Yesterday, I hosted my second annual Endometriosis March, and I am beyond grateful to everyone who came out, supported, and donated—your support means the world. 💛 Endometriosis affects 1 in 10 women worldwide, yet it remains underfunded, under-discussed, and misunderstood. My journey started in eighth grade when I was told my crippling pain was just “bad period cramps.” It took years of pushing through pain, countless dismissals, and a brutal surgery to finally get diagnosed with stage 4 endometriosis. This disease impacts every aspect of life—careers, relationships, and self-worth—but it doesn’t define me. It drives me. I share my story to show women and girls everywhere that you can live a life full of possibility, even with endo. I call it “normal-ish.” I work a full-time corporate career, own a business, and even went on reality TV. You can do anything—it just comes with good days and bad days. But I wouldn’t change a thing. Endo made me who I am today, and I am stronger for it...