Gotowe bibliografie tematyczne / Children suffering grief or loss

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Gotowa bibliografia na temat „Children suffering grief or loss”

Autor: Grafiati

Data publikacji: 23 sierpnia 2023

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Artykuły w czasopismach na temat "Children suffering grief or loss"

Polita, Naiara Barros, Francine de Montigny, Rhyquelle Rhibna Neris, Willyane de Andrade Alvarenga, Fernanda Machado Silva-Rodrigues, Ana Carolina Andrade Biaggi Leite i Lucila Castanheira Nascimento. "The Experiences of Bereaved Parents After the Loss of a Child to Cancer: A Qualitative Metasynthesis". Journal of Pediatric Oncology Nursing 37, nr 6 (27.07.2020): 444–57. http://dx.doi.org/10.1177/1043454220944059.

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This study aims to synthesize qualitative evidence about the bereavement experience of parents following the death of a child due to cancer. A qualitative metasynthesis was conducted from searching five databases. The search identified 650 articles that were independently assessed by two reviewers. Thirty-one articles were selected for full-text reading and assessed for eligibility; a total of 14 articles were included in the final sample and submitted to quality appraisal. The software NVivo® was used to organize the data and support the thematic analysis procedures. Two analytical themes were constructed: (1) losing a child and facing a rupture in identity and sense of life and (2) surviving grief and reengaging in life. The grief process was dynamic, continuous, and begun before the death of the child. Fathers and mothers reacted differently to the loss and experience of grief. The loss of a child definitively changed the parents’ life and caused identity crisis and loss of life’s purpose. During the process of survival, parents constructed new meanings that helped them cope with grief; they used strategies that allowed them to recover their sense of purpose in life. Synthesizing the experience of bereaved parents is essential to improve the support families of children with advanced cancer receive to better cope with their suffering and loss, before and after the child’s death.

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Windy, Windy. "Kajian Teologis Kitab Ayub 1-2 Dan Implikasi Psikologis Terhadap Keluarga Kristen Yang Mengalami Kematian Anak Di Gereja Toraja Klasis Makale Tengah Jemaat Imanuel Tampo". KAMASEAN: Jurnal Teologi Kristen 1, nr 2 (31.12.2020): 107–26. http://dx.doi.org/10.34307/kamasean.v1i2.32.

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This paper is motivated by a Christian family at Gereja Toraja Jemaat Imanuel Tampo who mourn the death of a child. The death of child causes parents to give different emotional reactions from one to others. Job 1-2 show that how Christians confronting with suffering. This is the author’s consideration to see the theological study of Job 1-2 and its implications for Christian families who experience child death at Gereja Toraja Klasis Makale Tengah Jemaat Imanuel Tampo. The research method that the authors use in this research is a narrative study qualitative. This narrative study is developed to describe the theological studies of Job 1-2 and the implications for Christian family who experience child death at Gereja Toraja Klasis Makale Tengah Jemaat Imanuel Tampo. Job confronted the suffering that occurs by surrendering to God and accepts that suffering humbly. Job 1-2 teaches to understand God’s sovereignty that occurs through suffering. Christian families who grieve over the loss of their children also accept the suffering they endure. Theory of Kubler Ross regards 5 stages of grief, namely denial of anger, bargaining, depression, and acceptance as a process to be accepted the suffering. In the end the Christian family in the Gereja Toraja Klasis Makale tengah Jemaat Imanuel Tampo can through the suffering of the death of a child by surrending to God and accepting it.

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Szczepańska, Joanna. "Doświadczenia emocjonalne rodziców w procesie diagnozy dziecka ze spektrum zaburzeń autystycznych". Psychologia Rozwojowa 27, nr 2 (2022): 45–55. http://dx.doi.org/10.4467/20843879pr.22.010.17467.

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As the population of children who are diagnosed as being on autism spectrum grows in number, so does the interest of scientists in this subject. Specialists in various fields increasingly not only focus on the children themselves but also examine their families’ situation and functioning. By doing so, they aim to understand the family as a system. Numerous empirical studies have demonstrated that when a baby with a disability is born or when it develops in an abnormal way, this becomes a source of suffering, anxiety, grief, or hostility towards the outside world. Such a situation is viewed as a crisis, a loss, and a process of mourning; working through these experiences is difficult, requires tremendous work, and requires external support in many cases. For these reasons, this paper provides a brief overview of parents’ experiences in the process of diagnosing a child; it cites the literature on the topic and shows the different paths of these experiences.

