Experiences Of Injustice Research Articles

Silenced Echoes: Revenge Fantasies Toward Unjust Events in Drawings and Narratives of Indian Hindu Women.

The study explored revenge fantasies as a response to perceived injustices among Indian Hindu women amid the prevalent gender-based violence. A mixed-method design with 52 women (18-56 years) was used to collect their drawings and narratives depicting revenge fantasies, demographics, the Traumatic Events Questionnaire, and the Injustice Experiences Questionnaire. Participants highlighted non-family events with strangers as perpetrators, preferring avoidance as the common revenge fantasy. Dominant themes included gender bias, sexual violence, body shaming, and feelings of inferiority. Passive aggression/forgiveness as a drawing indicator correlated negatively with Injustice Experiences Questionnaire, offering insights into revenge fantasies toward unjust events among Hindu women.

Stress and Quality of Life of Parents of Children With POLR3-Related Leukodystrophy: A Cross-Sectional Pilot Study.

Background: RNA polymerase III (POLR3)-related leukodystrophy is a rare, neurodegenerative disorder characterized by hypomyelination, hypodontia, and hypogonadotropic hypogonadism. Despite the challenges of caring for a child with POLR3-related leukodystrophy, few studies have examined parents' disease burden. We sought to investigate quality of life and stress levels amongst parents of children with POLR3-related leukodystrophy. Methods: 43 parents of 32 children completed questionnaires on demographics, stress, quality of life, coping mechanisms, and experience of injustice. Detailed clinical data was collected from all patients. Results: Mothers (t[27] = -8.66, P < .001) and fathers (t[16] = -4.47, P < .001) had lower quality of life scores compared to the normative population, yet 80% of parents' stress scores fell within the normal stress range. Parents' experience of injustice scores were high (>60). Correlations were found between and within parents' scores. Years since disease onset and certain life circumstances correlated to mothers' quality of life scores; however, no correlation was found between modifiable factors and fathers' quality of life scores. Helpful coping mechanisms included those that allowed parents to be involved in their child's life. Conclusions: This is the first study to assess stress and quality of life in this population. These results shed light on the importance of implementing services and social support to improve the well-being of parents.

Franz Kafka and Antisemitism: The Historical Context of Der Prozess

Abstract Franz Kafka’s novel The Trial (1915) is open to many interpretations. One aspect, however, which has not been taken sufficiently into account, is its relation to the antisemitic trials of his times, where Jews were accused of treason or ‘ritual murder’: the trials of Tisza (Austro-Hungary, 1882, in what is now Hungary), Dreyfus (France, 1894–9), Hilsner (Austro-Hungary, 1899–1900, in what is now the Czech Republic), and Beiliss (Imperial Russia, 1912–13, in what is now Ukraine). Kafka knew about them and made comments in his correspondence or diaries. This ‘Jewish moment’ is essential for the understanding of the novel. However, Joseph K. has no religious or ethnic identity: Kafka discovers in the Jewish experience the quintessential human experience of Injustice.

Children’s Plight to Life of Poverty and Injustice Captured in F.H. Batacan’s Smaller and Smaller Circles

This research paper analyzes how children's experiences of poverty and injustice are imagined and articulated in F. H. Batacan's novel Smaller and Smaller Circles. By employing content analysis, passages and excerpts from the novel were identified and subjected to in-depth analysis using sociological and philosophical approaches to literary criticism. The study aims to explore the novel’s portrayal of the causes and effects of these experiences, and how it reflects the broader discourse on the morality of children's suffering. The findings reveal that the novel imagines children's experiences of poverty and injustice as resulting from a complex interplay of societal norms, such as generational responsibility, the culture of silence, and toxic masculinity. Institutional failures, including the church’s complicity, inefficient law enforcement, and barangay deficiencies, further exacerbate these conditions. Additionally, media and societal attitudes, particularly misplaced faith and victim blaming, contribute to the perpetuation of these harmful conditions. The novel portrays these imagined experiences as leading to psychosocial trauma, delayed or denied justice, delinquency, and even suicide. Through this portrayal, the novel positions itself within the discourse on the morality of children's suffering, raising questions about the ethical implications of these societal failures.

The Relationship of Pain Intensity, Perceived Injustice, and Pain Catastrophizing to Heart Rate Variability In Naturally Occurring Acute Pain.

