Food First: Nutrition as the Foundation for Health

2015 ◽  
Vol 21 (4) ◽  
pp. 213-221 ◽  
Author(s):  
Laura Sandquist
Keyword(s):  
Health Care Professionals ◽  
Well Being ◽  
The Body ◽  
Biological Functions ◽  
Gastrointestinal Dysfunction ◽  
Physiological Processes ◽  
Novel Approach ◽  
Whole Person ◽  
Whole Systems ◽  
Health And Well Being

The principles of integrative nursing advocate that food be considered as a primary intervention for health promotion, risk reduction, and generally improved well-being. Food provides information to the body, signaling basic biological functions and normalizing physiological processes. Health care professionals should query patients about their nutritional intake, recognizing that adjustments in the types of foods consumed can often address long-standing symptoms that create distress, including pain, fatigue, anxiety, and gastrointestinal dysfunction. A Food First approach to care offers a novel approach that champions whole person/whole systems emergent health and well-being.

Whole-Systems Healing

2014 ◽  
pp. 47-55 ◽  
Author(s):  
Mary Jo Kreitzer ◽  
Jayne Felgen ◽  
Patricia A. Roach
Keyword(s):  
Systems Approach ◽  
World View ◽  
Well Being ◽  
Complexity Science ◽  
Whole Person ◽  
Adaptive Action ◽  
Systems Leadership ◽  
Whole Systems ◽  
Deep Listening ◽  
Health And Well Being

Integrative nursing embodies a whole person/whole systems approach to advancing the health and well-being of people, organizations, communities and the environment. It is based on a whole systems world view, an approach that recognizes that a change in any part of the systems causes a change in the whole system. Whole systems thinking and leadership draws from concepts and principles of complexity science, social networks, social change and gentle action. Whole systems leadership embodies competencies of deep listening, awareness of systems, awareness of self, seeking diverse perspectives, suspending certainty and embracing uncertainty, and taking adaptive action.

scholarly journals Transition from Emotional to Rational Advertising for Food Products on the Romanian Market

2017 ◽  
Vol 50 (1) ◽  
pp. 101-108
Author(s):  
A.F. Jităreanu ◽  
Elena Leonte ◽  
A. Chiran ◽  
Benedicta Drobotă
Keyword(s):  
Urban Areas ◽  
Eating Habits ◽  
Well Being ◽  
Point Of View ◽  
The Body ◽  
Positive Effects ◽  
New Methods ◽  
Brand Advertising ◽  
Tangible Evidence ◽  
Health And Well Being

Abstract Advertising helps to establish a set of assumptions that the consumer will bring to all other aspects of their engagement with a given brand. Advertising provides tangible evidence of the financial credibility and competitive presence of an organization. Persuasion is becoming more important in advertising. In marketing, persuasive advertising acts to establish wants/motivations and beliefs/attitudes by helping to formulate a conception of the brand as being one which people like those in the target audience would or should prefer. Considering the changes in lifestyle and eating habits of a significant part of the population in urban areas in Romania, the paper aims to analyse how brands manage to differentiate themselves from competitors, to reposition themselves on the market and influence consumers, meeting their increasingly varied needs. Food brands on the Romanian market are trying, lately, to identify new methods of differentiation and new benefits for their buyers. Given that more and more consumers are becoming increasingly concerned about what they eat and the products’ health effects, brands struggle to highlight the fact that their products offer real benefits for the body. The advertisements have become more diversified and underline the positive effects, from the health and well - being point of view, that those foods offer (no additives and preservatives, use of natural ingredients, various vitamins and minerals or the fact that they are dietary). Advertising messages’ diversification is obvious on the Romanian market, in the context of an increasing concern of the population for the growing level of information of some major consumer segments.

scholarly journals Psychological Consequences of the Delay in the Silent Mentor Programme During the COVID-19 Pandemic: Perspectives From Family Members of Silent Mentors