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Black, Helen K., i Robert L. Rubinstein. "Narratives of Three Elderly African-American Women Living in Poverty Who have Lost an Adult Child to Horrendous Death". OMEGA - Journal of Death and Dying 38, nr 2 (marzec 1999): 143–61. http://dx.doi.org/10.2190/1nkp-axbp-9rla-a5uh.

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Fifty Elderly African-American Women Living In Poverty Were Interviewed For A Research Project Entitled “Chronic Poverty And The Self In Later Life” Which Studies The Effects Of Long-Term Poverty On Women's Self-Concepts. The Fact That Ten Women Out Of The Forty-Five Women In Our Sample Who Bore Children Lost Them To Murder, drugs, or other forms of violence made the subject of horrendous death (Leviton, 1995) salient during data analysis. Interview transcripts from three women who lost children to horrendous death were examined for reactions to the children's deaths and subsequent thoughts and feelings about their own deaths. Key themes emerging from the women's narratives were: 1) women's experience with poverty and abandonment, their expectation that life includes suffering, and their religious faith assisted them in grief work; 2) currently, women focused on present joys and concerns rather than on past sorrows; 3) women did not articulate thoughts about their own deaths in light of their child(ren)‘s deaths; and 4) women doubted or negated the concept of an afterlife, which contradicts traditional African beliefs and may speak to the loss they endured.

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Etinosa, Egharevba Matthew, Adejomo Gbadebo, Olonade Yunusa Olawale, Ugbenu Oke i Kasa Adamu Gayus. "COVID-19 and the state of mental health challenges among Women, Girls and Children: the case of Nigeria". Advances in Social Sciences Research Journal 9, nr 7 (2.08.2022): 648–67. http://dx.doi.org/10.14738/assrj.97.12759.

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Health is a resource for daily existence and wellbeing. Mental, social, emotional, spiritual, psychological and physical health constitute an overall essence of that well-being. The COVID-19 epidemic has had a profoundly negative impact on women, children, and society as a whole by causing unfathomable loss, grief, pain, and solitude. The pandemic has pushed many families into poverty and exacerbated conditions of inequality with women and children exposed to violence and other deprivation which deeply impacted on their mental health. The study employed the use of content analysis of secondary sources of data, and the social stress, social model and general strain theories constituting the theoretical framework for examining the subject under investigation. The findings of the study demonstrated that the prevalence of mental disorders among women and children is rising, with serious human rights and socio-economic repercussions as a result of poverty and gender inequality. Furthermore, the majority of those suffering from mental health issues are unable to get the crucial medical and social care they need. The study's recommendation emphasized the need to address issues of poverty, inequality, and gender inequality as well as make sure that Nigeria's national and sustainable development policies and programmes must address the serious mental health problems that women and children currently face as well as those that will arise after the post-Covid-19 era.

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Murray, Rianna T., Laura Briggs Drew, Christina Memmott, Ya-Maila Bangura i Elisabeth F. Maring. "A community’s experience during and after the Ebola epidemic of 2014—2016 in Sierra Leone: A qualitative study". PLOS Neglected Tropical Diseases 15, nr 2 (25.02.2021): e0009203. http://dx.doi.org/10.1371/journal.pntd.0009203.

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Background The 2014–2016 Ebola epidemic devastated families and communities throughout West Africa. Due to its high mortality rate and infectious nature, most Ebola research to date has focused on healthcare response and interventions; however, little is known about the experiences of Ebola survivors and communities. This qualitative study aimed to better understand the lived experiences of community members, including children, during and after the Ebola epidemic in Sierra Leone. Methods During June 2016 and June 2017, we conducted four focus groups comprised of primary school students, female caretakers, male caretakers, and teachers, and two individual in-depth interviews with local nurses in Calaba Town, a small village outside of Freetown. Interviews were recorded, transcribed verbatim, and coded using a modified grounded theory methodology. Findings All participants shared that they experienced significant challenges during and after the Ebola epidemic. During the epidemic, participants endured daily life challenges pertaining to fear, financial distress, and school closures. They also experienced suffering, loss, isolation, grief, and compromised culture. Confusion and distrust were also prevalent during the epidemic, with participants reporting confusion around Ebola transmission and distrust in the government and healthcare services. We also found that the struggle for food and grief stemming from the loss of loved ones continued more than a year after the epidemic ended. Despite Sierra Leone being declared Ebola-free, stigma and fear persisted and community members shared their continuing distrust of the government due to their actions during and after the epidemic. Conclusions The findings of this qualitative study reveal that the Ebola epidemic was a traumatizing period for the Calaba Town community, and that confusion and distrust toward the government health care system have continued. Future studies should explore the extended impact of the epidemic on communities, including long-term psychological, social, and economic consequences of this outbreak.

