scholarly journals Promoting the health and well being of older carers: A proactive strategy

2003 ◽  
Vol 26 (2) ◽  
pp. 78 ◽  
Author(s):  
Bev O'Connell ◽  
Susan Bailey ◽  
Arlene Walker
Keyword(s):  
Health Care ◽  
Health Care Professionals ◽  
Well Being ◽  
Care Recipient ◽  
Health Care Needs ◽  
Physical And Mental Health ◽  
Care Needs ◽  
Health Related ◽  
Mental And Physical Health ◽  
Health And Well Being

Research has indicated that carers are concerned about their ageing status, their deteriorating health and their abilityto continue to care for their dependants. Given that the health care system will become increasingly reliant on carersthe health care needs of carers should be a concern for all health care professionals. This paper describes the first stageof a project designed to enhance older carers health promotion knowledge and skills and improve their healthpromoting behaviors. This stage investigated the mental and physical health status of older carers. It also soughtinformation on older carers' levels of participation in health related and social activities and identification of barriersto participation in these types of activities. The results highlighted that carers responding to the survey experiencedcompromised physical and mental health. Many carers reported being unable to participate in social and health-typeactivities as they were unable to leave the care recipient. Of note, is that carers identified their own mental fragilityand felt they needed further emotional support.

scholarly journals HEALTH IMPLICATIONS OF SOCIAL ROLES AND ROLE TRANSITIONS IN MIDLIFE AND LATER LIFE

2019 ◽  
Vol 3 (Supplement_1) ◽  
pp. S797-S797
Author(s):  
Kelly E Cichy ◽  
Athena Koumoutzis
Keyword(s):  
Racial Differences ◽  
Social Roles ◽  
Later Life ◽  
Well Being ◽  
Care Recipient ◽  
Physical And Mental Health ◽  
Care Needs ◽  
Social Trends ◽  
Care Recipients ◽  
Health And Well Being

Abstract Demographic and social trends shape the timing, nature, and implications of social roles and transitions. With increased life expectancy and a changing world, expectations for work and retirement and the need for informal and formal caregiving continue to evolve. Families are also more heterogeneous and the population is becoming increasingly more racially/ethnically diverse. These changes underscore the need for research that focuses on the varied social roles individuals occupy in midlife and later adulthood and the implications of these roles for health and well-being. The current symposium features research that explores multiple roles, including romantic partner, grandparent, and employee/retiree, caregiver/care recipient while attending to individual differences in how these roles and transitions are associated with physical and mental health outcomes. Garcia, Donnelly, and Umberson utilize dyadic diary data from midlife men and women in gay, lesbian, and heterosexual marriages to consider how exposure and reactivity to daily stress varies across union types. Rickenbach and colleagues examine longitudinal changes in health and well-being associated with being a caregiving and non-caregiving grandparent. Cichy and Koumoutzis examine racial differences in the associations between providing care to a spouse/parent and daily health and well-being among African Americans and European Americans. Savla, Roberto, and Sands classify community-living older adults based on their care needs while considering the type of care they receive, predictors of this care, and its implications for care recipients’ health. Finally, Stawski and colleagues examine how mental, physical, and cognitive health change as a function of the transition to and through retirement.

A concept analysis of children’s agency within the health literature

2016 ◽  
Vol 20 (4) ◽  
pp. 503-511 ◽  
Author(s):  
Marjorie Montreuil ◽  
Franco A Carnevale
Keyword(s):  
Health Care ◽  
Health Care Needs ◽  
Social Worlds ◽  
Care Needs ◽  
Research And Practice ◽  
Related Literature ◽  
Health Literature ◽  
Children’S Agency ◽  
Health Related ◽  
Legal Contexts

