Relevant bibliographies by topics / Survivors

Academic literature on the topic 'Survivors'

Author: Grafiati
Published: 4 June 2021
Last updated: 29 July 2024

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Journal articles on the topic "Survivors"

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Reed, Mark D., and Jason Y. Greenwald. "Survivor‐Victim Status, Attachment, and Sudden Death Bereavement." Suicide and Life-Threatening Behavior 21, no. 4 (December 1991): 385–401. http://dx.doi.org/10.1111/j.1943-278x.1991.tb00576.x.

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ABSTRACT: This research examines the significance of the survivor‐victim relationship in understanding grief following sudden death bereavement. Data for this study come from medical examiner's reports and mailed self‐report surveys of survivors of suicide and accidental death. In general, the results show that survivor‐victim attachment is more important than survivor's status in explaining grief reactions. Also, suicide survivors experience significantly less emotional distress and shock, but greater feelings of guilt/shame and rejection, than survivors of accidental death. This paper concludes by directing future research to explore more fully the importance of survivor‐victim relationships in understanding grief following bereavement.
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Shepp, Veronica, Erin O’Callaghan, Anne Kirkner, Katherine Lorenz, and Sarah Ullman. "Sexual Assault Survivors Who Exchange Sex: Identity, Stigma, and Informal Responses From Support Providers." Affilia 35, no. 1 (August 18, 2019): 105–28. http://dx.doi.org/10.1177/0886109919866161.

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It is well established in the literature that individuals who engage in sex work are more likely to experience sexual trauma/violence, but little research has examined experiences of sexual assault survivors who exchange sex from the survivor’s perspective. Sexual assault survivors and their informal support providers (SPs; e.g., family, friends, romantic partners) were interviewed separately about disclosure, social reactions, and help-seeking following assault. Sixteen survivors mentioned experiences exchanging sex, which comprise the sample for the current study as well as comments from twelve SPs. Qualitative analysis revealed several themes including violence experienced engaging in sex work, navigating stigma and the identity of both sexual assault survivor and sex worker, and how survivors’ social supports impact their recovery. Survivors endorsed their sex worker identities at varying levels, and others used their identity as a sexual assault survivor to explain why they engaged in sex work. Social work implications regarding service provision and advocacy work are discussed.
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Quillen, Joanne, Yimei Li, Michele Demski, Claire Carlson, Holli Bradley, Lisa Schwartz, Jill P. Ginsberg, and Wendy Hobbie. "Comparing the Knowledge of Parents and Survivors Who Attend a Survivorship Clinic." Journal of Pediatric Oncology Nursing 35, no. 1 (November 2, 2017): 56–64. http://dx.doi.org/10.1177/1043454217735828.

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Background: This study underscores the importance of the survivor/parent dynamic in understanding the knowledge level of childhood cancer survivors and their parents with regard to cancer diagnosis, treatments, and potential late effects, and to assess the impact of parental knowledge on survivor’s knowledge. Procedure: A convenience sample (N = 219 dyads) consisting of childhood cancer survivors with a parent match was used. Survivors 2 years out from completion of therapy, aged 16 to 25 years, and fluent in English or Spanish completed 2 questionnaires to assess adolescent and young adult and parental knowledge regarding diagnosis, treatment, and long-term risks. Results: Data from the survivor/parent dyad confirm that parents are more knowledgeable than their child regarding treatment specifics. However, survivors are more accurate when assessing second tumor and fertility risk. More knowledgeable parents led to more knowledgeable survivors. Conclusions: Although parents were well-informed about treatment specifics, they were not as accurate in identifying risks appropriately. Therefore, education must be directed at both parent and survivors to maximize knowledge.
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Mertens, Ann, Rebecca Williamson, Jordan Gilleland-Marchak, Lillian R. Meacham, Brooke Cherven, and Paula Edwards. "Evaluation of the adoption, acceptance, and satisfaction of SurvivorLink as a communication tool for pediatric cancer survivors." Journal of Clinical Oncology 34, no. 3_suppl (January 20, 2016): 89. http://dx.doi.org/10.1200/jco.2016.34.3_suppl.89.

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89 Background: With the number of cancer survivors growing, focus on early recognition and treatment of late effects is even more imperative for life-long survivorship care. Electronic personal health records (PHR) potentially offer self-management and e-learning support which can empower the survivor, as well be used as a communication tool with healthcare providers (HCP). Methods: We developed a PHR, SurvivorLink (www.cancersurvivorlink.org), as a patient-centered tool to support pediatric cancer survivors, increase knowledge of late effects and survivor care, and promote communication between patients/parents and providers. Measures of success for a sustainable PHR implementation include adoption/use, acceptance, satisfaction and usability. The objectives of this feasibility study are to determine characteristics that predict the success of this PHR tool. An online pre-/post survey was administered to young adult survivors and parents of child survivors who registered on SurvivorLink. Results: Overall, 155 parents and 93 survivors completed the pre-test survey; 75% and 86% respectively have subsequently logged into SurvivorLink after initial registration. Individuals who used this PHR were more likely to be survivors (vs. parents; Odds Ratio (OR): 2.2, 95% CI: 1.1, 4.2). Other demographic variables were analyzed but no significant differences were found between users and non-users. Among users not aware of their need for specialized survivor care at the pre-survey, 52% reported awareness of the need for survivor care in the post-survey (vs 0% of non-users). Parents/survivors also reported high acceptance: 90% would use in the future, 82% stated it would help with advocating for survivor's health; and usability: 96% would recommend to other survivors/parents, 95% would recommend to their healthcare provider. Conclusions: SurvivorLink can improve knowledge around the importance of survivor care, and is both adopted and accepted by survivors/ parents independent of demographic differences. Research is underway to establish SurvivorLink's effectiveness as an advocacy/communication tool for survivor/parent with HCP in the self-management of their healthcare.
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Reynolds, Francoise M. T., and Peter Cimbolic. "Attitudes toward Suicide Survivors as a Function of Survivors' Relationship to the Victim." OMEGA - Journal of Death and Dying 19, no. 2 (October 1989): 125–33. http://dx.doi.org/10.2190/kr1x-qng3-2ygm-udyq.