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Schiefenhövel, Wulf. "Perception, Expression, and Social Function of Pain: A Human Ethological View". Science in Context 8, nr 1 (1995): 31–46. http://dx.doi.org/10.1017/s0269889700001885.

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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.

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Corral Trujillo, M. E., R. A. Cerda González, H. G. Martínez Sandoval, A. Carrazco Chapa, K. M. López Serna, J. C. Riega-Torres, L. Pérez Barbosa, C. M. Skinner Taylor i D. Á. Galarza-Delgado. "AB1839-HPR PERINATAL GRIEF IN WOMEN WITH AUTOIMMUNE RHEUMATIC DISEASES". Annals of the Rheumatic Diseases 82, Suppl 1 (30.05.2023): 2150.2–2151. http://dx.doi.org/10.1136/annrheumdis-2023-eular.4639.

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BackgroundPerinatal loss (PL), defined as a loss from any gestational age or in the neonatal period [1] lead women to the process of grieving. Perinatal Grief (PG) involves suffering and reaction such as sadness, disbelief and anger [2].PL and PG symptoms affect many women around the world; women with autoimmune rheumatic diseases (ARDs) have greater risk of PL. The Perinatal Grief Scale (PGS) can help health providers prevent complicated grief in their patients [3].ObjectivesDetermine which PL and sociodemographic variables are associated factors to a complicated grief in women with ARDs.MethodsDescriptive, cross-sectional, comparative study at the Hospital Universitario “Dr. José Eleuterio González” in México. We included women from the Pregnancy and Rheumatic Diseases Clinic (CEER) that answer a virtual survey with the PGS. The demographic, ARD and PL data were obtained from the clinical records. For the control group, women without ARD were invited to fill a virtual survey with the PGS, sociodemographic and PL data.The PGS is a Likert-type scale that consists of 27 items with four response options. The questions are distributed in four subscales: active grief (10 items), guilt (8 items), depression (6 items), acceptance (3 items). Scores greater than 50 points suggests a complicated grief comorbidity.The Kolmogorov-Smirnov test was used to determine normality; to analyze the differences between groups, Mann–Whitney U, Chi-square tests and T-test were employed. A p < 0.05 was considered statistically significant. The statistical analysis was performed with the statistical program SPSS version 25.ResultsA total of 50 women were included: 25 with ARD and 25 without ARD. The median age for the group with ARD was 42 (38.5-51) and 34 (26-42.5) for the without ARD group. In the ARD group the most frequent diagnosis were systemic lupus erythematosus (7/14%), rheumatoid arthritis (6/12%) and Antiphospholipid Syndrome (4/8%).For the PGS, twenty (40%) of the 50 women got a score >50; 11 (55%) were women without ARD and 9(45%) have ARD. The PL, suffered by these 20 women were 18 during the pregnancy (17/85% on the first trimester and 1/5% on the second trimester) and 2 (10%) after birth. No statistically differences were found in the total score and subscales of the PGS between groups. The sociodemographic and PL data and the PGS score for both groups are included intable 1.ConclusionEven though there were no significant differences between groups; we hypothesize that the greater number of PL in women with ARD serves as a protective factor and prevents that the PG evolve to a complicated grief. On the other hand, having the PL during the first trimester of the pregnancy can be a risk factor for complicated grief. Our limitation was the sample size for both groups.References[1] Côté-Arsenault D and Denney-Loelsch E (2016) “Have no regrets”: Parents’ experiences and developmental task in pregnancy with lethal fetal diagnosis. Social Sciences and Medicine 154, 100–109.[2] Bonanno GA and Kaltman S (2001) The varieties of grief experience. Clinical Psychology Review 21, 705–734.[3] Mota González C, Calleja Bello N, Aldana Calva E, Gómez López ME, Sánchez Pichardo MA. Escala de duelo perinatal: validación en mujeres mexicanas con pérdida gestacional. Revista latinoamericana de psicología. 2011 Sep;43(3):419-28.Table 1.Clinical characterizationPatients with ARD N=25Patients without ARD N=25P=0.05Years of education0.114>9 years21 (84%)15 (60%)<9 years4 (16%)10 (40%)Marital Status0.225Single2 (8%)2 (8%)Married/Common law20 (80%)15 (60%)Divorced3 (12%)8 (32%)Perinatal Losses0.387113 (52%)17 (68%)>112 (48%)3 (32%)Number of pregnancies, median (IQR)4 (2.5-5)3 (2-3.5)0.38Number of living children, median (IQR)2 (1-3)1 (0.5-2)0.123PGS score, median (IQR)43(37.5-60.0)46 (39.5-62.5)0.587PGS active grief subscale13 (10-18)14 (12-18.5)0.355PGS depression subscale12 (10-19)12 (10-22)0.782PGS guilt subscale12 (9-18.5)12 (8-17)0.815PGS acceptance subscale6 (6-8)7 (6-8)0.347Acknowledgements:NIL.Disclosure of InterestsNone Declared.