Behavioral factors of pain catastrophizing and perceived injustice are associated with pain intensity in chronic pain. Diminished heart rate variability (HRV) is also strongly associated with chronic pain. These factors have been less explored earlier in the pain experience and it is unclear whether they play a role in the transition from acute to chronic pain. The aim of this study was to determine the relationship between pain catastrophizing, perceived injustice, pain intensity, and HRV in naturally occurring acute pain. Ninety-seven patients were recruited from local outpatient physical therapy clinics. Seated HRV was captured on 94 patients via Polar chest strap while patients were taking a survey via iPad. In addition to sociodemographic data, the survey included the Pain Catastrophizing Scale (PCS), Injustice Experience Questionnaire (IEQ), and Numeric Pain Rating Scale (NPRS). The natural log of high-frequency power (lnHFP) HRV was used in the statistical analysis. Multiple linear regression modeling revealed that lower pain catastrophizing, higher perceived injustice, and lower pain intensity were associated with lower HRV, and accounted for 11.4% of the variance in HRV. While greater chronic pain intensity is associated with lower HRV, the relationship is reversed in the setting of acute pain. These findings highlight the need to better understand the unique factors that contribute to lower HRV in the acute phase.

Trauma Healing through Psalms 136–139: a Trauma-Informed Canon-Critical Framework

Abstract This article draws together insights from trauma theory and the conversation in Psalms scholarship known as “Psalmenexegese und Psalterexegese” or as the question of “shape and shaping” to propose a reading of Pss 136–139 as a pathway to trauma healing. This sequence of psalms moves participants toward healing by preparing them for the work of trauma healing through a mantra-like focus (Ps 136), unleashing the full range of human stress-responses to trauma (Ps 137), directly answering each of these stress-responses (Ps 138), and then—in a dramatic resolution—characterizing God as intimately concerned with human biology and life while continuing to acknowledge ongoing experiences of pain and injustice (Ps 139). The article illustrates the proposed framework for trauma healing with examples from pastoral work with asylum-seekers.

Taking the car out of the countryside: Understanding opposition to climate policy in rural Finland

There is an urgent need to decarbonize mobility. Yet, the necessary policies risk compounding existing vulnerabilities and controversies and creating new ones, potentially leading to political polarization. One affected population consists of people living in rural peripheries. Drawing from a Finnish public consultation survey (n = 18,378), we explore how rural participants (n = 4995) experience policies and proposals to decarbonize mobility: how they perceive the problem and what they propose as solutions. We draw on Noortje Marres' concept of attachments to understand the socio-material, discursive and subjective attachments that coalesce in rural experiences of policies and proposals to decarbonize mobility. We contribute to previous research on spatial inequalities in the mobility transition by showing how electric vehicles might not simply replace internal combustion engines in rural areas. We also show how distributive policies, i.e. subsidies, might not solve the problems, because different dimensions of attachments are intertwined and serve to maintain each other and thus reinforce existing experiences of inaccessibility and injustice. We conclude with suggestions for how to better address just and acceptable mobility transitions for rural dwellers.

We, the receptors: Planning and the politicization of local opposition to fracking in Britain

The British government used to herald shale gas as a bridge fuel to a zero-carbon economy, trying (and ultimately, failing) to incorporate this hydrocarbon into a punctuated energy transition that is still under way in the country. On the one hand, planning translated central political decisions into local priorities, but on the other hand, it politicized public opposition to fracking. Although, there have been considerable criticisms of the planning process for fracking in Great Britain, we still lack a grounded understanding of how planning influenced the wider dynamics of public engagement with shale gas development. Drawing on ethnographic and participatory research across three locations in northern England, I explore how the planning process was experienced by the public and how its local participants were impacted by it. The ways in which planning dealt with evidence, public perception and democratic legitimacy suggested that planning was reinforcing the governmental pro-fracking policies while simultaneously undermining its own legitimacy, as questions about validity, impartiality and democracy were being raised. Rather than merely a technocratic arena for adjudicating between private and public interests, planning had a transformative effect on local participants and served as an important moment for mobilizing more politicized forms of public opposition against fracking, which undermined the energy-transition narratives touted by the government. I use anthropological theorizations of ritual to explain the concrete local dynamics that led to this unintended effect. This case study suggests that centrally orchestrated energy transitions may fail when they are enacted through local processes that foster experiences of injustice and lack of local control among the opposing publics.