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This study examined attitudes toward suicide survivors. Two variables were assessed: the impact of information on attitudes toward suicide survivors and whether the survivor's relationship to the victim affects the attitudes of others towards the survivor. Sixty participants responded to one of three fictional case histories that described a child's suicide, a spouse's suicide, or a parent's suicide. Prior to reading case vignettes, thirty of the participants read an article about suicide; the other thirty read death-related but not suicide-related materials. Results indicated that suicide information did not affect attitudes toward survivors. Further results indicated that reactions to suicide survivors are generally negative and the relationship of survivors to victims affects these reactions. Children of victims were seen least negatively; parents of a child who died by suicide received the most negative reactions.
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Soley, Berta. "Engaging torture survivors in the global fight against torture." Torture Journal 31, no. 1 (May 11, 2021): 88–92. http://dx.doi.org/10.7146/torture.v31i1.125764.

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Lived experience can be emancipating and also paralysing, but foremost, it is immensely valuable to combat what has been suffered in first person (Henry, 2021). How to recognise that contribution and engage torture survivors in the global fight against torture? What role do survivors play in society? How to involve survivors in advocacy and policy-making processes? What are the existing power (in)balances at play? Who gets to decide whether a survivor should speak up or not? Acknowledging that it can prompt some organisational, therapeutic, and professional considerations, what are the limits? How do we ensure that the survivor’s well-being is protected along the process? To what extend should survivors be engaged in our organisation’s decision-making? In front of the current on-going debate on the need of actively engaging torture survivors in the global fight against torture, IRCT held a webinar to explore this topic. The webinar examined torture survivor engagement in the rehabilitation process of rebuilding lives, seeking justice and torture prevention. This article summarises the discussion held during the webinar with the presentations from Léonce Byimana[1], Feride Rushiti[2], Kolbassia Haoussou[3] and Vasfije Karsniqi-Goodman[4] and further inputs from other IRCT-members. [1] Executive Director of Torture Abolition and Survivors Support Coalition (TASSC) [2] Executive Director of the Kosova Rehabilitation Center for Torture Victims (KRCTV) [3] Director of Survivor Empowerment at Freedom From Torture [4] Survivor and member of the Kosovan parliament
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Hoffman, Barbara, and Ellen Stovall. "Survivorship Perspectives and Advocacy." Journal of Clinical Oncology 24, no. 32 (November 10, 2006): 5154–59. http://dx.doi.org/10.1200/jco.2006.06.5300.

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From the moment of diagnosis, a cancer survivor faces serious life-altering decisions. Survivors who are informed about their options and who feel they have personal control over decision making generally perceive a higher quality of life than those who feel less informed and less in control. Health care providers are in a unique position to define a survivor's cancer care and to guide a survivor through treatment and post-treatment care. By implementing survivorship care plans and directing their patients to survivorship resources, health care providers can advocate for survivors and teach them to be effective self-advocates.
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Huemmer, Jennifer, Bryan McLaughlin, and Lindsey E. Blumell. "Leaving the Past (Self) Behind: Non-Reporting Rape Survivors’ Narratives of Self and Action." Sociology 53, no. 3 (May 24, 2018): 435–50. http://dx.doi.org/10.1177/0038038518773926.

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Using a symbolic interactionist framework, this study considers the narratives of non-reporting rape survivors. We use interviews to examine the complex processes that inform a survivor’s decision not to report. Rape is not interpreted as an isolated event; it is something that is seen as caused by, connected to, and affecting the survivor’s sense of self and agency. Rape forces the survivor to reconstruct a sense of agency in the aftermath of the traumatic attack. Rather than report the rape, the survivors constructed narratives that direct blame and accountability toward the “old self”. This less visible, yet still agentic strategy, allows the survivors to regain a sense of agency and control. As a result, a more positive, optimistic self can be constructed, while pursuing legal justice would force them to reenact an “old” self that cannot be disentangled from the rape.
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Elam, Jerome. "The OSCE/ODIHR Code of Practice for Ensuring the Rights of Victims and Survivors of Human Trafficking: A Survivor's Perspective." Journal of Human Trafficking, Enslavement and Conflict-Related Sexual Violence 4, no. 1 (July 7, 2023): 47–57. http://dx.doi.org/10.7590/266644723x16875292791265.