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Fieldsend, Megumi, i Jonathan A. Smith. "‘Either stay grieving, or deal with it’: the psychological impact of involuntary childlessness for women living in midlife". Human Reproduction 35, nr 4 (kwiecień 2020): 876–85. http://dx.doi.org/10.1093/humrep/deaa033.

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Abstract STUDY QUESTION What is it like for women to be involuntarily childless in midlife? SUMMARY ANSWER Involuntarily childless women may be suffering from prolonged grief due to its ambiguous and intangible nature; however, they are also striving to find ways of dealing with their internal pain in order to live with their loss. WHAT IS KNOWN ALREADY Many studies examining issues around human reproduction have tended to place childlessness in the realm of medicalised infertility and report generalised mental issues, such as depression and psychological distress, existing amongst women undergoing fertility treatments. Few studies, however, have focused on the individual with regard to the experiential significance of involuntary childlessness and living beyond the phase of trying for a baby. STUDY DESIGN, SIZE, DURATION A phenomenologically oriented person-centred qualitative design was used. In-depth semi-structured interviews were conducted with 12 White British women, who identified themselves as involuntarily childless, recruited via three leading childless support networks in the UK. PARTICIPANTS/MATERIALS, SETTING, METHODS In order to retain an idiographic commitment to the detailed account of a person’s experience, a homogeneous and purposive sampling was used applying the following criteria: women aged between 45 and 55; in long-term heterosexual relationships with no adopted children, stepchildren or children of a partner from a previous marriage or relationship; and no longer trying to have a child. Considering the homogeneity of ethnic background and wishing to respect cultural differences, this study focused on White British women living in the UK. Of the 12, one woman was found to not meet the criteria, and therefore, the experiential data of 11 interviews were used for the study and analysed using interpretative phenomenological analysis (IPA). MAIN RESULTS AND THE ROLE OF CHANCE Two higher-order levels of themes that illustrate intrapersonal features were identified: the intrapersonal consequences of loss and confronting internal pain. The former explicated the depth of internal pain while the latter revealed ways in which the participants deal with it in their everyday lives. The important finding here is that both themes are co-existing internal features and dynamically experienced by the participants as they live with the absence of much-hoped-for children. LIMITATIONS, REASONS FOR CAUTION Given the homogeneous sampling and the small number of participants, which is consistent with IPA, we want to be cautious in generalising our study findings. WIDER IMPLICATIONS OF THE FINDINGS This study offers the view that there might be potential mental health issues surrounding involuntary childlessness that are currently overlooked. Particularly because the loss of hope cannot be pathologised, and the grief is ambiguous and intangible, it might make people’s grieving process more complicated. An ongoing sense of uncertainty also may persist in that involuntarily childless people may develop symptoms similar to those diagnosed with prolonged grief disorder (PGD). The overall findings elucidate the need for clinicians, counsellors and health professionals to be aware of the possible association with PGD and promote long-term support and care in helping to maintain psychological well-being for people dealing with involuntary childlessness. Furthermore, this research points to an educational application for younger people by offering information beyond an explanation of infertility and fertility treatment, helping to understand the lived experience of involuntary childlessness. STUDY FUNDING/COMPETING INTEREST(S) No funding was obtained for this study. The authors have no conflicts of interest to declare. TRIAL REGISTRATION NUMBER Not applicable.

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Gerhardstein, Alphonse. "Making a Buck While Making a Difference". Michigan Journal of Race & Law, nr 21.2 (2016): 251. http://dx.doi.org/10.36643/mjrl.21.2.making.

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It is not right for children to die before their parents. It is not right for peaceful, unarmed citizens to die at the hands of the police. In my civil rights practice, I have met many mothers, fathers, and family members who are struggling to recover after a law enforcement officer caused the death of their loved one. Sure, they want fair compensation. But money does little to reduce their loss or make the grief more bearable. They often want to do something that will ensure that their loved one did not die in vain. They want to prevent other families from suffering the same loss. This Article will show that even without standing to seek injunctive relief, these plaintiffs can indeed secure significant reform. This Article will also share suggestions for the practitioner on how to litigate these cases economically and efficiently. Part I explores avenues for relief other than compensatory and punitive damages. Part II shares language to include in retainer agreements to encourage clients to share any settlement they reach with the public to increase awareness of police misconduct. Part III explains that researching local police policies and practices helps to inform where meaningful opportunities for reform exist. Part IV then provides examples of resolutions that require the officers involved and their supervisors to personally engage with the victims’ families or that commemorate victims in their respective communities. Finally, Part V reviews techniques for case selection, case theory, and working within a budget so the small office practitioner can make enough money to carry the work forward.

