We argue that many of these issues would be alleviated by prioritizing microservices and access to modular data in smaller chunks or summarized form. Here, we argue that these difficulties are systemic and emerge from incentives that encourage development effort on self-sufficient platforms and data repositories instead of interoperable microservices. The global push to develop biomedical cloud platforms has led to new challenges, including platform lock-in, difficulty integrating across platforms, and duplicated effort for both users and developers. However, despite their advantages, cloud platforms in and of themselves do not automatically support FAIRness. Cloud computing holds great promise for addressing challenges with big data and ensuring reproducibility in biology. Findings will potentially benefit HIV researchers and care providers, those interested in the phenomenon of resilience, social researchers, thanatologists, grief counselors, and survivors of HIV, as well as people such as friends and family who are also impacted by HIV.The biomedical research community is investing heavily in biomedical cloud platforms. I believe the narrative of those with HIV, which may include the transformative dimensions of this experience, has the potential to benefit multiple fields of research and practice and to provide insight for those who provide care and support to HIV/AIDS patients. My personal experience with HIV and my subsequent journey from overwhelming fear and hopelessness to understanding, acceptance, and even appreciation for who I am today as a result of diagnosis compelled me to undertake this study in order to benefit others. However, a great deal of fear, misinformation, and stigmatization still exists, resulting in unnecessary suffering. HIV is now identified as a chronic rather than a terminal illness-or as the “death sentence” it once was thought to be. It was anticipated that this research would reveal personal as well as shared experiences relative to coming to terms with this unique psychological trauma. Themes illuminated the core inquiry, which explores the potential for positive or transformative experiences in the face of life threatening illness. Interviews were transcribed and common units of text, aligned with each of the interview queries, were identified and coded. Interviewees were invited to reflect on their experiences with and beliefs about HIV prior to diagnosis, their personal experience of receiving a diagnosis, and their social, emotional, and spiritual experiences following diagnosis. This study is a narrative analysis of the lived experiences of individuals diagnosed with human immunodeficiency virus (HIV). The purpose of this study is to explore the experiences of people coming to terms with HIV diagnosis and come to a greater understanding of the trajectory of adjustment and beyond.
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