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The Organization for Security and Cooperation in Europe (OSCE) Office for Democratic Institutions and Human Rights (ODIHR) officially launched the Code of Practice for Ensuring the Rights of Victims and Survivors of Human Trafficking on 18 April 2023 at the 23rd Alliance Conference Against Trafficking in Persons in Vienna, Austria. Developed from survivor leader Jerome Elam's idea for a Victim and Survivor's Bill of Rights, the Code of Practice seeks to extend relevant international and regional standards for the protection of victims and survivors. To accomplish this, the Code of Practice offers specific guidance to Member States of the OSCE in the treatment, engagement and empowerment of victims and survivors of human trafficking. Drafted in collaboration with the Inaugural OSCE Office for Democratic Institutions and Human Rights (ODIHR) International Survivors of Trafficking Advisory Board (ISTAC), the 'Code of Practice' relies on the lived experience of ISTAC to create an umbrella of knowledge and support to protect victims and survivors. In addition, the Code of Practice seeks to minimize any additional trauma imparted upon victims and survivors upon their engagement by anti-trafficking stakeholders, including governmental organizations, the media and civil society. This is primarily accomplished by giving specific guidance on using trauma informed care in all aspects of victim and survivor identification and recovery and during their involvement with the legal system. The Code of Practice also offers recommendations for gender sensitive, disability sensitive, cultural and religious considerations to be employed by the anti-trafficking community. The role of survivor leaders is highlighted by the Code of Practice and member states are advised to foster the inclusion of survivor leaders in the development and refurbishment of legislation, policies and protocols for addressing the crime of human trafficking. The OSCE/ODIHR Code of Practice is an extension of existing policies and broadens the scope of protecting victim and survivors' rights so that the opportunity to reclaim their lives is allowed into full bloom. The unique nature of the Code of Practice in using the lived experience of survivor leaders adds a new dimension to the tools used by the anti-trafficking community and expands the reach of the fight against the darkness of human trafficking.
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Eng, Xue Wen, Sandra G. Brauer, Suzanne S. Kuys, Matthew Lord, and Kathryn S. Hayward. "Factors Affecting the Ability of the Stroke Survivor to Drive Their Own Recovery outside of Therapy during Inpatient Stroke Rehabilitation." Stroke Research and Treatment 2014 (2014): 1–8. http://dx.doi.org/10.1155/2014/626538.

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Aim. To explore factors affecting the ability of the stroke survivor to drive their own recovery outside of therapy during inpatient rehabilitation.Method. One-on-one, in-depth interviews with stroke survivors (n=7) and their main carer (n=6), along with two focus groups with clinical staff (n=20). Data was thematically analysed according to group.Results. Stroke survivors perceived “dealing with loss,” whilst concurrently “building motivation and hope” for recovery affected their ability to drive their own recovery outside of therapy. In addition, they reported a “lack of opportunities” outside of therapy, with subsequent time described as “dead and wasted.” Main carers perceived stroke survivors felt “out of control … at everyone’s mercy” and lacked knowledge of “what to do and why” outside of therapy. Clinical staff perceived the stroke survivor’s ability to drive their own recovery was limited by the lack of “another place to go” and the “passive rehab culture and environment.”Discussion. To enable the stroke survivor to drive their own recovery outside of therapy, there is a need to increase opportunities for practice and promote active engagement. Suggested strategies include building the stroke survivor’s motivation and knowledge, creating an enriched environment, and developing daily routines to provide structure outside of therapy time.
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Dissertations / Theses on the topic "Survivors"

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Buegel, Angela Lila. "Nutrition-Related Disease Risk in Pediatric Cancer Survivors." The Ohio State University, 2009. http://rave.ohiolink.edu/etdc/view?acc_num=osu1250544679.

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Pieters, Huibrie. "From 'Cancer Patient' to 'Cancer Survivor' oldest breast cancer survivors in transition /." Diss., Restricted to subscribing institutions, 2009. http://proquest.umi.com/pqdweb?did=2023818721&sid=1&Fmt=2&clientId=1564&RQT=309&VName=PQD.

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Skinner, Julie Margaret. "Coping with survivors and surviving : a study of how survivors, mothers of survivors, and teachers of survivors cope in the aftermath of child sexual abuse." Thesis, University of York, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.387547.

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Euteneuer, Jacob. "The survivors' affair." Thesis, Kansas State University, 2012. http://hdl.handle.net/2097/13727.

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Master of Arts
Department of English
Daniel A. Hoyt
In this project, the opening chapters of a novel, a fifty-foot man falls to the ground in Athens, Ohio. He is pronounced dead at the scene. What begins as a bizarre happening in a small college town soon spirals into an event with global repercussions. The federal government puts together a team of four scientists: Peter, a biologist; Jonathon, an archaeologist; Alexa, a forensic scientist; and Carly, a geneticist. As politicians, the media, and religious figures latch on to the giant man, the scientists try to determine if the body is real. Meanwhile, a religious cult develops in Athens. The cult believes the body is the Judeo-Christian God because it resembles images of God in popular and classic works of art. The giant man came from up in the clouds, has a white, billowing beard, and is old. Cult members tie bandanas around their eyes because they believe humans are not meant to look upon the body of God. The novel is told from a third-person omniscient point of view and shows the far-reaching consequences of such a fantastic event in our contemporary world. The novel delves into the mind of the Pope, a mortician, a lawyer, clergymen, students at Ohio University, the mayor of Athens, and a four-year-old boy, among many others. These characters try to come to terms with what it means to have the unreal and the impossible happen in their ordinary lives.
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Faubert, Joël. "Zombies and Survivors." Thesis, Université d'Ottawa / University of Ottawa, 2020. http://hdl.handle.net/10393/41077.

