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The expectation for universities to support students' employability through work-integrated learning placements demands investigation into how opportunities are inclusive to students from a diversity of backgrounds. In this paper, we explore the experiences of students with disabilities during work placements, drawing on qualitative data collected through six focus groups with students (n = 27). Analysed through the frame of stigma, the results show how students bear an unfair burden of responsibility in their placement experiences, as they shoulder consequential decisions to disclose and/or request accommodations to support their learning. In this study, work placement environments were often somewhat hostile, both in relation to their built environments but also through the bias and/or prejudice of others. The results shed light on the difficulties that students with disabilities face in their placements and underscore how educational equity is multi-layered, requiring scrutiny of the student life-course including access to opportunities in professional fields. Points of interest: Despite work integrated placements often being positioned as opportunities for students to 'try out' authentic work experiences during their time at university, placements are not inclusive to students with disabilities. Students with disabilities shoulder an unfair responsibility in their work placement experiences, where they must negotiate the decision of disclosure and/or request for accommodations. Students reported hostile work placement environments, and cultures of exclusion, demanding more investigation into how universities can ensure safe and appropriate learning environments for students on placement. Students recommend greater education and training for placement teams (i.e., academic unit chairs, professional coordinators) and industry supervisors to reduce stigma and combat entrenched assumptions about disability. Universities themselves must also reflect and act on how to support inclusive cultures, including supporting training and policy that embed a strengths-based lens of disabilities. [ABSTRACT FROM AUTHOR]

In this article we study the concept of 'belonging' within the context of inclusive education. We see inclusion and belonging as two entangled concepts and focus on inclusion as an ethical process. We do this by analyzing the Flemish documentary Inclusief [Inclusive] to investigate the idea of belonging as building and finding roots. As a method we carry out a close reading of two episodes of the documentary and plug in theory to gain a deeper sense about the meaning of belonging in two students' life stories. In our writing process these fragments become tangible. Through the stories, we see how belonging emerges. We come to understand belonging in inclusive education as connected to the dynamic interplay with the context; listening with care; and radical relationality. By combining these elements schools can invest in becoming inclusive communities of care, and contribute to every student having a feeling of belonging. This paper explores the relation between inclusion in educational contexts and the sense of belonging of disabled students. The authors argue for a system approach to aim for inclusion instead of through case-by-case assessment. Through close reading of two episodes of the Flemish documentary Inclusief, the authors find that belonging is enhanced through the teachers' careful attention to the students' relations with each other. The authors state that creating space to enhance every student's belonging is carried out through listening with care and being open to many connections between the student and others. The interplay with the environment proves very important to stimulate a sense of belonging with every student. The authors argue that caring communities arise through close connections. [ABSTRACT FROM AUTHOR]

People with disabilities have an inviolable right to equitable access and participation in tertiary education and support systems are known to be indispensable in making this right a reality. This article presents the voices of students with disabilities regarding aspects that influence their successful access and participation in tertiary education in Ghana. A qualitative approach was adopted for the study with data collected through interviews with 12 students with disabilities in three public universities. From the perspective of these students, successful inclusion of people with disabilities in tertiary education in Ghana is influenced by enrolment practices, the built environment, teaching and learning approaches, and assessment provisions. The context influenced provisions and support provided. Attitudes of the university community and lack of knowledge of inclusive practices such as Universal Design play a role in students' access and participation. Comprehensive awareness-raising on disability and inclusive practices is recommended to address this issue. This paper explores inclusion practices in three Ghanaian public universities focussing on the combined voices of students with disabilities. The context of the three universities influences the provisions and support available for people with disabilities. The students with disabilities involved in the study reported that access to the university environment and support for academic engagement impact their university experience. The attitude of the university community is a factor in ensuring access, participation and success of people with disabilities in higher education. Creating awareness of disability issues within the university community is pivotal in building and sustaining inclusive culture. The application of universal design principles is essential to improving access and participation of people with disabilities in higher education institutions. [ABSTRACT FROM AUTHOR]

