2.1. Motherhood and the Responsibility of Caregiving of Children with Intellectual Disabilities
Intellectual disability is a developmental disease that manifests throughout the formative years as substantial limitations in cognitive functioning and adaptive behavior (American Association on Intellectual and Developmental Disabilities [
7]). Individuals with intellectual disabilities often face challenges with communication, social skills, and daily living skills in addition to having difficulties with learning, thinking, and problem-solving skills (Centers for Disease Control and Prevention [
19]). Intellectual disability is a complex disorder with various degrees of severity and underlying causes. Genetic abnormalities, brain injury, and metabolic disorders are the most common causes of intellectual disability [
20]. Autism spectrum disorder, attention deficit hyperactivity disorder, and epilepsy are all conditions associated with intellectual disability [
19]. Individuals with intellectual disabilities are affected throughout their lives, and this can have a significant impact on their education, career, and social participation.
Motherhood is an important part of many women’s lives, including through their variety of responsibilities such as providing emotional and physical care, nurturing, and guiding their children [
13,
15,
21]. Mothers who are caregivers of children with disabilities may have more complex and numerous caregiving responsibilities, such as providing specialized care, advocating for their children’s needs, and coordinating multiple services and lines of support [
22]. Mothers of disabled children frequently shoulder a disproportionate number of caregiving tasks and may experience substantial difficulty in balancing these responsibilities with their own needs and other life demands, such as work [
11]. Therefore, caregivers’ physical and mental health, social relationships, and overall well-being can all suffer as a result of the responsibilities of caregiving [
23]. The impact of caregiving on mothers of disabled children can potentially affect their employment opportunities and outcomes [
24]. Mothers may experience job difficulties due to the need to provide care, a lack of access to flexible work arrangements, and workplace prejudice or stigma [
18]. These obstacles can lead to decreased employment rates, lower incomes, and financial insecurity [
25]. Despite these obstacles, many mothers of disabled children continue to work, either out of necessity or by choice. They may, however, require additional assistance and accommodation in order to reconcile their caregiving responsibilities with their employment responsibilities. Flexible work arrangements, access to leave, and workplace policies that encourage inclusivity and understanding are examples of such assistance [
11,
26].
Mothers of children with intellectual disabilities are more likely to face workplace harassment and stigma, and they are frequently excluded from job prospects and professional advancement [
21,
27]. They also encounter challenges in obtaining flexible work arrangements, paid leave, and inexpensive childcare, which can influence their work–life balance and general well-being [
4,
28]. On the other hand, several studies have found that mothers of children with intellectual disabilities are extremely motivated to work and resilient in overcoming career restrictions [
29,
30]. It should be noted that mothers of children with intellectual disabilities reported higher levels of job satisfaction when they had access to flexible work arrangements, supportive supervisors, and inclusive workplace environments [
31]. Another study indicated that mothers who engaged in peer support groups had higher work satisfaction and better mental health [
32]. Previous studies have highlighted the demand for broader policies and strategies to support mothers who look after their children with intellectual disabilities in finding work. For example, [
29] indicated that mothers who had access to cheap daycare were more successful in managing their caregiving and job duties. For mothers with disabled children, their work experience isn't always clearly recognized, as evidenced [
6]. [
3] focused on the experiences of women who had children with intellectual disabilities. The author used interpretive phenomenological analysis in a qualitative study to investigate the experiences of these mothers. The study allowed in-depth assessment of mothers’ experiences, and the results show that the mothers experienced a variety of feelings, including love, joy, and fulfillment, as well as stress, guilt, and anxiety. The author also discovered that these mothers faced several problems, such as navigating complex care systems, dealing with societal stigma, and balancing the demands of their children and family.