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Cops and Robbers on Graphs (C & R) is a vertex-to-vertex pursuit game played on graphs first introduced by Quilliot (in 1978) and Nowakowski (in 1983). The cop player starts the game by choosing a set of vertices which will be the cops’ starting positions. The robber player responds by choosing its own start vertex. On each player’s turn, the player may move its tokens to adjacent vertices. The cops win if the robber is captured (they occupy the same vertex). The robber wins if it can avoid capture indefinitely. The question, then, is to determine the smallest number of cops required to guarantee the robber will be captured. A variation of C & R called Zombies and Survivors (Z & S) was recently proposed and studied by Fitzpatrick. Z & S is the same as C & R with the added twist that the zombies are required to move closer to the survivor (by following a shortest path from the zombie to the survivor). Whenever multiple shortest paths exist, the zombies are free to choose which one to follow. As in C & R, we are interested in the minimum number of zombies required to guarantee the survivor will be caught. Chapter 1 summarizes important results in vertex-pursuit games. In Chapter 2 we give an example of a planar graph where 3 zombies always lose, whereas Aigner and Fromme showed in 1984 that three cops have a winning strategy on planar graphs. In Chapter 3 we show how two zombies can win on a cycle with one chord.
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Clarke, Philippa J. "Handicap in stroke survivors." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1996. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/MQ51554.pdf.

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Ralph, Andrea Jayne. "Acquired brain injury : the public's understanding of survivors and survivors' perceptions of stigma." Thesis, University of Hull, 2012. http://hydra.hull.ac.uk/resources/hull:6303.

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The portfolio has three parts: a systematic literature review, an empirical paper and a set of appendixes. Part 1 is a systematic literature review, in which the empirical literature assessing the public’s knowledge of acquired brain injury (ABI) and attitudes towards survivors is reviewed and critically evaluated. The review aims to identify the misconceptions commonly endorsed by the public and identify their attitudes towards survivors, to determine whether the stigmatisation of this population is likely. Part 2 is an empirical paper which aimed to explore whether survivors of ABI perceived stigma and anticipated discrimination. To achieve this, participants with ABI completed either an online (n= 114) or paper version (n= 36) of a questionnaire designed to assess their level of perceived stigma. This study further aimed to determine whether perceived stigma was associated with reduced self-efficacy and unemployment, given their negative impact on rehabilitation outcomes, continued recovery and quality of life post-injury. The findings and clinical implications are discussed and highlight the need for government and media campaigns to prioritise fighting the stigma of ABI and promoting the inclusion of survivors. Part 3 comprises the appendices, including a reflective account of the research process and additional information relating to Part 1 and Part 2 of the portfolio.
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Pepper, Sarah E. "Self Blame in Sexual Assault Survivors and Attributions to Other Sexual Assault Survivors." Thesis, University of North Texas, 2009. https://digital.library.unt.edu/ark:/67531/metadc12181/.

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Previous research indicates that survivors of sexual assault often blame themselves for the assault. Research has also shown that people blame the perpetrator in some situations and the survivor in other situations involving sexual assault. The purpose of this study was to discover if survivors of sexual assault who blame themselves tend to blame other survivors (survivor blame) in situations different from their own. Another purpose was to assess whether or not sexual assault survivors who do not blame themselves for their attack tend to blame other survivors. The participants' attributional style was also assessed in order to understand the relations between self-blame and survivor blame in situations involving sexual assault. Findings indicated that certain types of attributional style are related to self-blame in sexual assault survivors and blame toward sexual assault survivors depicted in vignettes. This indicates that attributional style may have important implications in the clinical setting to aid sexual assault survivors who experience self-blame, as well in educating society about sexual assault and the ultimate responsibility of perpetrators.
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Pepper, Sarah E. Sewell Kenneth W. "Self blame in sexual assault survivors and attributions to other sexual assault survivors." [Denton, Tex.] : University of North Texas, 2009. http://digital.library.unt.edu/ark:/67531/metadc12181.

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Abolio, Bolukaoto. "The Experiences of female rape survivors seen at Bopanang Centre, Northern Cape." Thesis, University of Limpopo (Medunsa Campus), 2009. http://hdl.handle.net/10386/278.

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Thesis(M Med.(Family Medicine))--University of Limpopo, 2009.
Aim: The aim of this research was to explore the experiences of female rape survivors seen at Bopanang Centre in Upington, Northern Cape Province. The objectives of the study were: 1 To describe the experiences of female rape survivors who received health care at Bopanang Centre Upington, Northern Cape. 2 To enable caregivers understand the experiences of women who survived rape. Design: The design was a descriptive exploratory qualitative study using in depth interviews on females who survived rape. The interviews were conducted in both English and Afrikaans and recorded on audio tapes while field notes and a research diary were documented by the researcher. Setting: The setting was Bopanang Centre in Upington town in the Northern Cape. Study population: The study population was all female rape survivors seen at Bopanang Centre, Upington in the Northern Cape Province. The sample size of women interviewed was 10 participants. Results: Most female rape survivors recall exceptionally well the events leading to the rape. All the survivors experienced various post rape distressful feelings ranging from anger, bitterness, humiliation, sadness, and confusion, self-blame and guilt, lack of trust and fear of men to the most extreme feelings such as crushed dignity and dead inside even considering committing suicide. Variable and inconsistent care of services had been offered to them, without fully considering their specific needs and experiences of females who had survived rape. Victimization and stigma were barriers for disclosure and reporting of the rape. Excessive alcohol use and abuse of sleeping pills had been reported by some of the survivors as a means to alleviate the post rape distress. From the study disclosure was the most important factor in determining how one was able to cope with distress following the rape. All those survivors who had good family support could cope reasonably well to deal with post rape distress. Conclusion: The study concludes that the experiences of female rape survivors seenat Bopanang Centre in Upington Northern Cape have not been adequately addressed by health care providers and stakeholders, health care and post rape services offered to them. Female rape survivors having a good family support cope reasonably well despite the distressful post rape feelings experiences they experience on a daily basis.
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Books on the topic "Survivors"