This paper examines how an intersection of critical cultural disability studies and rhetorical studies can inform a critical education on 'mental health (problems)' for psychology students. Building on cultural theories of disability/impairment, a conception of 'mental health (problems)' as culturally constituted is introduced. We propose the rhetorical perspective as a particularly relevant analytical and pedagogical approach to enable students to critically reflect on the cultural assumptions underpinning various (professional) understandings of 'mental health (problems)'. Our contribution is based on a research project in which clinical psychology students rhetorically analysed cultural constructions of 'mental health (problems)' in a graphic novel on 'bipolar disorder'. Based on a qualitative analysis of students' reflective reports, we argue that rhetorical perspectives enable students to develop reflexive stances towards the different cultural logics, and the ethical and political ramifications of these logics, in which psychological practice and knowledge on 'mental health (problems)' are inevitably embedded. This article argues that clinical psychology students need to think critically about the language they use to think and talk about mental health problems because this language has an impact on their beliefs, attitudes and actions towards people experiencing mental health problems. Educators can support students in this endeavour by introducing them to stories that challenge some of the dominant ways society thinks and talks about mental health problems, for example by working with stories or art work of survivors. In this study, clinical psychology students read an autobiographical graphic novel on 'bipolar disorder'. The graphic novel made students reflect on how the main character in the novel experiences mental health problems, on their personal and professional assumptions about mental health problems, and on dominant societal assumptions about mental health problems and their impact. [ABSTRACT FROM AUTHOR]

This paper explores the experiences of students with chronic illnesses in UK universities. Sixty-seven students with chronic illnesses completed an online survey with open-ended questions about their experiences in higher education. Questions covered four main topics: academic work; university staff; social and extracurricular activities; and participants' miscellaneous opinions. Using thematic analysis, the data were analysed with references to the social model of disability and social representations of chronic illness. Participants wrote of misconceptions surrounding chronic illnesses, a sense of inequality, and feeling undervalued. Many staff members seemed to lack understanding and so 'policed' academic regulations rather than accommodating for their chronic illnesses. However, some participants wrote of social and academic 'allies' who offered understanding and proactive support. The findings add substance to the chronic illness literature with the focus on students at university, and we offer recommendations to universities for improving inclusivity for students with chronic illnesses. Disabled students with energy-limiting chronic illnesses are frustrated by a lack of support and feel that they have fewer opportunities than non-disabled students. Some university staff may hold negative views of disabled individuals, and so provide inadequate support. This can lead to students' reluctance to disclose chronic illnesses. Students with chronic illnesses felt that some staff and peers did not class chronic illnesses as 'real' disabilities and felt that they were perceived lesser than those with visible disabilities. Some students proudly owned the label of 'disabled' to educate others, including staff, who sometimes used university regulations inappropriately to excuse not adjusting support for disabled students. Some staff and students were perceived as supportive allies. Universities must listen to disabled students and those with chronic illnesses to ensure they fulfil their legal and moral obligations of providing equality of opportunity, enabling all students to succeed. [ABSTRACT FROM AUTHOR]

From 2016-17, academics at a leading Irish university collaborated with a group of self- advocates with intellectual disabilities to co-design, co-deliver, and co-assess an entire disability module for third-year undergraduate social work students. There are few, if any, reports of university modules of this type, involving adults with intellectual disabilities, in the existing literature. Alongside and after the module, our group of academics and self-advocates conducted inclusive research regarding relevant stakeholders' experiences of the initiative. This paper relates to university students' experiences of being taught and assessed by adults with intellectual disabilities. These experiences were overwhelmingly positive with reported benefits including increased comfort around disability and greater empathy with people with people with disabilities. This said, some aspects of being taught and assessed by self-advocates with intellectual disabilities also provoked considerable anxiety among students. From 2016 to 2017, academics at a leading Irish university collaborated with a group of self-advocates with intellectual disabilities to design, teach and mark a disability module for social work students. The group also conducted inclusive research regarding people's experiences of the module This paper explores how university students experienced being taught and marked by adults with intellectual disabilities. Students' experiences were generally very positive. They said the module led to more empathy with disabled people and reduced their discomfort around disability At the same time, some aspects of the module, particularly the idea of being marked by adults with intellectual disabilities, made them very nervous. We hope that our research might encourage others to employ adults with intellectual disabilities as university lecturers and markers. [ABSTRACT FROM AUTHOR]