In the context of Saudi Arabia, a handful of studies have been conducted on this topic. For example, [
33] interviewed 84 parents of autistic children to assess their quality of life. They found that this was lower for those families of children with autism than those of neurotypical children or children with other disabilities. In addition, [
15] studied the effect of having a disabled child on the quality of life of Saudi women. The findings revealed that having a disabled child had a detrimental impact on the mothers’ quality of life. The study suggested that greater support services be provided to mothers of disabled children in Saudi Arabia in order to improve their quality of life. Many mothers who care for individuals with disabilities have indicated that they face extreme fatigue and burnout to the extent that working outside the home becomes nearly impossible. They also pointed out that the healthcare services their children need often require them to attend appointments that are typically scheduled during regular work hours [
34] (p. 165). As a result, many mothers of children with disabilities either leave their jobs, seek positions below their actual qualifications, decline promotions due to additional responsibilities conflicting with their caregiving duties for their disabled children, or opt to transition from full-time to part-time positions to achieve a balance between caregiving and providing financial support [
34]. Research has indicated that several factors influence how mothers of children with disabilities navigate the work environment and whether they are capable of engaging in paid employment. These factors include the level of care required by the child’s disability, the type of disability, the mother’s health, the support she receives from extended family, and the availability and quality of childcare services [
34]. Despite the challenges they face, some mothers choose to continue working, for various reasons, and succeed in their endeavors. However, others struggle to strike a balance between the demands of their job and fitting into the work environment. This, in turn, leads to feelings of isolation, self-esteem issues, and a sense of reduced accomplishment, especially for those with higher educational qualifications [
35]. Moreover, those who engage in paid employment highly value their positions and report that their working life affords them the opportunity to shape their sense of self, distinct from that associated with their roles as mothers [
35]. Some working mothers of children with disabilities perceive that employment provides them with a temporary respite from family worries and caregiving responsibilities. It also offers a sense of independence and an opportunity for engagement and conversation with others in addition to utilizing their skills and abilities to a greater extent [
36]. Despite these advantages that employment brings to working mothers, some may feel guilty due to the perception that engaging in paid work is a self-indulgent act [
36]. Consequently, some may face pressure to leave their jobs due to societal constraints that confine mothers to the primary caregiving role for their child, or they may struggle to balance the demands of work and the demands of caregiving for their child with a disability [
6]. This balance is often not fair, especially in the absence of adequate support and the fragility of the systems that protect mothers of children with disabilities in developing societies [
11].
Through reviewing the published research on the experiences of mothers of children with disabilities in the Kingdom of Saudi Arabia, it is observed that some of these studies relied on surveys to gather their experiences. This approach deprives the mothers of the opportunity to express their experiences more clearly and overlooks the psychological reality and human experience of these mothers. Furthermore, the qualitative study undertaken centered on on the mother’s experience of caring for the child, with an emphasis on the services provided for the disability, while neglecting the personal challenges, social obstacles, and psychological barriers that these mothers faced. Additionally, there was little attention given to the challenges of the work environment that these mothers encountered.
2.2. Work–Life Balance
According to [
37], work–life balance (WLB) refers to the fact that having rewarding experiences in some aspects of life influences a range of resources, such as energy, time, and dedication, and that these resources are scattered throughout all areas. WLB research began in the 1960s, with a number of studies concentrating on working mothers and families with multiple incomes due to day-to-day engagement. A growing number of women are entering the labor force [
38]. Different theories of WLB have been proposed at the theoretical level, including segmentation theory, overflow theory, compensation theory, enrichment theory, facilitation theory, and work–life conflict theory [
39]. Ref. [
40] developed the conflict theory, suggesting that elements of work and life are inherently distinct, and both vie for an individual's focus because of the time and effort required. And that the two struggle for an individual’s attention due to the effort and time needed. Many human resource practitioners began to see work–life balance as a “business issue” in the late 1980s, and firms at all levels realized that spending resources on WLB is in the greater interest of the corporation and its workers [
41]. Although work–life balance was originally considered a minor issue, it has grown in importance in recent years because it influences everyone, whether positively or negatively. Both work and family life are crucial aspects of living.[
42]. WLB is now acknowledged as a critical management problem for both businesses and employees. Many WLB issues (including stress, absenteeism, employee retention, bad health, and morale) can be attributed to unsuitable WLB management [
43]. A range of complementing variables, including equality, job security, labor market flexibility, and affordability, have been added to the present policy mix in the field of work–life balance [
44]. Concerning practices, like in many Arab nations, there are signs that Saudi Arabia's Work-Life Balance (WLB) practices to aid parents of disabled children in the workplace are inadequate. [45,46].
2.3. Work–Family Fit in the Context of Disability
The challenges faced by parents of children with disabilities in balancing work and family responsibilities have garnered significant attention in the literature, such as the paper by [
47]. They argued that, while many organizations have introduced family-friendly policies, these policies often do not meet the needs of parents of disabled children. Moreover, [
48] refer to the challenges and opportunities faced by families that have one or more children with autism spectrum disorder in the workplace that have not been investigated in depth. Their qualitative study provides evidence of how the family domain can greatly impact experiences and decisions made in the work domain for families with special needs. Therefore, organizations need to provide flexible work arrangements, such as telecommuting and flextime, as well as on-site childcare and respite care. It is also necessary to provide training for managers and colleagues on how to support parents of children with ASD. Ref. [
49] also examine the work–family fit for parents of children with emotional and behavioral disorders (EBD). They conducted focus groups with 41 employed parents of children with EBD to gain insights into the challenges they face in balancing work and family responsibilities. The authors argue that these challenges can have a significant impact on the parents’ mental and physical health as well as their work performance. They also argue that these challenges can lead to financial strain, as parents may have to take on additional childcare expenses or reduce their work hours. In addition, [
28] assert that parents of individuals with disabilities encounter similar challenges.
