Women's Healthcare: A Full Spectrum View

Introduction from Dr. LeRoy Robinson, Guest Editor of the Special Collection

Incorporating lived experiences into public health strategies can significantly amplify the effectiveness and inclusivity of health initiatives. While the advantages of utilizing these rich insights are considerable, this approach can present unique challenges for individuals invited to apply their personal experiences within a health intervention context. This presentation will spotlight three research initiatives that have demonstrated promising outcomes in enhancing the health of minority and marginalized populations through Community Health Workers. Additionally, it will tackle the challenges that must be addressed to protect and promote the health and well-being of Community Health Workers who harness their lived experiences to foster the health of their communities.

Reproductive health research in transgender health has grown exponentially over the past decade. Despite this, gaps still remain in addressing key patient questions and concerns. We will delve into the state of the research and opportunities to address gaps.

This talk delves into the significant disparities in infertility knowledge and outcomes among African American women, focusing on the impact of sexually transmitted infections (STIs) and tubal factor infertility. African American women experience disproportionately high rates of STIs, such as Gonorrhea and Chlamydia, which contribute to pelvic inflammatory disease (PID) and subsequent tubal damage. Despite these challenges, limited access to education, screening, and care exacerbates the problem. I will discuss the historical context, the contemporary landscape of tubal infertility, and the critical need for tailored educational initiatives and healthcare interventions to address these inequities and empower reproductive autonomy within this community.

Racial and gender disparities in autism spectrum disorder (ASD) diagnosis disproportionately affect Black and Brown women and LGBTQIA+ individuals, leading to delayed interventions and poorer long-term outcomes. This meta-analysis examines these groups' intersectional challenges, focusing on cultural biases, inadequate representation in diagnostic tools, and socioeconomic barriers to timely diagnosis. The project aims to propose modifications to the autism diagnostic process, enhancing fairness and accuracy for individuals of all races, genders, and sexual orientations. By synthesizing findings on diagnostic disparities and exploring policy frameworks, this study intends to improve healthcare equity. Researching autism diagnosis in marginalized populations is crucial for advancing social justice. Ultimately, this work paves the way for future research and policy changes to promote more inclusive and equitable diagnostic practices within the autism community.