Abstract
Although substantial recent research addresses the importance of higher education (HE) for students with disabilities, this sector has remained under-researched in Botswana. The struggle of female students with disabilities to access and participate in HE remains an issue of great concern for disability activists and researchers. The purpose of this phenomenological study was to explore and describe the lived experiences of female students with disabilities in their struggle to access and participate in three HE institutions in Botswana. Seven female students with disabilities participated in this research. Multiple methods, such as focus group discussions, photovoice and solicited journals, were used to collect data. The data were analysed using Atlas.ti 7.5 qualitative data analysis software. Three themes emerged, and they are (a) socio-cultural issues and disability identity, (b) access and participation in HE and (c) empowerment of female students. These findings served to inform Botwana’s HE institutions that include female students with disabilities, to help them to promote participation as well as quality of experiences.
Keywords
Introduction
Female students with disabilities are marginalised when it comes to health and social services, particularly higher education (HE), and this has a significant impact on their quality of life (Peña, 2014). Widening access and participation of students with disabilities in HE has been found to increase the chances of (a) obtaining and maintaining a higher income, and (b) creating a means for lifelong independence and quality of life (Wehman, 2013). Success in HE depends on various micro and macro factors, such as policy, strong political will, institutional support services and programmes, assistive technology, favourable attitudes, accessible facilities and instructional accommodation (Chataika, 2010). However, students with disabilities, particularly in an African context, struggle to access these services. In order to understand their struggle the social model of disability (SMD) was used as a theoretical framework.
Theoretical Framework
In this article, we used the SMD to critically analyse the experiences of female students with disabilities who were enrolled in Botswana’s institutions of higher learning. SMD challenges the predominant discourses that tend to promote the ‘deficit model’ that brands people with disabilities as abnormal, and that they should be corrected. SMD does not view nor portray persons with disabilities as passive victims, and thus it promotes the understanding of persons with disabilities as persons endowed with the agency to confront and resist exclusion and oppression (Adam & Kreps, 2006; Devlin & Pothier, 2006; Lepofsky, 2004). Social scientists such as Mike Oliver (1990, pp. 112–131) situated disability within the social arrangements of the society. In this context, disability is a social–political construct which results from barriers which are attitudinal, structural and political as well as from curriculum factors nested in social arrangements which limit the access and participation of female students with disabilities in HE. As a result, these individuals continue to face challenges in employment, housing and transportation that arise from socio-political arrangements and not from their medical condition. Thus, these individuals cannot be ‘fixed’ but their human rights need to be protected through legislation and mainstreamed in the political process (Bickenbach, Chatterji, Badley, & Ustun, 2008). Proponents of SMD call for the creation of a barrier-free society to promote access and participation in society for individuals with disabilities and reduce the dominant exclusion tendencies (Campbell & Oliver, 1996).
This study seeks to explore the access to and participation in HE of female students with disabilities. Therefore, their experiences were central to this study for which SMD was used. SMD as an embodied theory emerges from the lived experiences of persons with disabilities; hence, it enabled the researcher to explore the experiences of female students with disabilities enrolled in higher education institutions (HEIs) and better understand how they are affected by contextual factors.
Review of Literature
Education of Students with Disabilities in HE
Global debates on democratising HE have raised pertinent questions about participation as well as representation in HE. These questions have a bearing on issues such as diversity and the inclusion of groups whose rights were not recognised. HE is, therefore, viewed as a critical site forthe acquisition of skills, competencies and knowledge necessary for socio-economic development (Morley, Leach, & Lugg, 2009). Similar conclusions were made by the World Bank (2009) report on the role of HE in the context of the sub-Saharan region. The report articulates an overt and direct link between rates of return in investing in HE and poverty education. Rearticulating the point of access and participation of students with disabilities in HE, studies (Moswela, 2016; Tuomi, Lehtomäki, & Matonya, 2015; Wehman, 2013) are unanimous that HE increases these students’ chances of (a) obtaining and maintaining a higher income, and (b) creating a means for lifelong independence and quality of life.
Educational provision for students with disabilities in HE is shaped by multiple factors, such as economic, political, social and cultural conditions. However, the governments’ affirmative action programmes and/or policy initiatives have been linked to the widening access and participation of students with disabilities in HE (Shevlin, Kenny, & McNeela, 2004). Although progressive legislations (IDEA, Disability Discrimination Act) in developed countries have led to their greater access and participation in HE, the participation in and access to HEIs for students with disabilities is still a contentious issue. For example, a significant body of research (Shevlin et al., 2004; Stodden, Whelley, Chang, & Harding, 2001) has identified several barriers restricting the participation, progress and success of students with disabilities in HE. These barriers are attitudinal and structural, and include the transport system, career prospects and appropriate skills development for competitive tertiary education and the world of work (Momin, 2004). Individuals with disabilities require intra-individual skills such as motivation, self-determination and self-advocacy in order to remain and persist in HE (Getzel, 2008). These critical factors for the successful participation and progress in HE for students with disabilities have also been documented in similar studies exploring factors that limit access to and success within post-secondary education programmes (Stodden et al., 2001). However, factors which limit participation and progress in HE for female students with disabilities were quite different from the experiences of male students with disabilities.
