AUTHOR] |
