scholarly journals Helping Families Affected by Depression: Incorporating Prosocial and Caregiving Literature

2016 ◽  
Vol 9 (12) ◽  
pp. 23 ◽  
Author(s):  
Magdalena Cismaru ◽  
Audrey Le Pioufle

<p>In this study, we use prosocial and caregiving literature to strengthen the family section of anti-depression campaigns. We suggest that the addition of the prosocial and caregiving insights bring a new perspective on depression caregiving of family members that goes beyond a mere description of the family’s reactions and coping abilities. Built on essential components such as empathy, knowledge and skills instead of fear or anxiety, the development of a specific theoretical framework for designers of anti-depression campaigns targeting people caring for family members suffering from depression increases our understanding of family member behavior as caregivers. It provides families with a comprehensive tool that includes motivational and determining factors in one’s will and ability to deliver appropriate help in the face of family illness. Specific recommendations for designers of social marketing campaigns are provided. In addition, we exemplify how an anti-depression campaign targeting family members of depressed people is consistent with the prosocial and caregiving literature, while waiting for a formal evaluation of the effectiveness of the model presented in this article.</p>

RAINBOW ◽  
2017 ◽  
pp. 77-80
Author(s):  
Amy E. West ◽  
Sally M. Weinstein ◽  
Mani N. Pavuluri

Session 9 of the RAINBOW treatment protocol focuses on improving family problem-solving and coping (ingredient O: Oh, how do we solve this problem? of RAINBOW), and is conducted with the parent/caregiver(s), child, and siblings. It is important for all family members to have opportunities to talk about their experiences and to have that experience respected by the family. The therapist works with the family to improve interactions at home by problem-solving difficult situations and developing a family plan to minimize behavioral escalation once it occurs. In addition, the session aims to foster affiliation among family members through emphasizing shared experiences, positive feelings, and common goals.


2013 ◽  
Vol 12 (4) ◽  
pp. 317-329 ◽  
Author(s):  
Trude Aamotsmo ◽  
Kari E. Bugge

AbstractObjectives:The aim of this review was to provide a systematic overview of knowledge on how advanced cancer in a parent impacts the healthy parent's role in a family with children aged 6–12 years, and the types of help that they require in order to cope. Despite the large number of families living with a parent affected by cancer, the literature is limited concerning the needs and outcomes for the healthy parents and their need for support in managing their children's needs, when the partner is seriously ill or is in the palliative phase of cancer.Method:Comprehensive literature searches were undertaken by systematically searching for qualitative articles published during the period 1989–2009. The quality assessment was evaluated using a predefined “checklist to assess qualitative research.”Results:Seven articles met our eligibility criteria. Four distinct themes emerged that describe the healthy parent's role in the family, whose life is now characterized by uncertainty and who is attempting to maintain a balance between the needs of their children, the patient, and themselves: (1) new roles without a script, (2) attempting to maintain a safe and normal life, (3) feeling alone even within the family, and (4) support to help young family members.Significance of results:The present review provides new knowledge and insight into how healthy parents manage the challenges in parenting young children, coping with their everyday lives, and taking on new roles when their partner has advanced cancer or is dying. The healthy parent cannot balance the needs of all family members. To reach the goals of palliative care, nurses and other health professionals are encouraged to offer the patient, the healthy parent, and the children practical and emotional support.


2017 ◽  
Vol 11 (2) ◽  
pp. 91
Author(s):  
Menik Winiharti ◽  
Triana Salihah Salihah