An Analysis of the Time Travel Device for Exploring Black-White Race Relations in Octavia E. Butler’s Kindred

The thesis focuses on Octavia E. Butler’s novel Kindred and employs close reading and textual analysis to explore the depiction of black-white race relations through the time travel device. It points out that Butler cleverly uses the method of temporal rescue to break the “grandmother paradox.” The dual-time setting allows Dana, while saving her white ancestors, to witness the harsh realities faced by her African American ancestors in American history. On this basis, the thesis reveals and critiques the historical roots of racial issues, highlighting the physiological and psychological experiences of racial injustice endured by African Americans, as well as the persistence and improvement of the legacy of slavery. It emphasizes the importance of African Americans confronting history to break the cycle of oppression and shape a more equitable future.

Experience of Institutionalization &amp; Occupational Injustice Among Boys at a Residential School &amp; Treatment Center

Abstract Date Presented 03/21/24 This research project explores the experience of occupational injustice (OI) among children in institutionalized care. It delves into implementation of occupation-centered care in institutionalized settings as a means to mitigate the effects of OI. Primary Author and Speaker: Lindsey Warren

Predictors of Delayed Recovery in Japanese Patients With Whiplash-Associated Disorders: The Role of Initial Catastrophizing and Disability Levels.

Background Whiplash-associated disorders are sequelae of traffic accidents that frequently result in sustained pain and disability due to a broader spectrum of symptoms than typical neck pain. Several studies have used the length of time from injury to the completion of insurance claims as a measure of recovery time for patients with whiplash-associated disorders. However, studies on the initial factors in patients whose treatment exceeds 90 days are lacking. Therefore, this study aimed to identify key factors predicting prolonged treatment duration in Japanese patients with whiplash-associated disorders. Methodology We included 103 outpatients who presented with neck pain after a motor vehicle accident. During their initial visits, various factors were comprehensively assessed, including pain intensity, Neck Disability Index (NDI), six items of the Pain Catastrophizing Scale (PCS-6), a short version of the Tampa Scale of Kinesiophobia, the Injustice Experience Questionnaire, cervical range of motion, and radiographic findings. Patients were categorized into "early recovery" or "delayed recovery" groups based on the time elapsed between the first assessment and the end of the treatment period. Logistic regression analysis identified cut-off values from receiver operating characteristic curves to help identify factors contributing to delays in the recovery process. Results Analysis showed that initial NDI and PCS-6 scores of ≥35% and ≥12, respectively, were significant predictors of delayed recovery, increasing the odds of delay by factors of 3.19 and 4.46, respectively. Conclusions Our findings may aid in appropriate clinical decision-making and lead to interventions to minimize the negative impact of prolonged treatment duration on patient recovery.

(086) MEDICAL GASLIGHTING AND VULVOVAGINAL PAIN DISORDERS

Abstract Introduction Gaslighting is a form of epistemic injustice that involves testimonial injustice, in which patient’s experiences are discounted by others. The incidence of epistemic injustice has been described in a number of pain conditions including chronic fatigue syndrome and fibromyalgia, as well as in marginalized obstetric populations. Little research has been directed towards epistemic injustice in populations seeking treatment for benign gynecologic conditions or the unique context of vulvovaginal pain conditions. Additionally, little is known about the consequence of this type of injustice on patient’s perception of their care or willingness to seek care. Objective The purpose of this study was to develop a patient-validated instrument to measure patient experience of epistemic injustice in their past gynecologic care and to use the instrument to explore patient experiences in a vulvovaginal pain referral center. Methods An instrument was designed by the study team to quantify the incidence and distressed caused by gaslighting in patients seek care for vulvovaginal pain conditions. This was created based on common themes from written testimonials of patients available from National Vulvodynia Association. After construction, the instrument was submitted for feedback to officers from two vulvovaginal pain disorder patient societies. The survey was modified to include the feedback from these sources. The survey was then completed by patients establishing care with the clinic prior to their first appointment. Results 187 patients completed the survey in part or in full. Patients reported having seen an average of 5.7 providers prior to presentation. Patients felt supported by only 42% of past providers. Patients felt belittled by 27% of past providers. Patients felt 21% of past providers did not believe their symptoms. 45% of patients were told they “just needed to relax more”; 18% percent were recommended to drink alcohol to improve their condition; 55% considered giving up seeking care because they felt their concerns were not being addressed; 31% were told their symptoms were caused by high levels of anxiety; 22% were referred to psychiatry without other medical treatment for their symptoms; 19% felt unsafe during a medical encounter. 39% percent of patients were made to feel they were “crazy” and this was the most distressing of the questions asked (average 7.3/10 on a likert scale for distress for patients who had experienced this). Conclusions A survey based on patient concerns and validated by patients affected by vulvovaginal pain conditions has not been previously reported. This instrument was applied to a patient population at a large referral center for vulvovaginal pain conditions and the results showed that patients commonly experienced many forms of epistemic injustice, and greater than half of patients consider cessation of care for their condition because of these experiences. Disclosure Any of the authors act as a consultant, employee or shareholder of an industry for: Dr. Jill Krapf is a medical advisor for Evvy. Dr. Andrew Goldstein is a part time Employee of Daré Bioscience. He is a member of the board of directors of The Gynecologic Cancers Research Foundation. He is an advisor for: AbbVie, Incyte, and the National Vulvodynia Association. He has received research funding from Incyte.