The voice of disabled students in higher education (HE) has been widely explored in the global North but relatively little is known about the experiences of their counterparts in the global South. The paper attempts to address this lacuna by focusing on disabled students in HE in India. A part of the author's doctoral study in 2013–14 explored the lived experiences and aspirations of 29 students with a visual impairment using phenomenological methodology. Their access to courses and subsequently, career opportunities were found to be restricted by an interplay of systemic exclusion, lack of information, internalised oppression, pedagogy, and employment opportunities. While disability legislation in India focuses on widening participation in HE, the issue of access to courses for students with a visual impairment has received little attention. This paper emphasises the importance of facilitating their access to their desired courses in HE and to this end, provision of support in school. This article highlights the experiences of students with a visual impairment regarding enrolling in different courses in higher education (HE) in India. The research found that four main factors prevented many students with a visual impairment from pursuing science-and mathematics-based courses in HE. These were i) exclusion from science and mathematics in early education, ii) inadequate support systems, iii) inaccessible teaching practices, and iv) limited work opportunities. Little or no support and motivation was available for them to study these subjects. The research recommended that HE authorities must recognise the ability of students with a visual impairment to learn visual-based subjects. It also highlighted the need to provide support for learning mathematics and science to these students in school so that they can study mathematics- and science-based courses in HE. [ABSTRACT FROM AUTHOR]

Providing an inclusive education to students with intellectual disability in higher education is an emerging challenge. This paper presents the results of a research study that analyses the perceptions of graduates from the Promentor Programme (Universidad Autónoma de Madrid, Spain). The study follows a phenomenological design and employs qualitative research methodology. Two focus groups are conducted, with 14 participants in total. The participants' perspective is structured around the following categories: (a) Quality of life and training received; (b) barriers encountered; (c) supports received; and (d) lecturers' competences. In general, participants give their experience a positive assessment in relation to aspects such as social inclusion, professional and personal development or self-esteem. The study's conclusions highlight the convenience of an inclusive and qualitative research design that will serve to hear the voices of persons with intellectual disability, as well as their perception of the positive impact of university education on their lives. This article focuses on the perspective of Spanish university students with intellectual disability in order to understand their perceptions of their training experience in an inclusive higher education course. An inclusive research design is adopted which seeks to give voice to people with intellectual disability not only as participants, but also as members of the research team. The study confirms that, from the students' perspective, university environments can be suitable for the education of students with intellectual disability; therefore, the creation of inclusive higher education programmes should be encouraged. University lecturers should receive training in inclusive education. Higher education institutions must take into account the voices of vulnerable groups of students in order to effectively eliminate existing barriers. [ABSTRACT FROM AUTHOR]

Although established for decades now, inclusive education remains a complex process that creates difficulties for the educators and children involved. With a collaborative and comprehensive focus, this study examined the point of view of 12 French secondary-school students about inclusion upon the recent opening of a localised educational inclusion unit (ULIS) at their school. The students' point of view was captured by means of a participative photography workshop entitled "Photovoice." The photos and their associated verbatim comments were analysed according to two indicators: social participation and pedagogical accessibility. With respect to social participation, the results revealed no distinction between the students, whether or not they have a disability. With respect to pedagogical accessibility, the students acknowledged that the ULIS supports access to learning for students with a disability. This study sought to build knowledge of inclusive education, particularly in schools, by focusing on the point of view of French secondary-school students. It aims to identify the barriers and facilitators related to the implementation of inclusive education. We consider inclusive education as a developmental process of all students. It involves the creation of a society that fights exclusion and marginalisation. Faced with the lack of relevant information given from the point of view of students, we wanted to give them a voice and thereby highlight the impact of implementing inclusive education. This data encourages reflection on inclusive education with the goal of helping all education professionals take into account diversity. [ABSTRACT FROM AUTHOR]