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Rozprawy doktorskie na temat "Children suffering grief or loss"

Lewis, Danielle Kirsten. "Grief and Loss: Supportive Stories for Children with Autism". BYU ScholarsArchive, 2019. https://scholarsarchive.byu.edu/etd/8478.

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The effect of grief on children with autism is an under-researched area of study. Until recently, it was often assumed that individuals with autism did not have the capacity to grieve. Because of deficits in social skills, interpersonal relationships, and language and communication skills, these individuals are especially vulnerable as they navigate the challenging social and emotional aspects associated with bereavement and grief. Bibliotherapy is offered as supportive strategy for bereaved children, providing them with structure and guidance through a time of uncertainty and change. This study is based on two focus groups, one with teachers of children with autism (n = 8) and one with parents of children with autism (n = 5). Researchers focused on the purpose of supporting children in grades K–3 through the death of a loved one or pet. Focus group participants discussed their perceptions of how this special population of children grieves and how to support them following a significant loss, such as the death of a loved one or beloved pet. After reviewing selected resources (supportive stories), participants offered their impressions regarding the appropriateness and potential effectiveness of the resources. Focus groups were audiotaped and later transcribed. Transcriptions were carefully reviewed and discussed by two individuals to identify and summarize themes. After summarizing the information from the transcriptions and organizing the information, one individual served as a quality check, to verify the accuracy of the findings. Additionally, a member check was offered to participants to assure accuracy in the typed transcripts (for intended meaning and content). The following information and recommendations are presented based on the input from the focus group participants. Three overarching themes were identified in this study, as well as some specific cautions and warnings. Participants emphasized the importance of individualization in the selection of stories for children with autism. Readers should be aware of the child’s specific needs and circumstances when they are selecting a story. The stories should be developmentally appropriate and should help support the child through the specific type of death or loss that has occurred. Participants also discussed the importance of selecting books that are concrete, simple, and structured. As children with autism often have difficulty with abstract concepts, the topic of death and loss should be approached in a concrete and literal way. Books that present information in this manner will best help the child to understand their experience. Practitioners who use bibliotherapy to support children with autism through a death or loss should be sensitive to family beliefs. Open communication should be used with the child’s family in order to select a book that best fits that child’s needs. Children with autism will also benefit from stories that help to normalize their experience and that help them to understand the emotions that they or their family and friends may experience. Future research is recommended to further explore the use of supportive stories in aiding a child with autism through the grief and loss process. It is important to examine how children with autism respond to the selected stories and to understand how effective the stories are in their coping and understanding process.

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McKegney, Sherrie. "Silenced suffering : the disenfranchised grief of birthmothers compulsorily separated from their children". Thesis, McGill University, 2003. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=81253.

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Few efforts have been made to understand the subjective experiences of birthparents involved in the child welfare system, especially of those who have had their parental rights permanently removed. The research undertaken seeks an initial investigation of this neglected issue, providing accounts of four birthmothers' experiences of having one or more of their children involuntarily and permanently removed from their care as a result of child neglect. Implicit in this research is the assumption that these mothers do indeed suffer tremendous grief over the loss of their children, regardless of child welfare agencies' assessments of their parenting capacities. Furthermore, the research critically evaluates how child welfare practice and policy might serve to exacerbate incumbent issues of loss, ultimately disenfranchising this already isolated and stigmatized population. Therefore, this qualitative study endeavours to assist not only child protection workers, but also the greater community in better understanding what it is like to be a "child welfare parent" who has had her parental rights terminated, and to be aware of the existing imbalance of power between child welfare agencies and the clientele they serve. The study ultimately aims to help ensure that human dignity and genuine respect are not lost in the work of child protection.

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Huepenbecker, Valerie Anne. "A time to grieve children and loss /". Menomonie, WI : University of Wisconsin--Stout, 2005. http://www.uwstout.edu/lib/thesis/2005/2005huepenbeckerv.pdf.

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Louie, Benedict L. "Application of a grief model and Buddhist psychology in dealing with grieving, loss, and suffering". Thesis, California Institute of Integral Studies, 2013. http://pqdtopen.proquest.com/#viewpdf?dispub=3557739.

