scholarly journals Meaning and inconsistencies of meaning – exploring the perspectives of Norwegian veterans in Afghanistan

2016 ◽  
Vol 7 (1) ◽  
pp. 31-43 ◽  
Author(s):  
Roger Lien ◽  
Kristian Firing ◽  
Mons Bendixen ◽  
Leif Edward Ottesen Kennair

Abstract This qualitative study explores the meaning-making process of veterans to address the positive aspects of military service in international operations. Thirteen veterans from a Force Protection Unit in Norway were interviewed about their deployment to Afghanistan. A thematic analysis revealed three main themes reflecting meaningful aspects of the service. “Confirmation of ability” refers to finding meaning by coping with stressful situations and being recognized for it. “Cohesion of peers” refers to finding meaning by belonging to a team and giving mutual support within the team, such as backing up each other and caring. “Significance of effort” refers to finding meaning by seeing their efforts as a contribution, as well as by receiving recognition and gaining status for their efforts. The analysis also revealed accompanying themes of inconsistencies, which in turn activated different coping strategies. The findings have been substantiated through a functional exposition of meaning: purpose, value, efficacy, and self-worth, as advocated by Baumeister (1991), and are discussed in the context of previous research and a theoretical concept of meaning making. Steps for future research are proposed.

2021 ◽  
pp. 193672442110356
Author(s):  
Elmira Jangjou

In response to students’ food insecurity, a number of colleges and universities have taken action and established campus food pantries as part of their intervention plans. However, many of these pantries ceased operation due to COVID-19 campus shutdowns. The purpose of this study is to illustrate the short-term impacts of the COVID-19 pandemic on postsecondary students, who use a university-provided food pantry. Drawing from semi-structured interviews with 12 participants, the thematic analysis explored the initial coping strategies these students used to endure the pandemic. Findings revealed that many students experienced the immediate effects of the pandemic in the form of income loss, self-isolation, anxiety, and appetite change. Although the pandemic interrupted these students’ journeys to continue their studies and become independent in various ways, the affected students implemented various coping strategies, including seeking help from family or friends, using available resources, cooking at home, and even trying to save money. However, considering that the targeted population in this study was already at risk because of their basic needs insecurity, these postsecondary students require extra attention from their higher education institutions in the case of emergencies, such as a global pandemic. In addition to its timely and relevant findings, this study provides important avenues for future research and intervention efforts.


2021 ◽  
Vol 10 (4) ◽  
pp. 880
Author(s):  
Fery AM Mendrofa ◽  
Umi Hani ◽  
Yuni Nurhidayat

A pandemic of a novel coronavirus-infected disease is currently ongoing in the world. Most patients have to be isolated due to the treatments. This study aimed to make sense of how patients with coronavirus-infected disease understand and experience infectious isolation. The research used a qualitative design with a phenomenological approach. Data collection was conducted with in-depth interviews of nine patients with coronavirus disease-2019 (COVID-19) confirmed who had been in the isolation room. The analysis was conducted on interview transcripts by organizing keywords found into categories, sub-themes, and themes based on Colaizzi's approach. The results indicated that the participants experienced fright due to the isolation and attempted to integrate their isolation experiences. Isolation highlighted a sense of threat posed by cross-infection, a threat that participants experienced as originating from others and from themselves to others. Participants described feeling changes experienced after several days of treatment. Participants reported various symptoms of the disease and received careful care while in isolation. They still communicate with family. Isolated patients are able to deal with the treatment by improving their coping strategies. Participants reported the most support from their families, even from a distance. Future research could explore experiences of isolation from family and staff perspectives and identify the psychological aspect in caring for the COVID-19 patients.


BMJ Open ◽  
2017 ◽  
Vol 7 (8) ◽  
pp. e015023 ◽  
Author(s):  
Wouter Schakel ◽  
Christina Bode ◽  
Hilde P A van der Aa ◽  
Carel T J Hulshof ◽  
Judith E Bosmans ◽  
...  

ObjectivesFatigue is an often mentioned symptom by patients with irreversible visual impairment. This study explored the patient perspective of fatigue in visually impaired adults with a focus on symptoms of fatigue, causes, consequences and coping strategies.SettingTwo large Dutch low vision multidisciplinary rehabilitation organisations.Participants16 visually impaired adults with severe symptoms of fatigue selected by purposive sampling.MethodsA qualitative study involving semistructured interviews. A total of four first-level codes were top–down predetermined in correspondence with the topics of the research question. Verbatim transcribed interviews were analysed with a combination of a deductive and inductive approach using open and axial coding.ResultsParticipants often described the symptoms of fatigue as a mental, daily and physical experience. The most often mentioned causes of fatigue were a high cognitive load, the intensity and amount of activities, the high effort necessary to establish visual perception, difficulty with light intensity and negative cognitions. Fatigue had the greatest impact on the ability to carry out social roles and participation, emotional functioning and cognitive functioning. The most common coping strategies were relaxation, external support, socialising and physical exercise and the acceptance of fatigue.ConclusionsOur results indicate that low vision-related fatigue is mainly caused by population specific determinants that seem different from the fatigue experience described in studies with other patient populations. Fatigue may be central to the way patients react, adapt and compensate to the consequences of vision loss. These findings indicate a need for future research aimed at interventions specifically tailored to the unique aspects of fatigue related to vision loss.