The capacity of children to act as agents is being increasingly recognized and has important implications for health research and practice. However, there are various discrepancies in how children’s agency is defined in the literature. The aim of this analysis was to examine the concept of children’s agency within the health-related literature, using Rodgers evolutionary method. The following questions were addressed: How did the concept of agency become associated with children in the health-related literature? What are the sociocultural and legal contexts that surround the concept of children’s agency? What is the meaning of children’s agency? Forty-five articles were included in the analysis. An inductive approach was used to identify the attributes of children’s agency as well as the temporal, disciplinary, and paradigmatic trends in its conceptualization. The concept of children’s agency first appeared in the health literature in the 1980s and was defined as an ability children could gradually develop. Later on, children’s agency was used to refer to the capacity of all children to influence their own and others’ health-care needs and is now increasingly used to refer to children as active agents who reflect on and construct their social worlds.

scholarly journals How Can Psychologists and Psychiatrists Help COVID-19 Bereaved Persons: Five propositions to Understanding Contextual Challenges

2020 ◽  
Vol 20 (2) ◽  
pp. 121-128
Author(s):  
Cyrille Kossigan KOKOU-KPOLOU ◽  
Jude Mary CENAT ◽  
María Nieves PEREZ-MARFIL ◽  
Manuel FERNANDEZ-ALCANTARA
Keyword(s):  
Health Care ◽  
Health Care Professionals ◽  
Social Inequalities ◽  
Global Perspective ◽  
Health Care Needs ◽  
Care Needs ◽  
Therapeutic Alliances ◽  
Dsm 5 ◽  
Health Measures ◽  
Online Platforms

The COVID-19 pandemic is causing unprecedented cumulative deaths and leaving behind millions of bereaved families and individuals. Moreover, the pandemic is disrupting social fabrics in the conventional way we mourn our deads. In this context therefore, how can psychologists, psychiatrists and other health care professionals help bereaved families and individuals more effectively? This opinion paper proposed five recommendations that cover mental health care needs and challenges which may emerge from the management of these traumatic deaths. In all, efforts to comply with either DSM-5 or ICD-11 PGD guidelines could help COVID-19 bereaved persons with overwhelming distress, as they ensure therapists' use of appropriate terminologies in therapeutic alliances. However, clinicians need to have a global perspective of COVID-19 bereavement courses, political and public health measures due to the pandemic, and flexible attitudes about the ICD-11 and of DSM-5 time-criterion for diagnosis. This paper emphasizes the importance of social and collective recognition of COVID-19 deaths through various symbolic and materialized forms to free up collective and individual capacities for resilience. The necessity of individual and group interventions through online platforms is underscored, however these modes of therapies may not reinforce social inequalities by excluding bereaved individuals who really need them.

scholarly journals In What Ways Does Health Related Stigma Affect Sustainable Employment and Well-Being at Work? A Systematic Review

2021 ◽  
Author(s):  
I. E. van Beukering ◽  
S. J. C. Smits ◽  
K. M. E. Janssens ◽  
R. I. Bogaers ◽  
M. C. W. Joosen ◽  
...  
Keyword(s):  
Systematic Review ◽  
Health Care ◽  
Health Care Professionals ◽  
People With Disabilities ◽  
Well Being ◽  
Screening Process ◽  
Related Stigma ◽  
Health Related ◽  
Sustainable Employment ◽  
Anticipated Stigma

Abstract Purpose Studies are increasingly showing that health related stigma is a barrier to employment, but it is not known how. The aim of this systematic review is to identify, appraise and analyse studies that have directly or indirectly addressed ways in which stigma affects sustainable employment and well-being at work of people with disabilities. Methods Using a multiphase screening process, this review is based on a comprehensive literature search (2000–2019) carried out in six electronic databases: Embase, Web of Science, Medline Ovid, Cochrane CENTRAL, PsycINFO and Google Scholar. Results 7.263 publications were identified; 96 studies were found eligible to be included in the review. 72% of the studies were conducted in North America or Europe. Few studies directly assessed how stigma affects the employment of people with disabilities. Most studies highlighted that attitudes and behaviour of employers formed a barrier to employment, as well as anticipated stigma and self-stigma in people with health problems. However, the findings also showed that the attitudes and behaviour of co-workers, health care professionals, reintegration professionals, customers, and family and friends could act as a barrier to employment although these influences are under-researched. Although many similarities were seen in the relevant findings of studies about both physical and mental disabilities, several nuances were found. Conclusion Stigma hampers sustainable employment and well-being in multiple ways. Whereas the number of publications on this topic is rapidly increasing, the roles of health care professionals, reintegration professionals, co-workers, customers, and family and friends particularly warrant more attention.

