I’ve been seeing more and more people bring this up lately, and it really hit me how little it’s talked about. Yes, endo can stick around after menopause. Some of us are still dealing with flares, pain, fatigue, the whole thing… and for some, symptoms are just now showing up.
If this is something you’ve gone through (or are going through), I’d love to hear from you.
Like… what’s helped? What’s made it harder? Did your doctors actually listen? Or act like it wasn’t possible?
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