This essay explores endometriosis from a sociological perspective, with a focus on its impact on women in their everyday lives, work, and social contexts. Endometriosis, a condition affecting approximately 10 percent of women during their reproductive years, is a prevalent but incurable disease, with treatments only alleviating symptoms. Despite its prevalence, it remains relatively unknown to the general public, leading to lengthy diagnostic processes and a lack of understanding of the experiences of those affected. With this essay we want to shed light on how endometriosis affects women’s opportunities in the job market and private life, as well as its interaction with gender aspects within medical research and treatment. Through interviews and digital ethnography, we investigate how individuals with endometriosis experience interactions with healthcare providers, employers, and social relationships, as well as how the disease contributes to stigma and shame. The authors conclude that endometriosis significantly impacts women’s lives, both personally and professionally. The disease often leads to physical and emotional challenges that can limit their participation in the workforce and social activities. They emphasize the need for increased awareness and understanding of endometriosis, as well as improved healthcare strategies to support affected women. Further research is necessary to explore and address the unique challenges faced by women with endometriosis. Regarding future research, the thesis highlights the importance of continued investigation in this field to develop better treatment methods and support structures. This includes exploring the effects of endometriosis on women’s mental health, their ability to maintain employment, and how the disease affects their social relationships and overall quality of life.