Experiences of Female Students with Disabilities in HE
The World Report on Disability (World Health Organization, 2011) revealed that persons with disabilities in developing countries continue to face barriers to accessing education. Globally, literacy rate of persons with disabilities is estimated at 3 per cent, whereas the literacy rate of women and girls with disabilities stands at 1 per cent (Arnade & Haefner, 2006; Groce, 2003; Moodley, 2017). The majority of these students rarely receive HE, and those who manage to gain access to HE face significant obstacles to equal participation in HE; they tend to live with two ‘minority’ identities—female and disability. It is not the single category of ‘female’ that shapes the lives of female students, but the combination of gender and disability. As a result, their subjective experiences could be entirely different from that of male students with disabilities. It is, therefore, important to view disability through a gender lens in order to conceptualise women’s subjective experiences of disability. The problem is that traditional gender beliefs still prevail in Africa. As a result, notwithstanding the benefits of HE, research set in the context of the sub-Saharan region unveils a glaring marginalisation of female students with disabilities in HE sectors (Opini, 2010; Osongo, 2006; Tuomi et al., 2015). Compounding this issue is a set of socio-cultural factors that act as exclusion structures to produce and maintain the marginalisation of female students with disabilities when it comes to access to HE (Morley et al., 2009).
Set in a Kenyan context, studies (Opini, 2010, 2012) documenting the experiences of female students with disabilities in university education indicate that participation of female students with disabilities in HE is limited by factors such as poverty, sexual abuse, discrimination, inadequate learning resources and structural access. Opini (2012) concluded that female students with disabilities were driven to succeed in HE by a determination to challenge their ‘subjugated position in society’. However, the study failed to interrogate critical issues such as the empowerment of this group of students to ensure that they continued in HE.
A phenomenological study by Williams (2016) explored the lived experiences of 11 female student veterans with disabilities entering HE in the United State of America. The purpose of the study was to identify the services, resources and support systems accessible to them. The several transitional challenges identified by female students which varied from individual to individual due to their special needs and their experiences, qualifications and academic goals. The study concluded that female student veterans with disabilities had their own special needs which were different from those of male student veterans with disabilities, and that there were no strong support structures for these students. Interestingly, the factors motivating these students to enter HE included being the role model for their families, changing careers and attaining lifetime goals, for which education was considered important.
Set in an Ethiopian HE context, using in-depth semi-structured interviews, Tefera and Van Engen (2016) documented the experiences of 13 female students with physical disabilities. Findings revealed that the challenges that female students with disabilities faced were the result of their disabilities and, in fact, motivated them to attain high levels of education. Furthermore, participants of the study indicated that the struggle served to develop their self-confidence and self-reliance. Most of the participants indicated that they faced negative attitudes as well as problems in accessing assistive technology, and that they put in extra effort to prove themselves to employers and co-workers. Participants indicated that too much family support made them dependent while exclusion made them stronger.
The findings of a qualitative study by Tobias and Mukhopadhyay (2017), whichexplored the day-to-day experiences of individuals with visual impairments in the Oshana and Oshikoto regions of Namibia, indicate that most female persons with visual impairment have limited access to education. The few that managed to access education dropped out before completing primary school. The study further documented the negative attitudes of peers towards female individuals with visual impairment. Low educational attainment impacted negatively on the employment of participants of the study.
Although studies have shed light on the lived experiences of female students with disabilities in HE (Tuomi et al., 2015), there has been little evidence in the African context. Very few studies have revealed the impact of social culture and practice on female students with disabilities. Even though substantial recent research (Opini, 2010; Osongo, 2006; Tuomi et al., 2015) addresses the importance of HE for students with disabilities, this sector has remained under-researched in the context of Botswana. In Botswana, very little is known about the experiences of female students with disabilities in HE. Therefore, an in-depth exploration of their experiences is needed, and the aim of this study was to understand the academic and social experiences of female students with disabilities and how they can be included in institutions of higher learning. Broadly, we sought an answer to the question of ‘How do female students with disabilities experience higher education in Botswana?’
