March is Endometriosis Awareness Month, and while it’s encouraging to see more conversations happening about diagnosis delays and wait times, the reality of living with endometriosis goes far beyond that.

In this short episode, I’m sharing some reflections on the parts of endometriosis that still don’t get talked about enough — the daily impact, the emotional toll, and the invisible experiences behind the awareness campaigns.

Because awareness is important… but so is telling the whole story.

If you live with endometriosis, what’s something you wish people understood about it?

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