Comparison Between Disability, Physical Performance, and Other Biopsychosocial Factors in Full-Duty Career Firefighters Working With and Without Current Low Back Pain.

Low back pain (LBP) is highly prevalent and a top cause of disability-related early retirement in firefighters. Those with a lifetime history of LBP have various deficiencies that are associated with increased injury risk and absenteeism. However, the influence of working with current LBP on disability, physical performance, and other biopsychosocial factors has not been fully characterized in this population. The purpose of this study was to compare anthropometric measures, exercise habits, physical fitness/performance, disability/work ability, and other biopsychosocial factors of firefighters working with and without current LBP. A cross-sectional study was conducted using baseline assessments from 419 full-duty career firefighters without documented work restrictions (age: 37.6 ± 8.8 y; 5 F, 414 M) who were enrolled in a regional wellness initiative in Southern California, USA. Current LBP status was determined by a questionnaire and confirmed by an interview. Anthropometric measures, patient-reported outcomes, and physical fitness tests were used to assess body mass index; body fat %; waist circumference; strengthening, cardiovascular, and flexibility exercise frequency; back and core muscular endurance; functional movement quality, perceived back-related disability, lift and carry ability, and firefighter task ability; sleep quality; and perceptions of fear and fatigue and catastrophic injustice experience. Scores for participants with and without current LBP were compared using analysis of variance and chi-square analysis. The point prevalence of current LBP was 19.81% (83/419). For the entire cohort, those with current LBP had significantly worse scores than those without current LBP for all assessed variables, except core muscular endurance and functional movement quality. These trends held up when analyses were stratified by age and obesity categories, and approximately half of the comparisons retained statistical significance. A significantly greater percentage of participants with current LBP were working with some level of back-related disability and/or perceived physical demand characteristics of work level below the required very heavy job demands. Nearly one-fifth of full-duty career firefighters without documented work restrictions reported having current LBP, and these individuals had deficits in several modifiable biopsychosocial factors across five health domains. These findings can help guide future research and implementation efforts in the fire service designed to improve performance, resiliency, work readiness, recovery, and quality of life, as well as to reduce impairment, disability, and absenteeism and increase presenteeism.

An Interpretative Phenomenological Analysis of Residence Permit Appeals at the Administrative Courts of Finland: Acquiescence Bias by Legalised Judicial Injustices in Finland

Arctic law and politics are heavily focused on citizens and their welfare. In recent times, migration has led to an increase in immigrants to the Arctic region, expanding discussions on diversity, equality, and inclusion. This article analyses immigrant experiences of the wheels of justice when appealing extended-residence decisions in Finland. There has been research on residence applications but there is no previous research on appealing residence decisions in Finland. Using interpretative phenomenological analysis (IPA), the article analyses four Africans’ experiences of (in)justice during residence permit decision appeals lodged through the administrative courts in Finland 2011–2020. The article uses the Renault concept to argue and underscore the experiences of injustice and to underscore the gathered, analysed emerging themes and the patterns observed in the handling of the residence permit appeal cases from a legal and political perspective. The information was gathered through in-depth interviews using open-ended, structured questions, and the analysis of personal text and information was collated using MAXQDA software. The article highlights the incidences of human rights violations, injustice, mental health and well-being issues, inadequate information and distrust of the administrative justice system, and the risk that this poses to Arctic law and politics as right-wing politics are on the rise.