Methods
Using qualitative phenomenological inquiry, the focus of the study was the life experiences of female students with disabilities at three institutions of HE in Botswana. Pugach (2001) explains that qualitative research has the strength to advocate for addressing disability-related issues by giving a voice to those who have been marginalised. McCarthy (2003) also posits that a change in attitude towards people with disabilities can occur mainly through exposure to the voices and visions of the individuals. Since the objective of this research was to gain an insight into how female students with disabilities interpret their lived experiences, phenomenological approach was judged to be the most appropriate research design (Smith, Flower, & Larkin, 2009). Phenomenological approach is data driven and so provided an opportunity for participants to explore and make sense of their own experiences (Reid, Flowers, & Larkin, 2005) and also gave them a voice (Murray & Harrison, 2004; Reynolds & Prior, 2003).
Research Settings
This study was carried out at three university college campuses in Gaborone. Two (UCA and UCC) are public institutions while the third (UCD) is privately owned. UCA and UCC offer both part-time and full-time undergraduate and graduate courses. UCD offers only undergraduate courses.
UCA is a large public HEI that offers programmes in various academic disciplines such as Social Sciences, Business, Science and Engineering. Its student enrolment is close to 15,000. The campus has well-established Disability Support Services catering to 90 students with various disabilities.
UCC is the oldest public HEI offering specialised programmes in Agriculture, such as Mechanisation, Soil Science, Economics, Crop Science and Veterinary Science. This institution has enrolled approximately 2,000 students. Support services for students with disabilities here were relatively new and coordinated by the Student Affairs office. In total, UCC had registered less than five students with disabilities.
UCD is a privately owned institution that offers programmes in Business Management with a total student enrolment of 4,000. Like UCC, UCD had a limited number of students with disabilities (10 in all, mostly with visual impairments). The student support services office was in the initial stages of disability-service delivery.
Only these three HEIs enrolled students with disabilities and had facilities in place for them. Hence these campuses were the research sites for the study.
Participants
The study applied the purposive sampling approach for locating information-rich key informants, the process beginning with questioning well-situated people (Smith et al., 2009). The first author of this research is Manager, Disability Support Services, at one of the three institutions of HE selected for the study, and works very closely with the students with disabilities and had prior knowledge about female students with disabilities. Seven female students with disabilities voluntarily participated in the study (see Table 1). While selecting the participants, the researchers firstly obtained permission from the Institutional Review Board of the institution; and secondly, the researchers contacted the participants by telephone to make personal appointments. The researchers explained the nature and purpose of the study and maintained anonymity and data confidentiality. This process helped the researcher build relationships with the participants of the study (Chilisa & Preece, 2005).
Participant’s Characteristics
Data-collection Instruments and Procedure
Focus Group Discussions
A semi-structured interview guide was used to collect data for the study. The focus group interview was conducted to capture the general experiences or ‘typical challenges’ of female students with disabilities. The interview guide focused on themes such as access and participation, instructional delivery, socio-cultural beliefs and issues of relationships. All interviews were audio recorded and later transcribed for analysis.
Photovoice
Photovoice is a social science method that emphasises social justice. It is commonly used to give voice to disempowered people, such as the homeless, children, HIV/AIDS patients and women, as it has the potential to illustrate and exhibit the daily realities (Darbyshire, MacDougall, & Schiller, 2005) which the eyes social scientists cannot reach (Packard, 2008). In this research, photovoice provided an opportunity to the participants to portray their struggle and gave meaning to and interpreted the images (Agarwal, Moya, Yasui, & Seymour, 2015).
Before collecting data, researchers organised two training sessions on data capturing. Specific issues were discussed during photovoice training workshops, such as ethics, power, camera use and the potential risks and overcoming them (Wang, 1999; Wang, Yi, Tao, & Carovano, 1998). The researchers gave disposable cameras to the participants and asked them to document their life experiences in HE for a period of two weeks. Thereafter, participants went into a group discussion session. The purpose of the discussion was to critically reflect upon their experiences using visual narratives. To guide them in reflecting critically on their stance regarding their collection of pictures were the following questions: What do you see here? What is really happening here? How does this relate to your life? Why does this problem exist? What can we do about this? By engaging in critical reflection, the participants tried to make sense of the photos that they had taken of their day-to-day academic and social life. In doing so participants become advocates for change in their own lives (Wang, 1999).
Solicited Diaries
In addition, researchers gathered substantial data from solicited diaries on the academic and social experiences of students with disabilities in Botswana’s HEIs over a period of two weeks. Bijoux and Myers (2006) describe these narrative tools as ‘an account produced specifically at the researcher’s request by an informant or informants and are written with the full knowledge that the text will be used for research purposes’. The researchers provided general guidelines to the participants for areas to explore in their everyday life, but what they included was up to the participants. In this way, participants diarised and gave meaning to their daily experiences, emotions and the events that characterised their lives in the social context of HE (Bijoux & Myers, 2006; Jacelon & Imperio, 2005).