2021 ◽  
pp. 003022282110009
Author(s):  
Li Ping Wong ◽  
Sik Loo Tan ◽  
Haridah Alias ◽  
Thiam Eng Sia ◽  
Aik Saw
Keyword(s):  
Mental Health ◽  
Qualitative Interviews ◽  
Psychological Impact ◽  
Family Members ◽  
Well Being ◽  
The Body ◽  
Functional Health ◽  
Psychological Consequences ◽  
Negative Effect ◽  
Health And Well Being

The COVID-19 pandemic has put a hold on the Silent Mentor Programme (SMP); this pause has not only caused unprecedented challenges for the delivery of medical education but has forced changes in the programme ceremony sessions. We aimed to describe the psychological impact and experiences of family members of silent mentors during the COVID-19 pandemic using qualitative interviews. Many expressed feelings of remorse and unrest about the unprecedented delay of the SMP. The delay increased negative emotions particularly among some elderly family members; however, there was no prominent negative effect on their functional health and well-being. Several participants relayed the belief that the soul cannot rest until the body receives a proper burial while some worried about the deterioration of the physical condition of the mentors. In conclusion, findings provide insights into the importance of not overlooking the mental health implications of delaying the SMP in future outbreaks or crises.

scholarly journals New Frontiers in Caregiving Research: Biopsychosocial Perspectives and Interventions

2020 ◽  
Vol 4 (Supplement_1) ◽  
pp. 615-615
Author(s):  
Jyoti Savla ◽  
Karen Roberto ◽  
Mamta Sapra
Keyword(s):  
Family Caregivers ◽  
Memory Loss ◽  
Well Being ◽  
Psychoeducational Intervention ◽  
Loved One ◽  
Daily Diary Study ◽  
Physiological Processes ◽  
And Coping ◽  
With Memory ◽  
Health And Well Being

Abstract Although families embrace the opportunity to care for a loved one, caregiving is stressful and takes a toll on the caregiver’s health and well-being. Earlier studies of stress and coping among family caregivers focused on psychological outcomes and emotional well-being. In the last decade, stress researchers have broadened their focus to include biomarkers and health outcomes. Data from two studies of caregivers of persons with memory loss will be used to discuss two new frontiers of caregiving research. First, a daily-diary study will be used to identify the mechanism by which stress disrupts the physiological processes and proliferates into serious psychopathology and pre-clinical and clinical health conditions. Second, a mindfulness-based psychoeducational intervention study will be utilized to identify malleable factors that can be harnessed to lower stress and improve the well-being of family caregivers. Next steps for caregiving research in the context of demographic and technological trends will be discussed.

scholarly journals ‘The fact that she just looked at me…’ – Narrations on shame in South African workplaces

2017 ◽  
Vol 43 (0) ◽  
Author(s):  
Claude-Hélène Mayer ◽  
Rian Viviers ◽  
Louise Tonelli
Keyword(s):  
Mental Health ◽  
Higher Education ◽  
South African ◽  
Well Being ◽  
The Body ◽  
Theory And Practice ◽  
Work Context ◽  
Negative Effects ◽  
Managerial Implications ◽  
Health And Well Being

Orientation: Shame has been internationally researched in various cultural and societal contexts as well as across cultures in the workplace, schools and institutions of higher education. It is an emotional signal that refers to experienced incongruence of identity goals and the judgement of others.Research purpose: The purpose of this study was to focus on experiences of shame in the South African (SA) workplace, to provide emic, in-depth insights into the experiences of shame of employees.Motivation for the study: Shame in the workplace often occurs and might impact negatively on mental health and well-being, capability, freedom and human rights. This article aims at gaining some in-depth understanding of shame experiences in SA workplaces. Building on this understanding the aim is to develop awareness in Industrial and Organisational Psychologists (IOPs), employees and organisations to cope with shame constructively in addition to add to the apparent void in the body of knowledge on shame in SA workplaces.Research design, approach and method: An interpretative hermeneutical research paradigm, based on Dilthey’s modern hermeneutics was applied. Data were collected through semistructured interviews of 11 employees narrating their experiences from various workplaces, including the military, consulting organisations and higher education institutions. Content analysis was used for data analysis and interpretation.Main findings: The major themes around which shameful experiences evolved included loss of face, mistreatment by others, low work quality, exclusion, lifestyle and internalised shame on failure in the workplace. Shame is experienced as a disturbing emotion that impacts negatively on the self within the work context. It is also experienced as reducing mental health and well-being at work.Practical/managerial implications: SA organisations need to be more aware of shame in the workplace, to address the potential negative effects of shame on employees, particularly if they are not prepared to reframe shame into a constructively and positively used emotion. Safe spaces should be made available to talk about shame. Strategies should be applied to deal with shame constructively.Contribution/value-add: This article expands an in-depth understanding of shame from emic and culture-specific perspectives within SA workplaces. The findings are beneficial to IOPs and organisations to understand what shame is from the perspective of SA employees across cultural groups. The article thereby adds value to theory and practice, offering IOPs a deeper understanding of shame in the work context.

