Methods:Data came from an NIMH-funded ethnographic study on family, sociocultural resources, and strengths of Mexican immigrant clients with SMI and their key family members. Twelve in-depth semi structured interviews were conducted and transcribed. The sample consisted of seven clients and five family members. Transcripts were analyzed using template analysis methods. After developing predetermined codes based on intersectionality theory, a code template was developed and updated as more themes emerged from the qualitative data.
Results:Analysis revealed four thematic domains in which perceptions of relationships were most salient: (1) experiences and perceptions of marriage (e.g., “My husband was bothered that my mother [with SMI] was not doing anything”); (2) experiences and perceptions of other relationships such as parenting (e.g., “Since I had my son I always told myself, how can a mother leave her children?”); (3) a sense of being alone and loneliness (e.g., “I know I have to take care of myself so that I don’t lose my mind again. Because now I am alone”); and (4) perceptions of gender normative roles (e.g., “There’s washing and ironing and making tortillas. … A woman doesn’t rest”).
Implications:Results indicate that clients and key family members have varying perceptions of marriage and other personal relationships that depend on their role of as a caregiver or client; however, for both types of participants, relational conflicts emerged as a consequence of the client’s illness. Several participants expressed an inability to maintain romantic relationships or avoid relationship conflict due to the responsibility of caring for a family member with SMI and a lack of support or understanding from their spouse or other significant family members. These findings underscore the importance of addressing personal relationships in assessment and treatment services for Latinos with SMI and family members. There is also a need for more purposeful involvement of not only key family members but also other family members such as partners or spouses of those with the illness and family caregivers.