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This study researches the journey of transformative learning experiences of adult men and women who have adopted a positive attitude in dealing with challenging and life-threatening issues. By applying a Western grief model and the principles of “living the present moment” and “letting go” derived from Buddhist psychology, this study aims to identify ways to transform mental suffering and grieving into positive energy that may help to provide comfort to individuals in despair.

The research paradigm is transpersonal and the method of this study is narrative analysis. A combination of face-to-face and telephone interviews as well as email exchanges with eight individuals who shared their personal experiences in adopting a positive attitude in overcoming difficult situations were employed. These participants have battled and conquered their unique life-challenging situations.

The stories of these individuals document their challenges with grief and include insights learned from these experiences and the ways in which they transformed these experiences into catalysts for positive energy. Seven themes became evident and significant in their journey in coping with suffering, and paved the way for their transformational learning experiences. They are: a) Reaching acceptance, b) the importance of a support network, c) making meanings of suffering, d) impermanence, e) letting go of the past, f) living in the present moment, and g) spirituality. It is hoped that this transformational learning experience will enable other people from diverse demographic, professional, and cultural backgrounds to embrace a Western grief model in combination with Buddhist psychology to better cope with their loss or grieving, and help them to understand the opportunity for growth these life challenges can present.

Everyone experiences loss and difficult challenges in the course of a lifetime. How we view and react to them determines the effect they have on the rest of our lives. This study will contribute to the need for more research in this area by asking the following question: “How do actions derived from Buddhist principles help to alleviate suffering among people facing challenges of change?”

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Budzinski, Erica L. "An investigation of Wisconsin public schools' grief and loss support programs". Online version, 1998. http://www.uwstout.edu/lib/thesis/1998/1998budzinskie.pdf.

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Spiegelberg, Mandi. "Coping with loss supporting school-aged children who are dealing with bereavement /". Menomonie, WI : University of Wisconsin--Stout, 2006. http://www.uwstout.edu/lib/thesis/2006/2006spiegelbergm.pdf.

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Sha, Wei, i 沙卫. "Grief experience of bereaved mothers who loss of children in Sichuan earthquake 2008". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2014. http://hdl.handle.net/10722/206428.

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Bereavement, an unavoidable event in everyone’s life, brings endless missing, grief, and suffering to people. Among all kinds of bereavement, losing a child is considered the most sorrowful and traumatizing. It is extremely difficult for parents who lose a child to recover from their deepest pain. On May 12, 2008, an earthquake, measuring 8.0 Ms, occurred in Wenchuan, Sichuan province, China. The earthquake killed more than 70,000 people and left about 20,000 missing. During the earthquake, some school buildings collapsed and as a result, hundreds of students died. Their parents experienced overwhelming bereavement. To understand what bereaved mothers experience and how they cope with bereavement after the loss of children, the author conducted this longitudinal study based on the dual process model of coping with bereavement (DPM), and applied qualitative inquiry using interpretative phenomenological analysis. In this study, the author has reported on her 4 waves of interviews with these parents, regarding how they coped with grief over 2 years. The author conducted 4 waves of in-depth, face-to-face interviews with mothers who lost their children during the Wenchuan earthquake (N= 43). The findings reveal that three levels of stresses exist in these bereaved mothers’ (BMs) grief experiences, including individual, family, and society levels. On the individual level, they experienced not only emotional distress, such as overwhelming grief, despair, and anger, but they also experienced cognitive distresses, such as regret, guilt, meaninglessness and hopelessness. On the family level, BMs experienced various stresses, such as family incompleteness, despair of their family life, and tensions with their spouses. On the society level, these BMs experienced pressure from social expectations and public opinion. They felt segregated and detached from their social networks. Life became meaningless to these BMs, resulting in suicidal thoughts. These BMs practiced a variety of coping strategies to deal with their endless grief and stresses in their daily lives. These BMs actively worked through their grief and negative emotions. They adjusted their cognition to deal with their children’s deaths, and made efforts to reconstruct their lives; through things like having another child, rebuilding their life purpose, and rebuilding relationships with others. Avoidance strategies included proactive avoidance and reactive avoidance coping. Respite was manifested in the BMs temporarily devoting themselves to other things in order to distract themselves from tremendous bereavement. This study verifies and enriches the DPM in the Chinese socio-cultural context, while indicating suggestions for social work practice and social policy.
published_or_final_version
Social Work and Social Administration
Doctoral
Doctor of Philosophy

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Martell, Mary M. "Bereavement and Loss: Using Bowlby's Grief Stages to Analyze Books for Preschool Children". University of Akron / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=akron1320799352.

