Meaning Making in Wartime Bereavement: Lessons Learned From Bereaved Parents and Siblings

2016 ◽  
Vol 76 (2) ◽  
pp. 103-121 ◽  
Author(s):  
Christina Harrington

Wartime deaths are traumatic and leave many grieving families in their wake. Yet, the unique, nuanced bereavement needs and experiences of those who remain are largely unknown. This Canadian, qualitative study examined the bereavement experiences of family of origin, bereaved during the mission to Afghanistan. The findings provide rich data on the predominant ways in which family members found and made meaning following the death and the ways in which military culture influenced the meanings made.

2019 ◽  
Author(s):  
Marcela D. Rodríguez ◽  
Juan-Pablo Garcia-Vazquez ◽  
Angel G. Andrade

BACKGROUND The most common reasons for the lack of adherence among older adults is the forgetfulness due to the multiple cognitive processes associated with prospective memory involved in remembering to follow a medication regimen. Problems with prospective memory increase the demands for care. Therefore, family members play an essential role in supporting patients in activities that involve: helping with medication adherence, transmitting knowledge about medications, and helping to refill their prescriptions. To address some of these medication problems, we designed a Medication Ambient Display (MAD) to support education, motivation, and measurement of medication-taking behaviors in older adults. The functionality of MAD consists of providing external cues to convey information through abstract and stylized representations of older adults’ medication adherence. Specifically, MAD is placed as a portrait in the elderly’s home. It shows a virtual birdcage to raise elders’ consciousness about their responsibility for caring for their health, in a similar way that they gladly take care of their pets OBJECTIVE This study aimed to assess the effect of MAD’s external cues on the involvement of family members in the management of medications for the elderly. METHODS We conducted a qualitative study consisting of semi-structured interviews with older adults and their relatives identified as informal caregivers. The study lasted ten (10) weeks. We visited participants weekly to collect data about: older adults’ medication problems, help received, and their perception about older adults’ medication adherence. The first five (5) weeks of the study was used to establish baseline data to understand the involvement of relatives on medication management activities. Afterward, we introduced MAD to be used for the successive five (5) weeks. RESULTS We found that new patterns of interaction among older adults and their relatives arose while using MAD. Participants perceived that MAD reinforced the care functions of family caregivers. For instance, it made them aware of older adults' medication adherence and encouraged youngest family members to help older adults. CONCLUSIONS We identified that the external cues provided through ambient displays did not overwhelm family members, but motivated their social connectedness with older adults. We conclude this paper with a set of lessons learned from this qualitative assessment, which may help designers to develop assistive technology for older adults.


BMJ Open ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. e049734
Author(s):  
Katya Galactionova ◽  
Maitreyi Sahu ◽  
Samuel Paul Gideon ◽  
Saravanakumar Puthupalayam Kaliappan ◽  
Chloe Morozoff ◽  
...  

ObjectiveTo present a costing study integrated within the DeWorm3 multi-country field trial of community-wide mass drug administration (cMDA) for elimination of soil-transmitted helminths.DesignTailored data collection instruments covering resource use, expenditure and operational details were developed for each site. These were populated alongside field activities by on-site staff. Data quality control and validation processes were established. Programmed routines were used to clean, standardise and analyse data to derive costs of cMDA and supportive activities.SettingField site and collaborating research institutions.Primary and secondary outcome measuresA strategy for costing interventions in parallel with field activities was discussed. Interim estimates of cMDA costs obtained with the strategy were presented for one of the trial sites.ResultsThe study demonstrated that it was both feasible and advantageous to collect data alongside field activities. Practical decisions on implementing the strategy and the trade-offs involved varied by site; trialists and local partners were key to tailoring data collection to the technical and operational realities in the field. The strategy capitalised on the established processes for routine financial reporting at sites, benefitted from high recall and gathered operational insight that facilitated interpretation of the estimates derived. The methodology produced granular costs that aligned with the literature and allowed exploration of relevant scenarios. In the first year of the trial, net of drugs, the incremental financial cost of extending deworming of school-aged children to the whole community in India site averaged US$1.14 (USD, 2018) per person per round. A hypothesised at-scale routine implementation scenario yielded a much lower estimate of US$0.11 per person treated per round.ConclusionsWe showed that costing interventions alongside field activities offers unique opportunities for collecting rich data to inform policy toward optimising health interventions and for facilitating transfer of economic evidence from the field to the programme.Trial registration numberNCT03014167; Pre-results.


Author(s):  
Courtney Brown ◽  
Katharine J. Head ◽  
Jane Hartsock ◽  
Katelyn Burns ◽  
Theodore E. Wilson ◽  
...  

2009 ◽  
Vol 25 (4) ◽  
pp. 190-198 ◽  
Author(s):  
Kristin Dahle Olsen ◽  
Elin Dysvik ◽  
Britt Sætre Hansen

2020 ◽  
pp. 250-262
Author(s):  
Adelina Ruiz-Guerrero

The coronavirus pandemic has without a doubt had an enormous impact on every possible way of our lives. We have felt its effects on an individual personal level and as family members, at work, as members of a community, and particularly as students and teachers. Even in institutions and departments such as ours where online education has been at the forefront of our work for years now, the challenge to survive a fully virtual new reality has left us with a lot of lessons learned and has opened doors to more opportunities for growth. For years now, the Language Department at ITESO has had its language courses in LMS platforms and has offered courses in blended and fully virtual options alongside face-to-face classes. In the English Certificate Programme, we have regular teletandem sessions with universities in other countries. The Language Hub, our self-access centre, offers writing support through an emailing writing desk service and we run virtual conversation clubs on Zoom alongside face-to-face sessions. We are certainly no strangers to online work, but up until now, that was just an option both students and teachers could consider. As of March, this year, our whole university had to move to online classes and the services of our self-access centre had to be adapted to virtual options as well. This report presents our answer to the questions posed by SISAL for this open call to the special issue on how we have lived the experience of self-access during the pandemic.


Rev Rene ◽  
2021 ◽  
Vol 22 ◽  
pp. e62550
Author(s):  
Aline Malaquias de Oliveira ◽  
Maria de Lourdes Custódio Duarte ◽  
Daniela Giotti da Silva ◽  
Larissa Gomes de Mattos

Objective: to understand family members’ perceptions of nursing care for people with psychiatric symptoms. Methods: qualitative study, with 13 family members, in five clinical inpatient units linked to the clinical nursing service of a general hospital. Data were collected through semi-structured interviews. Results: the challenges perceived by family members were turnover of professionals in the work schedules and difficulty in specialized management. The participants suggested training of the team, greater multi-professional integration, improved management and reduced turnover of professionals during care. Conclusion: family members verbalized difficulties and suggestions to support reflection on the care offered to people with psychiatric symptoms hospitalized in clinical units, in order to improve work practices and qualify care.


2012 ◽  
Vol 7 (1) ◽  
pp. 142-148
Author(s):  
Kazue Komura ◽  
Tatsuya Morita ◽  
Terukazu Akazawa ◽  
Makiko Sanjo ◽  
Satoru Tsuneto ◽  
...  

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