scholarly journals As Representações Sociais da Dança: um Mergulho no Universo dos Estudantes de Bacharelado em Educação Física

2021 ◽  
Vol 22 (2) ◽  
pp. 231-235
Author(s):  
Felipe da Silva Triani ◽  
Glhevysson dos Santos Barros
Keyword(s):  
Social Representations ◽  
Free Association ◽  
Well Being ◽  
Bachelor's Degree ◽  
Social Representation ◽  
The Body ◽  
Rhythmic Movements ◽  
Technical Procedure ◽  
The Social ◽  
Health And Well Being

ResumoA dança é a arte de movimentar expressivamente o corpo seguindo movimentos ritmados, em geral ao som de música. Dessa forma, o significado da dança vai além da expressão artística, podendo ser vista como um meio para adquirir conhecimentos ou como opção de lazer. No campo de atuação do bacharelado, as investigações acadêmicas ainda são tímidas, urgindo de produções científicas que possam alimentar o campo científico sobre o tema. Dessa forma, o objetivo do estudo foi identificar e analisar as representações sociais que um grupo de bacharelandos do curso em Educação Física compartilha sobre a dança. A metodologia da pesquisa envolve uma abordagem qualitativa, tendo o estudo de campo como procedimento técnico. A amostra foi constituída por 200 indivíduos, sendo 85 homens e 115 mulheres com médias de idade entre 17 a 45 anos. A coleta de dados ocorreu através de questionário com associação livre de palavras, cujo termo indutor foi ”dança”. A análise foi feita por meio dos conteúdos das respostas. O resultado principal do estudo apontou que a maioria dos estudantes emprega sentido de dança como uma atividade técnica e a associam com saúde mental e bem-estar. Palavras-chave: Representação Social. Educação Física. Dança. AbstractDance is the art of expressively moving the body following rhythmic movements, usually to the sound of music. Thus, the meaning of dance goes beyond artistic expression, and can be seen as a means to acquire knowledge or as a leisure option. In the field of performance of the bachelor's degree, academic investigations are still timid, urging scientific productions that can feed the scientific field on the theme. Thus, the objective of the study was to identify and analyze the social representations that a group of Physical Education course bachelors shares about dance. The research methodology is a qualitative approach, with the field study as a technical procedure. The sample consisted of 200 individuals, 85 men and 115 women with a mean age between 17 and 45 years. Data collection was carried out through a questionnaire with free association of words, whose inducing term was, "dance". The analysis was done through the responses content. The main result of the study pointed out that most students use dance as a technical activity and associate it with mental health and well-being. Keywords: Social Representation. PE. Dance.

scholarly journals Team Focus: Occupational Therapist

2008 ◽  
Vol 10 (3) ◽  
pp. 94-98
Author(s):  
Susan J. Forwell ◽  
Kathleen M. Zackowski
Keyword(s):  
Occupational Therapy ◽  
Health Care Professionals ◽  
Occupational Therapists ◽  
Well Being ◽  
Therapy Process ◽  
Functional Difficulties ◽  
Care And Support ◽  
Symptomatic Management ◽  
Home Work ◽  
Health And Well Being