This paper is an exploration of social work placements with students who are living with a disability. The paper discusses hurdles including censoring placements and opportunities, equal access, strategies for building a belief in ability and self-esteem. Field education is a significant part of the social work degree internationally. It allows social work students to further develop their social work identity and to apply their knowledge to professional practice through real-life learning. The paper broadens the conversation on social work placements and ability, adding some personal narratives and sharing some insights from an Australian university context. [ABSTRACT FROM AUTHOR]

Spanish universities must guarantee optimum accessibility to facilitate the teaching-learning process of students with disabilities. The objective of this study was to investigate how Spanish students with disabilities perceive access to Higher Education and the day-to-day of their academic life. A qualitative design was performed, using sequential discourse analysis adapted to the area of studies with people with disabilities. Two focus groups and sixteen interviews with university students with disabilities were analyzed. The discursive strategies of the students presented an asymmetry between the normative and the factual, although within a framework of inclusion and integration into university life. Six types of barriers were identified: computer, bureaucratic, and architectural -more intense in the traditional universities-, and learning, personal, and social barriers -stronger in online universities. To ensure the inclusion of students with disabilities, there is a need to increase information and training and to establish common procedures across Higher Education institutions. Despite the legislative measures regarding inclusion in Higher Education, the representativeness of students with disabilities in Spain is low. Students with disabilities found six different types of barriers in accessing university studies in Spain. Research shows that Spanish university students with disabilities consider dropping out of Higher Education due to the difficulties they encounter on a day-to-day basis. Spanish university students with disabilities detect barriers that are specific to society, in general, and to the university system, in particular, that prevent a real equality beyond the deficits of their disabilities. Improvements should be oriented towards the training and awareness of the entire university community and its standards of practice. [ABSTRACT FROM AUTHOR]

This paper studies barriers and support affecting access, experience and performance as identified by students with disabilities at the University of Seville. Biographical-narrative research methodology is employed and the study is limited to an analysis of the design and development of subjects across the curriculum. Findings, which give voice to the students themselves, are organized in four topic areas: subject structure, methodology, tutorials, and assessment. The paper concludes with a review and discussion of key findings as well as suggestions for improvement and policy-making. [ABSTRACT FROM AUTHOR]

Research on transition to higher education and young people with disabilities has increased in recent years. However, there is still limited understanding of transition issues and how digital technologies, such as social media and mobile devices, are used by this group of students to manage these issues. This article presents the findings of an empirical study that addressed this matter based on young people's views and experiences. The qualitative study was conducted in the context of a group of students with vision impairments transitioning to a New Zealand university. The findings draw from observations, a researcher diary, focus groups, individual interviews, and data from social media. The study shows that, like their non-disabled peers, the students actively engaged with interactive and collaborative digital technologies to make sense, individually and collectively, of different transition issues before, during and after the first academic trimester of their university journey. This research shows that, from the perspective of students with vision impairments, key issues for transitioning to higher education include the academic system, social connections, disability support, family involvement and their own impairment(s). Transition issues in higher education, in the context of disability, are complex and interconnected. Students with vision impairments actively engage with and adapt digital technologies to manage transition issues. These findings expand the current understanding of transition as well as student retention in higher education in the context of disability and the role of digital technologies. This research recommends tertiary institutions use creatively collaborative and interactive digital technologies to complement transition services and activities for students with disabilities so their participation and inclusion in higher education can be encouraged. [ABSTRACT FROM AUTHOR]

This article focuses on access of students with disabilities to education in Ethiopia and, in particular, on the role of inclusive education resource centres (IERCs). A mixed-methods approach was used to collect both quantitative and qualitative data. The participants were school administrators, itinerant teachers, special educators, regular classroom teachers, and school directors. It was identified that a large number of students and teachers benefitted from the support provided by IERCs. The target schools are equipped with materials that support inclusive pedagogy. The awareness of parents and communities is gradually changing, except in some unreached communities. As a result, the number of students with disabilities enrolled is increasing. There were some barriers observed, such as assignment of itinerant teachers to a large number of satellite schools, high turnover of local government officials, and whether there was investment in the sustainability of IERCs and the positive outcomes observed. [ABSTRACT FROM AUTHOR]