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Dunsford, Cathie. Survivors. Münster: Wurf, 1990.

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Nation, Terry. Survivors. Leicester: Ulverscroft, 2010.

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Peck, Abraham J. Survivors. New York, N.Y: Union of American Hebrew Congregations, 1985.

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Jonah, Zion Ben. Survivors. Sydney South: [Jesus Christians], 2002.

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Lorrah, Jean. Survivors. London: Titan Books, 1989.

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Lorrah, Jean. Survivors. New York, N.Y: Pocket Books, 1989.

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Campbell, Andrew. Innocent Survivors (Innocent Survivor). iUniverse, 2000.

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Survivors of Trauma: Survivor's Stories. Tellwell Talent, 2021.

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Wesley, Rawles James, and Dick Hill. Survivors. Brilliance Audio, 2014.

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Lawrence. Survivors. Lulu.com, 2005.

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Book chapters on the topic "Survivors"

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Johnson, Julia, Sheena Rolph, and Randall Smith. "Survivors and Non-Survivors." In Residential Care Transformed, 63–84. London: Palgrave Macmillan UK, 2010. http://dx.doi.org/10.1057/9780230290303_4.

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Kolff, Willem J., Belding H. Scribner, Thomas Starzl, and Eli A. Friedman. "Survivors." In Strength and Compassion in Kidney Failure, 21–24. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5296-9_5.

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Borruso, Paolo. "Survivors." In Debre Libanos 1937, 109–42. London: Routledge, 2023. http://dx.doi.org/10.4324/9781003367222-4.

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Deppa, Joan, Maria Russell, Dona Hayes, and Elizabeth Lynne Flocke. "Survivors." In The Media and Disasters, 12–68. London: Routledge, 2023. http://dx.doi.org/10.4324/9781003379478-4.

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Newins, Amie R., and Laura C. Wilson. "The Role of Reactions to Disclosure in Mental Health Among Survivors of Sexual Assault." In A Clinician's Guide to Disclosures of Sexual Assault, 23–34. Oxford University Press, 2021. http://dx.doi.org/10.1093/med-psych/9780197523643.003.0003.

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Although services and support have the potential to be helpful, a survivor’s trajectory toward recovery is contingent on the social reactions they receive. Given that fear of negative social reactions is the primary reason that sexual assault survivors delay disclosing or fail to disclose their victimization to others, we review numerous correlates of when and why survivors disclose their assault, typical social reactions survivors receive, the psychosocial impact of social reactions on survivors, and recommendations for ways providers can provide services that are more survivor-centered. Because nondisclosure limits the resources, services, and support available to survivors, it is important to understand what contributes to survivors’ decisions regarding if and when they tell others about their victimization. Furthermore, given the link between negative reactions and psychosocial difficulties, it is important to minimize the potential for a survivor to receive a harmful response from a provider.
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Newins, Amie R., and Laura C. Wilson. "Labels and Language Related to Sexual Assault." In A Clinician's Guide to Disclosures of Sexual Assault, 13–22. Oxford University Press, 2021. http://dx.doi.org/10.1093/med-psych/9780197523643.003.0002.

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Professionals need to critically consider the language they use when working with survivors of sexual assault because it can convey they are empathic helpers or, conversely, may inadvertently alienate survivors. This chapter discusses the inconsistencies in definitions within the literature, the importance of clarifying how others use terms, the significance of particular words (e.g., survivor vs. victim), the role of the survivor’s conceptualization of the incident(s), and the influence of sociocultural factors on our understanding of sexual violence. Professionals need to recognize that people’s knowledge and use of particular words and definitions will vary widely and that beliefs engrained in our society (e.g., gender roles, masculinity) create barriers to care for many survivors. Ultimately, intentional work focused on the language that professionals use is fundamental to providing survivor-centered support because it serves as an indicator of nonjudgmental and affirming services.
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"Survivors Helping Survivors." In Tracing and Documenting Nazi Victims Past and Present, 131–54. De Gruyter Oldenbourg, 2020. http://dx.doi.org/10.1515/9783110665376-008.

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"Survivors." In Surface and Destroy, 131–45. The University Press of Kentucky, 2011. http://dx.doi.org/10.2307/j.ctt2jcr03.14.

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"Survivors." In Warplane 04, 45–48. Amsterdam University Press, 2017. http://dx.doi.org/10.1515/9789086163243-008.

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"Survivors." In Pioneer Urbanites, 44–58. University of California Press, 2023. http://dx.doi.org/10.2307/jj.8501203.10.

