In Tracey Lindeman’s new book BLEED: Destroying Myths and Misogyny in Endometriosis Care, Stephanie Lepage wonders how different her life could have been if only the doctors had bothered to look for endometriosis before her mid-30s. She had developed constant pain in her right lower abdomen that was so intense that rolling onto her side would shoot her out of a dead sleep on an almost nightly basis. When Lepage finally got in to see a gynecologist about it, that doctor said it was little more than a red herring. She remained in agony for two years without reprieve until it mysteriously subsided.
“The thing that stood out to me the most was like, unless I was trying to conceive, no one even cared about bleeding and pain.”