Getting diagnosed with endometriosis or adenomyosis isn’t just about medical tests—it’s an emotional rollercoaster filled with frustration, pain, and perseverance. In this episode, Sarah and Nicole share their deeply personal journeys—from years of being dismissed by doctors to finally getting answers.

We open up about the daily realities of living with these conditions—chronic pain, heavy periods, fertility struggles—and how they impact everything from relationships to mental health. We also talk about what kept us going, the importance of advocating for ourselves, and the incredible strength we’ve found in the community.

Beyond our stories, we explore why diagnosis takes 7-10 years for so many, how gaps in medical education leave patients in limbo, and what needs to change to ensure people get the care they deserve—sooner.

💡 Whether you're on your own journey, supporting a loved one, or just want to understand these conditions better, this episode is for you. You’re not alone—we’re in this together.