Data Analysis
Data gathered through three processes were transcribed and then de-identified; following the transcription of the primary data (focus group interview), they were imported into ATLAS.ti 7.5 together with secondary data (pictures generated through photovoice and solicited diaries). Data were de-identified and pseudonym were used. Researchers read all the data numerous times and analysed them to identify recurring patterns and themes (Frankena, Naaldenberg, Cardol, Linehan, & van Schrojenstein Lantman-de Valk, 2015). A list of codes was developed and the initial phase yielded 12 families (codes) that were merged into four major themes. The next section discusses these themes in detail.
Findings
Socio-cultural Beliefs and Disability Identity
The study concluded that disability is deeply rooted within the social–cultural fabric of the society and it influences the experiences of female students with disabilities. In the context of HE, disability influences policies, shapes access and participation of this group of students in curricular as well as co-curricular activities. Socio-cultural beliefs influence the broader social context of HE and influence peers and faculty–student social relations. The dynamics of how this intra-relationship occurs can best be understood under three sub-themes: body image, self-acceptance and peer acceptance.
Body Image and Disability
Data seem to position the social relations of female students with disabilities as overlapping other cultural contextual issues as well as psycho-medical traits. The female body in the case of students with mobility limitations appeared to arouse curiosity as a spectacle in the context of cultural expectations of femininity. Unlike Bonani, a female student with mobility limitations, Chedza had resorted to being ‘a disappearing body’ by avoiding spaces that were likely to expose her body deviance as defined by cultural norms.
One interesting commonality between the body images of Bonani and Chedza was the urge to strive towards cultural expectations regarding the female body and its functions. The issue of body image and social relations seemed to be common among female students with mobility limitations, but not so among their male counterparts. It could be deduced from this that the body of a female student with mobility limitations is a site of struggle in the realm of social relations. Our study revealed that gender, disability and socio-cultural factors interact to influence the social relations of this group of students enrolled at Botswana’s HEIs. What appeared to be a ‘kind gesture’ of male students without disabilities to push them in a wheelchair was social attraction to a body that symbolised ‘asexual notions’ that was masked by an act of kindness. It was this body spectacle that male students wanted to explore, its construct and the asexual cultural conformity to cultural idealised expectations and norms of the body of a female person. Its conformity lay in female sexual and reproductive expectations of an ideal female body. Bonani said she found herself under pressure of conform to manage tensions that interfered with appearance expectations. This clearly reveals her effort to conform to the set cultural expectations of the dominant group. In sharp contrast to her earlier beliefs, the pressure to conform led Bonani to surrender power to her male peers, allowing them to push her in a manual wheelchair, though this was something that she had always resisted as undermining her confidence and self-esteem.
Self-acceptance and Disability
Self-acceptance is a personal perception of one’s own value; it is a multi-dimensional concept and influenced by the social context. Participants in the study were preoccupied by thoughts about themselves. Chiyapo, for example, described having had an extremely negative body image, but that slowly changed as she learnt to accept herself:
As deformed body [nervous laughter], and it’s and I’m not like others and that … ah … that’s taken me a long time … to accept myself … kind of given up now …’cause when I was young, children used to make fun of me … now people give me that look … It does not bother me.
Una also described suffering from anxiety and depression, which likely explains some of her extremely negative body-image experiences. She stressed the importance of self-acceptance, saying:
No one! Absolutely no one other than you who can help you. My body changed from girl to woman, people look at you differently … I wonder, do they look at me sexually … I am sexually attractive … I love my body.
Peer Interaction and Disability
Participants described peer support in varied and rich metaphors to show how their peers enabled them to overcome nested exclusion and marginalisation in Botswana’s HEIs. The success of students with disabilities in the complex processes of access and participation in curricular and co-curricular activities was to a large extent driven by peer support as social capital for these students. Bonani, who uses a wheelchair, provided an interesting foundation for peer interactions. She said:
People in this school are nice. I don’t know if it’s this 2016 thing, the just, compassionate and caring stuff. One thing I have noticed is that people like to be all chummy, chummy with me, especially guys. They would come to me and introduce themselves and start talking, about nothing really. Some are just so gentle; they step back and ask me to go first. Some, they even offer to buy for me, how cute? When it comes to social interaction it is very easy for me to connect with other fellow students.
On the issue of peer support, Mbaki (a student with cerebral palsy) expressed her views about peer support: ‘My schoolmates help me because most of my lecturers are failing. That’s how I keep moving forward’. Peer support extended to strategic lobbying for mainstream disability issues. Chedza noted:
With the help of other students and the lecturers, we were able to convince the academic department to change the location of the class. At least some people are starting to understand my needs as a student.
