“There is no specific law regulating patients’ rights in Sweden, as opposed to in other Nordic countries. Instead, different rights for patients, such as patient choice or the right to information, are incorporated in other legislation and are formulated in policy agreements between the state and the county councils through the SALAR. Regulations are mainly targeted at the behaviour of personnel and only indirectly at patients’ rights. For instance, personnel are obliged to provide individually tailored information but patients have no articulated right to receive such information (Winblad & Ringard 2009). In March 2001, however, the government appointed a committee…