Publications by authors named "Lauren F Cardoso"

Endometriosis is a debilitating and highly stigmatized chronic condition. The relationship between stigma and depressive symptoms among college-attending women with endometriosis symptoms was examined. Data were analyzed from a cross-sectional online survey of undergraduate women (N = 424).

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To describe how an innovative, community-engaged survey illuminated previously unmeasured pandemic inequities and informed health equity investments. The methodological approach of Massachusetts' COVID-19 Community Impact Survey, a cross-sectional online survey, was driven by key health equity principles: prioritizing community engagement, gathering granular and intersectional data, capturing root causes, elevating community voices, expediting analysis for timeliness, and creating data-to-action pathways. Data collection was deployed statewide in 11 languages from 2020 to 2021.

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Background: The purpose of this study is to examine the frequency of "period poverty," or not being able to afford sanitary products, among university students, and associations with poor mental health.

Methods: An online survey was conducted with a nationally-drawn sample (N = 471) of college-attending women to assess the association between period poverty and depression. Period poverty was measured via two questions designed for this study; depression was measured with the standard PHQ-9.

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Article Synopsis
  • Endometriosis is a condition affecting around 10% of women globally, but there's limited awareness and knowledge of it in low- and middle-income countries.
  • A study analyzed data from low-income women in Mexico City who experienced intimate partner violence, revealing that over half reported symptoms suggestive of endometriosis, while only 12.5% had ever heard of the condition.
  • The findings emphasize the need for better education about endometriosis as part of global reproductive health initiatives, especially since awareness is low even among women experiencing pain-related symptoms.
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Introduction: Women living with disabilities are disproportionately vulnerable to intimate partner violence (IPV). Existing research on the topic largely takes place in high-income settings and treats disability as a dichotomous experience-an individual either has a disability or does not. Disability experiences, however, are diverse such that some individuals face minimal impairment, while for others impairment can be severe.

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Introduction: Emerging research has linked women's sanitation and menstrual hygiene experiences with increased vulnerability to violence outside the home. Few studies, however, have investigated the relationship between menstruation and violence perpetrated by family members. This type of violence may be linked specifically to restrictions placed on women during menstruation, which are common in some regions of Nepal owing to shared power differentials that disfavour women, and societal norms that stigmatise menstruation.

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Objective: Symptoms of endometriosis, including pelvic pain, back and nerve pain, and gastrointestinal pain, often begin in adolescence. Yet, research on the experience of these debilitating symptoms among young people is scarce. Of particular concern is the influence of adolescent girls' social context.

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Objectives: To examine the relationship between household ownership of information and communication technologies (ICTs) and justifications for wife beating.

Methods: Women aged 15 to 49 years in 20 countries were surveyed via UNICEF's Multiple Indicator Cluster Surveys between 2006 and 2014. Multivariate logistic regressions accounted for individual-, household-, and structural-level variables.

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Background: Men and women's perceptions of intimate partner violence (IPV) within crisis-affected populations are not well understood. This mixed-methods study examined the frequency of IPV against women in urban Cote d'Ivoire, and qualitatively explored how men and women perceive the impact of various forms of IPV on health, everyday activities, and feelings of shame.

Methods: A survey was administered to Ivorian women (N = 80) to measure the frequency of IPV, and ten focus group discussions were conducted with women (n = 46) and men (n = 45) to explore perceptions of different forms of IPV, including its impacts on disruptions to health, everyday activities, and experiences of shame.

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