Occupational therapists (OTs) have a unique and valued role in the health and functional recovery of individuals with multiple sclerosis (MS). To maximize the benefit of occupational therapy by both health care professionals who refer patients and the patients who use the services, an understanding of the scope of services that OTs offer is essential. This article describes the breadth of the OT evaluation and intervention specific to the treatment of individuals who have MS. As an overriding goal, the OT assists clients in processing the implications of physical, cognitive, and emotional changes and creatively developing strategies to cope with and, when appropriate, minimize the effects of these changes. The occupational therapy process is described, beginning with evaluation and providing guidelines and resources for appropriate client-centered goal setting. The OT and client then discuss intervention that ensures optimal functional outcome and includes symptomatic management, according to the specific functional difficulties and implications and the particular symptoms of each patient. Through discussion, the OT helps each client achieve health and well-being with remedial and compensatory techniques that enable participation in meaningful activities and roles in the home, work, and community. OT services are essential to the appropriate and optimal delivery of comprehensive care and support to individuals with MS.

Perception, Expression, and Social Function of Pain: A Human Ethological View

1995 ◽  
Vol 8 (1) ◽  
pp. 31-46 ◽  
Author(s):  
Wulf Schiefenhövel
Keyword(s):  
Evolutionary Biology ◽  
Well Being ◽  
Building Blocks ◽  
Field Work ◽  
The Body ◽  
Human Interaction ◽  
Small Children ◽  
Body Postures ◽  
Culture Independent ◽  
Health And Well Being

The ArgumentPain has important biomedical socioanthropological, semiotic, and other facets. In this contribution pain and the experssion of pain are looked at from the perspective of evolutionary biology, utilizing, among others, cross-cultural data from field work in Melanesia.No other being cares for sick and suffering conspecifics in the way humans do. Notwithstanding aggression and neglect, common in all cultures, human societies can be characterized as empathic, comforting, and promoting the health and well-being of their members. One important stimulus triggering this caring response in others is the expression of pain. The nonverbal channel of communication, particularly certain universal — i.e., culture-independent facial expressions, gestures, and body postures, convey much of the message from the painstricken person to the group.These behaviors signal the person's physical and psychical pain, sadness, grief, and despair in ways very similar to the signs given by infants and small children: the body loses tonus and sinks or drops to the ground, the gestures are those of helplessness. Pain and grief may be so strong that control is lost not only over the body's posture but also over the mind's awareness. In such cases the afflicted person may carry out actions endangering himself or others. In general, these behavior patterns resemble those of infants in situations of distress and danger, and it is not surprising that the response of the members of the group is basically parental: taking care, assisting and consoling.Perceptive and behavioral patterns which developed in the course of avian and mammalian phylogeny to serve the well-being of the young have proven, as was shown by Eibl-Eibesfeldt (1989), to be powerful building blocks for actions in other spheres of human interaction. Love is one such field, the reactions to a conspecific suffering pain is another.

Subcutaneous Immunoglobulin Substitutions in Previously Untreated (PUPs) and Treated Patients (PTPs) Result in Rapid Improvement of Total and Serum IgG Levels - a Novel Substitution Protocol for PUPs.

Blood ◽  
2004 ◽  
Vol 104 (11) ◽  
pp. 3832-3832
Author(s):  
Christoph Königs ◽  
Dominik Dunsch ◽  
Richard Linde ◽  
Thomas Klingebiel ◽  
Wolfhart Kreuz
Keyword(s):  
Outpatient Clinic ◽  
Well Being ◽  
Igg Subclasses ◽  
The Body ◽  
Loading Dose ◽  
Therapeutic Concept ◽  
Cell Counts ◽  
Serum Igg ◽  
Novel Approach ◽  
Trough Levels