Betawi language still exists today. It is particularly used in the suburb area of Jakarta. The typical of this language is changing the suffix /a/ to /e/, as in the words 'siape', 'di mane', 'ade ape', and 'kenape'. The emphasis of suffix /e/ in Betawi language makes this language sound louder or sharper. However, people who are unfamiliar with Betawi ethnic and its language and rarely hear the conversation in Betawinese, usually assume that Betawi language is rude. The paradigm in the society is corroborated by the use of ‘lu’ and 'gua' as the synonyms of 'you' and ‘I’ respectively. In terms of conversation in a Betawinese family, politeness plays a significant role. Every member of the family uses the strategy of politeness. The goals of this study are to find the politeness strategies used by the members of a Betawinese family in their daily conversation. It is also expected to describe the extent to which the family members apply politeness in everyday conversation. The research is conducted by observing the family members when they speak to other members. The data are analyzed based on the speaker and addressee in applying the politeness strategy. The result shows that there are four politeness strategies used: Bald on record, Off record, Positive politeness and Negative politeness. The speakers who have a higher status in the family potentially threaten the 'face' of the hearers who have a lower status. This study has also found that the selection of politeness strategies is determined by two factors; (a) the status of the family members within the family itself and (b) the intensity of inter-speaker meeting. Generally, it is proven that a Betawinese family apply politeness strategies in their daily conversation. Keywords: Politeness strategy, family member, family status, conversation 


Author(s):  
Sugeng Mashudi ◽  
Ah. Yusuf ◽  
Rika Subarniati Triyoga

Aim: This study aims to determine the effect of health services on coping mechanisms of families with schizophrenia. Methode: The sample consisted of 260 family carers of individuals with schizophrenia in Ponorogo, East Java, Indonesia. Caregivers of families completed filling in the service factor questionnaire and coping mechanism questionnaire. Results: Community Value for Service Factor 0.662 and Family Coping 0.670 which means valid and strong. Community Value for Service Factor 0.853 and Family Coping 0.800 means Reliability. T-Statistics value of 0.205, which means there is an influence between service factors on family coping. Conclusiaon: Research on improving health services for coping mechanisms in family members of individuals with schizophrenia will help design interventions to improve coping mechanisms.


2020 ◽  
Vol 16 (1) ◽  
pp. 100-118
Author(s):  
Żaneta Nieckarz

The article focuses on the situation of a child in a family with the drinking problem and describes the concept of family dysfunctionality resulting from the emergence of such problem. It also highlights the family functioning system. Furthermore, it presents an analysis of the roles performed in a dysfunctional family taking into account the spheres of activity of family members. In the face of the adopted facts, assistance and support in getting out of the specific role assumed by a family member are presented.


Author(s):  
Brent M. S. Campney

Scholarly literature on racist violence has typically focused on the experiences of young males who suffer a disproportionate share of the police violence directed at their communities. This study widens our view of the effects of racist violence by examining the experiences of the family members of these men, and particularly the wives, children, parents, and siblings. The article shows that family members often witnessed the abuse of their loved ones, endured feelings of helplessness in the face of these acts of violence, confronted threats (or worse) from these officers at the time or subsequently, and experienced firsthand the injustice of the justice system. The article builds on a recent scholarship on racist violence—primarily lynchings—that focuses on the effects of this violence on the families and communities of the victims.


2020 ◽  
Vol 5 ◽  
pp. 99
Author(s):  
Andrea Roxana Macías Ávila ◽  
Grey Zita Zambrano Intriago