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Conference papers on the topic "Survivors"

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Gamber, Cayo. "AI Technology, Holocaust Survivors, and Human Interactions at Holocaust Museums." In 10th International Conference on Human Interaction and Emerging Technologies (IHIET 2023). AHFE International, 2023. http://dx.doi.org/10.54941/ahfe1004005.

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In this presentation, I will focus primarily on three constituencies: the individuals who developed the strategies for using AI technologies to tell survivors' personal stories; the survivors who were willing to participate in the Dimensions in Testimony (DiT) project to use volumetric capture in order to record the narrative of their (and their extended family's) experience of the Shoah, and the audience members who visit with the interactive DiT survivor recordings.Currently in use at over a dozen museums worldwide, pre-recorded interviews with individual Holocaust survivors incorporate specialized display technology and natural language processing in order to generate interactive conversations between survivors and visitors. The video recordings are prepared to answer well over 1,000 possible questions visitors might ask of them. In addition, a limited number of these AI recordings also are available to visitors to the Dimensions in Testimony (DiT) website.Members of the public who “visit with” individual survivor AIs are able to interact with eyewitnesses to history to learn from those who actually were there. Given that, these conversations are directed by the visitors to specific Holocaust museums and/or the DiT website themselves, visitors participate in a highly-personalized, inquiry-based educational interaction.For the past five years, I have studied both the responses of survivors who participated in this effort and I have engaged in observational study of individuals interacting with the DiT recordings both in a museum setting (asking questions of Renée Firestone at the Holocaust Museum Los Angeles [HMLA]) and students interacting with the DiT recordings available through the USC Shoah Foundation website (in particular, how students interact with the interactive DiT recording of Pinchas Gutter).In order to evaluate how this particular technology has been “accepted,” I will address the following points of inquiry:1.How might engaging in interactions that feel like self-directed interviews encourage greater empathy and/or compassion on the part of interlocutors? Or, conversely, is it possible that “users” will try to “game” the recordings by asking questions the recording cannot answer?2.What were the ground rules for capturing the testimony of the survivors?3.How do survivors themselves feel about participating in this innovative technology/project? 4.What do we learn about ourselves as a result of engaging in these interactions with the DiT recordings?5.How might these interactions redefine Holocaust education?
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Matthews, Tara, Kathleen O'Leary, Anna Turner, Manya Sleeper, Jill Palzkill Woelfer, Martin Shelton, Cori Manthorne, Elizabeth F. Churchill, and Sunny Consolvo. "Stories from Survivors." In CHI '17: CHI Conference on Human Factors in Computing Systems. New York, NY, USA: ACM, 2017. http://dx.doi.org/10.1145/3025453.3025875.

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Yalda, Mayada. "The Ten-Year Survival Rate for Breast Cancer Females in Kurdistan/Iraq: Special Facts and Features." In 3rd Scientific Conference on Women’s Health. Hawler Medical University, 2022. http://dx.doi.org/10.15218/crewh.2022.03.

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Background and objective: Worldwide, breast cancer varies widely in survival rate and age at first diagnosis. Owing to the limited follow up database in developing areas, this study aimed to estimate the 10-years survival rate for breast cancer in Kurdistan/Iraq and correlate it with clinicopathological variables. Methodology: This follow-up study included 160 breast cancer patients diagnosed before 2010. Their data were obtained from Duhok/central lab. Survivors and families of deceased cases were contacted to approve the survivor. Cases were reviewed for variables including estrogen and HER-2 status. Results: The mean age of patients was 44.9 years. Only 66 of them (41.2%) survived for 10-years. None of the survivors was below 30 or above 70 years. Death rate was significantly high between 30-39 years. The survival rate was highest (75.8%) between 40-49 years. The lymph nodes involvement was seen in 61.87% with statistically higher mortality rate. Estrogen was positive in > ¾ of patients (76.9%) which was statistically high among survivors. However, in deceased group estrogen positivity was also high (41.88%), while HER-2 were only significant between 40-49 years. Conclusion: The relatively low survival rate, the young age at first diagnosis, despite the high estrogen receptors positivity are facts can’t be explained by delay treatment and need thorough search for a possible genetic or other underling rezone.
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Tan, Huey, Matthew Cramp, and Ashwin Dhanda. "P026 Differential epigenetic regulation in survivors and non-survivors from severe alcoholic hepatitis." In Abstracts of the British Association for the Study of the Liver Annual Meeting, 22–24 November 2021. BMJ Publishing Group Ltd and British Society of Gastroenterology, 2021. http://dx.doi.org/10.1136/gutjnl-2021-basl.35.

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Kalpathy, Ravi, Hosam M. Mahmoud, and Walter Rosenkrantz. "Survivors in Leader Election Algorithms." In 2014 Proceedings of the Eleventh Workshop on Analytic Algorithmics and Combinatorics (ANALCO). Philadelphia, PA: Society for Industrial and Applied Mathematics, 2013. http://dx.doi.org/10.1137/1.9781611973204.11.

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Magnusson, Charlotte, Héctor A. Caltenco, David McGookin, Mikko Kytö, Ingibjörg Hjaltadóttir, Thóra B. Hafsteinsdóttir, Helga Jónsdóttir, and Ingibjörg Bjartmarz. "Tangible Interaction for Stroke Survivors." In TEI '17: Eleventh International Conference on Tangible, Embedded, and Embodied Interaction. New York, NY, USA: ACM, 2017. http://dx.doi.org/10.1145/3024969.3025073.