Perceived Injustice and Anger in Fibromyalgia With and Without Comorbid Mental Health Conditions: A Hebrew Validation of the Injustice Experience Questionnaire.

Perceived injustice (PI), assessed by the Injustice Experience Questionnaire (IEQ), is an important trigger of anger. Both PI and anger are associated with adverse chronic pain outcomes, and with comorbid mental health severity. We aimed examined the roles of PI and anger in mediating pain across Fibromyalgia patients, with and without comorbid anxiety/depression (FM+A/D, FM-A/D, respectively), as well as rheumatoid arthritis (RA), and pain-free controls (PFC). We hypothesized the highest levels of PI, anger, and pain in FM+A/D patients, followed by FM-A/D, RA, and PFC, thus also validating a Hebrew version of the IEQ. We translated the IEQ using the forward-backward method and collected data online. Based on self-reported anxiety/depression, the sample comprised 66 FM+A/D patients, 64 FM-A/D, 34 RA, and 32 PFCs. Assessments included the IEQ, state and trait anger, pain intensity, anxiety, depression, and pain catastrophizing. The structure and reliability of the Hebrew IEQ were examined using factor analysis and Cronbach alpha. Bootstrapped-based modeling was used to test the roles of state and trait anger in mediating and moderating the relationship between PI and pain intensity. We confirmed a one-factor structure of the IEQ, with excellent reliability. FM+A/D patients demonstrated the highest scores in all measures. Within this group, trait anger moderated the mediating effect of state anger in the relationship between PI and pain intensity. Our findings validate a Hebrew IEQ and highlight the importance of PI and state and trait anger in the differential manifestation of mental health comorbidity in FM.

Epistemic injustice and unwellness in the classroom: Creating knowledge like we matter

In this essay, I reflect on my experience teaching graduate classes on social justice in Yerevan. Here, an important part of the experience of injustice is epistemic. By this, I mean that students’ discourses of injustice often centre around their perception of other peoples’ lack of and/or refusal of their knowledge and consequent misrepresentation of current – and past – events. This form of epistemic injustice is layered upon experiences of war, loss, and dislocation which drive many students to take up graduate studies in social justice. In response, I consider the nature of the unwellness created by the intertwining of this experience and the epistemic injustice perpetuated around and about it. I discuss troubles in the reception and misuse of context. Subsequently, I think about how we can challenge this unwellness through how we create knowledge as a learning community. Rather than producing rules, I propose touchstones which might guide us to create knowledge as though our ‘ we’ – in community of difference – matters, and as though we, in fact, matter.

Indigenous climate justice in Aotearoa New Zealand: the dangers of (mis)recognition within climate policymaking

This paper explores Indigenous climate justice in the settler-colonial context of Aotearoa New Zealand. We adopt the interdisciplinary approach of Critical Discourse Analysis (CDA) to examine the extent to which Māori knowledge systems (mātauranga Māori) and Māori status as Treaty partners with the Crown (New Zealand Government) were recognised included in New Zealand’s Zero Carbon Act (ZCA). Through our exploration we reflect on and explore Māori experiences of climate injustice through lack of recognition or misrecognition. CDA helps to identify whose voices dominated the ZCA process, revealing unequal power relations between stakeholder groups, the Crown, and Māori. By analysing policy documents, long-form submissions from Māori, and interviews with Māori we shed light on the power dynamics which shaped the ZCA process and the implicit assumptions regarding Māori participation in climate policy decision-making. The misrepresentation of Māori as stakeholders rather than treaty partners perpetuates historical legacies of colonization. By applying CDA within the context of climate justice, we highlight tensions between Māori aspirations for partnership and the actual treatment of Māori as stakeholders rather than Treaty partners. By closely examining the narratives surrounding the formation of the ZCA, CDA reveals the ways in which Māori voices are side-lined, their aspirations and concerns dismissed, their Indigenous knowledge systems (mātauranga-a-iwi and mātauranga-a-hapu) marginalized, and their rights to retain their tino rangatiratanga (sovereignty) violated.