The findings indicate that positive student social relations were a product of the interplay of intrinsic factors (such as self-acceptance/self-awareness, self-motivation, social class and self-advocacy skills) and extrinsic factors (such as agency, attitudes of peers and availability of a disability support structure, which was unique to UCA). The study established that positive peer social relations at UCD were maintained by the long-established social capital of peers who had previously interacted with these students at high school.
Negative attitudes of mature students towards a fellow mature-age female student with mobility limitations were reported at UCA. This finding was context specific to UCA only, and demonstrated that agency for mature-age students with disabilities opened space to resist the social stigma imposed on them. Negative attitudes were not context specific to UCA only. At UCC, a female student with mobility limitations experienced negative attitudes from some sections of the student community because of the type and degree of her disability. Her body self-image seemed to make her uncomfortable, forcing her to be ‘disappearing body’ in some instances.
Structural Access and Participation of Female Students with Disabilities
Participants of the study explicitly narrated how spatiality interacted with female students with disabilities to shape their experiences in Botswana’s HEIs. Characteristically, students’ experiences resulted from their interaction with key spaces of student life in the setting of Botswana’s HEIs. It is important to underscore that structural access contributes to positive experiences as is evidenced by the independent access and participation in all activities taking place in these spaces. The positive experiences of students were a result of their interaction with spaces that were organised with ramps, double doors, sidewalks, ‘reserved parking’ areas and accessible buildings (lecture halls, halls of residence and student-services buildings) with lifts. Thus, these spaces were welcoming, and relayed the powerful and socially positive messages of ‘you belong here’ and ‘we value diversity’. From the students’ standpoint, these messages brought limitless social and academic experiences, leading to dignified participation in these institutions. Participants hailed the provision of these accessible spaces as a clear commitment to the creation of a barrier-free environment that widens access and enhances participation. The independent participation of students with disabilities in student-centred spaces mitigated the unequal power relations between students with and without disabilities. This was exemplified by innumerable instances in which access and participation were not negotiated through students without disabilities.
Notwithstanding these positive experiences, students equally narrated their negative experiences, where space was socially and culturally marked to maintain values of normalcy, thus creating social divisions between students with and without disabilities. The following excerpt illustrates the experiences of students with mobility limitations in academic spaces.
One has to worry where classes are, because not all the buildings in this school are wheelchair friendly. The other time the lift was not working and I was forced to miss class. … the laboratories are mostly upstairs computer labs, so I had to miss lots of classes, labs practice just because I couldn’t access it, and right now, yes, there are students willing to help me … there is no how they can help me, you know, carry me upstairs …
Structural barriers emerged as a major concern. Because of her physical disabilities, Chedza narrated her experience of structural barriers as follows: ‘… like the cafeteria. It is not easy to access if there is a queue as I am unable to queue using a wheelchair. So, I have to wait for someone to get food for me’. Structural barriers were also evident in lecture halls where Chedza attended her lessons during lesson observation.
This foregrounded the challenges students with mobility limitations contend within Botswana’s HEIs. Whereas their peers’ interaction with space was unaccompanied by worries about classroom design, for female students with mobility limitations it was a huge concern and adversely affected their ability to succeed in their studies. Students like Bonani devised student-initiated reasonable accommodations to address the ‘fit-in’ structural barriers that were pervasive in HEIs environments by identifying accessible space themselves. Repeatedly the pervasive nature of structural access was also brought up and further articulated during the photovoice workshop. Chiyapo, as a female with physical disabilities, succinctly captured the issue of structural barriers at UCA:
They are excluding us; I don’t even go there. They are upstairs; I have to see people go and get me this and that. I make people tired. I call the lecturer downstairs; it’s just a shadow consultation. Have to go through other people when I have a lecture; it’s a cumbersome experience. I don’t even bother.
Echoing similar sentiments, Bonani said:
Restrooms within the academic space have no provisions for students with disabilities. My dignity has been compromised and I have to ask people to pass quickly. New buildings have subtle exclusion tendencies such as heavy [difficult to operate] doors.
Another dimension of space that remained socio-culturally marked as a ‘no-go area’ for students with disabilities comprised the leisure and recreational facilities in all the three institutions. Koga, a student with visual impairment, summed up this issue by saying, ‘We don’t have resources that cater to leisure … despite having those university courts, we don’t have access to them because we don’t have the sporting facilities that cater to people with disabilities’.
