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The purpose of this paper is to provide a concise, selective review of the current status of service provision for male survivors of sexual assault in the UK.

This paper explored to what extent services are equipped to support the specific and complex needs of the male survivor and highlighted key implications for research, policy and practice.

The review outlined the historical backdrop to how and why services for male survivors have been consistently lacking, the current status of UK service provision is reported and suggestions for continued research in this developing area are made.

Despite a flurry of research in this area in recent years, UK service provision for male sexual assault survivors is inconsistent across locale. The value of the current paper is that it provides an outline of relevant work to date, and provides important suggestions for future directions.

The aim of the present study was to compare psychological functioning in male rape survivors who had been raped either by strangers or acquaintances, and to test differences between the functioning of gay versus heterosexual survivors. Thirty‐eight male rape survivors completed a range of measures relating to their perceptions about the nature of the effects of their assault, their general health, self‐esteem and world assumptions. Results revealed that survivors of stranger rapes had lower psychological functioning overall than survivors of acquaintance rapes. Gay survivors were more likely to have crises about their sexual identity than heterosexual survivors. Suggestions for future work are proposed.

Contemporaneously, the crime of rape has experienced an increase in reporting. The majority of rape survivors continue to experience, however, extensive victimisation due to biased attitudes held by many people and organisations within the general population. The paper aims to discuss these issues.

In a quantitative study with a sample of 176 participants, this research aimed to explore sexuality and religiosity as factors that affect attitudes towards survivors of rape.

Results indicated that negative attitudes towards rape survivors could be predicted by rape myth acceptance. While the sexuality of the victim affected attitudes towards rape survivors and negative attitudes towards survivors were also found to be predicted by high religiosity scores, analyses concluded that both males and females perceived gay male victims with more negative attitudes in comparison to lesbian rape survivors. Male participants demonstrated, overall, more negative attitudes towards rape survivors than their female counterparts. In sum, sexuality and religiosity were concluded to be crucial factors in explaining blame attributions.

This study indicates: (1) the effect of social correlates other than gender on rape myths; (2) the effect sexuality has on the perception of rape myths; and (3) the effect religiosity has on the perception of rape myths. This study also reveals implications for the reporting, prosecution and conviction of rape cases that may be subject to bias and discrimination due to victim characteristics other than gender.

Attitudes towards rape survivors based on social correlates other than gender have received little attention within existing literature and research. This paper adds to this discussion by considering the affects of sexuality and religiosity which have implications for the reporting of such a crime.

The purpose of this paper is to explore whether the voluntary sector meets male rape victims’ needs in England, UK. The author’s contribution represents an attempt to piece together some of the voluntary sector’s responses to male rape victims in England, UK and examine whether they meet male rape victims’ needs.

The author draws on data collected from semi-structured interviews and qualitative questionnaires with male rape counsellors, therapists and voluntary agency caseworkers (n=70).

The findings reveal nuanced themes that have been overlooked in the existing literature of male rape: first, male rape victims are not given a choice of their voluntary agency practitioner (regarding gender) to serve them; second, there is no specific training on male rape in voluntary agencies; third, the impact of limited resources and funding in the voluntary sector means that many male rape victims’ needs are unmet; and finally, there is ageism and discrimination in some voluntary agencies, whereby male rape victims are prioritised in terms of their age.

Methodologically, the author’s sample size was not considerably large (n=70), making it difficult to generalise the findings to all voluntary agency practitioners in a British context.

At a time of scarce funding and scant resources for the third sector, the impact of limited resources and funding in the voluntary sector could mean that male rape victims may not receive proper care and treatment. Budget cuts in the third sector are problematic, in that voluntary agencies may be unable to get access to robust training programs for male rape or to resources that can help shape and develop the ways in which they serve male rape victims. The needs of male rape victims, therefore, are unlikely to be met at the local, regional and national levels.

Some practitioners are misinformed about male rape and do not have the tools to be able to adequately and efficiently handle male rape victims. Not only can their lack of understanding of male rape worsen male rape victims’ trauma through inappropriate ways of handling them, but also the practitioners may implicitly reinforce male rape myths, such as “male rape is solely a homosexual issue” or “men cannot be raped”.

Whilst previous contributions have recognised the third sector’s responses to female rape victims, little work has been done to identify their treatment of male rape victims. The author attempts to fill some of this lacuna. In particular, The author draws attention to some of the issues and dilemmas that arise when voluntary agencies provide services for male victims of rape. The author’s concern is that many male rape victims’ needs may be neglected or ignored because of the rise in neoliberalism, as there appears to be a financial meltdown in the voluntary sector.

Information seeking can be used to make sense of a situation or solve a problem. Information seeking can be considered a coping strategy when facing illness, crisis or other life-changing events. Cancer is a globally occurring, life-threatening disease, and this review aims to provide an overview of the existing literature on the active information seeking behaviour of cancer patients specifically focussing on how active information seeking serves as a coping strategy.

This study adheres to current guidelines for conducting systematic reviews and consequently, thorough literature searches were conducted in four databases: Medline, Embase, CINAHL and Scopus which resulted in 7,179 publications. Following a careful screening process, this systematic review identifies 14 studies on the use of information seeking to cope with cancer.

