Worthy Warriors, this one’s for you!
We know how exhausting it is to constantly explain endo—how it’s more than “just a bad period,” how it impacts EVERYTHING, how it feels to not be believed.
But here’s the thing: your. voice. matters. Your story could be the one that finally makes someone feel seen, understood, and less alone.
So, if you could tell the world one thing to help them truly understand endometriosis, what would it be? If you could tell the world how you are TRULY feeling - the words you always hold back - this is your chance.
This is your space to speak your truth. No pressure, no judgment—just your experience, shared in a way that feels right to you.
Speak Your Truth Here
Bowel Endo endometriosis is the worst. I have to get a MRI contrast this upcoming Wed. I am nervous. I know my symptoms in that area are worse l can’t eat much at one time. I have to use ducolax to get my poop to get through my intestines . I have a colonoscopy that showed no invasion in that area. It could be on the outside of my bowel.
I know that sometimes Endo patients develop ulcerative colitis. I hope that’s not it because l don’t need another health problem
That sounds incredibly tough, I’m really sorry you’re going through this. The uncertainty and tests are so stressful. I hope it’s not ulcerative colitis and that you get some answers soon. You’re not alone in this. Your community is here if you need to talk.
Yeah l have heard ulcerative colitis can be with emdometrios. So much pain l can’t think of type. I’m sure you been there