The three sites were nested around the socio-spatial attributes of the dominant design principles of space. Inherently, these are spaces clearly designed for the ‘perfect’ and ‘normal’ body. For this study, students catalogued markers of social exclusion, such as the absence of ramps, double doors, sidewalks, spaces marked as ‘reserved parking’, accessible buildings (lecture halls, halls of residence and student-services buildings) with lifts. Instead, there were open trenches next to walkways and the wheelchair transfer and landing areas. These socially marked spaces of exclusion systematically marginalised students with mobility limitations and excluded them from participation in the wider activities of the institution. Space at institutions of HE was found to be constitutive of overt social dualities with regard to how students with mobility limitations would interact with it.
It is important to acknowledge that a few new buildings and the spaces around them at UCA had associations with accessibility features. Old buildings at UCA as well as the spaces around them were predominantly inaccessible as these buildings had staircases and the lifts were nonoperational for most of the time, and there were open trenches, either no ramps with rails or ramps that were too steep, a lack of adaptable toilets, and narrow doorways in the halls of residence. Interaction with these spaces rendered students with mobility limitations powerless and made them feel unwelcome in these areas. These were negative experiences for such students. In fact, they avoided these spaces, resulting in students with mobility limitations being viewed as ‘disappearing bodies’. The design features of these spaces seemed to be socially and culturally marked to sustain cultural values of ‘ideal perfect bodies’, which did not include the ‘imperfect bodies’ of students with disabilities.
Social divisions among students were evident in these spaces and those with mobility limitations were constantly reminded that they ‘don’t belong here’. They would need to navigate circuitous routes to access and interact with these spaces, which were illustrative of the fact that disability is spatially constructed. Missing lessons as a result of spaces designed on principles based on ‘ideal students’ was a recurring theme at UCA. Spatial design manifested the unequal power between students with disabilities and those that were able bodied, with the former’s constant struggle to access and participate in student activities occurring in these spaces. Unique to the context of UCA were concerns raised by students with visual impairments that centred on being marginalised as a result of structural barriers. Some students with mobility limitations, who were empowered, repeatedly rejected offers to be lifted while on wheelchairs to access these structures. Empowerment positioned them to resist power and formed agency to call for the creation of a barrierfree environment at HEIs, where independent and full participation in student-life activities is a value.
Empowerment of Female Students
When reflecting on empowerment during a focus group discussion with nuances of social justice, Mbaki, a female student with visual impairment, contended:
Like CCTV, where we can use it for reading … and also at the computer labs, there should be software that will help us use the computers just like other students, software that helps zoom in and be able to read your material.
To her, empowerment implies being helped and/or assisted by the other in order to succeed in studies. This understanding feeds into the deficit view of self and suggests that the student sees herself as having little control over her life. The findings demonstrate the extent to which students have internalised and conformed to the deficit view of disability. However, Mbaki’s understanding of empowerment was investing in assistive technology for students with disabilities to address the institutionalised marginalisation of such students and promoting their inclusion in Botswana’s HEIs. Her views on empowerment seemed to challenge institutional culture by advocating equity of opportunity. The scope of empowerment did not subsume critical areas such as knowledge about self, rights, effective communication, how to request for accommodations, or negotiation and leadership skills. Their views on access and participation appeared to be organically linked to these students’ inability to self-advocate or engage in a dialogue that could change institutional policies and practices. While students openly talked about self-motivation, this did not translate into confronting institutionalised marginalisation. It was this institutional culture and value system that seemed to compromise these students’ quality of experiences and success in studies.
Extending the concept of empowerment, Lukudzo, a female student with mobility limitation, narrated her story, which illustrated how she was empowered through her own agency and through the help of the disability office:
Since I joined the disability support group, the disability department has empowered me; now I know how to stand up for my rights. If someone tries to step on my toes, I’ll tell them, ‘No, not me.’
Data seemed to indicate that a good number of female students clearly demonstrated knowledge about their rights and self and could effectively communicate. This group of students would often self-advocate with faculty, requesting for reasonable accommodations. These self-advocates had developed such skills through agency, involvement in movements for persons with disabilities and their upper social status. The outcomes of their self-advocacy enabled them to self-advocate, to succeed in their studies, to access, participate and remain in their studies, and to develop a positive attitude towards learning. Commenting on the issue of empowerment, female students with visual impairments repeatedly referred to ‘being crushed’, ‘so crushed’ and ‘confidence flies out of the window’. This gendered way of viewing the self was highly prevalent among the younger female students with visual impairments compared to other categories such as mobility limitations. Despite the fact that some students knew their rights, it was difficult for them to start a dialogue that would help promote their inclusion in a HE, a space that seemed to be reserved for traditional students. This was because of the intersection of internal and external factors in social relations, namely power relations and the deficit view of the self. This rendered these students powerless to define themselves, hold effective dialogue with faculty about diversity, or request for reasonable accommodations and negotiate with faculty. All these factors crystallised into low self-esteem and maintained the deficit psycho-medical construction of a student with a disability.
