“…For example, there is ample evidence that inadequacy of information that patients receive about their disease and treatment options contribute to distress [22] and frustration [23], especially with regard to chronic disorders in childhood [24], and specifically to sickle-cell anaemia [25]. And employing quality-of-life parameters to study patients with Hodgkin's disease, it was found that a group treated and given information through bulletin for 3 months benefitted more in areas such as anxiety, depression, and life disruption than the group that received the standard care only [26]. Furthermore, lack of or inadequate information on a disorder can lead to a limitless variety of conceptions of causation, many of which are based on societal norms, ethos, superstitions, and religio-philosophical speculations, and may, in consequence, instigate interpersonal conflicts and lifestyle, which can potentially aggravate the effects of the focal disorder.…”