Effects of Mindful Self-Compassion Training on Increasing Self-Compassion in Health Care Professionals

2021 ◽  
Vol 75 (Supplement_2) ◽  
pp. 7512515315p1-7512515315p1
Author(s):  
Susan M. Knier ◽  
Julie L. Watson ◽  
Jennifer O’Connor Duffy
Keyword(s):  
Health Care ◽  
Health Care Professionals ◽  
Well Being ◽  
Self Compassion ◽  
The Impact ◽  
Health And Well Being ◽  
Primary Author

Abstract Date Presented 04/22/21 Health care professionals are vulnerable to stress overload and risks that threaten health and well-being. This study investigated the impact of mindful self-compassion (MSC) training on people working in health care. Overall, self-compassion and subscale scores showed significant improvement. Participants indicated that self-compassion and positive mind states were integrated into their lives. OTs could assimilate MSC as an adjunct approach for their clients and their selves. Primary Author and Speaker: Susan M. Knier

Exploring Rehabilitation and Wellness Needs of People with MS Living in South Florida: A Pilot Study

2004 ◽  
Vol 6 (1) ◽  
pp. 26-31 ◽  
Author(s):  
Sherrilene Classen ◽  
Jennie Q. Lou
Keyword(s):  
Health Care ◽  
Health Care Professionals ◽  
South Florida ◽  
The Self ◽  
Health Care Needs ◽  
Care Needs ◽  
Client Experience ◽  
Qualitative Research Design ◽  
Illness Experiences ◽  
Client Expectations

Multiple sclerosis is a neurological disorder with an unpredictable course that affects each person uniquely. Health care professionals must understand the illness experiences of clients with MS and their health care needs before planning interventions. This study illustrates the process of exploring the rehabilitation and wellness needs of people with MS through a qualitative research design utilizing a focus group. Through content analysis we established three central themes from the data: client experience, client perceived concerns and needs, and client expectations. The self-reflections of people with MS in South Florida enhanced our understanding of their illness experiences and health care needs.

scholarly journals “A prison with extra flavours”: experiences of immigrants in Swedish immigration detention centres

2015 ◽  
Vol 11 (2) ◽  
pp. 73-85 ◽  
Author(s):  
Soorej Jose Puthoopparambil ◽  
Beth Maina Ahlberg ◽  
Magdalena Bjerneld
Keyword(s):  
Health Care ◽  
Health Care Professionals ◽  
Health Care Services ◽  
Well Being ◽  
Structured Interviews ◽  
Immigration Detention ◽  
Content Type ◽  
Care Services ◽  
Lack Of Control ◽  
Health And Well Being

Purpose – The immigration detention environment largely influences the health and well-being of detainees by either aggravating medical conditions or contributing to new illness. There is limited research on how detainees experience and try to cope with this environment. The purpose of this paper is to describe experiences of detainees in Swedish immigration detention centres. Design/methodology/approach – Semi-structured interviews were conducted in three detention centres with a total of 21 detainees who had been detained for at least two weeks. Interview transcripts were analysed using thematic analysis. Findings – The detainees likened immigration detention to imprisonment. They experienced lack of control over their life situation mainly through arbitrary restrictions and lack of proper response from authorities making it appear futile to seek help. This perceived lack of control forced them into passivity. Differences in amenities provided in the centres were observed and some of these were reported to assist in making detention more bearable. Research limitations/implications – This study provides only one stakeholder perspective. The perspectives of other stakeholders, such as detention staff, health care professionals and volunteers must be explored to improve understanding and mitigate the effects of detention. Originality/value – Irrespective of the better standards of detention in Sweden, the detainees considered detention as imprisonment affecting their health and well-being. If states deem detention to be necessary, improved staff-detainee interaction should be ensured through proper staff training, arbitrary restrictions within detention should be avoided and health care services should be improved.

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