Este documento presenta el proceso y los resultados de la investigación “Comportamiento de los familiares de los usuarios menores de 5 años con patologías diferentes ingresados en el servicio de Pediatría del Hospital Verdi Cevallos Balda”. Es importante mencionar que la psicología, desde los diferentes ámbitos de aplicación, ha establecido la necesidad de identificarlos factores que protegen o vulneran a la persona frente a condiciones críticas. El objetivo de este trabajo investigativo planteó identificar el comportamiento de los familiares de los usuarios ingresados en el servicio hospitalario. Los métodos utilizados fueron: estudio descriptivo, con análisis cualitativo y cuantitativo de los datos. La población de estudio constituyo 35 familiares de los usuarios, se aplicó encuestas estructuradas. La aparición de una enfermedad aguda, crónica o terminal en alguno de los miembros de la familia representa un serio problema tanto en su estructura como en su comportamiento. Los cuidadores obtuvieron valores en Ansiedad, Tristeza y Estrés; mientras las madres puntuaron un nivel más alto de tristeza que los demás cuidadores. Cuando los niveles de Ansiedad materna son elevados también lo son los paternos de ansiedad y depresión. Conocer los comportamiento de cada miembro del grupo familiar para afrontar el proceso de enfermedad y los tratamientos, permite adecuar las intervenciones que faciliten la adaptación a la situación adversa por la que atraviesan. Estos resultados obtenidos conducen al planteamiento de la propuesta de intervención con la familia de los usuarios menores de 5 años ingresado con patologías diferentes en el servicio de pediatría del Hospital Verdi Cevallos Balda. PALABRAS CLAVE: comportamiento familiar; condiciones; triste; estresado. BEHAVIOR OF THE FAMILY MEMBERS OF CHILDREN UNDER FIVE YEARS INCOME IN THE PEDIATRIC SERVICE OF THE VERDI CEVALLOS BALDA HOSPITAL FROM MANABÍ ABSTRACT This document presents the process and the results of the research "Behavior of the relatives of users under 5 years old with different pathologies admitted to the pediatric service of the Verdi Cevallos Balda Hospital". It is important to mention that psychology, from different areas of application, has established the need to identify factors that protect or harm the person in the face of critical conditions. The objective of this research work was to identify the behavior of family members of users admitted to the hospital service. The methods used were: descriptive study, with qualitative and quantitative analysis of the data. The study population constituted 35 family members of the users, structured surveys were applied. The appearance of an acute, chronic or terminal illness in one of the members of the family represents a serious problem both in its structure and in its behavior. The caregivers obtained values ​​in Anxiety, Sadness and Stress; while mothers scored a higher level of sadness than other caregivers. When the levels of maternal anxiety are high, so are the paternal anxiety and depression. Knowing the behavior of each member of the family group to deal with the disease process and treatments, allows adapting interventions that facilitate adaptation to the adverse situation they are going through. These results lead to the proposal of intervention proposal with the family of users under 5 years admitted to the pediatric service of the Verdi Cevallos Balda Hospital. KEYWORDS: family behavior; terms; sad; stressed.


2019 ◽  
Vol 20 (2) ◽  
pp. 283-298
Author(s):  
Kholid Mawardi ◽  
Cucu Nurzakiyah

The results of the study found that the responsibility of religious education of children in the family of Tablighi Jama'ah differed in terms of several conditions, namely first, when parents were not going to khuruj where both parents were responsible for children's education; secondly, when the father goes khuruj, then the mother is responsible for everything including children's education; third, when both parents go khuruj, then the responsibility of the child is left to other family members such as grandparents or their first adult children; and fourth, when the child goes to khuruj, where parents are responsible for children's religious education both mother and father. The pattern of the religious education in the Tablighi Jama'ah family in the village of Bolang is formed from several similarities held in the implementation of religious education, one of which is the daily activity that is carried out by the Tablighi Jama'at family. Al-Qur'an becomes one of the material given to children in the ta'lim. Children are taught how to read the Qur'an and memorize short letters such as Surat al-Falaq, al-Ikhlas, and so on. In addition to al-Qur'an, in this ta'lim there is a special study in the Tablighi Jama'ah, which is reading the book of fadhilah ‘amal, and the last is mudzakarah six characteristics.


Author(s):  
Khuan Seow ◽  
Nadia Caidi

Canada has an aging population with the fastest growing age groups (80 and 45-64 years old) vulnerable to age-related diseases such as Alzheimer’s disease. Caregiving responsibilities often fall to the family members of the afflicted without much attention and consideration being placed on the information needs of these caregivers. We call for a better understanding of these caregivers' information needs and uses by social policy makers as well as information providers.La population du Canada a tendance à vieillir considérablement, avec la hausse la plus rapide dans les groupes d’âge (80 et 45 à 64 ans). Les personnes âges sont très vulnérables à toute sorte de maladies, telles que la maladie d’Alzheimer. La responsabilité revient souvent aux membres de la famille qui doivent prendre soin des personnes atteintes de cette maladie. Or, nous ne connaissons que peu de chose sur les besoins en information des personnes qui prennent soin de ces malades de l’Alzheimer : qui sont-ils ? Quelles sont leurs sources... 


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