Other work-related issues may accrue through daily interaction with work colleagues, and feelings of workplace stigma and shame may present [
27], which refer to the workplace stigma the parents face when they choose to disclose their family member’s special needs and care demands to obtain support. Moreover, [
5] discuss the challenges that parents face in maintaining employment while caring for a child with a chronic illness. Also presented in the findings were the negative impact of these parents’ caring responsibilities on their work life and the increased stress they experience trying to maintain full-time employment. In addition, [
50] examines the impact of family care responsibilities on employment. The author concludes that family care responsibilities can have a significant impact on employment. Additionally, [
51] investigated the impact of child disability on parental employment and labor income in Norway, with the results showing that caring for children with disabilities has a negative effect on mothers’ labor market participation, working hours, and labor income. The employment effect is more pronounced among mothers of children with more severe disabilities. Although their labor income is lower, the employment probabilities and working hours of fathers of children with more severe disabilities remain consistent in the after-birth period. The authors deduce that providing care for children with disabilities significantly affects parental employment and labor income. This effect is more noticeable for mothers compared to fathers.Ref. [
13] investigated the experiences of mothers caring for children with disabilities in Canada. The author found that the challenges they face significantly impact their mental and physical health, as well as their work performance. This can lead to financial strain, as they may have to meet additional childcare expenses or reduce their work hours. The author also stated that these mothers are normally invisible in society, which means their struggles and experiences are overlooked and not taken seriously. As part of the shifting of gender roles, in masculine cultures such as most Arab cultures, the responsibilities of caregiving for children in general, and the disabled in particular, fall more on the mothers’ shoulders [
1,
52]. This causes mothers to be more influenced by the disability than fathers. Ref. [
53] examines the role of gender in caring for a child with a disability. Their results show that caring for a child with a disability is a complex position that has at least three meanings: (1) Caring for, which refers to the caregiving work that is involved in raising a child with a disability. This work can be physically and emotionally stressful, and it can take up a great amount of time. (2) Caring about, which refers to the love and care that mothers feel for their children with disabilities. This love is often unconditional, and it can be a source of great strength for mothers. (3) The extended caring role, which refers to the ways in which mothers of children with disabilities extend their caring to broader societal fear and anxiety. This can include advocacy work, fundraising, or even raising awareness about disability issues. In the families [
53] studied, mothers were the primary caregivers for their children with disabilities. Fathers, on the other hand, were more likely to be involved in financial and emotional support. These conventional gender expectations concerning the division of duties between parents might adversely affect mothers of children with disabilities. This caregiving role can lead to feelings of isolation, stress, and burnout, which can also make it difficult for mothers to access the support they need. The findings of [
53] are important because they challenge the traditional assumption that mothers are the only ones who can care for children with disabilities.
Moreover, [
25] examine the negative impact of work–family conflict on working mothers’ career development. They review a number of studies that found that work–family conflict can lead to a number of negative outcomes for working mothers. Therefore, they argue that work–family conflict is a complex issue that is caused by a number of factors, including the increasing number of women in the workforce, the traditional gender roles that still exist in many societies, the lack of workplace flexibility, and support for working parents. In Saudi Arabia, [
16] investigated Saudi mothers living with a child with cerebral palsy (CP) and their perceptions of disability. The study concluded that the mothers’ perceptions of disability were influenced by different factors, including their cultural beliefs, their religious beliefs, and their personal experiences. They also concluded that the mothers’ perceptions of disability had a significant impact on their lives. Their study findings facilitate understanding of the influence of the cultural context in which a person lives and how it impacts perceptions of disability. The study highlights the need for policymakers and service providers to be sensitive to the cultural context when developing policies and services for people with disabilities. In addition, [
15] provide a comprehensive overview of the quality of life, needs, and fears of mothers of children with disabilities in Saudi Arabia during the COVID-19 lockdown. Their findings show that mothers of children with disabilities experienced a significant decline in quality of life during the COVID-19 lockdown.