22 years. That’s how long it took me to finally hear the words “you have endometriosis.” In that time, I was dismissed, misdiagnosed, gaslit, and left to figure it out on my own. If you’re newly diagnosed, still searching for answers, or feeling completely alone in your pain—this post is for you. These are the 6 things I wish someone had told me sooner. 💛 Let’s keep breaking the silence and stigma around invisible illness. You deserve real answers, real care, and real validation. 🎗️ If this resonates, share it with someone who needs to see it.