Turning to the context of specific processes and student support structures at the three HEIs, there were no inherent empowerment reinforcement features for female students with disabilities to deal with issues of structural and systematic exclusion. Empowerment would enable these students to develop self-advocacy, increase their cultural capital, confront their marginalisation and demand change towards inclusivity.
Across all three settings students reported neither participation nor engagement in empowerment processes. Statements documented during one-on-one interviews, which were corroborated by data from solicited diaries, paint a picture of students who have not been empowered. Chedza, a female student with mobility limitations at UCC repeatedly used phrases such as ‘being shy’ to engage lecturers, and ‘Aah, I don’t bother anybody’. This illustrates that students were not empowered to deal with the intersection of issues and the structures that ostracise them.
In summary, the majority of the students with disabilities who participated in this study had entered HEIs without the cultural capital required to succeed in their studies. These students lacked self-advocacy skills to navigate their way through HE and experience success in their studies. Social class interacted with other socio-cultural factors to disadvantage students from the lower social classes. The three Botswana institutions of HE were not culturally sensitive to this class gap and did not address cultural aspects of non-traditional students. Very few female students with disabilities enter HEIs empowered with the cultural capital needed to successfully self-advocate and succeed in their studies.
Discussion
Although the number of female students with disabilities entering HE in Botswana is increasing (Moswela, 2016; Moswela & Mukhopadhyay, 2011), these students face barriers to accessing and participating in the curricular and co-curricular activities. This study identified three predominant barriers: (a) socio-cultural beliefs towards disability, (b) structural access and participation and (c) empowerment of female students.
Socio-cultural Beliefs About Disabilities
The findings of this research suggest that disability is a stigmatising phenomenon and its impact on female students with disabilities can be profound. The negative social–cultural beliefs cemented discrimination against these students. Oppressive socio-cultural beliefs marginalise female students in HE and force them to live with a double ‘minority’ status in the African context—being women as well as persons with disabilities. As a result, female students with disabilities are forced to embrace a negative identity (Evans-Lacko, Brohan, Moitaba, & Thorncroft, 2012; Halzenbuehler, Phelan, & Link, 2013) and body image. These negative images are further affected by powerful social expectations of specific physical size and shape; thus, disabled bodies are subjected to negative evaluation by the self and by others (Banks, 2014).
The SMD helped in comprehending the female students’ struggles against established norms in society. Stereotyped social norms perceived them as sick, helpless, incompetent and asexual—and as powerless. This could be attributed to the stigma and prejudices linked to ‘witchcraft’ in traditional African society. Female students with disabilities experienced stress related to social exclusion and other forms of victimisation. It is clear that disability discrimination persists not only in the university system but also in Botswana society as a whole, as what occurs in HEIs reflects the wider society. Findings of this study suggest that female students with disabilities frequently encounter the negative societal attitude that they are in ‘need of help’, which further devalues them in the society.
It is important to underscore that as African society is predominantly both ableist and patriarchal, ‘ableism’ and ‘sexism’ uniquely interact in its socio-cultural beliefs. Coincidentally, this did not greatly influence peer interaction in HE, which could be attributed to the inclusive primary and secondary education systems in Botswana. Students with physical disabilities are integrated in regular school; therefore, students without disabilities usually accept students with disabilities.
Structural Access and Participation
The interaction of disability and spatiality has a bearing on the academic and social experiences of female students with disabilities enrolled in Botswana’s HEIs. These students indicated both positive and negative experiences. Research (Fidzani, 2015; Goode, 2007; Hadjikakou, Polycarpou, & Hadjilja, 2010; Haihambo, 2010; Kenyon, 2011; Milic Babic & Dowling, 2015; Nkoane, 2006; Shevlin et al., 2004) has confirmed that physical access, particularly to restrooms, affects the experiences of female students with disabilities. Female students with disabilities complained of the restroom doors which compromised their privacy. This suggests that the physical spaces were created for people without disability and people with disabilities were mostly an ‘add-on’. The SMD theoretical framework as outlined in the first section of this article places emphasis on examining how social arrangements create barriers to participation by students with disabilities. This theoretical framework was the lens used to study the social arrangements and how space is constituted in Botswana’s HEIs to exclude female students with disabilities.