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Tozeland, Judith C. "Working through grief and loss with children and their families, group and individual approaches". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk2/tape15/PQDD_0004/MQ32269.pdf.

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Ener, Liz D. "A Canonical Correlational Analysis Exploring Characteristics of Children Presenting to Counseling for Grief and Loss". Thesis, University of North Texas, 2015. https://digital.library.unt.edu/ark:/67531/metadc804937/.

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To date, researchers who have explored the complexity of childhood bereavement have utilized unstandardized assessment instruments and/or have independently evaluated specific constructs rather than factoring in the dimensionality of loss. The purpose of this study was to use parents' completion of established instruments--the Child Behavior Checklist and the Parenting Stress Index--to examine the multivariate shared relationship between characteristics of bereaved children referred for counseling--their ages, genders, ethnicities, types of loss, and life stressors--and their behavioral manifestations as well as the relationship between these characteristics and levels of parent-child relational stress. Utilizing archival clinical files, I examined these characteristics from bereaved children (N = 98) whose parents sought counseling services from two university-based counseling clinics. The sample consisted of 67 boys and 31 girls between the ages 3 and 11 years old (M = 6.28). The majority of participants (67%, n = 66) identified as Caucasian, 10% (n = 10) as African American, 10% (n = 10) as Hispanic/Latino, 6% as Bi-racial (n = 6), 4% as Native American (n = 4), and 2% as Asian (n = 2). A canonical correlational analyses (CCA) was conducted to examine relationship between characteristics of children and their subsequent behavioral manifestations. The full model was found to be statistically significant using the Wilks’s λ = .611 criterion, F(25, 328.41) = 1.862, p = .008. The R2 type effect size was .389, which indicates the full model explains about 39% of the variance shared between the two variable sets. A second CCA was conducted to explore the relationship between characteristics of bereaved children and levels of parent-child relational stress. The full model was found statistically to be significant using the Wilks’s λ = .790 criterion, F(10, 154) = 1.926, p = .045. The R2 type effect size was .210, which indicates the full model explains about 21% of the variance shared between the two variable sets. Overall, correlational findings from this study provided insight into bereaved children’s manifestations of loss and levels of parent-child relational stress as contingent upon specific characteristics. Specifically, results indicated a strong relationship between age and bereaved children’s behavioral manifestations. This finding reinforced the importance for clinicians to understand developmental implications when working with bereaved children. Furthermore, caregivers who reported minimal overall external stressors also reported less parent-child relational interference. This finding further emphasizes the importance for caregivers to maintain utmost stability for bereaved children.

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Książki na temat "Children suffering grief or loss"

Kanyer, Laurie A. 25 things to do when grandpa passes away, mom and dad get divorced, or the dog dies: Activities to help children suffering loss or change. Seattle, Wash: Parenting Press, 2004.

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Stroh, Diana. On eagle's wings: A mother's story of hope and healing amidst suffering and loss. [Charleston, SC]: [publisher not identified], 2010.

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Golden bubbles: Learning through loss : a grandmother's insight into childhood cancer. Huntsville, Ala: Pub. Designs, 2007.

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Krauss, Pesach. Why me?: Coping with grief, loss, and change. Toronto: Bantam Books, 1988.

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Robert, DeBellis, red. Suffering: Psychological and social aspects in loss, grief, and care. New York: Haworth Press, 1986.

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Sauceda, Carol T. From the seeds of affliction: The fruits of suffering. Salt Lake City: Millennial Mind Pub. ., 2014.

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Chronic pain, loss, and suffering. Toronto: University of Toronto Press, 2004.

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Bruce, Lindsay, i Elsegood John, red. Working with children in grief and loss. London: Baillière Tindall, 1996.

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Overcoming loss: Activities and stories to help transform children's grief and loss. London: Jessica Kingsley Publishers, 2008.

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Reason for the season: Ministerial reflections on personal grief, suffering and loss. Cape Coral, Fla: Founders Press, 2010.

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Części książek na temat "Children suffering grief or loss"

Kroll, Brynna. "Children and Divorce". W Loss and Grief, 111–24. London: Macmillan Education UK, 2002. http://dx.doi.org/10.1007/978-1-4039-1404-0_8.

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Rankin, Hollie. "Grief". W Guide to Supporting Children through Bereavement and Loss, 3–6. Abingdon, Oxon ; New York, NY : Routledge, 2019.: Routledge, 2019. http://dx.doi.org/10.4324/9780429433160-3.

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Rabenstein, Stephanie. "Assessing Grief and Loss in Children and Adolescents". W Understanding Child and Adolescent Grief, 19–33. New York, NY : Routledge, 2017. | Series: Death, dying, and bereavement: Routledge, 2017. http://dx.doi.org/10.4324/9781315164250-3.