The included studies consist of both qualitative and quantitative approaches to analysing the use of information seeking to cope with cancer. The included studies have focussed primarily on demographic factors, the impact of affect, information needs, sources and coping strategies.

A number of research gaps within library and information science are identified. Bringing research in this field into information science could allow for a greater understanding of information literacy, the use of existing information and the process of information searching when using information seeking to cope with serious illness.

This systematic review focusses on how information seeking serves as a coping strategy for cancer patients and provides an overview of the recent literature.

Research has found that African-Americans and women have opportunities for advancement in the traditional corporate environment through resources embedded in their social networks. However, layoffs can affect the composition of their social networks, their positions in the networks, and rewards from those networks. I suggest that the racial, cultural, and gender differences between African-American and women layoff survivors and White and male layoff survivors will negatively affect their access to and benefits from social capital resources. Yet, strong tie relationships with White and male layoff survivors in key strategic positions can help African-American and women survivors maintain their existing job position because they can then borrow the social capital resources of the White and male survivors. Thus, while research has found that weak ties help individuals advance in their workplaces, strong tie relationships with majority groups may be more beneficial to minority groups in maintaining their position after a layoff.

To examine associations by gender between cancer history and major health insurance transitions (gains and losses), and relationships between insurance transitions and access to care.

Longitudinal 2008–2013 Medical Expenditure Panel Survey data were pooled yielding 2,223 cancer survivors and 50,692 individuals with no cancer history ages 18–63 years upon survey entry, with gender-specific sub-analyses. Access-to-care implications of insurance loss or gain were compared by cancer history and gender.

Initially uninsured cancer survivors were significantly more likely to gain insurance coverage than individuals with no cancer history (RR: 1.25; 95% CI: 1.08–1.44). Females in particular were significantly more likely to gain insurance (unmarried RR: 1.16; 95% CI: 1.06–1.28; married RR: 1.09; 95% CI: 1.02–1.16). Significantly higher rates of difficulty accessing needed medical care and prescription medications were reported by those remaining uninsured, those who lost insurance, and women in general. Remaining uninsured, losing insurance, and male gender were associated with lack of a usual source of care.

Additional outreach to disadvantaged populations is needed to improve access to affordable insurance and medical care. Future longitudinal studies should assess whether major Affordable Care Act (ACA) provisions enacted after the 2008–2013 study period (or those of ACA’s replacement) are addressing these important issues.

Loss of health insurance coverage can reduce health care access resulting in poor health outcomes. Cancer survivors may be particularly at risk of insurance coverage gaps due to the long-term chronic disease trajectory. This study is novel in exploring associations between cancer history by gender and health insurance transitions, both gains and losses, in a national non-elderly adult sample.

The study aimed to listen to refugee survivors of sexual and gender-based violence (SGBV) and/or torture and explore what justice meant to them in exile. This study argues that what the survivors who participated in this research wanted was “viable justice”. The research was funded by the British Academy and Leverhulme Trust.

Using a survivor-focussed justice lens combined with a trauma-informed approach, narrative interviews were held with 41 women and 20 men refugee survivors living in refugee settlements in Northern Uganda. The researchers also conducted semi-structured interviews with 37 key informants including refugee welfare councils, the UN, civil society, non-government and government organisations. Thematic analysis of the data resulted in the following themes being identified: no hope of formal justice for atrocities that occurred in South Sudan; insecurity; lack of confidence in transitional justice processes in Ugandan refugee settlements; abuse and loss of freedom in refugee settlements; and lack of access to health and justice services in refugee settlements.

This study argues that what the survivors who participated in this research wanted was “viable justice”. That is justice that is survivor-centred and includes elements of traditional and transitional justice, underpinned by social justice. By including the voices of both men and women survivors of SGBV and/or torture and getting the views of service providers and other stakeholders, this paper offers an alternative form of justice to the internationally accepted types of justice, which offer little relevance or restitution to refugees, particularly where the crime has been committed in a different country and where there is little chance that perpetrators will be prosecuted in a formal court of law.

The research findings are based on a small sample of South Sudanese refugees living in three refugee settlements in Northern Uganda. Thus, wider conclusions should not be drawn. However, the research does suggest that a “viable justice” approach should be implemented that is gender and culturally sensitive and which could also be trialled in different refugee contexts.

Improvements in refugee survivors’ dignity, resilience and recovery are dependent upon the active engagement of refugees themselves using a “survivor-focussed approach” which combines formal and community-based health services with traditional and transitional justice responses.

The provision of a “viable justice approach” ensures those who have experienced SGBV and/or torture, and their families, feel validated. It will assist them to use their internal, cultural and traditional resilience and agency in the process of recovery.

The research findings are original in that data was collected from men and women survivors of SGBV and/or torture and service providers. The empirical evidence supports this study’s recommendation for an approach that combines both formal and survivor-focussed approaches towards health and viable justice services to meet the needs of refugees living in refugee settlements. This is a response that listens to and responds to the needs of refugee survivors in a way that continues to build their resilience and agency and restores their dignity.