This article draws from an ethnographic study of a group of school-aged disabled white working-class and self-proclaimed 'bad boys' in one Alternative Provision (AP) in an English further education college. These young disabled students' disabilities contribute to the formation of their revalorised – yet stigmatised – identities. Stigma also facilitates the governance of their educational careers. The article considers how this group understands its precarious existence in and beyond AP and how these young men resist the conditions of their devaluation. Despite multiple, stigmatising experiences, the article shows how they appropriate space and (social) capital, often in tension with other students and college staff. The article suggests that there are questions about AP as an appropriate means to confer value upon young disabled students. White, disabled, working-class male students are increasingly placed into Alternative Provisions intended for young people who would otherwise not receive suitable education for various reasons. The experiences of such students have received limited research attention. This article is based on research conducted with young people who attend a provision located within an English further education college. The research found that these young people experience a lack of support, low trust and disregard from peers and some professionals at a crucial time in their educational careers. It is important to understand disability in relation to other social differences – social class and gender, for example – as the combined impact of these in educational settings may undermine future career prospects and life chances. The article emphasises the importance of education practices that develop reciprocity, trust and cooperation in improving the often oppressive circumstances young disabled people face in post-school settings. [ABSTRACT FROM AUTHOR]

This article considers the inclusion of mental health service users' experiences and perspectives in professional education classrooms. After brief introductions to the authors' backgrounds, the article discusses professional expertise and knowledge and the accreditation of professional education courses. It then goes on to explore service users' understandings of mental and emotional distress and the development of Mad Studies, which, at first sight, may appear incompatible with professional education courses. Discussion then turns to the development and trial of a living experience learning resource, which portrays the first author's knowledge and understanding of having voices. The article concludes by arguing for the inclusion of Mad Studies knowledges in professional education classrooms. This article discusses including mental health service users' experiences and knowledges in professional education classrooms. The article discusses service users' own understandings of mental and emotional distress and the international development of Mad Studies – the cooperative study of mental health service users' experiential knowledges. The article also describes how we produced a learning resource (video film) which portrays the first author's understanding of having or hearing voices. The learning resource was used in research with seven first-year social work students and we found that the students' understandings of mental illness changed after viewing the resource. Mad Studies offers mental health service users hope and the possibility of change. It is therefore important that Mad Studies knowledges are included in professional education. [ABSTRACT FROM AUTHOR]

The article offers instructions for authors when submitting articles for the Student Perspectives section of the academic journal "Disability & Society," such as following all instructions for submitting a peer-reviewed paper, paying attention to the journal's policy on language, and uploading all submissions at Student Perspectives in the ScholarOne system at http://mc.manuscriptcentral.com/cdso.

The article presents guidelines for authors when submitting articles for the Student Perspectives section of the journal "Disability & Society," including following instructions for submitting a peer-reviewed paper to the journal, paying attention to the journal's policy on language, and uploading all submissions as Student Perspectives in the ScholarOne system.

This paper reports findings from a 12-month Australian study exploring beliefs and experiences of disclosure and course success in post-compulsory education for 20 students with mental illness. Enrolled students with disclosed or non-disclosed mental illness, teaching and support staff, and institutional practices across four sites providing vocational education and training were the three cases selected for this collective case study. Students participated in two semi-structured interviews over the course of one academic year. Disclosure was not preferred by students, most fearing that it would negatively impact upon their capacity to obtain employment in the occupation for which they were training. Further research exploring the processes, timing and outcomes of disclosure, in a wide range of post-secondary settings and with larger numbers of students, would allow for a deeper exploration of issues raised by this small study. [ABSTRACT FROM AUTHOR]

The article presents guidelines for student perspectives section like from 2014 student perspective papers will be free to access along with peer review and work can be submitted as a student perspectives paper during course of study.

The article presents guidelines for submitting papers for the BreakThrough Scholars section of the journal "Disability & Society."

