A full package of gains Lay perspectives on a bioeconomic transition in Norway

2021 ◽  
Vol 13 (2) ◽  
pp. 73
Author(s):  
Pia Piroschka Otte ◽  
Maja Farstad
Keyword(s):  
2020 ◽  
pp. 002224292098327
Author(s):  
Yanmei Zheng ◽  
Joseph W. Alba

The authors argue that appreciation of the biological underpinnings of human behavior can alter the beliefs and actions of multiple marketing stakeholders in ways that have immense welfare implications. However, a biological perspective often deviates from the lay perspective. The realization of improved welfare depends in part on narrowing this gap. The authors review biological evidence on self-control and report 10 empirical studies that examine lay response to biological characterizations of self-control. The authors contrast lay response with scientific understanding and then offer implications of biology—as well as the gap between the scientific and lay perspectives—for policymakers, firms, consumers, marketing educators, and scholars. The authors also identify opportunities for future research. The authors conclude that marketing scholars can and should play an active role in narrowing the gap between the scientific and lay perspectives in the service of both theory development and human welfare.


2011 ◽  
Vol 6 (1) ◽  
pp. 71-79 ◽  
Author(s):  
David L. Mount ◽  
Darin M. Johnson ◽  
Maria Isabel Rego ◽  
Kandyce Schofield ◽  
Alethea Amponsah ◽  
...  

The unequal discussion of Black males’ health is a pressing social problem. This study addressed Black males’ lay perspectives regarding their health, illness, and mortality, with attention to the determinants of men’s health, prevention, lifestyle, and opportunities for health promotion using an exploratory/qualitative research methodology. Participants were 68 Black males aged 15 to 68 years, with an average age of 44 years ( SD = 14.5). The narratives represented a complex interplay of biopsychosocial factors, ranging from intrapersonal attitudes, interpersonal experiences to discussions about community and public policy injustices. Five prominent themes emerged: (a) lack of chronic disease awareness, (b) fatalism, (c) fear and anxiety of academic–medical settings, (d) hyperactive masculinity fatigue, and (e) the gay–straight divide. The term Tired Black Male Health syndrome was coined in the forum. Implications of these findings are discussed in the context of culturally relevant strategies for improving Black male community health engagement.


Author(s):  
Jennie A. Abrahamson ◽  
Victoria L. Rubin

We investigate health care provider and lay consumer perspectives in online health communication, information sharing, and use to improve communication that supports healthy everyday life behavior. With Rhetorical Structure Theory analysis, we differentiate discourse structure patterns and communicative goals in provider and consumer answers regarding a chronic condition - diabetes.Nous investiguons les perspectives des professionnels et des usagers du système de soins de santé en matière de communications en ligne, d’échange et d’utilisation d’information médicale pour améliorer les comportements quotidiens sains. À l’aide d’une analyse des réponses basée sur la théorie de la structure rhétorique, nous discriminons les modèles de structure de discours et les objectifs communicationnels des fournisseurs et des usagers concernant une maladie chronique : le diabète. 


2006 ◽  
Vol 8 (4) ◽  
pp. 309-330 ◽  
Author(s):  
Anders Blok ◽  
Mette Jensen ◽  
Pernille Kaltoft
Keyword(s):  

Author(s):  
Julia Frost ◽  
Jane Grose ◽  
Nicky Britten

This article explores how people with progressive multiple sclerosis give meaning to their experiences. It builds upon the self-management literature, which has captured the tension between the desire for retaining normalcy and the increasing burden of self-management associated with chronic disease progression. This repeat interview study is empirically grounded in 28 interviews with 14 people with progressive multiple sclerosis. We identified gender differences in diagnosis-seeking which impacted subsequent sense-making. Male respondents found a diagnosis of multiple sclerosis difficult to come to terms with, and an enduring sense of loss or anger could inhibit further sense-making. A diagnosis of multiple sclerosis was more difficult to obtain for women respondents, and any sense of certainty that diagnosis provided framed their subsequent sense-making strategies. The complex sequelae of multiple sclerosis require that self-management strategies are both contextual and timely, although even the most accomplished self-managers can lose their sense of self with neurodegeneration. Disease progression can be associated with suicidal ideation, suggesting the need for greater dialogue to ensure that people with multiple sclerosis are adequately supported to fulfil their quality of life at all stages of neurodegeneration. These lay perspectives emphasise the articulation of affect rather than the rendering of a medical diagnosis, although diagnosis may provide a degree of certainty in the short term. The ethos of self-management ensures people attempt to retain their sense of ‘normality’ and existent social roles for as long as possible, but this ethos can negate both one’s ability to self-manage and the management of self.


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