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Aim and objectives: To describe the FGM/C experiences of young women living in Nigeria. Background: Globally, several activities have been targeted at ending female genital mutilation/cutting (FGM/C). However, the practice is ongoing, especially in countries such as Nigeria, which is reported to be having a population boom. Therefore, there is a need to investigate the FGM/C experiences of young women in such countries so that efforts towards ending it can be accelerated using evidence-based, community-led interventions. Design: A qualitative descriptive design. Methods: The study took place in two states of southeastern Nigeria with a high prevalence of FGM/C. The snowball sampling method was used to recruit 22 women, aged 20-40, who had undergone FGM/C. Participant's experiences were explored through semi-structured interviews, and the qualitative content analysis was used for data analysis. The consolidated checklist for reporting of qualitative studies guided the reporting of this study. Findings: Three themes and seven subthemes emerged from the data. The themes were as follows: cultural issues, life as a circumcised woman and the future with FGM/C. Half of the participants could not recall their experiences on the day of their circumcision, as they were circumcised at infancy. However, those who were older when circumcised experienced it as a painful, traumatic experience forced upon them. Some of the participants experienced sexual and childbirth problems due to this procedure, and this was of great concern to them. Conclusion: Female genital mutilation/cutting was a traumatic experience forced on the participants. They felt helpless as they could not choose and had to do the "right thing." Despite the trauma and complications caused by the cutting, some still supported the continuation of the practice. Relevance to clinical practice: Understanding the experiences of genitally mutilated women could assist healthcare practitioners in rendering quality, and contextualised services to these women.

Background: Infant feeding is an integral part of the reproductive process with important implications for the health of mothers and their babies. However, various practices exist in different communities. It is therefore pertinent to know the infant feeding practices among rural dwellers, as well as the factors that influence them.Methods: This study was a cross sectional survey. A total of 372 volunteering parturient women were recruited using a multi-stage stratified sampling technique. Ethical approval and respondents’ informed consent was obtained. A self-developed and validated questionnaire was used to collect data. Descriptive and inferential statistics was used to analyse data.Results: Findings revealed that majority (84.4%) of the respondents were aware of exclusive breastfeeding (EBF), but only about half (50.5%) ever practiced exclusive breastfeeding. Also, a significant percentage of the respondents introduced complimentary feeding to the baby immediately after birth while 29.3% of participants reported drinking palm wine which is mainly alcoholic to stimulate breast milk secretion. Occupation of parturient women was associated with the practice of EBF (p=0.002).Conclusions: Almost half of our studied parturient women do not engage in EBF. There is need for health care workers to strategically educate parturient women and their significant others on the numerous benefits of exclusive breast feeding.

The aim of the review is to map the existing evidence regarding the data-sharing practices of health researchers in African countries. This review will also identify perceptions; barriers; facilitators; ethical-, legal-, and author-reported recommendations; as well as institutional-and funding-related aspects that are being considered by African health researchers on data sharing in Africa and, as a result, identify areas for development and improvement in health care on the continent. Introduction:The sharing of health-related data has been widely discussed in the literature. However, sharing health-related data has yet to become a common practice among health researchers in Africa, which bears a large burden of health diseases globally. The sharing of health research data could lead to greater development and improvement in health care in Africa.Inclusion criteria: This review will incorporate studies that report on data sharing among health researchers in Africa. All primary, secondary, and gray literature will be considered for inclusion. Studies on data sharing on topics other than health-related data will be excluded. No language restrictions will be applied. Methods:The JBI scoping review methodological framework will be adopted. An initial search of databases such as MEDLINE, Scopus, LILACS, and Web of Science will be conducted. All search results will be screened and relevant data extracted by two independent reviewers. The findings will be presented in the final scoping review report and illustrated in a Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for Scoping Reviews flow diagram.

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