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Waterman, Jill, Audra K. Langley, Jeanne Miranda i Debbie B. Riley. "Module 3: Loss and grief issues in adoption." W Adoption-specific therapy: A guide to helping adopted children and their families thrive., 123–42. Washington: American Psychological Association, 2018. http://dx.doi.org/10.1037/0000096-006.

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Bowman, Mary-Ann Sontag. "Final Gifts: Lessons Children Can Learn from Dogs About End-of-Life, Loss, and Grief". W Children, Dogs and Education, 131–49. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-77845-7_7.

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Ward, Harriet, Lynne Moggach, Susan Tregeagle i Helen Trivedi. "The Children". W Outcomes of Open Adoption from Care, 63–100. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-76429-6_3.

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AbstractThe children’s early experiences provide a context for assessing subsequent outcomes. Data collected from case files and records presented to the courts show that before separation from birth parents, almost all 210 adoptees had experienced serious and often multiple forms of maltreatment; this was the primary reason for removal. Before entering their adoptive homes, 69% of the adoptees had had four or more adverse childhood experiences (ACEs), 32% had experienced failed reunifications and 48% had had three or more foster placements. Adverse childhood experiences before entry to care, harmful experiences in care and repeated exposure to grief and loss are likely to have contributed to the high prevalence of emotional and behavioural difficulties, displayed by 49% of the adoptees. According to our classification, 57% were at high risk of experiencing adverse outcomes in adulthood.

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"9. Grief Therapy". W Chronic Pain, Loss, and Suffering. Toronto: University of Toronto Press, 2004. http://dx.doi.org/10.3138/9781442672949-011.

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Loscalzo, Matthew, Marshall Forstein i Linda A. Klein. "Conclusion Loss". W Loss and Grief, 223–32. Oxford University PressNew York, 2022. http://dx.doi.org/10.1093/med/9780197524534.003.0019.

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Abstract Loss and Grief: Personal Stories of Doctors and Other Health Care Professionals presents unflinching, deeply personal stories by doctors and other health care professionals, who did not take the “escape” of writing about walking in our patient’s shoes. They had the audacity to walk in their own shoes. A consistent theme was that professional training/identity offered no immunity/direction for a loss that is deeply personal. The professional veneer was too thin to be instructive or protective. This was a surprise. Perhaps, it should not have been. The psychological barriers for individuals who cannot share their own losses and distress with colleagues, reflects a society that denies the impact of loss and minimizes the emotional components of vulnerabilities. It does not have to be this way. It is our hope that such openly shared feelings of isolation and suffering will humanize the loss experience, ignite prospective discussions, and illuminate opportunities for education, research and interventions to prepare us for multiple loss experiences endemic to life. Paradoxically, in some of the most supportive health systems, the very professionals who compassionately care for patients feel so alone when they experience their own losses. Perhaps our most immediate goal could be to create an infrastructure within health care to best support professionals manage the relentless professional stream of losses and personal suffering? Ultimately, we must accept that if doctors and other health care professionals are not at the vanguard of making a world filled with loss and grief more realistic, loving, and kind, who will be?

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"Children in Distress". W Loss, Change and Grief, 75–100. David Fulton Publishers, 2012. http://dx.doi.org/10.4324/9780203064696-9.

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"1. Loss and Grief: An Overview". W Chronic Pain, Loss, and Suffering, 1–20. Toronto: University of Toronto Press, 2004. http://dx.doi.org/10.3138/9781442672949-003.

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Raporty organizacyjne na temat "Children suffering grief or loss"

Clarke, Alison, Sherry Hutchinson i Ellen Weiss. Psychosocial support for children. Population Council, 2005. http://dx.doi.org/10.31899/hiv14.1003.

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Masiye Camp in Matopos National Park, and Kids’ Clubs in downtown Bulawayo, Zimbabwe, are examples of a growing number of programs in Africa and elsewhere that focus on the psychological and social needs of AIDS-affected children. Given the traumatic effects of grief, loss, and other hardships faced by these children, there is increasing recognition of the importance of programs to help them strengthen their social and emotional support systems. This Horizons Report describes findings from operations research in Zimbabwe and Rwanda that examines the psychosocial well-being of orphans and vulnerable children and ways to increase their ability to adapt and cope in the face of adversity. In these studies, a person’s psychosocial well-being refers to his/her emotional and mental state and his/her network of human relationships and connections. A total of 1,258 youth were interviewed. All were deemed vulnerable by their communities because they had been affected by HIV/AIDS and/or other factors such as severe poverty.

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