Empowerment of Female Students with Disabilities
In the current study, empowerment is equated with an individual’s sense of worth, knowledge about adequacy and self-respect. It was found that contextual factors play a critical role and influence the process of empowerment of female students with disabilities. As a result, female students with disabilities are not empowered and hardly have a voice. This could be attributed to the service–delivery models in these institutions. For example, HEIs provide ‘reasonable accommodations’ for students with disabilities (e.g., extending their assignments’ due dates as well as examination time) and adaptive technologies (such as recorders and Zoomtext). The provision of accommodations and adaptive technologies is built on the premise of creating a ‘level playing field’ for those with disabilities (Devlin & Pothier, 2006). The current service delivery operates from charity perspectives (depending mostly on external support), and female students with disabilities are not consulted.
Although Botswana HEIs have numerous student-support structures, these structures do not increase the variety of learning opportunities or related support that would reinforce the concept of self-determination and self-advocacy (Moswela, 2016). As a result, female students with disabilities are dependent on the system and unable to continue to create successes in their lives. Our study identified several contextual factors that limit the empowerment of female students with disabilities in Botswana HEIs, and include the lack of structure to empower students with disabilities, lack of self-advocacy skills, the negative attitude of lecturers, lack of negotiation skills in students, inadequate communication skills and low levels of self-confidence. These factors interplayed with the institutional power hierarchy that resides with faculty members to limit the opportunities of this group of students with disabilities from engaging in power-sensitive communication with the faculty to request for reasonable accommodations. The lack of empowerment of female students with disabilities retarded the transformation process of the power hierarchy in Botswana’s HEIs (Madriaga, 2007; Morrison, Sansosti, & Hadley, 2009). In order to address this issue, it is important to develop curricula that promote self-advocacy to build life skills that offer positive post-secondary experiences. The findings of this study bring to light deeply buried issues which have resulted in the marginalisation of female students with disabilities in their interaction with HE cultures. Academic culture reflects how society functions; inequalities in ‘cultural capital’ occur when there is limited responsiveness in educational systems. Seale (2013) defines cultural capital as ‘the possession of cultural competencies and knowledge that enable people to be cultural consumers in ways that are valued and expected in the society’. It would seem that female students with disabilities enter the enclave Botswana’s HEIs devoid of self-advocacy skills or the knowledge to succeed in HE; at the same time these institutions are unresponsive to the needs of female students with disabilities whose culture is inconsistent with the mainstream culture of the institutions. The lack of ‘cultural capital’ in female students with disabilities thus limited their access and participation in HE’s curricular and co-curricular activities. In addition, with no cultural capital and only limited self-advocacy skills female students with disabilities are rendered powerless to confront and question the dominant culture. Studies that are critical about this status quo have pressed HEIs to develop personal-development models to equip students with disabilities with a set of life skills that would empower these students to succeed in their courses as well as gain the skills for employability (Butterwick & Benjamin, 2006).
Conclusion and Recommendations
The findings of this research tend to suggest that the lack of institutional support challenges students with disabilities and compromise their experiences in HE (Brinckerhoff, McGuire, & Shaw, 2002; Getzel, Briel, & McManus, 2006; Gil, 2007). In addition, adjusting to a HE environment presents challenges for all students; however, the responsibility of managing their accommodations along with their academic course work is challenges unique to female students with disabilities. Often, students with disabilities enter HE unprepared to disclose their disability or without an understanding of how to access services on campus (Brinckerhoff et al., 2002; Getzel et al., 2006; Wagner, Newman, Cameto, Garza, & Levine, 2005). Students with disabilities must self-identify to the university to request reasonable accommodations and support. For varying reasons, some students do not self-disclose; these students, perhaps anxious for a ‘new beginning’ in an educational setting, may not want to deal with being labelled. Others may decide to delay disclosure until they experience academic problems (Getzel et al., 2006). In many instances, students were made to feel that they did not belong in HE. Females with disabilities found themselves in a double-jeopardy status socially constructed from being discriminated against for being women and for having a disability. It is taken for granted that students with disabilities are a homogenous group, that the needs of all students with disabilities are same, and that ‘females with disabilities’ do not exist.
This study revealed that access to and participation in HE for female students with disabilities in Botswana is limited by negative socio-cultural issues and the lack of support systems to empower this group. The findings are similar to those of studies done in southern Africa (Chataika, 2010; Howell, 2006; Howell & Lazarus, 2003; Matshedisho, 2007; Nkoane, 2006). The present research suggests that the university needs to be proactive when it comes to enhancing the access and participation of female students with disabilities in HE. In addition, intensifying disability-awareness initiatives for staff and students would further enhance the access and participation of female students with disabilities in HE. It is hoped that the findings of this study will give a direction for widening access and participation for these students. Female students with disabilities reported positive social relations in a space characterised by representation and practices free from stigma.
Declaration of Conflicting Interests
The authors declared no potential conflicts of interest with respect to the research, authorship and/or publication of this article.
Funding
The authors received no financial support for the research, authorship and/or publication of this article.