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Sudirman, Nur Andini, and Alif Aulia Masfufah. "Coping Strategy among Bullying Survivors." In Proceedings of the 4th ASEAN Conference on Psychology, Counselling, and Humanities (ACPCH 2018). Paris, France: Atlantis Press, 2019. http://dx.doi.org/10.2991/acpch-18.2019.5.

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Ferro, D., F. Violi, C. Quintarelli, M. Saliola, C. Alessandri, and C. Cordova. "INFLUENCE OF HYPERFIBRINOLYSIS ON THE PROGNOSTIC VALUE OF FACTOR VII IN PATIENTS WITH LIVER INSUFFICIENCY." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643066.

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As the most coagulation factors are sintethized by liver cel1,patients with liver failure (LF) have low values of coagulation factors. These latter were investigated to assess their prognostic value in LF patients,but none was proved to be useful in the individual assessment of LF. A previous study showed that in fulminant hepatitis,factor VII,whose half-life is very short,was a marker of imminent death;a further investigation supported this finding in patients with chronic LF. We evaluated the influence of hyperfibrinolysis on the prognostic value of factor VII in 37 consecutive patients affected by liver cirrhosis (LC) in severe decompensated state. 16 died within 30-50 days from the hospitalization,2 1 suvived and was discharged 30-80 days from the hospitalization. Positive FDP ( >10pgr/ml;Thrombo-Wellcotest) was found in both survivors (6) and non survivors (7) patients. Factor VII activity (Mariani's method) clear-cut differentiated survivors and non survivors indipen-dently if they had or not positive FDP. Factor VII activity of non survivors was significant lower and did not overlap that of survivors. The absence of influence of hyperfibrino1ysis on the prognostic value of .factor VII further supports the importance of evaluating this clotting factor on patients with LF.
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Garzke, William H., and Kenneth M. Smith. "RMS Lusitania - A Design History and Forensic Analysis of Her Sinking." In SNAME Maritime Convention. SNAME, 2022. http://dx.doi.org/10.5957/smc-2022-064.

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This paper represents a final report of the review of evidence from wreck site of the RMS Lusitania based on material compiled by the late Gregg Bemis, owner of the wreck. It also discusses new evidence from the cargo manifest of Lusitania that was classified for almost 100 years as well as survivor’s accounts from several different sources and the results from previous expeditions to the wreck site. In this forensics analysis several considerations will be made from the study of the documents, testimony, and wreckage: 1. The conclusions will be consistent with witnesses and survivors during the sinkage of this ship 2. The probable cause will be consistent with the normal laws of physics 3. The cause reported is what actually happened, to a reasonable degree of engineering certainty.
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Eisinger, François, Jérôme Viguier, Xavier Pivot, Jean-Yves Blay, Yvan Coscas, Claire Roussel, and Jean-François Morère. "Abstract B33: Cancer survivors as messengers." In Abstracts: AACR International Conference on Frontiers in Cancer Prevention Research‐‐ Oct 22-25, 2011; Boston, MA. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1940-6207.prev-11-b33.

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Reports on the topic "Survivors"

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Snyder, Claire, Christina T. Yuan, Renee F. Wilson, Katherine Smith, Youngjee Choi, Paul C. Nathan, Allen Zhang, and Karen A. Robinson. Models of Care That Include Primary Care for Adult Survivors of Childhood Cancer: A Realist Review. Agency for Healthcare Research and Quality (AHRQ), February 2022. http://dx.doi.org/10.23970/ahrqepcrealistmodelsofcare.

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Objectives. We had two aims: (1) identify and analyze models of survivorship care for adult survivors of childhood cancer that include primary care, and (2) identify available tools, training, and other resources for adult survivors of childhood cancer. Methods. For each aim, we used realist synthesis to provide insights on how and for whom, in what contexts, and via what mechanisms the models of care and resources we identified can be effective for adult survivors of childhood cancer. We developed an initial program theory through searches of the literature and discussions with Stakeholders. We then identified and summarized quantitative evidence that supported or refuted the theory and developed specific hypotheses about how contexts and mechanisms may interact to produce outcomes (i.e., “CMO” hypotheses). The final program theory and CMO hypotheses were presented to Stakeholders for feedback. Results. Our final refined theory describes how, within the overall environment, survivor and provider characteristics and facilitators/barriers interact to produce intermediate and final outcomes. We focus on the role of models of care and resources (e.g., care plans) in these interactions. The program theory variables seen most consistently in the literature include oncology care versus primary care, survivor and provider knowledge (i.e., survivor risks and needs), provider comfort treating childhood cancer survivors, communication and coordination between and among providers and survivors, and delivery/receipt of prevention and surveillance of late effects of original cancer treatment. In turn, these variables played the most prominent role in the seven CMO hypotheses (4 focused on survivors and 3 focused on providers) regarding what works for whom and in what circumstances. Conclusions. To enable models of care that include primary care for adult survivors of childhood cancer, there needs to be communication of knowledge to both survivors and primary care providers. Our program theory provides guidance on the ways this knowledge could be shared, including the role of resources in doing so, and our CMO hypotheses suggest how the relationships illustrated in our theory could be associated with survivors living longer and feeling better through high-value care.
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Idris, Iffat. Documentation of Survivors of Gender-based Violence (GBV). Institute of Development Studies (IDS), July 2021. http://dx.doi.org/10.19088/k4d.2021.103.