Abstract In primary immunodeficiencies the substitution of human immunoglobulins (Ig) is a major therapeutic concept. In Germany, Ig substitutions relied on various Ig formulations for intravenous (iv) substitutions. From December 2002 Ig preparations for subcutaneous (sc) home treatment were licensed in Germany. In the Frankfurt cohort several PID PTPs decided to switch from intravenous therapy (ivIg) in our outpatient clinic to subcutaneous infusions (scIg) at home. For PUPs current protocols suggest an iv loading dose prior to scIg or daily scIg infusions for one week. In a Pediatric cohort, daily infusions seem not feasible, therefore a novel approach was developed to rapidly achieve sufficient IgG levels sparing an iv loading dose and daily infusions. In a longitudinal analysis, immune parameters were monitored for PTPs changed to scIg and PUPs starting on scIg primarily. In a prospective study we report about 12 patients at the age of 14 to 58 years that have been switched to or were started on scIg. These are pediatric as well as adult patients. Their conditions include IgG2-IgA deficiencies, IgG3 deficiency, CVID, hypo- and agammaglobulinemia. Trough levels of total IgG, IgG subclasses, markers of infection and white blood cell counts were monitored under ivIg for at least one year prior to changing to scIg for PTPs retrospectively. Identical parameters have been monitored for 3 to 16 months since the start of scIg prospectively. Monitoring also included the history of any infections, general well-being and the body weight. For all patients the monthly scIg dose was identical to the respective ivIg dose at the time of switching therapy (200-400mg/kg bw). For PUPs a protocol of infusions on every other day was established changing to weekly intervals when sufficient IgG levels were achieved. The scIg infusions were well tolerated by all patients besides initial local swelling and slight pain on the following day. Before starting home therapy, patients were trained for a period of 4 weeks and were able to safely perform infusions. For PTPs, after switching to scIg the IgG trough levels increased. Also serum IgG subclasses increased and reached physiological levels in all subclasses. Patients that did not have a sufficient amount of IgG of any subclasses under ivIg reached normal levels after scIg was initiated within a maximum of 6 weeks (average of 3,5 weeks). We saw a tendency to a decrease in the frequency of infections. For PUPs, patients with subclass deficiencies reached normal IgG levels in total and in the respective subclasses after 2 to 3 infusions. A PUP with CVID needed 4 infusions (1 week) to achieve sufficient levels to change to weekly infusions. In summary at the Frankfurt immunodeficiency outpatient clinic switching from ivIg to self-administered scIg was well tolerated. In all PTPs higher IgG trough levels were reached with the same amount of substituted IgG. Patients with subclass deficiencies under ivIg reached physiological levels after changing to scIg. For PUPs a novel protocol was established with infusions on every second day for one week to achieve sufficient IgG levels without iv loading dose. In comparison to established protocols, this novel approach spares daily visits and infusions. Additionally this prevents injections into still painful tissues, which is highly relevant especially for the treatment and adherence of pediatric patients.

scholarly journals Improving access to a multi-component intervention for caregivers and people with dementia

Dementia ◽  
2016 ◽  
Vol 18 (1) ◽  
pp. 347-359 ◽  
Author(s):  
Maarten Milders ◽  
Stephen Bell ◽  
Angus Lorimer ◽  
Heather Jackson ◽  
Paul McNamee
Keyword(s):  
Health Care Professionals ◽  
Cost Effective ◽  
Well Being ◽  
Pharmacological Interventions ◽  
Sense Of Competence ◽  
Support Organizations ◽  
People With Dementia ◽  
Novel Approach ◽  
Present Part ◽  
Intervention Costs

Due to the increasing social and economic costs of dementia, there are urgent calls to develop accessible and sustainable care for people with dementia and their caregivers. Multi-component non-pharmacological interventions (NPIs) appear effective in improving or maintaining daily functioning and well-being, but are typically labour-intensive for health care professionals, thus hindering access. The current study aimed to explore the feasibility and acceptability of a novel approach to widen access to NPI by involving caregivers to present part of the intervention and with staff from local support organizations instructed to train the caregivers. Trainers and caregivers were shown to comply with training instructions and the direct intervention costs were low. Feedback from trainers and caregivers was positive and well-being ratings from people with dementia and caregivers remained stable over time and caregivers’ sense of competence improved. The findings suggest that involving caregivers and trained non-professionals to provide the intervention is feasible and acceptable and could be a cost-effective solution to improve access to care.

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