The article presents guidelines for submitting papers for the BreakThrough Scholars section of the journal "Disability & Society."

By blending the conceptual frameworks of epistemic injustice and ethical loneliness and applying them to campus-based practices of 'risk' identification and 'referral', this article describes how Mad students come to be abandoned as knowers and learners. I then dwell in and politicize the condition of (ethical) loneliness these harms produce by seeking to 'practise' it as a form of Mad knowing, and as a framework for visioning justice. Framing Mad student experiences in this way opens up several possibilities for epistemic justice. First, it offers additional language and interpretive resources for naming and protesting our experiences of violence. Second, it compels us to understand and attend to Mad student experiences of epistemic harm and to recognize how Mad knowledges are routinely generated in their wake. Third, it invites new ways of understanding and responding to these harms, and imagining redress. [ABSTRACT FROM AUTHOR]

The article offers instructions for submitting articles in the Student Perspective section of the journal "Disability & Society."

The article offers guidelines related to Student Perspective papers which will be Free to Access including peer-review of papers, submission of papers by students pursuing Bachelors, Masters, or Doctorate degree at any university, and paying attention to the Journal's policy on language.

The article invites research papers from the students of Bachelors, Masters, or Doctorate degree at any university for the Student Perspective section of the journal "Disability & Society."

This article reports the findings of two small-scale qualitative studies at an English university which engaged service users and carers (SUACs) as researchers in co-production with an academic researcher. Findings were that SUAC participants reported considerable levels of self-transformation via involvement in training health and social work professionals. Students reported heightened empathy and having had their perceptions about disability challenged. Further research regarding whether any learned values and attitudes regarding disability are carried through to the world of practice is recommended. [ABSTRACT FROM AUTHOR]

The article offers submission guidelines for the Student Perspective section of the periodical. It mentions the need for Student Perspective papers to undergo peer review, the eligibility requirements for university students interested in submitting their paper and the submission criteria which include observance of the policy of the periodical on language, the upload of the submissions and the need for the papers not to be a straight reproduction of another work made for academic assessment.

The article provides guidelines for authors submitting articles for the Student Perspective section of the journal "Disability & Society."

There are limited comparisons between the experience of disabled students in higher education and their non-disabled peers, particularly on practice placements. This article presents the results of such a comparison, across six professional disciplines in one UK university. The results revealed that both disabled and non-disabled students reported positive placement experiences and also similar difficulties. Such difficulties were exacerbated for some disabled students, however, including as a consequence of the attitudes of others to disability. Recommendations for practice are identified that aim to enhance the placement experience of all students and to remove barriers to access. [ABSTRACT FROM PUBLISHER]

Disabled young people in many low and middle-income countries experience significant levels of educational exclusion due to disabling social and physical environments and are more likely to be illiterate than their non-disabled peers. Most social sciences and development literature, however, tends to homogenise the educational trajectories of disabled young people and focuses predominantly on the perspectives of educationalists, development experts and carers in assessing educational needs and institutions. Consequently, the experiences of young people across multiple categories of social difference, and their agency in shaping their own educational trajectories, remain largely unknown. This article contributes to filling this gap by exploring the educational narratives of young people with different impairments in mainstream, special and integrated schools in Ghana. The article shows how exploring individual narratives provides new insights into the educational needs of and ‘appropriate’ education for disabled young people in the Global South. [ABSTRACT FROM PUBLISHER]

An ongoing interest in disabled learners’ voices has been reflected in a number of studies that explore students’ experiences of schooling, as part of the quest to understand how inclusive education can be achieved. These studies, however, have been conducted mainly in industrially developed countries, while very few studies exist from industrially developing countries such as Greece in which disabled people’s voices are under-represented not only in political processes but in research as well. The aim of this study was to investigate disabled students’ educational experience, their social interactions with peers and teachers, the choice of school and the support they received for responding to curricular demands and complexities. The results of the study confirmed that disabled students can provide invaluable information on matters involving their education, and showed how personal experiences of disability are influenced by the socio-cultural experiences lived in different social arenas, such as that of education. [ABSTRACT FROM PUBLISHER]