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This review is largely based on grey literature, in particular policy documents and reports by international development organizations. While there was substantial literature on approaches and principles to GBV documentation, there was less on remote service delivery such as helplines – much of this only in the wake of the COVID-19 pandemic. In addition, very little was found on actual examples of GBV documentation in developing contexts. By definition, gender featured strongly in the available literature; the particular needs of persons with disabilities were also addressed in discussions of overall GBV responses, but far less in GBV documentation. GBV documentation refers to the recording of data on individual GBV incidents in order to provide/refer survivors with/to appropriate support, and the collection of data of GBV incidents for analysis and to improve GBV responses. The literature notes that there are significant risks associated with GBV documentation, in relation to data protection. Failure to ensure information security can expose survivors, in particular, to harm, e.g. reprisal attacks by perpetrators, stigma, and ostracism by their families/ communities. This means that GBV documentation must be carried out with great care. A number of principles should always be applied when documenting GBV cases in order to protect survivors and prevent potential negative effects: do no harm, survivor-centered approach, survivor autonomy, informed consent, non-discrimination, confidentiality, and data protection (information security).
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Tangka, Florence K. L., Sujha Subramanian, Madeleine Jones, Patrick Edwards, Sonja Hoover, Tim Flanigan, Jenya Kaganova, et al. Young Breast Cancer Survivors: Employment Experience and Financial Well-Being. RTI Press, July 2020. http://dx.doi.org/10.3768/rtipress.2020.rr.0041.2007.

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The economic burden of breast cancer for women under 50 in the United States remains largely unexplored, in part because young women make up a small proportion of breast cancer cases overall. To address this knowledge gap, we conducted a web-based survey to compare data from breast cancer survivors 18–39 years of age at first diagnosis and 40–49 years of age at first diagnosis. We administered a survey to a national convenience sample of 416 women who were 18–49 years of age at the time of their breast cancer diagnosis. We analyzed factors associated with financial decline using multivariate regression. Survivors 18–39 years of age at first diagnosis were more likely to report Stage II–IV breast cancer (P<0.01). They also quit their jobs more often (14.6%) than older survivors (4.4%; P<0.01) and faced more job performance issues (55.7% and 42.8%, respectively; P=0.02). For respondents in both groups, financial decline was more likely if the survivor had at least one comorbid condition (odds ratios: 2.36–3.21) or was diagnosed at Stage II–IV breast cancer (odds ratios: 2.04–3.51).
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Ganz, Patricia A. Managing Menopausal Symptoms in Breast Cancer Survivors. Fort Belvoir, VA: Defense Technical Information Center, October 1998. http://dx.doi.org/10.21236/ada368408.

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Ganz, Patricia A. Managing Menopausal Symptoms in Breast Cancer Survivors. Fort Belvoir, VA: Defense Technical Information Center, October 1995. http://dx.doi.org/10.21236/ada303160.

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Ganz, Patricia A. Managing Menopausal Symptoms in Breast Cancer Survivors. Fort Belvoir, VA: Defense Technical Information Center, October 1997. http://dx.doi.org/10.21236/ada341366.

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Hendricks, Sam. Video: Better care for childhood cancer survivors. Monash University, February 2024. http://dx.doi.org/10.54377/696b-2665.

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Lin, Cian-Cian, and Yu-Ning Her. Demoralization in cancer survivors － An updated systematic review and meta-analysis for quantitative studies. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, December 2022. http://dx.doi.org/10.37766/inplasy2022.12.0048.

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Review question / Objective: The mean demoralization level among cancer survivors. Rationale: Demoralization often results in functional impairments across all stages of cancer patients. Cancer patients are not only vulnerable during hospice but also vulnerable during their survivorship. The purpose of this review is to examine the risk of demoralization and associated risk factors among cancer survivors. Condition being studied: Demoralization in cancer survivors.
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Sripad, Pooja. Exploring barriers and enablers of service provision for survivors of human trafficking in the Bay Area: An action research study. Population Council, 2021. http://dx.doi.org/10.31899/sbsr2021.1067.

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Despite increasing recognition of public health and rights issues associated with human trafficking globally and in the United States following the Trafficking Victims Protection Act of 2000, there has been limited research on how to systematically strengthen service access for survivors of sex and labor trafficking. The experience of service providers may provide insight into how trafficking survivor responses and service networks function in California’s Bay Area. This study explores provider perspectives on existing service networks and collaboration dynamics, including the barriers to and enablers of long-term service provision and survivor follow-up. A participatory research design included qualitative interviews with key informants working at nongovernmental organizations, organizational website reviews, and consultation with network service providers in the Greater San Francisco Bay Area. This study approach allowed for eliciting in-depth reflections of service provision, collective generation of stakeholder mapping, and consensus-driven recommendations arising from barriers and enablers to anti-trafficking service provision. This report enhances stakeholder awareness of existing organizational and policy resources and offers insights into research and programming on how anti-trafficking service response networks can be strengthened to provide survivor-centric support in the long-term.
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González-Prats, Maria Carolina. Examining the Narratives of Military Sexual Trauma Survivors. Portland State University Library, January 2000. http://dx.doi.org/10.15760/etd.7385.

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