2020 ◽  
Vol 4 (4) ◽  
pp. 109-116
Author(s):  
La Rakhmat Wabula ◽  
Syahfitrah Umamity ◽  
Ellen Lombonaung

Resilience was a dynamic process that adapts positively to the difficulties it has. This term was often used by researchers in cancer patients. Controversy often occurs in its conception and little is known by patients in the use of the term resilience in their lives. The subject of this paper was cancer patients. The literature review was conducted by examining qualitative studies that discuss the use of terms in cancer patients and the use of themes used in terms of resilience. A systematic review of reviews through SCOPUS, MEDLINE, Psyc INFO and CINAHL reviewed from 2000 to 2017. Thematic analysis was used to encode themes in the studio and produce analytical themes, and resolution resolutions in the studio. After being invited to 573 citations, there were only 32 suitable studies. Four categories emerged, including coping strategies, social support, spirituality, and growth. The conclusion is no use of the term resilience in cancer patients, but cancer patients more often use other terms with the same meaning as resilience. Cancer patients rarely use the term direct resilience, but more often use terms such as coping strategies, social support, growth, and spiritual as terms related to resilience. Keywords: resilience; cancer patients


2021 ◽  
Author(s):  
Yael Benn ◽  
Mark Jayes ◽  
Martin Casassus ◽  
Marney Williams ◽  
Colin Jenkinson ◽  
...  

Acalculia, an acquired disability following a stroke or brain injury, involves difficulty processing numerical information and/ or calculations. Acalculia is not routinely screened for, and as a result there is a lack of understanding about the nature and prevalence and the impact of the condition. This qualitative study was initiated by stroke survivors with a strong interest in acalculia. Sixteen stroke/brain injury survivors with acalculia and seven carers were interviewed using semi-structured online interviews. Participants ranged in age, gender, time post onset, country of residence and numeracy level prior to brain injury. Data were analysed using thematic analysis. Three main themes were identified: Awareness and Diagnosis; Emotional and Practical Impact (independence); Support, Coping Strategies and Self-training. Participants and carers repeatedly referred to the lack of awareness and treatment for acalculia and the impact acalculia has had on their lives and independence. Practical impacts included managing money, making appointments, using timetables, organising social activities and employment, and managing medication. Our results highlight the urgent need to develop suitable assessments and interventions for acalculia and the scope for this to be PCPI-led. The data also reveal useful strategies and suggestions regarding effective timing, targets and approaches for intervention.


Author(s):  
Melanie Rose Dixon ◽  
Isabelle Giroux ◽  
Christian Jacques ◽  
Philippe Grégoire

Excessive online stock trading appears to share similarities with gambling disorder. However, using gambling disorder criteria to assess excessive trading may not allow a full understanding of this phenomenon as specific aspects of the trading context that differ from gambling may be overlooked. This study explores the manifestations and consequences of excessive trading and its links with gambling disorder via the perceptions of online stock traders themselves. Data for thematic analysis were collected from a sample of online stock traders (N = 13) divided into two focus groups based on trading frequency (i.e., on a regular or occasional basis). Perceived manifestations of excessive trading included excessive preoccupation and frequent behaviors, and consequences that affect finances, relationships, work and health. Perceived links between gambling disorder and excessive trading concerned a shared incapacity to control behaviors, and chasing losses. Though excessive trading and gambling disorder are similar on many grounds, the assessment of trading behaviors should consider specific aspects such as the context within which they occur (e.g., state of the market). Implications for future research on excessive trading behaviors are discussed. RésuméLes transactions d’actions excessives peuvent présenter des similitudes avec le jeu pathologique. Cependant, appliquer des critères propres au jeu pathologique à des pratiques de transactions excessives en ligne ne permet pas nécessairement de bien comprendre ce phénomène, car il pourrait arriver qu’on néglige certains aspects particuliers du contexte transactionnel qui diffèrent du contexte du jeu. Cette étude explore les manifestations et les conséquences de pratiques transactionnelles excessives et ses liens avec le jeu pathologique, en se penchant sur les perceptions personnelles des négociateurs. Les données ont été recueillies pour une analyse thématique à partir d’un échantillon de négociateurs en ligne (N = 13), divisé en deux groupes de discussion en fonction de la fréquence des transactions (soit sur une base régulière ou occasionnelle). Parmi les manifestations perçues à propos de transactions excessives, on a pu voir des préoccupations excessives et de fréquents comportements et leurs conséquences sur les finances, les relations, le travail et la santé. Les liens communs perçus entre les troubles du jeu et la négociation excessive étaient l’incapacité à contrôler ses comportements et la récupération des pertes. Bien que la négociation excessive et les problèmes du jeu soient semblables sous divers aspects, l’évaluation de comportements de négociateurs devrait prendre en compte des aspects particuliers tels que le contexte dans lequel ces comportements se manifestent (par exemple, l’état du marché). Dans l’étude, on aborde aussi la portée de futures recherches sur les comportements de négociation excessive.