From Collective Identity to Counter-Hegemony

In mass media, such as films, the Papuan region and people are still regarded as “the other", for example, portrayed as a people and region that needs to be civilized through various approaches. In addition, Papua is rich in natural wealth and culture, but instead of bringing prosperity, it become a source of new conflicts that threaten the existence and survival of the environment and the Papuan. This condition encourages young Papuan filmmakers and members of the Papuan Voices (PV) community to create an alternative narrative about Papua. Through documentaries produced collectively, they aim to present another side of Papua from the perspective of the Papuans. Using a poststructuralism approach elaborated with Gramsci's theory of hegemony, this study aims to explore the dynamics of collective identity formation and efforts to create counter-narratives as part of a counter-hegemony movement, namely by criticizing inequality and instilling solidarity for Papua. The analysis shows that the formation of PV’s collective identity is based on the history of Papuan suffering memories (memoria passionis) related to the experiences of injustice.

Exploring the Experience of Healthcare-Related Epistemic Injustice among People with Myalgic Encephalomyelitis / Chronic Fatigue Syndrome

Myalgic encephalomyelitis / chronic fatigue syndrome (ME/CFS) is a chronic, disabling yet clinically “contested” condition, previously theorised through a lens of epistemic injustice. Phenomena conceptually close to epistemic injustice, including stigma, are known to have deleterious consequences on a person’s health and life-world. Yet, no known primary studies have explored how people with ME/CFS experience healthcare through a lens of epistemic injustice, whilst a dearth of research explicitly exploring healthcare-related injustice from a patient perspective has been noted. This qualitative study seeks to address this gap. Semi-structured interviews and interpretative phenomenological analysis (IPA) were used to explore the experiences of five people with ME/CFS in the UK, vis-à-vis healthcare-related epistemic injustice. One superordinate theme is presented, “Being de-centred in patient-centred care,” alongside two sub-themes: “Struggling for epistemic-existential validation” and “Negotiating socio-epistemic hierarchies, politics and ‘power’.” Findings suggest that healthcare-related epistemic injustice may differentially impact according to the patient’s social positionality (here, notably gender), and that a potential pathway of existential harm operates through threats to identity and personhood. Findings also indicate that cultural and political factors may further epistemic injustice in healthcare. Finally, epistemic injustice impacting as a chronic stressor cannot be ruled out and is worthy of further research. The experience of healthcare-related epistemic injustice can carry far-reaching yet varied consequences for patients. Future research should consider drawing upon more socio-demographically diverse samples and an intersectional approach is recommended. Further exploration of structural drivers of epistemic injustice may highlight a need for politically and socio-culturally cognisant clinical approaches.

Translation and adaptation of the Arabic version of the injustice experience questionnaire in patients with chronic musculoskeletal pain.

The objectives of this study were to (1) translate the short version of the Injustice Experience Questionnaire (IEQ-SF) from English to Arabic and (2) test the validity and reliability of the translated Arabic version of the IEQ-SF. A cross-sectional study in which the original English version of the IEQ-SF was translated into Arabic was conducted in accordance with Beaton's translation process. Internal consistency, reproducibility (retest within 5 days), and validity of the translated Arabic version of the IEQ-SF were tested in Arabic-speaking participants (n = 20). Individuals with chronic pain (n = 99) completed the Arabic versions of the IEQ-SF and the Musculoskeletal Health Questionnaire (MSK-HQ) from June to August 2021. The main analyses included Cronbach's alpha (α), Intraclass Correlation Coefficients (ICC), and Spearman's rank correlations (ρ). The internal consistency (α = 0.74) and test-retest reliability (ICC = 0.88, 0.83-0.92 95% CI) for the translated Arabic version of IEQ-SF were high. There was also a high correlation between the translated Arabic version of the IEQ-SF and different health-related questionnaires such as the MSK-HQ (ρ = -0.738; p < 0.001), Hospital Anxiety and Depression Scale (ρ = 0.701-0.791; all, p < 0.001), and Pain Catastrophizing Scale (ρ = 0.762; p < 0.001). The Arabic version of the IEQ-SF demonstrated high reliability and validity and would be useful for clinicians and researchers studying Arabic-speaking individuals with chronic pain.