Endometriosis
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I say yes, because that’s exactly what happened to me. I had onset of symptoms in middle school for all of my issues, and only migraines were acknowledged. None of the many symptoms of endo were even acknowledged for years, and I even had a few doctors lecture me about the fact that I was not in fact experiencing pain and that I should stop exaggerating.
Why is the the first question we’re asked, does it cause pain with sex? Like it’s the top priority, because then it becomes a man’s problem
I think so. After diagnosis and excision I asked my (now former ) doctor why doctors never ask patients to describe an average period. It would have quickly identified my endo 20 years before I was diagnosed. Her response? “Why would we ask? It’s subjective. That won’t tell anyone anything.”
Um… hospitals use subjective 1-10 pain scales for treatment constantly. Isn’t ALL pain and feeling itself subjective?