2021 ◽  
Vol 0 ◽  
pp. 1-7
Author(s):  
Fahisham Taib ◽  
Khoo Teik Beng ◽  
Lee Chee Chan

Objective: Parents who have children with complex lifelong and life-limiting neurological conditions experienced many stresses and anxieties throughout their lives as caregivers. However, this information is still very limited. The study aimed to explore the challenges faced by parents with children who have complex neurological conditions, their coping strategies, needs, and expectations. Materials and Methods: A semi-structured, in-depth interviews were conducted in the either Malay or English language among the parents of children with complex lifelong neurological conditions and have been on long-term in-patient hospital care. The interviews were audio-recorded and transcribed for thematic analysis. The qualitative study was conducted from October to November 2016 at the Paediatric Institute of Hospital Kuala Lumpur. Grounded theory was used to examine the qualitative data with inductive and deductive types of coding. The transcripts were read repeatedly to allow familiarity to the themes presented by the participants. Further discussions were conducted among the researchers to triangulate the information. Results: A total of 11 parents were interviewed for this study. The thematic analysis resulted in 8 challenges: Physical wellbeing, Environment, Relationship, Financial, Occupational, Rational, Mental, and Spiritual. Coping strategies comprised problem focused issues related to the key challenges in the caregivers’ context. Similar to the needs and expectations, the key themes were derived from the key understandings of the challenges and looking at the palliative care impacts for these children. Conclusion: There are various challenges faced by parents of children with life-limiting neurological disorders. Physical, Environment, Relationship, Financial, Occupational, Rational, Mental, and Spiritual Wellbeing can be a platform for the assessment of the caregivers’ needs and the planning for palliative care support.


Author(s):  
T.S.M. Fernando ◽  
H.M.J.P. Vidanapathirana

Key populations are at the highest risk of acquiring and transmitting the Human Immuno-deficiency Virus (HIV). Due to the stigma vested upon them, they have become least accessible for preventive and curative services for HIV. Therefore, coping strategies are essential to minimize stigma to end AIDS by 2025, five years ahead of the global target of ending AIDS in 2030. The objective was to describe the coping strategies adopted by key-populations to overcome behavior-related stigma. Data from thirty-two in-depth interviews were analyzed using the thematic analysis method.


2018 ◽  
Vol 15 (4) ◽  
pp. 293-305
Author(s):  
M Anderson ◽  
MK Tulloch-Reid

Objective To determine the challenges, coping strategies and needs of urban and rural Jamaican caregivers of adolescents with diabetes, and suggest ways to assist coping. Methods This qualitative study comprised four focus groups (two urban and two rural) with a total of nineteen caregivers of adolescents with diabetes. Thematic analysis was conducted on the data. Results The main challenges caregivers faced were keeping their children healthy, managing conflict with their children, and financial concerns. They met these challenges with problem-focused and emotion-focused coping strategies. Caregivers used the problem-focused strategies of vigilance, advocacy, minimising their children’s negative emotions, coercion, education, and seeking support, and the emotion-focused strategies of relying on their identity as parents and turning to their faith. Caregivers wanted assistance acquiring medication and equipment, increased diabetes education, and support groups. Discussion More resources should be channelled toward provision of diabetes supplies. Diabetes education is necessary in schools and for the general public. Healthcare practitioners should explore issues beyond diabetes management, such as caregivers’ coping and the caregiver-child relationship. Support groups are needed to facilitate learning. Special attention must be paid to rural areas: rural residents appeared to be in greater need than their urban counterparts.


2021 ◽  
Vol 12 ◽  
Author(s):  
José Devís-Devís ◽  
José Serrano-Durá ◽  
Pere Molina

Referees are essential participants in the sport of football. They are responsible for enforcing the rules and achieving the necessary impartiality for the matches. Referees are often target of hostile reactions from fans, players, and coaches. However, few studies have focused on these experiences and the strategies they use to manage them. In order to fill this gap, a qualitative interview-based study was developed to explore the experiences of a group of football referees (four males and four females) on aggression, violence, and coping. A thematic analysis was developed combining inductive and deductive processes. Results indicated that the most frequent aggressions experienced were verbal abuse. Most of the aggressions from spectators were of a sexist nature. When aggressions were considered normal by referees, symbolic violence emerged. Racist aggressions were directed to the two Moroccan participants. Problem and emotional-focused coping strategies were identified. The two most common referee responses to coaches’ and players’ verbal abuse were penalties and send-off calls. Smiling and not considering insults as a personal matter were two emotional-focused coping strategies used toward spectator aggressions. Implications for the referees’ job and well-being as well as the quality of football competitions were highlighted to reduce aggressions and violence and to help referees to cope with hostile behaviors.


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